Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 151651 |
| ensemblid | ENSG00000163576.18 |
| hgncid | 26330 |
| symbol | EFHB |
| name | EF-hand domain family member B |
| refseq_nuc | NM_144715.4 |
| refseq_prot | NP_653316.3 |
| ensembl_nuc | ENST00000295824.14 |
| ensembl_prot | ENSP00000295824.9 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 19879472 |
| end | 19934217 |
| strand | - |
| ver | v1.2 |
| region | chr3:19879472-19934217 |
| region5000 | chr3:19874472-19939217 |
| regionname0 | EFHB_chr3_19879472_19934217 |
| regionname5000 | EFHB_chr3_19874472_19939217 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 833 | 100 | 5 | 23 | 54 | 5 | 12 | 41 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0002 | 0/1 | 833 | 93 | 31 | 26 | 20 | 6 | 9 | 15 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0003 | 0/0 | 833 | 34 | 3 | 10 | 15 | 3 | 3 | 11 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0004 | 0/0 | 833 | 21 | 0 | 0 | 16 | 0 | 5 | 12 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0005 | 0/0 | 833 | 15 | 10 | 1 | 0 | 1 | 3 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0006 | 0/0 | 833 | 15 | 6 | 6 | 0 | 0 | 3 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0007 | 0/0 | 833 | 15 | 15 | 0 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0008 | 0/0 | 833 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMET others(828): Show |
chr3 | 19874472 | 19939217 |
| a0009 | 0/0 | 833 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0010 | 0/0 | 833 | 5 | 2 | 1 | 1 | 0 | 1 | 1 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0011 | 0/0 | 833 | 5 | 2 | 0 | 2 | 1 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0012 | 0/0 | 833 | 4 | 0 | 2 | 0 | 0 | 2 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0013 | 0/0 | 833 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0014 | 0/0 | 833 | 3 | 0 | 2 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0015 | 0/0 | 833 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0016 | 0/0 | 833 | 2 | 0 | 1 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0017 | 0/0 | 833 | 2 | 1 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0018 | 0/0 | 833 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0019 | 0/0 | 833 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0020 | 0/0 | 833 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMET others(828): Show |
chr3 | 19874472 | 19939217 |
| a0021 | 0/0 | 833 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0022 | 0/0 | 833 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0023 | 0/0 | 833 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0024 | 0/0 | 441 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(436): Show |
chr3 | 19874472 | 19939217 |
| a0025 | 0/0 | 833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0026 | 0/0 | 833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| a0027 | 0/0 | 833 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | MNMEI others(828): Show |
chr3 | 19874472 | 19939217 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2499 | 98 | 5 | 22 | 54 | 5 | 11 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0001c0026 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0001c0028 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0002 | 0/0 | 2499 | 35 | 9 | 3 | 16 | 1 | 6 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0003 | 0/1 | 2499 | 33 | 0 | 20 | 4 | 5 | 3 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0009 | 0/0 | 2499 | 13 | 13 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0010 | 0/0 | 2499 | 9 | 8 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0019 | 0/0 | 2499 | 2 | 1 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0002c0024 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0003c0004 | 0/0 | 2499 | 33 | 3 | 10 | 14 | 3 | 3 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0003c0039 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0004c0005 | 0/0 | 2499 | 20 | 0 | 0 | 15 | 0 | 5 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0004c0035 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0005c0006 | 0/0 | 2499 | 15 | 10 | 1 | 0 | 1 | 3 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0006c0007 | 0/0 | 2499 | 14 | 6 | 6 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0006c0029 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0007c0008 | 0/0 | 2499 | 14 | 14 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0007c0027 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0008c0011 | 0/0 | 2499 | 8 | 8 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0009c0012 | 0/0 | 2499 | 6 | 5 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0010c0018 | 0/0 | 2499 | 3 | 2 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0010c0020 | 0/0 | 2499 | 2 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0011c0013 | 0/0 | 2499 | 5 | 2 | 0 | 2 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0012c0014 | 0/0 | 2499 | 4 | 0 | 2 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0013c0016 | 0/0 | 2499 | 3 | 2 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0014c0017 | 0/0 | 2499 | 3 | 0 | 2 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0015c0015 | 0/0 | 2499 | 3 | 3 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0016c0022 | 0/0 | 2499 | 2 | 0 | 1 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0017c0021 | 0/0 | 2499 | 2 | 1 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0018c0025 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0019c0033 | 0/0 | 2499 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0020c0023 | 0/0 | 2499 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0021c0036 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0022c0034 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0023c0030 | 0/0 | 2499 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0024c0037 | 0/0 | 2405 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2400): Show |
chr3 | 19874472 | 19939217 | ||
| a0025c0032 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0026c0031 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 | ||
| a0027c0038 | 0/0 | 2499 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | ATGAA others(2494): Show |
chr3 | 19874472 | 19939217 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002 | 1/0 | 2860 | 98 | 5 | 22 | 54 | 5 | 11 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0001c0026t0001 | 0/0 | 2860 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0001c0028t0002 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0002t0001 | 0/0 | 2860 | 32 | 8 | 2 | 15 | 1 | 6 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0002t0002 | 0/0 | 2860 | 3 | 1 | 1 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0003t0001 | 0/1 | 2860 | 33 | 0 | 20 | 4 | 5 | 3 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0009t0001 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0009t0002 | 0/0 | 2860 | 12 | 12 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0010t0001 | 0/0 | 2860 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0010t0002 | 0/0 | 2860 | 7 | 6 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0019t0001 | 0/0 | 2860 | 2 | 1 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0002c0024t0001 | 0/0 | 2860 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0003c0004t0001 | 0/0 | 2860 | 33 | 3 | 10 | 14 | 3 | 3 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0003c0039t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0004c0005t0001 | 0/0 | 2860 | 20 | 0 | 0 | 15 | 0 | 5 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0004c0035t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0005c0006t0001 | 0/0 | 2860 | 14 | 9 | 1 | 0 | 1 | 3 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0005c0006t0003 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0006c0007t0002 | 0/0 | 2860 | 14 | 6 | 6 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0006c0029t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0007c0008t0001 | 0/0 | 2860 | 6 | 6 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0007c0008t0002 | 0/0 | 2860 | 8 | 8 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0007c0027t0002 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0008c0011t0001 | 0/0 | 2860 | 8 | 8 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0009c0012t0002 | 0/0 | 2860 | 6 | 5 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0010c0018t0002 | 0/0 | 2860 | 3 | 2 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0010c0020t0001 | 0/0 | 2860 | 2 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0011c0013t0001 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0011c0013t0002 | 0/0 | 2860 | 4 | 1 | 0 | 2 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0012c0014t0001 | 0/0 | 2860 | 4 | 0 | 2 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0013c0016t0001 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0013c0016t0002 | 0/0 | 2860 | 2 | 1 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0014c0017t0001 | 0/0 | 2860 | 3 | 0 | 2 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0015c0015t0002 | 0/0 | 2860 | 3 | 3 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0016c0022t0001 | 0/0 | 2860 | 2 | 0 | 1 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0017c0021t0001 | 0/0 | 2860 | 2 | 1 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0018c0025t0001 | 0/0 | 2860 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0019c0033t0001 | 0/0 | 2860 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0020c0023t0001 | 0/0 | 2860 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0021c0036t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0022c0034t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0023c0030t0001 | 0/0 | 2860 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0024c0037t0001 | 0/0 | 2766 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2761): Show |
chr3 | 19874472 | 19939217 |
| a0025c0032t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0026c0031t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| a0027c0038t0001 | 0/0 | 2860 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | AGACT others(2855): Show |
chr3 | 19874472 | 19939217 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0002g0001 | 0/0 | 9 | 0 | 1 | 5 | 0 | 3 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0002 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0009 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0026t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0001c0028t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0067 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0003t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0009t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0010t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0019t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0019t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0002c0024t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0003c0039t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0008 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0005t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0004c0035t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0005c0006t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0007t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0006c0029t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0008t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0007c0027t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0008c0011t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0009c0012t0002g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0009c0012t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0009c0012t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0009c0012t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0009c0012t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0010c0018t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0010c0018t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0010c0018t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0010c0020t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0010c0020t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0011c0013t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0011c0013t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0011c0013t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0011c0013t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0011c0013t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0012c0014t0001g0007 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0012c0014t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0013c0016t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0013c0016t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0013c0016t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0014c0017t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0014c0017t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0014c0017t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0015c0015t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0016c0022t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0016c0022t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0017c0021t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0017c0021t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0018c0025t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0019c0033t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0020c0023t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0021c0036t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0022c0034t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0023c0030t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0024c0037t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0025c0032t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0026c0031t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| a0027c0038t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | GBR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00099 | hp2 | a0002 | c0003 | t0001 | g0017 | EUR | GBR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0105 | EUR | GBR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0064 | EUR | GBR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00280 | hp1 | a0005 | c0006 | t0001 | g0081 | EUR | FIN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0228 | EUR | FIN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00323 | hp1 | a0002 | c0003 | t0001 | g0048 | EUR | FIN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0264 | EUR | FIN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00544 | hp2 | a0004 | c0005 | t0001 | g0003 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00642 | hp1 | a0010 | c0020 | t0001 | g0050 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00642 | hp2 | a0002 | c0019 | t0001 | g0053 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00673 | hp2 | a0003 | c0004 | t0001 | g0166 | EAS | CHS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0023 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0199 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0170 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00738 | hp2 | a0006 | c0007 | t0002 | g0272 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0147 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0241 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01069 | hp2 | a0003 | c0004 | t0001 | g0024 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01070 | hp1 | a0003 | c0004 | t0001 | g0025 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01070 | hp2 | a0012 | c0014 | t0001 | g0078 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01071 | hp1 | a0012 | c0014 | t0001 | g0007 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01071 | hp2 | a0003 | c0004 | t0001 | g0024 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01074 | hp1 | a0002 | c0003 | t0001 | g0051 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01074 | hp2 | a0005 | c0006 | t0001 | g0082 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01081 | hp1 | a0013 | c0016 | t0002 | g0271 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01099 | hp2 | a0003 | c0004 | t0001 | g0157 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01106 | hp1 | a0002 | c0003 | t0001 | g0071 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0194 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01109 | hp2 | a0006 | c0007 | t0002 | g0190 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01168 | hp1 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01169 | hp1 | a0001 | c0026 | t0001 | g0066 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0015 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01175 | hp1 | a0006 | c0007 | t0002 | g0203 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0016 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0055 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01192 | hp2 | a0006 | c0007 | t0002 | g0267 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01243 | hp1 | a0002 | c0010 | t0002 | g0179 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01255 | hp1 | a0006 | c0007 | t0002 | g0039 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01255 | hp2 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01256 | hp2 | a0002 | c0024 | t0001 | g0046 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01257 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01257 | hp2 | a0003 | c0004 | t0001 | g0171 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0016 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01346 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01361 | hp1 | a0018 | c0025 | t0001 | g0047 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01361 | hp2 | a0014 | c0017 | t0001 | g0122 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01433 | hp2 | a0019 | c0033 | t0001 | g0143 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01515 | hp2 | a0002 | c0003 | t0001 | g0058 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01516 | hp1 | a0003 | c0004 | t0001 | g0149 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01516 | hp2 | a0011 | c0013 | t0002 | g0208 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01517 | hp1 | a0003 | c0004 | t0001 | g0135 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01884 | hp1 | a0002 | c0009 | t0002 | g0276 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01884 | hp2 | a0007 | c0008 | t0002 | g0027 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01891 | hp1 | a0002 | c0009 | t0002 | g0006 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0085 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01934 | hp1 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01934 | hp2 | a0009 | c0012 | t0002 | g0259 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01943 | hp1 | a0002 | c0003 | t0001 | g0052 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01943 | hp2 | a0016 | c0022 | t0001 | g0172 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0216 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01975 | hp2 | a0002 | c0003 | t0001 | g0063 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0073 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01981 | hp2 | a0003 | c0004 | t0001 | g0023 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01993 | hp1 | a0014 | c0017 | t0001 | g0096 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0062 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02027 | hp2 | a0004 | c0005 | t0001 | g0137 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02040 | hp1 | a0003 | c0004 | t0001 | g0148 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0256 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02080 | hp1 | a0014 | c0017 | t0001 | g0095 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02080 | hp2 | a0003 | c0004 | t0001 | g0176 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02145 | hp1 | a0007 | c0008 | t0001 | g0087 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02145 | hp2 | a0002 | c0010 | t0002 | g0184 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CDX | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | CDX | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02165 | hp1 | a0004 | c0005 | t0001 | g0151 | EAS | CDX | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CDX | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0215 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02257 | hp2 | a0002 | c0009 | t0002 | g0011 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02258 | hp1 | a0013 | c0016 | t0001 | g0076 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02258 | hp2 | a0015 | c0015 | t0002 | g0012 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0111 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02280 | hp1 | a0011 | c0013 | t0002 | g0255 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02280 | hp2 | a0005 | c0006 | t0001 | g0119 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0069 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02293 | hp2 | a0006 | c0007 | t0002 | g0268 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02300 | hp2 | a0002 | c0003 | t0001 | g0004 | AMR | PEL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02523 | hp1 | a0004 | c0005 | t0001 | g0003 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02572 | hp1 | a0005 | c0006 | t0001 | g0090 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02572 | hp2 | a0007 | c0008 | t0002 | g0193 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02602 | hp1 | a0003 | c0004 | t0001 | g0159 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02615 | hp1 | a0005 | c0006 | t0001 | g0103 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02615 | hp2 | a0002 | c0009 | t0002 | g0006 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02622 | hp1 | a0007 | c0008 | t0002 | g0196 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02622 | hp2 | a0007 | c0008 | t0001 | g0020 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02630 | hp1 | a0005 | c0006 | t0001 | g0118 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02630 | hp2 | a0002 | c0009 | t0002 | g0006 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02647 | hp1 | a0005 | c0006 | t0001 | g0126 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02647 | hp2 | a0002 | c0009 | t0002 | g0278 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02683 | hp2 | a0006 | c0007 | t0002 | g0266 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0112 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02698 | hp2 | a0004 | c0005 | t0001 | g0008 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02717 | hp1 | a0009 | c0012 | t0002 | g0261 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02723 | hp1 | a0008 | c0011 | t0001 | g0043 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02723 | hp2 | a0002 | c0009 | t0002 | g0275 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02735 | hp2 | a0002 | c0003 | t0001 | g0057 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02738 | hp1 | a0005 | c0006 | t0001 | g0088 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0099 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02809 | hp1 | a0010 | c0018 | t0002 | g0257 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02809 | hp2 | a0006 | c0007 | t0002 | g0265 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02818 | hp1 | a0020 | c0023 | t0001 | g0041 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02818 | hp2 | a0015 | c0015 | t0002 | g0012 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02886 | hp1 | a0002 | c0009 | t0002 | g0274 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02895 | hp2 | a0002 | c0010 | t0002 | g0185 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02896 | hp1 | a0002 | c0010 | t0002 | g0181 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02896 | hp2 | a0002 | c0010 | t0001 | g0127 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02922 | hp1 | a0006 | c0007 | t0002 | g0191 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02922 | hp2 | a0006 | c0007 | t0002 | g0038 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02965 | hp1 | a0006 | c0007 | t0002 | g0189 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02965 | hp2 | a0005 | c0006 | t0001 | g0079 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0174 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02976 | hp1 | a0007 | c0008 | t0001 | g0083 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02976 | hp2 | a0008 | c0011 | t0001 | g0042 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03017 | hp1 | a0001 | c0028 | t0002 | g0211 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03041 | hp1 | a0005 | c0006 | t0001 | g0080 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03041 | hp2 | a0009 | c0012 | t0002 | g0037 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03098 | hp1 | a0011 | c0013 | t0001 | g0074 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03098 | hp2 | a0002 | c0010 | t0002 | g0182 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03130 | hp1 | a0008 | c0011 | t0001 | g0044 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03130 | hp2 | a0005 | c0006 | t0003 | g0040 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03139 | hp1 | a0007 | c0008 | t0001 | g0020 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03139 | hp2 | a0006 | c0007 | t0002 | g0038 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03195 | hp1 | a0002 | c0009 | t0002 | g0006 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03195 | hp2 | a0008 | c0011 | t0001 | g0014 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03209 | hp1 | a0007 | c0008 | t0002 | g0027 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03209 | hp2 | a0002 | c0009 | t0002 | g0277 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03225 | hp1 | a0002 | c0009 | t0001 | g0128 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03225 | hp2 | a0005 | c0006 | t0001 | g0104 