Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25861 |
| ensemblid | ENSG00000095397.17 |
| hgncid | 16361 |
| symbol | WHRN |
| name | whirlin |
| refseq_nuc | NM_015404.4 |
| refseq_prot | NP_056219.3 |
| ensembl_nuc | ENST00000362057.4 |
| ensembl_prot | ENSP00000354623.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 114402080 |
| end | 114505473 |
| strand | - |
| ver | v1.2 |
| region | chr9:114402080-114505473 |
| region5000 | chr9:114397080-114510473 |
| regionname0 | WHRN_chr9_114402080_114505473 |
| regionname5000 | WHRN_chr9_114397080_114510473 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 907 | 112 | 30 | 25 | 36 | 7 | 13 | 21 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0002 | 0/1 | 907 | 77 | 4 | 15 | 50 | 0 | 7 | 40 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0003 | 0/0 | 907 | 61 | 15 | 15 | 23 | 3 | 5 | 21 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0004 | 0/0 | 907 | 23 | 17 | 3 | 1 | 0 | 2 | 1 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0005 | 0/0 | 907 | 10 | 0 | 6 | 1 | 3 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0006 | 0/0 | 907 | 7 | 0 | 0 | 6 | 0 | 1 | 3 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0007 | 0/0 | 907 | 6 | 0 | 0 | 6 | 0 | 0 | 5 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0008 | 0/0 | 907 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0009 | 0/0 | 907 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0010 | 0/0 | 907 | 2 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0011 | 0/0 | 907 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0012 | 0/0 | 907 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0013 | 0/0 | 907 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0014 | 0/0 | 907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0015 | 0/0 | 907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0016 | 0/0 | 907 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0017 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0018 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0019 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0020 | 0/0 | 907 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0021 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0022 | 0/0 | 907 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0023 | 0/0 | 907 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0024 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| a0025 | 0/0 | 907 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | MNAPL others(902): Show |
chr9 | 114397080 | 114510473 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002 | 0/0 | 2721 | 53 | 8 | 8 | 27 | 2 | 8 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0006 | 1/0 | 2721 | 17 | 6 | 1 | 5 | 1 | 3 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0008 | 0/0 | 2721 | 12 | 8 | 1 | 3 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0009 | 0/0 | 2721 | 10 | 0 | 7 | 0 | 2 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0010 | 0/0 | 2721 | 10 | 5 | 2 | 0 | 2 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0012 | 0/0 | 2721 | 8 | 2 | 6 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0028 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0001c0040 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0002c0001 | 0/1 | 2721 | 53 | 0 | 12 | 35 | 0 | 5 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0002c0004 | 0/0 | 2721 | 23 | 4 | 3 | 15 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0002c0031 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0003c0003 | 0/0 | 2721 | 45 | 10 | 9 | 21 | 2 | 3 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0003c0007 | 0/0 | 2721 | 16 | 5 | 6 | 2 | 1 | 2 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0004c0005 | 0/0 | 2721 | 17 | 13 | 1 | 1 | 0 | 2 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0004c0018 | 0/0 | 2721 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0004c0019 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0004c0026 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0004c0042 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0005c0011 | 0/0 | 2721 | 9 | 0 | 5 | 1 | 3 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0005c0039 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0006c0013 | 0/0 | 2721 | 6 | 0 | 0 | 5 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0006c0027 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0007c0015 | 0/0 | 2721 | 5 | 0 | 0 | 5 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0007c0025 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0008c0016 | 0/0 | 2721 | 5 | 5 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0008c0030 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0009c0014 | 0/0 | 2721 | 5 | 0 | 5 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0010c0024 | 0/0 | 2721 | 2 | 1 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0011c0033 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0011c0034 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0012c0022 | 0/0 | 2721 | 2 | 1 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0013c0020 | 0/0 | 2721 | 2 | 0 | 0 | 2 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0014c0023 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0015c0021 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0016c0017 | 0/0 | 2721 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0017c0029 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0018c0032 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0019c0036 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0020c0043 | 0/0 | 2721 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0021c0038 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0022c0035 | 0/0 | 2721 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0023c0041 | 0/0 | 2721 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0024c0044 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 | ||
| a0025c0037 | 0/0 | 2721 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | ATGAA others(2716): Show |
chr9 | 114397080 | 114510473 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001 | 0/0 | 4070 | 49 | 5 | 7 | 27 | 2 | 8 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0002t0003 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0002t0004 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0002t0008 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0006t0001 | 1/0 | 4070 | 14 | 5 | 1 | 3 | 1 | 3 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0006t0003 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0006t0009 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0008t0002 | 0/0 | 4062 | 7 | 3 | 1 | 3 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0008t0007 | 0/0 | 4062 | 3 | 3 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0008t0010 | 0/0 | 4062 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0009t0002 | 0/0 | 4062 | 10 | 0 | 7 | 0 | 2 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0010t0001 | 0/0 | 4070 | 5 | 1 | 1 | 0 | 2 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0010t0003 | 0/0 | 4070 | 5 | 4 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0001c0012t0002 | 0/0 | 4062 | 8 | 2 | 6 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0028t0002 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0001c0040t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0002c0001t0001 | 0/1 | 4070 | 51 | 0 | 12 | 33 | 0 | 5 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0002c0001t0005 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0002c0001t0012 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0002c0004t0002 | 0/0 | 4062 | 23 | 4 | 3 | 15 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0002c0031t0002 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0003c0003t0001 | 0/0 | 4070 | 44 | 9 | 9 | 21 | 2 | 3 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0003c0003t0006 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0003c0007t0002 | 0/0 | 4062 | 14 | 5 | 5 | 2 | 1 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0003c0007t0011 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0003c0007t0013 | 0/0 | 4062 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0004c0005t0001 | 0/0 | 4070 | 12 | 9 | 0 | 1 | 0 | 2 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0005t0003 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0005t0004 | 0/0 | 4070 | 2 | 1 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0005t0006 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0018t0001 | 0/0 | 4070 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0019t0001 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0004c0026t0002 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0004c0042t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0005c0011t0001 | 0/0 | 4070 | 9 | 0 | 5 | 1 | 3 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0005c0039t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0006c0013t0001 | 0/0 | 4070 | 6 | 0 | 0 | 5 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0006c0027t0002 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0007c0015t0001 | 0/0 | 4070 | 5 | 0 | 0 | 5 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0007c0025t0002 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0008c0016t0001 | 0/0 | 4070 | 5 | 5 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0008c0030t0002 | 0/0 | 4062 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0009c0014t0005 | 0/0 | 4062 | 5 | 0 | 5 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0010c0024t0001 | 0/0 | 4070 | 2 | 1 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0011c0033t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0011c0034t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0012c0022t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0012c0022t0004 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0013c0020t0001 | 0/0 | 4070 | 2 | 0 | 0 | 2 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0014c0023t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0014c0023t0004 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0015c0021t0004 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0016c0017t0004 | 0/0 | 4070 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0017c0029t0002 | 0/0 | 4062 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0018c0032t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0019c0036t0001 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0020c0043t0001 | 0/0 | 4070 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0021c0038t0005 | 0/0 | 4062 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4057): Show |
chr9 | 114397080 | 114510473 |
| a0022c0035t0003 | 0/0 | 4070 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0023c0041t0001 | 0/0 | 4070 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0024c0044t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| a0025c0037t0001 | 0/0 | 4070 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | AGACT others(4065): Show |
chr9 | 114397080 | 114510473 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0004g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0008g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0002t0008g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0001g0209 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0009g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0006t0009g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0007g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0007g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0007g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0010g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0008t0010g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0009t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0010t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0012t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0028t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0001c0040t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0005g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0001t0012g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0004t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0002c0031t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0003t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0011g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0003c0007t0013g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0004g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0005t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0018t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0018t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0019t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0019t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0026t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0004c0042t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0011t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0005c0039t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0006c0027t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0015t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0015t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0015t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0015t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0015t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0007c0025t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0008c0016t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0008c0016t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0008c0016t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0008c0016t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0008c0030t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0009c0014t0005g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0009c0014t0005g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0009c0014t0005g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0009c0014t0005g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0009c0014t0005g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0010c0024t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0010c0024t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0011c0033t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0011c0034t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0012c0022t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0012c0022t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0013c0020t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0013c0020t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0014c0023t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0014c0023t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0015c0021t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0015c0021t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0016c0017t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0016c0017t0004g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0017c0029t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0018c0032t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0019c0036t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0020c0043t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0021c0038t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0022c0035t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0023c0041t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0024c0044t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| a0025c0037t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0010 | c0024 | t0001 | g0217 | EUR | GBR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00140 | hp2 | a0005 | c0011 | t0001 | g0007 | EUR | GBR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00280 | hp1 | a0001 | c0006 | t0001 | g0164 | EUR | FIN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0088 | EUR | FIN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00323 | hp1 | a0001 | c0010 | t0001 | g0111 | EUR | FIN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00323 | hp2 | a0001 | c0009 | t0002 | g0287 | EUR | FIN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00408 | hp1 | a0017 | c0029 | t0002 | g0306 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00408 | hp2 | a0007 | c0015 | t0001 | g0142 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00423 | hp1 | a0003 | c0003 | t0001 | g0187 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00423 | hp2 | a0011 | c0034 | t0001 | g0087 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00438 | hp1 | a0001 | c0008 | t0002 | g0303 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00544 | hp1 | a0006 | c0013 | t0001 | g0174 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00544 | hp2 | a0002 | c0001 | t0001 | g0168 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00558 | hp1 | a0018 | c0032 | t0001 | g0084 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00558 | hp2 | a0002 | c0001 | t0001 | g0029 | EAS | CHS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00642 | hp1 | a0005 | c0039 | t0001 | g0060 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00642 | hp2 | a0002 | c0001 | t0001 | g0114 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00733 | hp1 | a0002 | c0004 | t0002 | g0311 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00733 | hp2 | a0003 | c0007 | t0002 | g0270 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00738 | hp1 | a0003 | c0007 | t0011 | g0011 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00738 | hp2 | a0001 | c0009 | t0002 | g0260 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00741 | hp1 | a0004 | c0018 | t0001 | g0161 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG00741 | hp2 | a0005 | c0011 | t0001 | g0007 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01069 | hp1 | a0005 | c0011 | t0001 | g0081 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01069 | hp2 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01070 | hp1 | a0001 | c0002 | t0001 | g0202 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01070 | hp2 | a0001 | c0012 | t0002 | g0286 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0008 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01074 | hp1 | a0002 | c0001 | t0001 | g0055 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01074 | hp2 | a0004 | c0018 | t0001 | g0094 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01099 | hp1 | a0003 | c0003 | t0001 | g0093 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01099 | hp2 | a0001 | c0009 | t0002 | g0261 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0232 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01109 | hp2 | a0008 | c0030 | t0002 | g0292 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01167 | hp1 | a0002 | c0001 | t0001 | g0014 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0216 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0163 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01168 | hp2 | a0001 | c0012 | t0002 | g0278 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01169 | hp1 | a0002 | c0001 | t0001 | g0013 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01169 | hp2 | a0001 | c0012 | t0002 | g0010 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01175 | hp1 | a0003 | c0007 | t0002 | g0263 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0124 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01192 | hp2 | a0001 | c0010 | t0003 | g0223 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01243 | hp1 | a0004 | c0005 | t0004 | g0237 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01243 | hp2 | a0012 | c0022 | t0001 | g0213 | AMR | PUR | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01255 | hp1 | a0003 | c0007 | t0002 | g0254 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01255 | hp2 | a0009 | c0014 | t0005 | g0248 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01257 | hp1 | a0001 | c0009 | t0002 | g0280 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01257 | hp2 | a0009 | c0014 | t0005 | g0247 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01258 | hp1 | a0002 | c0004 | t0002 | g0312 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01258 | hp2 | a0001 | c0009 | t0002 | g0279 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01261 | hp1 | a0001 | c0009 | t0002 | g0256 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0120 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01358 | hp1 | a0001 | c0012 | t0002 | g0010 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01358 | hp2 | a0002 | c0001 | t0001 | g0017 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0134 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01433 | hp2 | a0009 | c0014 | t0005 | g0244 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0129 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01496 | hp2 | a0001 | c0006 | t0001 | g0067 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0183 | EUR | IBS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01516 | hp2 | a0001 | c0009 | t0002 | g0257 | EUR | IBS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0182 | EUR | IBS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01517 | hp2 | a0003 | c0003 | t0001 | g0162 | EUR | IBS | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01884 | hp1 | a0001 | c0010 | t0003 | g0224 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0228 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01891 | hp1 | a0001 | c0008 | t0002 | g0274 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01891 | hp2 | a0001 | c0010 | t0003 | g0226 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01934 | hp1 | a0001 | c0009 | t0002 | g0262 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01934 | hp2 | a0002 | c0001 | t0001 | g0097 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0099 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01943 | hp2 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01952 | hp1 | a0003 | c0007 | t0002 | g0251 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01952 | hp2 | a0002 | c0001 | t0001 | g0016 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01975 | hp1 | a0001 | c0009 | t0002 | g0294 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01975 | hp2 | a0009 | c0014 | t0005 | g0249 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01978 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01981 | hp1 | a0001 | c0010 | t0001 | g0096 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01981 | hp2 | a0001 | c0008 | t0002 | g0267 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01993 | hp1 | a0002 | c0001 | t0001 | g0002 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01993 | hp2 | a0003 | c0007 | t0002 | g0253 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02004 | hp1 | a0005 | c0011 | t0001 | g0086 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02004 | hp2 | a0001 | c0012 | t0002 | g0276 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02027 | hp2 | a0002 | c0001 | t0001 | g0035 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02040 | hp2 | a0001 | c0006 | t0009 | g0242 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02055 | hp1 | a0001 | c0012 | t0002 | g0277 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02055 | hp2 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02056 | hp1 | a0002 | c0001 | t0001 | g0033 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0022 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02080 | hp1 | a0001 | c0028 | t0002 | g0301 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02080 | hp2 | a0013 | c0020 | t0001 | g0139 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02083 | hp2 | a0002 | c0004 | t0002 | g0309 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0020 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02129 | hp2 | a0002 | c0004 | t0002 | g0313 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02132 | hp2 | a0002 | c0001 | t0001 | g0172 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02135 | hp1 | a0006 | c0013 | t0001 | g0153 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02135 | hp2 | a0002 | c0001 | t0001 | g0052 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02145 | hp1 | a0014 | c0023 | t0004 | g0233 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02145 | hp2 | a0004 | c0005 | t0001 | g0206 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02148 | hp1 | a0003 | c0003 | t0001 | g0175 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02148 | hp2 | a0009 | c0014 | t0005 | g0250 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02155 | hp1 | a0001 | c0006 | t0001 | g0173 | EAS | CDX | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02155 | hp2 | a0001 | c0008 | t0002 | g0258 | EAS | CDX | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02165 | hp1 | a0006 | c0027 | t0002 | g0310 | EAS | CDX | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02165 | hp2 | a0005 | c0011 | t0001 | g0065 | EAS | CDX | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02257 | hp1 | a0001 | c0006 | t0001 | g0193 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02257 | hp2 | a0001 | c0006 | t0001 | g0070 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02258 | hp1 | a0004 | c0026 | t0002 | g0273 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02258 | hp2 | a0019 | c0036 | t0001 | g0205 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02273 | hp1 | a0020 | c0043 | t0001 | g0100 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02273 | hp2 | a0002 | c0001 | t0001 | g0012 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02280 | hp1 | a0003 | c0007 | t0002 | g0314 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02280 | hp2 | a0001 | c0010 | t0001 | g0212 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02293 | hp1 | a0002 | c0004 | t0002 | g0307 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02293 | hp2 | a0005 | c0011 | t0001 | g0082 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02300 | hp1 | a0005 | c0011 | t0001 | g0135 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02300 | hp2 | a0002 | c0001 | t0001 | g0003 | AMR | PEL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02451 | hp1 | a0002 | c0004 | t0002 | g0291 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0192 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02523 | hp2 | a0002 | c0004 | t0002 | g0304 | EAS | KHV | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02572 | hp1 | a0004 | c0005 | t0001 | g0204 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02572 | hp2 | a0001 | c0006 | t0001 | g0072 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02615 | hp1 | a0001 | c0008 | t0007 | g0317 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02615 | hp2 | a0014 | c0023 | t0001 | g0089 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0078 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02622 | hp2 | a0015 | c0021 | t0004 | g0231 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02698 | hp1 | a0011 | c0033 | t0001 | g0085 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02735 | hp1 | a0002 | c0001 | t0001 | g0031 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02735 | hp2 | a0001 | c0009 | t0002 | g0269 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02738 | hp1 | a0001 | c0006 | t0001 | g0018 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0132 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02809 | hp1 | a0001 | c0006 | t0003 | g0225 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02809 | hp2 | a0003 | c0007 | t0002 | g0264 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02818 | hp1 | a0004 | c0042 | t0001 | g0063 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02818 | hp2 | a0003 | c0007 | t0002 | g0266 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02886 | hp1 | a0001 | c0008 | t0010 | g0252 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02895 | hp1 | a0004 | c0005 | t0006 | g0239 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02895 | hp2 | a0016 | c0017 | t0004 | g0235 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02896 | hp1 | a0002 | c0004 | t0002 | g0289 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0059 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02897 | hp1 | a0016 | c0017 | t0004 | g0236 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02897 | hp2 | a0002 | c0004 | t0002 | g0290 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02965 | hp1 | a0001 | c0008 | t0007 | g0318 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02965 | hp2 | a0003 | c0003 | t0001 | g0200 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02970 | hp1 | a0002 | c0004 | t0002 | g0283 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02970 | hp2 | a0021 | c0038 | t0005 | g0245 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03017 | hp1 | a0002 | c0001 | t0001 | g0040 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03041 | hp1 | a0008 | c0016 | t0001 | g0194 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03041 | hp2 | a0003 | c0007 | t0002 | g0315 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03098 | hp1 | a0004 | c0005 | t0001 | g0215 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0199 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03130 | hp1 | a0008 | c0016 | t0001 | g0198 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03130 | hp2 | a0015 | c0021 | t0004 | g0229 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03139 | hp1 | a0004 | c0005 | t0001 | g0006 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03139 | hp2 | a0022 | c0035 | t0003 | g0221 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03195 | hp1 | a0001 | c0010 | t0003 | g0222 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03195 | hp2 | a0004 | c0019 | t0001 | g0201 | AFR | ESN | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03209 | hp1 | a0001 | c0008 | t0010 | g0293 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03225 | hp1 | a0003 | c0003 | t0006 | g0238 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03225 | hp2 | a0004 | c0005 | t0001 | g0006 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03239 | hp1 | a0003 | c0007 | t0013 | g0243 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0068 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03453 | hp1 | a0008 | c0016 | t0001 | g0009 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03453 | hp2 | a0001 | c0008 | t0002 | g0284 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03486 | hp1 | a0001 | c0006 | t0001 | g0062 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0207 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03490 | hp1 | a0004 | c0005 | t0001 | g0106 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0113 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03492 | hp1 | a0002 | c0004 | t0002 | g0282 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03492 | hp2 | a0004 | c0005 | t0001 | g0108 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0066 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03540 | hp2 | a0004 | c0005 | t0001 | g0080 | AFR | GWD | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03579 | hp1 | a0003 | c0003 | t0001 | g0058 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03579 | hp2 | a0003 | c0003 | t0001 | g0197 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03704 | hp1 | a0003 | c0007 | t0002 | g0275 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03704 | hp2 | a0002 | c0001 | t0001 | g0112 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03710 | hp2 | a0001 | c0010 | t0001 | g0075 | SAS | PJL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03834 | hp1 | a0003 | c0003 | t0001 | g0090 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03834 | hp2 | a0001 | c0006 | t0001 | g0091 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0144 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03927 | hp2 | a0002 | c0001 | t0001 | g0005 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03942 | hp1 | a0003 | c0003 | t0001 | g0166 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03942 | hp2 | a0002 | c0001 | t0001 | g0165 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04184 | hp1 | a0003 | c0003 | t0001 | g0019 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04184 | hp2 | a0002 | c0031 | t0002 | g0285 | SAS | BEB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04199 | hp1 | a0001 | c0006 | t0001 | g0046 | SAS | STU | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04199 | hp2 | a0006 | c0013 | t0001 | g0043 | SAS | STU | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04228 | hp1 | a0023 | c0041 | t0001 | g0015 | SAS | STU | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0039 | SAS | STU | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0076 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18522 | hp2 | a0004 | c0005 | t0004 | g0234 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18612 | hp1 | a0002 | c0004 | t0002 | g0296 | EAS | CHB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0184 | EAS | CHB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18747 | hp1 | a0001 | c0006 | t0001 | g0119 | EAS | CHB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18747 | hp2 | a0001 | c0002 | t0001 | g0051 | EAS | CHB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18906 | hp1 | a0004 | c0019 | t0001 | g0064 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18906 | hp2 | a0008 | c0016 | t0001 | g0195 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18939 | hp1 | a0001 | c0002 | t0001 | g0156 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18939 | hp2 | a0002 | c0001 | t0001 | g0037 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18940 | hp1 | a0006 | c0013 | t0001 | g0140 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18940 | hp2 | a0002 | c0001 | t0001 | g0034 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18942 | hp1 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18942 | hp2 | a0004 | c0005 | t0001 | g0176 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18944 | hp1 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18947 | hp1 | a0002 | c0004 | t0002 | g0299 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18947 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18948 | hp1 | a0002 | c0001 | t0001 | g0103 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0181 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18949 | hp2 | a0002 | c0001 | t0001 | g0030 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18950 | hp1 | a0006 | c0013 | t0001 | g0169 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18950 | hp2 | a0002 | c0001 | t0001 | g0024 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18951 | hp1 | a0003 | c0007 | t0002 | g0259 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18951 | hp2 | a0002 | c0001 | t0001 | g0004 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18952 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18953 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18954 | hp1 | a0002 | c0004 | t0002 | g0272 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18956 | hp2 | a0002 | c0001 | t0001 | g0053 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18959 | hp1 | a0002 | c0001 | t0001 | g0048 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18959 | hp2 | a0003 | c0003 | t0001 | g0188 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18966 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18966 | hp2 | a0002 | c0001 | t0012 | g0054 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18967 | hp1 | a0001 | c0006 | t0001 | g0167 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18967 | hp2 | a0002 | c0004 | t0002 | g0271 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18969 | hp1 | a0002 | c0001 | t0001 | g0130 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18969 | hp2 | a0013 | c0020 | t0001 | g0151 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18970 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18971 | hp1 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18971 | hp2 | a0002 | c0001 | t0005 | g0246 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18975 | hp1 | a0001 | c0006 | t0009 | g0241 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18975 | hp2 | a0002 | c0001 | t0001 | g0026 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18979 | hp1 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18979 | hp2 | a0002 | c0001 | t0001 | g0036 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18980 | hp1 | a0002 | c0001 | t0001 | g0032 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18980 | hp2 | a0007 | c0015 | t0001 | g0136 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18984 | hp1 | a0002 | c0001 | t0001 | g0041 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0177 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18988 | hp2 | a0002 | c0001 | t0001 | g0044 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0160 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18992 | hp2 | a0002 | c0004 | t0002 | g0001 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18994 | hp1 | a0007 | c0015 | t0001 | g0138 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18994 | hp2 | a0003 | c0007 | t0002 | g0295 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18997 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19000 | hp1 | a0002 | c0001 | t0001 | g0179 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19004 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19004 | hp2 | a0002 | c0001 | t0001 | g0005 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19006 | hp2 | a0024 | c0044 | t0001 | g0219 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19009 | hp1 | a0002 | c0001 | t0001 | g0042 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19010 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19011 | hp1 | a0002 | c0004 | t0002 | g0305 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19043 | hp1 | a0003 | c0003 | t0001 | g0057 | AFR | LWK | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19043 | hp2 | a0001 | c0002 | t0008 | g0208 | AFR | LWK | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19054 | hp2 | a0002 | c0001 | t0001 | g0095 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19055 | hp1 | a0002 | c0001 | t0001 | g0104 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19055 | hp2 | a0002 | c0004 | t0002 | g0300 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19058 | hp1 | a0003 | c0003 | t0001 | g0137 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19058 | hp2 | a0002 | c0001 | t0001 | g0190 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19063 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19065 | hp1 | a0002 | c0001 | t0001 | g0050 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19066 | hp1 | a0006 | c0013 | t0001 | g0101 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19066 | hp2 | a0002 | c0001 | t0001 | g0191 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19068 | hp1 | a0002 | c0001 | t0001 | g0189 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19068 | hp2 | a0007 | c0025 | t0002 | g0302 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19070 | hp2 | a0002 | c0004 | t0002 | g0298 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19078 | hp1 | a0025 | c0037 | t0001 | g0069 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19078 | hp2 | a0002 | c0001 | t0001 | g0047 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19083 | hp1 | a0002 | c0001 | t0001 | g0023 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19083 | hp2 | a0007 | c0015 | t0001 | g0158 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19088 | hp1 | a0002 | c0004 | t0002 | g0308 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19091 | hp1 | a0002 | c0001 | t0001 | g0038 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19091 | hp2 | a0003 | c0003 | t0001 | g0118 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19240 | hp1 | a0003 | c0007 | t0002 | g0265 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA19240 | hp2 | a0012 | c0022 | t0004 | g0230 | AFR | YRI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20129 | hp1 | a0004 | c0005 | t0003 | g0220 | AFR | ASW | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20129 | hp2 | a0001 | c0040 | t0001 | g0214 | AFR | ASW | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20752 | hp1 | a0005 | c0011 | t0001 | g0083 | EUR | TSI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20752 | hp2 | a0001 | c0010 | t0001 | g0157 | EUR | TSI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20805 | hp1 | a0005 | c0011 | t0001 | g0074 | EUR | TSI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20805 | hp2 | a0003 | c0007 | t0002 | g0255 | EUR | TSI | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01123 | hp1 | a0003 | c0003 | t0001 | g0077 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG01123 | hp2 | a0001 | c0012 | t0002 | g0281 | AMR | CLM | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02109 | hp1 | a0001 | c0008 | t0002 | g0288 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02109 | hp2 | a0004 | c0005 | t0001 | g0079 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02486 | hp1 | a0003 | c0003 | t0001 | g0196 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02486 | hp2 | a0001 | c0012 | t0002 | g0268 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02559 | hp1 | a0004 | c0005 | t0001 | g0211 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG02559 | hp2 | a0008 | c0016 | t0001 | g0009 | AFR | ACB | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03471 | hp1 | a0001 | c0010 | t0003 | g0227 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| HG03471 | hp2 | a0004 | c0005 | t0006 | g0240 | AFR | MSL | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18955 | hp1 | a0001 | c0008 | t0002 | g0297 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA18955 | hp2 | a0007 | c0015 | t0001 | g0141 | EAS | JPT | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20300 | hp1 | a0001 | c0008 | t0007 | g0316 | AFR | USA | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA20300 | hp2 | a0010 | c0024 | t0001 | g0218 | AFR | USA | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA21309 | hp1 | a0004 | c0005 | t0001 | g0210 | AFR | LWK | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| NA21309 | hp2 | a0001 | c0006 | t0001 | g0071 | AFR | LWK | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| homoSapiens | chm13v2 | a0002 | c0001 | t0001 | g0107 | REF | REF | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0209 | REF | REF | WHRN_chr9_114397080_114510473 | WHRN | chr9 | 114397080 | 114510473 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114402892 | G | T | 1 | a0006 | 7 | HG00544.hp1 HG02135.hp1 HG02165.hp1 others(4): Show |
