Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22797 |
| ensemblid | ENSG00000105967.16 |
| hgncid | 11754 |
| symbol | TFEC |
| name | transcription factor EC |
| refseq_nuc | NM_012252.4 |
| refseq_prot | NP_036384.1 |
| ensembl_nuc | ENST00000265440.12 |
| ensembl_prot | ENSP00000265440.7 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 115935152 |
| end | 116030763 |
| strand | - |
| ver | v1.2 |
| region | chr7:115935152-116030763 |
| region5000 | chr7:115930152-116035763 |
| regionname0 | TFEC_chr7_115935152_116030763 |
| regionname5000 | TFEC_chr7_115930152_116035763 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 347 | 383 | 90 | 70 | 166 | 14 | 41 | 126 | TFEC_chr7_115930152_116035763 | TFEC | MTLDH others(342): Show |
chr7 | 115930152 | 116035763 |
| a0002 | 0/0 | 347 | 4 | 0 | 1 | 0 | 0 | 3 | 0 | TFEC_chr7_115930152_116035763 | TFEC | MTLDH others(342): Show |
chr7 | 115930152 | 116035763 |
| a0003 | 0/0 | 347 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | MTLDH others(342): Show |
chr7 | 115930152 | 116035763 |
| a0004 | 0/0 | 347 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | MTLDH others(342): Show |
chr7 | 115930152 | 116035763 |
| a0005 | 0/0 | 347 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TFEC_chr7_115930152_116035763 | TFEC | MTLDH others(342): Show |
chr7 | 115930152 | 116035763 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1041 | 366 | 77 | 68 | 164 | 14 | 41 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0002 | 0/0 | 1041 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0004 | 0/0 | 1041 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0005 | 0/0 | 1041 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0009 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0010 | 0/0 | 1041 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0001c0011 | 0/0 | 1041 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0002c0003 | 0/0 | 1041 | 4 | 0 | 1 | 0 | 0 | 3 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0003c0006 | 0/0 | 1041 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0004c0008 | 0/0 | 1041 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 | ||
| a0005c0007 | 0/0 | 1041 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | ATGAC others(1036): Show |
chr7 | 115930152 | 116035763 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 6646 | 102 | 27 | 16 | 43 | 4 | 11 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0002 | 0/0 | 6646 | 102 | 8 | 22 | 55 | 4 | 13 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0003 | 1/0 | 6646 | 63 | 6 | 15 | 36 | 1 | 4 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0004 | 0/0 | 6646 | 18 | 3 | 9 | 0 | 4 | 2 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0005 | 0/0 | 6646 | 13 | 0 | 0 | 13 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0006 | 0/0 | 6646 | 8 | 8 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0007 | 0/0 | 6646 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0008 | 0/0 | 6645 | 6 | 0 | 0 | 6 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6640): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0009 | 0/0 | 6646 | 4 | 0 | 0 | 0 | 1 | 3 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0010 | 0/0 | 6646 | 4 | 4 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0011 | 0/0 | 6646 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0012 | 0/0 | 6643 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6638): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0013 | 0/0 | 6646 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0014 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0015 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0016 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0017 | 0/0 | 6646 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0018 | 0/0 | 6646 | 2 | 1 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0019 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0020 | 0/0 | 6646 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0021 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0022 | 0/0 | 6646 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0024 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0025 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0026 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0027 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0028 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0030 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0031 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0033 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0034 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0035 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0036 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0001t0037 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0002t0001 | 0/0 | 6646 | 7 | 6 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0004t0001 | 0/0 | 6646 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0004t0029 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0005t0014 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0005t0032 | 0/0 | 6646 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0009t0003 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0010t0002 | 0/0 | 6646 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0001c0011t0004 | 0/0 | 6646 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0002c0003t0001 | 0/0 | 6646 | 3 | 0 | 1 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0002c0003t0021 | 0/0 | 6646 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0003c0006t0001 | 0/0 | 6646 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0004c0008t0023 | 0/0 | 6646 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| a0005c0007t0001 | 0/0 | 6646 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | ATTCA others(6641): Show |
chr7 | 115930152 | 116035763 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0001 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0003 | 0/0 | 6 | 0 | 0 | 3 | 0 | 3 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0066 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0002 | 0/0 | 6 | 2 | 1 | 0 | 3 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0007g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0008g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0008g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0009g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0009g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0009g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0010g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0010g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0010g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0010g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0011g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0011g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0011g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0012g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0012g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0012g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0013g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0014g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0015g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0016g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0017g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0017g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0018g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0018g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0019g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0020g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0021g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0022g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0024g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0025g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0026g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0027g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0028g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0030g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0031g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0033g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0034g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0035g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0036g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0001t0037g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0004t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0004t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0004t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0004t0029g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0005t0014g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0005t0014g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0005t0032g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0009t0003g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0010t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0001c0011t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0002c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0002c0003t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0002c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0002c0003t0021g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0003c0006t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0003c0006t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0003c0006t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0004c0008t0023g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0004c0008t0023g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0005c0007t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| a0005c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0317 | EUR | GBR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00140 | hp2 | a0001 | c0001 | t0009 | g0141 | EUR | GBR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0283 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00323 | hp1 | a0001 | c0001 | t0004 | g0002 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | FIN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0285 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0277 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0251 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0056 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0108 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00733 | hp2 | a0001 | c0001 | t0004 | g0263 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0137 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG00741 | hp2 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01069 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01071 | hp2 | a0001 | c0001 | t0013 | g0007 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01074 | hp1 | a0001 | c0001 | t0013 | g0007 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0295 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0293 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0143 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01256 | hp1 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01257 | hp1 | a0003 | c0006 | t0001 | g0039 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01258 | hp1 | a0003 | c0006 | t0001 | g0037 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01258 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01346 | hp2 | a0001 | c0001 | t0028 | g0250 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01361 | hp2 | a0001 | c0001 | t0007 | g0269 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01433 | hp2 | a0001 | c0001 | t0031 | g0158 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01517 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | IBS | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0058 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01943 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01978 | hp1 | a0003 | c0006 | t0001 | g0038 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01978 | hp2 | a0001 | c0001 | t0004 | g0164 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01993 | hp2 | a0001 | c0011 | t0004 | g0156 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0030 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02027 | hp2 | a0001 | c0001 | t0011 | g0151 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02055 | hp2 | a0001 | c0004 | t0001 | g0245 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02074 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0290 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02129 | hp1 | a0001 | c0009 | t0003 | g0296 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0132 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0102 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | CDX | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02257 | hp1 | a0004 | c0008 | t0023 | g0176 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02258 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0292 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PEL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02451 | hp1 | a0001 | c0001 | t0033 | g0179 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02451 | hp2 | a0001 | c0001 | t0016 | g0325 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0155 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0052 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02622 | hp1 | a0001 | c0001 | t0035 | g0175 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02630 | hp2 | a0001 | c0005 | t0014 | g0043 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02717 | hp1 | a0001 | c0001 | t0015 | g0323 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0266 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0271 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02738 | hp1 | a0001 | c0001 | t0009 | g0144 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02809 | hp1 | a0001 | c0001 | t0014 | g0234 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02818 | hp1 | a0001 | c0001 | t0034 | g0246 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0300 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02895 | hp1 | a0001 | c0001 | t0006 | g0240 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02895 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0031 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0051 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02922 | hp2 | a0001 | c0001 | t0030 | g0166 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02970 | hp1 | a0001 | c0001 | t0006 | g0241 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03017 | hp2 | a0005 | c0007 | t0001 | g0046 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03041 | hp2 | a0001 | c0001 | t0007 | g0267 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03098 | hp1 | a0001 | c0005 | t0014 | g0116 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03130 | hp2 | a0001 | c0005 | t0032 | g0115 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0049 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03195 | hp1 | a0001 | c0001 | t0024 | g0171 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03209 | hp2 | a0001 | c0004 | t0001 | g0243 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0161 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03239 | hp2 | a0001 | c0001 | t0026 | g0057 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03453 | hp2 | a0001 | c0001 | t0010 | g0167 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0023 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03490 | hp2 | a0002 | c0003 | t0021 | g0101 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03492 | hp1 | a0001 | c0001 | t0021 | g0107 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03516 | hp1 | a0004 | c0008 | t0023 | g0136 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0237 | AFR | ESN | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03540 | hp2 | a0001 | c0001 | t0016 | g0324 | AFR | GWD | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0169 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03654 | hp1 | a0002 | c0003 | t0001 | g0100 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03654 | hp2 | a0002 | c0003 | t0001 | g0118 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03669 | hp1 | a0001 | c0001 | t0009 | g0145 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0315 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0272 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03834 | hp1 | a0005 | c0007 | t0001 | g0045 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03834 | hp2 | a0001 | c0001 | t0018 | g0139 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03927 | hp2 | a0001 | c0001 | t0027 | g0247 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03942 | hp1 | a0001 | c0001 | t0022 | g0228 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0152 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04115 | hp2 | a0001 | c0001 | t0037 | g0122 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04184 | hp2 | a0001 | c0001 | t0025 | g0146 | SAS | BEB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04204 | hp2 | a0001 | c0001 | t0022 | g0089 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | STU | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0120 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18747 | hp1 | a0001 | c0001 | t0011 | g0148 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0153 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18906 | hp2 | a0001 | c0001 | t0016 | g0321 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18942 | hp2 | a0001 | c0001 | t0012 | g0309 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18945 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0318 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18949 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18956 | hp1 | a0001 | c0010 | t0002 | g0191 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18973 | hp1 | a0001 | c0001 | t0020 | g0016 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18979 | hp1 | a0001 | c0001 | t0017 | g0206 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18992 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18995 | hp1 | a0001 | c0001 | t0008 | g0232 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19030 | hp2 | a0001 | c0001 | t0015 | g0053 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0012 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19057 | hp2 | a0001 | c0001 | t0012 | g0308 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19062 | hp2 | a0001 | c0001 | t0011 | g0150 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0255 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19064 | hp2 | a0001 | c0001 | t0005 | g0260 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19066 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0257 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19075 | hp2 | a0001 | c0001 | t0012 | g0310 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19077 | hp2 | a0001 | c0001 | t0036 | g0302 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19082 | hp1 | a0001 | c0001 | t0008 | g0005 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19088 | hp1 | a0001 | c0001 | t0020 | g0016 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0259 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0261 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0168 | AFR | YRI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0149 | AFR | ASW | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0135 | AFR | ASW | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0002 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0163 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20905 | hp1 | a0001 | c0001 | t0009 | g0142 | SAS | GIH | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0160 | SAS | GIH | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02109 | hp1 | a0001 | c0004 | t0029 | g0238 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02486 | hp2 | a0001 | c0001 | t0019 | g0023 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0012 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG02559 | hp2 | a0001 | c0001 | t0018 | g0140 | AFR | ACB | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0172 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0235 | AFR | MSL | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0002 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA18955 | hp2 | a0001 | c0001 | t0005 | g0256 | EAS | JPT | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | USA | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0173 | AFR | LWK | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0066 | REF | REF | TFEC_chr7_115930152_116035763 | TFEC | chr7 | 115930152 | 116035763 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:115956763 | C | T | 1 | a0004 | 2 | HG02257.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.298G>A | p.Gly100Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 501/6646 | 298/1044 | 100/347 | chr7 | 115956763 | |||
| chr7:115984338 | C | T | 1 | a0005 | 2 | HG03017.hp2 HG03834.hp1 |
missense_variant | MODERATE | c.104G>A | p.Ser35Asn | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 307/6646 | 104/1044 | 35/347 | chr7 | 115984338 | |||
| chr7:115984342 | C | T | 1 | a0003 | 3 | HG01257.hp1 HG01258.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.100G>A | p.Asp34Asn | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 303/6646 | 100/1044 | 34/347 | chr7 | 115984342 | |||
| chr7:115984424 | C | G | 1 | a0002 | 4 | HG02148.hp2 HG03490.hp2 HG03654.hp1 others(1): Show |
missense_variant | MODERATE | c.18G>C | p.Gln6His | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 221/6646 | 18/1044 | 6/347 | chr7 | 115984424 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:115940623 | G | A | 1 | a0001c0010 | 1 | NA18956.hp1 | synonymous_variant | LOW | c.972C>T | p.Ala324Ala | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1175/6646 | 972/1044 | 324/347 | chr7 | 115940623 | |||
| chr7:115940839 | G | A | 1 | a0001c0011 | 1 | HG01993.hp2 | synonymous_variant | LOW | c.756C>T | p.Ser252Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 959/6646 | 756/1044 | 252/347 | chr7 | 115940839 | |||
| chr7:115956746 | T | G | 1 | a0001c0004 | 4 | HG02055.hp2 HG02109.hp1 HG03209.hp2 others(1): Show |
synonymous_variant | LOW | c.315A>C | p.Ser105Ser | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 518/6646 | 315/1044 | 105/347 | chr7 | 115956746 | |||
| chr7:115956767 | A | G | 1 | a0001c0009 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.294T>C | p.Tyr98Tyr | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/8 | 497/6646 | 294/1044 | 98/347 | chr7 | 115956767 | |||
| chr7:115984271 | T | C | 1 | a0001c0002 | 7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.171A>G | p.Ala57Ala | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 374/6646 | 171/1044 | 57/347 | chr7 | 115984271 | |||
| chr7:115984385 | C | T | 1 | a0001c0005 | 3 | HG02630.hp2 HG03098.hp1 HG03130.hp2 |
synonymous_variant | LOW | c.57G>A | p.Val19Val | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 260/6646 | 57/1044 | 19/347 | chr7 | 115984385 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:115935201 | C | T | 2 | a0001c0001t0010 a0004c0008t0023 |
6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5350G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5350 | chr7 | 115935201 | ||||||
| chr7:115935503 | G | T | 1 | a0001c0001t0028 | 1 | HG01346.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5048C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5048 | chr7 | 115935503 | ||||||
| chr7:115935515 | G | A | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5036C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 5036 | chr7 | 115935515 | ||||||
| chr7:115935688 | T | A | 3 | a0001c0001t0014 a0001c0005t0014 a0001c0005t0032 |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4863A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4863 | chr7 | 115935688 | ||||||
| chr7:115935688 | T | C | 1 | a0001c0001t0022 | 2 | HG03942.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4863A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4863 | chr7 | 115935688 | ||||||
| chr7:115935697 | A | T | 1 | a0001c0001t0025 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4854T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4854 | chr7 | 115935697 | ||||||
| chr7:115935712 | T | C | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4839A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4839 | chr7 | 115935712 | ||||||
| chr7:115935852 | C | T | 2 | a0001c0001t0021 a0002c0003t0021 |
2 | HG03490.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4699G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4699 | chr7 | 115935852 | ||||||
| chr7:115935883 | AC | A | 1 | a0001c0001t0008 | 6 | NA18945.hp1 NA18994.hp1 NA18995.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4667delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4667 | chr7 | 115935883 | ||||||
| chr7:115935903 | G | A | 1 | a0001c0001t0031 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4648C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4648 | chr7 | 115935903 | ||||||
| chr7:115935907 | A | G | 1 | a0001c0001t0020 | 2 | NA18973.hp1 NA19088.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4644T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4644 | chr7 | 115935907 | ||||||
| chr7:115936080 | A | C | 1 | a0001c0001t0013 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4471T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4471 | chr7 | 115936080 | ||||||
| chr7:115936165 | AATG | A | 1 | a0001c0001t0012 | 3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4383_*4385delCAT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4383 | chr7 | 115936165 | ||||||
| chr7:115936418 | G | A | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4133C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 4133 | chr7 | 115936418 | ||||||
