Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7138 |
| ensemblid | ENSG00000105048.18 |
| hgncid | 11948 |
| symbol | TNNT1 |
| name | troponin T1, slow skeletal type |
| refseq_nuc | NM_003283.6 |
| refseq_prot | NP_003274.3 |
| ensembl_nuc | ENST00000588981.6 |
| ensembl_prot | ENSP00000467176.1 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 55132698 |
| end | 55149206 |
| strand | - |
| ver | v1.2 |
| region | chr19:55132698-55149206 |
| region5000 | chr19:55127698-55154206 |
| regionname0 | TNNT1_chr19_55132698_55149206 |
| regionname5000 | TNNT1_chr19_55127698_55154206 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 278 | 306 | 86 | 59 | 112 | 11 | 36 | 75 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| a0002 | 0/0 | 278 | 10 | 2 | 5 | 0 | 1 | 2 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| a0003 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| a0004 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| a0005 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| a0006 | 0/0 | 278 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | MSDTE others(273): Show |
chr19 | 55127698 | 55154206 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 834 | 295 | 83 | 57 | 106 | 11 | 36 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0001c0003 | 0/0 | 834 | 8 | 0 | 2 | 6 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0001c0004 | 0/0 | 834 | 2 | 2 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0001c0007 | 0/0 | 834 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0002c0002 | 0/0 | 834 | 10 | 2 | 5 | 0 | 1 | 2 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0003c0006 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0004c0009 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0005c0005 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 | ||
| a0006c0008 | 0/0 | 834 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | ATGTC others(829): Show |
chr19 | 55127698 | 55154206 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1111 | 165 | 51 | 33 | 59 | 6 | 16 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0002 | 0/1 | 1111 | 78 | 20 | 14 | 22 | 4 | 17 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0003 | 1/0 | 1111 | 27 | 5 | 5 | 12 | 1 | 3 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0004 | 0/0 | 1111 | 21 | 5 | 4 | 12 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0005 | 0/0 | 1110 | 2 | 1 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1105): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0006 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0001t0007 | 0/0 | 1110 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1105): Show |
chr19 | 55127698 | 55154206 |
| a0001c0003t0001 | 0/0 | 1111 | 8 | 0 | 2 | 6 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0004t0001 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0004t0008 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0001c0007t0002 | 0/0 | 1111 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0002c0002t0001 | 0/0 | 1111 | 10 | 2 | 5 | 0 | 1 | 2 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0003c0006t0001 | 0/0 | 1111 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0004c0009t0002 | 0/0 | 1111 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0005c0005t0002 | 0/0 | 1111 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| a0006c0008t0003 | 0/0 | 1111 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | AGCAA others(1106): Show |
chr19 | 55127698 | 55154206 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0007 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0001 | 0/0 | 6 | 1 | 3 | 1 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0063 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0005g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0004t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0001c0007t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0002c0002t0001g0004 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0002c0002t0001g0010 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0003c0006t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0004c0009t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0005c0005t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| a0006c0008t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | GBR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0088 | EUR | FIN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0013 | EUR | FIN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | FIN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00408 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00621 | hp2 | a0001 | c0003 | t0001 | g0248 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0041 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0242 | EAS | CHS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0047 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0232 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0053 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0066 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0185 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0050 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | IBS | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01928 | hp1 | a0001 | c0001 | t0005 | g0262 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02071 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02080 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02083 | hp2 | a0003 | c0006 | t0001 | g0234 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0152 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PEL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0216 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0198 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03041 | hp1 | a0001 | c0007 | t0002 | g0145 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0166 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | ESN | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0151 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0231 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0032 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0123 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0217 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0059 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0161 | SAS | STU | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0272 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0052 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18966 | hp2 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18971 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18975 | hp2 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18982 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19005 | hp1 | a0004 | c0009 | t0002 | g0263 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19005 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19007 | hp2 | a0005 | c0005 | t0002 | g0218 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0055 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19030 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19043 | hp1 | a0001 | c0004 | t0008 | g0147 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19066 | hp2 | a0006 | c0008 | t0003 | g0036 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19074 | hp1 | a0001 | c0003 | t0001 | g0020 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | YRI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ASW | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | ASW | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20752 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | TSI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0061 | EUR | TSI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | GIH | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01123 | hp1 | a0001 | c0003 | t0001 | g0021 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | CLM | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0016 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0044 | AFR | MSL | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | USA | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | LWK | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0122 | REF | REF | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0063 | REF | REF | TNNT1_chr19_55127698_55154206 | TNNT1 | chr19 | 55127698 | 55154206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:55137121 | A | G | 1 | a0006 | 1 | NA19066.hp2 | missense_variant | MODERATE | c.593T>C | p.Met198Thr | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/14 | 650/1111 | 593/837 | 198/278 | chr19 | 55137121 | |||
| chr19:55137184 | G | T | 1 | a0004 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.530C>A | p.Thr177Lys | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/14 | 587/1111 | 530/837 | 177/278 | chr19 | 55137184 | |||
| chr19:55137185 | T | C | 1 | a0004 | 1 | NA19005.hp1 | missense_variant | MODERATE | c.529A>G | p.Thr177Ala | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/14 | 586/1111 | 529/837 | 177/278 | chr19 | 55137185 | |||
| chr19:55141918 | C | G | 1 | a0003 | 1 | HG02083.hp2 | missense_variant&splice_region_variant | MODERATE | c.131G>C | p.Arg44Pro | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/14 | 188/1111 | 131/837 | 44/278 | chr19 | 55141918 | |||
| chr19:55146681 | C | T | 1 | a0005 | 1 | NA19007.hp2 | missense_variant&splice_region_variant | MODERATE | c.73G>A | p.Ala25Thr | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 4/14 | 130/1111 | 73/837 | 25/278 | chr19 | 55146681 | |||
| chr19:55147019 | T | C | 1 | a0002 | 10 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
missense_variant&splice_region_variant | MODERATE | c.35A>G | p.Glu12Gly | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/14 | 92/1111 | 35/837 | 12/278 | chr19 | 55147019 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:55132957 | C | A | 1 | a0001c0003 | 8 | HG00621.hp2 HG01123.hp1 HG01261.hp2 others(5): Show |
synonymous_variant | LOW | c.795G>T | p.Arg265Arg | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 852/1111 | 795/837 | 265/278 | chr19 | 55132957 | |||
| chr19:55137183 | C | G | 1 | a0004c0009 | 1 | NA19005.hp1 | synonymous_variant | LOW | c.531G>C | p.Thr177Thr | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/14 | 588/1111 | 531/837 | 177/278 | chr19 | 55137183 | |||
| chr19:55141216 | T | C | 1 | a0001c0004 | 2 | HG02809.hp1 NA19043.hp1 |
synonymous_variant | LOW | c.279A>G | p.Glu93Glu | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/14 | 336/1111 | 279/837 | 93/278 | chr19 | 55141216 | |||
| chr19:55141893 | C | T | 1 | a0001c0007 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.156G>A | p.Pro52Pro | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/14 | 213/1111 | 156/837 | 52/278 | chr19 | 55141893 | |||
| chr19:55141917 | G | C | 1 | a0003c0006 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.132C>G | p.Arg44Arg | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/14 | 189/1111 | 132/837 | 44/278 | chr19 | 55141917 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:55132735 | G | A | 1 | a0001c0001t0006 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*180C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 180 | chr19 | 55132735 | ||||||
| chr19:55132736 | A | G | 1 | a0001c0001t0006 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*179T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 179 | chr19 | 55132736 | ||||||
| chr19:55132755 | G | C | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(3): Show |
102 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 160 | chr19 | 55132755 | ||||||
| chr19:55132805 | A | G | 1 | a0001c0004t0008 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 110 | chr19 | 55132805 | ||||||
| chr19:55132876 | TC | T | 2 | a0001c0001t0005 a0001c0001t0007 |
3 | HG01928.hp1 HG02071.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*38delG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 14/14 | 38 | chr19 | 55132876 | ||||||
| chr19:55149169 | T | C | 12 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(9): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
5_prime_UTR_variant | MODIFIER | c.-20A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/14 | 2012 | chr19 | 55149169 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:55133056 | A | G | 1 | a0001c0001t0003g0035 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.792-96T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133056 | |||||||
| chr19:55133071 | C | A | 2 | a0001c0001t0002g0143 a0001c0007t0002g0145 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.792-111G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133071 | |||||||
| chr19:55133074 | G | A | 75 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0013 others(72): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.792-114C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133074 | |||||||
| chr19:55133088 | C | G | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.792-128G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133088 | |||||||
| chr19:55133089 | A | C | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.792-129T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133089 | |||||||
| chr19:55133121 | C | T | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.792-161G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133121 | |||||||
| chr19:55133122 | T | C | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.792-162A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133122 | |||||||