missense_variant | MODERATE | c.2586C>A | p.His862Gln | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 12/12 | 3258/4070 | 2586/2724 | 862/907 | chr9 | 114402892 | |||
| chr9:114403897 | G | A | 1 | a0022 | 1 | HG03139.hp2 | missense_variant&splice_region_variant | MODERATE | c.2417C>T | p.Pro806Leu | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 3089/4070 | 2417/2724 | 806/907 | chr9 | 114403897 | |||
| chr9:114403926 | G | T | 3 | a0002 a0005 a0024 |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
missense_variant | MODERATE | c.2388C>A | p.Asn796Lys | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 3060/4070 | 2388/2724 | 796/907 | chr9 | 114403926 | |||
| chr9:114403930 | C | T | 1 | a0023 | 1 | HG04228.hp1 | missense_variant | MODERATE | c.2384G>A | p.Arg795Gln | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 3056/4070 | 2384/2724 | 795/907 | chr9 | 114403930 | |||
| chr9:114403966 | A | G | 8 | a0002 a0003 a0005 others(5): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
missense_variant | MODERATE | c.2348T>C | p.Val783Ala | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 3020/4070 | 2348/2724 | 783/907 | chr9 | 114403966 | |||
| chr9:114404058 | C | G | 2 | a0012 a0019 |
3 | HG01243.hp2 HG02258.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.2256G>C | p.Gln752His | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 2928/4070 | 2256/2724 | 752/907 | chr9 | 114404058 | |||
| chr9:114406699 | G | A | 1 | a0013 | 2 | HG02080.hp2 NA18969.hp2 |
missense_variant | MODERATE | c.1892C>T | p.Ala631Val | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/12 | 2564/4070 | 1892/2724 | 631/907 | chr9 | 114406699 | |||
| chr9:114406753 | A | G | 12 | a0002 a0003 a0004 others(9): Show |
180 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(177): Show |
missense_variant | MODERATE | c.1838T>C | p.Met613Thr | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/12 | 2510/4070 | 1838/2724 | 613/907 | chr9 | 114406753 | |||
| chr9:114407961 | G | C | 1 | a0005 | 10 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
missense_variant | MODERATE | c.1684C>G | p.Pro562Ala | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/12 | 2356/4070 | 1684/2724 | 562/907 | chr9 | 114407961 | |||
| chr9:114423486 | G | A | 1 | a0015 | 2 | HG02622.hp2 HG03130.hp2 |
missense_variant | MODERATE | c.1454C>T | p.Pro485Leu | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/12 | 2126/4070 | 1454/2724 | 485/907 | chr9 | 114423486 | |||
| chr9:114424398 | C | T | 1 | a0007 | 6 | HG00408.hp2 NA18955.hp2 NA18980.hp2 others(3): Show |
missense_variant | MODERATE | c.1352G>A | p.Gly451Asp | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/12 | 2024/4070 | 1352/2724 | 451/907 | chr9 | 114424398 | |||
| chr9:114424432 | C | T | 6 | a0002 a0005 a0009 others(3): Show |
94 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
missense_variant | MODERATE | c.1318G>A | p.Ala440Thr | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/12 | 1990/4070 | 1318/2724 | 440/907 | chr9 | 114424432 | |||
| chr9:114426242 | G | A | 1 | a0017 | 1 | HG00408.hp1 | missense_variant | MODERATE | c.1135C>T | p.Arg379Trp | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/12 | 1807/4070 | 1135/2724 | 379/907 | chr9 | 114426242 | |||
| chr9:114426286 | T | C | 2 | a0008 a0012 |
8 | HG01109.hp2 HG01243.hp2 HG02559.hp2 others(5): Show |
missense_variant | MODERATE | c.1091A>G | p.His364Arg | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/12 | 1763/4070 | 1091/2724 | 364/907 | chr9 | 114426286 | |||
| chr9:114426302 | C | T | 1 | a0019 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.1075G>A | p.Val359Ile | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/12 | 1747/4070 | 1075/2724 | 359/907 | chr9 | 114426302 | |||
| chr9:114426329 | G | A | 1 | a0014 | 2 | HG02145.hp1 HG02615.hp2 |
missense_variant | MODERATE | c.1048C>T | p.Arg350Trp | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/12 | 1720/4070 | 1048/2724 | 350/907 | chr9 | 114426329 | |||
| chr9:114426382 | C | T | 1 | a0022 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.995G>A | p.Arg332Gln | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/12 | 1667/4070 | 995/2724 | 332/907 | chr9 | 114426382 | |||
| chr9:114478626 | C | T | 1 | a0016 | 2 | HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.764G>A | p.Gly255Asp | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/12 | 1436/4070 | 764/2724 | 255/907 | chr9 | 114478626 | |||
| chr9:114478674 | G | A | 1 | a0020 | 1 | HG02273.hp1 | missense_variant | MODERATE | c.716C>T | p.Pro239Leu | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/12 | 1388/4070 | 716/2724 | 239/907 | chr9 | 114478674 | |||
| chr9:114478722 | C | T | 2 | a0011 a0018 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
missense_variant | MODERATE | c.668G>A | p.Arg223His | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/12 | 1340/4070 | 668/2724 | 223/907 | chr9 | 114478722 | |||
| chr9:114504573 | T | A | 1 | a0010 | 2 | HG00140.hp1 NA20300.hp2 |
missense_variant | MODERATE | c.229A>T | p.Thr77Ser | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 901/4070 | 229/2724 | 77/907 | chr9 | 114504573 | |||
| chr9:114504663 | T | C | 1 | a0024 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.139A>G | p.Thr47Ala | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 811/4070 | 139/2724 | 47/907 | chr9 | 114504663 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114403319 | C | T | 1 | a0001c0040 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2439G>A | p.Thr813Thr | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 11/12 | 3111/4070 | 2439/2724 | 813/907 | chr9 | 114403319 | |||
| chr9:114403935 | C | T | 1 | a0011c0033 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.2379G>A | p.Leu793Leu | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 3051/4070 | 2379/2724 | 793/907 | chr9 | 114403935 | |||
| chr9:114403992 | G | A | 1 | a0005c0039 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.2322C>T | p.Ser774Ser | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 2994/4070 | 2322/2724 | 774/907 | chr9 | 114403992 | |||
| chr9:114404031 | G | A | 3 | a0001c0010 a0001c0012 a0016c0017 |
20 | HG00323.hp1 HG01070.hp2 HG01123.hp2 others(17): Show |
synonymous_variant | LOW | c.2283C>T | p.Ser761Ser | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/12 | 2955/4070 | 2283/2724 | 761/907 | chr9 | 114404031 | |||
| chr9:114406545 | C | G | 1 | a0001c0040 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2046G>C | p.Arg682Arg | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/12 | 2718/4070 | 2046/2724 | 682/907 | chr9 | 114406545 | |||
| chr9:114406560 | G | A | 1 | a0001c0028 | 1 | HG02080.hp1 | synonymous_variant | LOW | c.2031C>T | p.Ile677Ile | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/12 | 2703/4070 | 2031/2724 | 677/907 | chr9 | 114406560 | |||
| chr9:114406599 | C | T | 1 | a0004c0019 | 2 | HG03195.hp2 NA18906.hp1 |
synonymous_variant | LOW | c.1992G>A | p.Pro664Pro | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/12 | 2664/4070 | 1992/2724 | 664/907 | chr9 | 114406599 | |||
| chr9:114423425 | C | T | 1 | a0004c0018 | 2 | HG00741.hp1 HG01074.hp2 |
synonymous_variant | LOW | c.1515G>A | p.Ala505Ala | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/12 | 2187/4070 | 1515/2724 | 505/907 | chr9 | 114423425 | |||
| chr9:114424397 | A | G | 35 | a0001c0002 a0001c0008 a0001c0010 others(32): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(285): Show |
synonymous_variant | LOW | c.1353T>C | p.Gly451Gly | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/12 | 2025/4070 | 1353/2724 | 451/907 | chr9 | 114424397 | |||
| chr9:114466297 | T | G | 1 | a0002c0031 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.933A>C | p.Pro311Pro | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/12 | 1605/4070 | 933/2724 | 311/907 | chr9 | 114466297 | |||
| chr9:114504685 | C | T | 12 | a0001c0008 a0001c0009 a0001c0012 others(9): Show |
76 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
synonymous_variant | LOW | c.117G>A | p.Val39Val | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 789/4070 | 117/2724 | 39/907 | chr9 | 114504685 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114402316 | A | C | 2 | a0001c0002t0008 a0001c0008t0010 |
4 | HG02886.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*438T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 12/12 | 438 | chr9 | 114402316 | ||||||
| chr9:114402429 | G | C | 1 | a0002c0001t0012 | 1 | NA18966.hp2 | 3_prime_UTR_variant | MODIFIER | c.*325C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 12/12 | 325 | chr9 | 114402429 | ||||||
| chr9:114504892 | G | A | 16 | a0001c0008t0002 a0001c0008t0007 a0001c0008t0010 others(13): Show |
76 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(73): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-91C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | chr9 | 114504892 | |||||||
| chr9:114505005 | G | C | 5 | a0001c0002t0003 a0001c0006t0003 a0001c0010t0003 others(2): Show |
9 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-204C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 204 | chr9 | 114505005 | ||||||
| chr9:114505058 | G | C | 6 | a0001c0002t0004 a0004c0005t0004 a0012c0022t0004 others(3): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-257C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 257 | chr9 | 114505058 | ||||||
| chr9:114505096 | G | C | 2 | a0003c0003t0006 a0004c0005t0006 |
3 | HG02895.hp1 HG03225.hp1 HG03471.hp2 |
5_prime_UTR_variant | MODIFIER | c.-295C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 295 | chr9 | 114505096 | ||||||
| chr9:114505115 | G | A | 1 | a0001c0006t0009 | 2 | HG02040.hp2 NA18975.hp1 |
5_prime_UTR_variant | MODIFIER | c.-314C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 314 | chr9 | 114505115 | ||||||
| chr9:114505192 | G | T | 19 | a0001c0008t0002 a0001c0008t0007 a0001c0008t0010 others(16): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-391C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 391 | chr9 | 114505192 | ||||||
| chr9:114505242 | C | T | 1 | a0003c0007t0013 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-441G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 441 | chr9 | 114505242 | ||||||
| chr9:114505252 | G | C | 1 | a0001c0008t0007 | 3 | HG02615.hp1 HG02965.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-451C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 451 | chr9 | 114505252 | ||||||
| chr9:114505311 | C | T | 19 | a0001c0008t0002 a0001c0008t0007 a0001c0008t0010 others(16): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-510G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 510 | chr9 | 114505311 | ||||||
| chr9:114505401 | AGCCTCCG others(1): Show |
A | 19 | a0001c0008t0002 a0001c0008t0007 a0001c0008t0010 others(16): Show |
83 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(80): Show |
5_prime_UTR_variant | MODIFIER | c.-608_-601delGCGGAG others(2): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 601 | chr9 | 114505401 | ||||||
| chr9:114505419 | C | T | 1 | a0003c0007t0011 | 1 | HG00738.hp1 | 5_prime_UTR_variant | MODIFIER | c.-618G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/12 | 618 | chr9 | 114505419 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:114403083 | G | A | 4 | a0001c0012t0002g0010 a0001c0012t0002g0277 a0001c0012t0002g0278 others(1): Show |
5 | HG01070.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.2541+134C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 11/11 | chr9 | 114403083 | |||||||
| chr9:114403097 | T | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0125 |
2 | NA18953.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.2541+120A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 11/11 | chr9 | 114403097 | |||||||
| chr9:114403457 | C | T | 65 | a0003c0003t0001g0008 a0003c0003t0001g0019 a0003c0003t0001g0022 others(62): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2419-118G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/11 | chr9 | 114403457 | |||||||
| chr9:114403754 | T | C | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2418+142A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 10/11 | chr9 | 114403754 | |||||||
| chr9:114404267 | A | G | 79 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(76): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2237-190T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404267 | |||||||
| chr9:114404489 | C | T | 4 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2237-412G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404489 | |||||||
| chr9:114404639 | T | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.2237-562A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404639 | |||||||
| chr9:114404824 | G | T | 65 | a0003c0003t0001g0008 a0003c0003t0001g0019 a0003c0003t0001g0022 others(62): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2237-747C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404824 | |||||||
| chr9:114404912 | T | C | 79 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(76): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.2237-835A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404912 | |||||||
| chr9:114404928 | C | G | 4 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0010g0252 others(1): Show |
4 | HG02886.hp1 HG03098.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2237-851G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404928 | |||||||
| chr9:114404932 | G | A | 1 | a0001c0008t0002g0274 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2237-855C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404932 | |||||||
| chr9:114404979 | G | C | 143 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(140): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.2237-902C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404979 | |||||||
| chr9:114404979 | G | T | 1 | a0003c0003t0001g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2237-902C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114404979 | |||||||
| chr9:114405059 | T | A | 3 | a0001c0008t0007g0316 a0001c0008t0007g0317 a0001c0008t0007g0318 |
3 | HG02615.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2237-982A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405059 | |||||||
| chr9:114405066 | CTCTCT | C | 13 | a0004c0005t0001g0006 a0004c0005t0001g0079 a0004c0005t0001g0080 others(10): Show |
14 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.2237-994_2237-990d others(7): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405066 | |||||||
| chr9:114405070 | C | CT | 9 | a0001c0002t0001g0056 a0001c0002t0001g0180 a0001c0002t0001g0182 others(6): Show |
9 | HG01071.hp2 HG01167.hp2 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.2237-994dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405070 | CT | C | 21 | a0001c0002t0001g0092 a0001c0002t0001g0099 a0001c0002t0001g0184 others(18): Show |
21 | HG00423.hp2 HG00741.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.2237-994delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405070 | CTT | C | 78 | a0001c0008t0002g0288 a0001c0040t0001g0214 a0002c0001t0001g0002 others(75): Show |
86 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.2237-995_2237-994d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405070 | CTTT | C | 55 | a0002c0001t0001g0041 a0002c0004t0002g0290 a0003c0003t0001g0008 others(52): Show |
56 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.2237-996_2237-994d others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405070 | CTTTT | C | 12 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0059 others(9): Show |
12 | HG02280.hp1 HG02486.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.2237-997_2237-994d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405070 | CTTTTTTT others(3): Show |
C | 2 | a0004c0005t0001g0210 a0004c0026t0002g0273 |
2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2237-1003_2237-994 others(13): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405070 | |||||||
| chr9:114405072 | T | C | 44 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0207 others(41): Show |
45 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.2237-995A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405072 | |||||||
| chr9:114405073 | T | C | 6 | a0001c0006t0001g0071 a0001c0006t0009g0242 a0001c0009t0002g0257 others(3): Show |
6 | HG01516.hp2 HG02040.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.2237-996A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405073 | |||||||
| chr9:114405074 | T | C | 76 | a0001c0040t0001g0214 a0002c0001t0001g0002 a0002c0001t0001g0003 others(73): Show |
84 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(81): Show |
intron_variant | MODIFIER | c.2237-997A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405074 | |||||||
| chr9:114405075 | T | C | 2 | a0002c0001t0001g0041 a0002c0004t0002g0290 |
2 | HG02897.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.2237-998A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405075 | |||||||
| chr9:114405076 | T | C | 1 | a0002c0004t0002g0304 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2237-999A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405076 | |||||||
| chr9:114405089 | T | A | 1 | a0003c0003t0001g0166 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2237-1012A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405089 | |||||||
| chr9:114405165 | C | T | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2237-1088G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405165 | |||||||
| chr9:114405186 | C | T | 65 | a0003c0003t0001g0008 a0003c0003t0001g0019 a0003c0003t0001g0022 others(62): Show |
66 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2237-1109G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405186 | |||||||
| chr9:114405243 | C | T | 5 | a0008c0016t0001g0009 a0008c0016t0001g0194 a0008c0016t0001g0195 others(2): Show |
6 | HG01109.hp2 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2236+1112G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405243 | |||||||
| chr9:114405265 | C | T | 1 | a0002c0001t0001g0104 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2236+1090G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405265 | |||||||
| chr9:114405328 | C | T | 3 | a0001c0009t0002g0260 a0001c0009t0002g0261 a0001c0009t0002g0262 |
3 | HG00738.hp2 HG01099.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.2236+1027G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405328 | |||||||
| chr9:114405611 | C | A | 1 | a0001c0002t0001g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2236+744G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405611 | |||||||
| chr9:114405621 | C | T | 1 | a0001c0012t0002g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2236+734G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405621 | |||||||
| chr9:114405664 | G | C | 145 | a0001c0002t0001g0102 a0002c0001t0001g0002 a0002c0001t0001g0003 others(142): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2236+691C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405664 | |||||||
| chr9:114405991 | C | G | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2236+364G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405991 | |||||||
| chr9:114405992 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2236+363C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114405992 | |||||||
| chr9:114406085 | C | T | 2 | a0001c0002t0001g0056 a0001c0008t0002g0297 |
2 | HG02027.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.2236+270G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114406085 | |||||||
| chr9:114406229 | C | T | 1 | a0003c0003t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2236+126G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114406229 | |||||||
| chr9:114406271 | C | A | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.2236+84G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114406271 | |||||||
| chr9:114406279 | C | T | 4 | a0003c0003t0001g0196 a0003c0003t0001g0197 a0003c0003t0006g0238 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2236+76G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 9/11 | chr9 | 114406279 | |||||||
| chr9:114406953 | G | A | 1 | a0001c0028t0002g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1699-61C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114406953 | |||||||
| chr9:114407020 | A | G | 237 | a0001c0002t0001g0073 a0001c0002t0001g0092 a0001c0002t0001g0134 others(234): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.1699-128T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407020 | |||||||
| chr9:114407070 | C | T | 5 | a0004c0005t0001g0006 a0004c0005t0001g0079 a0004c0005t0001g0080 others(2): Show |
6 | HG02109.hp2 HG02145.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1699-178G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407070 | |||||||
| chr9:114407171 | G | A | 2 | a0001c0006t0001g0018 a0001c0009t0002g0269 |
2 | HG02735.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1699-279C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407171 | |||||||
| chr9:114407655 | C | A | 79 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(76): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1698+292G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407655 | |||||||
| chr9:114407658 | C | T | 2 | a0002c0001t0001g0031 a0002c0001t0001g0055 |
2 | HG01074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1698+289G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407658 | |||||||
| chr9:114407693 | G | GGTCAAA | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1698+253_1698+254i others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407693 | |||||||
| chr9:114407737 | C | A | 2 | a0006c0013t0001g0101 a0006c0013t0001g0140 |
2 | NA18940.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1698+210G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407737 | |||||||
| chr9:114407829 | G | A | 1 | a0002c0004t0002g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1698+118C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407829 | |||||||
| chr9:114407900 | T | A | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1698+47A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 8/11 | chr9 | 114407900 | |||||||
| chr9:114408030 | C | T | 39 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0207 others(36): Show |
40 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1627-12G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408030 | |||||||
| chr9:114408211 | G | A | 1 | a0001c0002t0001g0110 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1627-193C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408211 | |||||||
| chr9:114408388 | G | C | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1627-370C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408388 | |||||||
| chr9:114408574 | G | A | 1 | a0001c0002t0001g0127 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1627-556C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408574 | |||||||
| chr9:114408608 | G | A | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1627-590C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408608 | |||||||
| chr9:114408726 | G | A | 7 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(4): Show |
7 | HG02257.hp2 HG02572.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1627-708C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408726 | |||||||
| chr9:114408862 | G | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627-844C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408862 | |||||||
| chr9:114408927 | G | A | 20 | a0001c0010t0001g0075 a0001c0010t0001g0096 a0001c0010t0001g0111 others(17): Show |
21 | HG00323.hp1 HG01070.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.1627-909C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408927 | |||||||
| chr9:114408929 | G | A | 79 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(76): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1627-911C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114408929 | |||||||
| chr9:114409051 | G | A | 2 | a0001c0006t0003g0225 a0015c0021t0004g0231 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1627-1033C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409051 | |||||||
| chr9:114409107 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1627-1089A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409107 | |||||||
| chr9:114409241 | A | AGAG | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1627-1226_1627-122 others(7): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409241 | |||||||
| chr9:114409630 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627-1612G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409630 | |||||||
| chr9:114409658 | C | T | 71 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(68): Show |
71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.1627-1640G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409658 | |||||||
| chr9:114409706 | C | G | 1 | a0001c0010t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1627-1688G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409706 | |||||||
| chr9:114409738 | C | T | 1 | a0001c0010t0003g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1627-1720G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409738 | |||||||
| chr9:114409763 | C | A | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-1745G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409763 | |||||||
| chr9:114409865 | C | T | 6 | a0004c0005t0001g0210 a0004c0005t0003g0220 a0004c0018t0001g0094 others(3): Show |
6 | HG00741.hp1 HG01074.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1627-1847G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114409865 | |||||||
| chr9:114410027 | G | A | 144 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(141): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1627-2009C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410027 | |||||||
| chr9:114410056 | C | G | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1627-2038G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410056 | |||||||
| chr9:114410181 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1627-2163A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410181 | |||||||
| chr9:114410289 | C | T | 4 | a0003c0003t0001g0008 a0003c0003t0001g0090 a0003c0003t0001g0175 others(1): Show |
5 | HG00733.hp2 HG01069.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627-2271G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410289 | |||||||
| chr9:114410365 | T | C | 1 | a0005c0039t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1627-2347A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410365 | |||||||
| chr9:114410405 | G | C | 1 | a0001c0006t0001g0067 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1627-2387C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410405 | |||||||
| chr9:114410417 | C | T | 5 | a0009c0014t0005g0244 a0009c0014t0005g0247 a0009c0014t0005g0248 others(2): Show |
5 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-2399G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410417 | |||||||
| chr9:114410459 | G | C | 2 | a0001c0002t0001g0056 a0001c0008t0002g0297 |
2 | HG02027.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1627-2441C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410459 | |||||||
| chr9:114410762 | C | G | 14 | a0004c0005t0001g0006 a0004c0005t0001g0079 a0004c0005t0001g0080 others(11): Show |
15 | HG01243.hp1 HG02109.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.1627-2744G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410762 | |||||||
| chr9:114410773 | C | T | 3 | a0001c0002t0001g0073 a0001c0002t0001g0207 a0001c0002t0003g0228 |
3 | HG01884.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1627-2755G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410773 | |||||||
| chr9:114410911 | C | T | 1 | a0009c0014t0005g0249 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1627-2893G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410911 | |||||||
| chr9:114410977 | T | A | 1 | a0001c0010t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1627-2959A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114410977 | |||||||
| chr9:114411067 | T | C | 2 | a0003c0003t0001g0154 a0003c0007t0002g0295 |
2 | NA18953.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.1627-3049A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411067 | |||||||
| chr9:114411131 | A | G | 1 | a0003c0003t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1627-3113T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411131 | |||||||
| chr9:114411222 | C | G | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-3204G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411222 | |||||||
| chr9:114411350 | C | G | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627-3332G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411350 | |||||||
| chr9:114411799 | T | C | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1627-3781A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411799 | |||||||
| chr9:114411844 | A | G | 71 | a0003c0003t0001g0008 a0003c0003t0001g0019 a0003c0003t0001g0022 others(68): Show |
72 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1627-3826T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411844 | |||||||
| chr9:114411893 | T | C | 67 | a0001c0040t0001g0214 a0003c0003t0001g0008 a0003c0003t0001g0019 others(64): Show |
68 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.1627-3875A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114411893 | |||||||
| chr9:114412044 | T | C | 7 | a0004c0005t0001g0210 a0004c0005t0003g0220 a0004c0005t0004g0234 others(4): Show |
7 | HG00741.hp1 HG01074.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1627-4026A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412044 | |||||||
| chr9:114412088 | A | G | 244 | a0001c0002t0001g0061 a0001c0002t0001g0073 a0001c0002t0001g0092 others(241): Show |
256 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.1627-4070T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412088 | |||||||
| chr9:114412236 | A | G | 1 | a0001c0006t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1627-4218T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412236 | |||||||
| chr9:114412327 | G | A | 3 | a0001c0006t0001g0070 a0001c0006t0001g0071 a0001c0006t0001g0072 |
3 | HG02257.hp2 HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1627-4309C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412327 | |||||||
| chr9:114412501 | G | A | 79 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(76): Show |
87 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.1627-4483C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412501 | |||||||
| chr9:114412970 | T | C | 149 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(146): Show |
158 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.1627-4952A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412970 | |||||||
| chr9:114412984 | C | T | 2 | a0001c0009t0002g0260 a0001c0009t0002g0262 |
2 | HG00738.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1627-4966G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412984 | |||||||
| chr9:114412998 | G | C | 5 | a0009c0014t0005g0244 a0009c0014t0005g0247 a0009c0014t0005g0248 others(2): Show |
5 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1627-4980C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114412998 | |||||||
| chr9:114413093 | C | T | 1 | a0001c0006t0003g0225 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1627-5075G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413093 | |||||||
| chr9:114413122 | C | T | 3 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0110 |
3 | NA19010.hp1 NA19054.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1627-5104G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413122 | |||||||
| chr9:114413670 | G | A | 1 | a0001c0009t0002g0260 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1627-5652C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413670 | |||||||
| chr9:114413687 | T | A | 1 | a0023c0041t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1627-5669A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413687 | |||||||
| chr9:114413730 | T | G | 1 | a0015c0021t0004g0229 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1627-5712A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413730 | |||||||
| chr9:114413780 | A | C | 3 | a0004c0005t0001g0210 a0004c0005t0003g0220 a0004c0026t0002g0273 |
3 | HG02258.hp1 NA20129.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1627-5762T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413780 | |||||||
| chr9:114413814 | A | C | 1 | a0001c0008t0010g0293 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1627-5796T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413814 | |||||||
| chr9:114413956 | AAGAG | A | 64 | a0003c0003t0001g0008 a0003c0003t0001g0019 a0003c0003t0001g0022 others(61): Show |
65 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.1627-5942_1627-593 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413956 | |||||||
| chr9:114413958 | G | T | 1 | a0001c0008t0002g0258 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1627-5940C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114413958 | |||||||
| chr9:114414026 | T | C | 148 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(145): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.1627-6008A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414026 | |||||||
| chr9:114414032 | T | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1627-6014A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414032 | |||||||
| chr9:114414052 | C | T | 1 | a0004c0005t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1627-6034G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414052 | |||||||
| chr9:114414160 | G | A | 9 | a0004c0005t0001g0006 a0004c0005t0001g0079 a0004c0005t0001g0080 others(6): Show |
10 | HG02109.hp2 HG02145.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1627-6142C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414160 | |||||||
| chr9:114414325 | G | A | 1 | a0005c0011t0001g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1627-6307C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414325 | |||||||
| chr9:114414669 | C | T | 84 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(81): Show |
92 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1627-6651G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414669 | |||||||
| chr9:114414955 | C | T | 1 | a0002c0001t0001g0033 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1627-6937G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114414955 | |||||||
| chr9:114415273 | T | TA | 21 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0059 others(18): Show |
21 | HG00741.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1627-7256dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114415273 | |||||||
| chr9:114415273 | TAA | T | 97 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0006t0001g0062 others(94): Show |
105 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.1627-7257_1627-725 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114415273 | |||||||
| chr9:114415286 | A | C | 26 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(23): Show |
26 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1627-7268T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114415286 | |||||||
| chr9:114415638 | A | G | 3 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 |
3 | HG01891.hp1 HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1627-7620T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114415638 | |||||||
| chr9:114416308 | G | A | 2 | a0001c0002t0001g0109 a0001c0002t0001g0125 |
2 | NA18953.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.1626+7006C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416308 | |||||||
| chr9:114416442 | C | T | 93 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(90): Show |
101 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1626+6872G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416442 | |||||||
| chr9:114416451 | C | A | 3 | a0001c0002t0001g0073 a0001c0002t0001g0207 a0001c0002t0003g0228 |
3 | HG01884.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1626+6863G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416451 | |||||||
| chr9:114416557 | C | T | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1626+6757G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416557 | |||||||
| chr9:114416745 | T | C | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1626+6569A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416745 | |||||||
| chr9:114416755 | G | C | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1626+6559C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416755 | |||||||
| chr9:114416764 | A | G | 3 | a0001c0006t0003g0225 a0004c0042t0001g0063 a0015c0021t0004g0231 |
3 | HG02622.hp2 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1626+6550T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416764 | |||||||
| chr9:114416773 | G | A | 1 | a0007c0015t0001g0136 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1626+6541C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416773 | |||||||
| chr9:114416904 | C | A | 8 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(5): Show |
8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1626+6410G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416904 | |||||||
| chr9:114416942 | A | G | 93 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(90): Show |
101 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1626+6372T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114416942 | |||||||
| chr9:114417066 | T | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+6248A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417066 | |||||||
