Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7270 |
| ensemblid | ENSG00000125482.13 |
| hgncid | 12397 |
| symbol | TTF1 |
| name | transcription termination factor 1 |
| refseq_nuc | NM_007344.4 |
| refseq_prot | NP_031370.2 |
| ensembl_nuc | ENST00000334270.3 |
| ensembl_prot | ENSP00000333920.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 132375548 |
| end | 132406840 |
| strand | - |
| ver | v1.2 |
| region | chr9:132375548-132406840 |
| region5000 | chr9:132370548-132411840 |
| regionname0 | TTF1_chr9_132375548_132406840 |
| regionname5000 | TTF1_chr9_132370548_132411840 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 905 | 215 | 64 | 37 | 77 | 11 | 24 | 61 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0002 | 0/0 | 905 | 66 | 6 | 6 | 48 | 2 | 4 | 40 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0003 | 0/0 | 905 | 52 | 0 | 4 | 45 | 0 | 3 | 37 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0004 | 0/0 | 905 | 32 | 5 | 7 | 12 | 2 | 6 | 9 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0005 | 0/0 | 905 | 16 | 1 | 2 | 8 | 1 | 4 | 8 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0006 | 0/0 | 905 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0007 | 0/0 | 905 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0008 | 0/0 | 905 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0009 | 0/0 | 905 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0010 | 0/0 | 905 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0011 | 0/0 | 905 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0012 | 0/0 | 901 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(896): Show |
chr9 | 132370548 | 132411840 |
| a0013 | 0/0 | 905 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| a0014 | 0/0 | 869 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(864): Show |
chr9 | 132370548 | 132411840 |
| a0015 | 0/0 | 905 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | MEGES others(900): Show |
chr9 | 132370548 | 132411840 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2715 | 165 | 35 | 32 | 68 | 8 | 21 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0005 | 0/0 | 2715 | 24 | 12 | 3 | 7 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0007 | 1/0 | 2715 | 9 | 7 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0009 | 0/0 | 2715 | 5 | 5 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0010 | 0/0 | 2715 | 4 | 4 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0013 | 0/0 | 2715 | 3 | 0 | 1 | 0 | 1 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0014 | 0/0 | 2715 | 2 | 0 | 0 | 0 | 2 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0018 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0022 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0001c0023 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0002c0002 | 0/0 | 2715 | 66 | 6 | 6 | 48 | 2 | 4 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0003c0003 | 0/0 | 2715 | 52 | 0 | 4 | 45 | 0 | 3 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0004c0004 | 0/0 | 2715 | 32 | 5 | 7 | 12 | 2 | 6 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0005c0006 | 0/0 | 2715 | 12 | 1 | 0 | 8 | 0 | 3 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0005c0011 | 0/0 | 2715 | 4 | 0 | 2 | 0 | 1 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0006c0008 | 0/0 | 2715 | 6 | 6 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0007c0012 | 0/0 | 2715 | 3 | 3 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0008c0015 | 0/0 | 2715 | 2 | 1 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0009c0016 | 0/0 | 2715 | 2 | 0 | 0 | 0 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0010c0025 | 0/0 | 2715 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0011c0024 | 0/0 | 2715 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0012c0017 | 0/0 | 2703 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2698): Show |
chr9 | 132370548 | 132411840 | ||
| a0013c0020 | 0/0 | 2715 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 | ||
| a0014c0021 | 0/0 | 2693 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2688): Show |
chr9 | 132370548 | 132411840 | ||
| a0015c0019 | 0/0 | 2715 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | ATGGA others(2710): Show |
chr9 | 132370548 | 132411840 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3143 | 160 | 31 | 31 | 68 | 8 | 21 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0001t0002 | 0/0 | 3143 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0001t0003 | 0/0 | 3143 | 4 | 4 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0005t0002 | 0/0 | 3143 | 24 | 12 | 3 | 7 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0007t0002 | 0/0 | 3143 | 4 | 3 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0007t0004 | 1/0 | 3143 | 2 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0007t0005 | 0/0 | 3145 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3140): Show |
chr9 | 132370548 | 132411840 |
| a0001c0007t0006 | 0/0 | 3145 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3140): Show |
chr9 | 132370548 | 132411840 |
| a0001c0009t0001 | 0/0 | 3143 | 5 | 5 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0010t0002 | 0/0 | 3143 | 4 | 4 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0013t0001 | 0/0 | 3143 | 3 | 0 | 1 | 0 | 1 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0014t0001 | 0/0 | 3143 | 2 | 0 | 0 | 0 | 2 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0018t0001 | 0/0 | 3143 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0022t0002 | 0/0 | 3143 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0001c0023t0002 | 0/0 | 3143 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0002c0002t0001 | 0/0 | 3143 | 8 | 6 | 2 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0002c0002t0002 | 0/0 | 3143 | 58 | 0 | 4 | 48 | 2 | 4 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0003c0003t0002 | 0/0 | 3143 | 52 | 0 | 4 | 45 | 0 | 3 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0004c0004t0002 | 0/0 | 3143 | 32 | 5 | 7 | 12 | 2 | 6 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0005c0006t0001 | 0/0 | 3143 | 12 | 1 | 0 | 8 | 0 | 3 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0005c0011t0001 | 0/0 | 3143 | 4 | 0 | 2 | 0 | 1 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0006c0008t0001 | 0/0 | 3143 | 6 | 6 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0007c0012t0002 | 0/0 | 3143 | 3 | 3 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0008c0015t0001 | 0/0 | 3143 | 2 | 1 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0009c0016t0002 | 0/0 | 3143 | 2 | 0 | 0 | 0 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0010c0025t0002 | 0/0 | 3143 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0011c0024t0002 | 0/0 | 3143 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0012c0017t0001 | 0/0 | 3131 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3126): Show |
chr9 | 132370548 | 132411840 |
| a0013c0020t0001 | 0/0 | 3143 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| a0014c0021t0001 | 0/0 | 3121 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3116): Show |
chr9 | 132370548 | 132411840 |
| a0015c0019t0001 | 0/0 | 3143 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | CTCAA others(3138): Show |
chr9 | 132370548 | 132411840 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 2 | 7 | 6 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0003 | 0/0 | 12 | 0 | 1 | 10 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 7 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 5 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0015 | 0/0 | 4 | 1 | 1 | 0 | 1 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0049 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0173 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0003g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0001t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0005t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0002g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0004g0132 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0007t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0009t0001g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0009t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0009t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0009t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0010t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0010t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0010t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0013t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0013t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0013t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0014t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0018t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0022t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0001c0023t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0004 | 0/0 | 9 | 0 | 2 | 6 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0010 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0002 | 0/0 | 13 | 0 | 3 | 8 | 0 | 2 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0022 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0023 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0004c0004t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0051 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0006t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0011t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0011t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0005c0011t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0006c0008t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0006c0008t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0006c0008t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0006c0008t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0006c0008t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0007c0012t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0007c0012t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0007c0012t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0008c0015t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0008c0015t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0009c0016t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0009c0016t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0010c0025t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0011c0024t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0012c0017t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0013c0020t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0014c0021t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| a0015c0019t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | GBR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0113 | EUR | GBR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0147 | EUR | GBR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00280 | hp2 | a0005 | c0011 | t0001 | g0233 | EUR | FIN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0121 | EUR | FIN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0209 | EUR | FIN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00544 | hp1 | a0003 | c0003 | t0002 | g0092 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00544 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00558 | hp2 | a0004 | c0004 | t0002 | g0014 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00597 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00639 | hp1 | a0004 | c0004 | t0002 | g0078 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00639 | hp2 | a0004 | c0004 | t0002 | g0101 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00673 | hp1 | a0004 | c0004 | t0002 | g0014 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00673 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | CHS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00735 | hp2 | a0001 | c0005 | t0002 | g0064 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00741 | hp1 | a0002 | c0002 | t0002 | g0114 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01074 | hp1 | a0004 | c0004 | t0002 | g0037 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01099 | hp1 | a0001 | c0005 | t0002 | g0062 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01167 | hp1 | a0001 | c0005 | t0002 | g0060 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01167 | hp2 | a0004 | c0004 | t0002 | g0023 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01169 | hp2 | a0004 | c0004 | t0002 | g0023 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01175 | hp1 | a0004 | c0004 | t0002 | g0037 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01175 | hp2 | a0001 | c0013 | t0001 | g0163 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01192 | hp1 | a0002 | c0002 | t0001 | g0141 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01243 | hp1 | a0005 | c0011 | t0001 | g0050 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01256 | hp2 | a0005 | c0011 | t0001 | g0050 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01361 | hp2 | a0010 | c0025 | t0002 | g0128 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0245 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01433 | hp2 | a0008 | c0015 | t0001 | g0250 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0186 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01515 | hp2 | a0001 | c0014 | t0001 | g0040 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01516 | hp2 | a0004 | c0004 | t0002 | g0030 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01517 | hp1 | a0004 | c0004 | t0002 | g0030 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01517 | hp2 | a0001 | c0014 | t0001 | g0040 | EUR | IBS | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01884 | hp2 | a0006 | c0008 | t0001 | g0041 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01928 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01943 | hp2 | a0001 | c0007 | t0002 | g0017 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01952 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01978 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01981 | hp1 | a0004 | c0004 | t0002 | g0022 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG01993 | hp2 | a0003 | c0003 | t0002 | g0089 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02015 | hp2 | a0011 | c0024 | t0002 | g0093 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02027 | hp2 | a0003 | c0003 | t0002 | g0031 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02055 | hp1 | a0006 | c0008 | t0001 | g0041 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02055 | hp2 | a0008 | c0015 | t0001 | g0206 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02074 | hp2 | a0004 | c0004 | t0002 | g0099 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02080 | hp1 | a0003 | c0003 | t0002 | g0031 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0090 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02135 | hp1 | a0001 | c0022 | t0002 | g0072 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02135 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02145 | hp2 | a0001 | c0005 | t0002 | g0018 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CDX | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02257 | hp1 | a0001 | c0005 | t0002 | g0018 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02258 | hp2 | a0006 | c0008 | t0001 | g0176 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02280 | hp1 | a0004 | c0004 | t0002 | g0098 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02280 | hp2 | a0001 | c0010 | t0002 | g0138 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02293 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02451 | hp1 | a0012 | c0017 | t0001 | g0159 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02451 | hp2 | a0007 | c0012 | t0002 | g0135 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0035 | EAS | KHV | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02572 | hp2 | a0001 | c0005 | t0002 | g0071 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02602 | hp2 | a0004 | c0004 | t0002 | g0106 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02615 | hp1 | a0006 | c0008 | t0001 | g0174 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02615 | hp2 | a0001 | c0005 | t0002 | g0063 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02622 | hp1 | a0001 | c0010 | t0002 | g0038 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02622 | hp2 | a0004 | c0004 | t0002 | g0105 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02630 | hp2 | a0001 | c0009 | t0001 | g0043 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02698 | hp2 | a0001 | c0005 | t0002 | g0065 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02735 | hp2 | a0004 | c0004 | t0002 | g0096 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02738 | hp1 | a0009 | c0016 | t0002 | g0094 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02809 | hp1 | a0001 | c0005 | t0002 | g0066 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02818 | hp1 | a0001 | c0007 | t0006 | g0167 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02886 | hp1 | a0001 | c0009 | t0001 | g0043 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02886 | hp2 | a0001 | c0009 | t0001 | g0222 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02895 | hp1 | a0001 | c0005 | t0002 | g0018 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0225 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02896 | hp2 | a0001 | c0005 | t0002 | g0061 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02922 | hp1 | a0001 | c0005 | t0002 | g0028 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02922 | hp2 | a0001 | c0007 | t0004 | g0131 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02965 | hp2 | a0004 | c0004 | t0002 | g0129 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02970 | hp1 | a0001 | c0005 | t0002 | g0029 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02970 | hp2 | a0001 | c0007 | t0002 | g0133 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02976 | hp1 | a0005 | c0006 | t0001 | g0232 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03017 | hp2 | a0001 | c0005 | t0002 | g0069 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03041 | hp1 | a0001 | c0007 | t0002 | g0017 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03041 | hp2 | a0001 | c0007 | t0005 | g0258 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03098 | hp1 | a0007 | c0012 | t0002 | g0134 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03098 | hp2 | a0007 | c0012 | t0002 | g0136 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03139 | hp2 | a0006 | c0008 | t0001 | g0226 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03209 | hp1 | a0001 | c0005 | t0002 | g0057 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03209 | hp2 | a0006 | c0008 | t0001 | g0175 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03225 | hp1 | a0001 | c0005 | t0002 | g0028 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03453 | hp2 | a0004 | c0004 | t0002 | g0104 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03492 | hp2 | a0003 | c0003 | t0002 | g0021 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03516 | hp1 | a0001 | c0005 | t0002 | g0029 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | GWD | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03579 | hp1 | a0001 | c0010 | t0002 | g0038 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03654 | hp2 | a0005 | c0006 | t0001 | g0051 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0002 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03669 | hp2 | a0005 | c0011 | t0001 | g0234 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03688 | hp1 | a0004 | c0004 | t0002 | g0102 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03710 | hp2 | a0004 | c0004 | t0002 | g0022 | SAS | PJL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03834 | hp1 | a0004 | c0004 | t0002 | g0023 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03942 | hp1 | a0001 | c0013 | t0001 | g0162 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04115 | hp1 | a0005 | c0006 | t0001 | g0237 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04115 | hp2 | a0009 | c0016 | t0002 | g0075 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04199 | hp2 | a0004 | c0004 | t0002 | g0097 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04204 | hp2 | a0005 | c0006 | t0001 | g0236 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0116 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18906 | hp1 | a0001 | c0007 | t0002 | g0017 | AFR | YRI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | YRI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18940 | hp1 | a0003 | c0003 | t0002 | g0130 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18940 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18941 | hp2 | a0002 | c0002 | t0002 | g0120 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18942 | hp1 | a0003 | c0003 | t0002 | g0033 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18943 | hp2 | a0003 | c0003 | t0002 | g0086 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18944 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18945 | hp1 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18950 | hp2 | a0005 | c0006 | t0001 | g0240 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18951 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18953 | hp1 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18954 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18961 | hp1 | a0003 | c0003 | t0002 | g0080 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0084 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18964 | hp2 | a0001 | c0005 | t0002 | g0068 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18966 | hp1 | a0005 | c0006 | t0001 | g0230 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18967 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18967 | hp2 | a0003 | c0003 | t0002 | g0091 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18968 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18968 | hp2 | a0001 | c0005 | t0002 | g0070 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18969 | hp1 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18970 | hp2 | a0005 | c0006 | t0001 | g0235 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18974 | hp2 | a0003 | c0003 | t0002 | g0085 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18975 | hp2 | a0003 | c0003 | t0002 | g0020 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18977 | hp1 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18979 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18981 | hp1 | a0005 | c0006 | t0001 | g0052 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18981 | hp2 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18983 | hp1 | a0003 | c0003 | t0002 | g0083 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0016 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18985 | hp1 | a0002 | c0002 | t0002 | g0110 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18986 | hp2 | a0003 | c0003 | t0002 | g0088 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18987 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18989 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18990 | hp2 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18992 | hp2 | a0005 | c0006 | t0001 | g0239 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18994 | hp2 | a0001 | c0005 | t0002 | g0012 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18995 | hp1 | a0004 | c0004 | t0002 | g0095 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18995 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18997 | hp2 | a0001 | c0005 | t0002 | g0067 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18998 | hp1 | a0003 | c0003 | t0002 | g0055 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18998 | hp2 | a0001 | c0023 | t0002 | g0073 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18999 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19000 | hp1 | a0004 | c0004 | t0002 | g0014 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19000 | hp2 | a0003 | c0003 | t0002 | g0032 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19007 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19009 | hp1 | a0005 | c0006 | t0001 | g0052 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0087 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19010 | hp2 | a0003 | c0003 | t0002 | g0082 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19011 | hp2 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19043 | hp2 | a0001 | c0018 | t0001 | g0231 | AFR | LWK | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19054 | hp2 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19058 | hp1 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19063 | hp2 | a0005 | c0006 | t0001 | g0238 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19064 | hp2 | a0004 | c0004 | t0002 | g0014 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19065 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19070 | hp2 | a0005 | c0006 | t0001 | g0051 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19072 | hp1 | a0003 | c0003 | t0002 | g0020 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19074 | hp1 | a0004 | c0004 | t0002 | g0100 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19081 | hp2 | a0004 | c0004 | t0002 | g0103 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19082 | hp1 | a0003 | c0003 | t0002 | g0019 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19083 | hp1 | a0014 | c0021 | t0001 | g0152 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19083 | hp2 | a0003 | c0003 | t0002 | g0081 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19085 | hp1 | a0003 | c0003 | t0002 | g0021 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19086 | hp1 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19086 | hp2 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19087 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19090 | hp1 | a0003 | c0003 | t0002 | g0009 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19091 | hp2 | a0003 | c0003 | t0002 | g0033 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19240 | hp1 | a0001 | c0009 | t0001 | g0194 | AFR | YRI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0224 | AFR | YRI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ASW | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ASW | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20752 | hp2 | a0001 | c0013 | t0001 | g0161 | EUR | TSI | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20905 | hp1 | a0015 | c0019 | t0001 | g0168 | SAS | GIH | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | GIH | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02559 | hp1 | a0004 | c0004 | t0002 | g0022 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03471 | hp1 | a0001 | c0009 | t0001 | g0218 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG03471 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | USA | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| HG06807 | hp2 | a0013 | c0020 | t0001 | g0157 | AFR | USA | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18955 | hp1 | a0004 | c0004 | t0002 | g0013 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | USA | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA20300 | hp2 | a0001 | c0010 | t0002 | g0137 | AFR | USA | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA21309 | hp1 | a0001 | c0007 | t0005 | g0259 | AFR | LWK | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0173 | REF | REF | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| homoSapiens | grch38p0 | a0001 | c0007 | t0004 | g0132 | REF | REF | TTF1_chr9_132370548_132411840 | TTF1 | chr9 | 132370548 | 132411840 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132375966 | AGCCATGC others(5): Show |
A | 1 | a0012 | 1 | HG02451.hp1 | disruptive_inframe_deletion | MODERATE | c.2655_2666delGCCATG others(6): Show |
p.Pro886_Ala889del | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 2724/3143 | 2655/2718 | 885/905 | chr9 | 132375966 | |||
| chr9:132375979 | G | A | 1 | a0008 | 2 | HG01433.hp2 HG02055.hp2 |
missense_variant | MODERATE | c.2654C>T | p.Ala885Val | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 2712/3143 | 2654/2718 | 885/905 | chr9 | 132375979 | |||
| chr9:132376024 | TCTTCATA others(15): Show |
T | 1 | a0014 | 1 | NA19083.hp1 | frameshift_variant | HIGH | c.2587_2608delCGAGAC others(16): Show |
p.Arg863fs | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 2666/3143 | 2587/2718 | 863/905 | chr9 | 132376024 | |||
| chr9:132379139 | A | G | 1 | a0013 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.2384T>C | p.Val795Ala | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/11 | 2442/3143 | 2384/2718 | 795/905 | chr9 | 132379139 | |||
| chr9:132386596 | T | C | 1 | a0009 | 2 | HG02738.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.2338A>G | p.Thr780Ala | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/11 | 2396/3143 | 2338/2718 | 780/905 | chr9 | 132386596 | |||
| chr9:132398210 | C | G | 2 | a0006 a0013 |
7 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(4): Show |
missense_variant | MODERATE | c.1708G>C | p.Asp570His | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/11 | 1766/3143 | 1708/2718 | 570/905 | chr9 | 132398210 | |||
| chr9:132400205 | A | G | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.1421T>C | p.Ile474Thr | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/11 | 1479/3143 | 1421/2718 | 474/905 | chr9 | 132400205 | |||
| chr9:132400209 | C | T | 1 | a0010 | 1 | HG01361.hp2 | missense_variant | MODERATE | c.1417G>A | p.Glu473Lys | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/11 | 1475/3143 | 1417/2718 | 473/905 | chr9 | 132400209 | |||
| chr9:132400231 | A | C | 1 | a0015 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1395T>G | p.Asn465Lys | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/11 | 1453/3143 | 1395/2718 | 465/905 | chr9 | 132400231 | |||
| chr9:132401570 | G | T | 2 | a0009 a0011 |
3 | HG02015.hp2 HG02738.hp1 HG04115.hp2 |
missense_variant | MODERATE | c.1252C>A | p.Leu418Ile | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1310/3143 | 1252/2718 | 418/905 | chr9 | 132401570 | |||
| chr9:132401620 | C | T | 1 | a0005 | 16 | HG00280.hp2 HG01243.hp1 HG01256.hp2 others(13): Show |
missense_variant | MODERATE | c.1202G>A | p.Arg401Gln | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1260/3143 | 1202/2718 | 401/905 | chr9 | 132401620 | |||
| chr9:132401743 | C | A | 1 | a0002 | 66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
missense_variant | MODERATE | c.1079G>T | p.Gly360Val | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1137/3143 | 1079/2718 | 360/905 | chr9 | 132401743 | |||
| chr9:132401882 | C | G | 1 | a0007 | 3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
missense_variant | MODERATE | c.940G>C | p.Val314Leu | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 998/3143 | 940/2718 | 314/905 | chr9 | 132401882 | |||
| chr9:132401914 | A | G | 1 | a0003 | 52 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(49): Show |
missense_variant | MODERATE | c.908T>C | p.Val303Ala | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 966/3143 | 908/2718 | 303/905 | chr9 | 132401914 | |||
| chr9:132401954 | C | A | 5 | a0003 a0004 a0009 others(2): Show |
88 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
missense_variant | MODERATE | c.868G>T | p.Ala290Ser | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 926/3143 | 868/2718 | 290/905 | chr9 | 132401954 | |||
| chr9:132402014 | T | C | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.808A>G | p.Thr270Ala | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 866/3143 | 808/2718 | 270/905 | chr9 | 132402014 | |||
| chr9:132402065 | A | G | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.757T>C | p.Ser253Pro | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 815/3143 | 757/2718 | 253/905 | chr9 | 132402065 | |||
| chr9:132402087 | C | A | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.735G>T | p.Glu245Asp | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 793/3143 | 735/2718 | 245/905 | chr9 | 132402087 | |||
| chr9:132402136 | C | T | 1 | a0012 | 1 | HG02451.hp1 | missense_variant | MODERATE | c.686G>A | p.Arg229Gln | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 744/3143 | 686/2718 | 229/905 | chr9 | 132402136 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132388186 | G | T | 18 | a0001c0001 a0001c0005 a0001c0013 others(15): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
synonymous_variant | LOW | c.2265C>A | p.Ile755Ile | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/11 | 2323/3143 | 2265/2718 | 755/905 | chr9 | 132388186 | |||
| chr9:132390626 | G | C | 1 | a0012c0017 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.2193C>G | p.Thr731Thr | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/11 | 2251/3143 | 2193/2718 | 731/905 | chr9 | 132390626 | |||
| chr9:132392191 | A | G | 1 | a0015c0019 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1872T>C | p.Asp624Asp | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/11 | 1930/3143 | 1872/2718 | 624/905 | chr9 | 132392191 | |||
| chr9:132398214 | G | A | 1 | a0001c0022 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1704C>T | p.Tyr568Tyr | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/11 | 1762/3143 | 1704/2718 | 568/905 | chr9 | 132398214 | |||
| chr9:132398220 | C | G | 13 | a0001c0001 a0001c0009 a0001c0013 others(10): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
synonymous_variant | LOW | c.1698G>C | p.Leu566Leu | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/11 | 1756/3143 | 1698/2718 | 566/905 | chr9 | 132398220 | |||
| chr9:132401613 | A | G | 1 | a0001c0013 | 3 | HG01175.hp2 HG03942.hp1 NA20752.hp2 |
synonymous_variant | LOW | c.1209T>C | p.Ser403Ser | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1267/3143 | 1209/2718 | 403/905 | chr9 | 132401613 | |||
| chr9:132401709 | T | C | 1 | a0007c0012 | 3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.1113A>G | p.Glu371Glu | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1171/3143 | 1113/2718 | 371/905 | chr9 | 132401709 | |||
| chr9:132401712 | C | T | 1 | a0001c0010 | 4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.1110G>A | p.Val370Val | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1168/3143 | 1110/2718 | 370/905 | chr9 | 132401712 | |||
| chr9:132401850 | T | C | 1 | a0001c0023 | 1 | NA18998.hp2 | synonymous_variant | LOW | c.972A>G | p.Pro324Pro | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 1030/3143 | 972/2718 | 324/905 | chr9 | 132401850 | |||
| chr9:132401910 | C | T | 1 | a0001c0014 | 2 | HG01515.hp2 HG01517.hp2 |
synonymous_variant | LOW | c.912G>A | p.Gly304Gly | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 970/3143 | 912/2718 | 304/905 | chr9 | 132401910 | |||
| chr9:132401940 | A | G | 1 | a0001c0018 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.882T>C | p.Pro294Pro | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/11 | 940/3143 | 882/2718 | 294/905 | chr9 | 132401940 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132375628 | T | C | 1 | a0001c0001t0003 | 4 | HG02896.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*287A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 287 | chr9 | 132375628 | ||||||
| chr9:132375721 | A | ATC | 2 | a0001c0007t0005 a0001c0007t0006 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192_*193dupGA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 193 | chr9 | 132375721 | ||||||
| chr9:132375854 | T | C | 30 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(27): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
3_prime_UTR_variant | MODIFIER | c.*61A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 11/11 | 61 | chr9 | 132375854 | ||||||
| chr9:132406801 | G | A | 16 | a0001c0001t0001 a0001c0001t0003 a0001c0007t0006 others(13): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
5_prime_UTR_variant | MODIFIER | c.-19C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/11 | 3980 | chr9 | 132406801 | ||||||
| chr9:132406811 | T | G | 1 | a0001c0007t0005 | 2 | HG03041.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-29A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/11 | 3990 | chr9 | 132406811 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:132376229 | G | A | 42 | a0002c0002t0002g0108 a0003c0003t0002g0002 a0003c0003t0002g0009 others(39): Show |
81 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2465-61C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376229 | |||||||
| chr9:132376343 | C | T | 2 | a0001c0001t0001g0181 a0001c0005t0002g0028 |
3 | HG02922.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2465-175G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376343 | |||||||
| chr9:132376359 | T | G | 1 | a0001c0005t0002g0065 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2465-191A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376359 | |||||||
| chr9:132376475 | C | T | 5 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0005t0002g0060 others(2): Show |
5 | HG01167.hp1 HG02615.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.2465-307G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376475 | |||||||