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03239 | hp1 | a0003 | c0004 | t0001 | g0162 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03239 | hp2 | a0012 | c0014 | t0001 | g0007 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03453 | hp2 | a0007 | c0008 | t0002 | g0036 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03486 | hp1 | a0009 | c0012 | t0002 | g0037 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03491 | hp1 | a0005 | c0006 | t0001 | g0019 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03491 | hp2 | a0003 | c0004 | t0001 | g0152 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03492 | hp1 | a0005 | c0006 | t0001 | g0019 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03492 | hp2 | a0021 | c0036 | t0001 | g0134 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03516 | hp1 | a0013 | c0016 | t0002 | g0270 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03516 | hp2 | a0008 | c0011 | t0001 | g0014 | AFR | ESN | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03540 | hp1 | a0002 | c0019 | t0001 | g0049 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03540 | hp2 | a0002 | c0010 | t0002 | g0183 | AFR | GWD | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03579 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03579 | hp2 | a0007 | c0008 | t0002 | g0036 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0093 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03669 | hp1 | a0022 | c0034 | t0001 | g0144 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03669 | hp2 | a0012 | c0014 | t0001 | g0007 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0110 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0017 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03704 | hp2 | a0004 | c0005 | t0001 | g0146 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03710 | hp2 | a0006 | c0007 | t0002 | g0039 | SAS | PJL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03831 | hp1 | a0023 | c0030 | t0001 | g0115 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03831 | hp2 | a0024 | c0037 | t0001 | g0140 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04184 | hp1 | a0004 | c0005 | t0001 | g0154 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04184 | hp2 | a0006 | c0029 | t0001 | g0123 | SAS | BEB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0092 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04204 | hp1 | a0004 | c0005 | t0001 | g0008 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0250 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG04228 | hp2 | a0010 | c0020 | t0001 | g0065 | SAS | STU | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18522 | hp1 | a0002 | c0010 | t0002 | g0180 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18522 | hp2 | a0008 | c0011 | t0001 | g0013 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18612 | hp1 | a0003 | c0039 | t0001 | g0178 | EAS | CHB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | CHB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18747 | hp1 | a0016 | c0022 | t0001 | g0164 | EAS | CHB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18906 | hp1 | a0007 | c0008 | t0001 | g0117 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18906 | hp2 | a0002 | c0010 | t0001 | g0075 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18940 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18940 | hp2 | a0011 | c0013 | t0002 | g0237 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18941 | hp1 | a0003 | c0004 | t0001 | g0173 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18944 | hp1 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18947 | hp1 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18947 | hp2 | a0011 | c0013 | t0002 | g0220 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18948 | hp1 | a0003 | c0004 | t0001 | g0165 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18948 | hp2 | a0003 | c0004 | t0001 | g0138 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18952 | hp1 | a0017 | c0021 | t0001 | g0136 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18959 | hp1 | a0004 | c0005 | t0001 | g0155 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18960 | hp2 | a0004 | c0035 | t0001 | g0142 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18961 | hp1 | a0002 | c0003 | t0001 | g0060 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18961 | hp2 | a0004 | c0005 | t0001 | g0141 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18964 | hp2 | a0025 | c0032 | t0001 | g0130 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18970 | hp1 | a0004 | c0005 | t0001 | g0003 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18979 | hp2 | a0004 | c0005 | t0001 | g0132 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18981 | hp1 | a0004 | c0005 | t0001 | g0003 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18984 | hp1 | a0004 | c0005 | t0001 | g0161 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18985 | hp1 | a0002 | c0003 | t0001 | g0070 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18985 | hp2 | a0004 | c0005 | t0001 | g0133 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18990 | hp2 | a0026 | c0031 | t0001 | g0129 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18991 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18991 | hp2 | a0004 | c0005 | t0001 | g0163 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0061 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19003 | hp2 | a0003 | c0004 | t0001 | g0168 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19006 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19010 | hp2 | a0027 | c0038 | t0001 | g0177 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19030 | hp1 | a0007 | c0008 | t0001 | g0097 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0120 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19043 | hp1 | a0007 | c0008 | t0002 | g0195 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19043 | hp2 | a0009 | c0012 | t0002 | g0258 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19058 | hp2 | a0003 | c0004 | t0001 | g0150 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19060 | hp2 | a0004 | c0005 | t0001 | g0131 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19064 | hp1 | a0003 | c0004 | t0001 | g0160 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19064 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19066 | hp2 | a0004 | c0005 | t0001 | g0003 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19068 | hp2 | a0002 | c0003 | t0001 | g0068 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19074 | hp1 | a0003 | c0004 | t0001 | g0153 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19077 | hp2 | a0010 | c0018 | t0002 | g0202 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19079 | hp2 | a0004 | c0005 | t0001 | g0145 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19083 | hp1 | a0003 | c0004 | t0001 | g0175 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19083 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19088 | hp2 | a0003 | c0004 | t0001 | g0167 | EAS | JPT | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19240 | hp1 | a0008 | c0011 | t0001 | g0013 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA19240 | hp2 | a0015 | c0015 | t0002 | g0012 | AFR | YRI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20129 | hp1 | a0002 | c0002 | t0001 | g0089 | AFR | ASW | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20129 | hp2 | a0017 | c0021 | t0001 | g0156 | AFR | ASW | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20752 | hp1 | a0002 | c0003 | t0001 | g0059 | EUR | TSI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20752 | hp2 | a0003 | c0004 | t0001 | g0169 | EUR | TSI | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20905 | hp1 | a0002 | c0003 | t0001 | g0056 | SAS | GIH | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20905 | hp2 | a0004 | c0005 | t0001 | g0008 | SAS | GIH | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01123 | hp1 | a0002 | c0003 | t0001 | g0072 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02109 | hp1 | a0002 | c0009 | t0002 | g0011 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02486 | hp1 | a0007 | c0027 | t0002 | g0273 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02486 | hp2 | a0008 | c0011 | t0001 | g0045 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02559 | hp1 | a0006 | c0007 | t0002 | g0240 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03471 | hp1 | a0002 | c0009 | t0002 | g0011 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG03471 | hp2 | a0007 | c0008 | t0002 | g0192 | AFR | MSL | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | USA | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| HG06807 | hp2 | a0009 | c0012 | t0002 | g0260 | AFR | USA | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20300 | hp1 | a0005 | c0006 | t0001 | g0094 | AFR | USA | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0026 | AFR | USA | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0077 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| NA21309 | hp2 | a0010 | c0018 | t0002 | g0188 | AFR | LWK | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| homoSapiens | chm13v2 | a0002 | c0003 | t0001 | g0067 | REF | REF | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0009 | REF | REF | EFHB_chr3_19874472_19939217 | EFHB | chr3 | 19874472 | 19939217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:19882566 | G | A | 2 | a0012 a0021 |
5 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(2): Show |
missense_variant | MODERATE | c.2312C>T | p.Thr771Ile | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/13 | 2511/2860 | 2312/2502 | 771/833 | chr3 | 19882566 | |||
| chr3:19882599 | C | T | 3 | a0007 a0009 a0020 |
22 | HG01884.hp2 HG01934.hp2 HG02145.hp1 others(19): Show |
missense_variant | MODERATE | c.2279G>A | p.Arg760Gln | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/13 | 2478/2860 | 2279/2502 | 760/833 | chr3 | 19882599 | |||
| chr3:19884561 | T | G | 3 | a0008 a0013 a0015 |
14 | HG01081.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
missense_variant | MODERATE | c.1988A>C | p.Gln663Pro | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/13 | 2187/2860 | 1988/2502 | 663/833 | chr3 | 19884561 | |||
| chr3:19884615 | C | T | 1 | a0023 | 1 | HG03831.hp1 | missense_variant&splice_region_variant | MODERATE | c.1934G>A | p.Gly645Asp | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/13 | 2133/2860 | 1934/2502 | 645/833 | chr3 | 19884615 | |||
| chr3:19888638 | A | T | 10 | a0004 a0005 a0011 others(7): Show |
53 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(50): Show |
missense_variant | MODERATE | c.1739T>A | p.Met580Lys | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/13 | 1938/2860 | 1739/2502 | 580/833 | chr3 | 19888638 | |||
| chr3:19896743 | T | G | 1 | a0022 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.1669A>C | p.Lys557Gln | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/13 | 1868/2860 | 1669/2502 | 557/833 | chr3 | 19896743 | |||
| chr3:19896835 | C | T | 2 | a0019 a0022 |
2 | HG01433.hp2 HG03669.hp1 |
missense_variant | MODERATE | c.1577G>A | p.Gly526Asp | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/13 | 1776/2860 | 1577/2502 | 526/833 | chr3 | 19896835 | |||
| chr3:19898793 | G | A | 1 | a0018 | 1 | HG01361.hp1 | missense_variant | MODERATE | c.1555C>T | p.Arg519Cys | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/13 | 1754/2860 | 1555/2502 | 519/833 | chr3 | 19898793 | |||
| chr3:19898823 | G | C | 1 | a0015 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
missense_variant | MODERATE | c.1525C>G | p.Pro509Ala | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/13 | 1724/2860 | 1525/2502 | 509/833 | chr3 | 19898823 | |||
| chr3:19905655 | CATGGCTC others(5159): Show |
C | 1 | a0024 | 1 | HG03831.hp2 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.1288+4482_1382del | p.Glu431fs | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/13 | 1581/2860 | 1289/2502 | 430/833 | chr3 | 19905655 | |||
| chr3:19918264 | G | A | 21 | a0002 a0003 a0004 others(18): Show |
219 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(216): Show |
missense_variant | MODERATE | c.1145C>T | p.Thr382Ile | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/13 | 1344/2860 | 1145/2502 | 382/833 | chr3 | 19918264 | |||
| chr3:19919838 | C | T | 21 | a0002 a0003 a0004 others(18): Show |
228 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(225): Show |
missense_variant | MODERATE | c.991G>A | p.Val331Ile | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/13 | 1190/2860 | 991/2502 | 331/833 | chr3 | 19919838 | |||
| chr3:19920552 | G | A | 10 | a0003 a0004 a0010 others(7): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
missense_variant | MODERATE | c.805C>T | p.Pro269Ser | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 2/13 | 1004/2860 | 805/2502 | 269/833 | chr3 | 19920552 | |||
| chr3:19933399 | T | A | 1 | a0027 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.620A>T | p.Asn207Ile | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 819/2860 | 620/2502 | 207/833 | chr3 | 19933399 | |||
| chr3:19933442 | C | T | 1 | a0025 | 1 | NA18964.hp2 | missense_variant | MODERATE | c.577G>A | p.Asp193Asn | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 776/2860 | 577/2502 | 193/833 | chr3 | 19933442 | |||
| chr3:19933723 | C | A | 10 | a0003 a0004 a0016 others(7): Show |
65 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
missense_variant | MODERATE | c.296G>T | p.Gly99Val | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 495/2860 | 296/2502 | 99/833 | chr3 | 19933723 | |||
| chr3:19934005 | A | G | 2 | a0008 a0020 |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
missense_variant | MODERATE | c.14T>C | p.Ile5Thr | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 213/2860 | 14/2502 | 5/833 | chr3 | 19934005 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:19882565 | G | C | 1 | a0004c0035 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.2313C>G | p.Thr771Thr | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/13 | 2512/2860 | 2313/2502 | 771/833 | chr3 | 19882565 | |||
| chr3:19888511 | G | A | 12 | a0001c0028 a0002c0003 a0002c0009 others(9): Show |
81 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(78): Show |
synonymous_variant | LOW | c.1866C>T | p.Phe622Phe | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/13 | 2065/2860 | 1866/2502 | 622/833 | chr3 | 19888511 | |||
| chr3:19919839 | T | C | 7 | a0002c0002 a0005c0006 a0006c0029 others(4): Show |
73 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(70): Show |
synonymous_variant | LOW | c.990A>G | p.Ser330Ser | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/13 | 1189/2860 | 990/2502 | 330/833 | chr3 | 19919839 | |||
| chr3:19933647 | C | T | 6 | a0001c0026 a0002c0003 a0002c0019 others(3): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
synonymous_variant | LOW | c.372G>A | p.Arg124Arg | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 571/2860 | 372/2502 | 124/833 | chr3 | 19933647 | |||
| chr3:19933662 | T | G | 1 | a0003c0039 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.357A>C | p.Gly119Gly | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 556/2860 | 357/2502 | 119/833 | chr3 | 19933662 | |||
| chr3:19933668 | A | G | 2 | a0002c0024 a0018c0025 |
2 | HG01256.hp2 HG01361.hp1 |
synonymous_variant | LOW | c.351T>C | p.Leu117Leu | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 550/2860 | 351/2502 | 117/833 | chr3 | 19933668 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:19934090 | A | G | 33 | a0001c0026t0001 a0002c0002t0001 a0002c0003t0001 others(30): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
5_prime_UTR_variant | MODIFIER | c.-72T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 72 | chr3 | 19934090 | ||||||
| chr3:19934093 | C | T | 1 | a0005c0006t0003 | 1 | HG03130.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/13 | 75 | chr3 | 19934093 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:19879890 | G | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0197 a0001c0001t0002g0219 others(3): Show |
7 | HG00544.hp1 NA18939.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2329-86C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19879890 | |||||||
| chr3:19879923 | T | C | 1 | a0008c0011t0001g0043 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2329-119A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19879923 | |||||||
| chr3:19880068 | T | C | 205 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0002g0199 others(202): Show |
244 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2329-264A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880068 | |||||||
| chr3:19880195 | G | A | 51 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(48): Show |
60 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.2329-391C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880195 | |||||||
| chr3:19880229 | C | CATTT | 11 | a0001c0001t0002g0215 a0001c0001t0002g0233 a0002c0002t0001g0124 others(8): Show |
12 | HG00642.hp2 HG00738.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.2329-429_2329-426d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | C | CATTTATT others(1): Show |
26 | a0002c0003t0001g0016 a0002c0003t0001g0054 a0002c0003t0001g0056 others(23): Show |
30 | HG00140.hp2 HG01106.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.2329-433_2329-426d others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | C | CATTTATT others(5): Show |
31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
40 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.2329-437_2329-426d others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | C | CATTTATT others(9): Show |
8 | a0002c0010t0001g0075 a0007c0008t0001g0020 a0007c0008t0002g0027 others(5): Show |
11 | HG01884.hp2 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2329-441_2329-426d others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | C | CATTTATT others(13): Show |
1 | a0007c0008t0002g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2329-445_2329-426d others(22): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | CATTT | C | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2329-429_2329-426d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | CATTTATT others(1): Show |
C | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2329-433_2329-426d others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880229 | CATTTATT others(5): Show |
C | 51 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(48): Show |
60 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.2329-437_2329-426d others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880229 | |||||||
| chr3:19880414 | C | T | 1 | a0013c0016t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2329-610G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880414 | |||||||
| chr3:19880748 | C | T | 61 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(58): Show |
74 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.2329-944G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880748 | |||||||
| chr3:19880833 | T | C | 1 | a0016c0022t0001g0164 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2329-1029A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880833 | |||||||
| chr3:19880846 | G | A | 10 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(7): Show |
14 | HG01081.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2329-1042C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880846 | |||||||
| chr3:19880911 | G | GAA | 7 | a0002c0010t0001g0075 a0008c0011t0001g0013 a0008c0011t0001g0014 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.2329-1109_2329-110 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880911 | |||||||
| chr3:19880949 | C | T | 1 | a0001c0001t0002g0243 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2329-1145G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19880949 | |||||||
| chr3:19881014 | A | C | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2329-1210T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881014 | |||||||
| chr3:19881239 | T | C | 51 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(48): Show |
60 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.2328+1311A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881239 | |||||||
| chr3:19881275 | C | T | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2328+1275G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881275 | |||||||
| chr3:19881453 | G | A | 1 | a0001c0001t0002g0246 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2328+1097C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881453 | |||||||
| chr3:19881479 | C | T | 1 | a0002c0003t0001g0073 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2328+1071G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881479 | |||||||
| chr3:19881507 | A | T | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2328+1043T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881507 | |||||||
| chr3:19881513 | A | G | 1 | a0002c0010t0001g0127 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2328+1037T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881513 | |||||||
| chr3:19881628 | A | C | 61 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(58): Show |
74 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.2328+922T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881628 | |||||||
| chr3:19881814 | T | C | 1 | a0003c0004t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2328+736A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881814 | |||||||
| chr3:19881840 | T | C | 61 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(58): Show |
74 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.2328+710A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881840 | |||||||
| chr3:19881864 | G | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2328+686C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881864 | |||||||
| chr3:19881952 | C | T | 2 | a0003c0004t0001g0175 a0003c0004t0001g0176 |
2 | HG02080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2328+598G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881952 | |||||||
| chr3:19881994 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2328+556C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19881994 | |||||||
| chr3:19882016 | A | AAAAT | 12 | a0001c0001t0002g0005 a0001c0001t0002g0187 a0001c0001t0002g0199 others(9): Show |
14 | HG00323.hp2 HG00597.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.2328+530_2328+533d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882016 | |||||||
| chr3:19882016 | AAAAT | A | 38 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0028 others(35): Show |
43 | HG00280.hp2 HG00408.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.2328+530_2328+533d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882016 | |||||||
| chr3:19882016 | AAAATAAA others(5): Show |
A | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.2328+522_2328+533d others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882016 | |||||||
| chr3:19882016 | AAAATAAA others(9): Show |
A | 2 | a0003c0004t0001g0026 a0003c0004t0001g0174 |
3 | HG02970.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2328+518_2328+533d others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882016 | |||||||
| chr3:19882047 | A | ATAAATAA others(1): Show |
28 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(25): Show |
35 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.2328+502_2328+503i others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882047 | |||||||
| chr3:19882047 | A | T | 1 | a0002c0003t0001g0057 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2328+503T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882047 | |||||||
| chr3:19882047 | ATAAATAA others(9): Show |
A | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
11 | HG02258.hp2 HG02486.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2328+487_2328+502d others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882047 | |||||||
| chr3:19882051 | ATAAATAA others(5): Show |
A | 2 | a0002c0002t0001g0120 a0005c0006t0001g0090 |
2 | HG02572.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2328+487_2328+498d others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882051 | |||||||
| chr3:19882055 | A | ATAAATAA others(1): Show |
3 | a0002c0003t0001g0072 a0002c0009t0002g0006 a0007c0008t0001g0083 |
3 | HG01123.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2328+487_2328+494d others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882055 | |||||||
| chr3:19882055 | A | ATAAT | 24 | a0002c0009t0001g0128 a0002c0009t0002g0006 a0002c0009t0002g0011 others(21): Show |
32 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(29): Show |
intron_variant | MODIFIER | c.2328+494_2328+495i others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882055 | |||||||
| chr3:19882055 | A | T | 35 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(32): Show |
42 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.2328+495T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882055 | |||||||
| chr3:19882055 | ATAAATAA others(1): Show |
A | 44 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(41): Show |
52 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.2328+487_2328+494d others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882055 | |||||||
| chr3:19882059 | ATAAT | A | 6 | a0004c0005t0001g0003 a0005c0006t0001g0079 a0005c0006t0001g0080 others(3): Show |
6 | HG00544.hp2 HG01516.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2328+487_2328+490d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882059 | |||||||
| chr3:19882067 | A | G | 50 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(47): Show |
59 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(56): Show |
intron_variant | MODIFIER | c.2328+483T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882067 | |||||||