| chr7:115936746 | T | G | 1 | a0001c0001t0026 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3805A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3805 | chr7 | 115936746 | ||||||
| chr7:115936827 | A | C | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3724T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3724 | chr7 | 115936827 | ||||||
| chr7:115937134 | A | T | 2 | a0001c0001t0009 a0001c0001t0018 |
6 | HG00140.hp2 HG02559.hp2 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3417T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3417 | chr7 | 115937134 | ||||||
| chr7:115937158 | G | A | 1 | a0001c0004t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3393C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3393 | chr7 | 115937158 | ||||||
| chr7:115937165 | G | A | 1 | a0001c0004t0029 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3386C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3386 | chr7 | 115937165 | ||||||
| chr7:115937369 | G | T | 1 | a0001c0001t0033 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3182C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 3182 | chr7 | 115937369 | ||||||
| chr7:115937608 | T | A | 4 | a0001c0001t0004 a0001c0001t0030 a0001c0001t0031 others(1): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2943A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2943 | chr7 | 115937608 | ||||||
| chr7:115937698 | A | G | 1 | a0001c0001t0027 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2853T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2853 | chr7 | 115937698 | ||||||
| chr7:115937760 | C | T | 1 | a0001c0001t0011 | 3 | HG02027.hp2 NA18747.hp1 NA19062.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2791G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2791 | chr7 | 115937760 | ||||||
| chr7:115938050 | T | C | 3 | a0001c0001t0004 a0001c0001t0031 a0001c0011t0004 |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2501A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2501 | chr7 | 115938050 | ||||||
| chr7:115938070 | G | T | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(36): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
3_prime_UTR_variant | MODIFIER | c.*2481C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2481 | chr7 | 115938070 | ||||||
| chr7:115938081 | T | C | 1 | a0001c0001t0030 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2470A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2470 | chr7 | 115938081 | ||||||
| chr7:115938387 | T | C | 3 | a0001c0001t0004 a0001c0001t0031 a0001c0011t0004 |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2164A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 2164 | chr7 | 115938387 | ||||||
| chr7:115938571 | C | A | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1980G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1980 | chr7 | 115938571 | ||||||
| chr7:115938613 | T | G | 26 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(23): Show |
172 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*1938A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1938 | chr7 | 115938613 | ||||||
| chr7:115938746 | T | A | 3 | a0001c0001t0004 a0001c0001t0031 a0001c0011t0004 |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1805A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1805 | chr7 | 115938746 | ||||||
| chr7:115938761 | A | G | 1 | a0001c0001t0005 | 13 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1790T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1790 | chr7 | 115938761 | ||||||
| chr7:115938950 | T | C | 1 | a0001c0005t0032 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1601A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1601 | chr7 | 115938950 | ||||||
| chr7:115939038 | G | A | 2 | a0001c0001t0033 a0001c0001t0034 |
2 | HG02451.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1513C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1513 | chr7 | 115939038 | ||||||
| chr7:115939202 | T | C | 1 | a0001c0001t0015 | 3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1349A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1349 | chr7 | 115939202 | ||||||
| chr7:115939264 | A | T | 1 | a0001c0001t0019 | 2 | HG02486.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1287T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1287 | chr7 | 115939264 | ||||||
| chr7:115939342 | G | T | 1 | a0001c0001t0018 | 2 | HG02559.hp2 HG03834.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1209C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1209 | chr7 | 115939342 | ||||||
| chr7:115939419 | T | C | 1 | a0001c0001t0006 | 8 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1132A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 1132 | chr7 | 115939419 | ||||||
| chr7:115939617 | C | T | 1 | a0001c0001t0017 | 2 | NA18949.hp1 NA18979.hp1 |
3_prime_UTR_variant | MODIFIER | c.*934G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 934 | chr7 | 115939617 | ||||||
| chr7:115939778 | G | A | 1 | a0001c0001t0035 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 773 | chr7 | 115939778 | ||||||
| chr7:115939818 | C | G | 1 | a0001c0001t0007 | 7 | HG01361.hp2 HG01891.hp1 HG02723.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*733G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 733 | chr7 | 115939818 | ||||||
| chr7:115939976 | T | C | 1 | a0001c0001t0016 | 3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*575A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 575 | chr7 | 115939976 | ||||||
| chr7:115939995 | T | C | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*556A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 556 | chr7 | 115939995 | ||||||
| chr7:115940059 | G | A | 1 | a0001c0001t0036 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*492C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 492 | chr7 | 115940059 | ||||||
| chr7:115940317 | T | C | 1 | a0004c0008t0023 | 2 | HG02257.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*234A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 8/8 | 234 | chr7 | 115940317 | ||||||
| chr7:115984497 | T | C | 1 | a0001c0001t0037 | 1 | HG04115.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 56 | chr7 | 115984497 | ||||||
| chr7:115984509 | G | T | 1 | a0001c0001t0024 | 1 | HG03195.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/8 | 68 | chr7 | 115984509 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:115941089 | C | T | 2 | a0004c0008t0023g0136 a0004c0008t0023g0176 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.664-158G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941089 | |||||||
| chr7:115941413 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(5): Show |
9 | HG02572.hp2 HG02622.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.663+480G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941413 | |||||||
| chr7:115941516 | G | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.663+377C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941516 | |||||||
| chr7:115941764 | G | A | 1 | a0001c0001t0003g0273 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.663+129C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941764 | |||||||
| chr7:115941805 | G | A | 1 | a0001c0001t0003g0034 | 2 | NA18991.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.663+88C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 7/7 | chr7 | 115941805 | |||||||
| chr7:115942277 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0222 |
4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-237C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942277 | |||||||
| chr7:115942303 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.516-263A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942303 | |||||||
| chr7:115942542 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.516-502A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942542 | |||||||
| chr7:115942715 | T | A | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516-675A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942715 | |||||||
| chr7:115942732 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.516-692C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942732 | |||||||
| chr7:115942776 | G | A | 2 | a0001c0001t0010g0167 a0001c0001t0010g0168 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.516-736C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942776 | |||||||
| chr7:115942902 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.516-862T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942902 | |||||||
| chr7:115942953 | C | T | 4 | a0001c0001t0001g0165 a0001c0001t0002g0020 a0001c0001t0002g0155 others(1): Show |
5 | HG01074.hp2 HG01192.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-913G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942953 | |||||||
| chr7:115942959 | G | A | 1 | a0001c0011t0004g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.516-919C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942959 | |||||||
| chr7:115942964 | T | C | 1 | a0001c0001t0002g0143 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.516-924A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942964 | |||||||
| chr7:115942985 | G | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-945C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942985 | |||||||
| chr7:115942986 | G | T | 1 | a0001c0001t0001g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.516-946C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115942986 | |||||||
| chr7:115943051 | T | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(91): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.516-1011A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943051 | |||||||
| chr7:115943145 | TCAATGGA others(5): Show |
T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-1117_516-1106d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943145 | |||||||
| chr7:115943206 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516-1166C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943206 | |||||||
| chr7:115943403 | G | A | 14 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.516-1363C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943403 | |||||||
| chr7:115943510 | ACACAATG others(4228): Show |
A | 5 | a0001c0001t0003g0273 a0001c0001t0003g0287 a0001c0001t0003g0291 others(2): Show |
5 | HG01099.hp2 HG02165.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.515+3129_516-1471d others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943510 | |||||||
| chr7:115943606 | T | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0091 others(4): Show |
7 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1566A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943606 | |||||||
| chr7:115943647 | T | C | 3 | a0001c0001t0001g0109 a0002c0003t0001g0100 a0002c0003t0001g0102 |
3 | HG02148.hp2 HG03490.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.516-1607A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943647 | |||||||
| chr7:115943659 | A | T | 1 | a0001c0001t0002g0001 | 4 | NA18943.hp1 NA18954.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1619T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943659 | |||||||
| chr7:115943758 | G | A | 1 | a0001c0001t0002g0214 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.516-1718C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943758 | |||||||
| chr7:115943868 | T | G | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-1828A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943868 | |||||||
| chr7:115943906 | GTACAATC | G | 7 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(4): Show |
7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1873_516-1867d others(9): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943906 | |||||||
| chr7:115943915 | G | T | 7 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(4): Show |
7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-1875C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943915 | |||||||
| chr7:115943965 | T | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.516-1925A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943965 | |||||||
| chr7:115943996 | T | A | 1 | a0001c0001t0003g0300 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.516-1956A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115943996 | |||||||
| chr7:115944013 | A | AT | 23 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0180 others(20): Show |
26 | HG01175.hp2 HG01361.hp2 HG01952.hp2 others(23): Show |
intron_variant | MODIFIER | c.516-1974dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATT | 6 | a0001c0001t0001g0177 a0001c0001t0003g0132 a0001c0001t0003g0307 others(3): Show |
8 | HG00673.hp1 HG02148.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.516-1975_516-1974d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTT | 9 | a0001c0001t0001g0073 a0001c0001t0001g0081 a0001c0001t0001g0084 others(6): Show |
9 | HG00741.hp2 HG01257.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.516-1978_516-1974d others(7): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(3): Show |
2 | a0001c0001t0001g0113 a0001c0001t0002g0195 |
2 | HG02145.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.516-1983_516-1974d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0157 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.516-1985_516-1974d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(6): Show |
4 | a0001c0001t0001g0036 a0001c0004t0001g0173 a0001c0004t0001g0243 others(1): Show |
4 | HG02055.hp2 HG03209.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-1986_516-1974d others(15): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(7): Show |
4 | a0001c0001t0004g0164 a0001c0001t0024g0171 a0001c0001t0028g0250 others(1): Show |
4 | HG01346.hp2 HG01978.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.516-1987_516-1974d others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(8): Show |
7 | a0001c0001t0001g0071 a0001c0001t0001g0114 a0001c0001t0004g0002 others(4): Show |
9 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.516-1988_516-1974d others(17): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(9): Show |
21 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0070 others(18): Show |
24 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.516-1989_516-1974d others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(10): Show |
23 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0054 others(20): Show |
23 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.516-1990_516-1974d others(19): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(11): Show |
13 | a0001c0001t0001g0042 a0001c0001t0001g0124 a0001c0001t0001g0130 others(10): Show |
14 | HG00741.hp1 HG01109.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-1991_516-1974d others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(12): Show |
22 | a0001c0001t0001g0129 a0001c0001t0002g0003 a0001c0001t0002g0004 others(19): Show |
26 | HG00558.hp1 HG00642.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.516-1992_516-1974d others(21): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(13): Show |
26 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0061 others(23): Show |
28 | HG00735.hp1 HG01099.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.516-1993_516-1974d others(22): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(14): Show |
16 | a0001c0001t0001g0326 a0001c0001t0001g0329 a0001c0001t0002g0003 others(13): Show |
17 | HG00423.hp1 HG00738.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.516-1994_516-1974d others(23): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(15): Show |
15 | a0001c0001t0001g0086 a0001c0001t0001g0233 a0001c0001t0001g0328 others(12): Show |
16 | HG00140.hp2 HG00673.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.516-1995_516-1974d others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(16): Show |
13 | a0001c0001t0001g0327 a0001c0001t0002g0008 a0001c0001t0002g0009 others(10): Show |
15 | HG00408.hp2 HG01106.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.516-1996_516-1974d others(25): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(17): Show |
9 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0153 others(6): Show |
10 | HG02630.hp2 HG03130.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.516-1997_516-1974d others(26): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(18): Show |
6 | a0001c0001t0001g0015 a0001c0001t0001g0330 a0001c0001t0002g0009 others(3): Show |
6 | HG01175.hp1 HG01243.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-1998_516-1974d others(27): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(19): Show |
4 | a0001c0001t0001g0015 a0001c0001t0002g0063 a0001c0001t0002g0202 others(1): Show |
4 | HG02027.hp2 HG03017.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.516-1999_516-1974d others(28): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(20): Show |
1 | a0001c0001t0002g0251 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.516-2000_516-1974d others(29): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(21): Show |
2 | a0001c0001t0002g0317 a0001c0001t0009g0144 |
2 | HG00140.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.516-1974_516-1973i others(30): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | A | ATTTTTTT others(23): Show |
1 | a0001c0005t0014g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.516-1974_516-1973i others(32): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | AT | A | 7 | a0001c0001t0002g0003 a0001c0001t0003g0034 a0001c0001t0003g0270 others(4): Show |
7 | HG02257.hp1 HG02818.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.516-1974delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | ATTTTTT | A | 31 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0067 others(28): Show |
34 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(31): Show |
intron_variant | MODIFIER | c.516-1979_516-1974d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944013 | ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.516-1985_516-1974d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944013 | |||||||
| chr7:115944047 | A | G | 2 | a0001c0001t0004g0021 a0001c0001t0004g0159 |
3 | HG01109.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.516-2007T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944047 | |||||||
| chr7:115944132 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.516-2092A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944132 | |||||||
| chr7:115944145 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-2105T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944145 | |||||||
| chr7:115944192 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.516-2152A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944192 | |||||||
| chr7:115944321 | A | C | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-2281T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944321 | |||||||
| chr7:115944381 | G | C | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516-2341C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944381 | |||||||
| chr7:115944392 | G | T | 1 | a0001c0001t0003g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.516-2352C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944392 | |||||||
| chr7:115944405 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.516-2365G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944405 | |||||||
| chr7:115944514 | T | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.516-2474A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944514 | |||||||
| chr7:115944791 | A | G | 7 | a0001c0001t0004g0002 a0001c0001t0004g0161 a0001c0001t0004g0162 others(4): Show |
11 | HG00323.hp1 HG00733.hp2 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-2751T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944791 | |||||||
| chr7:115944973 | G | A | 4 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0177 others(1): Show |
5 | HG02572.hp2 HG02809.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-2933C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115944973 | |||||||
| chr7:115945061 | A | G | 1 | a0001c0001t0003g0270 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.516-3021T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945061 | |||||||
| chr7:115945063 | T | A | 11 | a0001c0001t0003g0123 a0001c0001t0003g0127 a0001c0001t0003g0276 others(8): Show |
11 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.516-3023A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945063 | |||||||
| chr7:115945122 | AC | A | 96 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(93): Show |
130 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.516-3083delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945122 | |||||||
| chr7:115945140 | CT | C | 136 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(133): Show |
155 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.516-3101delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945140 | |||||||
| chr7:115945198 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.516-3158C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945198 | |||||||
| chr7:115945383 | A | G | 2 | a0001c0001t0033g0179 a0001c0001t0034g0246 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.516-3343T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945383 | |||||||
| chr7:115945503 | G | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0233 a0001c0001t0001g0326 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.516-3463C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945503 | |||||||
| chr7:115945601 | C | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.516-3561G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945601 | |||||||
| chr7:115945613 | T | C | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.516-3573A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945613 | |||||||
| chr7:115945634 | T | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(57): Show |
92 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.516-3594A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945634 | |||||||
| chr7:115945704 | C | A | 1 | a0001c0001t0003g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.516-3664G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945704 | |||||||
| chr7:115945718 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.516-3678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945718 | |||||||
| chr7:115945785 | T | C | 109 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(106): Show |
119 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.516-3745A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945785 | |||||||
| chr7:115945817 | C | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.516-3777G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945817 | |||||||
| chr7:115945890 | C | T | 1 | a0001c0001t0003g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.516-3850G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945890 | |||||||
| chr7:115945944 | G | A | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.516-3904C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945944 | |||||||
| chr7:115945983 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.516-3943G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115945983 | |||||||
| chr7:115946012 | A | G | 1 | a0001c0001t0002g0064 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.516-3972T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946012 | |||||||
| chr7:115946069 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.516-4029A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946069 | |||||||
| chr7:115946089 | T | A | 11 | a0001c0001t0001g0174 a0001c0001t0006g0012 a0001c0001t0006g0172 others(8): Show |
13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.516-4049A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946089 | |||||||
| chr7:115946095 | C | A | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.516-4055G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946095 | |||||||
| chr7:115946261 | C | T | 1 | a0001c0001t0016g0321 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516-4221G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946261 | |||||||
| chr7:115946275 | A | G | 11 | a0001c0001t0001g0174 a0001c0001t0006g0012 a0001c0001t0006g0172 others(8): Show |
13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.516-4235T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946275 | |||||||
| chr7:115946333 | T | A | 2 | a0004c0008t0023g0136 a0004c0008t0023g0176 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.516-4293A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946333 | |||||||
| chr7:115946380 | A | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.516-4340T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946380 | |||||||
| chr7:115946396 | C | CGT | 23 | a0001c0001t0001g0183 a0001c0001t0002g0001 a0001c0001t0002g0004 others(20): Show |
24 | HG02027.hp2 HG02071.hp2 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.516-4358_516-4357d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGT | 44 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(41): Show |
52 | HG00558.hp1 HG00673.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.516-4360_516-4357d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGTGT | 38 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(35): Show |
47 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(44): Show |
intron_variant | MODIFIER | c.516-4362_516-4357d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGTGTG others(1): Show |
5 | a0001c0001t0002g0003 a0001c0001t0002g0062 a0001c0001t0002g0182 others(2): Show |
5 | HG01981.hp2 HG02602.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-4364_516-4357d others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGTGTG others(3): Show |
11 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0010 others(8): Show |
14 | HG01261.hp2 HG01884.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.516-4366_516-4357d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGTGTG others(5): Show |
1 | a0001c0001t0008g0005 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.516-4368_516-4357d others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0009g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.516-4370_516-4357d others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | CGT | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0036 others(65): Show |