| chr9:132376662 | C | CT | 9 | a0001c0001t0001g0044 a0001c0001t0001g0156 a0001c0001t0001g0188 others(6): Show |
11 | HG00735.hp1 HG01361.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.2465-495dupA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376662 | |||||||
| chr9:132376662 | CT | C | 9 | a0001c0001t0001g0255 a0001c0005t0002g0061 a0002c0002t0002g0035 others(6): Show |
10 | HG02056.hp1 HG02451.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.2465-495delA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376662 | |||||||
| chr9:132376669 | T | G | 1 | a0002c0002t0002g0126 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2465-501A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376669 | |||||||
| chr9:132376694 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2465-526C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376694 | |||||||
| chr9:132376794 | C | G | 1 | a0011c0024t0002g0093 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2465-626G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376794 | |||||||
| chr9:132376825 | C | G | 1 | a0002c0002t0002g0117 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2465-657G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376825 | |||||||
| chr9:132376888 | G | T | 2 | a0007c0012t0002g0134 a0007c0012t0002g0135 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2465-720C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376888 | |||||||
| chr9:132376935 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0001g0169 a0001c0001t0001g0205 |
3 | HG02129.hp1 NA18987.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.2465-767T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132376935 | |||||||
| chr9:132377107 | T | G | 1 | a0002c0002t0002g0118 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2465-939A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377107 | |||||||
| chr9:132377116 | G | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2465-948C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377116 | |||||||
| chr9:132377119 | T | C | 2 | a0002c0002t0002g0119 a0002c0002t0002g0120 |
2 | NA18941.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.2465-951A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377119 | |||||||
| chr9:132377128 | A | G | 1 | a0001c0018t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2465-960T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377128 | |||||||
| chr9:132377136 | GGTGT | G | 5 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0005t0002g0060 others(2): Show |
5 | HG01167.hp1 HG02615.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.2465-972_2465-969d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377136 | |||||||
| chr9:132377178 | T | TGTGTGAG others(12): Show |
2 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.2465-1029_2465-101 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377178 | |||||||
| chr9:132377178 | TGTGTGAG others(12): Show |
T | 3 | a0001c0009t0001g0043 a0001c0009t0001g0218 a0007c0012t0002g0136 |
4 | HG02630.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2465-1029_2465-101 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377178 | |||||||
| chr9:132377208 | A | ATGCATGT others(8): Show |
3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2465-1055_2465-104 others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377208 | |||||||
| chr9:132377231 | GGTGTGAG others(12): Show |
G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2465-1082_2465-106 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377231 | |||||||
| chr9:132377264 | C | T | 2 | a0001c0001t0001g0197 a0001c0001t0001g0199 |
2 | HG00609.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.2465-1096G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377264 | |||||||
| chr9:132377265 | G | A | 52 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(49): Show |
80 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.2465-1097C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377265 | |||||||
| chr9:132377285 | GTGCATGT others(3): Show |
G | 1 | a0003c0003t0002g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2465-1127_2465-111 others(14): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377285 | |||||||
| chr9:132377307 | TGAGTGCA others(116): Show |
T | 7 | a0002c0002t0002g0108 a0004c0004t0002g0013 a0004c0004t0002g0014 others(4): Show |
13 | HG00558.hp2 HG00673.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.2465-1262_2465-114 others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377307 | |||||||
| chr9:132377339 | GGTGTGAG others(12): Show |
G | 3 | a0001c0001t0001g0015 a0001c0009t0001g0043 a0001c0009t0001g0218 |
4 | HG01361.hp1 HG02630.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2465-1190_2465-117 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377339 | |||||||
| chr9:132377346 | GTGCATGT others(88): Show |
G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2465-1273_2465-117 others(99): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377346 | |||||||
| chr9:132377358 | T | TGTGTGAG others(27): Show |
1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2465-1224_2465-119 others(38): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377358 | |||||||
| chr9:132377373 | GGTGT | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2465-1209_2465-120 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377373 | |||||||
| chr9:132377392 | GGTGTGAG others(54): Show |
G | 1 | a0005c0006t0001g0238 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2465-1285_2465-122 others(65): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377392 | |||||||
| chr9:132377395 | G | A | 2 | a0007c0012t0002g0134 a0007c0012t0002g0135 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2465-1227C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377395 | |||||||
| chr9:132377396 | TGAGTGCA others(27): Show |
T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2465-1262_2465-122 others(38): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377396 | |||||||
| chr9:132377399 | GTGCATGT others(73): Show |
G | 11 | a0004c0004t0002g0022 a0004c0004t0002g0023 a0004c0004t0002g0030 others(8): Show |
17 | HG00639.hp1 HG00639.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.2465-1311_2465-123 others(84): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377399 | |||||||
| chr9:132377404 | TGTG | T | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2465-1239_2465-123 others(7): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377404 | |||||||
| chr9:132377411 | TGTGTGAG others(12): Show |
T | 56 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(53): Show |
97 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.2465-1262_2465-124 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377411 | |||||||
| chr9:132377430 | GGTGTGAG others(16): Show |
G | 1 | a0001c0023t0002g0073 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2465-1285_2465-126 others(27): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377430 | |||||||
| chr9:132377436 | A | T | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2465-1268T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377436 | |||||||
| chr9:132377437 | GTGCA | G | 7 | a0002c0002t0002g0108 a0004c0004t0002g0013 a0004c0004t0002g0014 others(4): Show |
13 | HG00558.hp2 HG00673.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.2465-1273_2465-127 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377437 | |||||||
| chr9:132377440 | C | A | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2465-1272G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377440 | |||||||
| chr9:132377441 | A | G | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2465-1273T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377441 | |||||||
| chr9:132377449 | GGTGT | G | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2465-1285_2465-128 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377449 | |||||||
| chr9:132377460 | G | A | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2465-1292C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377460 | |||||||
| chr9:132377468 | GGTGT | G | 7 | a0002c0002t0002g0108 a0004c0004t0002g0013 a0004c0004t0002g0014 others(4): Show |
13 | HG00558.hp2 HG00673.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.2465-1304_2465-130 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377468 | |||||||
| chr9:132377472 | TGTGTGAA others(50): Show |
T | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2465-1361_2465-130 others(61): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377472 | |||||||
| chr9:132377479 | A | G | 9 | a0001c0001t0001g0045 a0001c0022t0002g0072 a0002c0002t0002g0108 others(6): Show |
16 | HG00558.hp2 HG00673.hp1 HG02074.hp2 others(13): Show |
intron_variant | MODIFIER | c.2465-1311T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377479 | |||||||
| chr9:132377484 | TGTG | T | 40 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(37): Show |
72 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.2465-1319_2465-131 others(7): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377484 | |||||||
| chr9:132377487 | GGTGT | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
231 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.2465-1323_2465-132 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377487 | |||||||
| chr9:132377491 | T | TGTGTGAA others(8): Show |
1 | a0001c0001t0001g0045 | 2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2465-1324_2465-132 others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377491 | |||||||
| chr9:132377494 | G | T | 1 | a0001c0001t0001g0189 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2465-1326C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377494 | |||||||
| chr9:132377501 | C | A | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2465-1333G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377501 | |||||||
| chr9:132377510 | GGTGTGAG others(12): Show |
G | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2465-1361_2465-134 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377510 | |||||||
| chr9:132377527 | GTAGTGTG others(81): Show |
G | 1 | a0001c0022t0002g0072 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2464+1444_2465-136 others(92): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377527 | |||||||
| chr9:132377559 | G | T | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2465-1391C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377559 | |||||||
| chr9:132377565 | GGTGAGTG others(12): Show |
G | 1 | a0001c0001t0001g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2465-1416_2465-139 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377565 | |||||||
| chr9:132377578 | G | GGT | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2465-1412_2465-141 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377578 | |||||||
| chr9:132377582 | T | C | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2465-1414A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377582 | |||||||
| chr9:132377589 | G | A | 165 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(162): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.2465-1421C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377589 | |||||||
| chr9:132377597 | GGTGTGT | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(159): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2465-1435_2465-143 others(10): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377597 | |||||||
| chr9:132377599 | T | TGTGAGTG others(6): Show |
1 | a0003c0003t0002g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2465-1432_2465-143 others(17): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377599 | |||||||
| chr9:132377603 | T | C | 1 | a0003c0003t0002g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2465-1435A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377603 | |||||||
| chr9:132377605 | T | A | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2465-1437A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377605 | |||||||
| chr9:132377609 | A | C | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2465-1441T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377609 | |||||||
| chr9:132377610 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(160): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.2465-1442T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377610 | |||||||
| chr9:132377618 | G | GGTGC | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(160): Show |
258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.2464+1440_2464+144 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377618 | |||||||
| chr9:132377622 | TGAGTGCA others(8): Show |
T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+1422_2464+143 others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377622 | |||||||
| chr9:132377625 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2464+1434C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377625 | |||||||
| chr9:132377633 | GGTGCGTG others(16): Show |
G | 1 | a0006c0008t0001g0175 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2464+1403_2464+142 others(27): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377633 | |||||||
| chr9:132377637 | C | T | 164 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(161): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.2464+1422G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377637 | |||||||
| chr9:132377638 | G | A | 1 | a0005c0011t0001g0234 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2464+1421C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377638 | |||||||
| chr9:132377644 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2464+1415T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377644 | |||||||
| chr9:132377652 | GGT | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.2464+1405_2464+140 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377652 | |||||||
| chr9:132377654 | T | TGTGTGTG others(10): Show |
74 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(71): Show |
118 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2464+1388_2464+140 others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377654 | |||||||
| chr9:132377680 | A | G | 6 | a0001c0001t0001g0242 a0001c0005t0002g0066 a0001c0010t0002g0038 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2464+1379T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377680 | |||||||
| chr9:132377688 | G | GGT | 4 | a0001c0001t0001g0242 a0001c0010t0002g0038 a0001c0010t0002g0137 others(1): Show |
5 | HG02280.hp2 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2464+1369_2464+137 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377688 | |||||||
| chr9:132377688 | GGTGTGAG others(26): Show |
G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1338_2464+137 others(37): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377688 | |||||||
| chr9:132377695 | G | A | 4 | a0001c0001t0001g0242 a0001c0010t0002g0038 a0001c0010t0002g0137 others(1): Show |
5 | HG02280.hp2 HG02622.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.2464+1364C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377695 | |||||||
| chr9:132377723 | TGTGTGAG others(8): Show |
T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0200 |
2 | HG01081.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2464+1321_2464+133 others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377723 | |||||||
| chr9:132377730 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1329C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377730 | |||||||
| chr9:132377757 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1302G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377757 | |||||||
| chr9:132377764 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1295T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377764 | |||||||
| chr9:132377775 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+1284C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377775 | |||||||
| chr9:132377776 | T | C | 42 | a0002c0002t0002g0108 a0003c0003t0002g0002 a0003c0003t0002g0009 others(39): Show |
81 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2464+1283A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377776 | |||||||
| chr9:132377797 | T | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1262A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377797 | |||||||
| chr9:132377808 | T | A | 2 | a0001c0009t0001g0194 a0001c0018t0001g0231 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2464+1251A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377808 | |||||||
| chr9:132377813 | GTGCATGT others(12): Show |
G | 4 | a0002c0002t0002g0114 a0007c0012t0002g0134 a0007c0012t0002g0135 others(1): Show |
4 | HG00741.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+1227_2464+124 others(23): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377813 | |||||||
| chr9:132377821 | GGT | G | 10 | a0001c0001t0001g0203 a0001c0009t0001g0222 a0005c0006t0001g0230 others(7): Show |
10 | HG01361.hp2 HG02886.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.2464+1236_2464+123 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377821 | |||||||
| chr9:132377829 | T | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1230A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377829 | |||||||
| chr9:132377831 | AATGCATG others(31): Show |
A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1190_2464+122 others(42): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377831 | |||||||
| chr9:132377832 | A | G | 1 | a0004c0004t0002g0013 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2464+1227T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377832 | |||||||
| chr9:132377878 | GGT | G | 3 | a0001c0005t0002g0012 a0001c0005t0002g0068 a0001c0023t0002g0073 |
6 | NA18945.hp1 NA18964.hp2 NA18981.hp2 others(3): Show |
intron_variant | MODIFIER | c.2464+1179_2464+118 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377878 | |||||||
| chr9:132377878 | GGTGT | G | 15 | a0001c0007t0002g0017 a0001c0007t0002g0133 a0001c0007t0005g0258 others(12): Show |
18 | HG01361.hp2 HG01943.hp2 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.2464+1177_2464+118 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377878 | |||||||
| chr9:132377894 | T | C | 1 | a0001c0018t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2464+1165A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377894 | |||||||
| chr9:132377908 | A | G | 1 | a0007c0012t0002g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2464+1151T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377908 | |||||||