| chr3:19882124 | C | T | 2 | a0002c0002t0001g0086 a0002c0002t0001g0100 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.2328+426G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882124 | |||||||
| chr3:19882136 | C | G | 2 | a0005c0006t0001g0079 a0005c0006t0001g0103 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2328+414G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882136 | |||||||
| chr3:19882191 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
11 | HG02258.hp2 HG02486.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2328+359G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882191 | |||||||
| chr3:19882230 | A | G | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
11 | HG02258.hp2 HG02486.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.2328+320T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882230 | |||||||
| chr3:19882330 | T | C | 60 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0002g0199 others(57): Show |
69 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.2328+220A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882330 | |||||||
| chr3:19882335 | T | A | 1 | a0006c0007t0002g0266 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2328+215A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882335 | |||||||
| chr3:19882520 | T | C | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.2328+30A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 12/12 | chr3 | 19882520 | |||||||
| chr3:19882791 | G | A | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.2147-60C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19882791 | |||||||
| chr3:19882880 | A | AC | 124 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(121): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2147-150_2147-149i others(3): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19882880 | |||||||
| chr3:19883039 | C | A | 4 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0089 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2147-308G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19883039 | |||||||
| chr3:19883727 | G | A | 30 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(27): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.2146+676C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19883727 | |||||||
| chr3:19884027 | A | G | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(1): Show |
4 | HG01168.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.2146+376T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884027 | |||||||
| chr3:19884104 | A | C | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2146+299T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884104 | |||||||
| chr3:19884191 | A | T | 1 | a0002c0002t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2146+212T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884191 | |||||||
| chr3:19884213 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2146+190T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884213 | |||||||
| chr3:19884315 | A | G | 124 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(121): Show |
153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.2146+88T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884315 | |||||||
| chr3:19884345 | A | C | 6 | a0007c0008t0002g0027 a0007c0008t0002g0036 a0007c0008t0002g0192 others(3): Show |
8 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.2146+58T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 11/12 | chr3 | 19884345 | |||||||
| chr3:19884717 | T | G | 1 | a0004c0005t0001g0161 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1934-102A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884717 | |||||||
| chr3:19884818 | A | C | 1 | a0001c0001t0002g0231 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1934-203T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884818 | |||||||
| chr3:19884905 | T | C | 51 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(48): Show |
60 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.1934-290A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884905 | |||||||
| chr3:19884915 | T | TA | 17 | a0001c0001t0002g0245 a0002c0002t0001g0105 a0002c0002t0001g0106 others(14): Show |
17 | HG00140.hp1 HG00642.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.1934-301dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884915 | |||||||
| chr3:19884915 | TA | T | 42 | a0001c0001t0002g0243 a0002c0003t0001g0004 a0002c0003t0001g0015 others(39): Show |
56 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(53): Show |
intron_variant | MODIFIER | c.1934-301delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884915 | |||||||
| chr3:19884915 | TAA | T | 10 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(7): Show |
12 | HG01109.hp2 HG02486.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.1934-302_1934-301d others(4): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884915 | |||||||
| chr3:19884959 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1934-344G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19884959 | |||||||
| chr3:19885074 | TAGTC | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
11 | HG02258.hp2 HG02486.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.1934-463_1934-460d others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885074 | |||||||
| chr3:19885132 | G | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1934-517C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885132 | |||||||
| chr3:19885221 | TC | T | 40 | a0004c0005t0001g0003 a0004c0005t0001g0008 a0004c0005t0001g0131 others(37): Show |
49 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1934-607delG | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885221 | |||||||
| chr3:19885221 | TCA | T | 3 | a0005c0006t0001g0118 a0005c0006t0001g0119 a0005c0006t0001g0126 |
3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1934-608_1934-607d others(4): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885221 | |||||||
| chr3:19885222 | C | CA | 57 | a0001c0001t0002g0010 a0001c0001t0002g0187 a0001c0028t0002g0211 others(54): Show |
66 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.1934-608dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885222 | |||||||
| chr3:19885222 | C | G | 1 | a0011c0013t0002g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1934-607G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885222 | |||||||
| chr3:19885222 | CA | C | 6 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0089 others(3): Show |
6 | HG01891.hp2 HG02895.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1934-608delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885222 | |||||||
| chr3:19885223 | A | G | 40 | a0004c0005t0001g0003 a0004c0005t0001g0008 a0004c0005t0001g0131 others(37): Show |
49 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.1934-608T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885223 | |||||||
| chr3:19885224 | A | G | 3 | a0005c0006t0001g0118 a0005c0006t0001g0119 a0005c0006t0001g0126 |
3 | HG02280.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1934-609T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885224 | |||||||
| chr3:19885346 | G | C | 51 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(48): Show |
60 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(57): Show |
intron_variant | MODIFIER | c.1934-731C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885346 | |||||||
| chr3:19885381 | T | A | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1934-766A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885381 | |||||||
| chr3:19885623 | G | T | 1 | a0002c0009t0001g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1934-1008C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885623 | |||||||
| chr3:19885686 | C | A | 2 | a0001c0001t0002g0224 a0001c0001t0002g0227 |
2 | HG02056.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1934-1071G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885686 | |||||||
| chr3:19885734 | C | T | 1 | a0001c0001t0002g0030 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1934-1119G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885734 | |||||||
| chr3:19885776 | G | C | 2 | a0001c0001t0002g0224 a0001c0001t0002g0227 |
2 | HG02056.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.1934-1161C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885776 | |||||||
| chr3:19885828 | C | A | 83 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(80): Show |
101 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(98): Show |
intron_variant | MODIFIER | c.1934-1213G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885828 | |||||||
| chr3:19885930 | G | A | 108 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(105): Show |
130 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.1934-1315C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885930 | |||||||
| chr3:19885974 | C | T | 4 | a0008c0011t0001g0013 a0008c0011t0001g0042 a0008c0011t0001g0043 others(1): Show |
5 | HG02723.hp1 HG02976.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1934-1359G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19885974 | |||||||
| chr3:19886036 | A | C | 2 | a0003c0004t0001g0167 a0003c0004t0001g0168 |
2 | NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1934-1421T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886036 | |||||||
| chr3:19886137 | T | C | 1 | a0023c0030t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1934-1522A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886137 | |||||||
| chr3:19886252 | T | C | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1934-1637A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886252 | |||||||
| chr3:19886328 | C | G | 1 | a0001c0001t0002g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1934-1713G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886328 | |||||||
| chr3:19886388 | C | T | 56 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(53): Show |
72 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.1934-1773G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886388 | |||||||
| chr3:19886425 | C | T | 111 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(108): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1934-1810G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886425 | |||||||
| chr3:19886520 | G | A | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1934-1905C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886520 | |||||||
| chr3:19886524 | C | T | 1 | a0004c0005t0001g0163 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1934-1909G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886524 | |||||||
| chr3:19886638 | T | C | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1933+1806A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886638 | |||||||
| chr3:19886674 | C | T | 1 | a0002c0002t0002g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1933+1770G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886674 | |||||||
| chr3:19886676 | CA | C | 122 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0005 others(119): Show |
153 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1933+1767delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886676 | |||||||
| chr3:19886676 | CAA | C | 34 | a0001c0001t0002g0204 a0001c0001t0002g0232 a0001c0001t0002g0236 others(31): Show |
41 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.1933+1766_1933+176 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886676 | |||||||
| chr3:19886676 | CAAA | C | 8 | a0002c0003t0001g0057 a0002c0009t0002g0277 a0004c0005t0001g0137 others(5): Show |
8 | HG01361.hp2 HG01934.hp2 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1933+1765_1933+176 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886676 | |||||||
| chr3:19886676 | CAAAA | C | 75 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(72): Show |
97 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(94): Show |
intron_variant | MODIFIER | c.1933+1764_1933+176 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19886676 | |||||||
| chr3:19887143 | G | A | 30 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(27): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1933+1301C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887143 | |||||||
| chr3:19887179 | G | A | 18 | a0007c0008t0001g0020 a0007c0008t0001g0083 a0007c0008t0001g0087 others(15): Show |
22 | HG01884.hp2 HG01934.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1933+1265C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887179 | |||||||
| chr3:19887268 | C | T | 1 | a0002c0009t0001g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1933+1176G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887268 | |||||||
| chr3:19887307 | C | A | 18 | a0007c0008t0001g0020 a0007c0008t0001g0083 a0007c0008t0001g0087 others(15): Show |
22 | HG01884.hp2 HG01934.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1933+1137G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887307 | |||||||
| chr3:19887344 | C | T | 62 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(59): Show |
80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.1933+1100G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887344 | |||||||
| chr3:19887382 | CAA | C | 37 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(34): Show |
49 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.1933+1060_1933+106 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887382 | |||||||
| chr3:19887382 | CAAA | C | 81 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(78): Show |
98 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(95): Show |
intron_variant | MODIFIER | c.1933+1059_1933+106 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887382 | |||||||
| chr3:19887396 | A | T | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1933+1048T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887396 | |||||||
| chr3:19887498 | T | C | 30 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(27): Show |
37 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.1933+946A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887498 | |||||||
| chr3:19887509 | A | G | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1933+935T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887509 | |||||||
| chr3:19887683 | G | A | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1933+761C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887683 | |||||||
| chr3:19887740 | G | A | 1 | a0002c0009t0001g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1933+704C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887740 | |||||||
| chr3:19887816 | A | G | 1 | a0002c0009t0001g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1933+628T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887816 | |||||||
| chr3:19887854 | T | A | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1933+590A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887854 | |||||||
| chr3:19887856 | C | A | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1933+588G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19887856 | |||||||
| chr3:19888019 | T | A | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1933+425A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888019 | |||||||
| chr3:19888062 | T | C | 1 | a0001c0001t0002g0252 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1933+382A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888062 | |||||||
| chr3:19888140 | C | G | 1 | a0001c0001t0002g0216 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1933+304G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888140 | |||||||
| chr3:19888185 | A | C | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1933+259T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888185 | |||||||
| chr3:19888317 | A | G | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1933+127T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888317 | |||||||
| chr3:19888411 | T | A | 4 | a0002c0010t0001g0075 a0013c0016t0001g0076 a0013c0016t0002g0270 others(1): Show |
4 | HG01081.hp1 HG02258.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1933+33A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 10/12 | chr3 | 19888411 | |||||||
| chr3:19888833 | A | G | 1 | a0005c0006t0001g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1726-182T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19888833 | |||||||
| chr3:19888972 | G | A | 4 | a0004c0005t0001g0131 a0004c0005t0001g0137 a0004c0005t0001g0145 others(1): Show |
4 | HG02027.hp2 NA18990.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1726-321C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19888972 | |||||||
| chr3:19888994 | A | G | 115 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(112): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1726-343T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19888994 | |||||||
| chr3:19889177 | G | A | 4 | a0002c0010t0001g0075 a0013c0016t0001g0076 a0013c0016t0002g0270 others(1): Show |
4 | HG01081.hp1 HG02258.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-526C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889177 | |||||||
| chr3:19889203 | G | A | 52 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(49): Show |
63 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.1726-552C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889203 | |||||||
| chr3:19889223 | A | G | 1 | a0002c0002t0001g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1726-572T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889223 | |||||||
| chr3:19889251 | T | G | 52 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(49): Show |
63 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.1726-600A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889251 | |||||||
| chr3:19889269 | G | C | 115 | a0001c0028t0002g0211 a0002c0002t0001g0077 a0002c0002t0001g0084 others(112): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1726-618C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889269 | |||||||
| chr3:19889426 | G | T | 1 | a0013c0016t0002g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1726-775C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889426 | |||||||
| chr3:19889570 | G | C | 52 | a0002c0002t0001g0077 a0002c0002t0001g0084 a0002c0002t0001g0085 others(49): Show |
63 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(60): Show |
intron_variant | MODIFIER | c.1726-919C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889570 | |||||||
| chr3:19889625 | C | G | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-974G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889625 | |||||||
| chr3:19889678 | T | C | 205 | a0001c0001t0002g0010 a0001c0001t0002g0029 a0001c0001t0002g0032 others(202): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.1726-1027A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889678 | |||||||
| chr3:19889762 | T | C | 1 | a0010c0020t0001g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1726-1111A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889762 | |||||||
| chr3:19889936 | G | A | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-1285C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19889936 | |||||||
| chr3:19890057 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1726-1406G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890057 | |||||||
| chr3:19890141 | T | C | 20 | a0006c0007t0002g0038 a0006c0007t0002g0265 a0007c0008t0001g0020 others(17): Show |
25 | HG01884.hp2 HG01934.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1726-1490A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890141 | |||||||
| chr3:19890260 | C | T | 36 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(33): Show |
45 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1726-1609G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890260 | |||||||
| chr3:19890330 | C | A | 1 | a0004c0005t0001g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1726-1679G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890330 | |||||||
| chr3:19890431 | G | C | 1 | a0005c0006t0001g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1726-1780C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890431 | |||||||
| chr3:19890476 | G | A | 1 | a0001c0001t0002g0269 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1726-1825C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890476 | |||||||
| chr3:19890520 | T | C | 1 | a0002c0010t0002g0179 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1726-1869A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890520 | |||||||
| chr3:19890688 | GT | G | 76 | a0001c0028t0002g0211 a0002c0002t0002g0194 a0002c0002t0002g0251 others(73): Show |
94 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.1726-2038delA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890688 | |||||||
| chr3:19890749 | C | T | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1726-2098G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890749 | |||||||
| chr3:19890818 | T | C | 6 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0135 others(3): Show |
8 | HG00733.hp1 HG00741.hp1 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.1726-2167A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890818 | |||||||
| chr3:19890898 | C | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726-2247G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890898 | |||||||
| chr3:19890899 | A | G | 149 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(146): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1726-2248T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890899 | |||||||
| chr3:19890927 | G | C | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1726-2276C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19890927 | |||||||
| chr3:19891007 | A | G | 72 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(69): Show |
82 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1726-2356T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891007 | |||||||
| chr3:19891071 | TTGC | T | 72 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(69): Show |
82 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1726-2423_1726-242 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891071 | |||||||
| chr3:19891085 | G | GCTGCTT | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1726-2435_1726-243 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891085 | |||||||
| chr3:19891085 | G | GCTT | 5 | a0002c0009t0001g0128 a0002c0010t0001g0075 a0013c0016t0001g0076 others(2): Show |
5 | HG01081.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1726-2435_1726-243 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891085 | |||||||
| chr3:19891100 | T | C | 1 | a0005c0006t0001g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1726-2449A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891100 | |||||||
| chr3:19891310 | C | A | 1 | a0001c0001t0002g0263 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1726-2659G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891310 | |||||||
| chr3:19891372 | G | GA | 72 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(69): Show |
82 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1726-2722dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891372 | |||||||
| chr3:19891372 | GA | G | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1726-2722delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891372 | |||||||
| chr3:19891383 | T | C | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1726-2732A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891383 | |||||||
| chr3:19891419 | G | A | 1 | a0002c0003t0001g0073 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1726-2768C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891419 | |||||||
| chr3:19891489 | A | G | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726-2838T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891489 | |||||||
| chr3:19891693 | T | C | 1 | a0004c0005t0001g0132 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1726-3042A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891693 | |||||||
| chr3:19891704 | G | A | 1 | a0002c0002t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1726-3053C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891704 | |||||||
| chr3:19891769 | T | A | 1 | a0002c0002t0001g0114 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1726-3118A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891769 | |||||||
| chr3:19891824 | G | A | 1 | a0002c0009t0001g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1726-3173C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891824 | |||||||
| chr3:19891909 | G | A | 1 | a0013c0016t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1726-3258C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19891909 | |||||||
| chr3:19892193 | C | T | 4 | a0002c0009t0001g0128 a0002c0010t0001g0075 a0013c0016t0002g0270 others(1): Show |
4 | HG01081.hp1 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-3542G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892193 | |||||||
| chr3:19892264 | C | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1726-3613G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892264 | |||||||
| chr3:19892461 | T | C | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1726-3810A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892461 | |||||||
| chr3:19892554 | G | A | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726-3903C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892554 | |||||||
| chr3:19892711 | T | C | 53 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(50): Show |
67 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1725+3976A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892711 | |||||||
| chr3:19892762 | G | A | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+3925C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892762 | |||||||
| chr3:19892855 | C | CTAAAATA others(3): Show |
