Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7110 |
| ensemblid | ENSG00000144747.17 |
| hgncid | 11870 |
| symbol | TMF1 |
| name | TATA element modulatory factor 1 |
| refseq_nuc | NM_007114.3 |
| refseq_prot | NP_009045.2 |
| ensembl_nuc | ENST00000398559.7 |
| ensembl_prot | ENSP00000381567.2 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 69019827 |
| end | 69052333 |
| strand | - |
| ver | v1.2 |
| region | chr3:69019827-69052333 |
| region5000 | chr3:69014827-69057333 |
| regionname0 | TMF1_chr3_69019827_69052333 |
| regionname5000 | TMF1_chr3_69014827_69057333 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1093 | 371 | 77 | 60 | 179 | 16 | 37 | 141 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0002 | 0/0 | 1093 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0003 | 0/0 | 1093 | 8 | 0 | 6 | 0 | 1 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0004 | 0/0 | 1093 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0005 | 0/0 | 1093 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0006 | 0/0 | 1093 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0007 | 0/0 | 1093 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0008 | 0/0 | 1093 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0009 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0010 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0011 | 0/0 | 1093 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| a0012 | 0/0 | 475 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(470): Show |
chr3 | 69014827 | 69057333 |
| a0013 | 0/0 | 1093 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | MSWFN others(1088): Show |
chr3 | 69014827 | 69057333 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3279 | 254 | 46 | 55 | 109 | 13 | 30 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0002 | 1/0 | 3279 | 101 | 18 | 4 | 70 | 2 | 6 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0005 | 0/0 | 3279 | 4 | 4 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0007 | 0/0 | 3279 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0008 | 0/0 | 3279 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0012 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0014 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0016 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0017 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0020 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0001c0023 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0002c0003 | 0/0 | 3279 | 9 | 8 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0003c0004 | 0/0 | 3279 | 8 | 0 | 6 | 0 | 1 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0004c0006 | 0/0 | 3279 | 3 | 0 | 0 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0005c0010 | 0/0 | 3279 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0006c0009 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0007c0018 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0008c0013 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0009c0019 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0010c0022 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0011c0015 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0012c0021 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 | ||
| a0013c0011 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | ATGAG others(3274): Show |
chr3 | 69014827 | 69057333 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6879 | 25 | 10 | 2 | 12 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0002 | 0/0 | 6879 | 88 | 5 | 14 | 58 | 3 | 8 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0003 | 0/1 | 6879 | 77 | 22 | 21 | 22 | 5 | 6 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0004 | 0/0 | 6880 | 18 | 0 | 5 | 0 | 2 | 11 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0006 | 0/0 | 6879 | 8 | 0 | 2 | 6 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0007 | 0/0 | 6879 | 6 | 0 | 2 | 0 | 1 | 3 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0009 | 0/0 | 6879 | 5 | 0 | 5 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0010 | 0/0 | 6879 | 4 | 0 | 0 | 4 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0011 | 0/0 | 6879 | 4 | 4 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0012 | 0/0 | 6879 | 4 | 0 | 0 | 4 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0015 | 0/0 | 6880 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0017 | 0/0 | 6879 | 2 | 0 | 0 | 0 | 2 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0018 | 0/0 | 6879 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0019 | 0/0 | 6879 | 2 | 0 | 2 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0020 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0022 | 0/0 | 6880 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0024 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0026 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0027 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0029 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0030 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0001t0031 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0002t0001 | 1/0 | 6879 | 92 | 11 | 4 | 69 | 1 | 6 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0002t0002 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0002t0003 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0002t0004 | 0/0 | 6880 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0001c0002t0008 | 0/0 | 6879 | 6 | 6 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0005t0014 | 0/0 | 6879 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0005t0028 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0007t0016 | 0/0 | 6879 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0007t0025 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0008t0013 | 0/0 | 6879 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0012t0002 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0014t0001 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0016t0002 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0017t0007 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0020t0001 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0001c0023t0001 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0002c0003t0005 | 0/0 | 6880 | 8 | 7 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0002c0003t0021 | 0/0 | 6881 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6876): Show |
chr3 | 69014827 | 69057333 |
| a0003c0004t0001 | 0/0 | 6879 | 8 | 0 | 6 | 0 | 1 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0004c0006t0001 | 0/0 | 6879 | 3 | 0 | 0 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0005c0010t0003 | 0/0 | 6879 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0006c0009t0001 | 0/0 | 6879 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0007c0018t0003 | 0/0 | 6879 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0008c0013t0023 | 0/0 | 6879 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0009c0019t0002 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0010c0022t0002 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0011c0015t0001 | 0/0 | 6879 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| a0012c0021t0015 | 0/0 | 6880 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6875): Show |
chr3 | 69014827 | 69057333 |
| a0013c0011t0003 | 0/0 | 6879 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | GTAGA others(6874): Show |
chr3 | 69014827 | 69057333 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0002 | 0/0 | 28 | 0 | 2 | 24 | 0 | 2 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0020 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0040 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0003 | 0/0 | 13 | 6 | 1 | 6 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0004 | 0/1 | 10 | 0 | 6 | 0 | 3 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0007 | 0/0 | 7 | 0 | 4 | 0 | 1 | 2 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0013 | 0/0 | 5 | 4 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0011 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0012 | 0/0 | 5 | 0 | 2 | 0 | 1 | 2 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0006g0015 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0006g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0007g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0009g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0009g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0009g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0010g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0010g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0011g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0012g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0015g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0017g0045 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0018g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0019g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0020g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0022g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0024g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0026g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0027g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0029g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0030g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0001t0031g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0001 | 0/0 | 30 | 2 | 0 | 27 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0008 | 0/0 | 6 | 4 | 2 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0002t0008g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0005t0014g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0005t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0005t0014g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0005t0028g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0007t0016g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0007t0025g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0008t0013g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0008t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0012t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0014t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0016t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0017t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0020t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0001c0023t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0002c0003t0005g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0002c0003t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0002c0003t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0002c0003t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0002c0003t0021g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0003c0004t0001g0010 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0003c0004t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0003c0004t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0003c0004t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0004c0006t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0004c0006t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0004c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0005c0010t0003g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0006c0009t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0006c0009t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0007c0018t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0008c0013t0023g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0009c0019t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0010c0022t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0011c0015t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0012c0021t0015g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| a0013c0011t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0004 | g0012 | EUR | GBR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00140 | hp1 | a0001 | c0001 | t0007 | g0059 | EUR | GBR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | GBR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0202 | EUR | FIN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | FIN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0007 | EUR | FIN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00323 | hp2 | a0001 | c0017 | t0007 | g0060 | EUR | FIN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00544 | hp2 | a0001 | c0001 | t0010 | g0022 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0110 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00639 | hp1 | a0001 | c0001 | t0019 | g0037 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00642 | hp1 | a0001 | c0001 | t0007 | g0058 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | CHS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00735 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01074 | hp1 | a0001 | c0001 | t0026 | g0184 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01099 | hp2 | a0001 | c0001 | t0009 | g0225 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0062 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0200 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01168 | hp2 | a0001 | c0001 | t0004 | g0217 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01169 | hp1 | a0001 | c0001 | t0004 | g0212 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01169 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01192 | hp1 | a0001 | c0001 | t0019 | g0037 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01243 | hp1 | a0002 | c0003 | t0005 | g0009 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01243 | hp2 | a0007 | c0018 | t0003 | g0198 | AMR | PUR | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01256 | hp1 | a0003 | c0004 | t0001 | g0096 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0201 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01258 | hp2 | a0003 | c0004 | t0001 | g0095 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01261 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01515 | hp1 | a0008 | c0013 | t0023 | g0208 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01515 | hp2 | a0001 | c0001 | t0017 | g0045 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01517 | hp2 | a0001 | c0001 | t0017 | g0045 | EUR | IBS | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01928 | hp1 | a0001 | c0001 | t0006 | g0168 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0015 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01978 | hp2 | a0001 | c0023 | t0001 | g0109 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02004 | hp1 | a0001 | c0001 | t0024 | g0183 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02004 | hp2 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0146 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02132 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0082 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02135 | hp2 | a0001 | c0001 | t0029 | g0103 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02148 | hp1 | a0003 | c0004 | t0001 | g0010 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02148 | hp2 | a0001 | c0001 | t0009 | g0024 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0032 | EAS | CDX | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02257 | hp2 | a0001 | c0005 | t0014 | g0187 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02258 | hp2 | a0001 | c0001 | t0031 | g0230 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02273 | hp2 | a0001 | c0001 | t0009 | g0024 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02280 | hp2 | a0001 | c0002 | t0003 | g0209 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02300 | hp1 | a0003 | c0004 | t0001 | g0090 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02300 | hp2 | a0001 | c0001 | t0009 | g0024 | AMR | PEL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02451 | hp1 | a0001 | c0001 | t0011 | g0195 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02451 | hp2 | a0002 | c0003 | t0005 | g0009 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | KHV | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02572 | hp2 | a0002 | c0003 | t0021 | g0055 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02602 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0141 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02615 | hp2 | a0001 | c0005 | t0014 | g0189 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02622 | hp2 | a0001 | c0005 | t0028 | g0188 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02630 | hp1 | a0001 | c0002 | t0008 | g0176 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02630 | hp2 | a0002 | c0003 | t0005 | g0054 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02647 | hp2 | a0001 | c0002 | t0008 | g0181 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02683 | hp1 | a0001 | c0001 | t0004 | g0211 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0147 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0229 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02717 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02717 | hp2 | a0001 | c0007 | t0025 | g0111 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0031 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0092 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0204 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02895 | hp2 | a0001 | c0001 | t0018 | g0041 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02896 | hp2 | a0001 | c0007 | t0016 | g0034 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02897 | hp1 | a0001 | c0007 | t0016 | g0034 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02965 | hp1 | a0001 | c0002 | t0008 | g0177 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02965 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02970 | hp2 | a0001 | c0001 | t0020 | g0051 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03041 | hp1 | a0002 | c0003 | t0005 | g0009 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03041 | hp2 | a0001 | c0002 | t0008 | g0179 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03098 | hp2 | a0001 | c0002 | t0008 | g0178 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03195 | hp1 | a0001 | c0016 | t0002 | g0149 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03195 | hp2 | a0002 | c0003 | t0005 | g0009 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03209 | hp1 | a0005 | c0010 | t0003 | g0050 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0115 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03225 | hp1 | a0001 | c0008 | t0013 | g0025 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0013 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0080 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03486 | hp1 | a0005 | c0010 | t0003 | g0050 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03490 | hp2 | a0001 | c0001 | t0022 | g0063 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03491 | hp1 | a0001 | c0001 | t0004 | g0226 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0008 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03540 | hp1 | a0001 | c0014 | t0001 | g0117 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03579 | hp2 | a0001 | c0008 | t0013 | g0052 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0218 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0174 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03834 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0007 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03927 | hp1 | a0003 | c0004 | t0001 | g0010 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03927 | hp2 | a0001 | c0001 | t0007 | g0061 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03942 | hp1 | a0001 | c0001 | t0004 | g0227 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03942 | hp2 | a0001 | c0012 | t0002 | g0065 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04115 | hp1 | a0001 | c0001 | t0004 | g0012 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04115 | hp2 | a0001 | c0001 | t0007 | g0057 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0130 | SAS | BEB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04199 | hp1 | a0001 | c0001 | t0007 | g0064 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0137 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | STU | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18522 | hp1 | a0002 | c0003 | t0005 | g0056 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | CHB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | CHB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0213 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18943 | hp1 | a0001 | c0001 | t0012 | g0016 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18945 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18947 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18950 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18959 | hp2 | a0009 | c0019 | t0002 | g0159 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18963 | hp1 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18966 | hp1 | a0004 | c0006 | t0001 | g0085 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0165 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18973 | hp2 | a0010 | c0022 | t0002 | g0191 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18981 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18981 | hp2 | a0004 | c0006 | t0001 | g0084 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0166 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18982 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0205 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18985 | hp1 | a0001 | c0001 | t0012 | g0016 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18985 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18986 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18988 | hp1 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18989 | hp2 | a0011 | c0015 | t0001 | g0124 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0151 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18991 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18992 | hp2 | a0001 | c0001 | t0030 | g0139 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18993 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18993 | hp2 | a0001 | c0001 | t0012 | g0016 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18994 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19001 | hp1 | a0001 | c0001 | t0010 | g0022 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19007 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19011 | hp2 | a0006 | c0009 | t0001 | g0101 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19030 | hp2 | a0001 | c0005 | t0014 | g0190 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19043 | hp1 | a0001 | c0020 | t0001 | g0112 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19043 | hp2 | a0001 | c0001 | t0027 | g0194 