| chr9:132377923 | C | G | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2464+1136G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377923 | |||||||
| chr9:132377933 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+1126C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377933 | |||||||
| chr9:132377935 | G | A | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+1124C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377935 | |||||||
| chr9:132377996 | A | T | 1 | a0014c0021t0001g0152 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2464+1063T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377996 | |||||||
| chr9:132377997 | TGTG | T | 57 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(54): Show |
98 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.2464+1059_2464+106 others(7): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132377997 | |||||||
| chr9:132378019 | GGTGTGAG others(31): Show |
G | 1 | a0001c0013t0001g0162 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2464+1002_2464+103 others(42): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378019 | |||||||
| chr9:132378034 | G | T | 1 | a0014c0021t0001g0152 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2464+1025C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378034 | |||||||
| chr9:132378069 | TGTG | T | 58 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(55): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2464+987_2464+989d others(5): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378069 | |||||||
| chr9:132378076 | TGTGTGAG others(8): Show |
T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2464+968_2464+982d others(17): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378076 | |||||||
| chr9:132378077 | G | A | 1 | a0001c0001t0001g0049 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2464+982C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378077 | |||||||
| chr9:132378087 | A | G | 1 | a0007c0012t0002g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2464+972T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378087 | |||||||
| chr9:132378091 | GGTGTGAG others(12): Show |
G | 58 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(55): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2464+949_2464+967d others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378091 | |||||||
| chr9:132378121 | ATGCATGT others(12): Show |
A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0185 a0001c0001t0001g0203 others(3): Show |
10 | HG00099.hp1 HG01361.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.2464+919_2464+937d others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378121 | |||||||
| chr9:132378126 | TGTG | T | 2 | a0001c0007t0002g0017 a0001c0007t0002g0133 |
4 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+930_2464+932d others(5): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378126 | |||||||
| chr9:132378145 | TGTG | T | 5 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0201 others(2): Show |
6 | HG01261.hp1 HG01261.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2464+911_2464+913d others(5): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378145 | |||||||
| chr9:132378178 | A | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0013t0001g0162 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2464+881T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378178 | |||||||
| chr9:132378187 | G | A | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2464+872C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378187 | |||||||
| chr9:132378217 | G | GGT | 70 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0054 others(67): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2464+840_2464+841d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378217 | |||||||
| chr9:132378250 | TGTG | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
12 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(9): Show |
intron_variant | MODIFIER | c.2464+806_2464+808d others(5): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378250 | |||||||
| chr9:132378264 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2464+795C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378264 | |||||||
| chr9:132378264 | GTGCATGT others(10): Show |
G | 2 | a0004c0004t0002g0104 a0012c0017t0001g0159 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2464+778_2464+794d others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378264 | |||||||
| chr9:132378306 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2464+753A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378306 | |||||||
| chr9:132378309 | G | C | 1 | a0004c0004t0002g0096 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2464+750C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378309 | |||||||
| chr9:132378376 | GGTGT | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(163): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.2464+679_2464+682d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378376 | |||||||
| chr9:132378380 | TGTGTGAG others(12): Show |
T | 1 | a0007c0012t0002g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2464+660_2464+678d others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378380 | |||||||
| chr9:132378382 | T | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+677A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378382 | |||||||
| chr9:132378383 | GTGAGTGC others(1): Show |
G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+668_2464+675d others(10): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378383 | |||||||
| chr9:132378391 | ATGCATGT others(8): Show |
A | 13 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0151 others(10): Show |
13 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.2464+653_2464+667d others(17): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378391 | |||||||
| chr9:132378403 | TGAGTGCA others(4): Show |
T | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+645_2464+655d others(13): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378403 | |||||||
| chr9:132378414 | G | GGT | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+643_2464+644d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378414 | |||||||
| chr9:132378421 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+638C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378421 | |||||||
| chr9:132378421 | GTGCATGT others(10): Show |
G | 56 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(53): Show |
97 | HG00280.hp2 HG00609.hp1 HG00735.hp2 others(94): Show |
intron_variant | MODIFIER | c.2464+621_2464+637d others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378421 | |||||||
| chr9:132378433 | T | TGA | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+625_2464+626i others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378433 | |||||||
| chr9:132378438 | A | G | 9 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(6): Show |
10 | HG00099.hp2 HG00323.hp1 NA18959.hp2 others(7): Show |
intron_variant | MODIFIER | c.2464+621T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378438 | |||||||
| chr9:132378447 | G | A | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+612C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378447 | |||||||
| chr9:132378452 | A | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+607T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378452 | |||||||
| chr9:132378456 | C | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+603G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378456 | |||||||
| chr9:132378459 | G | GC | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+599_2464+600i others(3): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378459 | |||||||
| chr9:132378460 | T | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+599A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378460 | |||||||
| chr9:132378461 | G | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+598C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378461 | |||||||
| chr9:132378461 | GGT | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+596_2464+597d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378461 | |||||||
| chr9:132378461 | GGTGT | G | 4 | a0003c0003t0002g0016 a0003c0003t0002g0055 a0003c0003t0002g0085 others(1): Show |
6 | NA18943.hp2 NA18968.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.2464+594_2464+597d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378461 | |||||||
| chr9:132378464 | GT | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+594delA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378464 | |||||||
| chr9:132378465 | T | G | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+594A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378465 | |||||||
| chr9:132378472 | G | A | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+587C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378472 | |||||||
| chr9:132378480 | GGTGT | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+575_2464+578d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378480 | |||||||
| chr9:132378484 | T | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+575A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378484 | |||||||
| chr9:132378486 | T | A | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+573A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378486 | |||||||
| chr9:132378490 | A | C | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+569T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378490 | |||||||
| chr9:132378491 | A | G | 10 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(7): Show |
12 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(9): Show |
intron_variant | MODIFIER | c.2464+568T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378491 | |||||||
| chr9:132378498 | T | G | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+561A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378498 | |||||||
| chr9:132378499 | G | T | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+560C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378499 | |||||||
| chr9:132378500 | A | G | 71 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0054 others(68): Show |
114 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.2464+559T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378500 | |||||||
| chr9:132378506 | G | A | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+553C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378506 | |||||||
| chr9:132378516 | TGG | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+541_2464+542d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378516 | |||||||
| chr9:132378518 | G | T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+541C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378518 | |||||||
| chr9:132378525 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2464+534C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378525 | |||||||
| chr9:132378537 | TGAGTGCA others(53): Show |
T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+462_2464+521d others(62): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378537 | |||||||
| chr9:132378540 | G | A | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+519C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378540 | |||||||
| chr9:132378557 | A | G | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2464+502T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378557 | |||||||
| chr9:132378557 | ATGCATGT others(40): Show |
A | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2464+455_2464+501d others(49): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378557 | |||||||
| chr9:132378580 | G | GGTGTGAG others(10): Show |
8 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0252 others(5): Show |
10 | NA18906.hp2 NA18959.hp2 NA18961.hp2 others(7): Show |
intron_variant | MODIFIER | c.2464+478_2464+479i others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378580 | |||||||
| chr9:132378589 | A | G | 9 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0252 others(6): Show |
11 | NA18906.hp2 NA18959.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.2464+470T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378589 | |||||||
| chr9:132378597 | G | GGTGT | 9 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0252 others(6): Show |
11 | NA18906.hp2 NA18959.hp2 NA18961.hp2 others(8): Show |
intron_variant | MODIFIER | c.2464+458_2464+461d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378597 | |||||||
| chr9:132378604 | G | A | 12 | a0001c0001t0001g0049 a0001c0001t0001g0054 a0001c0001t0001g0252 others(9): Show |
15 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(12): Show |
intron_variant | MODIFIER | c.2464+455C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(42): Show |
1 | a0001c0007t0004g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2464+454_2464+455i others(51): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(46): Show |
3 | a0005c0006t0001g0230 a0005c0006t0001g0239 a0005c0006t0001g0240 |
3 | NA18950.hp2 NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.2464+454_2464+455i others(55): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(46): Show |
1 | a0004c0004t0002g0099 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2464+454_2464+455i others(55): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(47): Show |
1 | a0014c0021t0001g0152 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2464+454_2464+455i others(56): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(46): Show |
113 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0039 others(110): Show |
178 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.2464+454_2464+455i others(55): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378604 | G | GTGCATGT others(31): Show |
2 | a0001c0005t0002g0068 a0012c0017t0001g0159 |
2 | HG02451.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.2464+454_2464+455i others(40): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378604 | |||||||
| chr9:132378629 | T | TGTGAGTG others(7): Show |
1 | a0002c0002t0002g0010 | 5 | HG02135.hp2 HG03831.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.2464+429_2464+430i others(16): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378629 | |||||||
| chr9:132378629 | T | TGTGTGTG others(27): Show |
1 | a0001c0009t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2464+429_2464+430i others(36): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378629 | |||||||
| chr9:132378630 | T | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(36): Show |
67 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2464+429A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378630 | |||||||
| chr9:132378631 | G | GT | 1 | a0002c0002t0002g0010 | 5 | HG02135.hp2 HG03831.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.2464+427_2464+428i others(3): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378631 | |||||||
| chr9:132378631 | G | T | 39 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(36): Show |
67 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.2464+428C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378631 | |||||||
| chr9:132378638 | G | A | 1 | a0002c0002t0002g0010 | 5 | HG02135.hp2 HG03831.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.2464+421C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378638 | |||||||
| chr9:132378638 | G | GTGCATGT others(12): Show |
38 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(35): Show |
66 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.2464+420_2464+421i others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378638 | |||||||
| chr9:132378652 | A | T | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+407T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378652 | |||||||
| chr9:132378656 | C | A | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+403G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378656 | |||||||
| chr9:132378657 | A | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0013t0001g0162 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2464+402T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378657 | |||||||
| chr9:132378659 | A | G | 41 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(38): Show |
73 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.2464+400T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378659 | |||||||
| chr9:132378660 | C | T | 39 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(36): Show |
71 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2464+399G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378660 | |||||||
| chr9:132378661 | G | A | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+398C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378661 | |||||||
| chr9:132378661 | G | GGTT | 39 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(36): Show |
71 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2464+397_2464+398i others(5): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378661 | |||||||
| chr9:132378662 | T | G | 39 | a0001c0001t0001g0011 a0001c0001t0001g0144 a0001c0001t0001g0146 others(36): Show |
71 | HG00099.hp2 HG00323.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.2464+397A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378662 | |||||||
| chr9:132378673 | A | ATGTGGTT others(8): Show |
1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+385_2464+386i others(17): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378673 | |||||||
| chr9:132378673 | ATGCATGT others(12): Show |
A | 1 | a0001c0010t0002g0038 | 2 | HG02622.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2464+367_2464+385d others(21): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378673 | |||||||
| chr9:132378683 | T | TGTGTGCA others(3): Show |
1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2464+375_2464+376i others(12): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378683 | |||||||
| chr9:132378715 | GGTGT | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2464+340_2464+343d others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378715 | |||||||
| chr9:132378719 | T | G | 8 | a0001c0009t0001g0222 a0005c0006t0001g0230 a0005c0006t0001g0232 others(5): Show |
8 | HG02886.hp2 HG02976.hp1 HG04115.hp1 others(5): Show |
intron_variant | MODIFIER | c.2464+340A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378719 | |||||||
| chr9:132378873 | C | T | 1 | a0003c0003t0002g0085 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2464+186G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132378873 | |||||||