8 | a0001c0001t0002g0249 a0002c0002t0002g0194 a0002c0002t0002g0251 others(5): Show |
9 | HG01109.hp1 HG01934.hp2 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.1725+3822_1725+383 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892855 | |||||||
| chr3:19892855 | C | CTAAAATA others(8): Show |
5 | a0007c0008t0001g0020 a0007c0008t0001g0083 a0007c0008t0001g0087 others(2): Show |
6 | HG02145.hp1 HG02622.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1725+3817_1725+383 others(19): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892855 | |||||||
| chr3:19892855 | C | CTAAAATA others(13): Show |
12 | a0002c0010t0002g0180 a0002c0010t0002g0181 a0002c0010t0002g0183 others(9): Show |
14 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1725+3812_1725+383 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892855 | |||||||
| chr3:19892855 | C | CTAAAATA others(18): Show |
2 | a0002c0010t0002g0179 a0007c0027t0002g0273 |
2 | HG01243.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1725+3807_1725+383 others(29): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892855 | |||||||
| chr3:19892855 | CTAAAATA others(3): Show |
C | 1 | a0001c0001t0002g0230 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1725+3822_1725+383 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892855 | |||||||
| chr3:19892883 | A | AAATAAAA others(1): Show |
14 | a0002c0002t0001g0077 a0002c0002t0001g0120 a0005c0006t0001g0019 others(11): Show |
17 | HG00280.hp1 HG01074.hp2 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.1725+3803_1725+380 others(12): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892883 | |||||||
| chr3:19892883 | A | AAATAAAA others(6): Show |
50 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(47): Show |
61 | HG00544.hp2 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.1725+3803_1725+380 others(17): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892883 | |||||||
| chr3:19892883 | A | AAATAAAA others(11): Show |
38 | a0001c0028t0002g0211 a0002c0002t0001g0086 a0002c0002t0001g0092 others(35): Show |
45 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(42): Show |
intron_variant | MODIFIER | c.1725+3803_1725+380 others(22): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892883 | |||||||
| chr3:19892883 | A | AAATAAAA others(16): Show |
11 | a0002c0003t0001g0057 a0002c0003t0001g0062 a0002c0003t0001g0064 others(8): Show |
16 | HG00140.hp2 HG01109.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.1725+3803_1725+380 others(27): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892883 | |||||||
| chr3:19892883 | A | AAATAAAA others(21): Show |
3 | a0002c0009t0002g0275 a0002c0009t0002g0276 a0002c0009t0002g0277 |
3 | HG01884.hp1 HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1725+3803_1725+380 others(32): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892883 | |||||||
| chr3:19892889 | T | G | 144 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(141): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1725+3798A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892889 | |||||||
| chr3:19892889 | T | TAAG | 9 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0089 others(6): Show |
9 | HG01891.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1725+3797_1725+379 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892889 | |||||||
| chr3:19892902 | T | C | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+3785A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892902 | |||||||
| chr3:19892903 | G | A | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1725+3784C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892903 | |||||||
| chr3:19892914 | G | A | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+3773C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892914 | |||||||
| chr3:19892957 | CT | C | 31 | a0001c0026t0001g0066 a0002c0002t0002g0194 a0002c0002t0002g0251 others(28): Show |
35 | HG01109.hp1 HG01169.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.1725+3729delA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19892957 | |||||||
| chr3:19893005 | G | A | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1725+3682C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893005 | |||||||
| chr3:19893147 | C | T | 1 | a0003c0004t0001g0176 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1725+3540G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893147 | |||||||
| chr3:19893198 | C | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+3489G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893198 | |||||||
| chr3:19893256 | C | T | 4 | a0002c0002t0001g0085 a0002c0002t0001g0089 a0002c0002t0001g0091 others(1): Show |
4 | HG01891.hp2 HG02895.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+3431G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893256 | |||||||
| chr3:19893257 | G | A | 2 | a0007c0008t0001g0020 a0007c0008t0001g0097 |
3 | HG02622.hp2 HG03139.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1725+3430C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893257 | |||||||
| chr3:19893313 | A | G | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
8 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1725+3374T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893313 | |||||||
| chr3:19893331 | T | C | 5 | a0002c0009t0001g0128 a0002c0010t0001g0075 a0013c0016t0001g0076 others(2): Show |
5 | HG01081.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1725+3356A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893331 | |||||||
| chr3:19893336 | T | C | 53 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(50): Show |
67 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.1725+3351A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893336 | |||||||
| chr3:19893402 | G | A | 1 | a0001c0001t0002g0244 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1725+3285C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893402 | |||||||
| chr3:19893515 | C | G | 153 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(150): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1725+3172G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893515 | |||||||
| chr3:19893516 | A | G | 155 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(152): Show |
186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.1725+3171T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893516 | |||||||
| chr3:19893609 | C | T | 4 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0109 others(1): Show |
4 | HG02735.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1725+3078G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893609 | |||||||
| chr3:19893614 | G | A | 1 | a0019c0033t0001g0143 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1725+3073C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893614 | |||||||
| chr3:19893728 | T | C | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1725+2959A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893728 | |||||||
| chr3:19893837 | T | C | 153 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(150): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1725+2850A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893837 | |||||||
| chr3:19893877 | G | C | 6 | a0004c0005t0001g0133 a0004c0005t0001g0141 a0004c0005t0001g0155 others(3): Show |
6 | NA18959.hp1 NA18960.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.1725+2810C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19893877 | |||||||
| chr3:19894156 | C | T | 2 | a0002c0002t0001g0121 a0003c0004t0001g0175 |
2 | NA19083.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1725+2531G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894156 | |||||||
| chr3:19894287 | T | C | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1725+2400A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894287 | |||||||
| chr3:19894468 | T | C | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1725+2219A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894468 | |||||||
| chr3:19894671 | T | C | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+2016A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894671 | |||||||
| chr3:19894726 | T | C | 153 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(150): Show |
183 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.1725+1961A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894726 | |||||||
| chr3:19894802 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1725+1885G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894802 | |||||||
| chr3:19894832 | C | T | 1 | a0003c0004t0001g0148 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1725+1855G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894832 | |||||||
| chr3:19894940 | C | T | 1 | a0003c0004t0001g0157 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1725+1747G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894940 | |||||||
| chr3:19894989 | A | AAAAAAT | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1725+1697_1725+169 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AAAAAATA others(13): Show |
1 | a0008c0011t0001g0013 | 2 | NA18522.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1725+1697_1725+169 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AAAATATA others(13): Show |
2 | a0008c0011t0001g0042 a0008c0011t0001g0043 |
2 | HG02723.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1725+1697_1725+169 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AAT | 17 | a0002c0003t0001g0016 a0002c0003t0001g0054 a0002c0003t0001g0055 others(14): Show |
18 | HG01081.hp1 HG01106.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1725+1696_1725+169 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AATAT | 21 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(18): Show |
27 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.1725+1694_1725+169 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AATATATA others(17): Show |
1 | a0008c0011t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1725+1697_1725+169 others(28): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AATATATA others(25): Show |
1 | a0008c0011t0001g0014 | 2 | HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1725+1697_1725+169 others(36): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894989 | A | AATATATA others(27): Show |
1 | a0008c0011t0001g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1725+1697_1725+169 others(38): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894989 | |||||||
| chr3:19894991 | T | A | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+1696A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894991 | |||||||
| chr3:19894993 | T | A | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+1694A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894993 | |||||||
| chr3:19894995 | T | A | 1 | a0002c0010t0002g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1725+1692A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19894995 | |||||||
| chr3:19895000 | G | A | 79 | a0001c0028t0002g0211 a0002c0002t0002g0194 a0002c0002t0002g0251 others(76): Show |
97 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.1725+1687C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895000 | |||||||
| chr3:19895097 | C | A | 72 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(69): Show |
82 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(79): Show |
intron_variant | MODIFIER | c.1725+1590G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895097 | |||||||
| chr3:19895171 | T | C | 1 | a0010c0018t0002g0202 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1725+1516A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895171 | |||||||
| chr3:19895223 | C | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+1464G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895223 | |||||||
| chr3:19895231 | C | T | 9 | a0001c0001t0002g0199 a0003c0004t0001g0025 a0003c0004t0001g0026 others(6): Show |
11 | HG00733.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1725+1456G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895231 | |||||||
| chr3:19895250 | G | A | 1 | a0005c0006t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1725+1437C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895250 | |||||||
| chr3:19895405 | C | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1725+1282G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895405 | |||||||
| chr3:19895475 | G | A | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1725+1212C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895475 | |||||||
| chr3:19895480 | C | CA | 13 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(10): Show |
18 | HG01109.hp2 HG01884.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1725+1206dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19895480 | |||||||
| chr3:19896056 | G | A | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1725+631C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19896056 | |||||||
| chr3:19896164 | C | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1725+523G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19896164 | |||||||
| chr3:19896461 | A | G | 1 | a0002c0003t0001g0058 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1725+226T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19896461 | |||||||
| chr3:19896580 | G | A | 1 | a0007c0008t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1725+107C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 9/12 | chr3 | 19896580 | |||||||
| chr3:19896905 | T | A | 1 | a0001c0001t0002g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1571-64A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19896905 | |||||||
| chr3:19897102 | A | G | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1571-261T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897102 | |||||||
| chr3:19897213 | G | C | 1 | a0026c0031t0001g0129 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1571-372C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897213 | |||||||
| chr3:19897214 | G | T | 1 | a0007c0027t0002g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1571-373C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897214 | |||||||
| chr3:19897308 | G | A | 5 | a0002c0009t0001g0128 a0002c0010t0001g0075 a0013c0016t0001g0076 others(2): Show |
5 | HG01081.hp1 HG02258.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1571-467C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897308 | |||||||
| chr3:19897329 | C | G | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1571-488G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897329 | |||||||
| chr3:19897469 | T | A | 1 | a0002c0010t0002g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1571-628A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897469 | |||||||
| chr3:19897496 | C | G | 149 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(146): Show |
179 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1571-655G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897496 | |||||||
| chr3:19897501 | T | C | 2 | a0006c0007t0002g0038 a0006c0007t0002g0265 |
3 | HG02809.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1571-660A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897501 | |||||||
| chr3:19897562 | T | G | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1571-721A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897562 | |||||||
| chr3:19897788 | C | A | 21 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1571-947G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897788 | |||||||
| chr3:19897927 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1570+851T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897927 | |||||||
| chr3:19897996 | A | C | 124 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(121): Show |
148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1570+782T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19897996 | |||||||
| chr3:19898082 | A | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1570+696T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898082 | |||||||
| chr3:19898215 | T | G | 148 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(145): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1570+563A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898215 | |||||||
| chr3:19898280 | G | A | 21 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1570+498C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898280 | |||||||
| chr3:19898436 | C | A | 147 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(144): Show |
175 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.1570+342G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898436 | |||||||
| chr3:19898445 | T | C | 9 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(6): Show |
9 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1570+333A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898445 | |||||||
| chr3:19898632 | T | G | 6 | a0002c0003t0001g0004 a0002c0003t0001g0018 a0002c0003t0001g0052 others(3): Show |
10 | HG01255.hp2 HG01346.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.1570+146A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 8/12 | chr3 | 19898632 | |||||||
| chr3:19898927 | T | C | 2 | a0006c0007t0002g0038 a0006c0007t0002g0265 |
3 | HG02809.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1503-82A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 7/12 | chr3 | 19898927 | |||||||
| chr3:19898967 | C | A | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1503-122G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 7/12 | chr3 | 19898967 | |||||||
| chr3:19899235 | T | G | 2 | a0002c0009t0001g0128 a0002c0010t0001g0075 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1502+197A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 7/12 | chr3 | 19899235 | |||||||
| chr3:19899385 | A | G | 120 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(117): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1502+47T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 7/12 | chr3 | 19899385 | |||||||
| chr3:19899582 | A | G | 120 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(117): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1419-67T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899582 | |||||||
| chr3:19899605 | A | T | 1 | a0010c0018t0002g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1419-90T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899605 | |||||||
| chr3:19899639 | G | T | 4 | a0005c0006t0001g0080 a0005c0006t0001g0118 a0005c0006t0001g0119 others(1): Show |
4 | HG02280.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419-124C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899639 | |||||||
| chr3:19899729 | G | C | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-214C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899729 | |||||||
| chr3:19899745 | A | G | 148 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(145): Show |
178 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.1419-230T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899745 | |||||||
| chr3:19899865 | G | T | 109 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(106): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1419-350C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899865 | |||||||
| chr3:19899965 | C | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1419-450G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899965 | |||||||
| chr3:19899966 | G | A | 71 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0002c0002t0001g0022 others(68): Show |
81 | HG00280.hp1 HG00544.hp2 HG01070.hp2 others(78): Show |
intron_variant | MODIFIER | c.1419-451C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19899966 | |||||||
| chr3:19900144 | T | C | 2 | a0002c0002t0001g0086 a0002c0002t0001g0100 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1419-629A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900144 | |||||||
| chr3:19900175 | A | G | 2 | a0006c0007t0002g0038 a0006c0007t0002g0265 |
3 | HG02809.hp2 HG02922.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1419-660T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900175 | |||||||
| chr3:19900193 | CA | C | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1419-679delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900193 | |||||||
| chr3:19900195 | A | G | 1 | a0003c0004t0001g0147 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1419-680T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900195 | |||||||
| chr3:19900438 | T | C | 3 | a0013c0016t0001g0076 a0013c0016t0002g0270 a0013c0016t0002g0271 |
3 | HG01081.hp1 HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1419-923A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900438 | |||||||
| chr3:19900523 | G | A | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1419-1008C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900523 | |||||||
| chr3:19900617 | T | C | 1 | a0004c0005t0001g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1419-1102A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900617 | |||||||
| chr3:19900703 | C | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1419-1188G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900703 | |||||||
| chr3:19900727 | A | C | 1 | a0002c0010t0002g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1419-1212T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900727 | |||||||
| chr3:19900801 | C | T | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1419-1286G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900801 | |||||||
| chr3:19900893 | C | T | 2 | a0002c0009t0001g0128 a0002c0010t0001g0075 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1419-1378G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900893 | |||||||
| chr3:19900926 | C | CA | 114 | a0001c0001t0002g0209 a0001c0001t0002g0228 a0001c0001t0002g0236 others(111): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1419-1412dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900926 | |||||||
| chr3:19900953 | A | C | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-1438T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900953 | |||||||
| chr3:19900956 | T | C | 5 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(2): Show |
7 | HG01109.hp2 HG02258.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1419-1441A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19900956 | |||||||
| chr3:19901111 | A | G | 2 | a0007c0008t0001g0117 a0009c0012t0002g0261 |
2 | HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1419-1596T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901111 | |||||||
| chr3:19901181 | G | T | 21 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1419-1666C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901181 | |||||||
| chr3:19901528 | A | G | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1419-2013T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901528 | |||||||
| chr3:19901543 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0235 |
2 | NA18939.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1419-2028G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901543 | |||||||
| chr3:19901572 | C | T | 1 | a0013c0016t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1419-2057G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901572 | |||||||
| chr3:19901575 | G | C | 27 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(24): Show |
31 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1419-2060C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901575 | |||||||
| chr3:19901579 | G | A | 115 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(112): Show |
139 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1419-2064C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901579 | |||||||
| chr3:19901648 | A | C | 1 | a0001c0001t0002g0221 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1419-2133T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901648 | |||||||
| chr3:19901693 | A | C | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1419-2178T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901693 | |||||||
| chr3:19901741 | G | C | 1 | a0003c0004t0001g0174 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1419-2226C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901741 | |||||||
| chr3:19901764 | A | G | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1419-2249T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901764 | |||||||
| chr3:19901949 | C | CA | 11 | a0001c0001t0002g0010 a0001c0001t0002g0032 a0001c0001t0002g0225 others(8): Show |
15 | HG01069.hp2 HG01071.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.1419-2435dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19901949 | |||||||
| chr3:19902054 | G | T | 1 | a0001c0001t0002g0213 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1419-2539C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902054 | |||||||
| chr3:19902248 | C | A | 1 | a0004c0005t0001g0146 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1419-2733G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902248 | |||||||
| chr3:19902263 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1419-2748G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902263 | |||||||
| chr3:19902419 | A | G | 141 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(138): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1419-2904T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902419 | |||||||
| chr3:19902584 | C | T | 21 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418+3036G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902584 | |||||||
| chr3:19902723 | G | A | 114 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(111): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1418+2897C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902723 | |||||||
| chr3:19902730 | T | C | 6 | a0002c0002t0001g0077 a0002c0009t0001g0128 a0002c0010t0001g0075 others(3): Show |