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19056 | hp1 | a0004 | c0006 | t0001 | g0088 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0048 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0014 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19060 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19067 | hp1 | a0001 | c0001 | t0015 | g0157 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19067 | hp2 | a0006 | c0009 | t0001 | g0100 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19074 | hp1 | a0001 | c0002 | t0002 | g0129 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19083 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19083 | hp2 | a0012 | c0021 | t0015 | g0173 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19085 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19089 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19091 | hp1 | a0001 | c0001 | t0012 | g0016 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA19240 | hp2 | a0001 | c0002 | t0008 | g0180 | AFR | YRI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ASW | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ASW | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0093 | EUR | TSI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20752 | hp2 | a0001 | c0002 | t0004 | g0094 | EUR | TSI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20805 | hp1 | a0003 | c0004 | t0001 | g0010 | EUR | TSI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0011 | EUR | TSI | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG01123 | hp2 | a0001 | c0001 | t0009 | g0196 | AMR | CLM | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02109 | hp1 | a0002 | c0003 | t0005 | g0053 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0222 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0041 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02559 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG02559 | hp2 | a0001 | c0008 | t0013 | g0025 | AFR | ACB | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0003 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG03471 | hp2 | a0002 | c0003 | t0005 | g0009 | AFR | MSL | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | USA | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | USA | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20300 | hp1 | a0013 | c0011 | t0003 | g0228 | AFR | USA | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0043 | AFR | USA | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA21309 | hp1 | a0001 | c0001 | t0011 | g0021 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| NA21309 | hp2 | a0001 | c0002 | t0001 | g0008 | AFR | LWK | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0004 | REF | REF | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0081 | REF | REF | TMF1_chr3_69014827_69057333 | TMF1 | chr3 | 69014827 | 69057333 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:69023227 | T | G | 1 | a0005 | 2 | HG03209.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.3232A>C | p.Asn1078His | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 3479/6879 | 3232/3282 | 1078/1093 | chr3 | 69023227 | |||
| chr3:69025594 | A | G | 1 | a0007 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.2978T>C | p.Leu993Pro | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/17 | 3225/6879 | 2978/3282 | 993/1093 | chr3 | 69025594 | |||
| chr3:69025630 | G | A | 1 | a0009 | 1 | NA18959.hp2 | missense_variant | MODERATE | c.2942C>T | p.Ala981Val | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/17 | 3189/6879 | 2942/3282 | 981/1093 | chr3 | 69025630 | |||
| chr3:69029900 | G | T | 1 | a0011 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.2509C>A | p.Leu837Ile | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/17 | 2756/6879 | 2509/3282 | 837/1093 | chr3 | 69029900 | |||
| chr3:69033557 | C | G | 1 | a0003 | 8 | HG00735.hp2 HG01256.hp1 HG01258.hp2 others(5): Show |
missense_variant | MODERATE | c.2392G>C | p.Asp798His | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/17 | 2639/6879 | 2392/3282 | 798/1093 | chr3 | 69033557 | |||
| chr3:69033682 | C | T | 1 | a0006 | 2 | NA19011.hp2 NA19067.hp2 |
missense_variant | MODERATE | c.2267G>A | p.Arg756Gln | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/17 | 2514/6879 | 2267/3282 | 756/1093 | chr3 | 69033682 | |||
| chr3:69038670 | T | C | 1 | a0004 | 3 | NA18966.hp1 NA18981.hp2 NA19056.hp1 |
missense_variant | MODERATE | c.2045A>G | p.Gln682Arg | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/17 | 2292/6879 | 2045/3282 | 682/1093 | chr3 | 69038670 | |||
| chr3:69044517 | C | A | 1 | a0012 | 1 | NA19083.hp2 | stop_gained | HIGH | c.1426G>T | p.Glu476* | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/17 | 1673/6879 | 1426/3282 | 476/1093 | chr3 | 69044517 | |||
| chr3:69047362 | C | T | 1 | a0002 | 9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
missense_variant | MODERATE | c.1343G>A | p.Cys448Tyr | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 1590/6879 | 1343/3282 | 448/1093 | chr3 | 69047362 | |||
| chr3:69047989 | C | T | 1 | a0008 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.716G>A | p.Ser239Asn | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 963/6879 | 716/3282 | 239/1093 | chr3 | 69047989 | |||
| chr3:69048146 | T | C | 1 | a0010 | 1 | NA18973.hp2 | missense_variant | MODERATE | c.559A>G | p.Met187Val | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 806/6879 | 559/3282 | 187/1093 | chr3 | 69048146 | |||
| chr3:69048481 | A | G | 1 | a0013 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.224T>C | p.Ile75Thr | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 471/6879 | 224/3282 | 75/1093 | chr3 | 69048481 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:69023240 | G | A | 1 | a0002c0003 | 9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.3219C>T | p.Leu1073Leu | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 3466/6879 | 3219/3282 | 1073/1093 | chr3 | 69023240 | |||
| chr3:69024055 | T | C | 1 | a0001c0007 | 3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
splice_region_variant&synonymous_variant | LOW | c.3138A>G | p.Arg1046Arg | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/17 | 3385/6879 | 3138/3282 | 1046/1093 | chr3 | 69024055 | |||
| chr3:69029886 | T | C | 1 | a0001c0008 | 3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.2523A>G | p.Glu841Glu | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/17 | 2770/6879 | 2523/3282 | 841/1093 | chr3 | 69029886 | |||
| chr3:69033585 | C | T | 1 | a0001c0017 | 1 | HG00323.hp2 | synonymous_variant | LOW | c.2364G>A | p.Ser788Ser | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/17 | 2611/6879 | 2364/3282 | 788/1093 | chr3 | 69033585 | |||
| chr3:69033603 | C | T | 1 | a0001c0016 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2346G>A | p.Leu782Leu | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/17 | 2593/6879 | 2346/3282 | 782/1093 | chr3 | 69033603 | |||
| chr3:69038905 | T | C | 1 | a0001c0005 | 4 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
synonymous_variant | LOW | c.1932A>G | p.Val644Val | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 7/17 | 2179/6879 | 1932/3282 | 644/1093 | chr3 | 69038905 | |||
| chr3:69038926 | T | C | 1 | a0001c0020 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.1911A>G | p.Lys637Lys | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 7/17 | 2158/6879 | 1911/3282 | 637/1093 | chr3 | 69038926 | |||
| chr3:69047418 | C | T | 1 | a0001c0014 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.1287G>A | p.Glu429Glu | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 1534/6879 | 1287/3282 | 429/1093 | chr3 | 69047418 | |||
| chr3:69047463 | G | A | 16 | a0001c0001 a0001c0007 a0001c0008 others(13): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
synonymous_variant | LOW | c.1242C>T | p.Ser414Ser | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 1489/6879 | 1242/3282 | 414/1093 | chr3 | 69047463 | |||
| chr3:69048447 | C | T | 1 | a0001c0012 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.258G>A | p.Arg86Arg | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 505/6879 | 258/3282 | 86/1093 | chr3 | 69048447 | |||
| chr3:69048552 | G | A | 1 | a0001c0023 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.153C>T | p.Ser51Ser | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/17 | 400/6879 | 153/3282 | 51/1093 | chr3 | 69048552 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:69019928 | G | A | 1 | a0001c0001t0019 | 2 | HG00639.hp1 HG01192.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3249C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 3249 | chr3 | 69019928 | ||||||
| chr3:69020143 | A | G | 1 | a0001c0001t0029 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3034T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 3034 | chr3 | 69020143 | ||||||
| chr3:69020149 | A | G | 1 | a0001c0001t0018 | 2 | HG02486.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3028T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 3028 | chr3 | 69020149 | ||||||
| chr3:69020333 | A | G | 1 | a0001c0001t0027 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2844T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2844 | chr3 | 69020333 | ||||||
| chr3:69020446 | C | A | 1 | a0001c0001t0018 | 2 | HG02486.hp2 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2731G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2731 | chr3 | 69020446 | ||||||
| chr3:69020662 | A | C | 1 | a0001c0007t0025 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2515T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2515 | chr3 | 69020662 | ||||||
| chr3:69020688 | T | A | 1 | a0001c0005t0028 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2489A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2489 | chr3 | 69020688 | ||||||
| chr3:69020727 | A | C | 1 | a0001c0001t0010 | 4 | HG00544.hp2 NA18984.hp2 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2450T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2450 | chr3 | 69020727 | ||||||
| chr3:69020729 | A | T | 1 | a0001c0001t0010 | 4 | HG00544.hp2 NA18984.hp2 NA18988.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2448T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2448 | chr3 | 69020729 | ||||||
| chr3:69020751 | A | G | 3 | a0001c0001t0006 a0001c0001t0015 a0012c0021t0015 |
10 | HG01928.hp1 HG01952.hp2 NA18964.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2426T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2426 | chr3 | 69020751 | ||||||
| chr3:69020823 | G | A | 1 | a0001c0001t0011 | 4 | HG02451.hp1 HG02559.hp1 HG02717.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2354C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2354 | chr3 | 69020823 | ||||||
| chr3:69020899 | A | G | 1 | a0001c0001t0020 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2278T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 2278 | chr3 | 69020899 | ||||||
| chr3:69021248 | A | C | 18 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(15): Show |
131 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*1929T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1929 | chr3 | 69021248 | ||||||
| chr3:69021277 | C | T | 1 | a0001c0001t0017 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1900G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1900 | chr3 | 69021277 | ||||||
| chr3:69021306 | G | A | 13 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(10): Show |