79 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.516-4358_516-4357d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | CGTGT | C | 10 | a0001c0001t0001g0174 a0001c0001t0003g0032 a0001c0001t0006g0012 others(7): Show |
12 | HG02258.hp2 HG02451.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.516-4360_516-4357d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946396 | CGTGTGT | C | 4 | a0001c0001t0001g0239 a0001c0001t0004g0021 a0001c0001t0004g0022 others(1): Show |
6 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.516-4362_516-4357d others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946396 | |||||||
| chr7:115946419 | G | GTGTT | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.516-4380_516-4379i others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | |||||||
| chr7:115946419 | G | GTT | 67 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(64): Show |
74 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.516-4380_516-4379i others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | |||||||
| chr7:115946419 | G | T | 32 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0067 others(29): Show |
35 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.516-4379C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946419 | |||||||
| chr7:115946478 | C | T | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.515+4396G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946478 | |||||||
| chr7:115946510 | G | T | 2 | a0001c0001t0018g0139 a0001c0001t0018g0140 |
2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.515+4364C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946510 | |||||||
| chr7:115946622 | TTCTC | T | 122 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(119): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.515+4248_515+4251d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946622 | |||||||
| chr7:115946641 | TTTTC | T | 15 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(12): Show |
16 | HG02257.hp1 HG02572.hp2 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.515+4229_515+4232d others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946641 | |||||||
| chr7:115946650 | T | A | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.515+4224A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946650 | |||||||
| chr7:115946734 | G | A | 1 | a0001c0001t0001g0078 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.515+4140C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946734 | |||||||
| chr7:115946789 | T | C | 105 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(102): Show |
115 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.515+4085A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115946789 | |||||||
| chr7:115947027 | G | A | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.515+3847C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947027 | |||||||
| chr7:115947155 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3719C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947155 | |||||||
| chr7:115947210 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.515+3664C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947210 | |||||||
| chr7:115947367 | C | T | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0174 others(10): Show |
15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.515+3507G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947367 | |||||||
| chr7:115947368 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0174 others(10): Show |
15 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.515+3506A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947368 | |||||||
| chr7:115947482 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3392T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947482 | |||||||
| chr7:115947489 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+3385G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947489 | |||||||
| chr7:115947743 | G | A | 4 | a0001c0001t0009g0141 a0001c0001t0009g0142 a0001c0001t0009g0144 others(1): Show |
4 | HG00140.hp2 HG02738.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+3131C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947743 | |||||||
| chr7:115947771 | G | GT | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.515+3102dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947771 | |||||||
| chr7:115947913 | GT | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.515+2960delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115947913 | |||||||
| chr7:115948122 | T | C | 14 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.515+2752A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948122 | |||||||
| chr7:115948210 | C | T | 2 | a0001c0001t0033g0179 a0001c0001t0034g0246 |
2 | HG02451.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.515+2664G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948210 | |||||||
| chr7:115948364 | C | G | 7 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(4): Show |
7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+2510G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948364 | |||||||
| chr7:115948473 | A | C | 1 | a0001c0001t0002g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+2401T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948473 | |||||||
| chr7:115948474 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.515+2400C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948474 | |||||||
| chr7:115948561 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.515+2313A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948561 | |||||||
| chr7:115948581 | G | A | 1 | a0001c0001t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.515+2293C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948581 | |||||||
| chr7:115948692 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.515+2182G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948692 | |||||||
| chr7:115948855 | T | C | 3 | a0001c0001t0003g0235 a0001c0001t0003g0319 a0001c0001t0003g0320 |
3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.515+2019A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115948855 | |||||||
| chr7:115949064 | C | T | 2 | a0001c0001t0024g0171 a0001c0001t0030g0166 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.515+1810G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949064 | |||||||
| chr7:115949083 | T | C | 7 | a0001c0001t0001g0070 a0001c0001t0001g0233 a0001c0001t0001g0326 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+1791A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949083 | |||||||
| chr7:115949093 | T | C | 73 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(70): Show |
106 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.515+1781A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949093 | |||||||
| chr7:115949114 | A | T | 1 | a0001c0001t0016g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.515+1760T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949114 | |||||||
| chr7:115949178 | A | C | 94 | a0001c0001t0002g0001 a0001c0001t0002g0003 a0001c0001t0002g0004 others(91): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.515+1696T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949178 | |||||||
| chr7:115949188 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.515+1686C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949188 | |||||||
| chr7:115949245 | A | G | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0204 others(4): Show |
9 | HG00408.hp2 NA18942.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.515+1629T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949245 | |||||||
| chr7:115949265 | C | A | 1 | a0001c0001t0033g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.515+1609G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949265 | |||||||
| chr7:115949388 | C | T | 3 | a0001c0001t0003g0273 a0001c0001t0003g0287 a0001c0001t0003g0291 |
3 | HG02165.hp2 NA18951.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.515+1486G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949388 | |||||||
| chr7:115949438 | T | G | 1 | a0001c0001t0037g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.515+1436A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949438 | |||||||
| chr7:115949547 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.515+1327T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949547 | |||||||
| chr7:115949547 | A | T | 1 | a0001c0001t0003g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.515+1327T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949547 | |||||||
| chr7:115949650 | G | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+1224C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949650 | |||||||
| chr7:115949669 | C | A | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.515+1205G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949669 | |||||||
| chr7:115949938 | C | T | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.515+936G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115949938 | |||||||
| chr7:115950015 | C | CTT | 231 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(228): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.515+857_515+858dup others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950015 | |||||||
| chr7:115950015 | C | CTTT | 10 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0174 others(7): Show |
11 | HG02055.hp2 HG02622.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.515+856_515+858dup others(3): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950015 | |||||||
| chr7:115950077 | T | C | 6 | a0001c0002t0001g0024 a0001c0002t0001g0047 a0001c0002t0001g0048 others(3): Show |
7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.515+797A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950077 | |||||||
| chr7:115950105 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.515+769T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950105 | |||||||
| chr7:115950164 | A | C | 1 | a0001c0001t0006g0240 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.515+710T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950164 | |||||||
| chr7:115950202 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.515+672C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950202 | |||||||
| chr7:115950231 | T | C | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.515+643A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950231 | |||||||
| chr7:115950297 | C | T | 1 | a0002c0003t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.515+577G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950297 | |||||||
| chr7:115950416 | T | C | 5 | a0001c0001t0003g0235 a0001c0001t0003g0268 a0001c0001t0003g0271 others(2): Show |
5 | HG01433.hp1 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.515+458A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 6/7 | chr7 | 115950416 | |||||||
| chr7:115950950 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG00642.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.440-1G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115950950 | |||||||
| chr7:115951104 | C | T | 14 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.440-155G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951104 | |||||||
| chr7:115951246 | C | T | 14 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.440-297G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951246 | |||||||
| chr7:115951363 | C | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0180 a0001c0001t0001g0183 |
3 | HG02622.hp2 HG02970.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.440-414G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951363 | |||||||
| chr7:115951826 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.440-877C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951826 | |||||||
| chr7:115951945 | C | G | 3 | a0001c0001t0004g0021 a0001c0001t0004g0022 a0001c0001t0004g0159 |
5 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.440-996G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115951945 | |||||||
| chr7:115952264 | T | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.440-1315A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952264 | |||||||
| chr7:115952387 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.440-1438A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952387 | |||||||
| chr7:115952486 | T | G | 1 | a0001c0001t0003g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.440-1537A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952486 | |||||||
| chr7:115952503 | T | C | 2 | a0001c0002t0001g0047 a0001c0002t0001g0051 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.440-1554A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952503 | |||||||
| chr7:115952840 | G | T | 7 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(4): Show |
7 | HG02257.hp1 HG02622.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+1746C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952840 | |||||||
| chr7:115952940 | A | C | 1 | a0001c0001t0003g0289 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.439+1646T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952940 | |||||||
| chr7:115952981 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.439+1605C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115952981 | |||||||
| chr7:115953162 | G | GTGCAGAA others(15): Show |
8 | a0001c0001t0004g0002 a0001c0001t0004g0056 a0001c0001t0004g0161 others(5): Show |
13 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.439+1402_439+1423d others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953162 | |||||||
| chr7:115953226 | C | G | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.439+1360G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953226 | |||||||
| chr7:115953277 | CTTTATGA others(6): Show |
C | 1 | a0001c0001t0001g0227 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.439+1296_439+1308d others(15): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953277 | |||||||
| chr7:115953363 | T | C | 1 | a0001c0001t0010g0169 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.439+1223A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953363 | |||||||
| chr7:115953470 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.439+1116C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953470 | |||||||
| chr7:115953481 | T | G | 1 | a0001c0005t0014g0116 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.439+1105A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953481 | |||||||
| chr7:115953505 | T | A | 3 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.439+1081A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953505 | |||||||
| chr7:115953565 | C | T | 1 | a0001c0001t0003g0313 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.439+1021G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953565 | |||||||
| chr7:115953634 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.439+952C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953634 | |||||||
| chr7:115953708 | A | G | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.439+878T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953708 | |||||||
| chr7:115953732 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.439+854T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953732 | |||||||
| chr7:115953906 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.439+680G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115953906 | |||||||
| chr7:115954051 | C | T | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.439+535G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954051 | |||||||
| chr7:115954159 | G | A | 1 | a0001c0001t0009g0144 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.439+427C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954159 | |||||||
| chr7:115954384 | C | T | 5 | a0001c0001t0002g0147 a0001c0001t0011g0148 a0001c0001t0011g0150 others(2): Show |
5 | HG02027.hp2 HG04184.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.439+202G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954384 | |||||||
| chr7:115954468 | G | A | 2 | a0001c0001t0017g0206 a0001c0001t0017g0318 |
2 | NA18949.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.439+118C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 5/7 | chr7 | 115954468 | |||||||
| chr7:115954673 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.383-31G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954673 | |||||||
| chr7:115954719 | C | T | 65 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(62): Show |
98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.383-77G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954719 | |||||||
| chr7:115954840 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.383-198C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954840 | |||||||
| chr7:115954994 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.383-352T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115954994 | |||||||
| chr7:115955015 | A | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-373T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955015 | |||||||
| chr7:115955088 | C | A | 1 | a0001c0001t0006g0012 | 3 | HG02559.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.383-446G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955088 | |||||||
| chr7:115955111 | A | G | 2 | a0001c0001t0009g0144 a0001c0001t0009g0145 |
2 | HG02738.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.383-469T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955111 | |||||||
| chr7:115955144 | C | T | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.383-502G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955144 | |||||||
| chr7:115955431 | A | T | 1 | a0001c0001t0003g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.383-789T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955431 | |||||||
| chr7:115955493 | T | C | 5 | a0001c0001t0002g0143 a0001c0001t0009g0141 a0001c0001t0009g0142 others(2): Show |
5 | HG00140.hp2 HG01243.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-851A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955493 | |||||||
| chr7:115955509 | G | A | 1 | a0001c0001t0003g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.383-867C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955509 | |||||||
| chr7:115955676 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.382+1003A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955676 | |||||||
| chr7:115955936 | A | T | 1 | a0001c0001t0003g0304 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.382+743T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115955936 | |||||||
| chr7:115956012 | G | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.382+667C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956012 | |||||||
| chr7:115956191 | T | G | 34 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.382+488A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956191 | |||||||
| chr7:115956296 | T | A | 1 | a0001c0001t0006g0012 | 3 | HG02559.hp1 HG03195.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.382+383A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956296 | |||||||
| chr7:115956411 | A | G | 2 | a0001c0001t0003g0132 a0001c0001t0003g0133 |
2 | HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.382+268T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956411 | |||||||
| chr7:115956474 | A | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.382+205T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956474 | |||||||
| chr7:115956565 | T | C | 3 | a0001c0001t0005g0013 a0001c0001t0005g0255 a0001c0001t0005g0256 |
5 | NA18955.hp2 NA18992.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.382+114A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 4/7 | chr7 | 115956565 | |||||||
| chr7:115956834 | T | C | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-41A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115956834 | |||||||
| chr7:115956996 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-203G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115956996 | |||||||
| chr7:115957387 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.268-594A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957387 | |||||||
| chr7:115957708 | T | C | 2 | a0001c0005t0014g0116 a0001c0005t0032g0115 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.268-915A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957708 | |||||||
| chr7:115957804 | C | A | 1 | a0001c0001t0001g0088 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.268-1011G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957804 | |||||||
| chr7:115957881 | T | C | 1 | a0001c0001t0003g0288 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.268-1088A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957881 | |||||||
| chr7:115957985 | G | A | 1 | a0001c0001t0003g0291 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268-1192C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115957985 | |||||||
| chr7:115958118 | T | G | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.268-1325A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958118 | |||||||
| chr7:115958161 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-1368T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958161 | |||||||
| chr7:115958169 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-1376G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958169 | |||||||
| chr7:115958474 | C | A | 1 | a0001c0001t0003g0290 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.268-1681G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958474 | |||||||
| chr7:115958477 | G | A | 1 | a0001c0001t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.268-1684C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958477 | |||||||
| chr7:115958687 | A | G | 1 | a0001c0001t0022g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.268-1894T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958687 | |||||||
| chr7:115958710 | G | A | 1 | a0001c0001t0019g0023 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.268-1917C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958710 | |||||||
| chr7:115958710 | G | T | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.268-1917C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958710 | |||||||
| chr7:115958748 | G | A | 1 | a0001c0001t0003g0281 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.268-1955C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958748 | |||||||
| chr7:115958765 | T | C | 1 | a0001c0001t0002g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.268-1972A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958765 | |||||||
| chr7:115958876 | T | C | 1 | a0001c0001t0004g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.268-2083A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958876 | |||||||
| chr7:115958987 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.268-2194A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115958987 | |||||||
| chr7:115959060 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.268-2267A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959060 | |||||||
| chr7:115959168 | A | G | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.268-2375T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959168 | |||||||
| chr7:115959309 | C | G | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-2516G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959309 | |||||||
| chr7:115959321 | A | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-2528T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959321 | |||||||
| chr7:115959389 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.268-2596C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959389 | |||||||
| chr7:115959422 | C | T | 2 | a0001c0001t0001g0131 a0001c0001t0014g0234 |
2 | HG00642.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.268-2629G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959422 | |||||||
| chr7:115959755 | C | T | 1 | a0001c0001t0003g0293 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.268-2962G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959755 | |||||||
| chr7:115959867 | T | C | 2 | a0001c0001t0008g0005 a0001c0001t0008g0232 |
6 | NA18945.hp1 NA18994.hp1 NA18995.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-3074A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959867 | |||||||
| chr7:115959973 | G | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.268-3180C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959973 | |||||||
| chr7:115959986 | G | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-3193C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115959986 | |||||||
| chr7:115960052 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.268-3259C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960052 | |||||||
| chr7:115960119 | C | A | 1 | a0001c0001t0002g0014 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.268-3326G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960119 | |||||||
| chr7:115960203 | A | T | 34 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.268-3410T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960203 | |||||||
| chr7:115960267 | C | T | 1 | a0001c0001t0027g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268-3474G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960267 | |||||||
| chr7:115960373 | C | T | 2 | a0001c0001t0004g0163 a0001c0001t0004g0263 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.268-3580G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960373 | |||||||
| chr7:115960436 | A | G | 10 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0255 others(7): Show |
13 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.268-3643T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960436 | |||||||
| chr7:115960503 | T | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-3710A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960503 | |||||||