| chr9:132379002 | C | A | 2 | a0001c0001t0001g0177 a0006c0008t0001g0174 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2464+57G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 10/10 | chr9 | 132379002 | |||||||
| chr9:132379190 | T | C | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2379-46A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379190 | |||||||
| chr9:132379387 | T | C | 2 | a0001c0007t0002g0017 a0001c0007t0002g0133 |
4 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-243A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379387 | |||||||
| chr9:132379504 | G | A | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-360C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379504 | |||||||
| chr9:132379522 | C | T | 1 | a0002c0002t0002g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2379-378G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379522 | |||||||
| chr9:132379524 | C | G | 24 | a0003c0003t0002g0002 a0003c0003t0002g0009 a0003c0003t0002g0016 others(21): Show |
51 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.2379-380G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379524 | |||||||
| chr9:132379760 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2379-616C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379760 | |||||||
| chr9:132379781 | C | G | 58 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(55): Show |
99 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2379-637G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379781 | |||||||
| chr9:132379865 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2379-721T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379865 | |||||||
| chr9:132379983 | T | C | 1 | a0006c0008t0001g0176 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2379-839A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132379983 | |||||||
| chr9:132380163 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2379-1019T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380163 | |||||||
| chr9:132380196 | A | T | 1 | a0001c0005t0002g0064 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2379-1052T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380196 | |||||||
| chr9:132380213 | G | C | 13 | a0001c0007t0002g0017 a0001c0007t0002g0133 a0001c0009t0001g0222 others(10): Show |
17 | HG01943.hp2 HG02886.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.2379-1069C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380213 | |||||||
| chr9:132380221 | C | G | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2379-1077G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380221 | |||||||
| chr9:132380287 | C | T | 42 | a0002c0002t0002g0108 a0003c0003t0002g0002 a0003c0003t0002g0009 others(39): Show |
81 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2379-1143G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380287 | |||||||
| chr9:132380494 | CTA | C | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2379-1352_2379-135 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380494 | |||||||
| chr9:132380558 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2379-1414T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380558 | |||||||
| chr9:132380624 | T | C | 1 | a0004c0004t0002g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2379-1480A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380624 | |||||||
| chr9:132380839 | G | A | 13 | a0001c0007t0002g0017 a0001c0007t0002g0133 a0001c0009t0001g0222 others(10): Show |
17 | HG01943.hp2 HG02886.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.2379-1695C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380839 | |||||||
| chr9:132380851 | T | C | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2379-1707A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380851 | |||||||
| chr9:132380873 | C | A | 2 | a0006c0008t0001g0226 a0013c0020t0001g0157 |
2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2379-1729G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132380873 | |||||||
| chr9:132381197 | A | AT | 5 | a0001c0001t0001g0049 a0001c0001t0001g0195 a0001c0007t0005g0258 others(2): Show |
6 | HG02818.hp1 HG03041.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.2379-2054dupA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381197 | |||||||
| chr9:132381197 | AT | A | 12 | a0001c0001t0001g0054 a0001c0001t0001g0199 a0001c0001t0001g0252 others(9): Show |
16 | HG00558.hp2 HG00673.hp1 NA18941.hp2 others(13): Show |
intron_variant | MODIFIER | c.2379-2054delA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381197 | |||||||
| chr9:132381216 | T | C | 4 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 others(1): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2379-2072A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381216 | |||||||
| chr9:132381254 | C | T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-2110G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381254 | |||||||
| chr9:132381313 | C | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2379-2169G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381313 | |||||||
| chr9:132381336 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2379-2192T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381336 | |||||||
| chr9:132381371 | G | A | 1 | a0005c0006t0001g0230 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2379-2227C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381371 | |||||||
| chr9:132381385 | T | C | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2379-2241A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381385 | |||||||
| chr9:132381404 | G | A | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-2260C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381404 | |||||||
| chr9:132381437 | G | A | 1 | a0001c0005t0002g0069 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2379-2293C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381437 | |||||||
| chr9:132381489 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2379-2345G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381489 | |||||||
| chr9:132381632 | A | G | 70 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(67): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2379-2488T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381632 | |||||||
| chr9:132381677 | A | C | 4 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0013t0001g0162 others(1): Show |
4 | HG02451.hp2 HG02683.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-2533T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381677 | |||||||
| chr9:132381743 | C | A | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2379-2599G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381743 | |||||||
| chr9:132381767 | G | C | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-2623C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381767 | |||||||
| chr9:132381836 | C | T | 5 | a0001c0009t0001g0194 a0001c0018t0001g0231 a0007c0012t0002g0134 others(2): Show |
5 | HG02451.hp2 HG03098.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.2379-2692G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381836 | |||||||
| chr9:132381918 | C | T | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2379-2774G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132381918 | |||||||
| chr9:132382092 | C | T | 1 | a0002c0002t0002g0115 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2379-2948G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382092 | |||||||
| chr9:132382093 | G | A | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-2949C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382093 | |||||||
| chr9:132382316 | C | T | 70 | a0001c0001t0001g0011 a0001c0001t0001g0049 a0001c0001t0001g0144 others(67): Show |
113 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.2379-3172G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382316 | |||||||
| chr9:132382452 | G | A | 2 | a0001c0001t0001g0208 a0001c0001t0001g0212 |
2 | HG03942.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.2379-3308C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382452 | |||||||
| chr9:132382498 | G | A | 1 | a0003c0003t0002g0091 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2379-3354C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382498 | |||||||
| chr9:132382658 | A | G | 4 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 others(1): Show |
5 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2379-3514T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382658 | |||||||
| chr9:132382761 | CA | C | 19 | a0001c0001t0001g0054 a0001c0001t0001g0241 a0001c0001t0001g0252 others(16): Show |
24 | HG01943.hp2 HG02717.hp1 HG02970.hp2 others(21): Show |
intron_variant | MODIFIER | c.2379-3618delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382761 | |||||||
| chr9:132382761 | CAA | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.2379-3619_2379-361 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382761 | |||||||
| chr9:132382761 | CAAA | C | 6 | a0001c0009t0001g0194 a0001c0010t0002g0038 a0001c0010t0002g0137 others(3): Show |
7 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.2379-3620_2379-361 others(7): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382761 | |||||||
| chr9:132382771 | A | G | 2 | a0001c0007t0002g0017 a0001c0007t0002g0133 |
4 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-3627T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382771 | |||||||
| chr9:132382772 | A | G | 171 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
265 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.2379-3628T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382772 | |||||||
| chr9:132382773 | A | G | 2 | a0001c0009t0001g0194 a0001c0018t0001g0231 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2379-3629T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382773 | |||||||
| chr9:132382793 | T | C | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2379-3649A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382793 | |||||||
| chr9:132382927 | A | G | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18975.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.2378+3629T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132382927 | |||||||
| chr9:132383065 | CAA | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(250): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.2378+3489_2378+349 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383065 | |||||||
| chr9:132383089 | A | T | 162 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(159): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.2378+3467T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383089 | |||||||
| chr9:132383250 | CA | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(178): Show |
291 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.2378+3305delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383250 | |||||||
| chr9:132383250 | CAA | C | 55 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(52): Show |
82 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.2378+3304_2378+330 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383250 | |||||||
| chr9:132383449 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2378+3107T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383449 | |||||||
| chr9:132383486 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+3070C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383486 | |||||||
| chr9:132383601 | T | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2378+2955A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383601 | |||||||
| chr9:132383664 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2378+2892C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383664 | |||||||
| chr9:132383687 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2378+2869C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383687 | |||||||
| chr9:132383778 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+2778G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383778 | |||||||
| chr9:132383779 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2378+2777T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383779 | |||||||
| chr9:132383805 | C | T | 1 | a0001c0005t0002g0062 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2378+2751G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383805 | |||||||
| chr9:132383828 | G | A | 1 | a0001c0007t0005g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2378+2728C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132383828 | |||||||
| chr9:132384113 | T | C | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2378+2443A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384113 | |||||||
| chr9:132384126 | C | T | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2378+2430G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384126 | |||||||
| chr9:132384153 | G | A | 1 | a0004c0004t0002g0100 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.2378+2403C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384153 | |||||||
| chr9:132384272 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2378+2284C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384272 | |||||||
| chr9:132384333 | A | T | 1 | a0001c0001t0001g0252 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.2378+2223T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384333 | |||||||
| chr9:132384500 | T | C | 1 | a0002c0002t0002g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2378+2056A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384500 | |||||||
| chr9:132384707 | A | C | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2378+1849T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384707 | |||||||
| chr9:132384779 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2378+1777G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132384779 | |||||||
| chr9:132385058 | A | G | 1 | a0001c0018t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2378+1498T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385058 | |||||||
| chr9:132385145 | G | A | 1 | a0001c0005t0002g0071 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2378+1411C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385145 | |||||||
| chr9:132385170 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+1386C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385170 | |||||||
| chr9:132385444 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+1112C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385444 | |||||||
| chr9:132385452 | C | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+1104G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385452 | |||||||
| chr9:132385678 | G | A | 2 | a0003c0003t0002g0082 a0003c0003t0002g0130 |
2 | NA18940.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.2378+878C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385678 | |||||||
| chr9:132385779 | C | CAGGCACT others(6): Show |
256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2378+776_2378+777i others(15): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132385779 | |||||||
| chr9:132386214 | C | T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2378+342G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132386214 | |||||||
| chr9:132386244 | C | T | 8 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(5): Show |
9 | HG02451.hp1 NA18959.hp2 NA18961.hp2 others(6): Show |
intron_variant | MODIFIER | c.2378+312G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132386244 | |||||||
| chr9:132386302 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2378+254C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132386302 | |||||||
| chr9:132386496 | T | C | 1 | a0001c0018t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2378+60A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 9/10 | chr9 | 132386496 | |||||||
| chr9:132386626 | G | A | 2 | a0002c0002t0002g0113 a0002c0002t0002g0121 |
2 | HG00099.hp2 HG00323.hp1 |
splice_region_variant&intron_variant | LOW | c.2313-5C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386626 | |||||||
| chr9:132386686 | G | A | 1 | a0003c0003t0002g0031 | 2 | HG02027.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.2313-65C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386686 | |||||||
| chr9:132386723 | C | T | 1 | a0001c0009t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2313-102G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386723 | |||||||
| chr9:132386772 | C | G | 3 | a0001c0001t0001g0184 a0001c0001t0001g0248 a0001c0013t0001g0162 |
3 | HG02683.hp2 HG03942.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.2313-151G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386772 | |||||||
| chr9:132386838 | C | T | 1 | a0002c0002t0002g0109 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2313-217G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386838 | |||||||
| chr9:132386848 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2313-227C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386848 | |||||||
| chr9:132386857 | T | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(240): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.2313-236A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386857 | |||||||
| chr9:132386870 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2313-249G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386870 | |||||||
| chr9:132386967 | C | CT | 11 | a0001c0009t0001g0222 a0005c0006t0001g0051 a0005c0006t0001g0052 others(8): Show |
13 | HG02886.hp2 HG02976.hp1 HG03654.hp2 others(10): Show |
intron_variant | MODIFIER | c.2313-347dupA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386967 | |||||||
| chr9:132386978 | T | G | 1 | a0001c0001t0001g0158 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.2313-357A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132386978 | |||||||
| chr9:132387118 | C | T | 14 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0151 others(11): Show |
14 | HG00558.hp1 HG00609.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2313-497G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387118 | |||||||
| chr9:132387119 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2313-498C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387119 | |||||||
| chr9:132387170 | G | C | 1 | a0003c0003t0002g0019 | 3 | NA18989.hp1 NA19054.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.2313-549C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387170 | |||||||
| chr9:132387238 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2313-617G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387238 | |||||||
| chr9:132387295 | C | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2313-674G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387295 | |||||||