116 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*1871C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1871 | chr3 | 69021306 | ||||||
| chr3:69021400 | A | G | 1 | a0001c0001t0026 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1777T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1777 | chr3 | 69021400 | ||||||
| chr3:69021404 | C | A | 1 | a0001c0008t0013 | 3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1773G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1773 | chr3 | 69021404 | ||||||
| chr3:69021410 | C | A | 2 | a0001c0007t0016 a0001c0007t0025 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1767G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1767 | chr3 | 69021410 | ||||||
| chr3:69021412 | A | C | 21 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0007 others(18): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*1765T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1765 | chr3 | 69021412 | ||||||
| chr3:69021614 | A | G | 3 | a0001c0001t0024 a0001c0007t0016 a0001c0007t0025 |
4 | HG02004.hp1 HG02717.hp2 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1563T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1563 | chr3 | 69021614 | ||||||
| chr3:69021685 | G | GT | 6 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0022 others(3): Show |
23 | HG00099.hp1 HG00738.hp1 HG01168.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1491dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1491 | chr3 | 69021685 | ||||||
| chr3:69021689 | T | G | 1 | a0001c0002t0008 | 6 | HG02630.hp1 HG02647.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1488A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1488 | chr3 | 69021689 | ||||||
| chr3:69021788 | C | G | 1 | a0008c0013t0023 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1389G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1389 | chr3 | 69021788 | ||||||
| chr3:69022116 | T | C | 1 | a0001c0001t0030 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1061A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1061 | chr3 | 69022116 | ||||||
| chr3:69022150 | G | T | 1 | a0001c0001t0009 | 5 | HG01099.hp2 HG01123.hp2 HG02148.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1027C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 1027 | chr3 | 69022150 | ||||||
| chr3:69022840 | T | C | 1 | a0001c0001t0012 | 4 | NA18943.hp1 NA18985.hp1 NA18993.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*337A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 337 | chr3 | 69022840 | ||||||
| chr3:69023020 | A | C | 1 | a0001c0001t0020 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*157T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 17/17 | 157 | chr3 | 69023020 | ||||||
| chr3:69052218 | C | T | 3 | a0001c0001t0007 a0001c0001t0022 a0001c0017t0007 |
8 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-132G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/17 | 132 | chr3 | 69052218 | ||||||
| chr3:69052277 | A | AG | 2 | a0002c0003t0005 a0002c0003t0021 |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-192dupC | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/17 | 192 | chr3 | 69052277 | ||||||
| chr3:69052279 | G | T | 2 | a0001c0001t0020 a0001c0008t0013 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-193C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/17 | 193 | chr3 | 69052279 | ||||||
| chr3:69052301 | T | G | 1 | a0001c0001t0031 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-215A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/17 | 215 | chr3 | 69052301 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:69023330 | G | A | 5 | a0001c0001t0003g0023 a0001c0001t0003g0044 a0001c0001t0003g0047 others(2): Show |
9 | HG00733.hp1 HG01255.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.3139-10C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023330 | |||||||
| chr3:69023564 | C | G | 2 | a0001c0002t0001g0008 a0001c0002t0001g0031 |
8 | HG01167.hp1 HG01169.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3139-244G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023564 | |||||||
| chr3:69023576 | G | T | 1 | a0001c0001t0003g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3139-256C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023576 | |||||||
| chr3:69023610 | T | C | 84 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(81): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.3139-290A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023610 | |||||||
| chr3:69023621 | C | G | 1 | a0001c0001t0001g0114 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3139-301G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023621 | |||||||
| chr3:69023884 | A | C | 1 | a0001c0001t0018g0041 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3138+171T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 16/16 | chr3 | 69023884 | |||||||
| chr3:69024256 | A | C | 1 | a0001c0001t0007g0057 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3013-76T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024256 | |||||||
| chr3:69024259 | G | A | 59 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(56): Show |
100 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.3013-79C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024259 | |||||||
| chr3:69024268 | G | GT | 11 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0221 others(8): Show |
18 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.3013-89dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024268 | |||||||
| chr3:69024268 | GT | G | 17 | a0001c0001t0001g0107 a0001c0001t0001g0114 a0001c0001t0002g0150 others(14): Show |
18 | HG01109.hp2 HG01256.hp1 HG01515.hp1 others(15): Show |
intron_variant | MODIFIER | c.3013-89delA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024268 | |||||||
| chr3:69024268 | GTT | G | 55 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(52): Show |
99 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.3013-90_3013-89del others(2): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024268 | |||||||
| chr3:69024418 | ATTAT | A | 64 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(61): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.3013-242_3013-239d others(6): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024418 | |||||||
| chr3:69024444 | T | C | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.3013-264A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024444 | |||||||
| chr3:69024467 | T | G | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3013-287A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024467 | |||||||
| chr3:69024685 | A | G | 1 | a0002c0003t0005g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3013-505T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024685 | |||||||
| chr3:69024766 | A | G | 84 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(81): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.3013-586T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024766 | |||||||
| chr3:69024802 | C | CT | 102 | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0030 others(99): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.3013-623dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024802 | |||||||
| chr3:69024802 | C | CTT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0001g0102 others(17): Show |
31 | HG01192.hp2 HG01346.hp2 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.3013-624_3013-623d others(4): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024802 | |||||||
| chr3:69024802 | C | T | 1 | a0001c0001t0018g0041 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.3013-622G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024802 | |||||||
| chr3:69024802 | CT | C | 11 | a0001c0001t0002g0144 a0001c0001t0002g0158 a0001c0001t0002g0175 others(8): Show |
15 | HG00735.hp2 HG01070.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.3013-623delA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69024802 | |||||||
| chr3:69025070 | G | A | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | NA18959.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.3012+490C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69025070 | |||||||
| chr3:69025141 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3012+419C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69025141 | |||||||
| chr3:69025174 | A | G | 1 | a0001c0002t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3012+386T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69025174 | |||||||
| chr3:69025212 | T | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0001g0102 others(14): Show |
25 | HG01192.hp2 HG02135.hp2 HG02257.hp2 others(22): Show |
intron_variant | MODIFIER | c.3012+348A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 15/16 | chr3 | 69025212 | |||||||
| chr3:69025727 | A | G | 2 | a0001c0001t0002g0027 a0001c0001t0002g0068 |
3 | HG00642.hp2 HG00741.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2860-15T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 14/16 | chr3 | 69025727 | |||||||
| chr3:69025779 | G | A | 33 | a0001c0001t0003g0043 a0001c0002t0001g0001 a0001c0002t0001g0014 others(30): Show |
71 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2860-67C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 14/16 | chr3 | 69025779 | |||||||
| chr3:69026173 | G | A | 1 | a0002c0003t0005g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2758-76C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026173 | |||||||
| chr3:69026283 | A | C | 1 | a0001c0001t0018g0041 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2758-186T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026283 | |||||||
| chr3:69026337 | C | T | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2758-240G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026337 | |||||||
| chr3:69026572 | A | T | 1 | a0001c0001t0007g0062 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2758-475T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026572 | |||||||
| chr3:69026621 | C | A | 148 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(145): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2758-524G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026621 | |||||||
| chr3:69026640 | A | T | 78 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(75): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2758-543T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026640 | |||||||
| chr3:69026672 | CTAGACTT others(40): Show |
C | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2758-622_2758-576d others(49): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026672 | |||||||
| chr3:69026679 | T | C | 4 | a0002c0003t0005g0009 a0002c0003t0005g0054 a0002c0003t0005g0056 others(1): Show |
8 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.2758-582A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026679 | |||||||
| chr3:69026721 | T | G | 78 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(75): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2758-624A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026721 | |||||||
| chr3:69026767 | T | TA | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2758-671dupT | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69026767 | |||||||
| chr3:69027000 | A | T | 144 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(141): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.2757+900T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027000 | |||||||