| chr7:115960645 | A | C | 1 | a0001c0001t0015g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.268-3852T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960645 | |||||||
| chr7:115960902 | C | T | 169 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(166): Show |
183 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.268-4109G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115960902 | |||||||
| chr7:115961105 | A | G | 1 | a0001c0001t0027g0247 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.268-4312T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961105 | |||||||
| chr7:115961116 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-4323G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961116 | |||||||
| chr7:115961290 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-4497T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961290 | |||||||
| chr7:115961336 | T | C | 1 | a0001c0001t0003g0291 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.268-4543A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961336 | |||||||
| chr7:115961362 | C | A | 32 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0067 others(29): Show |
35 | HG00323.hp2 HG00423.hp2 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.268-4569G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961362 | |||||||
| chr7:115961399 | T | C | 8 | a0001c0001t0002g0001 a0001c0001t0002g0188 a0001c0001t0002g0192 others(5): Show |
14 | HG00639.hp1 HG01346.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.268-4606A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961399 | |||||||
| chr7:115961446 | G | A | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-4653C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961446 | |||||||
| chr7:115961471 | T | C | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-4678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961471 | |||||||
| chr7:115961473 | T | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0174 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-4680A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961473 | |||||||
| chr7:115961755 | A | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-4962T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961755 | |||||||
| chr7:115961849 | A | G | 1 | a0001c0001t0003g0268 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.268-5056T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961849 | |||||||
| chr7:115961955 | A | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(116): Show |
131 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.268-5162T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115961955 | |||||||
| chr7:115962068 | G | A | 1 | a0001c0001t0001g0025 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.268-5275C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962068 | |||||||
| chr7:115962070 | A | C | 6 | a0001c0002t0001g0024 a0001c0002t0001g0047 a0001c0002t0001g0048 others(3): Show |
7 | HG01496.hp1 HG01891.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.268-5277T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962070 | |||||||
| chr7:115962087 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5294G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962087 | |||||||
| chr7:115962162 | A | G | 2 | a0001c0001t0002g0182 a0001c0001t0002g0197 |
2 | HG02738.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.268-5369T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962162 | |||||||
| chr7:115962167 | A | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5374T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962167 | |||||||
| chr7:115962725 | T | A | 1 | a0005c0007t0001g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.268-5932A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962725 | |||||||
| chr7:115962760 | G | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.268-5967C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962760 | |||||||
| chr7:115962763 | C | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-5970G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962763 | |||||||
| chr7:115962828 | C | G | 1 | a0001c0001t0005g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.268-6035G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962828 | |||||||
| chr7:115962844 | C | T | 3 | a0001c0001t0003g0235 a0001c0001t0003g0319 a0001c0001t0003g0320 |
3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.268-6051G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962844 | |||||||
| chr7:115962894 | G | C | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.268-6101C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962894 | |||||||
| chr7:115962959 | G | C | 1 | a0001c0001t0001g0330 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.268-6166C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115962959 | |||||||
| chr7:115963243 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-6450G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963243 | |||||||
| chr7:115963284 | C | T | 1 | a0001c0001t0007g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.268-6491G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963284 | |||||||
| chr7:115963298 | G | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0174 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.268-6505C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963298 | |||||||
| chr7:115963321 | A | G | 1 | a0001c0001t0002g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.268-6528T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963321 | |||||||
| chr7:115963343 | G | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.268-6550C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963343 | |||||||
| chr7:115963392 | G | GT | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.268-6600dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963392 | |||||||
| chr7:115963439 | G | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-6646C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963439 | |||||||
| chr7:115963610 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0103 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.268-6817G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963610 | |||||||
| chr7:115963948 | A | G | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-7155T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115963948 | |||||||
| chr7:115964107 | G | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.268-7314C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964107 | |||||||
| chr7:115964155 | A | C | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.268-7362T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964155 | |||||||
| chr7:115964229 | T | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.268-7436A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964229 | |||||||
| chr7:115964279 | A | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.268-7486T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115964279 | |||||||
| chr7:115965101 | C | A | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.268-8308G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965101 | |||||||
| chr7:115965191 | T | C | 15 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(12): Show |
22 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.268-8398A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965191 | |||||||
| chr7:115965279 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.268-8486A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965279 | |||||||
| chr7:115965346 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.268-8553T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965346 | |||||||
| chr7:115965478 | G | A | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.268-8685C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965478 | |||||||
| chr7:115965509 | G | C | 1 | a0001c0001t0002g0199 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.267+8661C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965509 | |||||||
| chr7:115965527 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+8643G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965527 | |||||||
| chr7:115965884 | C | G | 34 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.267+8286G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965884 | |||||||
| chr7:115965922 | T | C | 1 | a0001c0001t0003g0297 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.267+8248A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115965922 | |||||||
| chr7:115966745 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.267+7425A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966745 | |||||||
| chr7:115966827 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0200 a0001c0001t0002g0211 others(2): Show |
7 | NA18612.hp1 NA18947.hp1 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.267+7343G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966827 | |||||||
| chr7:115966866 | C | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.267+7304G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966866 | |||||||
| chr7:115966946 | T | C | 3 | a0001c0004t0001g0173 a0001c0004t0001g0243 a0001c0004t0001g0245 |
3 | HG02055.hp2 HG03209.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.267+7224A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966946 | |||||||
| chr7:115966963 | G | T | 1 | a0001c0001t0002g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.267+7207C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115966963 | |||||||
| chr7:115967373 | A | G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.267+6797T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967373 | |||||||
| chr7:115967400 | T | A | 33 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(30): Show |
35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.267+6770A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967400 | |||||||
| chr7:115967433 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.267+6737T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967433 | |||||||
| chr7:115967441 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+6729A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967441 | |||||||
| chr7:115967818 | T | G | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.267+6352A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967818 | |||||||
| chr7:115967851 | C | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6319G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115967851 | |||||||
| chr7:115968104 | T | C | 4 | a0001c0001t0003g0059 a0001c0001t0003g0132 a0001c0001t0003g0133 others(1): Show |
4 | HG01071.hp1 HG01943.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.267+6066A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968104 | |||||||
| chr7:115968301 | T | G | 34 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.267+5869A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968301 | |||||||
| chr7:115968540 | T | A | 2 | a0001c0001t0006g0172 a0001c0001t0006g0242 |
2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.267+5630A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968540 | |||||||
| chr7:115968718 | G | T | 1 | a0001c0001t0003g0284 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.267+5452C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968718 | |||||||
| chr7:115968859 | T | G | 1 | a0001c0001t0002g0200 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.267+5311A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968859 | |||||||
| chr7:115968872 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.267+5298G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115968872 | |||||||
| chr7:115969029 | G | T | 1 | a0001c0001t0003g0297 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.267+5141C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969029 | |||||||
| chr7:115969124 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.267+5046C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969124 | |||||||
| chr7:115969635 | T | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0174 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.267+4535A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969635 | |||||||
| chr7:115969741 | T | C | 3 | a0001c0001t0003g0294 a0001c0001t0003g0311 a0001c0001t0003g0312 |
3 | NA18953.hp1 NA18971.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.267+4429A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969741 | |||||||
| chr7:115969771 | G | T | 65 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(62): Show |
98 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.267+4399C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969771 | |||||||
| chr7:115969794 | T | C | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.267+4376A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969794 | |||||||
| chr7:115969857 | A | C | 1 | a0001c0001t0003g0273 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.267+4313T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969857 | |||||||
| chr7:115969928 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.267+4242G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969928 | |||||||
| chr7:115969976 | C | T | 1 | a0001c0001t0019g0023 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.267+4194G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115969976 | |||||||
| chr7:115970206 | G | A | 5 | a0001c0001t0003g0235 a0001c0001t0003g0268 a0001c0001t0003g0271 others(2): Show |
5 | HG01433.hp1 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+3964C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115970206 | |||||||
| chr7:115970797 | C | T | 2 | a0001c0001t0003g0034 a0001c0001t0003g0304 |
3 | NA18991.hp1 NA19065.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.267+3373G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115970797 | |||||||
| chr7:115971241 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+2929A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971241 | |||||||
| chr7:115971255 | G | A | 54 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
60 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.267+2915C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971255 | |||||||
| chr7:115971372 | GA | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.267+2797delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971372 | |||||||
| chr7:115971471 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.267+2699A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971471 | |||||||
| chr7:115971637 | C | G | 3 | a0001c0001t0001g0187 a0001c0001t0001g0219 a0001c0001t0001g0220 |
3 | NA18941.hp1 NA18968.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.267+2533G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115971637 | |||||||
| chr7:115972060 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.267+2110G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972060 | |||||||
| chr7:115972215 | T | C | 1 | a0001c0009t0003g0296 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.267+1955A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972215 | |||||||
| chr7:115972271 | T | C | 1 | a0001c0001t0001g0041 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.267+1899A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972271 | |||||||
| chr7:115972396 | A | T | 1 | a0001c0001t0003g0279 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.267+1774T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972396 | |||||||
| chr7:115972585 | A | G | 3 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0003g0311 |
3 | NA18946.hp1 NA18953.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.267+1585T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972585 | |||||||
| chr7:115972686 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1484A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972686 | |||||||
| chr7:115972701 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1469T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972701 | |||||||
| chr7:115972791 | C | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0079 a0001c0001t0001g0082 others(6): Show |
10 | HG00621.hp1 HG02080.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.267+1379G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972791 | |||||||
| chr7:115972849 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.267+1321G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115972849 | |||||||
| chr7:115973088 | A | C | 1 | a0001c0001t0033g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.267+1082T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973088 | |||||||
| chr7:115973091 | A | G | 1 | a0001c0001t0019g0023 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.267+1079T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973091 | |||||||
| chr7:115973097 | GA | G | 68 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.267+1072delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973097 | |||||||
| chr7:115973513 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.267+657A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973513 | |||||||
| chr7:115973730 | T | C | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.267+440A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973730 | |||||||
| chr7:115973833 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0033g0179 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.267+337A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973833 | |||||||
| chr7:115973859 | T | C | 2 | a0001c0001t0003g0044 a0001c0001t0003g0108 |
2 | HG00733.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.267+311A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973859 | |||||||
| chr7:115973898 | T | C | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.267+272A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115973898 | |||||||
| chr7:115974087 | C | T | 1 | a0001c0001t0007g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.267+83G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 3/7 | chr7 | 115974087 | |||||||
| chr7:115974381 | T | A | 1 | a0001c0001t0016g0324 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.181-125A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974381 | |||||||
| chr7:115974405 | A | AATATATA others(3): Show |
1 | a0001c0001t0003g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-150_181-149ins others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974405 | |||||||
| chr7:115974406 | T | A | 1 | a0001c0001t0003g0295 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.181-150A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTA | 24 | a0001c0001t0001g0078 a0001c0001t0001g0104 a0001c0001t0001g0110 others(21): Show |
24 | HG00408.hp1 HG00733.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.181-152_181-151dup others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATA | 37 | a0001c0001t0001g0075 a0001c0001t0001g0079 a0001c0001t0001g0091 others(34): Show |
39 | HG01069.hp2 HG01071.hp1 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.181-154_181-151dup others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATA | 24 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0076 others(21): Show |
25 | HG00140.hp2 HG00738.hp1 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.181-156_181-151dup others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(1): Show |
24 | a0001c0001t0001g0092 a0001c0001t0001g0103 a0001c0001t0001g0111 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.181-158_181-151dup others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(3): Show |
25 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0040 others(22): Show |
29 | HG01109.hp2 HG01255.hp2 HG01346.hp2 others(26): Show |
intron_variant | MODIFIER | c.181-160_181-151dup others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(5): Show |
15 | a0001c0001t0001g0006 a0001c0001t0001g0067 a0001c0001t0001g0083 others(12): Show |
17 | HG00323.hp2 HG00642.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.181-162_181-151dup others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(7): Show |
13 | a0001c0001t0001g0019 a0001c0001t0001g0054 a0001c0001t0001g0084 others(10): Show |
15 | HG00423.hp2 HG00642.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.181-164_181-151dup others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(9): Show |
6 | a0001c0001t0001g0072 a0001c0001t0001g0085 a0001c0001t0001g0130 others(3): Show |
6 | HG00558.hp2 HG00621.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.181-166_181-151dup others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(11): Show |
1 | a0001c0001t0003g0294 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.181-168_181-151dup others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | T | TTATATAT others(13): Show |
1 | a0001c0001t0001g0086 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.181-170_181-151dup others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTA | T | 8 | a0001c0001t0003g0034 a0001c0001t0003g0235 a0001c0001t0003g0278 others(5): Show |
9 | HG03471.hp2 NA18942.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.181-152_181-151del others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTATA | T | 3 | a0001c0001t0003g0123 a0001c0001t0003g0265 a0001c0001t0003g0282 |
3 | HG00609.hp1 HG02155.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.181-154_181-151del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0007g0058 a0001c0001t0007g0269 a0001c0001t0019g0023 |
4 | HG01361.hp2 HG01891.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.181-158_181-151del others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTATATAT others(3): Show |
T | 1 | a0001c0001t0007g0031 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.181-160_181-151del others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0003g0277 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.181-162_181-151del others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974406 | TTATATAT others(13): Show |
T | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.181-170_181-151del others(20): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974406 | |||||||
| chr7:115974421 | TATATATA others(23): Show |
T | 68 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-195_181-166del others(30): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974421 | |||||||
| chr7:115974423 | TATATATA others(21): Show |
T | 1 | a0001c0001t0002g0201 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.181-195_181-168del others(28): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974423 | |||||||
| chr7:115974427 | TATATATA others(17): Show |
T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.181-195_181-172del others(24): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974427 | |||||||
| chr7:115974433 | TATATATA others(11): Show |
T | 3 | a0001c0005t0014g0043 a0001c0005t0014g0116 a0003c0006t0001g0038 |
3 | HG01978.hp1 HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.181-195_181-178del others(18): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974433 | |||||||
| chr7:115974435 | TATATATA others(9): Show |
T | 2 | a0001c0001t0004g0056 a0001c0005t0032g0115 |
2 | HG00639.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.181-195_181-180del others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974435 | |||||||
| chr7:115974437 | TATATATA others(7): Show |
T | 12 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(9): Show |
17 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.181-195_181-182del others(14): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974437 | |||||||
| chr7:115974439 | TATATATA others(5): Show |
T | 4 | a0001c0001t0001g0105 a0001c0001t0004g0002 a0001c0001t0004g0263 others(1): Show |
5 | HG00323.hp1 HG00733.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-195_181-184del others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974439 | |||||||
| chr7:115974441 | TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0153 a0001c0001t0031g0158 |
2 | HG01433.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.181-195_181-186del others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974441 | |||||||
| chr7:115974447 | T | TATATATA others(3): Show |
1 | a0001c0001t0016g0324 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.181-192_181-191ins others(10): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974447 | |||||||
| chr7:115974447 | TATAA | T | 7 | a0001c0001t0001g0036 a0001c0001t0001g0113 a0001c0001t0001g0114 others(4): Show |
7 | HG02055.hp2 HG02145.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-195_181-192del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974447 | |||||||
| chr7:115974449 | TAA | T | 13 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
16 | HG01074.hp2 HG01192.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.181-195_181-194del others(2): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974449 | |||||||
| chr7:115974450 | A | ATATATAT others(6): Show |
1 | a0001c0001t0007g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.181-195_181-194ins others(13): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974450 | |||||||
| chr7:115974450 | A | ATATATAT others(16): Show |
1 | a0001c0001t0003g0252 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.181-195_181-194ins others(23): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974450 | |||||||
| chr7:115974451 | A | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0018 others(133): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.181-195T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974451 | |||||||
| chr7:115974452 | A | T | 3 | a0001c0001t0003g0252 a0002c0003t0021g0101 a0003c0006t0001g0037 |
3 | HG01258.hp1 HG02074.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.181-196T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974452 | |||||||
| chr7:115974453 | A | T | 3 | a0001c0001t0001g0109 a0002c0003t0001g0100 a0002c0003t0001g0118 |
3 | HG03490.hp1 HG03654.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.181-197T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974453 | |||||||
| chr7:115974457 | C | G | 9 | a0001c0001t0002g0001 a0001c0001t0002g0188 a0001c0001t0002g0192 others(6): Show |