| chr9:114417103 | A | C | 1 | a0002c0001t0001g0053 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1626+6211T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417103 | |||||||
| chr9:114417118 | G | A | 4 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+6196C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417118 | |||||||
| chr9:114417270 | C | T | 21 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0059 others(18): Show |
21 | HG00741.hp1 HG01074.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.1626+6044G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417270 | |||||||
| chr9:114417338 | T | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0192 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1626+5976A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417338 | |||||||
| chr9:114417425 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+5889G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417425 | |||||||
| chr9:114417499 | T | C | 1 | a0004c0005t0001g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1626+5815A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417499 | |||||||
| chr9:114417533 | T | C | 1 | a0001c0040t0001g0214 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1626+5781A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417533 | |||||||
| chr9:114417725 | C | T | 90 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(87): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1626+5589G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417725 | |||||||
| chr9:114417728 | C | T | 90 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(87): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1626+5586G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417728 | |||||||
| chr9:114417872 | C | T | 1 | a0001c0010t0003g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1626+5442G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417872 | |||||||
| chr9:114417997 | G | C | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1626+5317C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114417997 | |||||||
| chr9:114418081 | G | A | 1 | a0002c0001t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1626+5233C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418081 | |||||||
| chr9:114418213 | G | A | 85 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(82): Show |
93 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1626+5101C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418213 | |||||||
| chr9:114418266 | C | T | 6 | a0002c0001t0001g0032 a0002c0001t0001g0038 a0002c0001t0001g0042 others(3): Show |
6 | NA18948.hp1 NA18971.hp2 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.1626+5048G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418266 | |||||||
| chr9:114418446 | G | A | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1626+4868C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418446 | |||||||
| chr9:114418616 | G | A | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1626+4698C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418616 | |||||||
| chr9:114418623 | C | T | 1 | a0003c0007t0002g0275 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1626+4691G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418623 | |||||||
| chr9:114418639 | T | C | 121 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.1626+4675A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418639 | |||||||
| chr9:114418910 | T | C | 114 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(111): Show |
122 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1626+4404A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418910 | |||||||
| chr9:114418917 | C | T | 1 | a0004c0018t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1626+4397G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418917 | |||||||
| chr9:114418957 | C | T | 85 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(82): Show |
93 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1626+4357G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418957 | |||||||
| chr9:114418979 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1626+4335T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114418979 | |||||||
| chr9:114419042 | G | A | 85 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(82): Show |
93 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1626+4272C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419042 | |||||||
| chr9:114419128 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+4186G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419128 | |||||||
| chr9:114419150 | A | G | 90 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(87): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1626+4164T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419150 | |||||||
| chr9:114419260 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+4054C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419260 | |||||||
| chr9:114419264 | T | G | 3 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 |
3 | HG01891.hp1 HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1626+4050A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419264 | |||||||
| chr9:114419264 | TCA | T | 26 | a0001c0010t0001g0075 a0001c0010t0001g0096 a0001c0010t0001g0111 others(23): Show |
27 | HG00323.hp1 HG01070.hp2 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.1626+4048_1626+404 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419264 | |||||||
| chr9:114419325 | T | C | 90 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(87): Show |
98 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1626+3989A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419325 | |||||||
| chr9:114419436 | G | A | 2 | a0001c0002t0001g0056 a0001c0008t0002g0297 |
2 | HG02027.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.1626+3878C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419436 | |||||||
| chr9:114419470 | A | G | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+3844T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419470 | |||||||
| chr9:114419556 | G | A | 1 | a0004c0005t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1626+3758C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419556 | |||||||
| chr9:114419562 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+3752C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419562 | |||||||
| chr9:114419742 | G | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+3572C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419742 | |||||||
| chr9:114419809 | A | C | 85 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(82): Show |
93 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.1626+3505T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419809 | |||||||
| chr9:114419852 | C | T | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.1626+3462G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114419852 | |||||||
| chr9:114420198 | G | A | 272 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(269): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1626+3116C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420198 | |||||||
| chr9:114420230 | T | C | 3 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0011c0033t0001g0085 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1626+3084A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420230 | |||||||
| chr9:114420272 | C | T | 3 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 |
3 | HG01891.hp1 HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1626+3042G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420272 | |||||||
| chr9:114420325 | C | G | 115 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(112): Show |
123 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1626+2989G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420325 | |||||||
| chr9:114420414 | C | T | 4 | a0004c0005t0001g0206 a0004c0005t0001g0210 a0004c0005t0003g0220 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1626+2900G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420414 | |||||||
| chr9:114420560 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1626+2754C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420560 | |||||||
| chr9:114420836 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+2478C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420836 | |||||||
| chr9:114420869 | A | G | 115 | a0001c0010t0001g0075 a0001c0010t0001g0096 a0001c0010t0001g0111 others(112): Show |
124 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.1626+2445T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420869 | |||||||
| chr9:114420886 | T | C | 114 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(111): Show |
122 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.1626+2428A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420886 | |||||||
| chr9:114420915 | C | T | 1 | a0001c0002t0001g0117 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1626+2399G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114420915 | |||||||
| chr9:114421127 | C | T | 1 | a0001c0009t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1626+2187G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421127 | |||||||
| chr9:114421328 | C | T | 1 | a0001c0002t0001g0127 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1626+1986G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421328 | |||||||
| chr9:114421516 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1626+1798G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421516 | |||||||
| chr9:114421532 | C | G | 1 | a0002c0001t0001g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1626+1782G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421532 | |||||||
| chr9:114421604 | C | T | 1 | a0001c0008t0002g0303 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1626+1710G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421604 | |||||||
| chr9:114421653 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1626+1661C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114421653 | |||||||
| chr9:114422077 | C | A | 3 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0011c0033t0001g0085 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1626+1237G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422077 | |||||||
| chr9:114422151 | C | A | 4 | a0004c0005t0001g0206 a0004c0005t0001g0210 a0004c0005t0003g0220 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1626+1163G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422151 | |||||||
| chr9:114422184 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1626+1130C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422184 | |||||||
| chr9:114422262 | C | T | 1 | a0006c0027t0002g0310 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1626+1052G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422262 | |||||||
| chr9:114422282 | A | T | 2 | a0014c0023t0001g0089 a0014c0023t0004g0233 |
2 | HG02145.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1626+1032T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422282 | |||||||
| chr9:114422315 | G | T | 3 | a0001c0002t0001g0073 a0001c0002t0001g0207 a0001c0002t0003g0228 |
3 | HG01884.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1626+999C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422315 | |||||||
| chr9:114422377 | A | G | 2 | a0002c0001t0001g0013 a0002c0001t0001g0014 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1626+937T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422377 | |||||||
| chr9:114422421 | G | C | 1 | a0018c0032t0001g0084 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1626+893C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422421 | |||||||
| chr9:114422521 | G | T | 1 | a0001c0002t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1626+793C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422521 | |||||||
| chr9:114422646 | T | C | 91 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(88): Show |
99 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1626+668A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422646 | |||||||
| chr9:114422663 | G | A | 7 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0007g0316 others(4): Show |
7 | HG02615.hp1 HG02886.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1626+651C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422663 | |||||||
| chr9:114422672 | C | A | 272 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(269): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1626+642G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422672 | |||||||
| chr9:114422693 | G | A | 1 | a0002c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1626+621C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422693 | |||||||
| chr9:114422718 | C | T | 3 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 |
3 | HG01109.hp1 HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1626+596G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422718 | |||||||
| chr9:114422725 | C | T | 1 | a0001c0010t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1626+589G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422725 | |||||||
| chr9:114422762 | G | GA | 86 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(83): Show |
94 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1626+551dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422762 | |||||||
| chr9:114422871 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0192 |
2 | HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1626+443G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114422871 | |||||||
| chr9:114423026 | CT | C | 23 | a0001c0008t0002g0297 a0002c0001t0001g0023 a0002c0001t0001g0190 others(20): Show |
23 | HG00741.hp1 HG01074.hp2 HG01123.hp1 others(20): Show |
intron_variant | MODIFIER | c.1626+287delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114423026 | |||||||
| chr9:114423115 | A | G | 228 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(225): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.1626+199T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114423115 | |||||||
| chr9:114423191 | A | G | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1626+123T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114423191 | |||||||
| chr9:114423240 | C | G | 1 | a0007c0015t0001g0141 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1626+74G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 7/11 | chr9 | 114423240 | |||||||
| chr9:114423681 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1417-158C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114423681 | |||||||
| chr9:114423711 | C | T | 1 | a0001c0006t0001g0167 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1417-188G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114423711 | |||||||
| chr9:114423747 | T | C | 91 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(88): Show |
99 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.1417-224A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114423747 | |||||||
| chr9:114423874 | C | T | 1 | a0004c0005t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1417-351G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114423874 | |||||||
| chr9:114424183 | T | C | 151 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(148): Show |
161 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1416+151A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114424183 | |||||||
| chr9:114424184 | G | A | 2 | a0002c0001t0001g0130 a0004c0042t0001g0063 |
2 | HG02818.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1416+150C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114424184 | |||||||
| chr9:114424312 | T | A | 86 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(83): Show |
94 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1416+22A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 6/11 | chr9 | 114424312 | |||||||
| chr9:114424579 | C | T | 4 | a0002c0001t0001g0004 a0002c0001t0001g0030 a0002c0001t0001g0034 others(1): Show |
5 | HG00544.hp2 NA18940.hp2 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-33G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 5/11 | chr9 | 114424579 | |||||||
| chr9:114424876 | CTGCCCAG others(2): Show |
C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.1203+103_1203+111d others(11): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 5/11 | chr9 | 114424876 | |||||||
| chr9:114424966 | T | TAC | 3 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 |
3 | HG01891.hp1 HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1203+20_1203+21dup others(2): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 5/11 | chr9 | 114424966 | |||||||
| chr9:114425114 | C | T | 6 | a0004c0005t0001g0006 a0004c0005t0001g0079 a0004c0005t0001g0080 others(3): Show |
7 | HG02109.hp2 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1167-90G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425114 | |||||||
| chr9:114425288 | C | T | 20 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0059 others(17): Show |
20 | HG00741.hp1 HG01074.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.1167-264G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425288 | |||||||
| chr9:114425289 | G | T | 86 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(83): Show |
94 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.1167-265C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425289 | |||||||
| chr9:114425442 | C | T | 1 | a0004c0005t0004g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1167-418G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425442 | |||||||
| chr9:114425470 | A | G | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1167-446T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425470 | |||||||
| chr9:114425489 | G | GT | 8 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1167-466dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425489 | |||||||
| chr9:114425586 | G | GAC | 21 | a0001c0002t0001g0102 a0001c0006t0001g0091 a0001c0006t0009g0242 others(18): Show |
21 | HG00544.hp1 HG02027.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1167-564_1167-563d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACAC | 56 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0056 others(53): Show |
61 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.1167-566_1167-563d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACAC | 64 | a0001c0002t0001g0039 a0001c0002t0001g0045 a0001c0002t0001g0099 others(61): Show |
70 | HG00323.hp1 HG00544.hp2 HG01069.hp1 others(67): Show |
intron_variant | MODIFIER | c.1167-568_1167-563d others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(1): Show |
32 | a0001c0002t0001g0073 a0001c0002t0001g0116 a0001c0002t0001g0132 others(29): Show |
32 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(29): Show |
intron_variant | MODIFIER | c.1167-570_1167-563d others(10): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(3): Show |
25 | a0001c0002t0001g0113 a0001c0002t0001g0123 a0001c0002t0001g0128 others(22): Show |
25 | HG00140.hp1 HG00323.hp2 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.1167-572_1167-563d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(5): Show |
26 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0129 others(23): Show |
26 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(23): Show |
intron_variant | MODIFIER | c.1167-574_1167-563d others(14): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(7): Show |
19 | a0001c0002t0001g0068 a0001c0002t0001g0105 a0001c0002t0001g0109 others(16): Show |
19 | HG01168.hp1 HG01192.hp1 HG01981.hp2 others(16): Show |
intron_variant | MODIFIER | c.1167-576_1167-563d others(16): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(9): Show |
12 | a0001c0002t0001g0049 a0001c0002t0001g0155 a0001c0002t0001g0170 others(9): Show |
12 | HG00423.hp1 HG00438.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1167-578_1167-563d others(18): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(11): Show |
3 | a0003c0003t0001g0188 a0004c0005t0004g0234 a0015c0021t0004g0231 |
3 | HG02622.hp2 NA18522.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.1167-580_1167-563d others(20): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | G | GACACACA others(13): Show |
1 | a0003c0007t0002g0270 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1167-582_1167-563d others(22): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | GAC | G | 4 | a0001c0002t0001g0098 a0002c0001t0001g0023 a0004c0005t0001g0210 others(1): Show |
4 | NA19011.hp2 NA19083.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1167-564_1167-563d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425586 | GACACACA others(3): Show |
G | 5 | a0001c0010t0003g0222 a0001c0010t0003g0223 a0001c0010t0003g0226 others(2): Show |
5 | HG01192.hp2 HG01891.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1167-572_1167-563d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425586 | |||||||
| chr9:114425628 | CACAG | C | 5 | a0001c0002t0001g0092 a0001c0008t0002g0274 a0003c0007t0002g0264 others(2): Show |
5 | HG01891.hp1 HG02809.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1166+579_1166+582d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425628 | |||||||
| chr9:114425630 | C | CACACACA others(5): Show |
1 | a0003c0003t0001g0154 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1166+580_1166+581i others(14): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425630 | |||||||
| chr9:114425630 | CAG | C | 13 | a0001c0002t0001g0061 a0003c0003t0001g0059 a0003c0003t0001g0066 others(10): Show |
14 | HG01123.hp1 HG02055.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1166+579_1166+580d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425630 | |||||||
| chr9:114425632 | G | C | 29 | a0001c0002t0001g0192 a0001c0002t0001g0202 a0001c0002t0001g0203 others(26): Show |
29 | HG00423.hp2 HG00741.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.1166+579C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425632 | |||||||
| chr9:114425634 | G | C | 1 | a0003c0007t0002g0265 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1166+577C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425634 | |||||||
| chr9:114425696 | C | G | 124 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(121): Show |
133 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(130): Show |
intron_variant | MODIFIER | c.1166+515G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425696 | |||||||
| chr9:114425790 | A | G | 1 | a0003c0003t0001g0147 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1166+421T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425790 | |||||||
| chr9:114425826 | G | A | 7 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0007g0316 others(4): Show |
7 | HG02615.hp1 HG02886.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1166+385C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425826 | |||||||
| chr9:114425922 | G | A | 1 | a0002c0001t0001g0035 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1166+289C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425922 | |||||||
| chr9:114425931 | T | C | 4 | a0004c0005t0001g0206 a0004c0005t0001g0210 a0004c0005t0003g0220 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.1166+280A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425931 | |||||||
| chr9:114425986 | T | C | 1 | a0003c0003t0001g0008 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1166+225A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114425986 | |||||||
| chr9:114426116 | G | C | 1 | a0002c0001t0001g0042 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1166+95C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114426116 | |||||||
| chr9:114426168 | T | A | 4 | a0001c0010t0001g0212 a0004c0005t0004g0237 a0016c0017t0004g0235 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1166+43A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114426168 | |||||||
| chr9:114426188 | T | C | 1 | a0005c0011t0001g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1166+23A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 4/11 | chr9 | 114426188 | |||||||
| chr9:114426434 | T | C | 125 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(122): Show |
134 | HG00140.hp2 HG00423.hp2 HG00544.hp2 others(131): Show |
intron_variant | MODIFIER | c.964-21A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114426434 | |||||||
| chr9:114426539 | G | C | 1 | a0001c0006t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-126C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114426539 | |||||||
| chr9:114426579 | C | T | 4 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 others(1): Show |
4 | HG01109.hp1 HG02109.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-166G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114426579 | |||||||
| chr9:114426760 | C | A | 8 | a0001c0010t0001g0075 a0001c0010t0001g0111 a0001c0010t0001g0157 others(5): Show |
9 | HG00323.hp1 HG01070.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-347G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114426760 | |||||||
| chr9:114426913 | G | A | 86 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0004 others(83): Show |
94 | HG00140.hp2 HG00544.hp2 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.964-500C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114426913 | |||||||
| chr9:114427114 | G | A | 20 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0059 others(17): Show |
20 | HG00741.hp1 HG01074.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.964-701C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114427114 | |||||||
| chr9:114427402 | T | G | 3 | a0001c0002t0004g0232 a0001c0008t0002g0284 a0001c0008t0002g0288 |
3 | HG01109.hp1 HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-989A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114427402 | |||||||
| chr9:114427479 | C | T | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.964-1066G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114427479 | |||||||
| chr9:114427779 | G | GAC | 106 | a0001c0008t0002g0303 a0002c0001t0001g0002 a0002c0001t0001g0003 others(103): Show |
115 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.964-1368_964-1367d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114427779 | |||||||
| chr9:114428048 | C | T | 1 | a0005c0011t0001g0007 | 2 | HG00140.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.964-1635G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428048 | |||||||
| chr9:114428050 | A | G | 129 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 others(126): Show |
138 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.964-1637T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428050 | |||||||
| chr9:114428084 | T | C | 32 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.964-1671A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428084 | |||||||
| chr9:114428186 | G | A | 7 | a0001c0002t0001g0068 a0001c0002t0001g0128 a0001c0002t0001g0129 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-1773C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428186 | |||||||
| chr9:114428188 | C | G | 1 | a0003c0003t0001g0057 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.964-1775G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428188 | |||||||
| chr9:114428189 | G | A | 3 | a0001c0002t0001g0061 a0001c0002t0001g0192 a0001c0008t0002g0274 |
3 | HG01891.hp1 HG02055.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.964-1776C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428189 | |||||||
| chr9:114428396 | G | T | 1 | a0001c0008t0002g0274 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.964-1983C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428396 | |||||||
| chr9:114428442 | A | G | 4 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0066 others(1): Show |
4 | HG02280.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-2029T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428442 | |||||||
| chr9:114428469 | A | G | 215 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(212): Show |
218 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.964-2056T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428469 | |||||||
| chr9:114428533 | T | A | 1 | a0001c0010t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.964-2120A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428533 | |||||||
| chr9:114428610 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.964-2197G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428610 | |||||||
| chr9:114428828 | CCT | C | 5 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(2): Show |
5 | HG01192.hp2 HG02809.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-2417_964-2416d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428828 | |||||||
| chr9:114428860 | G | A | 2 | a0004c0018t0001g0094 a0004c0018t0001g0161 |
2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.964-2447C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428860 | |||||||
| chr9:114428876 | C | T | 1 | a0001c0010t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.964-2463G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428876 | |||||||
| chr9:114428931 | CT | C | 293 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(290): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.964-2519delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428931 | |||||||
| chr9:114428931 | CTT | C | 8 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0007g0316 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-2520_964-2519d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114428931 | |||||||
| chr9:114429002 | C | T | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-2589G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429002 | |||||||
| chr9:114429081 | C | T | 73 | a0001c0002t0001g0049 a0001c0008t0002g0303 a0002c0001t0001g0002 others(70): Show |
80 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.964-2668G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429081 | |||||||
| chr9:114429107 | T | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-2694A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429107 | |||||||
| chr9:114429117 | G | C | 4 | a0001c0002t0001g0092 a0004c0005t0001g0006 a0004c0005t0001g0079 others(1): Show |
5 | HG02109.hp2 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-2704C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429117 | |||||||
| chr9:114429169 | G | A | 1 | a0002c0001t0001g0037 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.964-2756C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429169 | |||||||
| chr9:114429176 | G | A | 3 | a0001c0002t0001g0073 a0001c0006t0001g0067 a0004c0019t0001g0064 |
3 | HG01496.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.964-2763C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429176 | |||||||
| chr9:114429177 | C | T | 3 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0011c0033t0001g0085 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.964-2764G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429177 | |||||||
| chr9:114429226 | C | T | 8 | a0003c0003t0001g0066 a0004c0005t0001g0106 a0004c0005t0001g0108 others(5): Show |
8 | HG00423.hp2 HG02698.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-2813G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429226 | |||||||
| chr9:114429233 | T | C | 8 | a0003c0003t0001g0066 a0004c0005t0001g0106 a0004c0005t0001g0108 others(5): Show |
8 | HG00423.hp2 HG02698.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-2820A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429233 | |||||||
| chr9:114429283 | T | G | 1 | a0003c0007t0002g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.964-2870A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429283 | |||||||
| chr9:114429306 | T | C | 1 | a0003c0007t0011g0011 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.964-2893A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429306 | |||||||
| chr9:114429390 | T | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-2977A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429390 | |||||||
| chr9:114429405 | C | A | 1 | a0001c0002t0001g0131 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.964-2992G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429405 | |||||||
| chr9:114429428 | C | A | 3 | a0003c0003t0001g0120 a0003c0003t0001g0124 a0003c0007t0013g0243 |
3 | HG01192.hp1 HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.964-3015G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429428 | |||||||
| chr9:114429438 | G | A | 1 | a0001c0008t0007g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.964-3025C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429438 | |||||||
| chr9:114429487 | C | T | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-3074G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429487 | |||||||
| chr9:114429559 | C | T | 118 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(115): Show |
119 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.964-3146G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429559 | |||||||
| chr9:114429583 | G | A | 3 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0011c0033t0001g0085 |
3 | HG02698.hp1 HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.964-3170C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429583 | |||||||
| chr9:114429598 | G | T | 8 | a0001c0006t0001g0173 a0001c0006t0009g0241 a0001c0006t0009g0242 others(5): Show |
8 | HG00741.hp1 HG01074.hp2 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.964-3185C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429598 | |||||||
| chr9:114429822 | G | A | 2 | a0002c0001t0001g0031 a0002c0001t0001g0055 |
2 | HG01074.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.964-3409C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429822 | |||||||
| chr9:114429913 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-3500G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429913 | |||||||
| chr9:114429950 | A | G | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-3537T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114429950 | |||||||
| chr9:114430091 | T | C | 9 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(6): Show |
9 | HG02145.hp2 HG02257.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.964-3678A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430091 | |||||||
| chr9:114430235 | C | T | 14 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0006t0001g0173 others(11): Show |
14 | HG00741.hp1 HG01074.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.964-3822G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430235 | |||||||
| chr9:114430268 | G | A | 10 | a0001c0002t0001g0182 a0001c0002t0001g0183 a0001c0006t0001g0173 others(7): Show |
10 | HG00741.hp1 HG01074.hp2 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.964-3855C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430268 | |||||||
| chr9:114430281 | G | A | 1 | a0002c0001t0001g0052 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.964-3868C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430281 | |||||||
| chr9:114430320 | T | G | 4 | a0001c0006t0009g0241 a0001c0006t0009g0242 a0013c0020t0001g0139 others(1): Show |
4 | HG02040.hp2 HG02080.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-3907A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430320 | |||||||
| chr9:114430329 | T | G | 2 | a0001c0009t0002g0256 a0001c0009t0002g0257 |
2 | HG01261.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.964-3916A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430329 | |||||||
| chr9:114430378 | T | C | 1 | a0004c0005t0003g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.964-3965A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430378 | |||||||
| chr9:114430563 | T | C | 1 | a0003c0007t0002g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.964-4150A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430563 | |||||||
| chr9:114430690 | T | C | 1 | a0003c0003t0001g0186 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.964-4277A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430690 | |||||||
| chr9:114430756 | G | A | 1 | a0009c0014t0005g0247 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.964-4343C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430756 | |||||||
| chr9:114430926 | G | A | 142 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.964-4513C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114430926 | |||||||
| chr9:114431049 | T | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-4636A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114431049 | |||||||
| chr9:114431480 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-5067G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114431480 | |||||||
| chr9:114431549 | G | A | 1 | a0005c0011t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.964-5136C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114431549 | |||||||
| chr9:114431555 | G | A | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.964-5142C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114431555 | |||||||
| chr9:114431816 | T | C | 1 | a0022c0035t0003g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.964-5403A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114431816 | |||||||
| chr9:114432225 | G | A | 23 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0192 others(20): Show |
23 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.964-5812C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432225 | |||||||
| chr9:114432630 | A | G | 22 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0192 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-6217T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432630 | |||||||
| chr9:114432721 | T | G | 1 | a0002c0001t0001g0179 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.964-6308A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432721 | |||||||
| chr9:114432727 | C | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-6314G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432727 | |||||||
| chr9:114432748 | G | A | 1 | a0001c0002t0001g0051 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.964-6335C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432748 | |||||||
| chr9:114432783 | T | C | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.964-6370A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432783 | |||||||
| chr9:114432918 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-6505G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432918 | |||||||
| chr9:114432919 | G | A | 301 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(298): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.964-6506C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114432919 | |||||||
| chr9:114433016 | T | C | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.964-6603A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433016 | |||||||
| chr9:114433058 | C | T | 1 | a0001c0006t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.964-6645G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433058 | |||||||
| chr9:114433325 | C | T | 156 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0207 others(153): Show |
166 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(163): Show |
intron_variant | MODIFIER | c.964-6912G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433325 | |||||||
| chr9:114433344 | G | A | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.964-6931C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433344 | |||||||
| chr9:114433412 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-6999C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433412 | |||||||
| chr9:114433480 | T | A | 314 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(311): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.964-7067A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433480 | |||||||
| chr9:114433540 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-7127G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433540 | |||||||
| chr9:114433593 | G | GT | 9 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(6): Show |
9 | HG00423.hp2 HG02109.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-7181dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433593 | |||||||
| chr9:114433627 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-7214C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433627 | |||||||