| chr3:69027014 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2757+886C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027014 | |||||||
| chr3:69027054 | G | T | 3 | a0001c0002t0001g0126 a0001c0002t0001g0131 a0001c0002t0001g0138 |
3 | NA18951.hp1 NA18991.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2757+846C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027054 | |||||||
| chr3:69027059 | G | A | 8 | a0001c0001t0007g0057 a0001c0001t0007g0058 a0001c0001t0007g0059 others(5): Show |
8 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(5): Show |
intron_variant | MODIFIER | c.2757+841C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027059 | |||||||
| chr3:69027120 | C | T | 1 | a0001c0002t0001g0125 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2757+780G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027120 | |||||||
| chr3:69027392 | G | A | 1 | a0001c0002t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2757+508C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027392 | |||||||
| chr3:69027617 | C | A | 1 | a0001c0002t0001g0130 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2757+283G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027617 | |||||||
| chr3:69027628 | C | A | 1 | a0001c0001t0002g0169 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2757+272G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027628 | |||||||
| chr3:69027679 | TA | T | 64 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(61): Show |
110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2757+220delT | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027679 | |||||||
| chr3:69027881 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2757+19G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 13/16 | chr3 | 69027881 | |||||||
| chr3:69028046 | A | G | 22 | a0001c0001t0003g0003 a0001c0001t0003g0042 a0001c0001t0003g0043 others(19): Show |
49 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.2665-54T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 12/16 | chr3 | 69028046 | |||||||
| chr3:69028335 | A | G | 2 | a0001c0002t0001g0091 a0001c0002t0004g0094 |
2 | HG01261.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2595-40T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69028335 | |||||||
| chr3:69028622 | A | G | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2595-327T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69028622 | |||||||
| chr3:69028723 | GT | G | 152 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(149): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.2595-429delA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69028723 | |||||||
| chr3:69029038 | A | ATT | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2595-745_2595-744d others(4): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029038 | |||||||
| chr3:69029042 | A | AT | 72 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(69): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2595-748dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029042 | |||||||
| chr3:69029042 | A | T | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2595-747T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029042 | |||||||
| chr3:69029048 | T | TA | 11 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(8): Show |
15 | HG00438.hp2 HG01943.hp2 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.2595-754_2595-753i others(3): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029048 | |||||||
| chr3:69029076 | C | T | 1 | a0001c0001t0003g0222 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2594+739G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029076 | |||||||
| chr3:69029148 | C | T | 1 | a0001c0001t0002g0154 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2594+667G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029148 | |||||||
| chr3:69029240 | G | C | 1 | a0001c0002t0001g0131 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2594+575C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029240 | |||||||
| chr3:69029354 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0098 |
5 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2594+461G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029354 | |||||||
| chr3:69029417 | C | A | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2594+398G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029417 | |||||||
| chr3:69029449 | A | AT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0099 a0001c0001t0001g0102 others(9): Show |
19 | HG01192.hp2 HG02135.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2594+365dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029449 | |||||||
| chr3:69029449 | AT | A | 153 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(150): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2594+365delA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029449 | |||||||
| chr3:69029519 | A | C | 84 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(81): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2594+296T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029519 | |||||||
| chr3:69029530 | C | T | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2594+285G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029530 | |||||||
| chr3:69029540 | G | A | 1 | a0003c0004t0001g0090 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2594+275C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029540 | |||||||
| chr3:69029737 | G | A | 5 | a0001c0001t0007g0057 a0002c0003t0005g0009 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02451.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2594+78C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 11/16 | chr3 | 69029737 | |||||||
| chr3:69030105 | C | T | 2 | a0001c0002t0003g0209 a0001c0023t0001g0109 |
2 | HG01978.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.2402-98G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030105 | |||||||
| chr3:69030356 | T | C | 1 | a0001c0001t0003g0048 | 2 | HG02027.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2402-349A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030356 | |||||||
| chr3:69030555 | A | T | 2 | a0001c0007t0016g0034 a0001c0007t0025g0111 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2402-548T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030555 | |||||||
| chr3:69030744 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2402-737G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030744 | |||||||
| chr3:69030784 | T | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(206): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2402-777A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030784 | |||||||
| chr3:69030999 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2402-992G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69030999 | |||||||
| chr3:69031027 | T | A | 1 | a0001c0001t0003g0200 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.2402-1020A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031027 | |||||||
| chr3:69031030 | G | A | 147 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(144): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2402-1023C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031030 | |||||||
| chr3:69031231 | G | A | 5 | a0001c0001t0001g0114 a0001c0005t0014g0187 a0001c0005t0014g0189 others(2): Show |
5 | HG02257.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2402-1224C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031231 | |||||||
| chr3:69031256 | G | A | 1 | a0001c0001t0002g0038 | 2 | HG02109.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.2402-1249C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031256 | |||||||
| chr3:69031417 | T | TAC | 42 | a0001c0001t0002g0002 a0001c0001t0002g0027 a0001c0001t0002g0036 others(39): Show |
80 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.2402-1412_2402-141 others(6): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031417 | |||||||
| chr3:69031571 | A | G | 80 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(77): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2402-1564T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031571 | |||||||
| chr3:69031577 | G | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0076 others(1): Show |
6 | HG00438.hp2 NA18983.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.2402-1570C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031577 | |||||||
| chr3:69031628 | C | T | 209 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(206): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2402-1621G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031628 | |||||||
| chr3:69031665 | A | C | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2402-1658T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031665 | |||||||
| chr3:69031898 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0098 |
5 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2401+1650T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69031898 | |||||||
| chr3:69032095 | T | G | 1 | a0001c0001t0020g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2401+1453A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032095 | |||||||
| chr3:69032213 | G | C | 1 | a0001c0001t0003g0215 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2401+1335C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032213 | |||||||
| chr3:69032613 | C | CT | 152 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(149): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.2401+934dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032613 | |||||||
| chr3:69032685 | A | ACTG | 2 | a0001c0001t0003g0046 a0001c0001t0003g0049 |
4 | NA18944.hp1 NA18953.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+860_2401+862d others(5): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032685 | |||||||
| chr3:69032713 | G | A | 2 | a0001c0002t0001g0083 a0001c0020t0001g0112 |
2 | HG02132.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2401+835C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032713 | |||||||
| chr3:69032738 | T | C | 1 | a0001c0001t0011g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2401+810A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032738 | |||||||
| chr3:69032758 | C | T | 2 | a0001c0001t0001g0102 a0001c0020t0001g0112 |
2 | NA18971.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2401+790G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032758 | |||||||
| chr3:69032858 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2401+690C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69032858 | |||||||
| chr3:69033013 | C | A | 1 | a0001c0001t0007g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2401+535G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033013 | |||||||
| chr3:69033080 | A | G | 2 | a0001c0002t0001g0033 a0001c0002t0001g0113 |
3 | NA18949.hp1 NA18993.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.2401+468T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033080 | |||||||
| chr3:69033146 | C | T | 1 | a0002c0003t0005g0054 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2401+402G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033146 | |||||||
| chr3:69033147 | G | A | 2 | a0001c0001t0004g0212 a0001c0001t0004g0217 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2401+401C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033147 | |||||||
| chr3:69033209 | G | A | 1 | a0001c0002t0001g0132 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.2401+339C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033209 | |||||||