| chr19:55133122 | T | TG | 11 | a0001c0001t0001g0104 a0001c0001t0001g0118 a0001c0001t0001g0172 others(8): Show |
11 | HG01175.hp2 HG01192.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.792-163dupC | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133122 | |||||||
| chr19:55133132 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.792-172G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133132 | |||||||
| chr19:55133154 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.792-194A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133154 | |||||||
| chr19:55133174 | T | G | 4 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0188 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.792-214A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133174 | |||||||
| chr19:55133198 | TG | T | 4 | a0001c0001t0001g0137 a0001c0001t0002g0266 a0001c0001t0003g0060 others(1): Show |
4 | HG01975.hp1 NA18962.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.792-239delC | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133198 | |||||||
| chr19:55133203 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.792-243C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133203 | |||||||
| chr19:55133238 | G | C | 2 | a0001c0001t0001g0131 a0001c0004t0001g0198 |
2 | HG02809.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.792-278C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133238 | |||||||
| chr19:55133238 | G | T | 75 | a0001c0001t0002g0001 a0001c0001t0002g0009 a0001c0001t0002g0013 others(72): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.792-278C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133238 | |||||||
| chr19:55133282 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.792-322C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133282 | |||||||
| chr19:55133547 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.791+340C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133547 | |||||||
| chr19:55133615 | T | TTGCAGTG others(8): Show |
1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.791+257_791+271dup others(15): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133615 | |||||||
| chr19:55133680 | T | TA | 6 | a0001c0001t0001g0072 a0001c0001t0001g0230 a0001c0001t0001g0256 others(3): Show |
6 | HG01928.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.791+206dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133680 | |||||||
| chr19:55133680 | TA | T | 23 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0105 others(20): Show |
23 | HG01261.hp1 HG01358.hp2 HG01934.hp2 others(20): Show |
intron_variant | MODIFIER | c.791+206delT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133680 | |||||||
| chr19:55133681 | A | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0119 |
3 | HG02004.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.791+206T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133681 | |||||||
| chr19:55133844 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.791+43C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133844 | |||||||
| chr19:55133845 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.791+42T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133845 | |||||||
| chr19:55133849 | T | A | 1 | a0001c0001t0002g0089 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.791+38A>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 13/13 | chr19 | 55133849 | |||||||
| chr19:55133932 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | splice_region_variant&intron_variant | LOW | c.751-5C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133932 | |||||||
| chr19:55133943 | A | G | 11 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0109 others(8): Show |
11 | HG01109.hp1 HG01192.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.751-16T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133943 | |||||||
| chr19:55133950 | CTGGGACA others(4): Show |
C | 1 | a0001c0001t0004g0043 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.751-34_751-24delCG others(9): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133950 | |||||||
| chr19:55133961 | GGTGGGGA others(1): Show |
G | 57 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(54): Show |
62 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.751-42_751-35delGT others(6): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133961 | |||||||
| chr19:55133969 | C | T | 27 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(24): Show |
30 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(27): Show |
intron_variant | MODIFIER | c.751-42G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133969 | |||||||
| chr19:55133971 | T | TG | 4 | a0001c0001t0001g0172 a0001c0001t0002g0154 a0001c0001t0002g0184 others(1): Show |
4 | HG01496.hp1 HG02071.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.751-45dupC | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55133971 | |||||||
| chr19:55134024 | C | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0185 |
2 | HG01109.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.750+42G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 12/13 | chr19 | 55134024 | |||||||
| chr19:55134230 | TG | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0256 a0001c0003t0001g0248 |
3 | HG00621.hp2 NA18963.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.612-27delC | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134230 | |||||||
| chr19:55134420 | C | T | 4 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0188 others(1): Show |
4 | HG02145.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.612-216G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134420 | |||||||
| chr19:55134432 | T | C | 5 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG01192.hp1 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-228A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134432 | |||||||
| chr19:55134456 | C | G | 1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.612-252G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134456 | |||||||
| chr19:55134492 | C | A | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0117 others(32): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-288G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134492 | |||||||
| chr19:55134517 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612-313G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134517 | |||||||
| chr19:55134533 | TA | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0117 others(32): Show |
40 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.612-330delT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134533 | |||||||
| chr19:55134534 | A | T | 1 | a0001c0001t0001g0087 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.612-330T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134534 | |||||||
| chr19:55134679 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-475C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134679 | |||||||
| chr19:55134683 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-479T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134683 | |||||||
| chr19:55134687 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-483T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134687 | |||||||
| chr19:55134691 | T | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-487A>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134691 | |||||||
| chr19:55134692 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.612-488C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134692 | |||||||
| chr19:55134694 | G | GGAGGGGA others(13): Show |
15 | a0001c0001t0001g0197 a0001c0001t0001g0199 a0001c0001t0001g0236 others(12): Show |
15 | HG00323.hp1 HG01081.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.612-510_612-491dup others(20): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134694 | |||||||
| chr19:55134694 | G | GGAGGGGA others(33): Show |
4 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0215 others(1): Show |
6 | HG00639.hp1 HG01069.hp2 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.612-530_612-491dup others(40): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134694 | |||||||
| chr19:55134694 | G | GGGAGGGG others(14): Show |
1 | a0001c0001t0001g0239 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.612-491_612-490ins others(21): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134694 | |||||||
| chr19:55134697 | G | GGGGAGGG others(13): Show |
1 | a0001c0001t0001g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612-494_612-493ins others(20): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134697 | |||||||
| chr19:55134700 | G | A | 1 | a0001c0001t0002g0241 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.612-496C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134700 | |||||||
| chr19:55134701 | A | AGGGGAGA others(14): Show |
1 | a0001c0001t0001g0190 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.612-518_612-498dup others(21): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134701 | |||||||
| chr19:55134702 | G | A | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.612-498C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134702 | |||||||
| chr19:55134710 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-506C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134710 | |||||||
| chr19:55134711 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-507T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134711 | |||||||
| chr19:55134713 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-509T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134713 | |||||||
| chr19:55134717 | G | C | 34 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0117 others(31): Show |
39 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.612-513C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134717 | |||||||
| chr19:55134736 | A | AGGGGAGG others(14): Show |
1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.612-553_612-533dup others(21): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134736 | |||||||
| chr19:55134740 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-536C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134740 | |||||||
| chr19:55134741 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-537T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134741 | |||||||
| chr19:55134744 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-540C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134744 | |||||||
| chr19:55134744 | G | C | 1 | a0001c0001t0002g0086 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.612-540C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134744 | |||||||
| chr19:55134757 | G | A | 2 | a0001c0001t0001g0230 a0001c0001t0002g0157 |
2 | HG00738.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.612-553C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134757 | |||||||
| chr19:55134762 | G | GGGGAGAG others(12): Show |
1 | a0001c0001t0003g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.612-559_612-558ins others(19): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134762 | |||||||
| chr19:55134768 | A | AGGAGAAG others(268): Show |
5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-565_612-564ins others(275): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(292): Show |
1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(299): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(286): Show |
1 | a0001c0001t0001g0070 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(293): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(277): Show |
1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(284): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(288): Show |
1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(295): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(288): Show |
17 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0073 others(14): Show |
20 | HG00621.hp1 HG01952.hp1 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.612-565_612-564ins others(295): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(289): Show |
1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(296): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(270): Show |
4 | a0001c0001t0001g0235 a0002c0002t0001g0004 a0002c0002t0001g0231 others(1): Show |
7 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.612-565_612-564ins others(277): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(278): Show |
1 | a0001c0001t0002g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(285): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(266): Show |
1 | a0001c0001t0003g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(273): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(254): Show |
1 | a0001c0001t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(261): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(267): Show |
1 | a0001c0001t0001g0168 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(274): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(253): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0189 |
2 | HG00544.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.612-565_612-564ins others(260): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(267): Show |
1 | a0001c0001t0003g0037 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(274): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(268): Show |
20 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0081 others(17): Show |