| chr9:114433738 | C | T | 1 | a0009c0014t0005g0244 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.964-7325G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433738 | |||||||
| chr9:114433874 | G | A | 5 | a0004c0005t0004g0234 a0004c0005t0004g0237 a0015c0021t0004g0231 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-7461C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433874 | |||||||
| chr9:114433878 | T | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-7465A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433878 | |||||||
| chr9:114433900 | T | C | 8 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(5): Show |
8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-7487A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433900 | |||||||
| chr9:114433918 | C | T | 3 | a0001c0002t0001g0134 a0001c0009t0002g0256 a0001c0009t0002g0257 |
3 | HG01261.hp1 HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.964-7505G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114433918 | |||||||
| chr9:114434034 | G | A | 301 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(298): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.964-7621C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434034 | |||||||
| chr9:114434141 | A | AC | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-7729dupG | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434141 | |||||||
| chr9:114434230 | T | C | 6 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(3): Show |
6 | HG00423.hp2 HG02698.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-7817A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434230 | |||||||
| chr9:114434349 | C | T | 22 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0192 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-7936G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434349 | |||||||
| chr9:114434428 | TC | T | 8 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(5): Show |
8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-8016delG | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434428 | |||||||
| chr9:114434450 | C | T | 314 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(311): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.964-8037G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434450 | |||||||
| chr9:114434522 | A | ATCTTCTC others(4): Show |
1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-8110_964-8109i others(13): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434522 | |||||||
| chr9:114434523 | C | CCTTCTCC others(4): Show |
308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.964-8111_964-8110i others(13): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434523 | |||||||
| chr9:114434523 | C | T | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-8110G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434523 | |||||||
| chr9:114434687 | T | C | 149 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0207 others(146): Show |
159 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.964-8274A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434687 | |||||||
| chr9:114434855 | C | G | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-8442G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434855 | |||||||
| chr9:114434868 | A | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-8455T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434868 | |||||||
| chr9:114434877 | C | T | 17 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(14): Show |
17 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.964-8464G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434877 | |||||||
| chr9:114434878 | G | A | 3 | a0003c0003t0001g0197 a0003c0003t0006g0238 a0003c0007t0002g0264 |
3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.964-8465C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434878 | |||||||
| chr9:114434931 | T | C | 3 | a0001c0002t0001g0061 a0004c0005t0003g0220 a0014c0023t0004g0233 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.964-8518A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114434931 | |||||||
| chr9:114435146 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-8733G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435146 | |||||||
| chr9:114435213 | C | A | 160 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0207 others(157): Show |
170 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(167): Show |
intron_variant | MODIFIER | c.964-8800G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435213 | |||||||
| chr9:114435446 | G | A | 6 | a0002c0001t0001g0031 a0002c0001t0001g0055 a0002c0001t0001g0112 others(3): Show |
6 | HG00642.hp2 HG01074.hp1 HG02735.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-9033C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435446 | |||||||
| chr9:114435458 | A | C | 7 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(4): Show |
9 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-9045T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435458 | |||||||
| chr9:114435465 | A | G | 3 | a0003c0003t0001g0120 a0003c0003t0001g0124 a0003c0007t0013g0243 |
3 | HG01192.hp1 HG01261.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.964-9052T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435465 | |||||||
| chr9:114435526 | A | G | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-9113T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435526 | |||||||
| chr9:114435686 | A | G | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-9273T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435686 | |||||||
| chr9:114435710 | T | C | 2 | a0001c0002t0001g0051 a0020c0043t0001g0100 |
2 | HG02273.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.964-9297A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435710 | |||||||
| chr9:114435755 | T | A | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0008t0002g0303 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.964-9342A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435755 | |||||||
| chr9:114435768 | G | C | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-9355C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435768 | |||||||
| chr9:114435883 | C | T | 1 | a0001c0002t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.964-9470G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435883 | |||||||
| chr9:114435886 | TTCTAAAA others(3): Show |
T | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0008t0002g0303 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.964-9483_964-9474d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435886 | |||||||
| chr9:114435933 | C | T | 1 | a0004c0005t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.964-9520G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435933 | |||||||
| chr9:114435993 | T | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.964-9580A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114435993 | |||||||
| chr9:114436259 | G | C | 8 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(5): Show |
8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-9846C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436259 | |||||||
| chr9:114436331 | T | A | 8 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(5): Show |
8 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-9918A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436331 | |||||||
| chr9:114436337 | C | T | 1 | a0002c0001t0001g0017 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.964-9924G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436337 | |||||||
| chr9:114436355 | A | G | 8 | a0001c0010t0001g0075 a0001c0010t0001g0111 a0001c0010t0001g0157 others(5): Show |
9 | HG00323.hp1 HG01070.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-9942T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436355 | |||||||
| chr9:114436373 | C | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-9960G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436373 | |||||||
| chr9:114436448 | T | C | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-10035A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436448 | |||||||
| chr9:114436455 | C | T | 1 | a0004c0005t0004g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.964-10042G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436455 | |||||||
| chr9:114436552 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-10139C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436552 | |||||||
| chr9:114436583 | C | T | 1 | a0001c0010t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.964-10170G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436583 | |||||||
| chr9:114436590 | G | C | 22 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0192 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-10177C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436590 | |||||||
| chr9:114436626 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-10213G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436626 | |||||||
| chr9:114436759 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.964-10346C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436759 | |||||||
| chr9:114436790 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-10377G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436790 | |||||||
| chr9:114436913 | T | C | 1 | a0004c0005t0001g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.964-10500A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436913 | |||||||
| chr9:114436967 | C | A | 7 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(4): Show |
7 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-10554G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114436967 | |||||||
| chr9:114437068 | A | G | 7 | a0001c0010t0001g0212 a0004c0005t0001g0211 a0004c0005t0004g0234 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-10655T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437068 | |||||||
| chr9:114437127 | C | T | 2 | a0001c0002t0008g0208 a0008c0030t0002g0292 |
2 | HG01109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.964-10714G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437127 | |||||||
| chr9:114437342 | G | A | 1 | a0002c0001t0001g0189 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.964-10929C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437342 | |||||||
| chr9:114437354 | C | A | 6 | a0001c0002t0001g0020 a0001c0002t0001g0068 a0001c0002t0001g0132 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-10941G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437354 | |||||||
| chr9:114437369 | A | G | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-10956T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437369 | |||||||
| chr9:114437390 | T | C | 1 | a0004c0005t0003g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.964-10977A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437390 | |||||||
| chr9:114437408 | T | C | 1 | a0004c0018t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.964-10995A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437408 | |||||||
| chr9:114437421 | T | C | 9 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0007g0316 others(6): Show |
9 | HG01109.hp2 HG02615.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.964-11008A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437421 | |||||||
| chr9:114437494 | C | T | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.964-11081G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437494 | |||||||
| chr9:114437498 | C | G | 5 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0010g0252 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.964-11085G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437498 | |||||||
| chr9:114437669 | G | A | 301 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(298): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.964-11256C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437669 | |||||||
| chr9:114437773 | T | C | 1 | a0002c0001t0001g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.964-11360A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437773 | |||||||
| chr9:114437799 | T | C | 120 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(117): Show |
121 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.964-11386A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437799 | |||||||
| chr9:114437860 | T | C | 39 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(36): Show |
39 | HG00741.hp1 HG01074.hp2 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.964-11447A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437860 | |||||||
| chr9:114437930 | G | A | 1 | a0003c0007t0013g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.964-11517C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114437930 | |||||||
| chr9:114438092 | A | G | 1 | a0001c0002t0001g0051 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.964-11679T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438092 | |||||||
| chr9:114438187 | A | G | 1 | a0001c0010t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.964-11774T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438187 | |||||||
| chr9:114438197 | A | G | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.964-11784T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438197 | |||||||
| chr9:114438252 | A | G | 22 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0002t0001g0192 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.964-11839T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438252 | |||||||
| chr9:114438310 | G | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-11897C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438310 | |||||||
| chr9:114438341 | A | G | 3 | a0001c0002t0001g0073 a0001c0006t0001g0067 a0004c0019t0001g0064 |
3 | HG01496.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.964-11928T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438341 | |||||||
| chr9:114438403 | T | C | 6 | a0002c0004t0002g0282 a0004c0005t0001g0106 a0004c0005t0001g0108 others(3): Show |
6 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-11990A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438403 | |||||||
| chr9:114438445 | CTTTTTTT others(6): Show |
C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-12045_964-1203 others(17): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438445 | |||||||
| chr9:114438448 | T | C | 1 | a0001c0008t0002g0274 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.964-12035A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438448 | |||||||
| chr9:114438454 | C | T | 1 | a0003c0003t0001g0159 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.964-12041G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438454 | |||||||
| chr9:114438455 | T | C | 1 | a0003c0003t0001g0159 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.964-12042A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438455 | |||||||
| chr9:114438467 | T | G | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-12054A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438467 | |||||||
| chr9:114438694 | G | A | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-12281C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438694 | |||||||
| chr9:114438730 | C | T | 8 | a0001c0010t0001g0075 a0001c0010t0001g0111 a0001c0010t0001g0157 others(5): Show |
9 | HG00323.hp1 HG01070.hp2 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.964-12317G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438730 | |||||||
| chr9:114438742 | C | T | 6 | a0001c0006t0001g0173 a0001c0006t0009g0241 a0001c0006t0009g0242 others(3): Show |
6 | HG02040.hp2 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.964-12329G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114438742 | |||||||
| chr9:114439096 | C | CAA | 306 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(303): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.964-12684_964-1268 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439096 | |||||||
| chr9:114439119 | T | C | 89 | a0001c0002t0001g0049 a0001c0002t0001g0113 a0001c0008t0002g0303 others(86): Show |
98 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.964-12706A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439119 | |||||||
| chr9:114439177 | C | T | 5 | a0005c0011t0001g0007 a0005c0011t0001g0065 a0005c0011t0001g0074 others(2): Show |
6 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-12764G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439177 | |||||||
| chr9:114439178 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.964-12765C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439178 | |||||||
| chr9:114439441 | G | A | 1 | a0002c0004t0002g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.964-13028C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439441 | |||||||
| chr9:114439635 | T | TAC | 170 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(167): Show |
171 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.964-13223_964-1322 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439635 | |||||||
| chr9:114439636 | A | AGATATAT others(15): Show |
3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.964-13245_964-1322 others(26): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439636 | |||||||
| chr9:114439739 | C | A | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.964-13326G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114439739 | |||||||
| chr9:114440115 | G | A | 103 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(100): Show |
113 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.964-13702C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440115 | |||||||
| chr9:114440193 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-13780C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440193 | |||||||
| chr9:114440211 | C | A | 28 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0006t0001g0018 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.964-13798G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440211 | |||||||
| chr9:114440294 | C | T | 7 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(4): Show |
7 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.964-13881G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440294 | |||||||
| chr9:114440357 | G | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-13944C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440357 | |||||||
| chr9:114440482 | G | T | 6 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0003c0003t0001g0057 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-14069C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440482 | |||||||
| chr9:114440536 | C | T | 1 | a0003c0007t0002g0253 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.964-14123G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440536 | |||||||
| chr9:114440539 | C | T | 5 | a0005c0011t0001g0007 a0005c0011t0001g0065 a0005c0011t0001g0074 others(2): Show |
6 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-14126G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440539 | |||||||
| chr9:114440585 | A | G | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-14172T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440585 | |||||||
| chr9:114440721 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964-14308A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440721 | |||||||
| chr9:114440803 | T | C | 1 | a0015c0021t0004g0231 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.964-14390A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440803 | |||||||
| chr9:114440901 | T | C | 6 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(3): Show |
6 | HG01123.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-14488A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114440901 | |||||||
| chr9:114441063 | C | T | 10 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0006t0001g0193 others(7): Show |
10 | HG01109.hp2 HG02257.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.964-14650G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441063 | |||||||
| chr9:114441337 | T | G | 1 | a0002c0004t0002g0305 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.964-14924A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441337 | |||||||
| chr9:114441352 | T | C | 166 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(163): Show |
167 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(164): Show |
intron_variant | MODIFIER | c.964-14939A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441352 | |||||||
| chr9:114441353 | G | A | 1 | a0001c0002t0001g0184 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.964-14940C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441353 | |||||||
| chr9:114441636 | C | G | 1 | a0017c0029t0002g0306 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.964-15223G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441636 | |||||||
| chr9:114441681 | A | G | 103 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(100): Show |
113 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.964-15268T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114441681 | |||||||
| chr9:114442083 | A | G | 121 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.964-15670T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442083 | |||||||
| chr9:114442170 | A | G | 1 | a0002c0004t0002g0308 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.964-15757T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442170 | |||||||
| chr9:114442220 | T | A | 1 | a0001c0009t0002g0261 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.964-15807A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442220 | |||||||
| chr9:114442283 | G | T | 1 | a0003c0003t0001g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.964-15870C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442283 | |||||||
| chr9:114442383 | A | C | 1 | a0001c0010t0001g0111 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.964-15970T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442383 | |||||||
| chr9:114442528 | G | C | 6 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(3): Show |
6 | HG01123.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-16115C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442528 | |||||||
| chr9:114442593 | T | G | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-16180A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442593 | |||||||
| chr9:114442633 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-16220G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442633 | |||||||
| chr9:114442687 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-16274G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442687 | |||||||
| chr9:114442748 | A | G | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-16335T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442748 | |||||||
| chr9:114442764 | A | T | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.964-16351T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442764 | |||||||
| chr9:114442830 | T | A | 6 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0003c0003t0001g0057 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-16417A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114442830 | |||||||
| chr9:114443052 | A | G | 47 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(44): Show |
47 | HG00423.hp2 HG01109.hp2 HG01192.hp2 others(44): Show |
intron_variant | MODIFIER | c.964-16639T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443052 | |||||||
| chr9:114443123 | G | A | 1 | a0023c0041t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.964-16710C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443123 | |||||||
| chr9:114443180 | A | G | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-16767T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443180 | |||||||
| chr9:114443275 | G | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-16862C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443275 | |||||||
| chr9:114443288 | T | C | 124 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(121): Show |
125 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.964-16875A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443288 | |||||||
| chr9:114443309 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.964-16896G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443309 | |||||||
| chr9:114443318 | G | A | 314 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(311): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.964-16905C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443318 | |||||||
| chr9:114443425 | T | A | 164 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(161): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.964-17012A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443425 | |||||||
| chr9:114443429 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-17016G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443429 | |||||||
| chr9:114443473 | G | A | 2 | a0001c0002t0001g0073 a0001c0006t0001g0067 |
2 | HG01496.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.964-17060C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443473 | |||||||
| chr9:114443495 | C | T | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-17082G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443495 | |||||||
| chr9:114443554 | T | A | 1 | a0003c0003t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.964-17141A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443554 | |||||||
| chr9:114443572 | G | A | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-17159C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443572 | |||||||
| chr9:114443798 | ACTGCTGA others(7906): Show |
A | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+14556_964-1738 others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443798 | |||||||
| chr9:114443871 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-17458C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443871 | |||||||
| chr9:114443914 | G | A | 2 | a0001c0010t0001g0096 a0001c0012t0002g0276 |
2 | HG01981.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.964-17501C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443914 | |||||||
| chr9:114443983 | G | A | 305 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(302): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.964-17570C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114443983 | |||||||
| chr9:114444000 | C | T | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-17587G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444000 | |||||||
| chr9:114444038 | G | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-17625C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444038 | |||||||
| chr9:114444072 | G | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-17659C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444072 | |||||||
| chr9:114444133 | T | C | 3 | a0002c0004t0002g0001 a0002c0004t0002g0271 a0002c0004t0002g0272 |
6 | NA18952.hp2 NA18954.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.964-17720A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444133 | |||||||
| chr9:114444338 | C | T | 10 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(7): Show |
10 | HG00280.hp1 HG01261.hp1 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.964-17925G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444338 | |||||||
| chr9:114444367 | T | A | 1 | a0005c0011t0001g0065 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.964-17954A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444367 | |||||||
| chr9:114444557 | C | T | 1 | a0001c0008t0002g0284 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.964-18144G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444557 | |||||||
| chr9:114444579 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-18166G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444579 | |||||||
| chr9:114444745 | A | G | 1 | a0001c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.964-18332T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114444745 | |||||||
| chr9:114445022 | C | T | 3 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0021c0038t0005g0245 |
3 | HG02109.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.964-18609G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445022 | |||||||
| chr9:114445037 | G | GTTATTAT others(5): Show |
1 | a0001c0006t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.964-18636_964-1862 others(16): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445037 | |||||||
| chr9:114445037 | G | GTTATTAT others(8): Show |
2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-18639_964-1862 others(19): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445037 | |||||||
| chr9:114445083 | C | T | 2 | a0001c0002t0001g0056 a0001c0008t0002g0297 |
2 | HG02027.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.964-18670G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445083 | |||||||
| chr9:114445115 | C | T | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-18702G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445115 | |||||||
| chr9:114445238 | C | T | 1 | a0001c0006t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.964-18825G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445238 | |||||||
| chr9:114445391 | G | C | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0004c0005t0001g0106 others(5): Show |
8 | HG00423.hp2 HG02109.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.964-18978C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445391 | |||||||
| chr9:114445425 | T | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.964-19012A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445425 | |||||||
| chr9:114445531 | AT | A | 3 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0021c0038t0005g0245 |
3 | HG02109.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.964-19119delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445531 | |||||||
| chr9:114445536 | G | A | 3 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0021c0038t0005g0245 |
3 | HG02109.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.964-19123C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445536 | |||||||
| chr9:114445537 | A | C | 3 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0021c0038t0005g0245 |
3 | HG02109.hp1 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.964-19124T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445537 | |||||||
| chr9:114445595 | C | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.964-19182G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445595 | |||||||
| chr9:114445637 | G | T | 4 | a0002c0001t0001g0189 a0003c0003t0001g0122 a0003c0003t0001g0143 others(1): Show |
4 | NA18956.hp1 NA18966.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.964-19224C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445637 | |||||||
| chr9:114445681 | G | A | 36 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(33): Show |
36 | HG00408.hp2 HG00544.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.964-19268C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445681 | |||||||
| chr9:114445721 | C | T | 1 | a0002c0001t0001g0005 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.964-19308G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114445721 | |||||||
| chr9:114446247 | G | A | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-19834C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446247 | |||||||
| chr9:114446353 | T | TG | 40 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(37): Show |
40 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.963+19913dupC | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446353 | |||||||
| chr9:114446509 | A | G | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+19758T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446509 | |||||||
| chr9:114446556 | G | C | 1 | a0004c0005t0003g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.963+19711C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446556 | |||||||
| chr9:114446687 | G | A | 1 | a0002c0001t0001g0012 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.963+19580C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446687 | |||||||
| chr9:114446705 | G | A | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.963+19562C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446705 | |||||||
| chr9:114446727 | C | T | 1 | a0022c0035t0003g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963+19540G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446727 | |||||||
| chr9:114446831 | C | T | 1 | a0002c0004t0002g0298 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.963+19436G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446831 | |||||||
| chr9:114446919 | C | T | 1 | a0005c0011t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.963+19348G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446919 | |||||||
| chr9:114446951 | C | T | 121 | a0001c0002t0001g0020 a0001c0002t0001g0039 a0001c0002t0001g0061 others(118): Show |
122 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.963+19316G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446951 | |||||||
| chr9:114446957 | T | C | 302 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(299): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.963+19310A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446957 | |||||||
| chr9:114446981 | A | G | 38 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0006t0001g0018 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.963+19286T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114446981 | |||||||
| chr9:114447007 | T | C | 2 | a0001c0002t0001g0156 a0002c0001t0001g0104 |
2 | NA18939.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.963+19260A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447007 | |||||||
| chr9:114447424 | T | C | 6 | a0002c0001t0001g0035 a0002c0001t0001g0036 a0002c0001t0001g0037 others(3): Show |
6 | HG02027.hp2 NA18939.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+18843A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447424 | |||||||
| chr9:114447448 | G | A | 37 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(34): Show |
37 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+18819C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447448 | |||||||
| chr9:114447450 | A | T | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.963+18817T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447450 | |||||||
| chr9:114447464 | A | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+18803T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447464 | |||||||
| chr9:114447560 | T | C | 1 | a0002c0004t0002g0296 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.963+18707A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447560 | |||||||
| chr9:114447655 | T | C | 3 | a0004c0005t0004g0237 a0016c0017t0004g0235 a0016c0017t0004g0236 |
3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.963+18612A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447655 | |||||||
| chr9:114447690 | G | A | 2 | a0001c0002t0001g0109 a0003c0003t0001g0154 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.963+18577C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447690 | |||||||
| chr9:114447697 | C | T | 5 | a0004c0005t0001g0106 a0004c0005t0001g0108 a0004c0005t0001g0176 others(2): Show |
5 | HG00423.hp2 HG02698.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+18570G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447697 | |||||||
| chr9:114447738 | C | A | 1 | a0003c0007t0002g0295 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.963+18529G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447738 | |||||||
| chr9:114447760 | TTCTC | T | 198 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(195): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.963+18503_963+1850 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447760 | |||||||
| chr9:114447782 | GTCTC | G | 4 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(1): Show |
4 | HG01192.hp2 HG01891.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.963+18481_963+1848 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447782 | |||||||
| chr9:114447864 | T | C | 5 | a0001c0010t0003g0222 a0001c0010t0003g0223 a0001c0010t0003g0224 others(2): Show |
5 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+18403A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447864 | |||||||
| chr9:114447999 | C | T | 1 | a0002c0001t0001g0032 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.963+18268G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114447999 | |||||||
| chr9:114448038 | C | T | 263 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(260): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.963+18229G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448038 | |||||||
| chr9:114448151 | A | C | 1 | a0001c0002t0001g0028 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.963+18116T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448151 | |||||||
| chr9:114448303 | C | T | 2 | a0001c0002t0001g0039 a0001c0002t0001g0123 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.963+17964G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448303 | |||||||
| chr9:114448362 | G | A | 2 | a0008c0016t0001g0009 a0008c0016t0001g0194 |
3 | HG02559.hp2 HG03041.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.963+17905C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448362 | |||||||
| chr9:114448438 | G | A | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+17829C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448438 | |||||||
| chr9:114448540 | A | G | 1 | a0001c0002t0001g0127 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.963+17727T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448540 | |||||||
| chr9:114448730 | C | G | 1 | a0002c0001t0012g0054 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.963+17537G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114448730 | |||||||
| chr9:114449389 | A | G | 1 | a0001c0002t0001g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.963+16878T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449389 | |||||||
| chr9:114449443 | C | T | 1 | a0001c0012t0002g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.963+16824G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449443 | |||||||
| chr9:114449448 | C | A | 1 | a0002c0001t0001g0002 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.963+16819G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449448 | |||||||
| chr9:114449488 | G | A | 100 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(97): Show |
110 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.963+16779C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449488 | |||||||
| chr9:114449512 | G | T | 1 | a0004c0005t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.963+16755C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449512 | |||||||
| chr9:114449582 | G | T | 1 | a0002c0001t0001g0034 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.963+16685C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449582 | |||||||
| chr9:114449692 | G | C | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.963+16575C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449692 | |||||||
| chr9:114449733 | C | G | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.963+16534G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449733 | |||||||
| chr9:114449807 | C | A | 145 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(142): Show |
155 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.963+16460G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449807 | |||||||
| chr9:114449907 | A | G | 1 | a0023c0041t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.963+16360T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449907 | |||||||
| chr9:114449927 | T | C | 102 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(99): Show |
112 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.963+16340A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114449927 | |||||||
| chr9:114450082 | T | C | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.963+16185A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450082 | |||||||
| chr9:114450436 | T | C | 107 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(104): Show |