| chr3:69033265 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2401+283G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033265 | |||||||
| chr3:69033273 | CA | C | 137 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(134): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.2401+274delT | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033273 | |||||||
| chr3:69033506 | T | C | 66 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(63): Show |
115 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.2401+42A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033506 | |||||||
| chr3:69033518 | T | G | 1 | a0001c0001t0004g0218 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2401+30A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 10/16 | chr3 | 69033518 | |||||||
| chr3:69033709 | A | T | 1 | a0001c0001t0002g0148 | 1 | NA19055.hp1 | splice_region_variant&intron_variant | LOW | c.2245-5T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69033709 | |||||||
| chr3:69033722 | G | T | 61 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(58): Show |
109 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.2245-18C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69033722 | |||||||
| chr3:69033853 | C | CG | 4 | a0001c0001t0002g0147 a0001c0002t0008g0178 a0004c0006t0001g0084 others(1): Show |
4 | HG02683.hp2 HG03098.hp2 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.2245-150dupC | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69033853 | |||||||
| chr3:69033897 | C | G | 1 | a0001c0001t0003g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2245-193G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69033897 | |||||||
| chr3:69034024 | A | G | 84 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(81): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.2245-320T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034024 | |||||||
| chr3:69034106 | C | G | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2245-402G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034106 | |||||||
| chr3:69034292 | G | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0098 |
5 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2245-588C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034292 | |||||||
| chr3:69034298 | C | A | 1 | a0001c0001t0003g0044 | 2 | NA18969.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.2245-594G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034298 | |||||||
| chr3:69034587 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0020t0001g0112 |
5 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+436T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034587 | |||||||
| chr3:69034861 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2244+162C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034861 | |||||||
| chr3:69034911 | G | A | 3 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0020t0001g0112 |
5 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2244+112C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034911 | |||||||
| chr3:69034911 | G | C | 77 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(74): Show |
127 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.2244+112C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034911 | |||||||
| chr3:69034966 | T | C | 3 | a0001c0001t0002g0163 a0001c0001t0002g0164 a0010c0022t0002g0191 |
3 | NA18973.hp2 NA18991.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.2244+57A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69034966 | |||||||
| chr3:69035010 | C | A | 80 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(77): Show |
132 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.2244+13G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 9/16 | chr3 | 69035010 | |||||||
| chr3:69035156 | G | A | 3 | a0001c0001t0020g0051 a0001c0008t0013g0025 a0001c0008t0013g0052 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2152-41C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035156 | |||||||
| chr3:69035283 | T | C | 153 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(150): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.2152-168A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035283 | |||||||
| chr3:69035341 | C | T | 1 | a0001c0001t0002g0036 | 2 | NA18942.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.2152-226G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035341 | |||||||
| chr3:69035342 | G | A | 6 | a0001c0002t0001g0083 a0002c0003t0005g0009 a0002c0003t0005g0053 others(3): Show |
10 | HG01243.hp1 HG02109.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.2152-227C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035342 | |||||||
| chr3:69035383 | T | C | 2 | a0001c0001t0003g0185 a0001c0001t0003g0186 |
2 | HG01255.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.2152-268A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035383 | |||||||
| chr3:69035401 | G | A | 2 | a0001c0005t0014g0189 a0001c0005t0014g0190 |
2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.2152-286C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035401 | |||||||
| chr3:69035522 | G | A | 147 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(144): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2152-407C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035522 | |||||||
| chr3:69035597 | T | C | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01192.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.2152-482A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035597 | |||||||
| chr3:69035639 | T | C | 1 | a0001c0002t0001g0014 | 4 | HG00609.hp1 NA18961.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.2152-524A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035639 | |||||||
| chr3:69035756 | A | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2152-641T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035756 | |||||||
| chr3:69035958 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2152-843T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69035958 | |||||||
| chr3:69036012 | C | CAGTAATA others(4): Show |
75 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(72): Show |
131 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.2152-898_2152-897i others(13): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69036012 | |||||||
| chr3:69036102 | C | A | 1 | a0001c0002t0001g0079 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2152-987G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69036102 | |||||||
| chr3:69036667 | A | G | 1 | a0001c0001t0020g0051 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.2152-1552T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69036667 | |||||||
| chr3:69036694 | C | T | 69 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(66): Show |
125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.2152-1579G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69036694 | |||||||
| chr3:69037012 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2151+1552C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037012 | |||||||
| chr3:69037087 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.2151+1477G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037087 | |||||||
| chr3:69037088 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | NA18980.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.2151+1476C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037088 | |||||||
| chr3:69037197 | T | A | 2 | a0001c0001t0006g0165 a0001c0001t0006g0166 |
2 | NA18970.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.2151+1367A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037197 | |||||||
| chr3:69037216 | C | T | 1 | a0001c0002t0001g0123 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2151+1348G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037216 | |||||||
| chr3:69037310 | C | T | 1 | a0001c0001t0030g0139 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.2151+1254G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037310 | |||||||
| chr3:69037312 | C | T | 72 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(69): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2151+1252G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037312 | |||||||
| chr3:69037322 | A | G | 209 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(206): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.2151+1242T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037322 | |||||||
| chr3:69037535 | G | A | 2 | a0001c0002t0001g0122 a0001c0002t0001g0133 |
2 | NA18978.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2151+1029C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037535 | |||||||
| chr3:69037651 | A | G | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2151+913T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037651 | |||||||
| chr3:69037683 | G | A | 2 | a0001c0002t0001g0008 a0001c0002t0001g0031 |
8 | HG01167.hp1 HG01169.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.2151+881C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037683 | |||||||
| chr3:69037700 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2151+864C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037700 | |||||||
| chr3:69037919 | G | A | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2151+645C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037919 | |||||||
| chr3:69037926 | G | C | 72 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(69): Show |
126 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.2151+638C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69037926 | |||||||
| chr3:69038261 | T | G | 85 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(82): Show |
145 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(142): Show |
intron_variant | MODIFIER | c.2151+303A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69038261 | |||||||
| chr3:69038318 | G | GT | 2 | a0001c0002t0001g0035 a0001c0002t0001g0137 |
3 | HG03669.hp2 HG03710.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.2151+245dupA | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69038318 | |||||||
| chr3:69038497 | T | C | 1 | a0001c0007t0016g0034 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2151+67A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 8/16 | chr3 | 69038497 | |||||||
| chr3:69038795 | C | T | 1 | a0001c0002t0001g0122 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1994+48G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 7/16 | chr3 | 69038795 | |||||||
| chr3:69039107 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0097 a0001c0001t0001g0098 |
5 | HG02257.hp1 HG02622.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1828-98T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039107 | |||||||
| chr3:69039115 | G | T | 1 | a0001c0002t0001g0121 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1828-106C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039115 | |||||||
| chr3:69039294 | G | A | 1 | a0001c0001t0004g0219 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1827+257C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039294 | |||||||
| chr3:69039311 | G | A | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1827+240C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039311 | |||||||
| chr3:69039332 | C | G | 1 | a0002c0003t0005g0053 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1827+219G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039332 | |||||||