15 | HG00639.hp1 HG01346.hp1 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.181-201G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974457 | |||||||
| chr7:115974510 | C | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.181-254G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974510 | |||||||
| chr7:115974587 | GTATC | G | 68 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-335_181-332del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974587 | |||||||
| chr7:115974874 | A | C | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18965.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.181-618T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115974874 | |||||||
| chr7:115975057 | T | C | 1 | a0001c0001t0003g0300 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.181-801A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975057 | |||||||
| chr7:115975203 | T | TA | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-948dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975203 | |||||||
| chr7:115975508 | T | C | 2 | a0001c0001t0003g0123 a0001c0001t0003g0282 |
2 | HG00609.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.181-1252A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975508 | |||||||
| chr7:115975704 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.181-1448G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975704 | |||||||
| chr7:115975705 | G | A | 68 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.181-1449C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975705 | |||||||
| chr7:115975819 | C | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1563G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975819 | |||||||
| chr7:115975902 | G | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(196): Show |
244 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.181-1646C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115975902 | |||||||
| chr7:115976068 | C | T | 1 | a0001c0001t0001g0124 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.181-1812G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115976068 | |||||||
| chr7:115976069 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-1813C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115976069 | |||||||
| chr7:115977005 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.181-2749G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977005 | |||||||
| chr7:115977169 | A | T | 248 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(245): Show |
302 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(299): Show |
intron_variant | MODIFIER | c.181-2913T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977169 | |||||||
| chr7:115977548 | TA | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.181-3293delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977548 | |||||||
| chr7:115977673 | G | A | 2 | a0001c0001t0005g0260 a0001c0001t0005g0261 |
2 | NA19064.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.181-3417C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977673 | |||||||
| chr7:115977812 | G | C | 1 | a0001c0001t0003g0284 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.181-3556C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977812 | |||||||
| chr7:115977910 | AC | A | 234 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(231): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.181-3655delG | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977910 | |||||||
| chr7:115977952 | A | G | 1 | a0001c0001t0003g0273 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.181-3696T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115977952 | |||||||
| chr7:115978034 | T | C | 1 | a0001c0001t0002g0262 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.181-3778A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978034 | |||||||
| chr7:115978109 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.181-3853G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978109 | |||||||
| chr7:115978149 | A | C | 1 | a0001c0001t0019g0023 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.181-3893T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978149 | |||||||
| chr7:115978353 | G | T | 33 | a0001c0001t0002g0014 a0001c0001t0002g0020 a0001c0001t0002g0060 others(30): Show |
35 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.181-4097C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978353 | |||||||
| chr7:115978497 | C | T | 107 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(104): Show |
117 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.181-4241G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978497 | |||||||
| chr7:115978795 | T | A | 1 | a0001c0001t0001g0090 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.181-4539A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978795 | |||||||
| chr7:115978951 | A | G | 2 | a0001c0001t0002g0009 a0001c0001t0002g0222 |
4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.181-4695T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978951 | |||||||
| chr7:115978970 | G | A | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0091 others(4): Show |
7 | HG02015.hp1 NA18747.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.181-4714C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115978970 | |||||||
| chr7:115979241 | A | G | 1 | a0001c0004t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.181-4985T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979241 | |||||||
| chr7:115979244 | C | T | 54 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(51): Show |
60 | HG00280.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.181-4988G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979244 | |||||||
| chr7:115979576 | G | A | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.180+4686C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979576 | |||||||
| chr7:115979674 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.180+4588G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979674 | |||||||
| chr7:115979730 | G | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.180+4532C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979730 | |||||||
| chr7:115979800 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+4462G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115979800 | |||||||
| chr7:115980486 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.180+3776T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980486 | |||||||
| chr7:115980641 | C | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+3621G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980641 | |||||||
| chr7:115980680 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+3582C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980680 | |||||||
| chr7:115980747 | G | T | 250 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(247): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.180+3515C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980747 | |||||||
| chr7:115980769 | C | CA | 88 | a0001c0001t0001g0025 a0001c0001t0001g0154 a0001c0001t0001g0165 others(85): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.180+3492dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980769 | |||||||
| chr7:115980774 | A | C | 1 | a0001c0001t0003g0287 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.180+3488T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980774 | |||||||
| chr7:115980778 | C | A | 1 | a0001c0001t0002g0202 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.180+3484G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980778 | |||||||
| chr7:115980778 | C | CA | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0030g0166 others(3): Show |
6 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.180+3483dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980778 | |||||||
| chr7:115980951 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.180+3311T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115980951 | |||||||
| chr7:115981056 | A | G | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.180+3206T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981056 | |||||||
| chr7:115981306 | A | G | 1 | a0004c0008t0023g0176 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.180+2956T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981306 | |||||||
| chr7:115981341 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+2921T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981341 | |||||||
| chr7:115981345 | A | T | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.180+2917T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981345 | |||||||
| chr7:115981408 | C | T | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.180+2854G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981408 | |||||||
| chr7:115981425 | C | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0233 a0001c0001t0001g0326 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.180+2837G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981425 | |||||||
| chr7:115981459 | G | C | 1 | a0001c0001t0003g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.180+2803C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981459 | |||||||
| chr7:115981725 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.180+2537G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981725 | |||||||
| chr7:115981805 | C | A | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.180+2457G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981805 | |||||||
| chr7:115981833 | G | GT | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.180+2428dupA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981833 | |||||||
| chr7:115981966 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.180+2296C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115981966 | |||||||
| chr7:115982086 | C | A | 2 | a0001c0001t0003g0283 a0001c0001t0003g0284 |
2 | HG00280.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.180+2176G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982086 | |||||||
| chr7:115982138 | T | C | 3 | a0001c0001t0007g0120 a0001c0001t0007g0266 a0001c0001t0007g0267 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.180+2124A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982138 | |||||||
| chr7:115982257 | G | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.180+2005C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982257 | |||||||
| chr7:115982262 | C | A | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.180+2000G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982262 | |||||||
| chr7:115982507 | T | C | 122 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(119): Show |
134 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.180+1755A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982507 | |||||||
| chr7:115982701 | G | A | 38 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(35): Show |
40 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.180+1561C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982701 | |||||||
| chr7:115982722 | T | C | 1 | a0001c0001t0002g0205 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.180+1540A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982722 | |||||||
| chr7:115982793 | C | A | 1 | a0001c0001t0004g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.180+1469G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982793 | |||||||
| chr7:115982900 | AT | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+1361delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115982900 | |||||||
| chr7:115983135 | A | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+1127T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983135 | |||||||
| chr7:115983236 | G | A | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.180+1026C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983236 | |||||||
| chr7:115983292 | G | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.180+970C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983292 | |||||||
| chr7:115983313 | C | A | 235 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(232): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.180+949G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983313 | |||||||
| chr7:115983453 | A | G | 26 | a0001c0001t0003g0123 a0001c0001t0003g0127 a0001c0001t0003g0184 others(23): Show |
29 | HG00408.hp1 HG00609.hp1 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.180+809T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983453 | |||||||
| chr7:115983458 | C | G | 2 | a0001c0001t0003g0270 a0001c0001t0003g0313 |
2 | NA18978.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.180+804G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983458 | |||||||
| chr7:115983569 | T | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(98): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.180+693A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983569 | |||||||
| chr7:115983774 | T | C | 3 | a0001c0001t0015g0052 a0001c0001t0015g0053 a0001c0001t0015g0323 |
3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.180+488A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983774 | |||||||
| chr7:115983809 | G | T | 1 | a0001c0001t0003g0285 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.180+453C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983809 | |||||||
| chr7:115983913 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.180+349A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115983913 | |||||||
| chr7:115984098 | T | G | 1 | a0001c0001t0002g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.180+164A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984098 | |||||||
| chr7:115984113 | TAATA | T | 3 | a0001c0005t0014g0043 a0001c0005t0014g0116 a0001c0005t0032g0115 |
3 | HG02630.hp2 HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.180+145_180+148del others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984113 | |||||||
| chr7:115984157 | C | T | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.180+105G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984157 | |||||||
| chr7:115984234 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.180+28A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 2/7 | chr7 | 115984234 | |||||||
| chr7:115985014 | G | A | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-501C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985014 | |||||||
| chr7:115985021 | G | GA | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-509dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985021 | |||||||
| chr7:115985034 | A | T | 1 | a0001c0001t0003g0299 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-72-521T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985034 | |||||||
| chr7:115985085 | AT | A | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-573delA | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985085 | |||||||
| chr7:115985118 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
4 | HG01168.hp2 HG01169.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-605A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985118 | |||||||
| chr7:115985414 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-901C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985414 | |||||||
| chr7:115985488 | T | C | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-975A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985488 | |||||||
| chr7:115985491 | A | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-978T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985491 | |||||||
| chr7:115985560 | T | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-72-1047A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985560 | |||||||
| chr7:115985660 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-72-1147A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985660 | |||||||
| chr7:115985672 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-1159A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985672 | |||||||
| chr7:115985785 | T | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-72-1272A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985785 | |||||||
| chr7:115985848 | C | A | 3 | a0001c0001t0007g0120 a0001c0001t0007g0266 a0001c0001t0007g0267 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-72-1335G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985848 | |||||||
| chr7:115985890 | T | A | 5 | a0001c0001t0001g0233 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-1377A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985890 | |||||||
| chr7:115985986 | T | C | 35 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(32): Show |
37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-72-1473A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115985986 | |||||||
| chr7:115986235 | T | C | 26 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0001g0239 others(23): Show |
35 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(32): Show |
intron_variant | MODIFIER | c.-72-1722A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986235 | |||||||
| chr7:115986245 | T | G | 3 | a0001c0001t0007g0120 a0001c0001t0007g0266 a0001c0001t0007g0267 |
3 | HG02723.hp1 HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-72-1732A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986245 | |||||||
| chr7:115986275 | C | T | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-1762G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986275 | |||||||
| chr7:115986629 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(98): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-2116A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986629 | |||||||
| chr7:115986744 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0030g0166 |
2 | HG02922.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.-72-2231G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986744 | |||||||
| chr7:115986746 | C | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-2233G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986746 | |||||||
| chr7:115986918 | T | TA | 250 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(247): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.-72-2406dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986918 | |||||||
| chr7:115986939 | T | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-2426A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115986939 | |||||||
| chr7:115987115 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-2602G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987115 | |||||||
| chr7:115987116 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-2603C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987116 | |||||||
| chr7:115987164 | G | C | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-72-2651C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987164 | |||||||
| chr7:115987357 | T | C | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-2844A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987357 | |||||||
| chr7:115987430 | T | C | 7 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0204 others(4): Show |
9 | HG00408.hp2 NA18942.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.-72-2917A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987430 | |||||||
| chr7:115987462 | G | A | 7 | a0001c0001t0001g0070 a0001c0001t0001g0233 a0001c0001t0001g0326 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-2949C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987462 | |||||||
| chr7:115987485 | T | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-2972A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987485 | |||||||
| chr7:115987495 | G | A | 7 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0128 others(4): Show |
7 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.-72-2982C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987495 | |||||||
| chr7:115987511 | C | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-2998G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987511 | |||||||
| chr7:115987776 | G | A | 1 | a0001c0001t0003g0271 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-72-3263C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987776 | |||||||
| chr7:115987781 | T | A | 4 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0002g0011 others(1): Show |
6 | HG00423.hp1 HG02135.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-3268A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115987781 | |||||||
| chr7:115988018 | A | G | 1 | a0001c0001t0007g0031 | 2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-72-3505T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988018 | |||||||
| chr7:115988050 | T | C | 35 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(32): Show |
37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-72-3537A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988050 | |||||||
| chr7:115988084 | T | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(118): Show |
133 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.-72-3571A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988084 | |||||||
| chr7:115988208 | T | G | 1 | a0001c0002t0001g0024 | 2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-72-3695A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988208 | |||||||
| chr7:115988272 | A | G | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72-3759T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988272 | |||||||
| chr7:115988298 | G | C | 2 | a0004c0008t0023g0136 a0004c0008t0023g0176 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-72-3785C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988298 | |||||||
| chr7:115988353 | A | G | 1 | a0001c0001t0004g0164 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-72-3840T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988353 | |||||||
| chr7:115988394 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-72-3881A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988394 | |||||||
| chr7:115988502 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-3989T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988502 | |||||||
| chr7:115988535 | G | A | 1 | a0001c0004t0001g0243 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-72-4022C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988535 | |||||||
| chr7:115988735 | C | T | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-72-4222G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988735 | |||||||
| chr7:115988892 | G | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-72-4379C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988892 | |||||||
| chr7:115988894 | T | C | 1 | a0001c0001t0002g0027 | 2 | NA18957.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.-72-4381A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115988894 | |||||||
| chr7:115989238 | T | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(98): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-72-4725A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989238 | |||||||
| chr7:115989411 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-4898C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989411 | |||||||
| chr7:115989450 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0017g0206 others(3): Show |
6 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-4937C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989450 | |||||||
| chr7:115989475 | C | T | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-4962G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989475 | |||||||
| chr7:115989484 | C | G | 13 | a0001c0001t0001g0174 a0001c0001t0001g0183 a0001c0001t0001g0239 others(10): Show |
15 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.-72-4971G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989484 | |||||||
| chr7:115989564 | G | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-5051C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989564 | |||||||
| chr7:115989576 | T | A | 1 | a0001c0001t0002g0207 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-72-5063A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989576 | |||||||
| chr7:115989609 | G | A | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72-5096C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989609 | |||||||
| chr7:115989657 | C | T | 1 | a0001c0001t0003g0320 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-72-5144G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989657 | |||||||
| chr7:115989847 | C | A | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-5334G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115989847 | |||||||
| chr7:115990094 | T | A | 34 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-5581A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990094 | |||||||
| chr7:115990136 | A | T | 6 | a0001c0001t0006g0012 a0001c0001t0006g0172 a0001c0001t0006g0240 others(3): Show |
8 | HG02258.hp2 HG02559.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-72-5623T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990136 | |||||||
| chr7:115990170 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-5657A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990170 | |||||||
| chr7:115990249 | G | T | 1 | a0001c0001t0002g0189 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-72-5736C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990249 | |||||||
| chr7:115990335 | G | A | 235 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(232): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-72-5822C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990335 | |||||||
| chr7:115990574 | T | G | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-6061A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990574 | |||||||
| chr7:115990634 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-72-6121A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990634 | |||||||
| chr7:115990849 | G | A | 1 | a0001c0001t0002g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-72-6336C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990849 | |||||||
| chr7:115990874 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-72-6361G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990874 | |||||||