117 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.963+15831A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450436 | |||||||
| chr9:114450641 | G | C | 2 | a0003c0003t0001g0008 a0003c0003t0001g0090 |
3 | HG01069.hp2 HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.963+15626C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450641 | |||||||
| chr9:114450686 | A | C | 173 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(170): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.963+15581T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450686 | |||||||
| chr9:114450776 | C | A | 1 | a0024c0044t0001g0219 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.963+15491G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450776 | |||||||
| chr9:114450823 | G | GA | 9 | a0005c0011t0001g0007 a0005c0011t0001g0065 a0005c0011t0001g0074 others(6): Show |
10 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(7): Show |
intron_variant | MODIFIER | c.963+15443_963+1544 others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450823 | |||||||
| chr9:114450825 | T | TC | 24 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0006t0001g0062 others(21): Show |
24 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.963+15441_963+1544 others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450825 | |||||||
| chr9:114450826 | T | C | 47 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(44): Show |
48 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.963+15441A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450826 | |||||||
| chr9:114450826 | T | TC | 93 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(90): Show |
101 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.963+15440dupG | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450826 | |||||||
| chr9:114450834 | C | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.963+15433G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450834 | |||||||
| chr9:114450834 | C | CA | 8 | a0001c0002t0008g0199 a0001c0002t0008g0208 a0001c0008t0007g0316 others(5): Show |
8 | HG01109.hp2 HG02615.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+15432_963+1543 others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450834 | |||||||
| chr9:114450835 | G | A | 33 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(30): Show |
33 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.963+15432C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450835 | |||||||
| chr9:114450835 | G | C | 5 | a0001c0006t0001g0071 a0001c0006t0001g0072 a0004c0026t0002g0273 others(2): Show |
5 | HG02258.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+15432C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450835 | |||||||
| chr9:114450836 | C | A | 33 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(30): Show |
33 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.963+15431G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114450836 | |||||||
| chr9:114451278 | A | G | 302 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(299): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.963+14989T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451278 | |||||||
| chr9:114451284 | G | C | 302 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(299): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.963+14983C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451284 | |||||||
| chr9:114451548 | T | C | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+14719A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451548 | |||||||
| chr9:114451655 | C | T | 98 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(95): Show |
108 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.963+14612G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451655 | |||||||
| chr9:114451661 | C | T | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+14606G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451661 | |||||||
| chr9:114451674 | C | T | 1 | a0003c0007t0013g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.963+14593G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114451674 | |||||||
| chr9:114452049 | A | G | 6 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(3): Show |
6 | HG01123.hp1 HG02622.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+14218T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452049 | |||||||
| chr9:114452099 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+14168G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452099 | |||||||
| chr9:114452133 | T | A | 137 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(134): Show |
147 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(144): Show |
intron_variant | MODIFIER | c.963+14134A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452133 | |||||||
| chr9:114452165 | G | A | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.963+14102C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452165 | |||||||
| chr9:114452312 | T | G | 98 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(95): Show |
108 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.963+13955A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452312 | |||||||
| chr9:114452483 | G | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+13784C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452483 | |||||||
| chr9:114452540 | A | G | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.963+13727T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452540 | |||||||
| chr9:114452629 | C | A | 171 | a0001c0002t0001g0049 a0001c0002t0001g0073 a0001c0002t0001g0092 others(168): Show |
181 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.963+13638G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452629 | |||||||
| chr9:114452833 | C | T | 1 | a0001c0010t0003g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.963+13434G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452833 | |||||||
| chr9:114452847 | G | A | 1 | a0001c0002t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.963+13420C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452847 | |||||||
| chr9:114452848 | G | A | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+13419C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114452848 | |||||||
| chr9:114453135 | G | A | 8 | a0001c0006t0001g0173 a0001c0006t0009g0241 a0001c0006t0009g0242 others(5): Show |
8 | HG02040.hp2 HG02080.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+13132C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114453135 | |||||||
| chr9:114453630 | AT | A | 3 | a0001c0006t0001g0071 a0001c0006t0001g0072 a0004c0026t0002g0273 |
3 | HG02258.hp1 HG02572.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.963+12636delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114453630 | |||||||
| chr9:114453725 | T | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+12542A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114453725 | |||||||
| chr9:114453769 | A | C | 1 | a0023c0041t0001g0015 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.963+12498T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114453769 | |||||||
| chr9:114454031 | C | T | 1 | a0005c0011t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.963+12236G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454031 | |||||||
| chr9:114454083 | A | C | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.963+12184T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454083 | |||||||
| chr9:114454092 | G | T | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+12175C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454092 | |||||||
| chr9:114454110 | G | C | 274 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.963+12157C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454110 | |||||||
| chr9:114454212 | A | G | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+12055T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454212 | |||||||
| chr9:114454306 | A | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11961T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454306 | |||||||
| chr9:114454345 | C | CAA | 274 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.963+11921_963+1192 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454345 | |||||||
| chr9:114454539 | T | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11728A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454539 | |||||||
| chr9:114454592 | A | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11675T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454592 | |||||||
| chr9:114454611 | G | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11656C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454611 | |||||||
| chr9:114454631 | A | C | 2 | a0001c0002t0001g0056 a0001c0008t0002g0297 |
2 | HG02027.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.963+11636T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454631 | |||||||
| chr9:114454652 | T | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.963+11615A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454652 | |||||||
| chr9:114454685 | A | AT | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+11581dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454685 | |||||||
| chr9:114454687 | A | AT | 41 | a0001c0002t0001g0192 a0001c0002t0001g0207 a0001c0002t0003g0228 others(38): Show |
41 | HG00423.hp2 HG01109.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.963+11579dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454687 | |||||||
| chr9:114454687 | A | T | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+11580T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454687 | |||||||
| chr9:114454866 | G | A | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11401C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454866 | |||||||
| chr9:114454867 | T | C | 1 | a0003c0007t0002g0255 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.963+11400A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454867 | |||||||
| chr9:114454885 | T | C | 1 | a0003c0003t0001g0163 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.963+11382A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454885 | |||||||
| chr9:114454916 | C | A | 7 | a0001c0010t0001g0075 a0001c0010t0001g0111 a0001c0012t0002g0010 others(4): Show |
8 | HG00323.hp1 HG01070.hp2 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.963+11351G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454916 | |||||||
| chr9:114454960 | T | A | 274 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.963+11307A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454960 | |||||||
| chr9:114454975 | A | T | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+11292T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454975 | |||||||
| chr9:114454997 | G | A | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11270C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114454997 | |||||||
| chr9:114455006 | TA | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11260delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455006 | |||||||
| chr9:114455046 | G | A | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+11221C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455046 | |||||||
| chr9:114455163 | T | C | 7 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+11104A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455163 | |||||||
| chr9:114455172 | TAG | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+11093_963+1109 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455172 | |||||||
| chr9:114455201 | T | G | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.963+11066A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455201 | |||||||
| chr9:114455215 | T | TTTTG | 270 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(267): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.963+11048_963+1105 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455215 | |||||||
| chr9:114455348 | G | A | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+10919C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455348 | |||||||
| chr9:114455355 | T | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+10912A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455355 | |||||||
| chr9:114455436 | T | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+10831A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455436 | |||||||
| chr9:114455515 | A | G | 3 | a0001c0002t0001g0061 a0004c0005t0003g0220 a0014c0023t0004g0233 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.963+10752T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455515 | |||||||
| chr9:114455581 | G | A | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+10686C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455581 | |||||||
| chr9:114455643 | G | A | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+10624C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455643 | |||||||
| chr9:114455658 | A | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+10609T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455658 | |||||||
| chr9:114455713 | C | CA | 7 | a0003c0003t0001g0076 a0003c0003t0001g0077 a0003c0003t0001g0078 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+10553dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455713 | |||||||
| chr9:114455713 | CA | C | 129 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(126): Show |
130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.963+10553delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455713 | |||||||
| chr9:114455713 | CAA | C | 44 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(41): Show |
44 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.963+10552_963+1055 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455713 | |||||||
| chr9:114455713 | CAAA | C | 92 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(89): Show |
102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.963+10551_963+1055 others(7): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455713 | |||||||
| chr9:114455873 | A | C | 1 | a0003c0003t0001g0145 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.963+10394T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455873 | |||||||
| chr9:114455894 | T | C | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.963+10373A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455894 | |||||||
| chr9:114455972 | T | C | 22 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0006t0001g0018 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.963+10295A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114455972 | |||||||
| chr9:114456123 | TAA | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+10142_963+1014 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456123 | |||||||
| chr9:114456151 | A | AAAC | 263 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(260): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.963+10115_963+1011 others(7): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456151 | |||||||
| chr9:114456179 | A | G | 1 | a0012c0022t0004g0230 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.963+10088T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456179 | |||||||
| chr9:114456320 | A | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+9947T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456320 | |||||||
| chr9:114456331 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+9936G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456331 | |||||||
| chr9:114456372 | C | T | 1 | a0006c0013t0001g0043 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.963+9895G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456372 | |||||||
| chr9:114456404 | TA | T | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+9862delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456404 | |||||||
| chr9:114456406 | GA | G | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+9860delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456406 | |||||||
| chr9:114456407 | A | G | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+9860T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456407 | |||||||
| chr9:114456429 | G | A | 1 | a0006c0013t0001g0140 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.963+9838C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456429 | |||||||
| chr9:114456478 | A | G | 1 | a0004c0005t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.963+9789T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456478 | |||||||
| chr9:114456479 | G | T | 1 | a0004c0005t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.963+9788C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456479 | |||||||
| chr9:114456480 | A | C | 1 | a0004c0005t0001g0176 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.963+9787T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456480 | |||||||
| chr9:114456506 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+9761G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456506 | |||||||
| chr9:114456528 | A | C | 267 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(264): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.963+9739T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456528 | |||||||
| chr9:114456537 | T | C | 3 | a0002c0001t0001g0036 a0002c0001t0001g0037 a0002c0001t0001g0041 |
3 | NA18939.hp2 NA18979.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.963+9730A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456537 | |||||||
| chr9:114456539 | G | A | 3 | a0001c0002t0001g0134 a0001c0009t0002g0256 a0001c0009t0002g0257 |
3 | HG01261.hp1 HG01433.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.963+9728C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456539 | |||||||
| chr9:114456565 | C | T | 2 | a0001c0010t0001g0157 a0001c0012t0002g0268 |
2 | HG02486.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.963+9702G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456565 | |||||||
| chr9:114456602 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+9665G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456602 | |||||||
| chr9:114456621 | A | C | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+9646T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456621 | |||||||
| chr9:114456640 | C | T | 5 | a0001c0002t0001g0061 a0004c0005t0001g0176 a0004c0005t0003g0220 others(2): Show |
5 | HG00423.hp2 HG02055.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.963+9627G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456640 | |||||||
| chr9:114456743 | C | T | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+9524G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456743 | |||||||
| chr9:114456747 | T | C | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+9520A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456747 | |||||||
| chr9:114456826 | C | CA | 19 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.963+9440dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456826 | |||||||
| chr9:114456826 | CAA | C | 270 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(267): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.963+9439_963+9440d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456826 | |||||||
| chr9:114456994 | A | G | 2 | a0003c0003t0001g0019 a0003c0007t0002g0275 |
2 | HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.963+9273T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114456994 | |||||||
| chr9:114457389 | T | C | 1 | a0003c0003t0001g0162 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.963+8878A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457389 | |||||||
| chr9:114457440 | C | T | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+8827G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457440 | |||||||
| chr9:114457608 | T | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+8659A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457608 | |||||||
| chr9:114457720 | C | A | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+8547G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457720 | |||||||
| chr9:114457723 | C | T | 170 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(167): Show |
171 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.963+8544G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457723 | |||||||
| chr9:114457730 | A | G | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+8537T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457730 | |||||||
| chr9:114457731 | C | T | 95 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(92): Show |
105 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.963+8536G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457731 | |||||||
| chr9:114457809 | G | A | 1 | a0007c0025t0002g0302 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.963+8458C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457809 | |||||||
| chr9:114457865 | A | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+8402T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457865 | |||||||
| chr9:114457883 | T | C | 1 | a0022c0035t0003g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.963+8384A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457883 | |||||||
| chr9:114457914 | C | G | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+8353G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457914 | |||||||
| chr9:114457914 | CA | C | 255 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(252): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.963+8352delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457914 | |||||||
| chr9:114457914 | CAA | C | 9 | a0001c0002t0001g0183 a0001c0012t0002g0286 a0002c0001t0001g0048 others(6): Show |
9 | HG01070.hp2 HG01516.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.963+8351_963+8352d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457914 | |||||||
| chr9:114457939 | T | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.963+8328A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457939 | |||||||
| chr9:114457967 | T | G | 1 | a0005c0011t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.963+8300A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114457967 | |||||||
| chr9:114458048 | T | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+8219A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458048 | |||||||
| chr9:114458152 | G | A | 3 | a0002c0004t0002g0283 a0002c0004t0002g0289 a0002c0004t0002g0290 |
3 | HG02896.hp1 HG02897.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.963+8115C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458152 | |||||||
| chr9:114458357 | T | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+7910A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458357 | |||||||
| chr9:114458467 | C | T | 2 | a0004c0005t0001g0176 a0011c0034t0001g0087 |
2 | HG00423.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.963+7800G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458467 | |||||||
| chr9:114458493 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+7774G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458493 | |||||||
| chr9:114458702 | G | A | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.963+7565C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458702 | |||||||
| chr9:114458729 | C | T | 2 | a0002c0001t0001g0030 a0003c0003t0001g0122 |
2 | NA18949.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.963+7538G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458729 | |||||||
| chr9:114458849 | C | T | 3 | a0001c0002t0001g0073 a0001c0006t0001g0067 a0004c0019t0001g0064 |
3 | HG01496.hp2 HG03209.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.963+7418G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458849 | |||||||
| chr9:114458929 | G | A | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+7338C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114458929 | |||||||
| chr9:114459079 | A | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+7188T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459079 | |||||||
| chr9:114459135 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+7132G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459135 | |||||||
| chr9:114459303 | C | CA | 10 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0002c0001t0001g0026 others(7): Show |
10 | HG01123.hp1 HG02109.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.963+6963dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459303 | |||||||
| chr9:114459303 | C | CAA | 262 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(259): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.963+6962_963+6963d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459303 | |||||||
| chr9:114459409 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0003g0228 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.963+6858C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459409 | |||||||
| chr9:114459461 | T | TA | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+6805dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459461 | |||||||
| chr9:114459548 | A | G | 1 | a0014c0023t0004g0233 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.963+6719T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459548 | |||||||
| chr9:114459584 | A | G | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+6683T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459584 | |||||||
| chr9:114459617 | C | A | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+6650G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459617 | |||||||
| chr9:114459707 | G | A | 1 | a0005c0011t0001g0086 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.963+6560C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459707 | |||||||
| chr9:114459763 | C | T | 1 | a0004c0005t0001g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963+6504G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459763 | |||||||
| chr9:114459904 | T | G | 1 | a0001c0010t0001g0212 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.963+6363A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459904 | |||||||
| chr9:114459950 | A | G | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+6317T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114459950 | |||||||
| chr9:114460007 | G | A | 142 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(139): Show |
152 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.963+6260C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460007 | |||||||
| chr9:114460091 | G | A | 2 | a0002c0001t0001g0038 a0024c0044t0001g0219 |
2 | NA19006.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.963+6176C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460091 | |||||||
| chr9:114460108 | C | T | 6 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(3): Show |
6 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+6159G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460108 | |||||||
| chr9:114460289 | C | T | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+5978G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460289 | |||||||
| chr9:114460301 | T | G | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+5966A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460301 | |||||||
| chr9:114460395 | G | A | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+5872C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460395 | |||||||
| chr9:114460433 | T | G | 1 | a0004c0005t0001g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.963+5834A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460433 | |||||||
| chr9:114460465 | C | T | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.963+5802G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460465 | |||||||
| chr9:114460504 | G | A | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+5763C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460504 | |||||||
| chr9:114460797 | C | A | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.963+5470G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114460797 | |||||||
| chr9:114461030 | T | C | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+5237A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461030 | |||||||
| chr9:114461082 | C | T | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+5185G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461082 | |||||||
| chr9:114461149 | C | A | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+5118G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461149 | |||||||
| chr9:114461157 | C | T | 266 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(263): Show |
277 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.963+5110G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461157 | |||||||
| chr9:114461188 | C | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+5079G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461188 | |||||||
| chr9:114461334 | G | A | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.963+4933C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461334 | |||||||
| chr9:114461442 | A | G | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+4825T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461442 | |||||||
| chr9:114461484 | C | T | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+4783G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461484 | |||||||
| chr9:114461528 | A | G | 276 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(273): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.963+4739T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461528 | |||||||
| chr9:114461640 | G | C | 6 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(3): Show |
6 | HG02257.hp2 HG02258.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.963+4627C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461640 | |||||||
| chr9:114461669 | G | A | 1 | a0001c0012t0002g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.963+4598C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461669 | |||||||
| chr9:114461718 | T | G | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+4549A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461718 | |||||||
| chr9:114461727 | A | G | 20 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0006t0001g0018 others(17): Show |
20 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(17): Show |
intron_variant | MODIFIER | c.963+4540T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461727 | |||||||
| chr9:114461772 | T | G | 273 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(270): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.963+4495A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461772 | |||||||
| chr9:114461816 | C | T | 30 | a0001c0002t0001g0073 a0001c0002t0001g0134 a0001c0006t0001g0018 others(27): Show |
30 | HG00280.hp1 HG00323.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.963+4451G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114461816 | |||||||
| chr9:114462335 | T | C | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.963+3932A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462335 | |||||||
| chr9:114462398 | G | A | 1 | a0014c0023t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.963+3869C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462398 | |||||||
| chr9:114462405 | A | C | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3862T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462405 | |||||||
| chr9:114462447 | G | A | 38 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(35): Show |
38 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.963+3820C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462447 | |||||||
| chr9:114462477 | G | A | 94 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(91): Show |
104 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.963+3790C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462477 | |||||||
| chr9:114462501 | A | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+3766T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462501 | |||||||
| chr9:114462526 | C | T | 1 | a0003c0003t0001g0143 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.963+3741G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462526 | |||||||
| chr9:114462579 | G | A | 13 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(10): Show |
18 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(15): Show |
intron_variant | MODIFIER | c.963+3688C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462579 | |||||||
| chr9:114462626 | T | C | 133 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(130): Show |
134 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.963+3641A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462626 | |||||||
| chr9:114462633 | T | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+3634A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462633 | |||||||
| chr9:114462650 | T | C | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+3617A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462650 | |||||||
| chr9:114462682 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0003g0228 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.963+3585C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462682 | |||||||
| chr9:114462741 | T | C | 8 | a0001c0006t0001g0173 a0001c0006t0009g0241 a0001c0006t0009g0242 others(5): Show |
8 | HG02040.hp2 HG02080.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.963+3526A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462741 | |||||||
| chr9:114462880 | A | C | 39 | a0001c0002t0001g0192 a0001c0002t0001g0207 a0001c0002t0003g0228 others(36): Show |
39 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(36): Show |
intron_variant | MODIFIER | c.963+3387T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462880 | |||||||
| chr9:114462893 | A | C | 1 | a0003c0003t0001g0175 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.963+3374T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462893 | |||||||
| chr9:114462917 | T | G | 5 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0003c0003t0001g0066 others(2): Show |
5 | HG02109.hp1 HG02818.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+3350A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462917 | |||||||
| chr9:114462951 | G | T | 271 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(268): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.963+3316C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114462951 | |||||||
| chr9:114463144 | C | T | 1 | a0001c0010t0003g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.963+3123G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463144 | |||||||
| chr9:114463249 | C | G | 1 | a0006c0013t0001g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.963+3018G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463249 | |||||||
| chr9:114463265 | C | T | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+3002G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463265 | |||||||
| chr9:114463378 | C | T | 4 | a0005c0011t0001g0007 a0005c0011t0001g0074 a0005c0011t0001g0135 others(1): Show |
5 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+2889G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463378 | |||||||
| chr9:114463426 | T | C | 3 | a0001c0002t0001g0061 a0004c0005t0003g0220 a0014c0023t0004g0233 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.963+2841A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463426 | |||||||
| chr9:114463533 | A | G | 1 | a0006c0013t0001g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.963+2734T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463533 | |||||||
| chr9:114463600 | C | T | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.963+2667G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463600 | |||||||
| chr9:114463618 | A | G | 7 | a0001c0010t0001g0212 a0004c0005t0001g0211 a0004c0005t0004g0234 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+2649T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463618 | |||||||
| chr9:114463774 | T | C | 1 | a0002c0004t0002g0312 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.963+2493A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463774 | |||||||
| chr9:114463876 | G | A | 1 | a0003c0007t0002g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.963+2391C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114463876 | |||||||
| chr9:114464000 | A | T | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.963+2267T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464000 | |||||||
| chr9:114464081 | C | T | 1 | a0001c0006t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.963+2186G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464081 | |||||||
| chr9:114464173 | C | T | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.963+2094G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464173 | |||||||
| chr9:114464319 | C | T | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.963+1948G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464319 | |||||||
| chr9:114464353 | A | G | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+1914T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464353 | |||||||
| chr9:114464605 | A | G | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.963+1662T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464605 | |||||||
| chr9:114464656 | G | T | 19 | a0001c0002t0001g0134 a0001c0006t0001g0018 a0001c0006t0001g0046 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.963+1611C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464656 | |||||||
| chr9:114464739 | A | G | 2 | a0004c0005t0001g0106 a0004c0005t0001g0108 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.963+1528T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464739 | |||||||
| chr9:114464786 | G | A | 1 | a0001c0002t0001g0192 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.963+1481C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464786 | |||||||
| chr9:114464813 | CATAATGA others(11): Show |
C | 2 | a0004c0018t0001g0094 a0004c0018t0001g0161 |
2 | HG00741.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.963+1436_963+1453d others(20): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464813 | |||||||
| chr9:114464813 | CATAATGA others(20): Show |
C | 37 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(34): Show |
37 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+1427_963+1453d others(29): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464813 | |||||||
| chr9:114464816 | AATG | A | 20 | a0001c0002t0001g0073 a0001c0002t0001g0125 a0001c0006t0001g0067 others(17): Show |
21 | HG01123.hp1 HG01175.hp2 HG01496.hp2 others(18): Show |
intron_variant | MODIFIER | c.963+1448_963+1450d others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464816 | AATGATG | A | 106 | a0001c0002t0001g0020 a0001c0002t0001g0039 a0001c0002t0001g0061 others(103): Show |
106 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.963+1445_963+1450d others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464816 | AATGATGA others(2): Show |
A | 69 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(66): Show |
71 | HG00408.hp2 HG00544.hp1 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.963+1442_963+1450d others(11): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464816 | AATGATGA others(5): Show |
A | 68 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(65): Show |
76 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.963+1439_963+1450d others(14): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464816 | AATGATGA others(8): Show |
A | 7 | a0001c0010t0001g0212 a0004c0005t0001g0211 a0004c0005t0004g0234 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+1436_963+1450d others(17): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464816 | AATGATGA others(11): Show |
A | 2 | a0001c0002t0001g0160 a0021c0038t0005g0245 |
2 | HG02970.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.963+1433_963+1450d others(20): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464816 | |||||||
| chr9:114464854 | TGATGATG others(8): Show |
T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+1398_963+1412d others(17): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464854 | |||||||
| chr9:114464866 | TGTC | T | 37 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(34): Show |
37 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(34): Show |