| chr3:69039333 | C | T | 1 | a0001c0002t0001g0080 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1827+218G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039333 | |||||||
| chr3:69039382 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1827+169C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 6/16 | chr3 | 69039382 | |||||||
| chr3:69039767 | T | TC | 86 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(83): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.1685-75_1685-74ins others(1): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69039767 | |||||||
| chr3:69039791 | T | C | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1685-98A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69039791 | |||||||
| chr3:69039793 | T | C | 79 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(76): Show |
133 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1685-100A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69039793 | |||||||
| chr3:69039966 | C | A | 1 | a0001c0001t0001g0026 | 2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1685-273G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69039966 | |||||||
| chr3:69040039 | T | C | 1 | a0001c0001t0002g0167 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1685-346A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040039 | |||||||
| chr3:69040063 | T | G | 1 | a0001c0001t0003g0220 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1685-370A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040063 | |||||||
| chr3:69040280 | A | T | 5 | a0001c0002t0001g0018 a0001c0002t0001g0078 a0001c0002t0001g0079 others(2): Show |
7 | NA18942.hp1 NA18945.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.1685-587T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040280 | |||||||
| chr3:69040405 | C | T | 1 | a0001c0001t0017g0045 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1685-712G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040405 | |||||||
| chr3:69040426 | T | C | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | NA18957.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1685-733A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040426 | |||||||
| chr3:69040692 | C | G | 1 | a0001c0001t0002g0146 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1685-999G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040692 | |||||||
| chr3:69040696 | C | T | 65 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(62): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1685-1003G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040696 | |||||||
| chr3:69040787 | T | C | 1 | a0001c0001t0006g0168 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1685-1094A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040787 | |||||||
| chr3:69040813 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0077 |
3 | NA19065.hp2 NA19079.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1685-1120A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040813 | |||||||
| chr3:69040850 | A | C | 1 | a0001c0002t0001g0120 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1685-1157T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040850 | |||||||
| chr3:69040921 | CA | C | 7 | a0001c0001t0001g0099 a0001c0001t0002g0145 a0001c0001t0002g0171 others(4): Show |
8 | HG00639.hp2 HG01169.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1685-1229delT | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040921 | |||||||
| chr3:69040937 | A | T | 2 | a0001c0001t0002g0143 a0001c0001t0002g0144 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1685-1244T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040937 | |||||||
| chr3:69040953 | C | T | 1 | a0001c0001t0003g0197 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1685-1260G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69040953 | |||||||
| chr3:69041325 | C | G | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1684+1482G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69041325 | |||||||
| chr3:69041348 | T | G | 2 | a0001c0002t0001g0086 a0001c0002t0001g0087 |
2 | NA18950.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1684+1459A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69041348 | |||||||
| chr3:69041392 | G | A | 6 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0222 others(3): Show |
7 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1684+1415C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69041392 | |||||||
| chr3:69041413 | T | A | 65 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(62): Show |
111 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1684+1394A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69041413 | |||||||
| chr3:69041646 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1684+1161C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69041646 | |||||||
| chr3:69042057 | G | T | 73 | a0001c0001t0002g0017 a0001c0001t0002g0028 a0001c0001t0002g0029 others(70): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1684+750C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042057 | |||||||
| chr3:69042086 | C | G | 67 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(64): Show |
115 | HG00099.hp2 HG00280.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1684+721G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042086 | |||||||
| chr3:69042091 | C | T | 1 | a0001c0001t0004g0211 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1684+716G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042091 | |||||||
| chr3:69042125 | C | G | 1 | a0001c0001t0003g0210 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1684+682G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042125 | |||||||
| chr3:69042174 | T | C | 1 | a0001c0001t0002g0170 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1684+633A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042174 | |||||||
| chr3:69042187 | C | T | 1 | a0001c0002t0008g0177 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1684+620G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042187 | |||||||
| chr3:69042489 | C | T | 211 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(208): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1684+318G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042489 | |||||||
| chr3:69042545 | C | T | 1 | a0001c0002t0008g0176 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1684+262G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042545 | |||||||
| chr3:69042565 | T | C | 35 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0035 others(32): Show |
72 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1684+242A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 5/16 | chr3 | 69042565 | |||||||
| chr3:69043312 | C | T | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1579-400G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 4/16 | chr3 | 69043312 | |||||||
| chr3:69043367 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1578+383C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 4/16 | chr3 | 69043367 | |||||||
| chr3:69043605 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1578+145G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 4/16 | chr3 | 69043605 | |||||||
| chr3:69044010 | T | C | 2 | a0001c0001t0002g0171 a0001c0001t0002g0172 |
2 | NA18963.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1452-134A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044010 | |||||||
| chr3:69044035 | A | G | 3 | a0001c0001t0020g0051 a0001c0008t0013g0025 a0001c0008t0013g0052 |
4 | HG02559.hp2 HG02970.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1452-159T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044035 | |||||||
| chr3:69044078 | T | C | 1 | a0001c0012t0002g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1452-202A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044078 | |||||||
| chr3:69044121 | A | C | 1 | a0001c0002t0001g0118 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1452-245T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044121 | |||||||
| chr3:69044164 | A | G | 76 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(73): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1452-288T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044164 | |||||||
| chr3:69044226 | C | T | 76 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(73): Show |
128 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.1451+266G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044226 | |||||||
| chr3:69044240 | A | G | 74 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(71): Show |
124 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.1451+252T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044240 | |||||||
| chr3:69044241 | T | A | 1 | a0001c0001t0004g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1451+251A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044241 | |||||||
| chr3:69044447 | T | C | 178 | a0001c0001t0001g0005 a0001c0001t0001g0019 a0001c0001t0001g0026 others(175): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1451+45A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 3/16 | chr3 | 69044447 | |||||||
| chr3:69044627 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-32C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044627 | |||||||
| chr3:69044646 | C | T | 1 | a0001c0001t0010g0205 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1348-51G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044646 | |||||||
| chr3:69044671 | G | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0020t0001g0112 others(5): Show |
14 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1348-76C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044671 | |||||||
| chr3:69044846 | T | C | 82 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(79): Show |
140 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.1348-251A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044846 | |||||||
| chr3:69044858 | T | C | 1 | a0004c0006t0001g0088 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1348-263A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044858 | |||||||
| chr3:69044953 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-358G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69044953 | |||||||
| chr3:69045049 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-454C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045049 | |||||||
| chr3:69045055 | T | G | 1 | a0001c0001t0003g0224 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1348-460A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045055 | |||||||
| chr3:69045154 | T | C | 1 | a0001c0002t0001g0014 | 4 | HG00609.hp1 NA18961.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.1348-559A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045154 | |||||||
| chr3:69045165 | A | C | 1 | a0001c0001t0002g0142 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1348-570T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045165 | |||||||
| chr3:69045288 | T | C | 1 | a0001c0002t0001g0089 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1348-693A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045288 | |||||||
| chr3:69045393 | G | A | 1 | a0001c0001t0003g0202 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1348-798C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045393 | |||||||
| chr3:69045413 | C | A | 8 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0020t0001g0112 others(5): Show |