26 | HG00323.hp2 HG00642.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.612-565_612-564ins others(275): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(253): Show |
1 | a0001c0001t0001g0172 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(260): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(253): Show |
1 | a0001c0001t0001g0194 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(260): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(253): Show |
1 | a0001c0001t0002g0088 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(260): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(268): Show |
19 | a0001c0001t0001g0005 a0001c0001t0001g0071 a0001c0001t0001g0094 others(16): Show |
25 | HG00423.hp1 HG00597.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.612-565_612-564ins others(275): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(270): Show |
1 | a0001c0001t0001g0092 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(277): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(254): Show |
1 | a0001c0001t0001g0084 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(261): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(269): Show |
1 | a0001c0001t0001g0176 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(276): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(270): Show |
1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.612-565_612-564ins others(277): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | AGGAGAAG others(268): Show |
1 | a0001c0003t0001g0248 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.612-565_612-564ins others(275): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134768 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0002g0157 |
2 | HG00738.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.612-564T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134768 | |||||||
| chr19:55134774 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-570C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134774 | |||||||
| chr19:55134775 | A | G | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): Show |
106 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.612-571T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134775 | |||||||
| chr19:55134780 | GA | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(74): Show |
92 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.612-577delT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134780 | |||||||
| chr19:55134781 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.612-577T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134781 | |||||||
| chr19:55134782 | A | G | 8 | a0001c0001t0001g0081 a0001c0001t0001g0105 a0001c0001t0001g0235 others(5): Show |
11 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.612-578T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134782 | |||||||
| chr19:55134786 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(192): Show |
221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.612-582C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134786 | |||||||
| chr19:55134787 | A | AGGAGAGC others(219): Show |
1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.612-584_612-583ins others(226): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134787 | |||||||
| chr19:55134787 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0014 others(193): Show |
222 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(219): Show |
intron_variant | MODIFIER | c.612-583T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134787 | |||||||
| chr19:55134788 | GGGA | G | 73 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
88 | HG00323.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.612-587_612-585del others(3): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134788 | |||||||
| chr19:55134789 | G | GAGAGCGG others(254): Show |
1 | a0001c0001t0002g0157 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.612-586_612-585ins others(261): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134789 | |||||||
| chr19:55134791 | A | AGAAGAG | 6 | a0001c0001t0001g0108 a0001c0001t0001g0235 a0001c0001t0002g0088 others(3): Show |
9 | HG00280.hp1 HG01069.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(6): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGAAGAGG others(4): Show |
1 | a0001c0001t0001g0172 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(11): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(263): Show |
1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(270): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(238): Show |
1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(245): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(240): Show |
1 | a0001c0001t0004g0043 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(247): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(229): Show |
1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(236): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(282): Show |
1 | a0001c0001t0003g0060 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(289): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(238): Show |
1 | a0001c0001t0004g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(245): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(229): Show |
1 | a0001c0001t0001g0190 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(236): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(224): Show |
1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(231): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(263): Show |
1 | a0001c0001t0001g0188 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(270): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(240): Show |
1 | a0001c0001t0004g0055 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(247): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(239): Show |
55 | a0001c0001t0001g0093 a0001c0001t0001g0117 a0001c0001t0001g0126 others(52): Show |
60 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(246): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(244): Show |
27 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0019 others(24): Show |
29 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(251): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(259): Show |
1 | a0001c0001t0004g0045 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(266): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(264): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0276 |
2 | HG02970.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.612-588_612-587ins others(271): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(264): Show |
23 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0197 others(20): Show |
26 | HG00323.hp1 HG00639.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(271): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(284): Show |
1 | a0001c0003t0001g0021 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(291): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(269): Show |
2 | a0001c0001t0001g0275 a0001c0001t0003g0068 |
2 | HG03486.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.612-588_612-587ins others(276): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(245): Show |
1 | a0001c0001t0003g0058 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(252): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(252): Show |
1 | a0001c0001t0001g0019 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(259): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(279): Show |
26 | a0001c0001t0002g0001 a0001c0001t0002g0013 a0001c0001t0002g0078 others(23): Show |
31 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(286): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(280): Show |
1 | a0001c0001t0002g0001 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(287): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(282): Show |
1 | a0001c0001t0002g0191 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(289): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(282): Show |
1 | a0001c0001t0002g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(289): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(240): Show |
1 | a0001c0001t0003g0028 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(247): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(242): Show |
1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(249): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(244): Show |
1 | a0001c0001t0003g0025 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(251): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(234): Show |
1 | a0001c0001t0001g0003 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(241): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(246): Show |
1 | a0001c0001t0001g0127 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(253): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(243): Show |
1 | a0001c0001t0003g0034 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(250): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(244): Show |
19 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0120 others(16): Show |
22 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.612-588_612-587ins others(251): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(245): Show |
1 | a0001c0001t0001g0003 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(252): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(245): Show |
1 | a0001c0001t0003g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(252): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(245): Show |
1 | a0001c0001t0001g0131 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(252): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(254): Show |
2 | a0001c0001t0001g0181 a0001c0001t0001g0182 |
2 | HG02630.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.612-588_612-587ins others(261): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(248): Show |
1 | a0001c0001t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(255): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(241): Show |
1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(248): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(280): Show |
1 | a0001c0001t0002g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(287): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(240): Show |
1 | a0001c0001t0004g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(247): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(269): Show |
1 | a0001c0001t0001g0192 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(276): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(240): Show |
1 | a0001c0001t0002g0266 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(247): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGAGG others(243): Show |
1 | a0001c0001t0001g0137 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.612-588_612-587ins others(250): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | AGGGGGAG others(250): Show |
1 | a0001c0001t0001g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.612-588_612-587ins others(257): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134791 | A | G | 1 | a0001c0003t0001g0248 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.612-587T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134791 | |||||||
| chr19:55134792 | G | T | 1 | a0004c0009t0002g0263 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.612-588C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134792 | |||||||
| chr19:55134793 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.612-589C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134793 | |||||||
| chr19:55134793 | G | GGGAGGGA others(235): Show |
1 | a0004c0009t0002g0263 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.612-590_612-589ins others(242): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134793 | |||||||
| chr19:55134793 | G | GGGAGGGG others(266): Show |
1 | a0001c0001t0001g0116 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.612-590_612-589ins others(273): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134793 | |||||||
| chr19:55134793 | G | GGGAGGGG others(235): Show |
1 | a0001c0001t0001g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.612-590_612-589ins others(242): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134793 | |||||||
| chr19:55134794 | G | GGAGGGGA others(245): Show |
1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.612-591_612-590ins others(252): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134794 | |||||||
| chr19:55134795 | A | G | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.612-591T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134795 | |||||||
| chr19:55134795 | A | T | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.612-591T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134795 | |||||||
| chr19:55134801 | G | GAAGAGGG others(227): Show |
1 | a0001c0001t0001g0180 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.612-598_612-597ins others(234): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134801 | |||||||
| chr19:55134807 | A | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0195 a0001c0001t0001g0196 others(6): Show |
9 | HG00423.hp2 HG00597.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.612-603T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134807 | |||||||
| chr19:55134808 | C | G | 10 | a0001c0001t0001g0105 a0001c0001t0001g0117 a0001c0001t0001g0195 others(7): Show |