intron_variant | MODIFIER | c.963+1398_963+1400d others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114464866 | |||||||
| chr9:114465028 | C | T | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+1239G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465028 | |||||||
| chr9:114465123 | C | G | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.963+1144G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465123 | |||||||
| chr9:114465183 | A | T | 4 | a0001c0012t0002g0010 a0001c0012t0002g0277 a0001c0012t0002g0278 others(1): Show |
5 | HG01070.hp2 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.963+1084T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465183 | |||||||
| chr9:114465201 | C | G | 173 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(170): Show |
174 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.963+1066G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465201 | |||||||
| chr9:114465593 | A | G | 274 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.963+674T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465593 | |||||||
| chr9:114465597 | T | C | 274 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(271): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.963+670A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465597 | |||||||
| chr9:114465701 | A | G | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.963+566T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465701 | |||||||
| chr9:114465800 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0123 |
2 | HG03017.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.963+467C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465800 | |||||||
| chr9:114465835 | T | C | 81 | a0001c0002t0001g0049 a0001c0002t0001g0113 a0001c0006t0001g0091 others(78): Show |
90 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.963+432A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465835 | |||||||
| chr9:114465952 | C | G | 7 | a0001c0010t0001g0212 a0004c0005t0001g0211 a0004c0005t0004g0234 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+315G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465952 | |||||||
| chr9:114465953 | A | T | 7 | a0001c0010t0001g0212 a0004c0005t0001g0211 a0004c0005t0004g0234 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.963+314T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465953 | |||||||
| chr9:114465965 | T | A | 1 | a0003c0003t0001g0077 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.963+302A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114465965 | |||||||
| chr9:114466061 | C | T | 128 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(125): Show |
129 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.963+206G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 3/11 | chr9 | 114466061 | |||||||
| chr9:114466440 | T | G | 2 | a0001c0002t0001g0207 a0001c0002t0003g0228 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.838-48A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466440 | |||||||
| chr9:114466545 | T | G | 1 | a0006c0013t0001g0174 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.838-153A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466545 | |||||||
| chr9:114466704 | C | A | 1 | a0001c0008t0002g0274 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838-312G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466704 | |||||||
| chr9:114466756 | C | T | 1 | a0002c0001t0001g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.838-364G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466756 | |||||||
| chr9:114466771 | C | T | 1 | a0002c0001t0001g0040 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.838-379G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466771 | |||||||
| chr9:114466772 | G | A | 1 | a0001c0006t0001g0071 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.838-380C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466772 | |||||||
| chr9:114466778 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.838-386G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466778 | |||||||
| chr9:114466788 | A | G | 236 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(233): Show |
247 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.838-396T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466788 | |||||||
| chr9:114466936 | G | T | 3 | a0003c0003t0001g0197 a0003c0003t0006g0238 a0003c0007t0002g0264 |
3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.838-544C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466936 | |||||||
| chr9:114466979 | T | G | 6 | a0001c0002t0001g0045 a0001c0006t0001g0173 a0001c0006t0009g0241 others(3): Show |
6 | HG02040.hp2 HG02080.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.838-587A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114466979 | |||||||
| chr9:114467120 | T | G | 233 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(230): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.838-728A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467120 | |||||||
| chr9:114467169 | T | C | 131 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(128): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.838-777A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467169 | |||||||
| chr9:114467178 | C | T | 131 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(128): Show |
132 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.838-786G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467178 | |||||||
| chr9:114467385 | C | T | 2 | a0001c0040t0001g0214 a0004c0005t0001g0215 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-993G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467385 | |||||||
| chr9:114467388 | G | C | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.838-996C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467388 | |||||||
| chr9:114467403 | G | A | 3 | a0001c0002t0001g0155 a0001c0002t0001g0171 a0001c0002t0001g0180 |
3 | HG00438.hp2 NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.838-1011C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467403 | |||||||
| chr9:114467447 | G | T | 1 | a0001c0002t0001g0068 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.838-1055C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467447 | |||||||
| chr9:114467490 | G | A | 29 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0006t0001g0062 others(26): Show |
29 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.838-1098C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467490 | |||||||
| chr9:114467513 | G | A | 3 | a0001c0002t0001g0061 a0004c0005t0003g0220 a0014c0023t0004g0233 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.838-1121C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467513 | |||||||
| chr9:114467516 | G | T | 1 | a0001c0002t0001g0092 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.838-1124C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467516 | |||||||
| chr9:114467534 | G | A | 3 | a0003c0003t0001g0197 a0003c0003t0006g0238 a0003c0007t0002g0264 |
3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.838-1142C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467534 | |||||||
| chr9:114467614 | C | T | 1 | a0002c0001t0001g0097 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.838-1222G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467614 | |||||||
| chr9:114467736 | C | G | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.838-1344G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467736 | |||||||
| chr9:114467737 | T | C | 8 | a0005c0011t0001g0007 a0005c0011t0001g0074 a0005c0011t0001g0081 others(5): Show |
9 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.838-1345A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467737 | |||||||
| chr9:114467809 | G | A | 3 | a0004c0005t0001g0176 a0011c0033t0001g0085 a0011c0034t0001g0087 |
3 | HG00423.hp2 HG02698.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.838-1417C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467809 | |||||||
| chr9:114467867 | T | G | 2 | a0003c0003t0001g0197 a0003c0003t0006g0238 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.838-1475A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467867 | |||||||
| chr9:114467946 | A | G | 3 | a0002c0001t0001g0033 a0002c0001t0001g0052 a0002c0001t0001g0053 |
3 | HG02056.hp1 HG02135.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.838-1554T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467946 | |||||||
| chr9:114467957 | A | G | 38 | a0001c0002t0001g0192 a0001c0002t0001g0207 a0001c0002t0003g0228 others(35): Show |
38 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(35): Show |
intron_variant | MODIFIER | c.838-1565T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114467957 | |||||||
| chr9:114468052 | T | G | 3 | a0001c0002t0001g0105 a0001c0002t0001g0156 a0002c0001t0001g0104 |
3 | HG02040.hp1 NA18939.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.838-1660A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468052 | |||||||
| chr9:114468167 | A | C | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.838-1775T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468167 | |||||||
| chr9:114468287 | T | C | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.838-1895A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468287 | |||||||
| chr9:114468288 | T | G | 1 | a0011c0033t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.838-1896A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468288 | |||||||
| chr9:114468304 | C | A | 1 | a0002c0001t0001g0050 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.838-1912G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468304 | |||||||
| chr9:114468335 | C | T | 1 | a0001c0006t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.838-1943G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468335 | |||||||
| chr9:114468347 | A | G | 103 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(100): Show |
113 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.838-1955T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468347 | |||||||
| chr9:114468911 | T | C | 102 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(99): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.838-2519A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114468911 | |||||||
| chr9:114469007 | C | T | 2 | a0001c0010t0001g0212 a0004c0005t0001g0211 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.838-2615G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469007 | |||||||
| chr9:114469015 | C | G | 38 | a0001c0002t0001g0045 a0001c0002t0001g0061 a0001c0002t0001g0073 others(35): Show |
38 | HG00280.hp1 HG00323.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.838-2623G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469015 | |||||||
| chr9:114469032 | T | C | 102 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(99): Show |
112 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.838-2640A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469032 | |||||||
| chr9:114469061 | G | A | 1 | a0001c0002t0001g0116 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.838-2669C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469061 | |||||||
| chr9:114469133 | C | A | 178 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(175): Show |
179 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.838-2741G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469133 | |||||||
| chr9:114469202 | G | A | 3 | a0003c0003t0001g0197 a0003c0003t0006g0238 a0003c0007t0002g0264 |
3 | HG02809.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.838-2810C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469202 | |||||||
| chr9:114469248 | G | C | 29 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0002t0008g0199 others(26): Show |
29 | HG01109.hp2 HG01192.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.838-2856C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469248 | |||||||
| chr9:114469309 | G | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.838-2917C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469309 | |||||||
| chr9:114469409 | C | T | 1 | a0002c0001t0001g0004 | 2 | NA18944.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.838-3017G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469409 | |||||||
| chr9:114469443 | C | G | 98 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(95): Show |
108 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.838-3051G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469443 | |||||||
| chr9:114469512 | C | T | 3 | a0001c0040t0001g0214 a0004c0005t0001g0204 a0004c0005t0001g0215 |
3 | HG02572.hp1 HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.838-3120G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469512 | |||||||
| chr9:114469606 | A | G | 99 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(96): Show |
109 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.838-3214T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469606 | |||||||
| chr9:114469740 | C | A | 1 | a0003c0003t0001g0159 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.838-3348G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469740 | |||||||
| chr9:114469765 | T | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.838-3373A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469765 | |||||||
| chr9:114469842 | A | G | 131 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(128): Show |
141 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.838-3450T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469842 | |||||||
| chr9:114469848 | G | C | 3 | a0001c0002t0001g0113 a0002c0001t0001g0112 a0002c0001t0001g0165 |
3 | HG03490.hp2 HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.838-3456C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469848 | |||||||
| chr9:114469955 | T | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.838-3563A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114469955 | |||||||
| chr9:114470017 | C | A | 1 | a0001c0012t0002g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.838-3625G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470017 | |||||||
| chr9:114470071 | G | A | 124 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(121): Show |
132 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.838-3679C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470071 | |||||||
| chr9:114470091 | C | A | 1 | a0001c0008t0002g0274 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.838-3699G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470091 | |||||||
| chr9:114470143 | T | C | 132 | a0001c0002t0001g0049 a0001c0002t0001g0092 a0001c0002t0001g0113 others(129): Show |
142 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.838-3751A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470143 | |||||||
| chr9:114470439 | C | T | 2 | a0001c0008t0002g0284 a0001c0008t0002g0288 |
2 | HG02109.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.838-4047G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470439 | |||||||
| chr9:114470543 | G | C | 279 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(276): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.838-4151C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470543 | |||||||
| chr9:114470751 | C | A | 3 | a0001c0002t0001g0061 a0004c0005t0003g0220 a0014c0023t0004g0233 |
3 | HG02055.hp2 HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.838-4359G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470751 | |||||||
| chr9:114470921 | G | A | 1 | a0004c0005t0003g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.838-4529C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470921 | |||||||
| chr9:114470932 | C | T | 3 | a0003c0003t0001g0148 a0003c0003t0001g0149 a0003c0003t0001g0150 |
3 | NA18947.hp2 NA18979.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.838-4540G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114470932 | |||||||
| chr9:114471245 | G | A | 2 | a0002c0001t0005g0246 a0003c0003t0001g0181 |
2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.838-4853C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471245 | |||||||
| chr9:114471455 | G | C | 3 | a0003c0003t0001g0066 a0004c0019t0001g0201 a0004c0042t0001g0063 |
3 | HG02818.hp1 HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.838-5063C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471455 | |||||||
| chr9:114471575 | T | C | 18 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0001c0006t0001g0062 others(15): Show |
18 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.838-5183A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471575 | |||||||
| chr9:114471645 | C | T | 2 | a0001c0010t0001g0212 a0004c0005t0001g0211 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.838-5253G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471645 | |||||||
| chr9:114471688 | G | A | 3 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0007t0002g0314 |
3 | HG02280.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.838-5296C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471688 | |||||||
| chr9:114471785 | G | A | 1 | a0002c0001t0001g0038 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.838-5393C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471785 | |||||||
| chr9:114471903 | T | C | 1 | a0001c0008t0007g0317 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.838-5511A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471903 | |||||||
| chr9:114471913 | T | A | 159 | a0001c0002t0001g0049 a0001c0002t0001g0073 a0001c0002t0001g0092 others(156): Show |
169 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(166): Show |
intron_variant | MODIFIER | c.838-5521A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471913 | |||||||
| chr9:114471967 | C | T | 39 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0144 others(36): Show |
40 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(37): Show |
intron_variant | MODIFIER | c.838-5575G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114471967 | |||||||
| chr9:114472229 | T | C | 14 | a0001c0002t0001g0061 a0001c0002t0001g0073 a0001c0002t0001g0092 others(11): Show |
14 | HG01109.hp1 HG01496.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.838-5837A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472229 | |||||||
| chr9:114472231 | C | T | 2 | a0001c0008t0002g0274 a0004c0026t0002g0273 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.838-5839G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472231 | |||||||
| chr9:114472433 | C | T | 3 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0007t0002g0314 |
3 | HG02280.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.838-6041G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472433 | |||||||
| chr9:114472441 | A | G | 13 | a0001c0002t0001g0045 a0001c0002t0001g0049 a0001c0006t0001g0091 others(10): Show |
13 | HG02056.hp2 HG02970.hp2 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.838-6049T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472441 | |||||||
| chr9:114472496 | T | C | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.837+6057A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472496 | |||||||
| chr9:114472509 | T | C | 2 | a0001c0002t0001g0061 a0003c0003t0001g0200 |
2 | HG02055.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.837+6044A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472509 | |||||||
| chr9:114472654 | G | T | 1 | a0006c0013t0001g0140 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.837+5899C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472654 | |||||||
| chr9:114472814 | C | T | 5 | a0001c0010t0001g0111 a0001c0012t0002g0010 a0001c0012t0002g0277 others(2): Show |
6 | HG00323.hp1 HG01070.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+5739G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472814 | |||||||
| chr9:114472890 | A | G | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.837+5663T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472890 | |||||||
| chr9:114472900 | C | G | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.837+5653G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114472900 | |||||||
| chr9:114473049 | C | G | 6 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0003c0003t0001g0057 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+5504G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473049 | |||||||
| chr9:114473102 | G | A | 2 | a0001c0002t0001g0207 a0001c0002t0003g0228 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.837+5451C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473102 | |||||||
| chr9:114473146 | G | A | 5 | a0001c0002t0008g0208 a0001c0010t0001g0212 a0003c0007t0002g0264 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.837+5407C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473146 | |||||||
| chr9:114473147 | G | A | 1 | a0001c0006t0001g0167 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.837+5406C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473147 | |||||||
| chr9:114473151 | C | T | 1 | a0003c0007t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.837+5402G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473151 | |||||||
| chr9:114473203 | C | T | 6 | a0001c0002t0001g0207 a0001c0002t0003g0228 a0003c0003t0001g0057 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+5350G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473203 | |||||||
| chr9:114473270 | G | T | 3 | a0002c0004t0002g0001 a0002c0004t0002g0271 a0002c0004t0002g0272 |
6 | NA18952.hp2 NA18954.hp1 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+5283C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473270 | |||||||
| chr9:114473307 | G | C | 78 | a0001c0002t0001g0021 a0001c0002t0001g0028 a0001c0002t0001g0049 others(75): Show |
83 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.837+5246C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473307 | |||||||
| chr9:114473481 | G | T | 11 | a0001c0002t0001g0192 a0001c0006t0001g0193 a0003c0003t0001g0196 others(8): Show |
13 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.837+5072C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473481 | |||||||
| chr9:114473531 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.837+5022C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473531 | |||||||
| chr9:114473741 | G | A | 2 | a0011c0033t0001g0085 a0018c0032t0001g0084 |
2 | HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.837+4812C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473741 | |||||||
| chr9:114473922 | C | T | 8 | a0001c0002t0004g0232 a0004c0005t0004g0234 a0004c0005t0004g0237 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+4631G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114473922 | |||||||
| chr9:114474245 | C | T | 3 | a0001c0002t0008g0208 a0001c0010t0001g0212 a0004c0005t0001g0211 |
3 | HG02280.hp2 HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.837+4308G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474245 | |||||||
| chr9:114474277 | T | C | 159 | a0001c0002t0001g0020 a0001c0002t0001g0039 a0001c0002t0001g0045 others(156): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.837+4276A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474277 | |||||||
| chr9:114474321 | T | C | 1 | a0003c0003t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.837+4232A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474321 | |||||||
| chr9:114474450 | C | T | 81 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(78): Show |
86 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(83): Show |
intron_variant | MODIFIER | c.837+4103G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474450 | |||||||
| chr9:114474595 | C | T | 4 | a0001c0008t0007g0316 a0001c0008t0007g0317 a0001c0008t0007g0318 others(1): Show |
4 | HG02615.hp1 HG02886.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+3958G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474595 | |||||||
| chr9:114474653 | C | T | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.837+3900G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474653 | |||||||
| chr9:114474970 | G | A | 59 | a0001c0006t0003g0225 a0001c0008t0002g0267 a0001c0008t0002g0284 others(56): Show |
62 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(59): Show |
intron_variant | MODIFIER | c.837+3583C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474970 | |||||||
| chr9:114474997 | A | G | 2 | a0003c0007t0002g0265 a0003c0007t0002g0315 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.837+3556T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114474997 | |||||||
| chr9:114475051 | G | A | 2 | a0001c0002t0001g0192 a0001c0006t0001g0193 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.837+3502C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475051 | |||||||
| chr9:114475107 | T | G | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.837+3446A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475107 | |||||||
| chr9:114475273 | T | G | 19 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(16): Show |
21 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.837+3280A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475273 | |||||||
| chr9:114475304 | G | T | 16 | a0001c0002t0001g0068 a0001c0008t0002g0274 a0003c0003t0001g0076 others(13): Show |
16 | HG00642.hp1 HG01069.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.837+3249C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475304 | |||||||
| chr9:114475306 | G | A | 16 | a0001c0002t0001g0068 a0001c0008t0002g0274 a0003c0003t0001g0076 others(13): Show |
16 | HG00642.hp1 HG01069.hp1 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.837+3247C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475306 | |||||||
| chr9:114475306 | G | C | 1 | a0006c0013t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.837+3247C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475306 | |||||||
| chr9:114475317 | A | G | 1 | a0003c0007t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.837+3236T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475317 | |||||||
| chr9:114475474 | C | T | 127 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(124): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.837+3079G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475474 | |||||||
| chr9:114475587 | T | C | 22 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(19): Show |
24 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.837+2966A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475587 | |||||||
| chr9:114475776 | T | C | 2 | a0001c0010t0003g0222 a0001c0010t0003g0223 |
2 | HG01192.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.837+2777A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475776 | |||||||
| chr9:114475788 | A | G | 1 | a0001c0002t0001g0123 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.837+2765T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475788 | |||||||
| chr9:114475934 | C | T | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.837+2619G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114475934 | |||||||
| chr9:114476036 | C | T | 1 | a0001c0006t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.837+2517G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476036 | |||||||
| chr9:114476041 | T | G | 1 | a0006c0013t0001g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.837+2512A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476041 | |||||||
| chr9:114476115 | C | A | 84 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(81): Show |
89 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.837+2438G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476115 | |||||||
| chr9:114476125 | C | T | 127 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(124): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.837+2428G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476125 | |||||||
| chr9:114476375 | C | T | 127 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(124): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.837+2178G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476375 | |||||||
| chr9:114476468 | G | A | 12 | a0001c0002t0001g0068 a0004c0005t0001g0206 a0004c0005t0001g0210 others(9): Show |
12 | HG00642.hp1 HG01069.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+2085C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476468 | |||||||
| chr9:114476523 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.837+2030A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476523 | |||||||
| chr9:114476529 | T | C | 6 | a0002c0001t0005g0246 a0009c0014t0005g0244 a0009c0014t0005g0247 others(3): Show |
6 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.837+2024A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476529 | |||||||
| chr9:114476687 | C | T | 7 | a0001c0008t0002g0303 a0001c0028t0002g0301 a0002c0004t0002g0296 others(4): Show |
7 | HG00438.hp1 HG02080.hp1 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.837+1866G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114476687 | |||||||
| chr9:114477107 | C | A | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.837+1446G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477107 | |||||||
| chr9:114477178 | C | T | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.837+1375G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477178 | |||||||
| chr9:114477202 | C | T | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.837+1351G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477202 | |||||||
| chr9:114477413 | G | A | 1 | a0002c0001t0001g0053 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.837+1140C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477413 | |||||||
| chr9:114477500 | T | C | 82 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(79): Show |
87 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.837+1053A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477500 | |||||||
| chr9:114477597 | C | T | 132 | a0001c0002t0001g0020 a0001c0002t0001g0039 a0001c0002t0001g0092 others(129): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.837+956G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477597 | |||||||
| chr9:114477600 | A | G | 4 | a0001c0008t0002g0303 a0001c0028t0002g0301 a0002c0004t0002g0304 others(1): Show |
4 | HG00438.hp1 HG02080.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.837+953T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477600 | |||||||
| chr9:114477633 | C | T | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.837+920G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477633 | |||||||
| chr9:114477689 | C | T | 2 | a0001c0010t0001g0096 a0020c0043t0001g0100 |
2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.837+864G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477689 | |||||||
| chr9:114477730 | T | C | 12 | a0001c0002t0001g0068 a0001c0008t0002g0274 a0003c0003t0001g0076 others(9): Show |
12 | HG00642.hp1 HG01123.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.837+823A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477730 | |||||||
| chr9:114477743 | G | A | 82 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(79): Show |
87 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.837+810C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477743 | |||||||
| chr9:114477795 | C | T | 2 | a0001c0002t0001g0207 a0001c0002t0003g0228 |
2 | HG01884.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.837+758G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114477795 | |||||||
| chr9:114478124 | T | C | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.837+429A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478124 | |||||||
| chr9:114478160 | C | A | 1 | a0002c0001t0001g0038 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.837+393G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478160 | |||||||
| chr9:114478238 | G | A | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.837+315C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478238 | |||||||
| chr9:114478250 | C | T | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.837+303G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478250 | |||||||
| chr9:114478363 | T | C | 3 | a0004c0005t0001g0206 a0004c0005t0001g0210 a0019c0036t0001g0205 |
3 | HG02145.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.837+190A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478363 | |||||||
| chr9:114478530 | C | T | 2 | a0002c0001t0001g0032 a0002c0001t0001g0044 |
2 | NA18980.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.837+23G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 2/11 | chr9 | 114478530 | |||||||
| chr9:114478812 | C | T | 1 | a0005c0011t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.619-41G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114478812 | |||||||
| chr9:114478814 | G | T | 1 | a0006c0013t0001g0101 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.619-43C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114478814 | |||||||
| chr9:114478837 | C | A | 9 | a0001c0002t0004g0232 a0004c0005t0004g0234 a0004c0005t0004g0237 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.619-66G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114478837 | |||||||
| chr9:114478934 | A | C | 1 | a0005c0011t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.619-163T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114478934 | |||||||
| chr9:114479191 | T | G | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619-420A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479191 | |||||||
| chr9:114479275 | A | G | 19 | a0001c0002t0003g0228 a0001c0006t0003g0225 a0001c0010t0003g0222 others(16): Show |
21 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.619-504T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479275 | |||||||
| chr9:114479296 | C | T | 10 | a0002c0001t0005g0246 a0004c0005t0001g0206 a0004c0005t0001g0210 others(7): Show |
10 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-525G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479296 | |||||||
| chr9:114479299 | C | T | 19 | a0001c0002t0003g0228 a0001c0006t0003g0225 a0001c0010t0003g0222 others(16): Show |
21 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.619-528G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479299 | |||||||
| chr9:114479342 | T | C | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.619-571A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479342 | |||||||
| chr9:114479409 | G | A | 5 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-638C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479409 | |||||||
| chr9:114479459 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.619-688G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479459 | |||||||
| chr9:114479532 | T | C | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-761A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479532 | |||||||
| chr9:114479540 | T | C | 309 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(306): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.619-769A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479540 | |||||||
| chr9:114479543 | G | A | 1 | a0013c0020t0001g0139 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.619-772C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479543 | |||||||
| chr9:114479565 | C | T | 1 | a0003c0003t0001g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.619-794G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479565 | |||||||
| chr9:114479618 | G | A | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-847C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114479618 | |||||||
| chr9:114480000 | T | G | 1 | a0002c0001t0001g0044 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.619-1229A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480000 | |||||||
| chr9:114480084 | T | TA | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-1314dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480084 | |||||||
| chr9:114480085 | A | T | 1 | a0009c0014t0005g0248 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.619-1314T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480085 | |||||||
| chr9:114480218 | A | G | 82 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(79): Show |
87 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.619-1447T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480218 | |||||||
| chr9:114480251 | C | T | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-1480G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480251 | |||||||
| chr9:114480275 | T | C | 4 | a0006c0013t0001g0140 a0007c0015t0001g0141 a0007c0015t0001g0142 others(1): Show |
4 | HG00408.hp2 NA18940.hp1 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-1504A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480275 | |||||||
| chr9:114480295 | T | C | 109 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(106): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.619-1524A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480295 | |||||||
| chr9:114480319 | A | G | 22 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(19): Show |
24 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-1548T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480319 | |||||||
| chr9:114480404 | A | G | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.619-1633T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480404 | |||||||
| chr9:114480481 | A | AAGAG | 190 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(187): Show |
200 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.619-1714_619-1711d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480481 | |||||||
| chr9:114480565 | C | T | 109 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(106): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.619-1794G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480565 | |||||||
| chr9:114480569 | A | G | 1 | a0003c0007t0013g0243 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.619-1798T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480569 | |||||||
| chr9:114480918 | C | T | 4 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-2147G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480918 | |||||||
| chr9:114480971 | T | A | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.619-2200A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114480971 | |||||||
| chr9:114481088 | A | G | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-2317T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481088 | |||||||
| chr9:114481208 | C | T | 1 | a0001c0010t0001g0096 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.619-2437G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481208 | |||||||
| chr9:114481291 | T | C | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-2520A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481291 | |||||||
| chr9:114481312 | A | T | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619-2541T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481312 | |||||||
| chr9:114481340 | T | A | 22 | a0001c0002t0003g0228 a0001c0002t0008g0208 a0001c0006t0003g0225 others(19): Show |
24 | HG01167.hp1 HG01169.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-2569A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481340 | |||||||
| chr9:114481494 | A | G | 1 | a0013c0020t0001g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.619-2723T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481494 | |||||||
| chr9:114481527 | C | T | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-2756G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481527 | |||||||
| chr9:114481529 | T | C | 141 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(138): Show |
147 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.619-2758A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481529 | |||||||
| chr9:114481552 | C | G | 3 | a0004c0005t0001g0206 a0004c0005t0001g0210 a0019c0036t0001g0205 |
3 | HG02145.hp2 HG02258.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.619-2781G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481552 | |||||||
| chr9:114481683 | C | T | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-2912G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481683 | |||||||
| chr9:114481744 | C | T | 1 | a0003c0003t0001g0185 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.619-2973G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481744 | |||||||