14 | HG00735.hp1 HG01243.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1348-818G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045413 | |||||||
| chr3:69045573 | A | C | 1 | a0001c0002t0001g0078 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1348-978T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045573 | |||||||
| chr3:69045678 | G | C | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1348-1083C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045678 | |||||||
| chr3:69045741 | C | T | 2 | a0001c0007t0016g0034 a0001c0007t0025g0111 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1348-1146G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045741 | |||||||
| chr3:69045743 | C | T | 77 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(74): Show |
134 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.1348-1148G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045743 | |||||||
| chr3:69045849 | C | A | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1348-1254G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045849 | |||||||
| chr3:69045920 | G | A | 1 | a0001c0001t0002g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1348-1325C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045920 | |||||||
| chr3:69045934 | T | C | 1 | a0001c0001t0009g0225 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1348-1339A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045934 | |||||||
| chr3:69045961 | T | A | 5 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(2): Show |
9 | HG00735.hp2 HG01261.hp2 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.1348-1366A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69045961 | |||||||
| chr3:69046123 | C | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+1235G>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046123 | |||||||
| chr3:69046205 | G | T | 1 | a0001c0001t0002g0066 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1347+1153C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046205 | |||||||
| chr3:69046218 | T | A | 1 | a0001c0001t0002g0175 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1347+1140A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046218 | |||||||
| chr3:69046274 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+1084C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046274 | |||||||
| chr3:69046303 | T | TAA | 155 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(152): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1347+1054_1347+105 others(6): Show |
TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046303 | |||||||
| chr3:69046591 | T | C | 1 | a0001c0001t0004g0226 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1347+767A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046591 | |||||||
| chr3:69046600 | T | C | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0076 others(1): Show |
6 | HG00438.hp2 NA18983.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.1347+758A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046600 | |||||||
| chr3:69046813 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0001g0030 |
4 | HG00735.hp1 HG02615.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1347+545T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69046813 | |||||||
| chr3:69047143 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1347+215C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69047143 | |||||||
| chr3:69047289 | A | G | 2 | a0005c0010t0003g0050 a0013c0011t0003g0228 |
3 | HG03209.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1347+69T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 2/16 | chr3 | 69047289 | |||||||
| chr3:69048888 | C | T | 1 | a0001c0001t0003g0115 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.143-326G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69048888 | |||||||
| chr3:69049032 | T | C | 1 | a0001c0002t0001g0137 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.143-470A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049032 | |||||||
| chr3:69049150 | C | T | 1 | a0001c0002t0001g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.143-588G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049150 | |||||||
| chr3:69049215 | A | T | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-653T>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049215 | |||||||
| chr3:69049278 | G | A | 1 | a0001c0002t0001g0110 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.143-716C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049278 | |||||||
| chr3:69049284 | A | G | 76 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0002g0002 others(73): Show |
132 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.143-722T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049284 | |||||||
| chr3:69049329 | A | C | 2 | a0001c0001t0003g0023 a0001c0001t0003g0044 |
5 | NA18969.hp2 NA18972.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.143-767T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049329 | |||||||
| chr3:69049358 | A | G | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-796T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049358 | |||||||
| chr3:69049408 | G | T | 1 | a0001c0001t0003g0141 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.143-846C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049408 | |||||||
| chr3:69049570 | T | C | 2 | a0001c0007t0016g0034 a0001c0007t0025g0111 |
3 | HG02717.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.143-1008A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049570 | |||||||
| chr3:69049676 | C | T | 1 | a0001c0001t0002g0140 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.143-1114G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049676 | |||||||
| chr3:69049788 | A | C | 86 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0020 others(83): Show |
146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.143-1226T>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049788 | |||||||
| chr3:69049857 | G | C | 1 | a0001c0020t0001g0112 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.143-1295C>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69049857 | |||||||
| chr3:69050128 | C | T | 4 | a0001c0001t0003g0206 a0001c0001t0003g0207 a0001c0001t0010g0022 others(1): Show |
6 | HG00423.hp1 HG00544.hp2 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.143-1566G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050128 | |||||||
| chr3:69050177 | T | A | 3 | a0001c0001t0007g0061 a0001c0001t0007g0062 a0001c0017t0007g0060 |
3 | HG00323.hp2 HG01167.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.143-1615A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050177 | |||||||
| chr3:69050216 | C | G | 2 | a0001c0001t0003g0203 a0001c0001t0003g0204 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.143-1654G>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050216 | |||||||
| chr3:69050259 | C | CA | 10 | a0001c0001t0001g0114 a0001c0001t0002g0040 a0001c0001t0003g0049 others(7): Show |
13 | HG01074.hp2 HG02145.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.142+1685dupT | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050259 | |||||||
| chr3:69050281 | A | G | 1 | a0001c0001t0002g0192 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.142+1664T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050281 | |||||||
| chr3:69050400 | A | G | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+1545T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050400 | |||||||
| chr3:69050419 | T | C | 1 | a0010c0022t0002g0191 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.142+1526A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050419 | |||||||
| chr3:69050486 | T | G | 2 | a0001c0001t0002g0192 a0001c0001t0002g0193 |
2 | NA18959.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.142+1459A>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050486 | |||||||
| chr3:69050574 | C | T | 1 | a0001c0001t0030g0139 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.142+1371G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050574 | |||||||
| chr3:69050595 | G | A | 57 | a0001c0001t0003g0003 a0001c0001t0003g0013 a0001c0001t0003g0023 others(54): Show |
98 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(95): Show |
intron_variant | MODIFIER | c.142+1350C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050595 | |||||||
| chr3:69050728 | T | C | 2 | a0001c0008t0013g0025 a0001c0008t0013g0052 |
3 | HG02559.hp2 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.142+1217A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050728 | |||||||
| chr3:69050785 | T | C | 26 | a0001c0002t0001g0001 a0001c0002t0001g0014 a0001c0002t0001g0035 others(23): Show |
59 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.142+1160A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050785 | |||||||
| chr3:69050927 | A | G | 1 | a0001c0001t0009g0196 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.142+1018T>C | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050927 | |||||||
| chr3:69050957 | T | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0027 others(68): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.142+988A>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050957 | |||||||
| chr3:69050985 | T | C | 1 | a0001c0001t0018g0041 | 2 | HG02486.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.142+960A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69050985 | |||||||
| chr3:69051044 | G | T | 5 | a0001c0001t0003g0042 a0001c0001t0003g0043 a0001c0001t0011g0021 others(2): Show |
9 | HG01884.hp2 HG01952.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.142+901C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051044 | |||||||
| chr3:69051218 | T | C | 2 | a0005c0010t0003g0050 a0013c0011t0003g0228 |
3 | HG03209.hp1 HG03486.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.142+727A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051218 | |||||||
| chr3:69051234 | T | C | 2 | a0001c0001t0007g0064 a0001c0001t0022g0063 |
2 | HG03490.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.142+711A>G | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051234 | |||||||
| chr3:69051249 | G | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0066 a0001c0001t0002g0067 others(2): Show |
6 | HG00642.hp2 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.142+696C>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051249 | |||||||
| chr3:69051383 | G | A | 1 | a0001c0001t0003g0229 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.142+562C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051383 | |||||||
| chr3:69051397 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG02615.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.142+548G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051397 | |||||||
| chr3:69051480 | C | T | 1 | a0001c0012t0002g0065 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.142+465G>A | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051480 | |||||||
| chr3:69051739 | G | A | 63 | a0001c0001t0003g0003 a0001c0001t0003g0004 a0001c0001t0003g0013 others(60): Show |
112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.142+206C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051739 | |||||||
| chr3:69051820 | G | A | 5 | a0002c0003t0005g0009 a0002c0003t0005g0053 a0002c0003t0005g0054 others(2): Show |
9 | HG01243.hp1 HG02109.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.142+125C>T | TMF1 | ENSG00000144747.17 | transcript | ENST00000398559.7 | protein_coding | 1/16 | chr3 | 69051820 |