6 | HG01081.hp1 HG02258.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1418+2890A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902730 | |||||||
| chr3:19902754 | G | A | 141 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(138): Show |
168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1418+2866C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902754 | |||||||
| chr3:19902757 | T | C | 2 | a0002c0009t0001g0128 a0002c0010t0001g0075 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1418+2863A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902757 | |||||||
| chr3:19902775 | G | C | 1 | a0002c0002t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1418+2845C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19902775 | |||||||
| chr3:19903176 | CA | C | 35 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(32): Show |
42 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.1418+2443delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903176 | |||||||
| chr3:19903273 | C | T | 32 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1418+2347G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903273 | |||||||
| chr3:19903315 | G | A | 6 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(3): Show |
6 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1418+2305C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903315 | |||||||
| chr3:19903352 | G | A | 1 | a0002c0002t0001g0098 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1418+2268C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903352 | |||||||
| chr3:19903370 | A | G | 110 | a0001c0001t0002g0209 a0001c0001t0002g0236 a0001c0028t0002g0211 others(107): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1418+2250T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903370 | |||||||
| chr3:19903391 | T | G | 21 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(18): Show |
24 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1418+2229A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903391 | |||||||
| chr3:19903420 | T | C | 2 | a0002c0009t0001g0128 a0002c0010t0001g0075 |
2 | HG03225.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1418+2200A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903420 | |||||||
| chr3:19903553 | T | G | 1 | a0005c0006t0001g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1418+2067A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903553 | |||||||
| chr3:19903600 | C | T | 1 | a0016c0022t0001g0164 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1418+2020G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903600 | |||||||
| chr3:19903690 | T | C | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1418+1930A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903690 | |||||||
| chr3:19903874 | G | A | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1418+1746C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903874 | |||||||
| chr3:19903942 | A | G | 2 | a0001c0001t0002g0234 a0003c0004t0001g0160 |
2 | HG00597.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.1418+1678T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19903942 | |||||||
| chr3:19904135 | G | A | 1 | a0002c0010t0002g0180 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1418+1485C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904135 | |||||||
| chr3:19904204 | G | A | 22 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0010t0002g0179 others(19): Show |
25 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.1418+1416C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904204 | |||||||
| chr3:19904296 | A | C | 18 | a0007c0008t0001g0020 a0007c0008t0001g0083 a0007c0008t0001g0087 others(15): Show |
22 | HG01884.hp2 HG01934.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1418+1324T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904296 | |||||||
| chr3:19904319 | G | T | 1 | a0002c0010t0001g0127 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1418+1301C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904319 | |||||||
| chr3:19904555 | C | T | 1 | a0002c0010t0002g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1418+1065G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904555 | |||||||
| chr3:19904565 | G | A | 53 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(50): Show |
69 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(66): Show |
intron_variant | MODIFIER | c.1418+1055C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904565 | |||||||
| chr3:19904636 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1418+984G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904636 | |||||||
| chr3:19904820 | C | T | 1 | a0003c0004t0001g0162 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1418+800G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904820 | |||||||
| chr3:19904941 | G | A | 1 | a0008c0011t0001g0044 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1418+679C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904941 | |||||||
| chr3:19904957 | G | A | 1 | a0016c0022t0001g0172 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1418+663C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904957 | |||||||
| chr3:19904980 | C | T | 44 | a0001c0001t0002g0010 a0002c0002t0001g0099 a0003c0004t0001g0023 others(41): Show |
52 | HG00642.hp1 HG00673.hp2 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.1418+640G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19904980 | |||||||
| chr3:19905037 | A | G | 3 | a0012c0014t0001g0007 a0012c0014t0001g0078 a0021c0036t0001g0134 |
5 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1418+583T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905037 | |||||||
| chr3:19905314 | T | C | 2 | a0012c0014t0001g0007 a0012c0014t0001g0078 |
4 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.1418+306A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905314 | |||||||
| chr3:19905406 | G | GA | 16 | a0006c0007t0002g0038 a0006c0007t0002g0039 a0006c0007t0002g0203 others(13): Show |
20 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.1418+213dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905406 | |||||||
| chr3:19905480 | G | GT | 9 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(6): Show |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1418+139dupA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905480 | |||||||
| chr3:19905500 | G | A | 182 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0233 others(179): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.1418+120C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905500 | |||||||
| chr3:19905565 | T | C | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1418+55A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905565 | |||||||
| chr3:19905613 | A | C | 39 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(36): Show |
48 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(45): Show |
splice_region_variant&intron_variant | LOW | c.1418+7T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 6/12 | chr3 | 19905613 | |||||||
| chr3:19905804 | T | C | 104 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(101): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1289-55A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19905804 | |||||||
| chr3:19905945 | G | A | 1 | a0003c0004t0001g0023 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1289-196C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19905945 | |||||||
| chr3:19906014 | A | T | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1289-265T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906014 | |||||||
| chr3:19906138 | G | A | 64 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0002c0002t0001g0022 others(61): Show |
72 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1289-389C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906138 | |||||||
| chr3:19906223 | G | A | 9 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(6): Show |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1289-474C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906223 | |||||||
| chr3:19906328 | C | G | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-579G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906328 | |||||||
| chr3:19906350 | G | A | 113 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(110): Show |
132 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1289-601C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906350 | |||||||
| chr3:19906512 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-763G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906512 | |||||||
| chr3:19906561 | C | T | 104 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(101): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1289-812G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906561 | |||||||
| chr3:19906593 | T | C | 1 | a0010c0018t0002g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1289-844A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906593 | |||||||
| chr3:19906680 | G | A | 1 | a0002c0003t0001g0062 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1289-931C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906680 | |||||||
| chr3:19906698 | GA | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0233 others(176): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1289-950delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906698 | |||||||
| chr3:19906710 | T | C | 104 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(101): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1289-961A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906710 | |||||||
| chr3:19906771 | A | G | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1289-1022T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906771 | |||||||
| chr3:19906788 | A | G | 1 | a0003c0039t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1289-1039T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19906788 | |||||||
| chr3:19907011 | CA | C | 9 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(6): Show |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1289-1263delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907011 | |||||||
| chr3:19907031 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1289-1282T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907031 | |||||||
| chr3:19907045 | T | TA | 9 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0002c0002t0002g0194 others(6): Show |
14 | HG00323.hp2 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1289-1297dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907045 | |||||||
| chr3:19907329 | A | C | 1 | a0002c0002t0001g0111 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1289-1580T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907329 | |||||||
| chr3:19907442 | T | G | 2 | a0007c0008t0002g0193 a0007c0008t0002g0196 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1289-1693A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907442 | |||||||
| chr3:19907466 | G | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0035 a0001c0001t0002g0241 others(3): Show |
8 | HG01069.hp1 HG01099.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-1717C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907466 | |||||||
| chr3:19907863 | T | C | 32 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1289-2114A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907863 | |||||||
| chr3:19907959 | G | A | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-2210C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19907959 | |||||||
| chr3:19908312 | C | T | 104 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(101): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1289-2563G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908312 | |||||||
| chr3:19908378 | C | G | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1289-2629G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908378 | |||||||
| chr3:19908402 | G | A | 1 | a0005c0006t0001g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1289-2653C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908402 | |||||||
| chr3:19908528 | G | A | 7 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-2779C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908528 | |||||||
| chr3:19908542 | A | AAGAAAGA others(9): Show |
4 | a0008c0011t0001g0014 a0008c0011t0001g0043 a0008c0011t0001g0044 others(1): Show |
4 | HG02486.hp2 HG02723.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2809_1289-279 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908542 | |||||||
| chr3:19908542 | A | AAGAAAGA others(10): Show |
1 | a0002c0003t0001g0061 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1289-2794_1289-279 others(21): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908542 | |||||||
| chr3:19908554 | A | AAGAGAGA others(17): Show |
1 | a0005c0006t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1289-2806_1289-280 others(28): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908554 | |||||||
| chr3:19908554 | A | AGAGAGAG others(6): Show |
1 | a0002c0002t0001g0109 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1289-2806_1289-280 others(17): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908554 | |||||||
| chr3:19908554 | AAGAGAGA others(3): Show |
A | 1 | a0001c0001t0002g0009 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1289-2815_1289-280 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908554 | |||||||
| chr3:19908562 | A | AAG | 3 | a0002c0002t0001g0101 a0003c0004t0001g0173 a0025c0032t0001g0130 |
3 | NA18941.hp1 NA18964.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1289-2815_1289-281 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAG | 2 | a0003c0004t0001g0152 a0004c0005t0001g0003 |
3 | HG00544.hp2 HG02523.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1289-2817_1289-281 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(5): Show |
1 | a0005c0006t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(11): Show |
2 | a0008c0011t0001g0013 a0020c0023t0001g0041 |
2 | HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1289-2814_1289-281 others(22): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(9): Show |
2 | a0002c0002t0002g0194 a0008c0011t0001g0014 |
2 | HG01109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1289-2814_1289-281 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(15): Show |
1 | a0002c0002t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(26): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(19): Show |
3 | a0002c0002t0001g0120 a0005c0006t0001g0019 a0007c0008t0001g0083 |
3 | HG02976.hp1 HG03492.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1289-2814_1289-281 others(30): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(25): Show |
1 | a0005c0006t0001g0082 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(36): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(31): Show |
1 | a0005c0006t0001g0088 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(42): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(47): Show |
1 | a0005c0006t0001g0081 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(58): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(28): Show |
1 | a0005c0006t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(39): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(36): Show |
1 | a0007c0008t0001g0020 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(47): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(7): Show |
1 | a0013c0016t0002g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1289-2827_1289-281 others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(9): Show |
2 | a0002c0002t0001g0086 a0002c0002t0001g0113 |
2 | HG02717.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1289-2829_1289-281 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(13): Show |
6 | a0002c0002t0001g0085 a0002c0002t0001g0111 a0002c0002t0001g0114 others(3): Show |
6 | HG00544.hp1 HG01891.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-2833_1289-281 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(15): Show |
5 | a0002c0002t0001g0089 a0002c0002t0001g0091 a0002c0002t0001g0092 others(2): Show |
5 | HG02895.hp1 HG02965.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-2835_1289-281 others(26): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(17): Show |
5 | a0002c0002t0001g0110 a0005c0006t0001g0080 a0005c0006t0001g0118 others(2): Show |
5 | HG02630.hp1 HG03041.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-2837_1289-281 others(28): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(19): Show |
4 | a0002c0002t0001g0022 a0002c0002t0001g0106 a0005c0006t0001g0119 others(1): Show |
4 | HG00741.hp2 HG02280.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2839_1289-281 others(30): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(21): Show |
1 | a0012c0014t0001g0078 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1289-2841_1289-281 others(32): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(23): Show |
3 | a0002c0002t0001g0093 a0002c0002t0001g0098 a0012c0014t0001g0007 |
3 | HG01071.hp1 HG03654.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1289-2843_1289-281 others(34): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(27): Show |
1 | a0002c0002t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1289-2847_1289-281 others(38): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AAGAGAGA others(31): Show |
2 | a0002c0002t0001g0125 a0002c0002t0002g0256 |
2 | HG02056.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.1289-2851_1289-281 others(42): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AGAGAG | 4 | a0001c0001t0002g0239 a0001c0001t0002g0262 a0003c0004t0001g0150 others(1): Show |
4 | HG01978.hp1 HG03704.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.1289-2814_1289-281 others(9): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AGAGAGAG others(14): Show |
1 | a0002c0002t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(25): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AGAGAGAG others(22): Show |
2 | a0002c0002t0001g0084 a0002c0002t0001g0107 |
2 | HG00408.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1289-2814_1289-281 others(33): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AGAGAGAG others(30): Show |
1 | a0002c0002t0001g0121 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(41): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | AGAGAGAG others(34): Show |
1 | a0005c0006t0001g0104 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1289-2814_1289-281 others(45): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | A | G | 2 | a0002c0002t0001g0109 a0005c0006t0003g0040 |
2 | HG02735.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1289-2813T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAG | A | 16 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0187 others(13): Show |
17 | HG00738.hp1 HG00738.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1289-2815_1289-281 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAG | A | 10 | a0001c0001t0002g0002 a0001c0001t0002g0230 a0001c0001t0002g0252 others(7): Show |
11 | HG01099.hp2 HG01891.hp1 HG02165.hp1 others(8): Show |
intron_variant | MODIFIER | c.1289-2817_1289-281 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAG | A | 8 | a0001c0001t0002g0031 a0002c0002t0001g0108 a0003c0004t0001g0023 others(5): Show |
8 | HG00735.hp2 HG01109.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-2819_1289-281 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAGA others(1): Show |
A | 10 | a0001c0001t0002g0197 a0002c0009t0002g0006 a0002c0009t0002g0276 others(7): Show |
11 | HG01243.hp1 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1289-2821_1289-281 others(12): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAGA others(3): Show |
A | 5 | a0002c0009t0002g0006 a0006c0007t0002g0038 a0006c0007t0002g0039 others(2): Show |
6 | HG02615.hp2 HG02809.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1289-2823_1289-281 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAGA others(5): Show |
A | 6 | a0002c0009t0002g0274 a0002c0009t0002g0278 a0002c0010t0002g0184 others(3): Show |
7 | HG01934.hp2 HG02145.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-2825_1289-281 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAGA others(9): Show |
A | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1289-2829_1289-281 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908562 | AAGAGAGA others(13): Show |
A | 1 | a0007c0027t0002g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1289-2833_1289-281 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908562 | |||||||
| chr3:19908564 | G | GAGAGAA | 7 | a0001c0028t0002g0211 a0002c0003t0001g0018 a0002c0003t0001g0057 others(4): Show |
8 | HG01255.hp2 HG01346.hp1 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-2816_1289-281 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908564 | |||||||
| chr3:19908564 | G | GAGAGAAA others(7): Show |
8 | a0002c0003t0001g0060 a0002c0003t0001g0062 a0002c0003t0001g0068 others(5): Show |
8 | HG00642.hp2 HG02004.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-2816_1289-281 others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908564 | |||||||
| chr3:19908566 | G | GAGAAAGA others(13): Show |
1 | a0002c0003t0001g0015 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1289-2818_1289-281 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908566 | |||||||
| chr3:19908568 | G | GAA | 5 | a0002c0003t0001g0016 a0002c0003t0001g0054 a0002c0003t0001g0064 others(2): Show |
5 | HG00140.hp2 HG01123.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289-2820_1289-281 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908568 | |||||||
| chr3:19908568 | G | GAAAGAGA others(3): Show |
10 | a0002c0003t0001g0004 a0002c0003t0001g0016 a0002c0003t0001g0017 others(7): Show |
13 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1289-2820_1289-281 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908568 | |||||||
| chr3:19908568 | G | GAAAGAGA others(11): Show |
3 | a0002c0003t0001g0015 a0002c0003t0001g0052 a0018c0025t0001g0047 |
3 | HG01169.hp2 HG01361.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1289-2820_1289-281 others(22): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908568 | |||||||
| chr3:19908570 | G | A | 14 | a0002c0002t0002g0251 a0002c0003t0001g0071 a0002c0010t0001g0075 others(11): Show |
15 | HG01106.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.1289-2821C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908570 | |||||||
| chr3:19908572 | G | A | 13 | a0001c0028t0002g0211 a0002c0003t0001g0018 a0002c0003t0001g0057 others(10): Show |
14 | HG00642.hp2 HG01255.hp2 HG01346.hp1 others(11): Show |
intron_variant | MODIFIER | c.1289-2823C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908572 | |||||||
| chr3:19908576 | G | A | 14 | a0002c0003t0001g0004 a0002c0003t0001g0016 a0002c0003t0001g0017 others(11): Show |
18 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.1289-2827C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908576 | |||||||
| chr3:19908578 | G | A | 3 | a0002c0003t0001g0071 a0002c0010t0001g0075 a0002c0019t0001g0049 |
3 | HG01106.hp1 HG03540.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1289-2829C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908578 | |||||||
| chr3:19908580 | G | A | 6 | a0001c0028t0002g0211 a0002c0003t0001g0018 a0002c0003t0001g0057 others(3): Show |
7 | HG01255.hp2 HG01346.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-2831C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908580 | |||||||
| chr3:19908582 | G | A | 3 | a0009c0012t0002g0258 a0009c0012t0002g0260 a0015c0015t0002g0012 |
3 | HG02818.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1289-2833C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908582 | |||||||
| chr3:19908584 | G | A | 5 | a0002c0003t0001g0016 a0002c0003t0001g0054 a0002c0003t0001g0064 others(2): Show |
5 | HG00140.hp2 HG01123.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289-2835C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908584 | |||||||
| chr3:19908586 | G | A | 3 | a0009c0012t0002g0258 a0009c0012t0002g0260 a0015c0015t0002g0012 |
3 | HG02818.hp2 HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1289-2837C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908586 | |||||||
| chr3:19908586 | GAGAGAGA others(13): Show |
G | 1 | a0002c0009t0002g0011 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1289-2857_1289-283 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908586 | |||||||
| chr3:19908588 | GAGAGAGA others(7): Show |
G | 1 | a0002c0009t0002g0011 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1289-2853_1289-284 others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908588 | |||||||
| chr3:19908590 | G | A | 6 | a0002c0003t0001g0052 a0002c0009t0002g0011 a0009c0012t0002g0258 others(3): Show |
8 | HG01361.hp1 HG01943.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1289-2841C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908590 | |||||||
| chr3:19908590 | GAGAGAGA others(13): Show |
G | 3 | a0001c0001t0002g0028 a0001c0001t0002g0198 a0001c0001t0002g0247 |
4 | NA18939.hp2 NA18952.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2861_1289-284 others(24): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908590 | |||||||
| chr3:19908592 | GAGAGAGA others(3): Show |
G | 3 | a0003c0004t0001g0024 a0003c0004t0001g0148 a0006c0007t0002g0240 |
4 | HG01069.hp2 HG01071.hp2 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2853_1289-284 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908592 | |||||||
| chr3:19908592 | GAGAGAGA others(7): Show |
G | 1 | a0001c0001t0002g0001 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1289-2857_1289-284 others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908592 | |||||||
| chr3:19908592 | GAGAGAGA others(11): Show |
G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1289-2861_1289-284 others(22): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908592 | |||||||