10 | HG00423.hp2 HG00597.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.612-604G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134808 | |||||||
| chr19:55134808 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.612-604G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134808 | |||||||
| chr19:55134833 | C | T | 1 | a0001c0001t0003g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.612-629G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134833 | |||||||
| chr19:55134841 | A | G | 1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.612-637T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134841 | |||||||
| chr19:55134841 | A | T | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.612-637T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134841 | |||||||
| chr19:55134854 | G | A | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-650C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134854 | |||||||
| chr19:55134855 | A | G | 1 | a0001c0003t0001g0249 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.612-651T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134855 | |||||||
| chr19:55134857 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.612-653T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134857 | |||||||
| chr19:55134866 | A | G | 1 | a0001c0001t0004g0056 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.612-662T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134866 | |||||||
| chr19:55134969 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.612-765G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55134969 | |||||||
| chr19:55135096 | G | GA | 4 | a0001c0001t0001g0092 a0001c0001t0001g0181 a0001c0001t0002g0124 others(1): Show |
4 | HG01934.hp2 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-893dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135096 | |||||||
| chr19:55135166 | C | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0120 others(23): Show |
31 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.612-962G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135166 | |||||||
| chr19:55135196 | TC | T | 26 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(23): Show |
29 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(26): Show |
intron_variant | MODIFIER | c.612-993delG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135196 | |||||||
| chr19:55135377 | TTTCC | T | 71 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
82 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.612-1177_612-1174d others(6): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135377 | |||||||
| chr19:55135400 | C | A | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.612-1196G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135400 | |||||||
| chr19:55135413 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.612-1209A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135413 | |||||||
| chr19:55135414 | C | CT | 12 | a0001c0001t0001g0116 a0001c0001t0001g0118 a0001c0001t0001g0148 others(9): Show |
12 | HG02080.hp1 HG02145.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.612-1211dupA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135414 | |||||||
| chr19:55135414 | C | CTT | 11 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0109 others(8): Show |
11 | HG01109.hp1 HG01192.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-1212_612-1211d others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135414 | |||||||
| chr19:55135414 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.612-1210G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135414 | |||||||
| chr19:55135525 | C | CT | 125 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(122): Show |
141 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.612-1322dupA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135525 | |||||||
| chr19:55135525 | C | CTT | 27 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0113 others(24): Show |
27 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(24): Show |
intron_variant | MODIFIER | c.612-1323_612-1322d others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135525 | |||||||
| chr19:55135525 | CT | C | 6 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0230 others(3): Show |
6 | HG01070.hp2 HG01168.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.612-1322delA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135525 | |||||||
| chr19:55135568 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.612-1364G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135568 | |||||||
| chr19:55135593 | T | C | 1 | a0001c0001t0004g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.612-1389A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135593 | |||||||
| chr19:55135608 | A | C | 1 | a0001c0001t0003g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.612-1404T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135608 | |||||||
| chr19:55135620 | T | C | 1 | a0001c0001t0004g0045 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.612-1416A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135620 | |||||||
| chr19:55135672 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.611+1431C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135672 | |||||||
| chr19:55135813 | G | GC | 8 | a0001c0001t0001g0169 a0001c0001t0001g0176 a0001c0001t0001g0180 others(5): Show |
8 | HG01358.hp1 HG01934.hp1 NA18980.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+1289dupG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135813 | |||||||
| chr19:55135814 | C | A | 1 | a0001c0001t0002g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.611+1289G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135814 | |||||||
| chr19:55135816 | C | G | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.611+1287G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135816 | |||||||
| chr19:55135817 | G | C | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.611+1286C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135817 | |||||||
| chr19:55135818 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.611+1285G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135818 | |||||||
| chr19:55135833 | T | C | 1 | a0001c0001t0001g0195 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.611+1270A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135833 | |||||||
| chr19:55135837 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0278 |
2 | HG03453.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.611+1266G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135837 | |||||||
| chr19:55135922 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.611+1181G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135922 | |||||||
| chr19:55135923 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.611+1180T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135923 | |||||||
| chr19:55135924 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.611+1179G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55135924 | |||||||
| chr19:55136014 | GC | G | 4 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0002g0110 others(1): Show |
4 | HG02132.hp1 NA18950.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.611+1088delG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136014 | |||||||
| chr19:55136034 | T | G | 1 | a0001c0001t0001g0101 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.611+1069A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136034 | |||||||
| chr19:55136061 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.611+1042T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136061 | |||||||
| chr19:55136063 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.611+1040G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136063 | |||||||
| chr19:55136078 | T | TACGGACT others(12): Show |
1 | a0001c0001t0004g0043 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.611+1006_611+1024d others(21): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136078 | |||||||
| chr19:55136111 | TC | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0137 a0001c0001t0004g0052 |
3 | NA18522.hp1 NA18962.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.611+991delG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136111 | |||||||
| chr19:55136256 | A | C | 1 | a0001c0001t0003g0028 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.611+847T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136256 | |||||||
| chr19:55136289 | ATTGCCCA others(64): Show |
A | 1 | a0001c0001t0004g0052 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.611+743_611+813del others(71): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136289 | |||||||
| chr19:55136565 | C | T | 1 | a0001c0001t0003g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.611+538G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136565 | |||||||
| chr19:55136684 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.611+419G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136684 | |||||||
| chr19:55136685 | T | G | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.611+418A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136685 | |||||||
| chr19:55136686 | G | C | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.611+417C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136686 | |||||||
| chr19:55136781 | A | T | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.611+322T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136781 | |||||||
| chr19:55136902 | G | A | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.611+201C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136902 | |||||||
| chr19:55136920 | G | T | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.611+183C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136920 | |||||||
| chr19:55136930 | A | G | 2 | a0001c0001t0001g0170 a0001c0001t0001g0173 |
2 | NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.611+173T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55136930 | |||||||
| chr19:55137007 | C | T | 2 | a0001c0003t0001g0020 a0001c0003t0001g0257 |
3 | NA18975.hp2 NA18982.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.611+96G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55137007 | |||||||
| chr19:55137010 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.611+93C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 11/13 | chr19 | 55137010 | |||||||
| chr19:55137240 | A | C | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.502-28T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137240 | |||||||
| chr19:55137241 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.502-29G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137241 | |||||||
| chr19:55137337 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.502-125C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137337 | |||||||
| chr19:55137389 | T | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.502-177A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137389 | |||||||
| chr19:55137411 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.502-199C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137411 | |||||||
| chr19:55137411 | G | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
14 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.502-199C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137411 | |||||||
| chr19:55137476 | C | CCCAGCCC others(30): Show |
1 | a0001c0001t0002g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502-265_502-264ins others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137476 | |||||||
| chr19:55137485 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.502-273G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137485 | |||||||
| chr19:55137499 | G | A | 1 | a0001c0001t0003g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.502-287C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137499 | |||||||
| chr19:55137506 | A | AGACCCCA others(244): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0269 a0001c0001t0002g0268 |
3 | HG02647.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.502-295_502-294ins others(251): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137506 | |||||||
| chr19:55137506 | A | AGACCCCA others(207): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0230 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.502-295_502-294ins others(214): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137506 | |||||||
| chr19:55137506 | A | AGACCCCA others(459): Show |
1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502-295_502-294ins others(466): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137506 | |||||||
| chr19:55137506 | A | AGACCCCA others(278): Show |
13 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
14 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.502-295_502-294ins others(285): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137506 | |||||||
| chr19:55137508 | A | ACCCCAGC others(29): Show |
111 | a0001c0001t0001g0006 a0001c0001t0001g0069 a0001c0001t0001g0072 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.502-297_502-296ins others(36): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137508 | |||||||
| chr19:55137508 | A | ACCCCAGC others(281): Show |
3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02630.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.502-297_502-296ins others(288): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137508 | |||||||
| chr19:55137508 | A | ACCCCAGC others(244): Show |