| chr7:115990875 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-6362T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990875 | |||||||
| chr7:115990946 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-72-6433C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115990946 | |||||||
| chr7:115991032 | C | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-6519G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991032 | |||||||
| chr7:115991065 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6552C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991065 | |||||||
| chr7:115991105 | C | T | 2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | NA18965.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.-72-6592G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991105 | |||||||
| chr7:115991107 | A | C | 1 | a0001c0001t0001g0025 | 2 | HG02809.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-72-6594T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991107 | |||||||
| chr7:115991152 | A | T | 1 | a0001c0001t0002g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-72-6639T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991152 | |||||||
| chr7:115991161 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6648G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991161 | |||||||
| chr7:115991321 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6808G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991321 | |||||||
| chr7:115991391 | T | G | 1 | a0001c0001t0002g0028 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-72-6878A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991391 | |||||||
| chr7:115991442 | A | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-6929T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991442 | |||||||
| chr7:115991472 | A | G | 6 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0128 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-6959T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991472 | |||||||
| chr7:115991644 | G | A | 1 | a0001c0001t0002g0157 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-72-7131C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991644 | |||||||
| chr7:115991695 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-72-7182G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991695 | |||||||
| chr7:115991764 | T | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-7251A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991764 | |||||||
| chr7:115991972 | C | A | 1 | a0001c0001t0003g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-72-7459G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115991972 | |||||||
| chr7:115992066 | A | T | 3 | a0001c0001t0003g0034 a0001c0001t0003g0304 a0001c0001t0003g0305 |
4 | NA18984.hp2 NA18991.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-7553T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992066 | |||||||
| chr7:115992120 | G | A | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-72-7607C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992120 | |||||||
| chr7:115992175 | C | A | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-72-7662G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992175 | |||||||
| chr7:115992321 | T | C | 2 | a0001c0001t0002g0226 a0001c0009t0003g0296 |
2 | HG01261.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.-72-7808A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992321 | |||||||
| chr7:115992356 | C | A | 11 | a0001c0001t0001g0174 a0001c0001t0006g0012 a0001c0001t0006g0172 others(8): Show |
13 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.-72-7843G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992356 | |||||||
| chr7:115992474 | A | T | 6 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(3): Show |
6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-72-7961T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992474 | |||||||
| chr7:115992491 | T | A | 3 | a0001c0001t0012g0308 a0001c0001t0012g0309 a0001c0001t0012g0310 |
3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-72-7978A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992491 | |||||||
| chr7:115992580 | A | G | 1 | a0001c0001t0003g0184 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-72-8067T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992580 | |||||||
| chr7:115992634 | A | C | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-8121T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992634 | |||||||
| chr7:115992674 | T | C | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72-8161A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992674 | |||||||
| chr7:115992863 | C | A | 1 | a0001c0001t0013g0007 | 3 | HG01069.hp2 HG01071.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-72-8350G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992863 | |||||||
| chr7:115992973 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-8460C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115992973 | |||||||
| chr7:115993054 | G | A | 14 | a0001c0001t0001g0112 a0001c0001t0004g0002 a0001c0001t0004g0021 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-72-8541C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993054 | |||||||
| chr7:115993122 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-8609G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993122 | |||||||
| chr7:115993284 | T | C | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-72-8771A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993284 | |||||||
| chr7:115993380 | T | G | 5 | a0001c0001t0001g0174 a0001c0004t0001g0173 a0001c0004t0001g0243 others(2): Show |
5 | HG02055.hp2 HG02109.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-8867A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993380 | |||||||
| chr7:115993420 | C | A | 4 | a0001c0001t0003g0235 a0001c0001t0003g0268 a0001c0001t0003g0319 others(1): Show |
4 | HG01433.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-8907G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993420 | |||||||
| chr7:115993474 | A | G | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-8961T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993474 | |||||||
| chr7:115993578 | G | T | 125 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(122): Show |
137 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.-72-9065C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993578 | |||||||
| chr7:115993694 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-72-9181G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993694 | |||||||
| chr7:115993756 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-72-9243T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993756 | |||||||
| chr7:115993760 | C | T | 1 | a0001c0001t0003g0276 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-72-9247G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993760 | |||||||
| chr7:115993761 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0013g0007 |
4 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-9248C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993761 | |||||||
| chr7:115993816 | A | AG | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-9304dupC | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993816 | |||||||
| chr7:115993877 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-9364C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993877 | |||||||
| chr7:115993892 | T | C | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-72-9379A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115993892 | |||||||
| chr7:115994026 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0155 |
3 | HG01074.hp2 HG01192.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-72-9513C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994026 | |||||||
| chr7:115994143 | G | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-9630C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994143 | |||||||
| chr7:115994156 | T | G | 1 | a0001c0001t0001g0126 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-72-9643A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994156 | |||||||
| chr7:115994331 | GCAACAAA others(3): Show |
G | 2 | a0001c0001t0018g0139 a0001c0001t0018g0140 |
2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-72-9828_-72-9819d others(12): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994331 | |||||||
| chr7:115994346 | A | T | 2 | a0001c0001t0018g0139 a0001c0001t0018g0140 |
2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-72-9833T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994346 | |||||||
| chr7:115994382 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0299 |
2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-9869G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994382 | |||||||
| chr7:115994383 | G | A | 5 | a0001c0001t0003g0297 a0001c0001t0010g0135 a0001c0001t0010g0167 others(2): Show |
5 | HG03453.hp2 HG03579.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-9870C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994383 | |||||||
| chr7:115994469 | C | A | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-9956G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994469 | |||||||
| chr7:115994566 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-10053G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994566 | |||||||
| chr7:115994600 | C | A | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-10087G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994600 | |||||||
| chr7:115994701 | G | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-10188C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994701 | |||||||
| chr7:115994842 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(120): Show |
135 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.-72-10329C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994842 | |||||||
| chr7:115994907 | T | C | 7 | a0001c0001t0002g0143 a0001c0001t0009g0141 a0001c0001t0009g0142 others(4): Show |
7 | HG00140.hp2 HG01243.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-10394A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994907 | |||||||
| chr7:115994969 | T | C | 2 | a0001c0001t0003g0123 a0001c0001t0003g0282 |
2 | HG00609.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.-72-10456A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994969 | |||||||
| chr7:115994989 | C | T | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-10476G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115994989 | |||||||
| chr7:115995007 | T | C | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-10494A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995007 | |||||||
| chr7:115995045 | T | C | 1 | a0001c0001t0003g0298 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-72-10532A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995045 | |||||||
| chr7:115995135 | G | A | 2 | a0001c0001t0004g0163 a0001c0001t0004g0263 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-72-10622C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995135 | |||||||
| chr7:115995175 | C | G | 1 | a0001c0001t0002g0230 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.-72-10662G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995175 | |||||||
| chr7:115995266 | G | A | 34 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-10753C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995266 | |||||||
| chr7:115995338 | G | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-10825C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995338 | |||||||
| chr7:115995418 | T | C | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-10905A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995418 | |||||||
| chr7:115995421 | G | T | 5 | a0001c0001t0001g0233 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-10908C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995421 | |||||||
| chr7:115995451 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-10938G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995451 | |||||||
| chr7:115995750 | G | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-11237C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995750 | |||||||
| chr7:115995789 | C | T | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-11276G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115995789 | |||||||
| chr7:115996324 | T | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-72-11811A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996324 | |||||||
| chr7:115996405 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0170 |
3 | HG02615.hp2 HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-72-11892C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996405 | |||||||
| chr7:115996448 | G | A | 3 | a0001c0001t0003g0235 a0001c0001t0003g0319 a0001c0001t0003g0320 |
3 | HG02630.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-72-11935C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996448 | |||||||
| chr7:115996700 | A | T | 1 | a0001c0001t0007g0120 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-72-12187T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996700 | |||||||
| chr7:115996701 | C | G | 1 | a0001c0010t0002g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-12188G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996701 | |||||||
| chr7:115996796 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-72-12283C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996796 | |||||||
| chr7:115996844 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-12331C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115996844 | |||||||
| chr7:115997000 | G | A | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-72-12487C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997000 | |||||||
| chr7:115997065 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-12552C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997065 | |||||||
| chr7:115997175 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-72-12662A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997175 | |||||||
| chr7:115997308 | A | G | 3 | a0001c0001t0015g0052 a0001c0001t0015g0053 a0001c0001t0015g0323 |
3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-72-12795T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997308 | |||||||
| chr7:115997414 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0299 |
2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-12901C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997414 | |||||||
| chr7:115997516 | T | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(123): Show |
138 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.-72-13003A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997516 | |||||||
| chr7:115997527 | C | T | 34 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-13014G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997527 | |||||||
| chr7:115997645 | T | C | 1 | a0001c0001t0002g0149 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-72-13132A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997645 | |||||||
| chr7:115997677 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-72-13164A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997677 | |||||||
| chr7:115997714 | G | A | 3 | a0001c0001t0004g0162 a0001c0001t0004g0163 a0001c0001t0004g0263 |
3 | HG00733.hp2 HG01884.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-72-13201C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997714 | |||||||
| chr7:115997972 | A | G | 235 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(232): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.-72-13459T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115997972 | |||||||
| chr7:115998145 | C | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0299 |
2 | NA18955.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-72-13632G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998145 | |||||||
| chr7:115998146 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-72-13633G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998146 | |||||||
| chr7:115998193 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-13680C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998193 | |||||||
| chr7:115998558 | C | A | 1 | a0001c0001t0002g0014 | 2 | HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-72-14045G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998558 | |||||||
| chr7:115998561 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-14048T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998561 | |||||||
| chr7:115998610 | A | G | 1 | a0001c0001t0002g0214 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-72-14097T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998610 | |||||||
| chr7:115998849 | T | C | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-72-14336A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998849 | |||||||
| chr7:115998851 | AAGAG | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-72-14342_-72-1433 others(8): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998851 | |||||||
| chr7:115998852 | A | G | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-14339T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998852 | |||||||
| chr7:115998951 | A | G | 1 | a0001c0001t0025g0146 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-72-14438T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115998951 | |||||||
| chr7:115999191 | T | C | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-72-14678A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999191 | |||||||
| chr7:115999291 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-72-14778T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999291 | |||||||
| chr7:115999396 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-72-14883T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999396 | |||||||
| chr7:115999447 | G | T | 1 | a0001c0001t0002g0194 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-72-14934C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999447 | |||||||
| chr7:115999513 | T | C | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-15000A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999513 | |||||||
| chr7:115999653 | G | A | 1 | a0001c0001t0012g0308 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-72-15140C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999653 | |||||||
| chr7:115999844 | C | CA | 161 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(158): Show |
185 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-72-15332dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999844 | |||||||
| chr7:115999844 | C | CAA | 82 | a0001c0001t0001g0025 a0001c0001t0001g0040 a0001c0001t0001g0041 others(79): Show |
112 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-72-15333_-72-1533 others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 115999844 | |||||||
| chr7:116000022 | A | C | 1 | a0001c0001t0009g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-72-15509T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000022 | |||||||
| chr7:116000096 | C | A | 1 | a0001c0001t0003g0320 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-72-15583G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000096 | |||||||
| chr7:116000180 | T | C | 1 | a0001c0001t0004g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-72-15667A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000180 | |||||||
| chr7:116000205 | C | T | 1 | a0005c0007t0001g0045 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-72-15692G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000205 | |||||||
| chr7:116000261 | C | A | 2 | a0001c0001t0010g0167 a0001c0001t0010g0168 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-72-15748G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000261 | |||||||
| chr7:116000261 | C | T | 1 | a0001c0001t0003g0301 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-72-15748G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000261 | |||||||
| chr7:116000518 | T | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-16005A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000518 | |||||||
| chr7:116000662 | G | T | 2 | a0001c0001t0010g0167 a0001c0001t0010g0168 |
2 | HG03453.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-72-16149C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000662 | |||||||
| chr7:116000716 | T | G | 1 | a0001c0001t0003g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-72-16203A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000716 | |||||||
| chr7:116000803 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-72-16290T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000803 | |||||||
| chr7:116000882 | A | T | 1 | a0001c0001t0002g0020 | 2 | HG01074.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-72-16369T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000882 | |||||||
| chr7:116000940 | GA | G | 14 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.-72-16428delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000940 | |||||||
| chr7:116000959 | A | C | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72-16446T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116000959 | |||||||
| chr7:116001108 | C | G | 4 | a0002c0003t0001g0100 a0002c0003t0001g0102 a0002c0003t0001g0118 others(1): Show |
4 | HG02148.hp2 HG03490.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-16595G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001108 | |||||||
| chr7:116001111 | A | G | 1 | a0001c0001t0012g0309 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-72-16598T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001111 | |||||||
| chr7:116001444 | G | A | 3 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-72-16931C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001444 | |||||||
| chr7:116001486 | C | T | 1 | a0001c0001t0003g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-72-16973G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001486 | |||||||
| chr7:116001527 | A | C | 1 | a0001c0001t0031g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-72-17014T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001527 | |||||||
| chr7:116001578 | T | C | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-72-17065A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001578 | |||||||
| chr7:116001795 | T | C | 1 | a0001c0001t0011g0150 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-72-17282A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001795 | |||||||
| chr7:116001952 | G | A | 34 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(31): Show |
36 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.-72-17439C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001952 | |||||||
| chr7:116001960 | A | C | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-17447T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116001960 | |||||||
| chr7:116002035 | G | A | 1 | a0001c0001t0037g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-72-17522C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002035 | |||||||
| chr7:116002073 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-72-17560G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002073 | |||||||
| chr7:116002585 | A | G | 1 | a0001c0010t0002g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-18072T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002585 | |||||||
| chr7:116002888 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-72-18375T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002888 | |||||||
| chr7:116002916 | G | T | 1 | a0001c0001t0002g0192 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-72-18403C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116002916 | |||||||
| chr7:116003119 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-72-18606G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003119 | |||||||
| chr7:116003251 | TA | T | 233 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(230): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-72-18739delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003251 | |||||||
| chr7:116003257 | A | G | 11 | a0001c0001t0003g0123 a0001c0001t0003g0127 a0001c0001t0003g0276 others(8): Show |
11 | HG00609.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.-72-18744T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003257 | |||||||
| chr7:116003281 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-18768C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003281 | |||||||
| chr7:116003320 | A | G | 328 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(325): Show |
389 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(386): Show |
intron_variant | MODIFIER | c.-72-18807T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003320 | |||||||
| chr7:116003570 | G | T | 2 | a0005c0007t0001g0045 a0005c0007t0001g0046 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-72-19057C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003570 | |||||||
| chr7:116003615 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-72-19102G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003615 | |||||||
| chr7:116003681 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-72-19168A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003681 | |||||||
| chr7:116003721 | T | C | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-72-19208A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003721 | |||||||
| chr7:116003754 | C | T | 1 | a0001c0010t0002g0191 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-72-19241G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116003754 | |||||||
| chr7:116004254 | A | C | 1 | a0001c0001t0002g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-72-19741T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004254 | |||||||
| chr7:116004271 | T | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-19758A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004271 | |||||||
| chr7:116004330 | A | G | 1 | a0001c0001t0019g0023 | 2 | HG02486.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-72-19817T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004330 | |||||||