| chr3:19908594 | G | A | 35 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0224 others(32): Show |
39 | HG00642.hp2 HG00738.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.1289-2845C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAAGAAAG others(6): Show |
1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1289-2846_1289-284 others(17): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAGAA | 10 | a0001c0001t0002g0001 a0001c0001t0002g0200 a0001c0001t0002g0216 others(7): Show |
10 | HG01069.hp1 HG01433.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1289-2846_1289-284 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAGAAAGA others(1): Show |
9 | a0001c0001t0002g0002 a0001c0001t0002g0034 a0001c0001t0002g0217 others(6): Show |
10 | HG00597.hp2 HG01099.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.1289-2846_1289-284 others(12): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAGAAAGA others(5): Show |
3 | a0001c0001t0002g0035 a0001c0001t0002g0205 a0003c0039t0001g0178 |
3 | HG01106.hp2 HG02559.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1289-2846_1289-284 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAGAAAGA others(9): Show |
2 | a0001c0001t0002g0206 a0011c0013t0001g0074 |
2 | HG02109.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1289-2846_1289-284 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | G | GAGAAAGA others(5): Show |
1 | a0003c0004t0001g0171 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1289-2846_1289-284 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | GAGAGAGA others(1): Show |
G | 8 | a0001c0001t0002g0001 a0001c0001t0002g0034 a0003c0004t0001g0160 others(5): Show |
8 | HG00673.hp1 NA18959.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-2853_1289-284 others(12): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908594 | GAGAGAGA others(5): Show |
G | 4 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0003c0004t0001g0153 others(1): Show |
4 | HG00323.hp2 HG02300.hp1 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2857_1289-284 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908594 | |||||||
| chr3:19908596 | GAGAGAA | G | 3 | a0001c0001t0002g0001 a0001c0001t0002g0225 a0004c0005t0001g0161 |
3 | NA18984.hp1 NA18994.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1289-2853_1289-284 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908596 | |||||||
| chr3:19908597 | AGAGAAAG others(4): Show |
A | 2 | a0009c0012t0002g0258 a0009c0012t0002g0260 |
2 | HG06807.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1289-2859_1289-284 others(15): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908597 | |||||||
| chr3:19908598 | G | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0005 others(95): Show |
117 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.1289-2849C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAA | 5 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0035 others(2): Show |
8 | HG00423.hp1 HG02155.hp1 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAAAGAA | 3 | a0001c0001t0002g0005 a0001c0001t0002g0032 a0011c0013t0002g0237 |
3 | HG02155.hp2 NA18940.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAAAGAAA others(3): Show |
5 | a0001c0001t0002g0032 a0001c0001t0002g0223 a0001c0001t0002g0232 others(2): Show |
5 | HG00408.hp1 HG02523.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAA | 9 | a0001c0001t0002g0213 a0001c0001t0002g0226 a0001c0001t0002g0228 others(6): Show |
9 | HG00280.hp2 HG00597.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.1289-2853_1289-285 others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAAAGA others(1): Show |
5 | a0001c0001t0002g0031 a0001c0001t0002g0212 a0003c0004t0001g0167 others(2): Show |
5 | HG01123.hp2 HG02004.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289-2857_1289-285 others(12): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAAAGA others(5): Show |
2 | a0001c0001t0002g0002 a0003c0004t0001g0168 |
2 | HG01433.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.1289-2861_1289-285 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAAAGA others(9): Show |
1 | a0004c0005t0001g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1289-2865_1289-285 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAAGAA others(4): Show |
1 | a0003c0004t0001g0166 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(15): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAA | 7 | a0001c0001t0002g0207 a0001c0001t0002g0249 a0003c0004t0001g0026 others(4): Show |
7 | HG02040.hp2 HG02080.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAAA others(7): Show |
2 | a0003c0004t0001g0026 a0003c0004t0001g0175 |
2 | NA19083.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(18): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(5): Show |
1 | a0004c0005t0001g0008 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(8): Show |
1 | a0002c0002t0001g0102 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(19): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(15): Show |
2 | a0001c0001t0002g0033 a0001c0001t0002g0233 |
2 | NA19009.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.1289-2850_1289-284 others(26): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(23): Show |
1 | a0007c0008t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(34): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(23): Show |
1 | a0002c0002t0001g0112 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(34): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(23): Show |
1 | a0001c0001t0002g0033 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(34): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(27): Show |
1 | a0002c0002t0001g0124 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(38): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(57): Show |
1 | a0007c0008t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(68): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | G | GAGAGAGA others(36): Show |
1 | a0002c0002t0001g0105 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1289-2850_1289-284 others(47): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908598 | GAGAAAGA others(9): Show |
G | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1289-2865_1289-285 others(20): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908598 | |||||||
| chr3:19908600 | GAA | G | 4 | a0001c0001t0002g0215 a0004c0005t0001g0003 a0007c0008t0002g0036 others(1): Show |
4 | HG02257.hp1 HG03579.hp2 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1289-2853_1289-285 others(6): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908600 | |||||||
| chr3:19908600 | GAAAGAA | G | 2 | a0007c0008t0002g0027 a0007c0008t0002g0196 |
3 | HG01884.hp2 HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1289-2857_1289-285 others(10): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908600 | |||||||
| chr3:19908600 | GAAAGAAA others(3): Show |
G | 1 | a0007c0008t0002g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1289-2861_1289-285 others(14): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908600 | |||||||
| chr3:19908601 | A | AGAGAGAG others(22): Show |
1 | a0005c0006t0001g0019 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1289-2853_1289-285 others(33): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908601 | |||||||
| chr3:19908601 | A | AGAGAGAG others(44): Show |
1 | a0007c0008t0001g0020 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1289-2853_1289-285 others(55): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908601 | |||||||
| chr3:19908602 | A | G | 55 | a0001c0001t0002g0009 a0001c0001t0002g0214 a0002c0002t0001g0022 others(52): Show |
57 | HG00099.hp1 HG00140.hp2 HG00408.hp2 others(54): Show |
intron_variant | MODIFIER | c.1289-2853T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908602 | |||||||
| chr3:19908605 | A | AGAGAGAG others(20): Show |
1 | a0023c0030t0001g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1289-2857_1289-285 others(31): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908605 | |||||||
| chr3:19908606 | A | G | 30 | a0002c0002t0001g0084 a0002c0002t0001g0085 a0002c0002t0001g0086 others(27): Show |
33 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.1289-2857T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908606 | |||||||
| chr3:19908609 | AAAG | A | 4 | a0009c0012t0002g0037 a0009c0012t0002g0259 a0009c0012t0002g0261 others(1): Show |
6 | HG01934.hp2 HG02258.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1289-2863_1289-286 others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908609 | |||||||
| chr3:19908610 | A | G | 23 | a0002c0002t0001g0084 a0002c0002t0001g0086 a0002c0002t0001g0089 others(20): Show |
27 | HG01070.hp2 HG01071.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.1289-2861T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908610 | |||||||
| chr3:19908613 | A | AGAGAGAG others(16): Show |
1 | a0002c0002t0002g0251 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1289-2865_1289-286 others(27): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908613 | |||||||
| chr3:19908614 | A | G | 10 | a0005c0006t0003g0040 a0007c0008t0001g0117 a0007c0008t0002g0027 others(7): Show |
12 | HG01081.hp1 HG01884.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1289-2865T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908614 | |||||||
| chr3:19908618 | A | G | 6 | a0002c0010t0001g0075 a0007c0008t0002g0027 a0007c0008t0002g0036 others(3): Show |
7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1289-2869T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908618 | |||||||
| chr3:19908622 | A | G | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1289-2873T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908622 | |||||||
| chr3:19908648 | G | T | 1 | a0007c0008t0001g0087 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1289-2899C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908648 | |||||||
| chr3:19908654 | A | T | 6 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(3): Show |
7 | HG02486.hp2 HG02723.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-2905T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908654 | |||||||
| chr3:19908706 | A | G | 1 | a0006c0007t0002g0240 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1289-2957T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908706 | |||||||
| chr3:19908751 | G | A | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1289-3002C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908751 | |||||||
| chr3:19908866 | G | T | 1 | a0002c0002t0001g0099 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1289-3117C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908866 | |||||||
| chr3:19908893 | C | T | 15 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(12): Show |
21 | HG00099.hp2 HG00323.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.1289-3144G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908893 | |||||||
| chr3:19908907 | G | A | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1289-3158C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19908907 | |||||||
| chr3:19909028 | A | C | 1 | a0013c0016t0002g0271 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1289-3279T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909028 | |||||||
| chr3:19909034 | G | T | 6 | a0006c0007t0002g0039 a0006c0007t0002g0203 a0006c0007t0002g0266 others(3): Show |
7 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.1289-3285C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909034 | |||||||
| chr3:19909128 | T | G | 1 | a0001c0001t0002g0031 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1289-3379A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909128 | |||||||
| chr3:19909200 | C | G | 3 | a0005c0006t0001g0080 a0005c0006t0001g0118 a0005c0006t0001g0119 |
3 | HG02280.hp2 HG02630.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1289-3451G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909200 | |||||||
| chr3:19909511 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-3762G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909511 | |||||||
| chr3:19909512 | G | A | 6 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0275 others(3): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1289-3763C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909512 | |||||||
| chr3:19909537 | G | C | 1 | a0005c0006t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1289-3788C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909537 | |||||||
| chr3:19909567 | T | C | 198 | a0001c0001t0002g0010 a0001c0001t0002g0033 a0001c0001t0002g0233 others(195): Show |
237 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(234): Show |
intron_variant | MODIFIER | c.1289-3818A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909567 | |||||||
| chr3:19909655 | G | A | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1289-3906C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909655 | |||||||
| chr3:19909713 | G | A | 1 | a0002c0003t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1289-3964C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909713 | |||||||
| chr3:19909726 | C | T | 1 | a0020c0023t0001g0041 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1289-3977G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909726 | |||||||
| chr3:19909734 | T | C | 31 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1289-3985A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909734 | |||||||
| chr3:19909769 | T | C | 32 | a0001c0028t0002g0211 a0002c0003t0001g0004 a0002c0003t0001g0015 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.1289-4020A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909769 | |||||||
| chr3:19909816 | G | A | 48 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0002c0002t0001g0022 others(45): Show |
54 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.1289-4067C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909816 | |||||||
| chr3:19909851 | T | C | 9 | a0002c0009t0001g0128 a0002c0009t0002g0006 a0002c0009t0002g0011 others(6): Show |
14 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1289-4102A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19909851 | |||||||
| chr3:19910252 | C | A | 1 | a0018c0025t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1289-4503G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910252 | |||||||
| chr3:19910280 | T | C | 1 | a0002c0010t0001g0127 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1289-4531A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910280 | |||||||
| chr3:19910323 | C | T | 64 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0002c0002t0001g0022 others(61): Show |
72 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(69): Show |
intron_variant | MODIFIER | c.1289-4574G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910323 | |||||||
| chr3:19910351 | G | T | 9 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(6): Show |
11 | HG01243.hp1 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1289-4602C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910351 | |||||||
| chr3:19910529 | C | A | 1 | a0001c0001t0002g0005 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1288+4774G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910529 | |||||||
| chr3:19910578 | T | C | 107 | a0001c0001t0002g0033 a0001c0001t0002g0233 a0001c0028t0002g0211 others(104): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1288+4725A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910578 | |||||||
| chr3:19910605 | C | T | 4 | a0005c0006t0001g0019 a0005c0006t0001g0081 a0005c0006t0001g0082 others(1): Show |
5 | HG00280.hp1 HG01074.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1288+4698G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910605 | |||||||
| chr3:19910715 | G | T | 1 | a0002c0009t0002g0274 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1288+4588C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910715 | |||||||
| chr3:19910905 | C | A | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288+4398G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19910905 | |||||||
| chr3:19911031 | T | C | 31 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1288+4272A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911031 | |||||||
| chr3:19911063 | G | A | 198 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(195): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.1288+4240C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911063 | |||||||
| chr3:19911134 | G | T | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1288+4169C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911134 | |||||||
| chr3:19911282 | C | A | 1 | a0004c0005t0001g0154 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1288+4021G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911282 | |||||||
| chr3:19911287 | C | A | 1 | a0010c0018t0002g0257 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1288+4016G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911287 | |||||||
| chr3:19911328 | A | G | 118 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(115): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1288+3975T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911328 | |||||||
| chr3:19911539 | C | T | 1 | a0003c0004t0001g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1288+3764G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911539 | |||||||
| chr3:19911553 | A | G | 118 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(115): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1288+3750T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911553 | |||||||
| chr3:19911652 | A | G | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288+3651T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911652 | |||||||
| chr3:19911835 | G | C | 1 | a0001c0001t0002g0227 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1288+3468C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911835 | |||||||
| chr3:19911873 | G | A | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1288+3430C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911873 | |||||||
| chr3:19911923 | C | A | 8 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0007c0008t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+3380G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19911923 | |||||||
| chr3:19912056 | T | A | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1288+3247A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19912056 | |||||||
| chr3:19912668 | A | T | 24 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0092 others(21): Show |
26 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.1288+2635T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19912668 | |||||||
| chr3:19912791 | T | C | 7 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1288+2512A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19912791 | |||||||
| chr3:19912927 | A | C | 65 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(62): Show |
73 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(70): Show |
intron_variant | MODIFIER | c.1288+2376T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19912927 | |||||||
| chr3:19913117 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1288+2186G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913117 | |||||||
| chr3:19913169 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0217 |
2 | HG01952.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1288+2134C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913169 | |||||||
| chr3:19913257 | A | T | 8 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0007c0008t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1288+2046T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913257 | |||||||
| chr3:19913488 | C | T | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1288+1815G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913488 | |||||||
| chr3:19913507 | A | G | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1288+1796T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913507 | |||||||
| chr3:19913678 | C | G | 186 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(183): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1288+1625G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913678 | |||||||
| chr3:19913694 | T | A | 1 | a0011c0013t0002g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1288+1609A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913694 | |||||||
| chr3:19913706 | T | C | 1 | a0002c0010t0002g0182 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1288+1597A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913706 | |||||||
| chr3:19913842 | G | A | 66 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(63): Show |
74 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(71): Show |
intron_variant | MODIFIER | c.1288+1461C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913842 | |||||||
| chr3:19913942 | C | T | 1 | a0002c0002t0001g0107 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1288+1361G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913942 | |||||||
| chr3:19913987 | A | G | 118 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(115): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1288+1316T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19913987 | |||||||
| chr3:19914034 | A | G | 2 | a0001c0001t0002g0264 a0001c0001t0002g0269 |
2 | HG00323.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1288+1269T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914034 | |||||||
| chr3:19914058 | C | T | 56 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(53): Show |
62 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1288+1245G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914058 | |||||||
| chr3:19914090 | C | T | 1 | a0004c0005t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1288+1213G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914090 | |||||||
| chr3:19914091 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1288+1212C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914091 | |||||||
| chr3:19914135 | A | G | 1 | a0003c0004t0001g0139 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1288+1168T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914135 | |||||||
| chr3:19914190 | C | T | 2 | a0001c0001t0002g0210 a0001c0001t0002g0219 |
2 | HG03654.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1288+1113G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914190 | |||||||
| chr3:19914198 | A | G | 56 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(53): Show |
62 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1288+1105T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914198 | |||||||
| chr3:19914228 | C | A | 16 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0092 others(13): Show |
18 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.1288+1075G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914228 | |||||||
| chr3:19914322 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1288+981C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914322 | |||||||
| chr3:19914502 | C | T | 59 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(56): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1288+801G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914502 | |||||||
| chr3:19914531 | A | T | 7 | a0006c0007t0002g0038 a0006c0007t0002g0039 a0006c0007t0002g0203 others(4): Show |
9 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288+772T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914531 | |||||||
| chr3:19914533 | C | T | 5 | a0009c0012t0002g0037 a0009c0012t0002g0258 a0009c0012t0002g0259 others(2): Show |
6 | HG01934.hp2 HG02717.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+770G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914533 | |||||||
| chr3:19914610 | A | G | 3 | a0003c0004t0001g0166 a0003c0004t0001g0167 a0003c0004t0001g0168 |
3 | HG00673.hp2 NA19003.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1288+693T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914610 | |||||||
| chr3:19914626 | C | T | 6 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(3): Show |
6 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1288+677G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914626 | |||||||
| chr3:19914640 | C | T | 59 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(56): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1288+663G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914640 | |||||||
| chr3:19914681 | T | C | 1 | a0009c0012t0002g0260 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1288+622A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914681 | |||||||
| chr3:19914733 | C | G | 104 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(101): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.1288+570G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914733 | |||||||
| chr3:19914791 | A | G | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288+512T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914791 | |||||||
| chr3:19914832 | G | A | 31 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1288+471C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914832 | |||||||
| chr3:19914959 | G | A | 1 | a0001c0001t0002g0218 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1288+344C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914959 | |||||||
| chr3:19914963 | A | T | 4 | a0002c0010t0002g0181 a0002c0010t0002g0183 a0002c0010t0002g0184 others(1): Show |
4 | HG02145.hp2 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+340T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19914963 | |||||||
| chr3:19915038 | A | G | 186 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(183): Show |
221 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.1288+265T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19915038 | |||||||
| chr3:19915043 | G | A | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1288+260C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19915043 | |||||||