1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.502-297_502-296ins others(251): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137508 | |||||||
| chr19:55137512 | C | CAGCCCCT others(66): Show |
1 | a0001c0001t0001g0135 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.502-301_502-300ins others(73): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137512 | |||||||
| chr19:55137512 | C | CAGCCCCT others(66): Show |
27 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0120 others(24): Show |
32 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.502-301_502-300ins others(73): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137512 | |||||||
| chr19:55137512 | C | CAGCCCCT others(67): Show |
1 | a0001c0001t0003g0023 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.502-301_502-300ins others(74): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137512 | |||||||
| chr19:55137514 | G | GCCCCTCC others(30): Show |
1 | a0001c0001t0002g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.502-303_502-302ins others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137514 | |||||||
| chr19:55137529 | G | GCCCAGGA others(30): Show |
1 | a0004c0009t0002g0263 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.502-318_502-317ins others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137529 | |||||||
| chr19:55137538 | T | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
94 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.502-326A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137538 | |||||||
| chr19:55137540 | G | C | 1 | a0001c0001t0001g0259 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502-328C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137540 | |||||||
| chr19:55137540 | G | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(45): Show |
54 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.502-328C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137540 | |||||||
| chr19:55137544 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0259 |
2 | HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.502-332C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137544 | |||||||
| chr19:55137545 | C | CCCCCAGC others(67): Show |
1 | a0001c0001t0001g0259 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.502-334_502-333ins others(74): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137545 | |||||||
| chr19:55137545 | C | G | 48 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(45): Show |
54 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.502-333G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137545 | |||||||
| chr19:55137546 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02630.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.502-334G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137546 | |||||||
| chr19:55137549 | G | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(50): Show |
59 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.502-337C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137549 | |||||||
| chr19:55137577 | G | C | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02630.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.502-365C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137577 | |||||||
| chr19:55137577 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.502-365C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137577 | |||||||
| chr19:55137582 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.502-370G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137582 | |||||||
| chr19:55137635 | T | C | 13 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0071 others(10): Show |
14 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+326A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137635 | |||||||
| chr19:55137653 | C | T | 50 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(47): Show |
56 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.501+308G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137653 | |||||||
| chr19:55137663 | T | TCGCATTA others(30): Show |
6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+261_501+297dup others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137663 | |||||||
| chr19:55137677 | A | G | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02630.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.501+284T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137677 | |||||||
| chr19:55137716 | C | A | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+245G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137716 | |||||||
| chr19:55137724 | C | A | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+237G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137724 | |||||||
| chr19:55137727 | T | C | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+234A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137727 | |||||||
| chr19:55137745 | G | GACCCAGG others(31): Show |
1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+215_501+216ins others(38): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137745 | |||||||
| chr19:55137755 | C | G | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+206G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137755 | |||||||
| chr19:55137760 | A | C | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.501+201T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137760 | |||||||
| chr19:55137790 | G | A | 1 | a0001c0001t0005g0166 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.501+171C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137790 | |||||||
| chr19:55137890 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0269 a0001c0001t0002g0268 |
3 | HG02647.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.501+71C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 10/13 | chr19 | 55137890 | |||||||
| chr19:55138225 | A | C | 166 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
185 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.388-151T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138225 | |||||||
| chr19:55138280 | G | GT | 54 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0095 others(51): Show |
61 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.388-207dupA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138280 | |||||||
| chr19:55138280 | G | GTTT | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0120 others(22): Show |
30 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.388-209_388-207dup others(3): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138280 | |||||||
| chr19:55138280 | G | GTTTT | 10 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(7): Show |
10 | HG01192.hp2 HG02056.hp1 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.388-210_388-207dup others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138280 | |||||||
| chr19:55138334 | G | C | 16 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(13): Show |
16 | HG01109.hp1 HG01192.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.388-260C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138334 | |||||||
| chr19:55138341 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(15): Show |
21 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.388-267C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138341 | |||||||
| chr19:55138370 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02630.hp2 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.388-296G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138370 | |||||||
| chr19:55138430 | A | AC | 7 | a0001c0001t0001g0105 a0001c0001t0001g0131 a0001c0001t0001g0149 others(4): Show |
7 | HG01192.hp1 HG02132.hp2 HG04199.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-357dupG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138430 | |||||||
| chr19:55138506 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.388-432C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138506 | |||||||
| chr19:55138521 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0258 |
3 | HG00323.hp1 HG01106.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.388-447C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138521 | |||||||
| chr19:55138588 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.388-514C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138588 | |||||||
| chr19:55138703 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-629G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138703 | |||||||
| chr19:55138707 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-633T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138707 | |||||||
| chr19:55138806 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.388-732G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138806 | |||||||
| chr19:55138807 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.388-733A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138807 | |||||||
| chr19:55138808 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.388-734C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138808 | |||||||
| chr19:55138948 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0269 a0001c0001t0002g0268 |
3 | HG02647.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.388-874A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55138948 | |||||||
| chr19:55139001 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-927G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139001 | |||||||
| chr19:55139018 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.388-944C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139018 | |||||||
| chr19:55139022 | T | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0081 others(27): Show |
36 | HG00544.hp1 HG00642.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.388-948A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139022 | |||||||
| chr19:55139050 | A | C | 1 | a0001c0001t0001g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.388-976T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139050 | |||||||
| chr19:55139081 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-1007G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139081 | |||||||
| chr19:55139186 | A | G | 236 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
270 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.388-1112T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139186 | |||||||
| chr19:55139304 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.388-1230A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139304 | |||||||
| chr19:55139319 | G | A | 163 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.388-1245C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139319 | |||||||
| chr19:55139475 | T | A | 1 | a0001c0001t0003g0064 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.388-1401A>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139475 | |||||||
| chr19:55139620 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
194 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.387+1263C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139620 | |||||||
| chr19:55139691 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.387+1192C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139691 | |||||||
| chr19:55139724 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.387+1159G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139724 | |||||||
| chr19:55139754 | C | G | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.387+1129G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139754 | |||||||
| chr19:55139774 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.387+1109C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139774 | |||||||
| chr19:55139784 | T | C | 3 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0267 |
3 | HG03490.hp2 HG03492.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.387+1099A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139784 | |||||||
| chr19:55139804 | T | TA | 81 | a0001c0001t0001g0156 a0001c0001t0002g0001 a0001c0001t0002g0009 others(78): Show |
92 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.387+1078dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139804 | |||||||
| chr19:55139814 | T | A | 20 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(17): Show |
23 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.387+1069A>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139814 | |||||||
| chr19:55139981 | G | A | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.387+902C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55139981 | |||||||
| chr19:55140080 | G | A | 2 | a0001c0004t0001g0198 a0001c0004t0008g0147 |
2 | HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.387+803C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140080 | |||||||
| chr19:55140122 | G | GA | 6 | a0001c0001t0001g0131 a0001c0001t0001g0148 a0001c0001t0001g0222 others(3): Show |
6 | HG01192.hp1 HG02970.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+760dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140122 | |||||||
| chr19:55140223 | G | A | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.387+660C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140223 | |||||||
| chr19:55140312 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.387+571T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140312 | |||||||
| chr19:55140338 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0168 |
2 | NA18945.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.387+545C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140338 | |||||||