| chr9:114481823 | G | A | 1 | a0001c0002t0001g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.619-3052C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481823 | |||||||
| chr9:114481839 | C | T | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619-3068G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481839 | |||||||
| chr9:114481845 | G | C | 1 | a0024c0044t0001g0219 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.619-3074C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481845 | |||||||
| chr9:114481893 | A | G | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.619-3122T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481893 | |||||||
| chr9:114481962 | T | G | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.619-3191A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481962 | |||||||
| chr9:114481969 | C | T | 2 | a0001c0002t0001g0184 a0025c0037t0001g0069 |
2 | NA18612.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.619-3198G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481969 | |||||||
| chr9:114481988 | C | T | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.619-3217G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114481988 | |||||||
| chr9:114482075 | C | T | 6 | a0002c0001t0005g0246 a0009c0014t0005g0244 a0009c0014t0005g0247 others(3): Show |
6 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-3304G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482075 | |||||||
| chr9:114482090 | G | A | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.619-3319C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482090 | |||||||
| chr9:114482166 | A | G | 1 | a0001c0006t0001g0173 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.619-3395T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482166 | |||||||
| chr9:114482304 | T | C | 3 | a0003c0003t0001g0145 a0003c0003t0001g0146 a0003c0003t0001g0177 |
3 | NA18952.hp1 NA18988.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.619-3533A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482304 | |||||||
| chr9:114482333 | G | T | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619-3562C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482333 | |||||||
| chr9:114482463 | G | A | 1 | a0004c0019t0001g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.619-3692C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482463 | |||||||
| chr9:114482471 | C | T | 5 | a0003c0003t0001g0178 a0003c0003t0001g0185 a0003c0003t0001g0186 others(2): Show |
5 | HG00423.hp1 NA18954.hp2 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-3700G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482471 | |||||||
| chr9:114482536 | G | T | 4 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-3765C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482536 | |||||||
| chr9:114482656 | C | T | 2 | a0011c0033t0001g0085 a0018c0032t0001g0084 |
2 | HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-3885G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482656 | |||||||
| chr9:114482657 | G | A | 140 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(137): Show |
146 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.619-3886C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482657 | |||||||
| chr9:114482806 | A | C | 117 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(114): Show |
124 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(121): Show |
intron_variant | MODIFIER | c.619-4035T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482806 | |||||||
| chr9:114482852 | G | A | 24 | a0001c0002t0001g0113 a0001c0002t0001g0144 a0001c0006t0001g0091 others(21): Show |
25 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-4081C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482852 | |||||||
| chr9:114482876 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.619-4105C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482876 | |||||||
| chr9:114482934 | C | G | 5 | a0001c0008t0002g0274 a0003c0003t0001g0076 a0003c0003t0001g0077 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-4163G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482934 | |||||||
| chr9:114482972 | C | G | 186 | a0001c0002t0001g0021 a0001c0002t0001g0027 a0001c0002t0001g0028 others(183): Show |
196 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.619-4201G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482972 | |||||||
| chr9:114482988 | C | T | 5 | a0001c0002t0008g0208 a0001c0010t0001g0212 a0002c0001t0001g0179 others(2): Show |
5 | HG02280.hp2 HG02559.hp1 NA18997.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-4217G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114482988 | |||||||
| chr9:114483029 | A | G | 2 | a0002c0001t0001g0030 a0003c0003t0001g0122 |
2 | NA18949.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.619-4258T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483029 | |||||||
| chr9:114483080 | C | T | 1 | a0001c0002t0001g0102 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.619-4309G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483080 | |||||||
| chr9:114483091 | C | G | 3 | a0001c0009t0002g0287 a0001c0009t0002g0294 a0003c0003t0001g0093 |
3 | HG00323.hp2 HG01099.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.619-4320G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483091 | |||||||
| chr9:114483158 | G | A | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619-4387C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483158 | |||||||
| chr9:114483429 | G | A | 121 | a0001c0002t0001g0020 a0001c0002t0001g0092 a0001c0002t0001g0098 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.619-4658C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483429 | |||||||
| chr9:114483437 | C | A | 63 | a0001c0002t0001g0192 a0001c0002t0003g0228 a0001c0002t0004g0232 others(60): Show |
64 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.619-4666G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483437 | |||||||
| chr9:114483637 | G | C | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-4866C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483637 | |||||||
| chr9:114483680 | A | G | 163 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(160): Show |
171 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.619-4909T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483680 | |||||||
| chr9:114483908 | G | A | 111 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(108): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.619-5137C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483908 | |||||||
| chr9:114483926 | T | G | 3 | a0003c0003t0001g0145 a0003c0003t0001g0146 a0003c0003t0001g0177 |
3 | NA18952.hp1 NA18988.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.619-5155A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483926 | |||||||
| chr9:114483989 | G | T | 159 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(156): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.619-5218C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114483989 | |||||||
| chr9:114484144 | G | A | 136 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(133): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.619-5373C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484144 | |||||||
| chr9:114484224 | C | T | 126 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.619-5453G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484224 | |||||||
| chr9:114484294 | C | T | 126 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.619-5523G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484294 | |||||||
| chr9:114484446 | G | C | 1 | a0022c0035t0003g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.619-5675C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484446 | |||||||
| chr9:114484463 | C | G | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.619-5692G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484463 | |||||||
| chr9:114484516 | T | C | 295 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(292): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.619-5745A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484516 | |||||||
| chr9:114484588 | G | A | 2 | a0001c0002t0001g0192 a0001c0006t0001g0193 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.619-5817C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484588 | |||||||
| chr9:114484623 | G | A | 1 | a0002c0004t0002g0300 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.619-5852C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484623 | |||||||
| chr9:114484808 | G | A | 4 | a0002c0001t0001g0024 a0002c0001t0001g0042 a0003c0003t0001g0022 others(1): Show |
4 | HG02056.hp2 NA18942.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-6037C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484808 | |||||||
| chr9:114484861 | C | G | 3 | a0001c0002t0001g0207 a0004c0005t0001g0206 a0019c0036t0001g0205 |
3 | HG02145.hp2 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.619-6090G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484861 | |||||||
| chr9:114484875 | C | A | 1 | a0005c0039t0001g0060 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.619-6104G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114484875 | |||||||
| chr9:114485055 | T | C | 1 | a0003c0003t0001g0078 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.619-6284A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485055 | |||||||
| chr9:114485239 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.619-6468C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485239 | |||||||
| chr9:114485307 | A | T | 130 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(127): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.619-6536T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485307 | |||||||
| chr9:114485362 | T | C | 44 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0284 others(41): Show |
45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.619-6591A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485362 | |||||||
| chr9:114485615 | C | T | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-6844G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485615 | |||||||
| chr9:114485699 | A | T | 1 | a0001c0006t0009g0241 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.619-6928T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485699 | |||||||
| chr9:114485770 | AGAGGCAG others(11): Show |
A | 44 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0284 others(41): Show |
45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.619-7017_619-7000d others(20): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485770 | |||||||
| chr9:114485807 | G | A | 1 | a0003c0007t0002g0259 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.619-7036C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485807 | |||||||
| chr9:114485842 | A | T | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.619-7071T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485842 | |||||||
| chr9:114485843 | A | T | 20 | a0001c0002t0001g0207 a0001c0002t0008g0199 a0001c0008t0002g0274 others(17): Show |
20 | HG00423.hp2 HG00558.hp1 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.619-7072T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485843 | |||||||
| chr9:114485844 | T | A | 1 | a0003c0003t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.619-7073A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485844 | |||||||
| chr9:114485853 | TA | T | 2 | a0001c0012t0002g0278 a0002c0001t0001g0004 |
3 | HG01168.hp2 NA18944.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.619-7083delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485853 | |||||||
| chr9:114485854 | A | T | 301 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(298): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.619-7083T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485854 | |||||||
| chr9:114485858 | T | C | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-7087A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485858 | |||||||
| chr9:114485947 | G | A | 2 | a0001c0002t0001g0192 a0001c0006t0001g0193 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.619-7176C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485947 | |||||||
| chr9:114485959 | A | T | 1 | a0001c0002t0001g0121 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.619-7188T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114485959 | |||||||
| chr9:114486153 | G | C | 1 | a0003c0003t0001g0146 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.619-7382C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486153 | |||||||
| chr9:114486199 | G | A | 110 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(107): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.619-7428C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486199 | |||||||
| chr9:114486208 | A | G | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-7437T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486208 | |||||||
| chr9:114486255 | G | A | 1 | a0002c0001t0001g0103 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.619-7484C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486255 | |||||||
| chr9:114486262 | C | A | 2 | a0001c0002t0001g0020 a0003c0003t0001g0019 |
2 | HG02129.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.619-7491G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486262 | |||||||
| chr9:114486388 | C | T | 2 | a0001c0009t0002g0279 a0001c0009t0002g0280 |
2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.619-7617G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486388 | |||||||
| chr9:114486593 | A | G | 2 | a0001c0040t0001g0214 a0004c0005t0001g0215 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.619-7822T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486593 | |||||||
| chr9:114486693 | A | G | 2 | a0002c0001t0001g0004 a0002c0001t0001g0030 |
3 | NA18944.hp1 NA18949.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.619-7922T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486693 | |||||||
| chr9:114486814 | C | CA | 69 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0167 others(66): Show |
72 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.619-8044dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486814 | |||||||
| chr9:114486814 | C | CAA | 82 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(79): Show |
87 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.619-8045_619-8044d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486814 | |||||||
| chr9:114486814 | CA | C | 20 | a0001c0002t0001g0160 a0001c0002t0001g0202 a0001c0002t0003g0228 others(17): Show |
22 | HG00423.hp2 HG01070.hp1 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.619-8044delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486814 | |||||||
| chr9:114486814 | CAAAAAAA others(3): Show |
C | 1 | a0001c0010t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.619-8053_619-8044d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486814 | |||||||
| chr9:114486883 | TTAGTGTG others(2): Show |
T | 4 | a0003c0003t0001g0147 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8121_619-8113d others(11): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486883 | |||||||
| chr9:114486884 | TA | T | 136 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(133): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.619-8114delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486884 | |||||||
| chr9:114486884 | TAGTGTGT others(16): Show |
T | 2 | a0001c0040t0001g0214 a0004c0005t0001g0215 |
2 | HG03098.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.619-8136_619-8114d others(25): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486884 | |||||||
| chr9:114486885 | A | AGT | 40 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0274 others(37): Show |
41 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.619-8116_619-8115d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486885 | |||||||
| chr9:114486885 | A | AGTGT | 8 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0001c0009t0002g0256 others(5): Show |
8 | HG00642.hp1 HG01261.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-8118_619-8115d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486885 | |||||||
| chr9:114486885 | A | AGTGTGT | 4 | a0001c0006t0001g0062 a0001c0006t0001g0070 a0001c0006t0001g0071 others(1): Show |
4 | HG02257.hp2 HG02572.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-8120_619-8115d others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486885 | |||||||
| chr9:114486885 | A | T | 1 | a0012c0022t0001g0213 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.619-8114T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486885 | |||||||
| chr9:114486885 | AGT | A | 7 | a0001c0006t0003g0225 a0001c0008t0007g0316 a0001c0008t0007g0317 others(4): Show |
7 | HG01884.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.619-8116_619-8115d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486885 | |||||||
| chr9:114486886 | G | T | 1 | a0004c0005t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.619-8115C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486886 | |||||||
| chr9:114486893 | TGTGTGTG others(8): Show |
T | 1 | a0001c0002t0001g0039 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.619-8137_619-8123d others(17): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486893 | |||||||
| chr9:114486895 | TGTGTGTG others(6): Show |
T | 73 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(70): Show |
78 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(75): Show |
intron_variant | MODIFIER | c.619-8137_619-8125d others(15): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486895 | |||||||
| chr9:114486897 | T | TA | 122 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(119): Show |
124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.619-8127_619-8126i others(3): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486897 | |||||||
| chr9:114486897 | T | TAGA | 5 | a0001c0002t0001g0116 a0001c0010t0001g0096 a0003c0003t0001g0120 others(2): Show |
5 | HG01261.hp2 HG01981.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-8127_619-8126i others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486897 | |||||||
| chr9:114486897 | TG | T | 9 | a0001c0002t0001g0207 a0002c0001t0001g0002 a0002c0001t0001g0003 others(6): Show |
11 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.619-8127delC | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486897 | |||||||
| chr9:114486897 | TGTGTGTG others(4): Show |
T | 3 | a0002c0001t0001g0040 a0002c0001t0001g0044 a0002c0004t0002g0296 |
3 | HG03017.hp1 NA18612.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.619-8137_619-8127d others(13): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486897 | |||||||
| chr9:114486899 | T | A | 131 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(128): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.619-8128A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486899 | |||||||
| chr9:114486901 | T | A | 9 | a0001c0002t0001g0207 a0002c0001t0001g0002 a0002c0001t0001g0003 others(6): Show |
11 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.619-8130A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486901 | |||||||
| chr9:114486903 | T | A | 1 | a0001c0002t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.619-8132A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486903 | |||||||
| chr9:114486904 | G | A | 27 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(24): Show |
29 | HG01109.hp1 HG01192.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.619-8133C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486904 | |||||||
| chr9:114486905 | T | G | 27 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(24): Show |
29 | HG01109.hp1 HG01192.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.619-8134A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486905 | |||||||
| chr9:114486905 | TA | T | 114 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(111): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.619-8135delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486905 | |||||||
| chr9:114486905 | TAGA | T | 21 | a0001c0002t0008g0199 a0002c0001t0001g0002 a0002c0001t0001g0003 others(18): Show |
23 | HG01074.hp2 HG01167.hp1 HG01169.hp1 others(20): Show |
intron_variant | MODIFIER | c.619-8137_619-8135d others(5): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486905 | |||||||
| chr9:114486908 | A | AGT | 4 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0200 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-8139_619-8138d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486908 | |||||||
| chr9:114486908 | A | T | 143 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(140): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.619-8137T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486908 | |||||||
| chr9:114486910 | T | A | 1 | a0004c0005t0001g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.619-8139A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486910 | |||||||
| chr9:114486912 | TGTGTGTG others(8): Show |
T | 1 | a0001c0010t0003g0227 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.619-8156_619-8142d others(17): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486912 | |||||||
| chr9:114486924 | TA | T | 4 | a0003c0003t0001g0147 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8154delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486924 | |||||||
| chr9:114486925 | A | G | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-8154T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486925 | |||||||
| chr9:114486926 | G | T | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-8155C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486926 | |||||||
| chr9:114486927 | A | T | 4 | a0003c0003t0001g0147 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8156T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486927 | |||||||
| chr9:114486927 | AGTGT | A | 126 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.619-8160_619-8157d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486927 | |||||||
| chr9:114486929 | T | TA | 4 | a0003c0003t0001g0147 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8159_619-8158i others(3): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486929 | |||||||
| chr9:114486931 | T | A | 4 | a0003c0003t0001g0147 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
4 | HG00423.hp2 HG00558.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8160A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486931 | |||||||
| chr9:114486940 | G | T | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-8169C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486940 | |||||||
| chr9:114486941 | T | G | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-8170A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486941 | |||||||
| chr9:114486951 | GTGTGTGT others(13): Show |
G | 2 | a0004c0005t0004g0234 a0014c0023t0004g0233 |
2 | HG02145.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.619-8200_619-8181d others(22): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(15): Show |
G | 6 | a0001c0002t0004g0232 a0004c0005t0004g0237 a0012c0022t0004g0230 others(3): Show |
6 | HG01109.hp1 HG01243.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.619-8202_619-8181d others(24): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(17): Show |
G | 3 | a0004c0005t0001g0006 a0004c0005t0001g0080 a0015c0021t0004g0229 |
4 | HG03130.hp2 HG03139.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-8204_619-8181d others(26): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(19): Show |
G | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.619-8206_619-8181d others(28): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(25): Show |
G | 2 | a0001c0002t0001g0192 a0001c0006t0001g0193 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.619-8212_619-8181d others(34): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(29): Show |
G | 1 | a0008c0016t0001g0198 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.619-8216_619-8181d others(38): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486951 | GTGTGTGT others(31): Show |
G | 5 | a0003c0003t0001g0196 a0003c0003t0001g0197 a0008c0016t0001g0009 others(2): Show |
6 | HG02486.hp1 HG02559.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-8218_619-8181d others(40): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486951 | |||||||
| chr9:114486953 | GTGTGTGT others(17): Show |
G | 1 | a0004c0005t0001g0079 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.619-8206_619-8183d others(26): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486953 | |||||||
| chr9:114486953 | GTGTGTGT others(27): Show |
G | 10 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0049 others(7): Show |
10 | HG00558.hp2 HG02809.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-8216_619-8183d others(36): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486953 | |||||||
| chr9:114486953 | GTGTGTGT others(29): Show |
G | 120 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0039 others(117): Show |
126 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.619-8218_619-8183d others(38): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486953 | |||||||
| chr9:114486953 | GTGTGTGT others(31): Show |
G | 134 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(131): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.619-8220_619-8183d others(40): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486953 | |||||||
| chr9:114486953 | GTGTGTGT others(33): Show |
G | 1 | a0001c0002t0001g0170 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.619-8222_619-8183d others(42): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486953 | |||||||
| chr9:114486955 | GTGTGTAT others(29): Show |
G | 6 | a0001c0008t0002g0284 a0001c0008t0002g0288 a0001c0008t0007g0316 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-8220_619-8185d others(38): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486955 | |||||||
| chr9:114486955 | GTGTGTAT others(31): Show |
G | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.619-8222_619-8185d others(40): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486955 | |||||||
| chr9:114486957 | GTGTATAT others(31): Show |
G | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619-8224_619-8187d others(40): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486957 | |||||||
| chr9:114486959 | GTA | G | 6 | a0001c0010t0003g0222 a0001c0010t0003g0227 a0001c0040t0001g0214 others(3): Show |
6 | HG01243.hp2 HG03139.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-8190_619-8189d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486959 | |||||||
| chr9:114486959 | GTATATA | G | 4 | a0001c0002t0008g0208 a0001c0006t0003g0225 a0001c0010t0001g0212 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-8194_619-8189d others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486959 | |||||||
| chr9:114486959 | GTATATAT others(3): Show |
G | 2 | a0004c0005t0001g0204 a0004c0005t0001g0210 |
2 | HG02572.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.619-8198_619-8189d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486959 | |||||||
| chr9:114486959 | GTATATAT others(21): Show |
G | 4 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0200 others(1): Show |
4 | HG02280.hp1 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-8216_619-8189d others(30): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486959 | |||||||
| chr9:114486959 | GTATATAT others(23): Show |
G | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.619-8218_619-8189d others(32): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486959 | |||||||
| chr9:114486963 | A | G | 5 | a0001c0010t0003g0222 a0001c0010t0003g0227 a0001c0040t0001g0214 others(2): Show |
5 | HG01243.hp2 HG03195.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-8192T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486963 | |||||||
| chr9:114486965 | A | G | 2 | a0001c0010t0003g0223 a0004c0005t0001g0215 |
2 | HG01192.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.619-8194T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486965 | |||||||
| chr9:114486967 | A | G | 4 | a0001c0002t0008g0208 a0001c0006t0003g0225 a0001c0010t0001g0212 others(1): Show |
4 | HG01884.hp1 HG02280.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-8196T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486967 | |||||||
| chr9:114486969 | A | G | 1 | a0001c0010t0003g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.619-8198T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486969 | |||||||
| chr9:114486971 | A | G | 1 | a0004c0005t0001g0204 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.619-8200T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114486971 | |||||||
| chr9:114487052 | CA | C | 66 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(63): Show |
69 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.619-8282delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487052 | |||||||
| chr9:114487052 | CAA | C | 137 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(134): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.619-8283_619-8282d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487052 | |||||||
| chr9:114487188 | A | AT | 9 | a0001c0002t0001g0049 a0001c0002t0001g0061 a0001c0012t0002g0277 others(6): Show |
9 | HG01261.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.619-8418dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487188 | |||||||
| chr9:114487188 | AT | A | 61 | a0001c0002t0001g0039 a0001c0002t0001g0115 a0001c0002t0001g0117 others(58): Show |
65 | HG00738.hp1 HG00738.hp2 HG01099.hp2 others(62): Show |
intron_variant | MODIFIER | c.619-8418delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487188 | |||||||
| chr9:114487210 | A | G | 8 | a0002c0001t0005g0246 a0003c0007t0002g0264 a0009c0014t0005g0244 others(5): Show |
8 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-8439T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487210 | |||||||
| chr9:114487343 | C | T | 1 | a0001c0008t0002g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.619-8572G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487343 | |||||||
| chr9:114487376 | TA | T | 84 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(81): Show |
89 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(86): Show |
intron_variant | MODIFIER | c.619-8606delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487376 | |||||||
| chr9:114487526 | C | T | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-8755G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487526 | |||||||
| chr9:114487547 | A | G | 1 | a0002c0001t0001g0030 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.619-8776T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487547 | |||||||
| chr9:114487594 | G | A | 90 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(87): Show |
95 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.619-8823C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487594 | |||||||
| chr9:114487622 | G | A | 2 | a0003c0007t0002g0264 a0021c0038t0005g0245 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.619-8851C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487622 | |||||||
| chr9:114487696 | CACAG | C | 133 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(130): Show |
139 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.619-8929_619-8926d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487696 | |||||||
| chr9:114487826 | T | C | 1 | a0013c0020t0001g0151 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.619-9055A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487826 | |||||||
| chr9:114487828 | T | C | 13 | a0001c0002t0003g0228 a0001c0006t0003g0225 a0001c0010t0003g0222 others(10): Show |
13 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.619-9057A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487828 | |||||||
| chr9:114487998 | A | G | 44 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0284 others(41): Show |
45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.619-9227T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114487998 | |||||||
| chr9:114488027 | G | A | 1 | a0004c0005t0004g0234 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.619-9256C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488027 | |||||||
| chr9:114488052 | C | T | 5 | a0003c0007t0002g0253 a0003c0007t0002g0254 a0003c0007t0002g0255 others(2): Show |
5 | HG00738.hp1 HG01175.hp1 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.619-9281G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488052 | |||||||
| chr9:114488113 | A | G | 115 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.619-9342T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488113 | |||||||
| chr9:114488115 | T | C | 1 | a0001c0010t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.619-9344A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488115 | |||||||
| chr9:114488209 | T | C | 12 | a0001c0002t0001g0207 a0001c0002t0008g0199 a0002c0001t0005g0246 others(9): Show |
12 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(9): Show |
intron_variant | MODIFIER | c.619-9438A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488209 | |||||||
| chr9:114488248 | G | A | 1 | a0021c0038t0005g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.619-9477C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488248 | |||||||
| chr9:114488258 | G | A | 8 | a0002c0001t0005g0246 a0003c0007t0002g0264 a0009c0014t0005g0244 others(5): Show |
8 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-9487C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488258 | |||||||
| chr9:114488512 | C | T | 133 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(130): Show |
139 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.619-9741G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488512 | |||||||
| chr9:114488623 | G | A | 128 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(125): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.619-9852C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488623 | |||||||
| chr9:114488726 | T | A | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.619-9955A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488726 | |||||||
| chr9:114488899 | T | C | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.619-10128A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488899 | |||||||
| chr9:114488926 | C | T | 1 | a0002c0004t0002g0311 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.619-10155G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114488926 | |||||||
| chr9:114489048 | T | C | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.619-10277A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489048 | |||||||
| chr9:114489072 | C | T | 126 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(123): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.619-10301G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489072 | |||||||
| chr9:114489093 | G | A | 1 | a0003c0003t0001g0152 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.619-10322C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489093 | |||||||
| chr9:114489101 | C | G | 1 | a0003c0007t0002g0264 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.619-10330G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489101 | |||||||
| chr9:114489245 | G | A | 8 | a0002c0001t0005g0246 a0003c0007t0002g0264 a0009c0014t0005g0244 others(5): Show |
8 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.619-10474C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489245 | |||||||
| chr9:114489305 | G | A | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.619-10534C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489305 | |||||||
| chr9:114489463 | T | TAC | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-10694_619-1069 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489463 | |||||||
| chr9:114489463 | TAC | T | 159 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(156): Show |
167 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.619-10694_619-1069 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489463 | |||||||
| chr9:114489463 | TACAC | T | 3 | a0001c0002t0001g0113 a0002c0001t0001g0112 a0002c0001t0001g0165 |
3 | HG03490.hp2 HG03704.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.619-10696_619-1069 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489463 | |||||||
| chr9:114489479 | C | T | 6 | a0001c0002t0001g0109 a0001c0002t0001g0115 a0001c0002t0001g0117 others(3): Show |
6 | NA18747.hp1 NA18944.hp2 NA18949.hp1 others(3): Show |
intron_variant | MODIFIER | c.619-10708G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489479 | |||||||
| chr9:114489481 | C | T | 2 | a0001c0008t0010g0293 a0008c0030t0002g0292 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.619-10710G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489481 | |||||||
| chr9:114489491 | T | TAC | 22 | a0001c0002t0004g0232 a0001c0012t0002g0010 a0001c0012t0002g0277 others(19): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-10722_619-1072 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489491 | |||||||
| chr9:114489491 | TAC | T | 5 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-10722_619-1072 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489491 | |||||||
| chr9:114489491 | TACACACA others(23): Show |
T | 1 | a0001c0010t0003g0226 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.619-10750_619-1072 others(34): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489491 | |||||||
| chr9:114489502 | A | ACACG | 265 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(262): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.619-10732_619-1073 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489502 | |||||||
| chr9:114489502 | A | G | 2 | a0001c0008t0010g0293 a0008c0030t0002g0292 |
2 | HG01109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.619-10731T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489502 | |||||||
| chr9:114489504 | G | A | 267 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(264): Show |
275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.619-10733C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489504 | |||||||
| chr9:114489504 | G | GCA | 4 | a0003c0003t0001g0008 a0011c0033t0001g0085 a0011c0034t0001g0087 others(1): Show |
5 | HG00423.hp2 HG00558.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.619-10735_619-1073 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489504 | |||||||
| chr9:114489512 | G | A | 22 | a0001c0002t0004g0232 a0001c0012t0002g0010 a0001c0012t0002g0277 others(19): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-10741C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489512 | |||||||
| chr9:114489515 | T | C | 22 | a0001c0002t0004g0232 a0001c0012t0002g0010 a0001c0012t0002g0277 others(19): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-10744A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489515 | |||||||
| chr9:114489516 | GCA | G | 11 | a0001c0002t0003g0228 a0001c0006t0003g0225 a0001c0010t0003g0222 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.619-10747_619-1074 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489516 | |||||||
| chr9:114489516 | GCACA | G | 218 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(215): Show |
224 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.619-10749_619-1074 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489516 | |||||||
| chr9:114489516 | GCACACA | G | 56 | a0001c0002t0001g0105 a0001c0002t0001g0109 a0001c0002t0001g0115 others(53): Show |
59 | HG00140.hp2 HG00280.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.619-10751_619-1074 others(10): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489516 | |||||||
| chr9:114489517 | C | T | 22 | a0001c0002t0004g0232 a0001c0012t0002g0010 a0001c0012t0002g0277 others(19): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-10746G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489517 | |||||||
| chr9:114489518 | A | G | 22 | a0001c0002t0004g0232 a0001c0012t0002g0010 a0001c0012t0002g0277 others(19): Show |
25 | HG01070.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.619-10747T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489518 | |||||||
| chr9:114489811 | A | T | 1 | a0001c0002t0001g0117 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.619-11040T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489811 | |||||||