| chr3:19915045 | T | C | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1288+258A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19915045 | |||||||
| chr3:19915099 | T | A | 1 | a0003c0004t0001g0171 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1288+204A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19915099 | |||||||
| chr3:19915110 | T | A | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1288+193A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 5/12 | chr3 | 19915110 | |||||||
| chr3:19915423 | G | A | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1178-10C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915423 | |||||||
| chr3:19915470 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1178-57G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915470 | |||||||
| chr3:19915503 | G | A | 31 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1178-90C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915503 | |||||||
| chr3:19915674 | C | T | 59 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(56): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1178-261G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915674 | |||||||
| chr3:19915757 | T | TA | 16 | a0001c0001t0002g0034 a0001c0001t0002g0186 a0001c0001t0002g0229 others(13): Show |
17 | HG01109.hp2 HG01175.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.1178-345dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915757 | |||||||
| chr3:19915757 | TA | T | 108 | a0001c0001t0002g0201 a0002c0002t0001g0021 a0002c0002t0001g0022 others(105): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.1178-345delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915757 | |||||||
| chr3:19915796 | A | G | 1 | a0014c0017t0001g0122 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1178-383T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915796 | |||||||
| chr3:19915844 | G | A | 3 | a0001c0001t0002g0028 a0001c0001t0002g0198 a0001c0001t0002g0247 |
4 | NA18939.hp2 NA18952.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.1178-431C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915844 | |||||||
| chr3:19915957 | A | G | 118 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(115): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.1178-544T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915957 | |||||||
| chr3:19915965 | G | A | 56 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(53): Show |
62 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(59): Show |
intron_variant | MODIFIER | c.1178-552C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19915965 | |||||||
| chr3:19916027 | C | T | 1 | a0007c0008t0001g0083 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1178-614G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916027 | |||||||
| chr3:19916216 | C | A | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1178-803G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916216 | |||||||
| chr3:19916388 | G | C | 1 | a0010c0018t0002g0188 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1178-975C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916388 | |||||||
| chr3:19916423 | G | T | 1 | a0005c0006t0001g0081 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1178-1010C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916423 | |||||||
| chr3:19916434 | G | A | 1 | a0003c0039t0001g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1178-1021C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916434 | |||||||
| chr3:19916509 | C | T | 58 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(55): Show |
68 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.1178-1096G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916509 | |||||||
| chr3:19916527 | A | T | 1 | a0005c0006t0001g0126 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1178-1114T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916527 | |||||||
| chr3:19916531 | C | A | 248 | a0001c0001t0002g0001 a0001c0001t0002g0005 a0001c0001t0002g0010 others(245): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1178-1118G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916531 | |||||||
| chr3:19916547 | T | A | 59 | a0002c0010t0002g0182 a0003c0004t0001g0023 a0003c0004t0001g0024 others(56): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.1178-1134A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916547 | |||||||
| chr3:19916661 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1178-1248G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916661 | |||||||
| chr3:19916678 | G | C | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178-1265C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916678 | |||||||
| chr3:19916843 | G | A | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1177+1389C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916843 | |||||||
| chr3:19916937 | G | C | 180 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(177): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1177+1295C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916937 | |||||||
| chr3:19916948 | T | G | 180 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(177): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1177+1284A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19916948 | |||||||
| chr3:19917138 | A | G | 1 | a0001c0001t0002g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1177+1094T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917138 | |||||||
| chr3:19917140 | G | A | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1177+1092C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917140 | |||||||
| chr3:19917291 | C | G | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1177+941G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917291 | |||||||
| chr3:19917357 | A | T | 31 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.1177+875T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917357 | |||||||
| chr3:19917411 | C | T | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+821G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917411 | |||||||
| chr3:19917435 | C | T | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1177+797G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917435 | |||||||
| chr3:19917705 | G | A | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+527C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917705 | |||||||
| chr3:19917865 | C | T | 1 | a0003c0004t0001g0138 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1177+367G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917865 | |||||||
| chr3:19917887 | G | T | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1177+345C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19917887 | |||||||
| chr3:19918084 | G | A | 1 | a0002c0003t0001g0064 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1177+148C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19918084 | |||||||
| chr3:19918091 | T | A | 6 | a0007c0008t0002g0027 a0007c0008t0002g0036 a0007c0008t0002g0192 others(3): Show |
8 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1177+141A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 4/12 | chr3 | 19918091 | |||||||
| chr3:19918546 | CT | C | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.997-135delA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918546 | |||||||
| chr3:19918592 | G | T | 1 | a0001c0001t0002g0197 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.997-180C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918592 | |||||||
| chr3:19918648 | A | G | 1 | a0002c0002t0001g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.997-236T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918648 | |||||||
| chr3:19918812 | T | TA | 43 | a0001c0001t0002g0232 a0001c0001t0002g0233 a0001c0001t0002g0250 others(40): Show |
55 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.997-401dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918812 | |||||||
| chr3:19918812 | TA | T | 82 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(79): Show |
95 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.997-401delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918812 | |||||||
| chr3:19918835 | C | T | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.997-423G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918835 | |||||||
| chr3:19918837 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.997-425C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918837 | |||||||
| chr3:19918907 | T | G | 177 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(174): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.997-495A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918907 | |||||||
| chr3:19918979 | C | CAA | 7 | a0006c0007t0002g0038 a0006c0007t0002g0039 a0006c0007t0002g0265 others(4): Show |
9 | HG00738.hp2 HG01192.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.997-569_997-568dup others(2): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918979 | |||||||
| chr3:19918979 | CA | C | 95 | a0001c0001t0002g0241 a0002c0002t0001g0021 a0002c0002t0001g0022 others(92): Show |
114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.997-568delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918979 | |||||||
| chr3:19918979 | CAAAAAAA others(4): Show |
C | 1 | a0004c0005t0001g0137 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.997-578_997-568del others(11): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19918979 | |||||||
| chr3:19919026 | G | T | 2 | a0005c0006t0001g0081 a0005c0006t0001g0082 |
2 | HG00280.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.997-614C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919026 | |||||||
| chr3:19919040 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.997-628G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919040 | |||||||
| chr3:19919147 | A | G | 2 | a0012c0014t0001g0007 a0012c0014t0001g0078 |
4 | HG01070.hp2 HG01071.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.996+686T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919147 | |||||||
| chr3:19919197 | G | T | 103 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(100): Show |
123 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.996+636C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919197 | |||||||
| chr3:19919298 | G | T | 1 | a0005c0006t0001g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.996+535C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919298 | |||||||
| chr3:19919337 | C | T | 8 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0007c0008t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.996+496G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919337 | |||||||
| chr3:19919364 | C | CT | 6 | a0001c0001t0002g0234 a0001c0001t0002g0239 a0002c0002t0001g0098 others(3): Show |
6 | HG00597.hp1 HG00642.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.996+468dupA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919364 | |||||||
| chr3:19919492 | C | A | 1 | a0002c0002t0001g0116 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.996+341G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919492 | |||||||
| chr3:19919535 | A | G | 118 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(115): Show |
138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.996+298T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919535 | |||||||
| chr3:19919577 | C | G | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.996+256G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919577 | |||||||
| chr3:19919738 | G | C | 1 | a0010c0018t0002g0202 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.996+95C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919738 | |||||||
| chr3:19919804 | T | C | 1 | a0003c0004t0001g0173 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.996+29A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919804 | |||||||
| chr3:19919808 | C | G | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.996+25G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 3/12 | chr3 | 19919808 | |||||||
| chr3:19920070 | C | T | 30 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0092 others(27): Show |
32 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(29): Show |
intron_variant | MODIFIER | c.853-94G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 2/12 | chr3 | 19920070 | |||||||
| chr3:19920117 | A | T | 14 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(11): Show |
17 | HG01243.hp1 HG01934.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.853-141T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 2/12 | chr3 | 19920117 | |||||||
| chr3:19920431 | G | A | 2 | a0002c0010t0002g0181 a0002c0010t0002g0185 |
2 | HG02895.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.852+74C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 2/12 | chr3 | 19920431 | |||||||
| chr3:19920707 | G | C | 58 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(55): Show |
64 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.790-140C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920707 | |||||||
| chr3:19920731 | G | A | 59 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(56): Show |
69 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(66): Show |
intron_variant | MODIFIER | c.790-164C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920731 | |||||||
| chr3:19920766 | C | T | 1 | a0002c0003t0001g0051 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.790-199G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920766 | |||||||
| chr3:19920908 | T | G | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.790-341A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920908 | |||||||
| chr3:19920978 | C | T | 4 | a0001c0001t0002g0204 a0001c0001t0002g0205 a0001c0001t0002g0206 others(1): Show |
4 | HG01168.hp2 HG02109.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-411G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920978 | |||||||
| chr3:19920987 | A | T | 1 | a0005c0006t0001g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.790-420T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19920987 | |||||||
| chr3:19921013 | T | G | 1 | a0003c0004t0001g0160 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.790-446A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921013 | |||||||
| chr3:19921130 | G | C | 1 | a0001c0001t0002g0234 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.790-563C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921130 | |||||||
| chr3:19921284 | A | G | 7 | a0007c0027t0002g0273 a0009c0012t0002g0037 a0009c0012t0002g0258 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-717T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921284 | |||||||
| chr3:19921295 | TGA | T | 8 | a0006c0007t0002g0038 a0006c0007t0002g0039 a0006c0007t0002g0203 others(5): Show |
10 | HG00738.hp2 HG01175.hp1 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.790-730_790-729del others(2): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921295 | |||||||
| chr3:19921506 | G | T | 197 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(194): Show |
234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.790-939C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921506 | |||||||
| chr3:19921574 | G | C | 1 | a0005c0006t0001g0094 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.790-1007C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921574 | |||||||
| chr3:19921575 | G | A | 1 | a0005c0006t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.790-1008C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921575 | |||||||
| chr3:19921672 | T | C | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-1105A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921672 | |||||||
| chr3:19921786 | CAGTTGTA | C | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-1226_790-1220d others(9): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921786 | |||||||
| chr3:19921791 | G | A | 32 | a0002c0003t0001g0004 a0002c0003t0001g0015 a0002c0003t0001g0016 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.790-1224C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921791 | |||||||
| chr3:19921837 | C | A | 6 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0275 others(3): Show |
11 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.790-1270G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19921837 | |||||||
| chr3:19922113 | C | T | 68 | a0002c0009t0001g0128 a0002c0009t0002g0006 a0002c0009t0002g0011 others(65): Show |
83 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.790-1546G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922113 | |||||||
| chr3:19922114 | G | A | 1 | a0002c0002t0001g0121 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.790-1547C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922114 | |||||||
| chr3:19922115 | A | C | 1 | a0007c0008t0001g0097 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.790-1548T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922115 | |||||||
| chr3:19922250 | G | C | 2 | a0011c0013t0001g0074 a0011c0013t0002g0255 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.790-1683C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922250 | |||||||
| chr3:19922543 | G | A | 1 | a0025c0032t0001g0130 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.790-1976C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922543 | |||||||
| chr3:19922657 | T | C | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-2090A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922657 | |||||||
| chr3:19922859 | G | A | 2 | a0013c0016t0002g0270 a0013c0016t0002g0271 |
2 | HG01081.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.790-2292C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922859 | |||||||
| chr3:19922866 | C | G | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-2299G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19922866 | |||||||
| chr3:19923038 | C | T | 59 | a0001c0001t0002g0250 a0003c0004t0001g0023 a0003c0004t0001g0024 others(56): Show |
69 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.790-2471G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923038 | |||||||
| chr3:19923084 | G | A | 1 | a0002c0003t0001g0068 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.790-2517C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923084 | |||||||
| chr3:19923220 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.790-2653A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923220 | |||||||
| chr3:19923248 | A | C | 113 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(110): Show |
134 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.790-2681T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923248 | |||||||
| chr3:19923271 | A | T | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-2704T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923271 | |||||||
| chr3:19923432 | A | C | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-2865T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923432 | |||||||
| chr3:19923611 | G | A | 2 | a0007c0008t0002g0193 a0007c0008t0002g0196 |
2 | HG02572.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.790-3044C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923611 | |||||||
| chr3:19923679 | T | G | 7 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0039 others(4): Show |
8 | HG00323.hp2 HG00738.hp2 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.790-3112A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923679 | |||||||
| chr3:19923719 | G | T | 1 | a0013c0016t0001g0076 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.790-3152C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923719 | |||||||
| chr3:19923859 | C | T | 59 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(56): Show |
65 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(62): Show |
intron_variant | MODIFIER | c.790-3292G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923859 | |||||||
| chr3:19923919 | T | C | 4 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.790-3352A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923919 | |||||||
| chr3:19923937 | A | T | 1 | a0002c0019t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.790-3370T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19923937 | |||||||
| chr3:19924085 | C | G | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-3518G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924085 | |||||||
| chr3:19924136 | G | C | 1 | a0001c0001t0002g0236 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.790-3569C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924136 | |||||||
| chr3:19924216 | C | CT | 7 | a0001c0001t0002g0187 a0001c0001t0002g0201 a0001c0001t0002g0239 others(4): Show |
7 | HG03130.hp2 HG03654.hp2 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.790-3650dupA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924216 | |||||||
| chr3:19924218 | T | C | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-3651A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924218 | |||||||
| chr3:19924220 | T | C | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-3653A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924220 | |||||||
| chr3:19924255 | C | T | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.790-3688G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924255 | |||||||
| chr3:19924370 | C | T | 7 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.790-3803G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924370 | |||||||
| chr3:19924385 | T | C | 11 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(8): Show |
13 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.790-3818A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924385 | |||||||
| chr3:19924684 | G | T | 1 | a0015c0015t0002g0012 | 3 | HG02258.hp2 HG02818.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.790-4117C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924684 | |||||||
| chr3:19924707 | T | C | 11 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(8): Show |
13 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.790-4140A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924707 | |||||||
| chr3:19924732 | A | G | 1 | a0005c0006t0001g0079 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.790-4165T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19924732 | |||||||
| chr3:19925020 | C | A | 1 | a0011c0013t0002g0237 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.790-4453G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925020 | |||||||
| chr3:19925020 | C | T | 104 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0001c0026t0001g0066 others(101): Show |
125 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.790-4453G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925020 | |||||||
| chr3:19925028 | G | A | 3 | a0003c0004t0001g0173 a0003c0004t0001g0175 a0003c0004t0001g0176 |
3 | HG02080.hp2 NA18941.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.790-4461C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925028 | |||||||
| chr3:19925059 | A | C | 177 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(174): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.790-4492T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925059 | |||||||
| chr3:19925062 | G | A | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.790-4495C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925062 | |||||||
| chr3:19925085 | A | G | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-4518T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925085 | |||||||
| chr3:19925228 | C | A | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-4661G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925228 | |||||||
| chr3:19925241 | C | CA | 10 | a0001c0001t0002g0238 a0001c0001t0002g0245 a0002c0002t0001g0077 others(7): Show |
10 | HG01099.hp2 HG02293.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-4675dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925241 | |||||||
| chr3:19925241 | C | CAA | 16 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0002c0009t0002g0006 others(13): Show |
23 | HG01109.hp1 HG01109.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-4676_790-4675d others(4): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925241 | |||||||
| chr3:19925241 | CA | C | 6 | a0001c0001t0002g0200 a0001c0001t0002g0241 a0001c0001t0002g0264 others(3): Show |
6 | HG00323.hp2 HG01069.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.790-4675delT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925241 | |||||||
| chr3:19925293 | C | T | 1 | a0001c0001t0002g0199 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.790-4726G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925293 | |||||||
| chr3:19925402 | A | G | 155 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(152): Show |
180 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(177): Show |
intron_variant | MODIFIER | c.790-4835T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925402 | |||||||
| chr3:19925494 | T | C | 32 | a0001c0026t0001g0066 a0002c0003t0001g0004 a0002c0003t0001g0015 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.790-4927A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925494 | |||||||
| chr3:19925629 | G | A | 2 | a0003c0004t0001g0026 a0003c0004t0001g0174 |
3 | HG02970.hp1 HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.790-5062C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925629 | |||||||
| chr3:19925700 | C | G | 10 | a0002c0009t0001g0128 a0002c0010t0001g0127 a0002c0010t0002g0179 others(7): Show |
10 | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.790-5133G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925700 | |||||||
| chr3:19925770 | G | A | 1 | a0003c0004t0001g0158 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.790-5203C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925770 | |||||||