| chr19:55140499 | C | T | 1 | a0001c0001t0003g0038 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.387+384G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140499 | |||||||
| chr19:55140526 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.387+357G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140526 | |||||||
| chr19:55140554 | G | A | 3 | a0001c0001t0001g0148 a0001c0001t0001g0269 a0001c0001t0002g0268 |
3 | HG02647.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.387+329C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140554 | |||||||
| chr19:55140600 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.387+283G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140600 | |||||||
| chr19:55140603 | C | A | 1 | a0001c0001t0003g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387+280G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140603 | |||||||
| chr19:55140669 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.387+214C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140669 | |||||||
| chr19:55140718 | A | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0230 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.387+165T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140718 | |||||||
| chr19:55140731 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.387+152G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140731 | |||||||
| chr19:55140751 | T | C | 1 | a0001c0001t0002g0221 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.387+132A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140751 | |||||||
| chr19:55140794 | G | GTAA | 74 | a0001c0001t0001g0148 a0001c0001t0001g0156 a0001c0001t0001g0269 others(71): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.387+86_387+88dupTT others(1): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140794 | |||||||
| chr19:55140794 | G | GTAATAA | 4 | a0001c0001t0004g0012 a0001c0001t0004g0049 a0001c0001t0004g0056 others(1): Show |
5 | HG02071.hp1 HG02080.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.387+83_387+88dupTT others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140794 | |||||||
| chr19:55140794 | GTAA | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(25): Show |
31 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(28): Show |
intron_variant | MODIFIER | c.387+86_387+88delTT others(1): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140794 | |||||||
| chr19:55140794 | GTAATAA | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
6 | HG02451.hp2 HG02630.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+83_387+88delTT others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140794 | |||||||
| chr19:55140794 | GTAATAAT others(5): Show |
G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0112 others(36): Show |
44 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.387+77_387+88delTT others(10): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140794 | |||||||
| chr19:55140808 | A | AATAATC | 4 | a0001c0001t0001g0235 a0002c0002t0001g0004 a0002c0002t0001g0231 others(1): Show |
7 | HG01069.hp1 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+74_387+75insGA others(4): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140808 | |||||||
| chr19:55140808 | A | C | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.387+75T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 9/13 | chr19 | 55140808 | |||||||
| chr19:55140974 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.310-14T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55140974 | |||||||
| chr19:55141054 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.310-94C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55141054 | |||||||
| chr19:55141065 | A | T | 1 | a0001c0001t0002g0143 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.310-105T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55141065 | |||||||
| chr19:55141107 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.309+79G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55141107 | |||||||
| chr19:55141160 | G | C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0230 |
2 | HG02451.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.309+26C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55141160 | |||||||
| chr19:55141171 | G | C | 1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.309+15C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 8/13 | chr19 | 55141171 | |||||||
| chr19:55141326 | T | G | 3 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0002g0217 |
3 | HG03834.hp2 HG03927.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.193-24A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141326 | |||||||
| chr19:55141344 | G | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0136 a0001c0001t0001g0149 others(6): Show |
9 | HG00438.hp1 HG00642.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.193-42C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141344 | |||||||
| chr19:55141390 | A | G | 163 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(160): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.193-88T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141390 | |||||||
| chr19:55141476 | A | C | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.193-174T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141476 | |||||||
| chr19:55141476 | A | T | 42 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0069 others(39): Show |
45 | HG00621.hp1 HG01109.hp1 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-174T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141476 | |||||||
| chr19:55141497 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.193-195T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141497 | |||||||
| chr19:55141498 | C | A | 1 | a0001c0001t0001g0256 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.193-196G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141498 | |||||||
| chr19:55141505 | C | CT | 44 | a0001c0001t0001g0081 a0001c0001t0001g0105 a0001c0001t0001g0116 others(41): Show |
45 | HG00544.hp1 HG00642.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.193-204dupA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141505 | |||||||
| chr19:55141505 | CT | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0098 a0001c0001t0001g0107 others(5): Show |
10 | HG02074.hp2 HG02083.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.193-204delA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141505 | |||||||
| chr19:55141533 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.193-231C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141533 | |||||||
| chr19:55141552 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.193-250G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141552 | |||||||
| chr19:55141650 | A | T | 41 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0082 others(38): Show |
46 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+207T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141650 | |||||||
| chr19:55141692 | C | G | 1 | a0001c0001t0002g0210 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.192+165G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141692 | |||||||
| chr19:55141760 | A | G | 9 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG02145.hp2 HG02451.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+97T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141760 | |||||||
| chr19:55141776 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.192+81C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141776 | |||||||
| chr19:55141783 | G | A | 18 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(15): Show |
21 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+74C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 7/13 | chr19 | 55141783 | |||||||
| chr19:55141929 | A | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0017 a0001c0001t0001g0081 others(21): Show |
30 | HG00642.hp2 HG00741.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.129-9T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55141929 | |||||||
| chr19:55142019 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.129-99C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142019 | |||||||
| chr19:55142092 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.129-172G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142092 | |||||||
| chr19:55142151 | T | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-231A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142151 | |||||||
| chr19:55142160 | A | G | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-240T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142160 | |||||||
| chr19:55142189 | C | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0119 |
3 | HG02004.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129-269G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142189 | |||||||
| chr19:55142213 | T | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-293A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142213 | |||||||
| chr19:55142265 | C | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-345G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142265 | |||||||
| chr19:55142270 | A | G | 10 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(7): Show |
10 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.129-350T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142270 | |||||||
| chr19:55142277 | A | C | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-357T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142277 | |||||||
| chr19:55142291 | TTC | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-373_129-372del others(2): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142291 | |||||||
| chr19:55142295 | G | A | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-375C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142295 | |||||||
| chr19:55142311 | C | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-391G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142311 | |||||||
| chr19:55142315 | G | C | 1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129-395C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142315 | |||||||
| chr19:55142316 | C | T | 8 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(5): Show |
8 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.129-396G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142316 | |||||||
| chr19:55142546 | AT | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(75): Show |
89 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.129-627delA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142546 | |||||||
| chr19:55142546 | ATT | A | 9 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0108 others(6): Show |
9 | HG02451.hp1 HG02897.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-628_129-627del others(2): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142546 | |||||||
| chr19:55142546 | ATTT | A | 9 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(6): Show |
9 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.129-629_129-627del others(3): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142546 | |||||||
| chr19:55142650 | C | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.129-730G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142650 | |||||||
| chr19:55142673 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.129-753C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142673 | |||||||
| chr19:55142889 | C | T | 1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129-969G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142889 | |||||||
| chr19:55142947 | T | G | 1 | a0001c0001t0001g0222 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.129-1027A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55142947 | |||||||
| chr19:55143008 | T | TA | 15 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(12): Show |
15 | HG01109.hp1 HG01192.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.129-1089dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143008 | |||||||
| chr19:55143009 | A | T | 20 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(17): Show |
23 | HG00621.hp1 HG02027.hp1 HG02083.hp1 others(20): Show |
intron_variant | MODIFIER | c.129-1089T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143009 | |||||||
| chr19:55143010 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-1090T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143010 | |||||||
| chr19:55143043 | C | T | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129-1123G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143043 | |||||||
| chr19:55143083 | C | T | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129-1163G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143083 | |||||||
| chr19:55143102 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.129-1182C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143102 | |||||||
| chr19:55143148 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.129-1228C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143148 | |||||||
| chr19:55143168 | C | CA | 86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(83): Show |
100 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(97): Show |
intron_variant | MODIFIER | c.129-1249dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143168 | |||||||
| chr19:55143168 | CA | C | 16 | a0001c0001t0001g0075 a0001c0001t0001g0094 a0001c0001t0001g0126 others(13): Show |
16 | HG00544.hp1 HG00639.hp2 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.129-1249delT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143168 | |||||||