| chr7:116004482 | G | A | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-19969C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004482 | |||||||
| chr7:116004795 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-72-20282T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004795 | |||||||
| chr7:116004880 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-20367G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116004880 | |||||||
| chr7:116005063 | G | T | 5 | a0001c0001t0001g0233 a0001c0001t0001g0326 a0001c0001t0001g0327 others(2): Show |
5 | HG02109.hp2 HG02258.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-72-20550C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005063 | |||||||
| chr7:116005113 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-72-20600A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005113 | |||||||
| chr7:116005150 | G | T | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-20637C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005150 | |||||||
| chr7:116005156 | A | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-20643T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005156 | |||||||
| chr7:116005214 | C | T | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-20701G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005214 | |||||||
| chr7:116005253 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-20740A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005253 | |||||||
| chr7:116005302 | A | T | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-72-20789T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005302 | |||||||
| chr7:116005348 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-20835G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005348 | |||||||
| chr7:116005479 | T | C | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-20966A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005479 | |||||||
| chr7:116005716 | G | A | 38 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(35): Show |
40 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.-72-21203C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005716 | |||||||
| chr7:116005968 | C | A | 1 | a0001c0001t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-72-21455G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005968 | |||||||
| chr7:116005999 | C | T | 1 | a0001c0001t0003g0275 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-72-21486G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116005999 | |||||||
| chr7:116006000 | G | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-21487C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006000 | |||||||
| chr7:116006005 | T | A | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-72-21492A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006005 | |||||||
| chr7:116006006 | C | G | 234 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(231): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.-72-21493G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006006 | |||||||
| chr7:116006007 | A | T | 4 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0255 others(1): Show |
7 | HG00609.hp2 HG02027.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-21494T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006007 | |||||||
| chr7:116006103 | G | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-72-21590C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006103 | |||||||
| chr7:116006164 | G | A | 4 | a0001c0001t0001g0113 a0001c0004t0001g0173 a0001c0004t0001g0243 others(1): Show |
4 | HG02055.hp2 HG02145.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-72-21651C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006164 | |||||||
| chr7:116006180 | G | A | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-72-21667C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006180 | |||||||
| chr7:116006326 | A | G | 1 | a0001c0001t0001g0036 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-72-21813T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006326 | |||||||
| chr7:116006428 | T | C | 1 | a0001c0001t0008g0232 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-72-21915A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006428 | |||||||
| chr7:116006515 | G | A | 4 | a0001c0001t0014g0234 a0001c0005t0014g0043 a0001c0005t0014g0116 others(1): Show |
4 | HG02630.hp2 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-72-22002C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006515 | |||||||
| chr7:116006653 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-72-22140A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006653 | |||||||
| chr7:116006834 | T | C | 1 | a0001c0001t0003g0301 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-72-22321A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006834 | |||||||
| chr7:116006837 | G | A | 1 | a0001c0001t0003g0059 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-72-22324C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116006837 | |||||||
| chr7:116007117 | C | T | 2 | a0005c0007t0001g0045 a0005c0007t0001g0046 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-72-22604G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007117 | |||||||
| chr7:116007158 | G | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(97): Show |
110 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-72-22645C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007158 | |||||||
| chr7:116007223 | G | A | 2 | a0001c0001t0003g0307 a0001c0001t0036g0302 |
2 | HG00673.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-72-22710C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007223 | |||||||
| chr7:116007329 | A | G | 7 | a0001c0001t0001g0070 a0001c0001t0001g0233 a0001c0001t0001g0326 others(4): Show |
7 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.-72-22816T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007329 | |||||||
| chr7:116007410 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-72-22897G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007410 | |||||||
| chr7:116007447 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-22934C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007447 | |||||||
| chr7:116007449 | A | C | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-72-22936T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007449 | |||||||
| chr7:116007514 | C | T | 5 | a0001c0001t0002g0143 a0001c0001t0009g0141 a0001c0001t0009g0142 others(2): Show |
5 | HG00140.hp2 HG01243.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.-72-23001G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007514 | |||||||
| chr7:116007515 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-72-23002C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007515 | |||||||
| chr7:116007571 | T | C | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-72-23058A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007571 | |||||||
| chr7:116007772 | C | G | 9 | a0001c0001t0002g0014 a0001c0001t0002g0060 a0001c0001t0002g0061 others(6): Show |
10 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.-73+22861G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007772 | |||||||
| chr7:116007830 | T | G | 1 | a0001c0001t0002g0211 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-73+22803A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007830 | |||||||
| chr7:116007846 | A | G | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73+22787T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007846 | |||||||
| chr7:116007992 | GA | G | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+22640delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116007992 | |||||||
| chr7:116008166 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-73+22467A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008166 | |||||||
| chr7:116008251 | G | A | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-73+22382C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008251 | |||||||
| chr7:116008525 | T | A | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+22108A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008525 | |||||||
| chr7:116008578 | G | A | 1 | a0001c0001t0003g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-73+22055C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008578 | |||||||
| chr7:116008693 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-73+21940T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008693 | |||||||
| chr7:116008755 | G | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0174 a0001c0001t0001g0183 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+21878C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008755 | |||||||
| chr7:116008797 | C | T | 1 | a0001c0001t0004g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-73+21836G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008797 | |||||||
| chr7:116008853 | C | T | 13 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(10): Show |
20 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-73+21780G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008853 | |||||||
| chr7:116008860 | T | C | 68 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(65): Show |
101 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-73+21773A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008860 | |||||||
| chr7:116008920 | G | T | 1 | a0001c0001t0001g0331 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-73+21713C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008920 | |||||||
| chr7:116008977 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-73+21656T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116008977 | |||||||
| chr7:116009102 | T | G | 3 | a0001c0001t0030g0166 a0001c0001t0034g0246 a0001c0001t0035g0175 |
3 | HG02622.hp1 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-73+21531A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009102 | |||||||
| chr7:116009169 | C | T | 1 | a0001c0001t0033g0179 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-73+21464G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009169 | |||||||
| chr7:116009215 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-73+21418A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009215 | |||||||
| chr7:116009297 | C | G | 1 | a0001c0001t0002g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-73+21336G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009297 | |||||||
| chr7:116009311 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+21322G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009311 | |||||||
| chr7:116009400 | G | A | 1 | a0001c0001t0003g0303 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-73+21233C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009400 | |||||||
| chr7:116009431 | C | T | 1 | a0001c0001t0003g0274 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-73+21202G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009431 | |||||||
| chr7:116009572 | A | G | 2 | a0001c0002t0001g0047 a0001c0002t0001g0051 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-73+21061T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009572 | |||||||
| chr7:116009573 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-73+21060A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009573 | |||||||
| chr7:116009590 | A | G | 1 | a0001c0001t0002g0189 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-73+21043T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009590 | |||||||
| chr7:116009761 | T | C | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+20872A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009761 | |||||||
| chr7:116009969 | C | T | 35 | a0001c0001t0001g0154 a0001c0001t0002g0014 a0001c0001t0002g0020 others(32): Show |
37 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-73+20664G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116009969 | |||||||
| chr7:116010119 | G | A | 2 | a0001c0001t0002g0009 a0001c0001t0002g0222 |
4 | HG01175.hp1 HG01516.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+20514C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010119 | |||||||
| chr7:116010216 | G | A | 1 | a0001c0001t0002g0213 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-73+20417C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010216 | |||||||
| chr7:116010480 | G | A | 1 | a0004c0008t0023g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-73+20153C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010480 | |||||||
| chr7:116010544 | A | G | 2 | a0001c0002t0001g0047 a0001c0002t0001g0051 |
2 | HG01891.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-73+20089T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010544 | |||||||
| chr7:116010805 | T | A | 1 | a0001c0001t0001g0098 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-73+19828A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116010805 | |||||||
| chr7:116011286 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+19347A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011286 | |||||||
| chr7:116011292 | A | G | 1 | a0001c0001t0003g0273 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-73+19341T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011292 | |||||||
| chr7:116011344 | T | C | 37 | a0001c0001t0001g0035 a0001c0001t0001g0154 a0001c0001t0001g0236 others(34): Show |
39 | HG00140.hp2 HG00642.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.-73+19289A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011344 | |||||||
| chr7:116011446 | T | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+19187A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011446 | |||||||
| chr7:116011509 | T | C | 1 | a0001c0001t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+19124A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011509 | |||||||
| chr7:116011514 | T | C | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-73+19119A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011514 | |||||||
| chr7:116011562 | A | T | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+19071T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011562 | |||||||
| chr7:116011781 | C | T | 249 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(246): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.-73+18852G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011781 | |||||||
| chr7:116011824 | A | G | 1 | a0001c0001t0003g0272 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-73+18809T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011824 | |||||||
| chr7:116011853 | C | A | 1 | a0001c0001t0015g0052 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-73+18780G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011853 | |||||||
| chr7:116011913 | G | A | 14 | a0001c0001t0001g0036 a0001c0001t0001g0174 a0001c0001t0001g0183 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+18720C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011913 | |||||||
| chr7:116011935 | C | T | 2 | a0001c0001t0024g0171 a0001c0001t0030g0166 |
2 | HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-73+18698G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116011935 | |||||||
| chr7:116012211 | T | G | 15 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(12): Show |
22 | HG00323.hp1 HG00639.hp2 HG00733.hp2 others(19): Show |
intron_variant | MODIFIER | c.-73+18422A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012211 | |||||||
| chr7:116012302 | C | T | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+18331G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012302 | |||||||
| chr7:116012329 | C | T | 1 | a0001c0001t0001g0015 | 2 | NA19003.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-73+18304G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012329 | |||||||
| chr7:116012451 | C | G | 3 | a0001c0001t0010g0167 a0001c0001t0010g0168 a0001c0001t0010g0169 |
3 | HG03453.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-73+18182G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012451 | |||||||
| chr7:116012648 | A | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0174 a0001c0001t0001g0183 others(11): Show |
16 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.-73+17985T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012648 | |||||||
| chr7:116012783 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-73+17850A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012783 | |||||||
| chr7:116012816 | T | A | 1 | a0001c0001t0001g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-73+17817A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012816 | |||||||
| chr7:116012826 | GA | G | 184 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(181): Show |
235 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.-73+17806delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | |||||||
| chr7:116012826 | GAA | G | 50 | a0001c0001t0001g0035 a0001c0001t0001g0069 a0001c0001t0001g0154 others(47): Show |
53 | HG00140.hp2 HG00642.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.-73+17805_-73+1780 others(6): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | |||||||
| chr7:116012826 | GAAA | G | 14 | a0001c0001t0001g0036 a0001c0001t0001g0183 a0001c0001t0001g0239 others(11): Show |
16 | HG02109.hp1 HG02258.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.-73+17804_-73+1780 others(7): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012826 | |||||||
| chr7:116012961 | T | C | 4 | a0001c0004t0001g0173 a0001c0004t0001g0243 a0001c0004t0001g0245 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+17672A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116012961 | |||||||
| chr7:116013000 | T | C | 1 | a0001c0001t0002g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-73+17633A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013000 | |||||||
| chr7:116013124 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-73+17509A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013124 | |||||||
| chr7:116013216 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-73+17417A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013216 | |||||||
| chr7:116013233 | T | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(98): Show |
111 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(108): Show |
intron_variant | MODIFIER | c.-73+17400A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013233 | |||||||
| chr7:116013280 | T | G | 2 | a0001c0001t0002g0214 a0001c0001t0002g0215 |
2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.-73+17353A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013280 | |||||||
| chr7:116013288 | T | A | 80 | a0001c0001t0001g0025 a0001c0001t0001g0036 a0001c0001t0001g0165 others(77): Show |
115 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.-73+17345A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013288 | |||||||
| chr7:116013381 | A | C | 1 | a0001c0001t0003g0137 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-73+17252T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013381 | |||||||
| chr7:116013523 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+17110C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013523 | |||||||
| chr7:116013753 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+16880T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013753 | |||||||
| chr7:116013861 | T | C | 1 | a0001c0001t0022g0228 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-73+16772A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013861 | |||||||
| chr7:116013944 | A | G | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-73+16689T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013944 | |||||||
| chr7:116013945 | T | C | 1 | a0001c0001t0002g0216 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-73+16688A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116013945 | |||||||
| chr7:116014021 | C | T | 144 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0036 others(141): Show |
188 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-73+16612G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014021 | |||||||
| chr7:116014066 | C | T | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+16567G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014066 | |||||||
| chr7:116014092 | G | C | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+16541C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014092 | |||||||
| chr7:116014164 | T | C | 2 | a0004c0008t0023g0136 a0004c0008t0023g0176 |
2 | HG02257.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-73+16469A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014164 | |||||||
| chr7:116014270 | A | G | 3 | a0001c0001t0002g0060 a0001c0001t0002g0062 a0001c0001t0002g0063 |
3 | HG02602.hp1 HG03017.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-73+16363T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014270 | |||||||
| chr7:116014304 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-73+16329G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014304 | |||||||
| chr7:116014330 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-73+16303G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014330 | |||||||
| chr7:116014460 | C | A | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+16173G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014460 | |||||||
| chr7:116014510 | T | C | 4 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(1): Show |
4 | HG03453.hp2 HG03579.hp1 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+16123A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014510 | |||||||
| chr7:116014943 | A | G | 8 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(5): Show |
8 | HG02257.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+15690T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116014943 | |||||||
| chr7:116015068 | T | G | 3 | a0001c0001t0003g0034 a0001c0001t0003g0304 a0001c0001t0003g0305 |
4 | NA18984.hp2 NA18991.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.-73+15565A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015068 | |||||||
| chr7:116015107 | A | G | 2 | a0001c0005t0014g0116 a0001c0005t0032g0115 |
2 | HG03098.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-73+15526T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015107 | |||||||
| chr7:116015332 | A | G | 150 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(147): Show |
162 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.-73+15301T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015332 | |||||||
| chr7:116015341 | G | C | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+15292C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015341 | |||||||
| chr7:116015344 | A | G | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-73+15289T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015344 | |||||||
| chr7:116015572 | A | T | 1 | a0001c0001t0003g0264 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-73+15061T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015572 | |||||||
| chr7:116015632 | C | T | 165 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(162): Show |
184 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.-73+15001G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015632 | |||||||
| chr7:116015728 | G | T | 2 | a0001c0001t0001g0180 a0001c0001t0033g0179 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-73+14905C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015728 | |||||||
| chr7:116015924 | G | T | 245 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(242): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.-73+14709C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015924 | |||||||
| chr7:116015926 | G | A | 6 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(3): Show |
6 | HG02257.hp1 HG03453.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+14707C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015926 | |||||||
| chr7:116015987 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-73+14646A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116015987 | |||||||
| chr7:116016038 | C | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+14595G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016038 | |||||||
| chr7:116016054 | A | G | 2 | a0001c0001t0002g0026 a0001c0001t0002g0027 |
4 | HG00408.hp2 NA18957.hp2 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.-73+14579T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016054 | |||||||
| chr7:116016265 | C | T | 3 | a0001c0001t0014g0234 a0001c0001t0034g0246 a0001c0001t0035g0175 |
3 | HG02622.hp1 HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+14368G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016265 | |||||||
| chr7:116016266 | A | G | 250 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(247): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(302): Show |
intron_variant | MODIFIER | c.-73+14367T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016266 | |||||||
| chr7:116016432 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-73+14201T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016432 | |||||||
| chr7:116016536 | C | T | 1 | a0001c0001t0012g0308 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-73+14097G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016536 | |||||||
| chr7:116016614 | T | C | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+14019A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016614 | |||||||
| chr7:116016629 | T | A | 1 | a0001c0001t0002g0217 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-73+14004A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016629 | |||||||
| chr7:116016676 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-73+13957G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016676 | |||||||
| chr7:116016703 | G | A | 1 | a0001c0001t0003g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-73+13930C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016703 | |||||||
| chr7:116016845 | T | C | 1 | a0001c0001t0001g0314 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-73+13788A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016845 | |||||||