| chr9:132387296 | C | G | 6 | a0001c0009t0001g0194 a0001c0018t0001g0231 a0007c0012t0002g0134 others(3): Show |
6 | HG02451.hp1 HG02451.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313-675G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387296 | |||||||
| chr9:132387297 | C | G | 5 | a0004c0004t0002g0102 a0009c0016t0002g0075 a0009c0016t0002g0094 others(2): Show |
5 | HG02015.hp2 HG02451.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313-676G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387297 | |||||||
| chr9:132387461 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2312+678C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387461 | |||||||
| chr9:132387502 | AGGAAACC others(6): Show |
A | 43 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0025 others(40): Show |
68 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(65): Show |
intron_variant | MODIFIER | c.2312+624_2312+636d others(15): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387502 | |||||||
| chr9:132387504 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.2312+635C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387504 | |||||||
| chr9:132387557 | G | A | 1 | a0001c0001t0001g0026 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2312+582C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387557 | |||||||
| chr9:132387618 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(237): Show |
377 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(374): Show |
intron_variant | MODIFIER | c.2312+521A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387618 | |||||||
| chr9:132387650 | G | A | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2312+489C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387650 | |||||||
| chr9:132387667 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2312+472G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387667 | |||||||
| chr9:132387688 | A | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2312+451T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387688 | |||||||
| chr9:132387819 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2312+320G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387819 | |||||||
| chr9:132387870 | C | T | 13 | a0001c0007t0002g0017 a0001c0007t0002g0133 a0001c0009t0001g0222 others(10): Show |
17 | HG01943.hp2 HG02886.hp2 HG02970.hp2 others(14): Show |
intron_variant | MODIFIER | c.2312+269G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387870 | |||||||
| chr9:132387871 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2312+268C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387871 | |||||||
| chr9:132387981 | G | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2312+158C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132387981 | |||||||
| chr9:132388002 | T | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2312+137A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132388002 | |||||||
| chr9:132388009 | A | G | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2312+130T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132388009 | |||||||
| chr9:132388020 | A | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2312+119T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132388020 | |||||||
| chr9:132388020 | A | T | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2312+119T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 8/10 | chr9 | 132388020 | |||||||
| chr9:132388299 | T | C | 10 | a0003c0003t0002g0009 a0003c0003t0002g0020 a0003c0003t0002g0031 others(7): Show |
18 | HG00673.hp2 HG02027.hp2 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.2223-71A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388299 | |||||||
| chr9:132388362 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-134C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388362 | |||||||
| chr9:132388366 | T | C | 2 | a0001c0001t0001g0177 a0006c0008t0001g0174 |
2 | HG02258.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.2223-138A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388366 | |||||||
| chr9:132388389 | T | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-161A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388389 | |||||||
| chr9:132388414 | G | A | 1 | a0002c0002t0002g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2223-186C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388414 | |||||||
| chr9:132388429 | C | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(225): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.2223-201G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388429 | |||||||
| chr9:132388440 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-212C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388440 | |||||||
| chr9:132388462 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(226): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.2223-234C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388462 | |||||||
| chr9:132388483 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-255C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388483 | |||||||
| chr9:132388595 | C | T | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2223-367G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388595 | |||||||
| chr9:132388622 | T | A | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2223-394A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388622 | |||||||
| chr9:132388645 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2223-417T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388645 | |||||||
| chr9:132388652 | T | C | 2 | a0003c0003t0002g0087 a0003c0003t0002g0088 |
2 | NA18986.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.2223-424A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388652 | |||||||
| chr9:132388703 | G | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223-475C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132388703 | |||||||
| chr9:132389072 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(240): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.2223-844G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389072 | |||||||
| chr9:132389077 | T | C | 2 | a0003c0003t0002g0033 a0003c0003t0002g0084 |
3 | NA18942.hp1 NA18962.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2223-849A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389077 | |||||||
| chr9:132389095 | T | C | 1 | a0001c0007t0006g0167 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2223-867A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389095 | |||||||
| chr9:132389182 | C | CT | 22 | a0001c0001t0001g0054 a0001c0001t0001g0172 a0001c0001t0001g0183 others(19): Show |
29 | HG01361.hp2 HG01943.hp2 HG01981.hp2 others(26): Show |
intron_variant | MODIFIER | c.2223-955dupA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389182 | |||||||
| chr9:132389182 | CT | C | 8 | a0001c0001t0001g0144 a0001c0001t0001g0150 a0001c0001t0001g0154 others(5): Show |
8 | HG01256.hp1 HG03688.hp2 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223-955delA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389182 | |||||||
| chr9:132389206 | G | A | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2223-978C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389206 | |||||||
| chr9:132389224 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(253): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.2223-996A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389224 | |||||||
| chr9:132389269 | G | A | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2223-1041C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389269 | |||||||
| chr9:132389308 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-1080C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389308 | |||||||
| chr9:132389317 | G | GGATTACA others(3): Show |
1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2223-1099_2223-109 others(14): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389317 | |||||||
| chr9:132389331 | C | T | 4 | a0004c0004t0002g0102 a0009c0016t0002g0075 a0009c0016t0002g0094 others(1): Show |
4 | HG02015.hp2 HG02738.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.2223-1103G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389331 | |||||||
| chr9:132389479 | C | A | 1 | a0004c0004t0002g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2222+1118G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389479 | |||||||
| chr9:132389511 | A | C | 1 | a0004c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2222+1086T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389511 | |||||||
| chr9:132389587 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(240): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.2222+1010T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389587 | |||||||
| chr9:132389662 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.2222+935C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389662 | |||||||
| chr9:132389687 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2222+910C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389687 | |||||||
| chr9:132389690 | A | G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(240): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.2222+907T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389690 | |||||||
| chr9:132389782 | T | C | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2222+815A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389782 | |||||||
| chr9:132389821 | T | A | 239 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(236): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.2222+776A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389821 | |||||||
| chr9:132389821 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2222+776A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389821 | |||||||
| chr9:132389858 | C | T | 1 | a0001c0009t0001g0194 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2222+739G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389858 | |||||||
| chr9:132389967 | T | C | 1 | a0001c0001t0001g0216 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2222+630A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389967 | |||||||
| chr9:132389973 | C | A | 2 | a0004c0004t0002g0102 a0012c0017t0001g0159 |
2 | HG02451.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.2222+624G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389973 | |||||||
| chr9:132389975 | A | C | 223 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0011 others(220): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.2222+622T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132389975 | |||||||
| chr9:132390041 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2222+556A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390041 | |||||||
| chr9:132390127 | G | A | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2222+470C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390127 | |||||||
| chr9:132390136 | C | A | 2 | a0001c0009t0001g0194 a0001c0018t0001g0231 |
2 | NA19043.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2222+461G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390136 | |||||||
| chr9:132390167 | A | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0249 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.2222+430T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390167 | |||||||
| chr9:132390273 | C | T | 2 | a0004c0004t0002g0104 a0004c0004t0002g0105 |
2 | HG02622.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2222+324G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390273 | |||||||
| chr9:132390489 | T | C | 220 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(217): Show |
354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.2222+108A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 7/10 | chr9 | 132390489 | |||||||
| chr9:132390861 | A | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1988-30T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132390861 | |||||||
| chr9:132390933 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1988-102A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132390933 | |||||||
| chr9:132391000 | G | A | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(222): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.1988-169C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391000 | |||||||
| chr9:132391119 | G | A | 1 | a0001c0007t0005g0258 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1988-288C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391119 | |||||||
| chr9:132391212 | CATAGTGT others(10): Show |
C | 5 | a0003c0003t0002g0032 a0004c0004t0002g0102 a0009c0016t0002g0075 others(2): Show |
6 | HG00544.hp2 HG02015.hp2 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1988-398_1988-382d others(19): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391212 | |||||||
| chr9:132391251 | C | T | 1 | a0002c0002t0002g0139 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1988-420G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391251 | |||||||
| chr9:132391328 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1988-497G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391328 | |||||||
| chr9:132391333 | T | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0221 |
2 | HG01070.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1988-502A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391333 | |||||||
| chr9:132391408 | G | GC | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(233): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1988-578dupG | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391408 | |||||||
| chr9:132391433 | C | T | 41 | a0002c0002t0002g0108 a0003c0003t0002g0002 a0003c0003t0002g0009 others(38): Show |
79 | HG00423.hp2 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.1988-602G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391433 | |||||||
| chr9:132391477 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1987+599T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391477 | |||||||
| chr9:132391481 | GA | G | 9 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0230 others(6): Show |
11 | HG03654.hp2 HG04115.hp1 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.1987+594delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391481 | |||||||
| chr9:132391491 | T | A | 9 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0230 others(6): Show |
11 | HG03654.hp2 HG04115.hp1 HG04204.hp2 others(8): Show |
intron_variant | MODIFIER | c.1987+585A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391491 | |||||||
| chr9:132391589 | C | T | 2 | a0001c0009t0001g0043 a0001c0009t0001g0218 |
3 | HG02630.hp2 HG02886.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1987+487G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391589 | |||||||
| chr9:132391689 | A | G | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987+387T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391689 | |||||||
| chr9:132391737 | C | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1987+339G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391737 | |||||||
| chr9:132391760 | G | A | 4 | a0001c0001t0001g0165 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
4 | HG01884.hp1 HG02486.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1987+316C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391760 | |||||||
| chr9:132391865 | T | C | 1 | a0001c0001t0001g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1987+211A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391865 | |||||||
| chr9:132391993 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1987+83G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132391993 | |||||||
| chr9:132392014 | C | T | 1 | a0001c0005t0002g0061 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1987+62G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132392014 | |||||||
| chr9:132392046 | G | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1987+30C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 6/10 | chr9 | 132392046 | |||||||
| chr9:132392231 | C | T | 1 | a0005c0011t0001g0050 | 2 | HG01243.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.1857-25G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392231 | |||||||
| chr9:132392336 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-130G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392336 | |||||||
| chr9:132392348 | C | A | 4 | a0001c0009t0001g0043 a0001c0009t0001g0218 a0001c0010t0002g0038 others(1): Show |
6 | HG02280.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857-142G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392348 | |||||||
| chr9:132392378 | C | A | 4 | a0003c0003t0002g0009 a0003c0003t0002g0033 a0003c0003t0002g0084 others(1): Show |
9 | NA18942.hp1 NA18962.hp1 NA18967.hp2 others(6): Show |
intron_variant | MODIFIER | c.1857-172G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392378 | |||||||
| chr9:132392453 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-247G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392453 | |||||||
| chr9:132392477 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1857-271C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392477 | |||||||
| chr9:132392500 | G | C | 45 | a0001c0001t0001g0011 a0001c0001t0001g0140 a0001c0001t0001g0142 others(42): Show |
70 | HG00323.hp1 HG00621.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.1857-294C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392500 | |||||||
| chr9:132392545 | C | T | 255 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(252): Show |
396 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(393): Show |
intron_variant | MODIFIER | c.1857-339G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392545 | |||||||
| chr9:132392575 | T | C | 2 | a0007c0012t0002g0134 a0007c0012t0002g0135 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1857-369A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392575 | |||||||
| chr9:132392589 | C | CCT | 75 | a0001c0001t0001g0048 a0001c0001t0001g0053 a0001c0001t0001g0149 others(72): Show |
120 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.1857-384_1857-383i others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392589 | |||||||
| chr9:132392609 | C | G | 1 | a0001c0001t0001g0193 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1857-403G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392609 | |||||||
| chr9:132392688 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-482G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392688 | |||||||