| chr19:55143192 | G | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-1272C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143192 | |||||||
| chr19:55143282 | G | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0119 |
3 | HG02004.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.129-1362C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143282 | |||||||
| chr19:55143291 | C | T | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129-1371G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143291 | |||||||
| chr19:55143446 | G | C | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.129-1526C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143446 | |||||||
| chr19:55143463 | G | T | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.129-1543C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143463 | |||||||
| chr19:55143483 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.129-1563C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143483 | |||||||
| chr19:55143489 | G | C | 2 | a0001c0001t0001g0126 a0001c0001t0003g0032 |
2 | HG03669.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.129-1569C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143489 | |||||||
| chr19:55143499 | G | A | 7 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.129-1579C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143499 | |||||||
| chr19:55143662 | A | G | 1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.129-1742T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143662 | |||||||
| chr19:55143734 | C | G | 1 | a0001c0001t0002g0164 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.128+1810G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143734 | |||||||
| chr19:55143753 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0269 a0001c0001t0002g0268 |
3 | HG02647.hp2 HG02976.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.128+1791G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143753 | |||||||
| chr19:55143759 | C | A | 1 | a0001c0001t0001g0197 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.128+1785G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143759 | |||||||
| chr19:55143769 | T | C | 24 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(21): Show |
30 | HG00621.hp1 HG01069.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.128+1775A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143769 | |||||||
| chr19:55143886 | C | T | 44 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(41): Show |
49 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.128+1658G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143886 | |||||||
| chr19:55143958 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.128+1586T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55143958 | |||||||
| chr19:55144052 | CCCCCACC others(3): Show |
C | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+1482_128+1491d others(12): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144052 | |||||||
| chr19:55144072 | C | CT | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0125 others(32): Show |
43 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.128+1471dupA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144072 | |||||||
| chr19:55144072 | CT | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0098 a0001c0001t0001g0104 others(8): Show |
13 | HG01074.hp2 HG02647.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+1471delA | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144072 | |||||||
| chr19:55144073 | T | C | 6 | a0001c0001t0001g0014 a0001c0001t0001g0087 a0001c0001t0001g0228 others(3): Show |
7 | HG00733.hp2 HG01168.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.128+1471A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144073 | |||||||
| chr19:55144151 | C | T | 1 | a0001c0004t0001g0198 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.128+1393G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144151 | |||||||
| chr19:55144185 | A | C | 1 | a0001c0001t0001g0215 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.128+1359T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144185 | |||||||
| chr19:55144278 | C | T | 1 | a0001c0001t0001g0239 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.128+1266G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144278 | |||||||
| chr19:55144428 | G | A | 1 | a0001c0001t0002g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.128+1116C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144428 | |||||||
| chr19:55144553 | A | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.128+991T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144553 | |||||||
| chr19:55144576 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0120 a0001c0001t0001g0140 others(2): Show |
7 | HG00735.hp2 HG01081.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.128+968C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144576 | |||||||
| chr19:55144644 | C | T | 1 | a0001c0001t0002g0201 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.128+900G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144644 | |||||||
| chr19:55144721 | G | T | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.128+823C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144721 | |||||||
| chr19:55144781 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(41): Show |
49 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(46): Show |
intron_variant | MODIFIER | c.128+763C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144781 | |||||||
| chr19:55144857 | G | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(42): Show |
50 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.128+687C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144857 | |||||||
| chr19:55144933 | G | A | 5 | a0001c0001t0002g0008 a0001c0001t0002g0016 a0001c0001t0002g0146 others(2): Show |
8 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+611C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144933 | |||||||
| chr19:55144969 | C | T | 1 | a0001c0001t0002g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.128+575G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55144969 | |||||||
| chr19:55145136 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.128+408C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145136 | |||||||
| chr19:55145136 | G | GA | 13 | a0001c0001t0001g0092 a0001c0001t0001g0150 a0001c0001t0001g0199 others(10): Show |
13 | HG01106.hp1 HG01361.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.128+407dupT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145136 | |||||||
| chr19:55145136 | GA | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(90): Show |
107 | HG00323.hp2 HG00544.hp1 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.128+407delT | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145136 | |||||||
| chr19:55145136 | GAA | G | 66 | a0001c0001t0001g0019 a0001c0001t0001g0087 a0001c0001t0001g0156 others(63): Show |
78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.128+406_128+407del others(2): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145136 | |||||||
| chr19:55145152 | AAC | A | 12 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(9): Show |
12 | HG02055.hp2 HG02258.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.128+390_128+391del others(2): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145152 | |||||||
| chr19:55145153 | AC | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0112 others(22): Show |
29 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.128+390delG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145153 | |||||||
| chr19:55145154 | C | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0119 a0001c0001t0001g0131 others(5): Show |
8 | HG00735.hp1 HG02074.hp1 HG06807.hp2 others(5): Show |
intron_variant | MODIFIER | c.128+390G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145154 | |||||||
| chr19:55145205 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.128+339C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145205 | |||||||
| chr19:55145335 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.128+209C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145335 | |||||||
| chr19:55145389 | G | A | 1 | a0001c0004t0008g0147 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.128+155C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145389 | |||||||
| chr19:55145493 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.128+51C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145493 | |||||||
| chr19:55145527 | A | C | 1 | a0001c0001t0001g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.128+17T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 6/13 | chr19 | 55145527 | |||||||
| chr19:55145673 | C | A | 42 | a0001c0001t0001g0019 a0001c0001t0001g0208 a0001c0001t0002g0009 others(39): Show |
48 | HG00280.hp1 HG00408.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.107-108G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145673 | |||||||
| chr19:55145677 | G | C | 2 | a0001c0001t0002g0086 a0001c0001t0002g0209 |
2 | NA19043.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.107-112C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145677 | |||||||
| chr19:55145701 | T | A | 6 | a0001c0001t0001g0230 a0001c0001t0001g0235 a0002c0002t0001g0004 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.107-136A>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145701 | |||||||
| chr19:55145775 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.107-210G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145775 | |||||||
| chr19:55145847 | C | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0140 |
4 | HG00735.hp2 HG01081.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-282G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145847 | |||||||
| chr19:55145975 | GCCCACCG others(1): Show |
G | 40 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0069 others(37): Show |
48 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.107-418_107-411del others(8): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145975 | |||||||
| chr19:55145990 | G | GC | 13 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0149 others(10): Show |
14 | HG00423.hp1 HG00642.hp2 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.107-426dupG | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55145990 | |||||||
| chr19:55146037 | C | G | 19 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0069 others(16): Show |
22 | HG02027.hp1 HG02083.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.106+397G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55146037 | |||||||
| chr19:55146367 | C | T | 10 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(7): Show |
10 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.106+67G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55146367 | |||||||
| chr19:55146390 | G | C | 1 | a0003c0006t0001g0234 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+44C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55146390 | |||||||
| chr19:55146393 | C | G | 1 | a0003c0006t0001g0234 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.106+41G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55146393 | |||||||
| chr19:55146398 | G | A | 2 | a0001c0001t0002g0213 a0001c0001t0002g0214 |
2 | NA18975.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.106+36C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 5/13 | chr19 | 55146398 | |||||||
| chr19:55146545 | A | T | 1 | a0001c0001t0001g0233 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.74-79T>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 4/13 | chr19 | 55146545 | |||||||
| chr19:55146644 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.73+37G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 4/13 | chr19 | 55146644 | |||||||
| chr19:55146720 | G | A | 7 | a0001c0001t0001g0014 a0001c0001t0001g0075 a0001c0001t0001g0076 others(4): Show |
8 | HG00280.hp1 HG00733.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-13C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146720 | |||||||
| chr19:55146799 | G | C | 38 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(35): Show |
48 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-92C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146799 | |||||||
| chr19:55146854 | T | C | 51 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(48): Show |
62 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.47-147A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146854 | |||||||
| chr19:55146855 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.47-148C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146855 | |||||||
| chr19:55146867 | C | T | 1 | a0001c0001t0002g0124 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.46+141G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146867 | |||||||
| chr19:55146909 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.46+99C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 3/13 | chr19 | 55146909 | |||||||
| chr19:55147029 | C | T | 30 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0120 others(27): Show |
35 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(32): Show |
splice_region_variant&intron_variant | LOW | c.33-8G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 2/13 | chr19 | 55147029 | |||||||
| chr19:55147259 | CCTGGACT others(7): Show |
C | 1 | a0001c0001t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-11-105_-11-92delA others(13): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147259 | |||||||