| chr9:114489906 | CAT | C | 123 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(120): Show |
125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.619-11137_619-1113 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489906 | |||||||
| chr9:114489913 | T | C | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-11142A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489913 | |||||||
| chr9:114489935 | A | G | 2 | a0003c0007t0002g0264 a0021c0038t0005g0245 |
2 | HG02809.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.619-11164T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114489935 | |||||||
| chr9:114490076 | C | T | 1 | a0007c0025t0002g0302 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.619-11305G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490076 | |||||||
| chr9:114490116 | G | A | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-11345C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490116 | |||||||
| chr9:114490134 | C | T | 3 | a0011c0033t0001g0085 a0011c0034t0001g0087 a0018c0032t0001g0084 |
3 | HG00423.hp2 HG00558.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.619-11363G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490134 | |||||||
| chr9:114490242 | T | C | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.619-11471A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490242 | |||||||
| chr9:114490293 | C | T | 1 | a0004c0018t0001g0161 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.619-11522G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490293 | |||||||
| chr9:114490318 | C | T | 112 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.619-11547G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490318 | |||||||
| chr9:114490415 | G | A | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.619-11644C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490415 | |||||||
| chr9:114490570 | T | TTTTC | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.619-11800_619-1179 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490570 | |||||||
| chr9:114490972 | A | G | 22 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(19): Show |
24 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.619-12201T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490972 | |||||||
| chr9:114490984 | G | A | 1 | a0002c0001t0001g0041 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.619-12213C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114490984 | |||||||
| chr9:114491028 | T | G | 136 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(133): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.619-12257A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491028 | |||||||
| chr9:114491136 | T | A | 4 | a0005c0011t0001g0081 a0005c0011t0001g0082 a0005c0011t0001g0083 others(1): Show |
4 | HG01069.hp1 HG02004.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.619-12365A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491136 | |||||||
| chr9:114491154 | G | A | 137 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(134): Show |
143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.619-12383C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491154 | |||||||
| chr9:114491168 | T | C | 1 | a0001c0008t0002g0284 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.619-12397A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491168 | |||||||
| chr9:114491235 | T | C | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.619-12464A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491235 | |||||||
| chr9:114491346 | G | A | 1 | a0003c0003t0001g0093 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.619-12575C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491346 | |||||||
| chr9:114491392 | C | T | 3 | a0004c0005t0004g0237 a0016c0017t0004g0235 a0016c0017t0004g0236 |
3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.619-12621G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491392 | |||||||
| chr9:114491458 | A | AAC | 4 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(1): Show |
4 | HG01192.hp2 HG01891.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.619-12689_619-1268 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491458 | |||||||
| chr9:114491458 | AACAC | A | 44 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0284 others(41): Show |
45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.619-12691_619-1268 others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491458 | |||||||
| chr9:114491549 | C | T | 4 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0002c0001t0001g0026 others(1): Show |
4 | HG00558.hp2 NA18975.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+12635G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491549 | |||||||
| chr9:114491556 | A | G | 1 | a0001c0006t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.618+12628T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491556 | |||||||
| chr9:114491619 | C | T | 22 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(19): Show |
24 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.618+12565G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491619 | |||||||
| chr9:114491693 | T | C | 139 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(136): Show |
145 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.618+12491A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491693 | |||||||
| chr9:114491753 | C | T | 5 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(2): Show |
5 | HG01884.hp2 HG02280.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.618+12431G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491753 | |||||||
| chr9:114491934 | G | A | 111 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(108): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.618+12250C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114491934 | |||||||
| chr9:114492015 | G | GA | 144 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(141): Show |
151 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.618+12168dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492015 | |||||||
| chr9:114492015 | GA | G | 22 | a0001c0002t0001g0207 a0001c0002t0008g0199 a0002c0001t0005g0246 others(19): Show |
22 | HG00423.hp2 HG00558.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.618+12168delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492015 | |||||||
| chr9:114492015 | GAA | G | 105 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(102): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.618+12167_618+1216 others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492015 | |||||||
| chr9:114492132 | T | C | 2 | a0001c0008t0002g0274 a0004c0026t0002g0273 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.618+12052A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492132 | |||||||
| chr9:114492174 | G | A | 1 | a0001c0002t0001g0207 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.618+12010C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492174 | |||||||
| chr9:114492261 | G | A | 128 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(125): Show |
130 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.618+11923C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492261 | |||||||
| chr9:114492286 | A | G | 1 | a0002c0001t0001g0112 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.618+11898T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492286 | |||||||
| chr9:114492426 | A | G | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.618+11758T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492426 | |||||||
| chr9:114492451 | G | C | 44 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0284 others(41): Show |
45 | HG00323.hp1 HG00323.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.618+11733C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492451 | |||||||
| chr9:114492502 | G | A | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.618+11682C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492502 | |||||||
| chr9:114492703 | A | G | 4 | a0002c0001t0001g0024 a0002c0001t0001g0042 a0003c0003t0001g0022 others(1): Show |
4 | HG02056.hp2 NA18942.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+11481T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492703 | |||||||
| chr9:114492757 | G | A | 1 | a0005c0011t0001g0074 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.618+11427C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492757 | |||||||
| chr9:114492761 | A | G | 295 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(292): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.618+11423T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492761 | |||||||
| chr9:114492870 | T | C | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.618+11314A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492870 | |||||||
| chr9:114492886 | G | A | 1 | a0011c0034t0001g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.618+11298C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492886 | |||||||
| chr9:114492990 | C | T | 8 | a0002c0001t0005g0246 a0003c0007t0002g0264 a0009c0014t0005g0244 others(5): Show |
8 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+11194G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114492990 | |||||||
| chr9:114493037 | G | C | 1 | a0001c0010t0001g0157 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.618+11147C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493037 | |||||||
| chr9:114493173 | G | A | 4 | a0005c0011t0001g0081 a0005c0011t0001g0082 a0005c0011t0001g0083 others(1): Show |
4 | HG01069.hp1 HG02004.hp1 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+11011C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493173 | |||||||
| chr9:114493308 | G | A | 1 | a0002c0031t0002g0285 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.618+10876C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493308 | |||||||
| chr9:114493348 | CT | C | 4 | a0003c0003t0001g0076 a0003c0003t0001g0178 a0003c0003t0001g0200 others(1): Show |
4 | HG00558.hp1 HG02965.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+10835delA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493348 | |||||||
| chr9:114493354 | T | A | 4 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+10830A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493354 | |||||||
| chr9:114493355 | T | A | 9 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(6): Show |
9 | HG00423.hp2 HG01884.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.618+10829A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493355 | |||||||
| chr9:114493356 | T | A | 12 | a0001c0002t0003g0228 a0003c0003t0001g0057 a0003c0003t0001g0058 others(9): Show |
12 | HG00423.hp2 HG01123.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.618+10828A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493356 | |||||||
| chr9:114493356 | TA | T | 131 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(128): Show |
137 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.618+10827delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493356 | |||||||
| chr9:114493357 | A | T | 9 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(6): Show |
9 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.618+10827T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493357 | |||||||
| chr9:114493358 | A | T | 1 | a0001c0010t0003g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.618+10826T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493358 | |||||||
| chr9:114493379 | T | TG | 94 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(91): Show |
99 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.618+10804dupC | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493379 | |||||||
| chr9:114493380 | G | C | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.618+10804C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493380 | |||||||
| chr9:114493401 | G | A | 1 | a0003c0003t0001g0181 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.618+10783C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493401 | |||||||
| chr9:114493426 | T | A | 8 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(5): Show |
8 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+10758A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493426 | |||||||
| chr9:114493464 | C | T | 112 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(109): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.618+10720G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493464 | |||||||
| chr9:114493465 | C | T | 1 | a0001c0002t0003g0228 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.618+10719G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493465 | |||||||
| chr9:114493507 | C | A | 1 | a0001c0010t0001g0075 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.618+10677G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493507 | |||||||
| chr9:114493873 | T | C | 1 | a0001c0002t0001g0160 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.618+10311A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493873 | |||||||
| chr9:114493949 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.618+10235A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114493949 | |||||||
| chr9:114494095 | T | C | 116 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.618+10089A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494095 | |||||||
| chr9:114494133 | T | C | 2 | a0001c0002t0001g0182 a0001c0002t0001g0183 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.618+10051A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494133 | |||||||
| chr9:114494187 | A | G | 4 | a0001c0002t0001g0113 a0002c0001t0001g0112 a0002c0001t0001g0114 others(1): Show |
4 | HG00642.hp2 HG03490.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+9997T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494187 | |||||||
| chr9:114494390 | A | AT | 5 | a0001c0008t0002g0274 a0003c0003t0001g0076 a0003c0003t0001g0077 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+9793dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494390 | |||||||
| chr9:114494459 | T | C | 300 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(297): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.618+9725A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494459 | |||||||
| chr9:114494583 | T | A | 2 | a0004c0019t0001g0201 a0004c0042t0001g0063 |
2 | HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.618+9601A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494583 | |||||||
| chr9:114494592 | T | G | 1 | a0001c0006t0001g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618+9592A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494592 | |||||||
| chr9:114494602 | C | G | 1 | a0001c0012t0002g0276 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.618+9582G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494602 | |||||||
| chr9:114494616 | A | G | 137 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(134): Show |
143 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.618+9568T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494616 | |||||||
| chr9:114494620 | C | T | 1 | a0001c0006t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.618+9564G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494620 | |||||||
| chr9:114494723 | C | A | 1 | a0002c0001t0001g0042 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.618+9461G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494723 | |||||||
| chr9:114494764 | A | C | 1 | a0003c0003t0001g0059 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.618+9420T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494764 | |||||||
| chr9:114494792 | G | A | 292 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(289): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(299): Show |
intron_variant | MODIFIER | c.618+9392C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494792 | |||||||
| chr9:114494868 | AG | A | 121 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.618+9315delC | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494868 | |||||||
| chr9:114494927 | TG | T | 105 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(102): Show |
108 | HG00323.hp2 HG00558.hp2 HG00733.hp2 others(105): Show |
intron_variant | MODIFIER | c.618+9256delC | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494927 | |||||||
| chr9:114494927 | TGG | T | 24 | a0001c0008t0002g0297 a0001c0008t0002g0303 a0001c0028t0002g0301 others(21): Show |
27 | HG00408.hp1 HG00438.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.618+9255_618+9256d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494927 | |||||||
| chr9:114494929 | G | C | 121 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(118): Show |
123 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(120): Show |
intron_variant | MODIFIER | c.618+9255C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494929 | |||||||
| chr9:114494930 | G | A | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.618+9254C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494930 | |||||||
| chr9:114494930 | G | GT | 8 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(5): Show |
8 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+9253_618+9254i others(3): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114494930 | |||||||
| chr9:114495179 | T | C | 1 | a0001c0006t0001g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.618+9005A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495179 | |||||||
| chr9:114495373 | A | G | 8 | a0001c0006t0003g0225 a0001c0010t0003g0222 a0001c0010t0003g0223 others(5): Show |
8 | HG01192.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+8811T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495373 | |||||||
| chr9:114495418 | G | A | 1 | a0008c0016t0001g0198 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.618+8766C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495418 | |||||||
| chr9:114495523 | G | A | 1 | a0001c0002t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.618+8661C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495523 | |||||||
| chr9:114495525 | G | C | 1 | a0001c0028t0002g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.618+8659C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495525 | |||||||
| chr9:114495538 | G | A | 1 | a0014c0023t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.618+8646C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495538 | |||||||
| chr9:114495566 | C | A | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+8618G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495566 | |||||||
| chr9:114495654 | G | T | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+8530C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495654 | |||||||
| chr9:114495777 | A | G | 1 | a0002c0001t0001g0047 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.618+8407T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114495777 | |||||||
| chr9:114496070 | A | G | 2 | a0001c0002t0001g0109 a0001c0002t0001g0110 |
2 | NA18953.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.618+8114T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496070 | |||||||
| chr9:114496237 | G | A | 1 | a0001c0028t0002g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.618+7947C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496237 | |||||||
| chr9:114496273 | T | C | 3 | a0004c0005t0004g0237 a0016c0017t0004g0235 a0016c0017t0004g0236 |
3 | HG01243.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.618+7911A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496273 | |||||||
| chr9:114496367 | G | A | 18 | a0001c0002t0004g0232 a0003c0003t0001g0196 a0003c0003t0001g0197 others(15): Show |
20 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.618+7817C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496367 | |||||||
| chr9:114496433 | T | C | 2 | a0003c0003t0001g0057 a0003c0003t0001g0058 |
2 | HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.618+7751A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496433 | |||||||
| chr9:114496474 | G | A | 1 | a0002c0001t0001g0044 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.618+7710C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496474 | |||||||
| chr9:114496538 | CCAAA | C | 7 | a0002c0001t0005g0246 a0009c0014t0005g0244 a0009c0014t0005g0247 others(4): Show |
7 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+7642_618+7645d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496538 | |||||||
| chr9:114496542 | A | C | 4 | a0001c0002t0001g0092 a0001c0008t0002g0274 a0002c0001t0001g0004 others(1): Show |
4 | HG01891.hp1 HG02258.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+7642T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496542 | |||||||
| chr9:114496594 | C | T | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+7590G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496594 | |||||||
| chr9:114496757 | G | A | 1 | a0001c0028t0002g0301 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.618+7427C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496757 | |||||||
| chr9:114496782 | T | C | 114 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(111): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.618+7402A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496782 | |||||||
| chr9:114496972 | A | G | 2 | a0002c0001t0001g0013 a0002c0001t0001g0014 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.618+7212T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496972 | |||||||
| chr9:114496991 | A | G | 2 | a0004c0005t0001g0106 a0004c0005t0001g0108 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.618+7193T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114496991 | |||||||
| chr9:114497258 | A | C | 50 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0274 others(47): Show |
51 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.618+6926T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497258 | |||||||
| chr9:114497268 | A | G | 115 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(112): Show |
117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.618+6916T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497268 | |||||||
| chr9:114497282 | C | A | 7 | a0002c0001t0005g0246 a0009c0014t0005g0244 a0009c0014t0005g0247 others(4): Show |
7 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+6902G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497282 | |||||||
| chr9:114497494 | G | A | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.618+6690C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497494 | |||||||
| chr9:114497511 | G | GT | 12 | a0001c0002t0001g0098 a0001c0002t0001g0099 a0001c0002t0001g0102 others(9): Show |
12 | HG00544.hp2 HG01934.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.618+6672dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497511 | |||||||
| chr9:114497516 | T | C | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+6668A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497516 | |||||||
| chr9:114497516 | T | TA | 101 | a0001c0002t0001g0092 a0001c0002t0001g0109 a0001c0002t0001g0110 others(98): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.618+6667dupT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497516 | |||||||
| chr9:114497517 | A | T | 7 | a0001c0002t0001g0207 a0001c0002t0008g0199 a0003c0003t0001g0057 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+6667T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497517 | |||||||
| chr9:114497679 | G | C | 21 | a0001c0002t0001g0192 a0001c0002t0004g0232 a0001c0006t0001g0193 others(18): Show |
23 | HG01109.hp1 HG01243.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.618+6505C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497679 | |||||||
| chr9:114497871 | C | T | 2 | a0001c0010t0003g0222 a0001c0010t0003g0223 |
2 | HG01192.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.618+6313G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497871 | |||||||
| chr9:114497905 | C | T | 116 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.618+6279G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497905 | |||||||
| chr9:114497957 | G | A | 2 | a0001c0028t0002g0301 a0003c0003t0001g0059 |
2 | HG02080.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.618+6227C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497957 | |||||||
| chr9:114497986 | C | T | 131 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(128): Show |
140 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.618+6198G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114497986 | |||||||
| chr9:114498190 | G | A | 93 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(90): Show |
100 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.618+5994C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498190 | |||||||
| chr9:114498467 | C | G | 1 | a0003c0003t0001g0022 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.618+5717G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498467 | |||||||
| chr9:114498473 | C | A | 1 | a0002c0004t0002g0291 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+5711G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498473 | |||||||
| chr9:114498523 | C | T | 1 | a0008c0030t0002g0292 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.618+5661G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498523 | |||||||
| chr9:114498538 | G | C | 1 | a0001c0006t0001g0018 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.618+5646C>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498538 | |||||||
| chr9:114498554 | C | T | 116 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(113): Show |
118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.618+5630G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498554 | |||||||
| chr9:114498617 | A | G | 308 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(305): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.618+5567T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498617 | |||||||
| chr9:114498625 | T | G | 4 | a0003c0003t0001g0162 a0003c0003t0001g0163 a0004c0018t0001g0094 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.618+5559A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498625 | |||||||
| chr9:114498832 | G | A | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+5352C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498832 | |||||||
| chr9:114498845 | C | CGCCT | 3 | a0001c0002t0001g0207 a0004c0005t0001g0206 a0019c0036t0001g0205 |
3 | HG02145.hp2 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.618+5335_618+5338d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498845 | |||||||
| chr9:114498860 | C | G | 2 | a0005c0011t0001g0065 a0025c0037t0001g0069 |
2 | HG02165.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.618+5324G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498860 | |||||||
| chr9:114498900 | A | T | 1 | a0004c0018t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.618+5284T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114498900 | |||||||
| chr9:114499022 | C | T | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+5162G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499022 | |||||||
| chr9:114499133 | T | C | 1 | a0004c0005t0001g0206 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.618+5051A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499133 | |||||||
| chr9:114499251 | G | A | 8 | a0001c0002t0003g0228 a0002c0001t0005g0246 a0009c0014t0005g0244 others(5): Show |
8 | HG01255.hp2 HG01257.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+4933C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499251 | |||||||
| chr9:114499319 | G | A | 97 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(94): Show |
104 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.618+4865C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499319 | |||||||
| chr9:114499525 | C | T | 1 | a0004c0018t0001g0094 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.618+4659G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499525 | |||||||
| chr9:114499587 | G | A | 7 | a0001c0008t0002g0267 a0001c0009t0002g0269 a0001c0012t0002g0268 others(4): Show |
7 | HG00733.hp2 HG01981.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+4597C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499587 | |||||||
| chr9:114499592 | G | A | 1 | a0001c0006t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.618+4592C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499592 | |||||||
| chr9:114499677 | T | C | 3 | a0001c0002t0001g0045 a0001c0006t0009g0241 a0001c0006t0009g0242 |
3 | HG02040.hp2 NA18975.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.618+4507A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499677 | |||||||
| chr9:114499681 | C | T | 1 | a0014c0023t0001g0089 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.618+4503G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499681 | |||||||
| chr9:114499707 | C | T | 50 | a0001c0008t0002g0258 a0001c0008t0002g0267 a0001c0008t0002g0274 others(47): Show |
51 | HG00323.hp2 HG00733.hp2 HG00738.hp1 others(48): Show |
intron_variant | MODIFIER | c.618+4477G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499707 | |||||||
| chr9:114499977 | A | AT | 306 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(303): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.618+4206dupA | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114499977 | |||||||
| chr9:114500256 | G | T | 1 | a0003c0007t0002g0275 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.618+3928C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114500256 | |||||||
| chr9:114500299 | G | A | 1 | a0001c0006t0001g0167 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.618+3885C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114500299 | |||||||
| chr9:114500338 | T | C | 1 | a0001c0006t0001g0046 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.618+3846A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114500338 | |||||||
| chr9:114500597 | G | A | 102 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(99): Show |
109 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.618+3587C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114500597 | |||||||
| chr9:114501229 | T | C | 93 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(90): Show |
100 | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.618+2955A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501229 | |||||||
| chr9:114501293 | A | C | 1 | a0004c0019t0001g0064 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.618+2891T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501293 | |||||||
| chr9:114501361 | G | T | 5 | a0001c0008t0002g0274 a0003c0003t0001g0076 a0003c0003t0001g0077 others(2): Show |
5 | HG01123.hp1 HG01891.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.618+2823C>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501361 | |||||||
| chr9:114501546 | T | A | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+2638A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501546 | |||||||
| chr9:114501550 | T | A | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+2634A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501550 | |||||||
| chr9:114501551 | T | C | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+2633A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TAC | 59 | a0001c0002t0001g0020 a0001c0002t0001g0170 a0001c0002t0001g0171 others(56): Show |
63 | HG00544.hp1 HG00544.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.618+2631_618+2632d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACAC | 46 | a0001c0002t0001g0021 a0001c0002t0001g0184 a0001c0002t0003g0228 others(43): Show |
49 | HG00323.hp2 HG00423.hp1 HG00738.hp1 others(46): Show |
intron_variant | MODIFIER | c.618+2629_618+2632d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACAC | 52 | a0001c0002t0001g0027 a0001c0002t0001g0028 a0001c0002t0001g0039 others(49): Show |
55 | HG00558.hp2 HG01069.hp1 HG01074.hp1 others(52): Show |
intron_variant | MODIFIER | c.618+2627_618+2632d others(8): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACACA others(1): Show |
20 | a0001c0002t0001g0049 a0001c0006t0001g0062 a0001c0008t0002g0303 others(17): Show |
20 | HG00408.hp1 HG00438.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.618+2625_618+2632d others(10): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACACA others(3): Show |
18 | a0001c0002t0001g0051 a0001c0002t0001g0068 a0001c0002t0001g0192 others(15): Show |
18 | HG00558.hp1 HG00733.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.618+2623_618+2632d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACACA others(5): Show |
7 | a0001c0006t0001g0070 a0001c0006t0001g0071 a0001c0006t0001g0072 others(4): Show |
7 | HG00423.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.618+2621_618+2632d others(14): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACACA others(7): Show |
2 | a0001c0002t0001g0073 a0009c0014t0005g0247 |
2 | HG01257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.618+2619_618+2632d others(16): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | T | TACACACA others(9): Show |
3 | a0009c0014t0005g0248 a0009c0014t0005g0249 a0009c0014t0005g0250 |
3 | HG01255.hp2 HG01975.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.618+2617_618+2632d others(18): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | TAC | T | 8 | a0001c0002t0001g0092 a0001c0006t0001g0091 a0003c0003t0001g0090 others(5): Show |
8 | HG01099.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.618+2631_618+2632d others(4): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | TACAC | T | 7 | a0003c0003t0001g0059 a0003c0003t0001g0076 a0003c0003t0001g0077 others(4): Show |
7 | HG00280.hp2 HG01123.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+2629_618+2632d others(6): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501551 | TACACACA others(3): Show |
T | 1 | a0003c0007t0002g0251 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.618+2623_618+2632d others(12): Show |
WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501551 | |||||||
| chr9:114501598 | C | T | 111 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(108): Show |
113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.618+2586G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501598 | |||||||
| chr9:114501624 | C | T | 2 | a0004c0005t0006g0239 a0004c0005t0006g0240 |
2 | HG02895.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.618+2560G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501624 | |||||||
| chr9:114501735 | A | G | 1 | a0004c0005t0003g0220 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.618+2449T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501735 | |||||||
| chr9:114501803 | G | A | 109 | a0001c0002t0001g0092 a0001c0002t0001g0098 a0001c0002t0001g0099 others(106): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.618+2381C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501803 | |||||||
| chr9:114501815 | C | T | 1 | a0003c0003t0006g0238 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.618+2369G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114501815 | |||||||
| chr9:114502054 | C | A | 1 | a0002c0001t0001g0189 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.618+2130G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502054 | |||||||
| chr9:114502326 | C | T | 60 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(57): Show |
62 | HG00558.hp2 HG00642.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.618+1858G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502326 | |||||||
| chr9:114502364 | G | A | 1 | a0002c0001t0012g0054 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.618+1820C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502364 | |||||||
| chr9:114502497 | G | A | 1 | a0002c0004t0002g0313 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.618+1687C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502497 | |||||||
| chr9:114502868 | G | A | 3 | a0001c0008t0007g0316 a0001c0008t0007g0317 a0001c0008t0007g0318 |
3 | HG02615.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.618+1316C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502868 | |||||||
| chr9:114502933 | A | G | 3 | a0003c0003t0001g0057 a0003c0003t0001g0058 a0003c0003t0001g0200 |
3 | HG02965.hp2 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.618+1251T>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114502933 | |||||||
| chr9:114503126 | C | T | 73 | a0001c0002t0001g0056 a0001c0008t0002g0258 a0001c0008t0002g0267 others(70): Show |
77 | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.618+1058G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503126 | |||||||
| chr9:114503253 | C | A | 1 | a0002c0001t0001g0055 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.618+931G>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503253 | |||||||
| chr9:114503256 | T | C | 1 | a0002c0001t0001g0190 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.618+928A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503256 | |||||||
| chr9:114503302 | C | T | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+882G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503302 | |||||||
| chr9:114503303 | A | C | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+881T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503303 | |||||||
| chr9:114503305 | A | C | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+879T>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503305 | |||||||
| chr9:114503306 | C | G | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+878G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503306 | |||||||
| chr9:114503308 | C | G | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+876G>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503308 | |||||||
| chr9:114503309 | T | C | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+875A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503309 | |||||||
| chr9:114503311 | C | T | 43 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(40): Show |
45 | HG00558.hp2 HG01074.hp1 HG02027.hp2 others(42): Show |
intron_variant | MODIFIER | c.618+873G>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503311 | |||||||
| chr9:114503317 | T | G | 1 | a0002c0001t0001g0191 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.618+867A>C | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503317 | |||||||
| chr9:114503331 | G | A | 1 | a0003c0007t0002g0314 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.618+853C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503331 | |||||||
| chr9:114503438 | T | A | 2 | a0001c0002t0001g0192 a0001c0006t0001g0193 |
2 | HG02257.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.618+746A>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503438 | |||||||
| chr9:114503558 | T | C | 6 | a0003c0003t0001g0196 a0003c0003t0001g0197 a0008c0016t0001g0009 others(3): Show |
7 | HG02486.hp1 HG02559.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.618+626A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503558 | |||||||
| chr9:114503616 | G | A | 1 | a0001c0002t0008g0199 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.618+568C>T | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503616 | |||||||
| chr9:114503729 | T | C | 1 | a0003c0003t0001g0200 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.618+455A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503729 | |||||||
| chr9:114503906 | T | C | 1 | a0004c0019t0001g0201 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.618+278A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503906 | |||||||
| chr9:114503986 | T | C | 2 | a0001c0002t0001g0202 a0001c0002t0001g0203 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.618+198A>G | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114503986 | |||||||
| chr9:114504057 | TA | T | 303 | a0001c0002t0001g0020 a0001c0002t0001g0021 a0001c0002t0001g0027 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.618+126delT | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114504057 | |||||||
| chr9:114504059 | A | T | 8 | a0002c0001t0001g0002 a0002c0001t0001g0003 a0002c0001t0001g0012 others(5): Show |
10 | HG01167.hp1 HG01169.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.618+125T>A | WHRN | ENSG00000095397.17 | transcript | ENST00000362057.4 | protein_coding | 1/11 | chr9 | 114504059 |