| chr9:132392898 | C | A | 1 | a0010c0025t0002g0128 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1857-692G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132392898 | |||||||
| chr9:132393019 | T | A | 49 | a0003c0003t0002g0002 a0003c0003t0002g0009 a0003c0003t0002g0016 others(46): Show |
88 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1857-813A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393019 | |||||||
| chr9:132393024 | T | C | 1 | a0001c0005t0002g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1857-818A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393024 | |||||||
| chr9:132393152 | G | T | 1 | a0001c0001t0001g0049 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1857-946C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393152 | |||||||
| chr9:132393269 | G | GC | 117 | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0026 others(114): Show |
174 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.1857-1064dupG | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393269 | |||||||
| chr9:132393269 | G | GCC | 17 | a0001c0001t0001g0046 a0001c0001t0001g0243 a0001c0001t0001g0257 others(14): Show |
20 | HG00280.hp2 HG02145.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857-1065_1857-106 others(6): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393269 | |||||||
| chr9:132393276 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1857-1070G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393276 | |||||||
| chr9:132393277 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1857-1071G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393277 | |||||||
| chr9:132393278 | G | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(180): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.1857-1072C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393278 | |||||||
| chr9:132393298 | A | T | 4 | a0001c0001t0001g0053 a0001c0001t0001g0242 a0001c0001t0001g0243 others(1): Show |
5 | HG01106.hp2 HG02145.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857-1092T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393298 | |||||||
| chr9:132393324 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-1118A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393324 | |||||||
| chr9:132393385 | C | T | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857-1179G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393385 | |||||||
| chr9:132393392 | A | G | 182 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(179): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.1857-1186T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393392 | |||||||
| chr9:132393393 | C | G | 1 | a0002c0002t0002g0077 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1857-1187G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393393 | |||||||
| chr9:132393400 | C | T | 1 | a0001c0001t0001g0042 | 2 | NA18980.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1857-1194G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393400 | |||||||
| chr9:132393401 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1857-1195C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393401 | |||||||
| chr9:132393408 | C | T | 2 | a0004c0004t0002g0098 a0004c0004t0002g0129 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1857-1202G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393408 | |||||||
| chr9:132393509 | C | T | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1857-1303G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393509 | |||||||
| chr9:132393787 | T | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1857-1581A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393787 | |||||||
| chr9:132393922 | C | G | 1 | a0001c0001t0002g0059 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1857-1716G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393922 | |||||||
| chr9:132393931 | T | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1857-1725A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393931 | |||||||
| chr9:132393935 | T | TC | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1857-1730dupG | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132393935 | |||||||
| chr9:132394014 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
5 | HG01891.hp2 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1857-1808A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394014 | |||||||
| chr9:132394024 | C | T | 224 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(221): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.1857-1818G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394024 | |||||||
| chr9:132394114 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-1908C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394114 | |||||||
| chr9:132394279 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1857-2073G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394279 | |||||||
| chr9:132394303 | G | A | 1 | a0004c0004t0002g0030 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1857-2097C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394303 | |||||||
| chr9:132394437 | G | A | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1856+1996C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394437 | |||||||
| chr9:132394583 | C | T | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1856+1850G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394583 | |||||||
| chr9:132394722 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+1711T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394722 | |||||||
| chr9:132394879 | G | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(235): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1856+1554C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394879 | |||||||
| chr9:132394892 | C | CA | 12 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0217 others(9): Show |
12 | HG01192.hp1 HG01891.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.1856+1540dupT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394892 | |||||||
| chr9:132394908 | A | ATTG | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1856+1522_1856+152 others(7): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394908 | |||||||
| chr9:132394948 | G | A | 3 | a0002c0002t0002g0074 a0002c0002t0002g0123 a0002c0002t0002g0124 |
3 | NA18955.hp2 NA19058.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1856+1485C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132394948 | |||||||
| chr9:132395058 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+1375C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395058 | |||||||
| chr9:132395124 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+1309C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395124 | |||||||
| chr9:132395143 | G | C | 1 | a0007c0012t0002g0136 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1856+1290C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395143 | |||||||
| chr9:132395145 | T | C | 1 | a0001c0009t0001g0218 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1856+1288A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395145 | |||||||
| chr9:132395160 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0180 |
2 | HG00280.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.1856+1273G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395160 | |||||||
| chr9:132395266 | ACTTT | A | 3 | a0001c0022t0002g0072 a0002c0002t0002g0036 a0002c0002t0002g0125 |
4 | HG02132.hp1 HG02135.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1856+1163_1856+116 others(8): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395266 | |||||||
| chr9:132395308 | T | C | 1 | a0001c0001t0001g0026 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1856+1125A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395308 | |||||||
| chr9:132395371 | T | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+1062A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395371 | |||||||
| chr9:132395484 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+949C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395484 | |||||||
| chr9:132395661 | G | A | 1 | a0005c0006t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1856+772C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395661 | |||||||
| chr9:132395673 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+760T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395673 | |||||||
| chr9:132395749 | G | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+684C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395749 | |||||||
| chr9:132395869 | C | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+564G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395869 | |||||||
| chr9:132395927 | C | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1856+506G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395927 | |||||||
| chr9:132395928 | G | A | 1 | a0001c0007t0004g0131 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1856+505C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395928 | |||||||
| chr9:132395967 | C | T | 1 | a0003c0003t0002g0081 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1856+466G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132395967 | |||||||
| chr9:132396083 | T | G | 81 | a0001c0005t0002g0012 a0001c0005t0002g0018 a0001c0005t0002g0028 others(78): Show |
130 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1856+350A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396083 | |||||||
| chr9:132396095 | C | T | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1856+338G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396095 | |||||||
| chr9:132396132 | G | A | 1 | a0002c0002t0002g0077 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1856+301C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396132 | |||||||
| chr9:132396149 | T | C | 126 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(123): Show |
204 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.1856+284A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396149 | |||||||
| chr9:132396190 | C | T | 81 | a0001c0005t0002g0012 a0001c0005t0002g0018 a0001c0005t0002g0028 others(78): Show |
130 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(127): Show |
intron_variant | MODIFIER | c.1856+243G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396190 | |||||||
| chr9:132396204 | T | C | 80 | a0001c0005t0002g0012 a0001c0005t0002g0018 a0001c0005t0002g0028 others(77): Show |
129 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1856+229A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396204 | |||||||
| chr9:132396305 | C | T | 74 | a0001c0005t0002g0012 a0001c0005t0002g0018 a0001c0005t0002g0028 others(71): Show |
123 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.1856+128G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396305 | |||||||
| chr9:132396324 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1856+109G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396324 | |||||||
| chr9:132396338 | C | T | 80 | a0001c0005t0002g0012 a0001c0005t0002g0018 a0001c0005t0002g0028 others(77): Show |
129 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(126): Show |
intron_variant | MODIFIER | c.1856+95G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396338 | |||||||
| chr9:132396387 | A | G | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1856+46T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 5/10 | chr9 | 132396387 | |||||||
| chr9:132396600 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1778-89A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396600 | |||||||
| chr9:132396674 | G | T | 2 | a0001c0001t0001g0177 a0004c0004t0002g0097 |
2 | HG02258.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1778-163C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396674 | |||||||
| chr9:132396674 | GT | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(165): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1778-164delA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396674 | |||||||
| chr9:132396679 | T | G | 1 | a0001c0001t0001g0219 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1778-168A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396679 | |||||||
| chr9:132396693 | A | G | 2 | a0007c0012t0002g0134 a0007c0012t0002g0135 |
2 | HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1778-182T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396693 | |||||||
| chr9:132396720 | T | G | 1 | a0002c0002t0002g0108 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1778-209A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396720 | |||||||
| chr9:132396772 | A | C | 1 | a0002c0002t0002g0108 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1778-261T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396772 | |||||||
| chr9:132396818 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1778-307G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396818 | |||||||
| chr9:132396819 | C | A | 1 | a0003c0003t0002g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1778-308G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396819 | |||||||
| chr9:132396819 | C | T | 1 | a0013c0020t0001g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1778-308G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132396819 | |||||||
| chr9:132397034 | C | T | 1 | a0001c0018t0001g0231 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1778-523G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397034 | |||||||
| chr9:132397092 | C | T | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1778-581G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397092 | |||||||
| chr9:132397257 | C | G | 1 | a0001c0013t0001g0161 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1778-746G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397257 | |||||||
| chr9:132397319 | G | A | 3 | a0001c0013t0001g0161 a0001c0013t0001g0162 a0001c0013t0001g0163 |
3 | HG01175.hp2 HG03942.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1778-808C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397319 | |||||||
| chr9:132397509 | C | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1777+632G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397509 | |||||||
| chr9:132397517 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
194 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1777+624G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397517 | |||||||
| chr9:132397518 | G | A | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1777+623C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397518 | |||||||
| chr9:132397570 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1777+571C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397570 | |||||||
| chr9:132397582 | A | ACCACAAC others(25): Show |
1 | a0002c0002t0002g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1777+527_1777+558d others(34): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397582 | |||||||
| chr9:132397629 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1777+512A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397629 | |||||||
| chr9:132397633 | A | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1777+508T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397633 | |||||||
| chr9:132397645 | GGA | G | 3 | a0001c0001t0003g0047 a0001c0001t0003g0224 a0001c0001t0003g0225 |
4 | HG02896.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1777+494_1777+495d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397645 | |||||||
| chr9:132397653 | G | A | 1 | a0001c0001t0001g0039 | 2 | HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1777+488C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397653 | |||||||
| chr9:132397751 | C | T | 1 | a0003c0003t0002g0080 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1777+390G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397751 | |||||||
| chr9:132397753 | G | A | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1777+388C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397753 | |||||||
| chr9:132397777 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1777+364C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397777 | |||||||
| chr9:132397847 | G | A | 2 | a0001c0007t0005g0259 a0001c0007t0006g0167 |
2 | HG02818.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1777+294C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397847 | |||||||
| chr9:132397878 | C | T | 1 | a0006c0008t0001g0174 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1777+263G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397878 | |||||||
| chr9:132397879 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1777+262T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397879 | |||||||
| chr9:132397901 | A | G | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1777+240T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397901 | |||||||
| chr9:132397985 | CA | C | 8 | a0001c0001t0001g0146 a0001c0007t0005g0258 a0001c0007t0005g0259 others(5): Show |
8 | HG02451.hp1 HG02818.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1777+155delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132397985 | |||||||
| chr9:132398033 | G | A | 1 | a0002c0002t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1777+108C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132398033 | |||||||
| chr9:132398036 | G | A | 3 | a0001c0005t0002g0057 a0001c0007t0002g0017 a0001c0007t0002g0133 |
5 | HG01943.hp2 HG02970.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.1777+105C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132398036 | |||||||
| chr9:132398120 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1777+21C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132398120 | |||||||
| chr9:132398131 | C | T | 13 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0230 others(10): Show |
16 | HG00280.hp2 HG01243.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1777+10G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 4/10 | chr9 | 132398131 | |||||||
| chr9:132398372 | G | GA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(235): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1592-47dupT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398372 | |||||||
| chr9:132398474 | T | C | 1 | a0005c0006t0001g0232 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1592-148A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398474 | |||||||
| chr9:132398545 | A | G | 2 | a0005c0011t0001g0233 a0005c0011t0001g0234 |
2 | HG00280.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1592-219T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398545 | |||||||
| chr9:132398564 | A | T | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1592-238T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398564 | |||||||