| chr7:116016927 | T | G | 1 | a0001c0002t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-73+13706A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116016927 | |||||||
| chr7:116017096 | T | C | 114 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(111): Show |
124 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.-73+13537A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017096 | |||||||
| chr7:116017134 | T | A | 1 | a0001c0001t0006g0244 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-73+13499A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017134 | |||||||
| chr7:116017179 | A | T | 8 | a0001c0001t0010g0135 a0001c0001t0010g0167 a0001c0001t0010g0168 others(5): Show |
8 | HG02257.hp1 HG02922.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+13454T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017179 | |||||||
| chr7:116017231 | T | C | 106 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(103): Show |
116 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.-73+13402A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017231 | |||||||
| chr7:116017254 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-73+13379G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017254 | |||||||
| chr7:116017405 | G | T | 4 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0121 others(1): Show |
11 | HG00423.hp1 HG00673.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.-73+13228C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017405 | |||||||
| chr7:116017411 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-73+13222T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017411 | |||||||
| chr7:116017432 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+13201G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017432 | |||||||
| chr7:116017454 | C | T | 66 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0177 others(63): Show |
99 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.-73+13179G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017454 | |||||||
| chr7:116017699 | A | G | 1 | a0001c0001t0004g0159 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-73+12934T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017699 | |||||||
| chr7:116017981 | G | GTGCACAG others(5): Show |
148 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(145): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.-73+12651_-73+1265 others(16): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116017981 | |||||||
| chr7:116018199 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0002g0138 |
2 | HG03453.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-73+12434T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018199 | |||||||
| chr7:116018282 | A | G | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+12351T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018282 | |||||||
| chr7:116018358 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+12275G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018358 | |||||||
| chr7:116018389 | A | G | 1 | a0001c0001t0001g0067 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-73+12244T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018389 | |||||||
| chr7:116018610 | C | G | 143 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(140): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.-73+12023G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018610 | |||||||
| chr7:116018615 | G | A | 5 | a0001c0001t0002g0010 a0001c0001t0002g0223 a0001c0001t0002g0224 others(2): Show |
7 | HG00735.hp1 HG01123.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.-73+12018C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018615 | |||||||
| chr7:116018991 | A | C | 1 | a0001c0004t0029g0238 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-73+11642T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116018991 | |||||||
| chr7:116019073 | A | G | 2 | a0001c0001t0018g0139 a0001c0001t0018g0140 |
2 | HG02559.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-73+11560T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019073 | |||||||
| chr7:116019192 | C | T | 1 | a0001c0001t0002g0229 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-73+11441G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019192 | |||||||
| chr7:116019247 | C | A | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+11386G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019247 | |||||||
| chr7:116019315 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-73+11318G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019315 | |||||||
| chr7:116019753 | C | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01255.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-73+10880G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116019753 | |||||||
| chr7:116020203 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-73+10430A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020203 | |||||||
| chr7:116020279 | T | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0236 |
2 | HG02145.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-73+10354A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020279 | |||||||
| chr7:116020281 | G | A | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+10352C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020281 | |||||||
| chr7:116020471 | C | T | 1 | a0001c0001t0002g0188 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-73+10162G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020471 | |||||||
| chr7:116020483 | C | T | 6 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0128 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+10150G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020483 | |||||||
| chr7:116020555 | A | G | 5 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0003c0006t0001g0037 others(2): Show |
5 | HG01255.hp2 HG01257.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+10078T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020555 | |||||||
| chr7:116020660 | A | C | 1 | a0001c0001t0024g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-73+9973T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020660 | |||||||
| chr7:116020759 | C | T | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+9874G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020759 | |||||||
| chr7:116020785 | T | C | 3 | a0001c0001t0015g0052 a0001c0001t0015g0053 a0001c0001t0015g0323 |
3 | HG02615.hp1 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-73+9848A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020785 | |||||||
| chr7:116020795 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-73+9838T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020795 | |||||||
| chr7:116020875 | A | G | 1 | a0001c0001t0016g0324 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-73+9758T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020875 | |||||||
| chr7:116020912 | T | C | 1 | a0001c0001t0001g0154 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-73+9721A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020912 | |||||||
| chr7:116020971 | T | G | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+9662A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116020971 | |||||||
| chr7:116021193 | C | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0017 others(96): Show |
109 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-73+9440G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021193 | |||||||
| chr7:116021273 | C | T | 9 | a0001c0001t0005g0013 a0001c0001t0005g0030 a0001c0001t0005g0255 others(6): Show |
12 | HG00609.hp2 HG02027.hp1 NA18949.hp2 others(9): Show |
intron_variant | MODIFIER | c.-73+9360G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021273 | |||||||
| chr7:116021340 | T | A | 1 | a0001c0001t0014g0234 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-73+9293A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021340 | |||||||
| chr7:116021563 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0042 others(6): Show |
11 | HG00733.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73+9070A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021563 | |||||||
| chr7:116021635 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-73+8998A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021635 | |||||||
| chr7:116021899 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-73+8734A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021899 | |||||||
| chr7:116021953 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-73+8680C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021953 | |||||||
| chr7:116021960 | C | G | 1 | a0001c0001t0003g0254 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-73+8673G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021960 | |||||||
| chr7:116021991 | A | T | 71 | a0001c0001t0001g0025 a0001c0001t0001g0134 a0001c0001t0001g0165 others(68): Show |
102 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.-73+8642T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116021991 | |||||||
| chr7:116022075 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(3): Show |
6 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(3): Show |
intron_variant | MODIFIER | c.-73+8558G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022075 | |||||||
| chr7:116022078 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0236 a0001c0001t0003g0235 |
3 | HG02145.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-73+8555C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022078 | |||||||
| chr7:116022189 | T | C | 1 | a0001c0001t0003g0307 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-73+8444A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022189 | |||||||
| chr7:116022222 | C | A | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+8411G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022222 | |||||||
| chr7:116022306 | A | G | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+8327T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022306 | |||||||
| chr7:116022346 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0155 |
3 | HG01074.hp2 HG01192.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-73+8287C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022346 | |||||||
| chr7:116022375 | T | C | 3 | a0001c0001t0012g0308 a0001c0001t0012g0309 a0001c0001t0012g0310 |
3 | NA18942.hp2 NA19057.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.-73+8258A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022375 | |||||||
| chr7:116022498 | G | A | 15 | a0001c0001t0001g0114 a0001c0001t0001g0174 a0001c0001t0001g0183 others(12): Show |
17 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73+8135C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022498 | |||||||
| chr7:116022551 | G | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+8082C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022551 | |||||||
| chr7:116022568 | G | T | 1 | a0001c0001t0028g0250 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-73+8065C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022568 | |||||||
| chr7:116022584 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-73+8049T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022584 | |||||||
| chr7:116022899 | G | T | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-73+7734C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022899 | |||||||
| chr7:116022905 | G | C | 15 | a0001c0001t0001g0114 a0001c0001t0001g0174 a0001c0001t0001g0183 others(12): Show |
17 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.-73+7728C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116022905 | |||||||
| chr7:116023038 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0003g0127 |
3 | HG01928.hp1 HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-73+7595T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023038 | |||||||
| chr7:116023083 | C | CA | 25 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0154 others(22): Show |
26 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-73+7549dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023083 | |||||||
| chr7:116023083 | CA | C | 14 | a0001c0001t0001g0187 a0001c0001t0001g0249 a0001c0001t0004g0002 others(11): Show |
21 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-73+7549delT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023083 | |||||||
| chr7:116023206 | T | C | 2 | a0001c0001t0003g0311 a0001c0001t0003g0312 |
2 | NA18953.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-73+7427A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023206 | |||||||
| chr7:116023491 | G | A | 1 | a0001c0001t0035g0175 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-73+7142C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023491 | |||||||
| chr7:116023492 | A | G | 1 | a0001c0001t0030g0166 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-73+7141T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023492 | |||||||
| chr7:116023827 | A | C | 1 | a0001c0005t0032g0115 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-73+6806T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116023827 | |||||||
| chr7:116024077 | G | T | 1 | a0001c0001t0002g0186 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-73+6556C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024077 | |||||||
| chr7:116024129 | C | T | 1 | a0001c0001t0031g0158 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-73+6504G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024129 | |||||||
| chr7:116024345 | A | C | 3 | a0001c0001t0016g0321 a0001c0001t0016g0324 a0001c0001t0016g0325 |
3 | HG02451.hp2 HG03540.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-73+6288T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024345 | |||||||
| chr7:116024403 | G | A | 2 | a0001c0001t0001g0315 a0001c0001t0001g0316 |
2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-73+6230C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024403 | |||||||
| chr7:116024547 | T | A | 2 | a0001c0001t0034g0246 a0001c0001t0035g0175 |
2 | HG02622.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.-73+6086A>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024547 | |||||||
| chr7:116024638 | A | G | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+5995T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024638 | |||||||
| chr7:116024777 | A | G | 29 | a0001c0001t0001g0154 a0001c0001t0002g0020 a0001c0001t0002g0138 others(26): Show |
30 | HG00140.hp2 HG01074.hp2 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.-73+5856T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024777 | |||||||
| chr7:116024784 | ATTTCCAT others(69): Show |
A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0236 a0001c0001t0003g0235 |
3 | HG02145.hp1 HG02896.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-73+5773_-73+5848d others(78): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024784 | |||||||
| chr7:116024802 | A | G | 2 | a0001c0001t0003g0264 a0001c0001t0003g0297 |
2 | NA18954.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-73+5831T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024802 | |||||||
| chr7:116024900 | T | G | 10 | a0001c0001t0002g0004 a0001c0001t0002g0011 a0001c0001t0002g0029 others(7): Show |
22 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.-73+5733A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116024900 | |||||||
| chr7:116025370 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-73+5263C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025370 | |||||||
| chr7:116025489 | G | C | 1 | a0001c0001t0003g0313 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-73+5144C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025489 | |||||||
| chr7:116025634 | G | A | 24 | a0001c0001t0001g0035 a0001c0001t0001g0040 a0001c0001t0001g0041 others(21): Show |
31 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-73+4999C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025634 | |||||||
| chr7:116025858 | T | C | 1 | a0001c0001t0001g0114 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-73+4775A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025858 | |||||||
| chr7:116025879 | C | A | 78 | a0001c0001t0001g0025 a0001c0001t0001g0117 a0001c0001t0001g0134 others(75): Show |
111 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-73+4754G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116025879 | |||||||
| chr7:116026280 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0003g0248 |
2 | HG00621.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-73+4353G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026280 | |||||||
| chr7:116026325 | C | T | 85 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0002g0251 others(82): Show |
93 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.-73+4308G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026325 | |||||||
| chr7:116026455 | T | C | 1 | a0005c0007t0001g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-73+4178A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026455 | |||||||
| chr7:116026566 | C | T | 1 | a0001c0001t0026g0057 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-73+4067G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026566 | |||||||
| chr7:116026613 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-73+4020G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026613 | |||||||
| chr7:116026614 | T | G | 1 | a0001c0001t0001g0181 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-73+4019A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026614 | |||||||
| chr7:116026645 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-73+3988A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026645 | |||||||
| chr7:116026867 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.-73+3766G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026867 | |||||||
| chr7:116026891 | A | G | 12 | a0001c0001t0004g0002 a0001c0001t0004g0021 a0001c0001t0004g0022 others(9): Show |
19 | HG00323.hp1 HG00639.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.-73+3742T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026891 | |||||||
| chr7:116026937 | T | C | 1 | a0002c0003t0001g0118 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.-73+3696A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116026937 | |||||||
| chr7:116027019 | G | A | 89 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0185 others(86): Show |
124 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.-73+3614C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027019 | |||||||
| chr7:116027100 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-73+3533C>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027100 | |||||||
| chr7:116027173 | T | C | 180 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0041 others(177): Show |
222 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.-73+3460A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027173 | |||||||
| chr7:116027248 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0002g0157 |
3 | HG00738.hp2 HG01358.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.-73+3385T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027248 | |||||||
| chr7:116027337 | G | A | 2 | a0001c0001t0001g0233 a0004c0008t0023g0136 |
2 | HG02258.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-73+3296C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027337 | |||||||
| chr7:116027495 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0236 a0001c0001t0003g0235 others(2): Show |
5 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+3138C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027495 | |||||||
| chr7:116027503 | G | A | 1 | a0001c0001t0037g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-73+3130C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027503 | |||||||
| chr7:116027539 | G | T | 1 | a0001c0011t0004g0156 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-73+3094C>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027539 | |||||||
| chr7:116027603 | A | T | 28 | a0001c0001t0001g0154 a0001c0001t0002g0020 a0001c0001t0002g0138 others(25): Show |
29 | HG00140.hp2 HG00735.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.-73+3030T>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027603 | |||||||
| chr7:116027664 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0236 a0001c0001t0003g0235 others(2): Show |
5 | HG02145.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-73+2969G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027664 | |||||||
| chr7:116027677 | T | C | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+2956A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027677 | |||||||
| chr7:116027967 | T | G | 3 | a0001c0001t0003g0319 a0001c0001t0003g0320 a0001c0001t0016g0321 |
3 | HG02630.hp1 HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-73+2666A>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027967 | |||||||
| chr7:116027968 | C | T | 81 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0001g0314 others(78): Show |
88 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-73+2665G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116027968 | |||||||
| chr7:116028032 | G | A | 81 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0001g0314 others(78): Show |
88 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.-73+2601C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028032 | |||||||
| chr7:116028129 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-73+2504A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028129 | |||||||
| chr7:116028151 | C | T | 1 | a0004c0008t0023g0136 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-73+2482G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028151 | |||||||
| chr7:116028245 | C | A | 1 | a0001c0001t0003g0123 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-73+2388G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028245 | |||||||
| chr7:116028273 | G | A | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+2360C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028273 | |||||||
| chr7:116028274 | C | G | 1 | a0001c0001t0010g0135 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-73+2359G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028274 | |||||||
| chr7:116028426 | T | C | 1 | a0001c0005t0014g0043 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-73+2207A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028426 | |||||||
| chr7:116028932 | TAA | T | 82 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0001g0314 others(79): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+1699_-73+1700d others(4): Show |
TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028932 | |||||||
| chr7:116028943 | T | C | 1 | a0001c0001t0002g0237 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-73+1690A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116028943 | |||||||
| chr7:116029110 | G | A | 8 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+1523C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029110 | |||||||
| chr7:116029224 | T | C | 1 | a0001c0004t0001g0245 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-73+1409A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029224 | |||||||
| chr7:116029315 | C | G | 2 | a0005c0007t0001g0045 a0005c0007t0001g0046 |
2 | HG03017.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.-73+1318G>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029315 | |||||||
| chr7:116029378 | A | G | 82 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0001g0314 others(79): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+1255T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029378 | |||||||
| chr7:116029414 | G | A | 9 | a0001c0001t0001g0239 a0001c0001t0006g0012 a0001c0001t0006g0240 others(6): Show |
11 | HG02055.hp2 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-73+1219C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029414 | |||||||
| chr7:116029643 | A | G | 8 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+990T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029643 | |||||||
| chr7:116029763 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-73+870G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029763 | |||||||
| chr7:116029771 | C | A | 9 | a0001c0001t0001g0124 a0001c0001t0001g0126 a0001c0001t0001g0128 others(6): Show |
9 | HG00280.hp2 HG00642.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.-73+862G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029771 | |||||||
| chr7:116029771 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-73+862G>A | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029771 | |||||||
| chr7:116029904 | C | CA | 225 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0036 others(222): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(276): Show |
intron_variant | MODIFIER | c.-73+728dupT | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029904 | |||||||
| chr7:116029958 | T | C | 1 | a0001c0001t0034g0246 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-73+675A>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116029958 | |||||||
| chr7:116030002 | G | A | 82 | a0001c0001t0001g0249 a0001c0001t0001g0306 a0001c0001t0001g0314 others(79): Show |
89 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.-73+631C>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030002 | |||||||
| chr7:116030013 | C | A | 8 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 others(5): Show |
8 | HG01243.hp2 HG02109.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-73+620G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030013 | |||||||
| chr7:116030105 | C | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG00423.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.-73+528G>T | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030105 | |||||||
| chr7:116030319 | A | C | 8 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
8 | HG01109.hp2 HG01255.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.-73+314T>G | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030319 | |||||||
| chr7:116030383 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-73+250T>C | TFEC | ENSG00000105967.16 | transcript | ENST00000265440.12 | protein_coding | 1/7 | chr7 | 116030383 |