| chr3:19925786 | C | A | 1 | a0002c0002t0001g0091 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.790-5219G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925786 | |||||||
| chr3:19925856 | A | T | 11 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(8): Show |
13 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.790-5289T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19925856 | |||||||
| chr3:19926052 | A | G | 1 | a0013c0016t0002g0270 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.790-5485T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926052 | |||||||
| chr3:19926141 | CCCAAAA | C | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-5580_790-5575d others(8): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926141 | |||||||
| chr3:19926149 | AGCTGT | A | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.790-5587_790-5583d others(7): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926149 | |||||||
| chr3:19926238 | G | A | 1 | a0003c0004t0001g0159 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.790-5671C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926238 | |||||||
| chr3:19926249 | C | G | 4 | a0001c0001t0002g0028 a0001c0001t0002g0197 a0001c0001t0002g0198 others(1): Show |
5 | NA18939.hp2 NA18952.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.790-5682G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926249 | |||||||
| chr3:19926326 | G | T | 1 | a0002c0019t0001g0049 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.790-5759C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926326 | |||||||
| chr3:19926332 | T | C | 1 | a0001c0001t0002g0239 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.790-5765A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926332 | |||||||
| chr3:19926333 | T | G | 8 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0007c0008t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.790-5766A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926333 | |||||||
| chr3:19926337 | G | GT | 9 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(6): Show |
11 | HG00323.hp2 HG00738.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.790-5771dupA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926337 | |||||||
| chr3:19926337 | G | T | 2 | a0007c0008t0002g0036 a0007c0008t0002g0192 |
3 | HG03453.hp2 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.790-5770C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926337 | |||||||
| chr3:19926337 | GT | G | 162 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(159): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.790-5771delA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926337 | |||||||
| chr3:19926345 | T | G | 1 | a0002c0003t0001g0070 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.790-5778A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926345 | |||||||
| chr3:19926346 | G | T | 1 | a0002c0003t0001g0070 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.790-5779C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926346 | |||||||
| chr3:19926352 | T | G | 1 | a0002c0003t0001g0070 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.790-5785A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926352 | |||||||
| chr3:19926509 | G | A | 60 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(57): Show |
66 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.790-5942C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926509 | |||||||
| chr3:19926608 | T | C | 171 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(168): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.790-6041A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926608 | |||||||
| chr3:19926653 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.790-6086G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926653 | |||||||
| chr3:19926658 | C | A | 13 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0166 others(10): Show |
15 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.790-6091G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926658 | |||||||
| chr3:19926662 | C | CTTTTTTA | 191 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0001c0026t0001g0066 others(188): Show |
225 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.790-6102_790-6096d others(9): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926662 | |||||||
| chr3:19926662 | C | CTTTTTTA others(7): Show |
1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.790-6096_790-6095i others(16): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926662 | |||||||
| chr3:19926662 | C | CTTTTTTG | 2 | a0007c0027t0002g0273 a0015c0015t0002g0012 |
4 | HG02258.hp2 HG02486.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.790-6096_790-6095i others(9): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926662 | |||||||
| chr3:19926685 | C | CAG | 171 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(168): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.790-6120_790-6119d others(4): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926685 | |||||||
| chr3:19926883 | C | T | 57 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(54): Show |
63 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.790-6316G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926883 | |||||||
| chr3:19926952 | G | A | 16 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(13): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.789+6278C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19926952 | |||||||
| chr3:19927091 | C | T | 171 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(168): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.789+6139G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927091 | |||||||
| chr3:19927140 | A | G | 1 | a0001c0001t0002g0250 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.789+6090T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927140 | |||||||
| chr3:19927203 | T | A | 171 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(168): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.789+6027A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927203 | |||||||
| chr3:19927293 | T | C | 1 | a0005c0006t0003g0040 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.789+5937A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927293 | |||||||
| chr3:19927358 | T | A | 1 | a0003c0004t0001g0160 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.789+5872A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927358 | |||||||
| chr3:19927358 | T | C | 64 | a0001c0001t0002g0002 a0001c0001t0002g0035 a0001c0001t0002g0241 others(61): Show |
80 | HG00423.hp2 HG00544.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.789+5872A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927358 | |||||||
| chr3:19927407 | T | C | 57 | a0002c0002t0001g0021 a0002c0002t0001g0022 a0002c0002t0001g0077 others(54): Show |
63 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.789+5823A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927407 | |||||||
| chr3:19927422 | T | C | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+5808A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927422 | |||||||
| chr3:19927556 | T | G | 1 | a0009c0012t0002g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.789+5674A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927556 | |||||||
| chr3:19927576 | T | C | 1 | a0004c0005t0001g0161 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.789+5654A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927576 | |||||||
| chr3:19927961 | T | A | 11 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(8): Show |
13 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.789+5269A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19927961 | |||||||
| chr3:19928062 | A | G | 31 | a0001c0026t0001g0066 a0002c0003t0001g0004 a0002c0003t0001g0015 others(28): Show |
38 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.789+5168T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928062 | |||||||
| chr3:19928412 | A | G | 8 | a0002c0002t0002g0194 a0002c0002t0002g0251 a0007c0008t0002g0027 others(5): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.789+4818T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928412 | |||||||
| chr3:19928413 | T | G | 177 | a0001c0001t0002g0246 a0001c0026t0001g0066 a0002c0002t0001g0021 others(174): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.789+4817A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928413 | |||||||
| chr3:19928483 | G | T | 3 | a0006c0007t0002g0189 a0006c0007t0002g0190 a0006c0007t0002g0191 |
3 | HG01109.hp2 HG02922.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.789+4747C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928483 | |||||||
| chr3:19928490 | C | T | 40 | a0001c0026t0001g0066 a0002c0003t0001g0004 a0002c0003t0001g0015 others(37): Show |
49 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.789+4740G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928490 | |||||||
| chr3:19928501 | G | C | 154 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(151): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.789+4729C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928501 | |||||||
| chr3:19928570 | G | A | 176 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(173): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.789+4660C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928570 | |||||||
| chr3:19928619 | G | T | 176 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(173): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.789+4611C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928619 | |||||||
| chr3:19928648 | T | C | 1 | a0006c0007t0002g0272 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.789+4582A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928648 | |||||||
| chr3:19928723 | G | A | 7 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(4): Show |
12 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.789+4507C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928723 | |||||||
| chr3:19928741 | G | A | 7 | a0009c0012t0002g0037 a0009c0012t0002g0258 a0009c0012t0002g0259 others(4): Show |
10 | HG01934.hp2 HG02258.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.789+4489C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928741 | |||||||
| chr3:19928905 | T | C | 3 | a0002c0009t0001g0128 a0002c0010t0001g0127 a0013c0016t0001g0076 |
3 | HG02258.hp1 HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.789+4325A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19928905 | |||||||
| chr3:19929009 | T | C | 176 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(173): Show |
209 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.789+4221A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929009 | |||||||
| chr3:19929014 | C | A | 2 | a0008c0011t0001g0014 a0008c0011t0001g0045 |
3 | HG02486.hp2 HG03195.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.789+4216G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929014 | |||||||
| chr3:19929018 | T | C | 1 | a0001c0001t0002g0247 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.789+4212A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929018 | |||||||
| chr3:19929020 | A | T | 1 | a0002c0002t0001g0077 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.789+4210T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929020 | |||||||
| chr3:19929169 | C | G | 177 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(174): Show |
210 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.789+4061G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929169 | |||||||
| chr3:19929207 | CT | C | 153 | a0001c0001t0002g0248 a0001c0026t0001g0066 a0002c0002t0001g0021 others(150): Show |
178 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.789+4022delA | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929207 | |||||||
| chr3:19929453 | C | G | 8 | a0001c0001t0002g0250 a0009c0012t0002g0037 a0009c0012t0002g0258 others(5): Show |
9 | HG01934.hp2 HG02717.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+3777G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929453 | |||||||
| chr3:19929488 | G | A | 1 | a0001c0001t0002g0249 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.789+3742C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929488 | |||||||
| chr3:19929488 | G | C | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.789+3742C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929488 | |||||||
| chr3:19929659 | A | C | 1 | a0001c0001t0002g0187 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.789+3571T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929659 | |||||||
| chr3:19929708 | C | CA | 96 | a0001c0001t0002g0250 a0001c0001t0002g0252 a0002c0002t0001g0077 others(93): Show |
119 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.789+3521dupT | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929708 | |||||||
| chr3:19929708 | C | CAA | 71 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(68): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.789+3520_789+3521d others(4): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929708 | |||||||
| chr3:19929708 | C | CAAA | 10 | a0001c0001t0002g0253 a0002c0002t0001g0124 a0002c0002t0001g0125 others(7): Show |
11 | HG01106.hp1 HG01123.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.789+3519_789+3521d others(5): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929708 | |||||||
| chr3:19929929 | G | C | 1 | a0001c0001t0002g0254 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.789+3301C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19929929 | |||||||
| chr3:19930039 | G | A | 154 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(151): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.789+3191C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930039 | |||||||
| chr3:19930425 | T | C | 2 | a0011c0013t0001g0074 a0011c0013t0002g0255 |
2 | HG02280.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.789+2805A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930425 | |||||||
| chr3:19930835 | G | A | 1 | a0016c0022t0001g0164 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.789+2395C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930835 | |||||||
| chr3:19930853 | C | T | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+2377G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930853 | |||||||
| chr3:19930872 | C | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2358G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930872 | |||||||
| chr3:19930873 | C | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2357G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930873 | |||||||
| chr3:19930874 | T | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2356A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930874 | |||||||
| chr3:19930875 | G | A | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2355C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930875 | |||||||
| chr3:19930877 | A | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2353T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930877 | |||||||
| chr3:19930880 | C | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2350G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930880 | |||||||
| chr3:19930884 | G | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2346C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930884 | |||||||
| chr3:19930896 | G | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2334C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930896 | |||||||
| chr3:19930899 | A | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2331T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930899 | |||||||
| chr3:19930902 | G | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2328C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930902 | |||||||
| chr3:19930903 | T | A | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2327A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930903 | |||||||
| chr3:19930908 | C | A | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2322G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930908 | |||||||
| chr3:19930910 | A | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2320T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930910 | |||||||
| chr3:19930912 | C | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2318G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930912 | |||||||
| chr3:19930913 | A | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2317T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930913 | |||||||
| chr3:19930914 | C | A | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2316G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930914 | |||||||
| chr3:19930921 | T | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2309A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930921 | |||||||
| chr3:19930929 | A | T | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2301T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930929 | |||||||
| chr3:19930930 | G | T | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2300C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930930 | |||||||
| chr3:19930932 | G | T | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2298C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930932 | |||||||
| chr3:19930933 | G | C | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2297C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930933 | |||||||
| chr3:19930935 | C | T | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2295G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930935 | |||||||
| chr3:19930941 | T | G | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2289A>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930941 | |||||||
| chr3:19930951 | G | A | 1 | a0003c0004t0001g0165 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.789+2279C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930951 | |||||||
| chr3:19930954 | G | A | 55 | a0003c0004t0001g0023 a0003c0004t0001g0024 a0003c0004t0001g0025 others(52): Show |
65 | HG00544.hp2 HG00673.hp2 HG00733.hp1 others(62): Show |
intron_variant | MODIFIER | c.789+2276C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19930954 | |||||||
| chr3:19931018 | G | C | 9 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(6): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.789+2212C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931018 | |||||||
| chr3:19931128 | A | ACTGGGTG others(4): Show |
1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2101_789+2102i others(13): Show |
EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931128 | |||||||
| chr3:19931143 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2087T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931143 | |||||||
| chr3:19931146 | G | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2084C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931146 | |||||||
| chr3:19931151 | A | T | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2079T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931151 | |||||||
| chr3:19931152 | G | A | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2078C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931152 | |||||||
| chr3:19931157 | T | A | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2073A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931157 | |||||||
| chr3:19931159 | T | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2071A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931159 | |||||||
| chr3:19931163 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2067T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931163 | |||||||
| chr3:19931165 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2065T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931165 | |||||||
| chr3:19931166 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2064T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931166 | |||||||
| chr3:19931167 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2063T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931167 | |||||||
| chr3:19931168 | A | T | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2062T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931168 | |||||||
| chr3:19931169 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2061G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931169 | |||||||
| chr3:19931173 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2057T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931173 | |||||||
| chr3:19931175 | A | G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2055T>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931175 | |||||||
| chr3:19931177 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2053T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931177 | |||||||
| chr3:19931178 | A | C | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2052T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931178 | |||||||
| chr3:19931186 | A | T | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2044T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931186 | |||||||
| chr3:19931187 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2043G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931187 | |||||||
| chr3:19931191 | C | A | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2039G>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931191 | |||||||
| chr3:19931192 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.789+2038G>C | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931192 | |||||||
| chr3:19931300 | G | A | 32 | a0001c0026t0001g0066 a0002c0003t0001g0004 a0002c0003t0001g0015 others(29): Show |
39 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.789+1930C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931300 | |||||||
| chr3:19931300 | G | C | 2 | a0002c0009t0001g0128 a0002c0010t0001g0127 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.789+1930C>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931300 | |||||||
| chr3:19931334 | T | A | 2 | a0003c0004t0001g0175 a0003c0004t0001g0176 |
2 | HG02080.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.789+1896A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931334 | |||||||
| chr3:19931335 | G | A | 13 | a0003c0004t0001g0025 a0003c0004t0001g0026 a0003c0004t0001g0166 others(10): Show |
15 | HG00673.hp2 HG00735.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.789+1895C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931335 | |||||||
| chr3:19931353 | T | C | 1 | a0002c0002t0002g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.789+1877A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931353 | |||||||
| chr3:19931423 | G | A | 15 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(12): Show |
23 | HG01884.hp1 HG01891.hp1 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.789+1807C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931423 | |||||||
| chr3:19931455 | C | T | 7 | a0002c0010t0002g0179 a0002c0010t0002g0180 a0002c0010t0002g0181 others(4): Show |
7 | HG01243.hp1 HG02145.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.789+1775G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931455 | |||||||
| chr3:19931555 | T | A | 154 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(151): Show |
179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.789+1675A>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931555 | |||||||
| chr3:19931556 | C | T | 2 | a0002c0010t0002g0179 a0002c0010t0002g0180 |
2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.789+1674G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931556 | |||||||
| chr3:19931567 | G | A | 4 | a0001c0001t0002g0005 a0001c0001t0002g0010 a0001c0001t0002g0262 others(1): Show |
9 | HG01978.hp1 HG02155.hp1 HG03017.hp2 others(6): Show |
intron_variant | MODIFIER | c.789+1663C>T | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931567 | |||||||
| chr3:19931694 | A | T | 1 | a0002c0010t0001g0075 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.789+1536T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19931694 | |||||||
| chr3:19932168 | G | T | 1 | a0004c0005t0001g0131 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.789+1062C>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932168 | |||||||
| chr3:19932338 | T | C | 11 | a0001c0001t0002g0264 a0001c0001t0002g0269 a0006c0007t0002g0038 others(8): Show |
13 | HG00323.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.789+892A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932338 | |||||||
| chr3:19932382 | A | C | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+848T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932382 | |||||||
| chr3:19932679 | T | C | 7 | a0008c0011t0001g0013 a0008c0011t0001g0014 a0008c0011t0001g0042 others(4): Show |
9 | HG02486.hp2 HG02723.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.789+551A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932679 | |||||||
| chr3:19932695 | A | T | 163 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(160): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.789+535T>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932695 | |||||||
| chr3:19932696 | A | C | 163 | a0001c0026t0001g0066 a0002c0002t0001g0021 a0002c0002t0001g0022 others(160): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.789+534T>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19932696 | |||||||
| chr3:19933009 | C | T | 9 | a0002c0009t0002g0006 a0002c0009t0002g0011 a0002c0009t0002g0274 others(6): Show |
16 | HG01884.hp1 HG01891.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.789+221G>A | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19933009 | |||||||
| chr3:19933208 | T | C | 165 | a0001c0001t0002g0279 a0001c0026t0001g0066 a0002c0002t0001g0021 others(162): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.789+22A>G | EFHB | ENSG00000163576.18 | transcript | ENST00000295824.14 | protein_coding | 1/12 | chr3 | 19933208 |