| chr9:132398732 | C | CT | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.1592-407dupA | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398732 | |||||||
| chr9:132398809 | T | C | 3 | a0001c0001t0003g0047 a0001c0001t0003g0224 a0001c0001t0003g0225 |
4 | HG02896.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1592-483A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398809 | |||||||
| chr9:132398889 | C | T | 1 | a0002c0002t0002g0126 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1592-563G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398889 | |||||||
| chr9:132398954 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1592-628A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398954 | |||||||
| chr9:132398990 | G | A | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1592-664C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132398990 | |||||||
| chr9:132399005 | G | A | 1 | a0003c0003t0002g0055 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1592-679C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399005 | |||||||
| chr9:132399083 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1592-757G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399083 | |||||||
| chr9:132399086 | C | A | 1 | a0001c0009t0001g0222 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1592-760G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399086 | |||||||
| chr9:132399177 | C | A | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1592-851G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399177 | |||||||
| chr9:132399198 | CA | C | 5 | a0001c0005t0002g0060 a0001c0010t0002g0038 a0001c0010t0002g0137 others(2): Show |
6 | HG01167.hp1 HG02280.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1591+836delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399198 | |||||||
| chr9:132399202 | AAAAAAAA others(6): Show |
A | 1 | a0002c0002t0002g0074 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1591+820_1591+832d others(15): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399202 | |||||||
| chr9:132399215 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0241 a0012c0017t0001g0159 |
3 | HG02451.hp1 HG02717.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1591+820C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399215 | |||||||
| chr9:132399215 | GA | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.1591+819delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399215 | |||||||
| chr9:132399215 | GAA | G | 6 | a0001c0001t0001g0054 a0001c0001t0001g0253 a0001c0001t0001g0254 others(3): Show |
7 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.1591+818_1591+819d others(4): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399215 | |||||||
| chr9:132399216 | A | G | 6 | a0001c0001t0001g0143 a0001c0001t0001g0171 a0001c0001t0001g0172 others(3): Show |
6 | HG02451.hp1 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1591+819T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399216 | |||||||
| chr9:132399217 | A | G | 1 | a0001c0001t0001g0252 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.1591+818T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399217 | |||||||
| chr9:132399285 | C | A | 2 | a0002c0002t0002g0126 a0002c0002t0002g0127 |
2 | NA18997.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1591+750G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399285 | |||||||
| chr9:132399310 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1591+725G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399310 | |||||||
| chr9:132399441 | C | T | 5 | a0004c0004t0002g0022 a0004c0004t0002g0030 a0004c0004t0002g0037 others(2): Show |
9 | HG00639.hp1 HG01074.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1591+594G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399441 | |||||||
| chr9:132399493 | C | T | 1 | a0004c0004t0002g0095 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1591+542G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399493 | |||||||
| chr9:132399512 | A | C | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(114): Show |
177 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1591+523T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399512 | |||||||
| chr9:132399521 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1591+514T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399521 | |||||||
| chr9:132399928 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1591+107T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399928 | |||||||
| chr9:132399944 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1591+91C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399944 | |||||||
| chr9:132399944 | G | C | 1 | a0001c0001t0001g0223 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1591+91C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399944 | |||||||
| chr9:132399973 | A | G | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1591+62T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399973 | |||||||
| chr9:132399978 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1591+57A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 3/10 | chr9 | 132399978 | |||||||
| chr9:132400387 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1368-129C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400387 | |||||||
| chr9:132400484 | G | A | 13 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0230 others(10): Show |
16 | HG00280.hp2 HG01243.hp1 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1368-226C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400484 | |||||||
| chr9:132400732 | A | G | 3 | a0001c0007t0005g0258 a0001c0007t0005g0259 a0001c0007t0006g0167 |
3 | HG02818.hp1 HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1368-474T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400732 | |||||||
| chr9:132400745 | A | C | 1 | a0001c0001t0001g0026 | 3 | HG02717.hp2 HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1368-487T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400745 | |||||||
| chr9:132400753 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1368-495C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400753 | |||||||
| chr9:132400773 | T | C | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1368-515A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400773 | |||||||
| chr9:132400973 | T | C | 4 | a0001c0001t0001g0048 a0001c0001t0001g0227 a0001c0001t0001g0228 others(1): Show |
5 | HG01891.hp2 HG02965.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1367+482A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400973 | |||||||
| chr9:132400986 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1367+469T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132400986 | |||||||
| chr9:132401026 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1367+429G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401026 | |||||||
| chr9:132401057 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1367+398G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401057 | |||||||
| chr9:132401158 | C | T | 1 | a0001c0005t0002g0057 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1367+297G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401158 | |||||||
| chr9:132401159 | G | A | 38 | a0002c0002t0001g0007 a0002c0002t0001g0141 a0002c0002t0001g0245 others(35): Show |
66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.1367+296C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401159 | |||||||
| chr9:132401219 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.1367+236T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401219 | |||||||
| chr9:132401248 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1367+207G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401248 | |||||||
| chr9:132401250 | C | T | 2 | a0001c0007t0005g0258 a0001c0007t0005g0259 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1367+205G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401250 | |||||||
| chr9:132401323 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(235): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(369): Show |
intron_variant | MODIFIER | c.1367+132G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401323 | |||||||
| chr9:132401397 | T | C | 12 | a0005c0006t0001g0051 a0005c0006t0001g0052 a0005c0006t0001g0230 others(9): Show |
15 | HG00280.hp2 HG01243.hp1 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.1367+58A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 2/10 | chr9 | 132401397 | |||||||
| chr9:132402980 | C | T | 1 | a0007c0012t0002g0134 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7-152G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132402980 | |||||||
| chr9:132403017 | A | G | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-189T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403017 | |||||||
| chr9:132403081 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0039 others(16): Show |
35 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-7-253C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403081 | |||||||
| chr9:132403095 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(174): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.-7-267T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403095 | |||||||
| chr9:132403099 | T | G | 2 | a0001c0007t0005g0258 a0001c0007t0005g0259 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-271A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403099 | |||||||
| chr9:132403102 | G | A | 3 | a0001c0001t0003g0047 a0001c0001t0003g0224 a0001c0001t0003g0225 |
4 | HG02896.hp1 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7-274C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403102 | |||||||
| chr9:132403188 | G | A | 38 | a0002c0002t0001g0007 a0002c0002t0001g0141 a0002c0002t0001g0245 others(35): Show |
66 | HG00099.hp2 HG00323.hp1 HG00558.hp1 others(63): Show |
intron_variant | MODIFIER | c.-7-360C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403188 | |||||||
| chr9:132403382 | C | G | 1 | a0002c0002t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-7-554G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403382 | |||||||
| chr9:132403453 | C | T | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-625G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403453 | |||||||
| chr9:132403499 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-7-671T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403499 | |||||||
| chr9:132403592 | C | G | 2 | a0001c0007t0005g0258 a0001c0007t0005g0259 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-764G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403592 | |||||||
| chr9:132403669 | TA | T | 84 | a0001c0001t0001g0144 a0002c0002t0002g0004 a0002c0002t0002g0006 others(81): Show |
146 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-7-842delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403669 | |||||||
| chr9:132403694 | A | G | 2 | a0004c0004t0002g0030 a0004c0004t0002g0078 |
3 | HG00639.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.-7-866T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403694 | |||||||
| chr9:132403759 | C | T | 2 | a0002c0002t0002g0076 a0002c0002t0002g0077 |
2 | NA19055.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-7-931G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403759 | |||||||
| chr9:132403765 | A | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0252 a0001c0001t0001g0253 others(4): Show |
8 | NA18959.hp2 NA18961.hp2 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7-937T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403765 | |||||||
| chr9:132403804 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-976A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403804 | |||||||
| chr9:132403844 | G | C | 1 | a0004c0004t0002g0037 | 2 | HG01074.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-7-1016C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403844 | |||||||
| chr9:132403898 | C | T | 1 | a0009c0016t0002g0075 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7-1070G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403898 | |||||||
| chr9:132403915 | G | C | 2 | a0006c0008t0001g0226 a0013c0020t0001g0157 |
2 | HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7-1087C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132403915 | |||||||
| chr9:132404071 | T | C | 2 | a0001c0007t0005g0258 a0001c0007t0005g0259 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-7-1243A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404071 | |||||||
| chr9:132404107 | G | A | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-7-1279C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404107 | |||||||
| chr9:132404117 | C | T | 1 | a0001c0001t0001g0049 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-7-1289G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404117 | |||||||
| chr9:132404118 | G | A | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-1290C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404118 | |||||||
| chr9:132404179 | T | C | 1 | a0012c0017t0001g0159 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-7-1351A>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404179 | |||||||
| chr9:132404350 | C | T | 1 | a0005c0006t0001g0230 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-7-1522G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404350 | |||||||
| chr9:132404385 | C | CCT | 3 | a0001c0001t0001g0160 a0001c0001t0001g0248 a0001c0001t0001g0249 |
3 | HG03492.hp1 HG04184.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.-7-1559_-7-1558dup others(2): Show |
TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404385 | |||||||
| chr9:132404398 | G | C | 237 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(234): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(368): Show |
intron_variant | MODIFIER | c.-7-1570C>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404398 | |||||||
| chr9:132404399 | T | G | 3 | a0007c0012t0002g0134 a0007c0012t0002g0135 a0007c0012t0002g0136 |
3 | HG02451.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-7-1571A>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404399 | |||||||
| chr9:132404601 | TA | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0158 a0001c0001t0001g0227 others(4): Show |
8 | HG01891.hp2 HG02451.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7-1774delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404601 | |||||||
| chr9:132404892 | T | A | 3 | a0001c0010t0002g0038 a0001c0010t0002g0137 a0001c0010t0002g0138 |
4 | HG02280.hp2 HG02622.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8+1898A>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404892 | |||||||
| chr9:132404979 | G | A | 84 | a0002c0002t0002g0004 a0002c0002t0002g0006 a0002c0002t0002g0010 others(81): Show |
146 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8+1811C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132404979 | |||||||
| chr9:132405073 | G | A | 1 | a0004c0004t0002g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-8+1717C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405073 | |||||||
| chr9:132405089 | G | A | 1 | a0003c0003t0002g0130 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-8+1701C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405089 | |||||||
| chr9:132405138 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(129): Show |
195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.-8+1652G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405138 | |||||||
| chr9:132405230 | A | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.-8+1560T>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405230 | |||||||
| chr9:132405328 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-8+1462G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405328 | |||||||
| chr9:132405352 | C | T | 84 | a0002c0002t0002g0004 a0002c0002t0002g0006 a0002c0002t0002g0010 others(81): Show |
146 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.-8+1438G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405352 | |||||||
| chr9:132405353 | G | A | 1 | a0001c0010t0002g0138 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-8+1437C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405353 | |||||||
| chr9:132405396 | C | T | 1 | a0013c0020t0001g0157 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-8+1394G>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405396 | |||||||
| chr9:132405473 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-8+1317C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405473 | |||||||
| chr9:132405980 | A | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0039 others(16): Show |
35 | HG00140.hp1 HG00597.hp2 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.-8+810T>G | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132405980 | |||||||
| chr9:132406038 | C | G | 19 | a0001c0001t0002g0059 a0001c0005t0002g0012 a0001c0005t0002g0018 others(16): Show |
26 | HG00735.hp2 HG01099.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.-8+752G>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406038 | |||||||
| chr9:132406377 | G | A | 2 | a0001c0007t0005g0258 a0001c0007t0005g0259 |
2 | HG03041.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-8+413C>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406377 | |||||||
| chr9:132406500 | G | T | 1 | a0001c0001t0001g0143 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-8+290C>A | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406500 | |||||||
| chr9:132406585 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-8+205T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406585 | |||||||
| chr9:132406590 | A | G | 2 | a0002c0002t0002g0027 a0002c0002t0002g0058 |
3 | NA18964.hp1 NA19054.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-8+200T>C | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406590 | |||||||
| chr9:132406603 | TA | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(128): Show |
198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.-8+186delT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406603 | |||||||
| chr9:132406603 | TAA | T | 5 | a0001c0001t0001g0140 a0001c0007t0005g0258 a0001c0007t0005g0259 others(2): Show |
10 | HG01192.hp1 HG02572.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.-8+185_-8+186delTT | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406603 | |||||||
| chr9:132406668 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(139): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.-8+122G>T | TTF1 | ENSG00000125482.13 | transcript | ENST00000334270.3 | protein_coding | 1/10 | chr9 | 132406668 |