| chr19:55147301 | AGCTGGGG others(102): Show |
A | 39 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(36): Show |
42 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.-11-242_-11-134del | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147301 | |||||||
| chr19:55147309 | TCTGGACT others(138): Show |
T | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11-286_-11-142del | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147309 | |||||||
| chr19:55147324 | G | C | 6 | a0001c0001t0001g0230 a0002c0002t0001g0004 a0002c0002t0001g0010 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-156C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147324 | |||||||
| chr19:55147329 | A | G | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(46): Show |
62 | HG00438.hp1 HG00544.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.-11-161T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147329 | |||||||
| chr19:55147345 | CCTGGACT others(66): Show |
C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0017 others(123): Show |
145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-11-250_-11-178del others(73): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147345 | |||||||
| chr19:55147366 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-11-198T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147366 | |||||||
| chr19:55147373 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-11-205C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147373 | |||||||
| chr19:55147377 | GGGGGCCT others(65): Show |
G | 1 | a0001c0007t0002g0145 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-11-281_-11-210del others(72): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147377 | |||||||
| chr19:55147403 | G | A | 36 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0112 others(33): Show |
44 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.-11-235C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147403 | |||||||
| chr19:55147403 | GAGGAGGG others(65): Show |
G | 13 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(10): Show |
18 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11-307_-11-236del others(72): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147403 | |||||||
| chr19:55147410 | G | GGCTGGGG others(185): Show |
1 | a0002c0002t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11-243_-11-242ins others(192): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147410 | |||||||
| chr19:55147414 | GGGGTCTG others(64): Show |
G | 35 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0113 others(32): Show |
43 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.-11-317_-11-247del others(71): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147414 | |||||||
| chr19:55147418 | T | C | 21 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0095 others(18): Show |
21 | HG00408.hp1 HG00558.hp1 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.-11-250A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147418 | |||||||
| chr19:55147431 | G | A | 1 | a0002c0002t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11-263C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147431 | |||||||
| chr19:55147446 | A | G | 1 | a0002c0002t0001g0077 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-11-278T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147446 | |||||||
| chr19:55147475 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-11-307T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147475 | |||||||
| chr19:55147493 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-11-325C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147493 | |||||||
| chr19:55147533 | CTCCTGGA others(29): Show |
C | 1 | a0001c0001t0001g0267 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11-401_-11-366del others(36): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147533 | |||||||
| chr19:55147548 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11-380C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147548 | |||||||
| chr19:55147645 | T | TCCTGGAC others(36): Show |
1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-11-478_-11-477ins others(43): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147645 | |||||||
| chr19:55147668 | A | AGGAGGGG others(31): Show |
2 | a0001c0001t0001g0149 a0001c0001t0003g0031 |
2 | HG00438.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-11-501_-11-500ins others(38): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147668 | |||||||
| chr19:55147668 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-11-500T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147668 | |||||||
| chr19:55147674 | G | A | 13 | a0001c0001t0001g0093 a0001c0001t0001g0148 a0001c0001t0001g0230 others(10): Show |
18 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.-11-506C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147674 | |||||||
| chr19:55147677 | T | C | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(205): Show |
238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-11-509A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147677 | |||||||
| chr19:55147678 | G | GC | 45 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(42): Show |
53 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-511_-11-510ins others(1): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147678 | |||||||
| chr19:55147678 | G | GCGGGTCT others(68): Show |
2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-11-511_-11-510ins others(75): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147678 | |||||||
| chr19:55147679 | G | C | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(158): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-11-511C>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147679 | |||||||
| chr19:55147679 | G | GA | 3 | a0001c0001t0001g0105 a0001c0001t0001g0149 a0001c0001t0003g0031 |
3 | HG00438.hp2 NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-11-512_-11-511ins others(1): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147679 | |||||||
| chr19:55147682 | T | C | 7 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0105 others(4): Show |
7 | HG00438.hp2 HG01069.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11-514A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147682 | |||||||
| chr19:55147682 | T | G | 161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(158): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-11-514A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147682 | |||||||
| chr19:55147682 | TCTGGACT others(30): Show |
T | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11-551_-11-515del others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147682 | |||||||
| chr19:55147683 | C | CCTGGACA others(31): Show |
161 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0014 others(158): Show |
183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-11-516_-11-515ins others(38): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147683 | |||||||
| chr19:55147683 | C | CTGGACAC others(30): Show |
2 | a0001c0001t0001g0075 a0001c0001t0001g0076 |
2 | HG01069.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.-11-516_-11-515ins others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147683 | |||||||
| chr19:55147683 | C | CTGGACTC others(30): Show |
1 | a0001c0001t0001g0148 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-11-516_-11-515ins others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147683 | |||||||
| chr19:55147683 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0149 a0001c0001t0003g0031 |
3 | HG00438.hp2 NA18960.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.-11-515G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147683 | |||||||
| chr19:55147695 | A | G | 45 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0069 others(42): Show |
53 | HG00438.hp1 HG00544.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-11-527T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147695 | |||||||
| chr19:55147695 | ATCTGAGG others(30): Show |
A | 5 | a0001c0001t0001g0230 a0002c0002t0001g0004 a0002c0002t0001g0010 others(2): Show |
10 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-564_-11-528del others(37): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147695 | |||||||
| chr19:55147713 | C | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-545G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147713 | |||||||
| chr19:55147714 | A | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-546T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147714 | |||||||
| chr19:55147724 | A | C | 8 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-556T>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147724 | |||||||
| chr19:55147726 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-11-558C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147726 | |||||||
| chr19:55147726 | G | T | 8 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-558C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147726 | |||||||
| chr19:55147762 | C | T | 5 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(2): Show |
5 | HG02145.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.-11-594G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147762 | |||||||
| chr19:55147763 | G | A | 5 | a0001c0001t0001g0230 a0002c0002t0001g0004 a0002c0002t0001g0010 others(2): Show |
10 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-595C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147763 | |||||||
| chr19:55147771 | C | G | 8 | a0001c0001t0001g0069 a0001c0001t0001g0072 a0001c0001t0001g0073 others(5): Show |
8 | HG01109.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11-603G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147771 | |||||||
| chr19:55147778 | A | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0002c0002t0001g0004 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-610T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147778 | |||||||
| chr19:55147785 | T | G | 6 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0002c0002t0001g0004 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-617A>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147785 | |||||||
| chr19:55147790 | G | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0002c0002t0001g0004 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-622C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147790 | |||||||
| chr19:55147794 | C | T | 7 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0001c0001t0002g0123 others(4): Show |
12 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.-11-626G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147794 | |||||||
| chr19:55147798 | C | A | 6 | a0001c0001t0001g0093 a0001c0001t0001g0230 a0002c0002t0001g0004 others(3): Show |
11 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.-11-630G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147798 | |||||||
| chr19:55147806 | G | A | 5 | a0001c0001t0001g0230 a0002c0002t0001g0004 a0002c0002t0001g0010 others(2): Show |
10 | HG00639.hp1 HG01069.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-11-638C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147806 | |||||||
| chr19:55147869 | A | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(218): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.-11-701T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147869 | |||||||
| chr19:55147878 | AGTCTGAG others(31): Show |
A | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-11-748_-11-711del others(38): Show |
TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147878 | |||||||
| chr19:55147893 | C | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(217): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.-11-725G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147893 | |||||||
| chr19:55147932 | G | T | 1 | a0001c0001t0003g0031 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-11-764C>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55147932 | |||||||
| chr19:55148047 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-11-879G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148047 | |||||||
| chr19:55148055 | C | G | 1 | a0001c0001t0001g0120 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-11-887G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148055 | |||||||
| chr19:55148387 | C | T | 5 | a0001c0001t0001g0094 a0001c0001t0001g0116 a0001c0001t0001g0117 others(2): Show |
5 | HG02145.hp1 HG02965.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-12+774G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148387 | |||||||
| chr19:55148412 | C | T | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0099 |
3 | HG02083.hp1 NA18982.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.-12+749G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148412 | |||||||
| chr19:55148731 | T | C | 31 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0070 others(28): Show |
34 | HG02027.hp1 HG02083.hp1 HG02145.hp2 others(31): Show |
intron_variant | MODIFIER | c.-12+430A>G | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148731 | |||||||
| chr19:55148741 | C | T | 11 | a0001c0001t0001g0015 a0001c0001t0001g0070 a0001c0001t0001g0071 others(8): Show |
12 | HG02027.hp1 HG02083.hp1 HG02809.hp2 others(9): Show |
intron_variant | MODIFIER | c.-12+420G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148741 | |||||||
| chr19:55148828 | C | A | 14 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0099 others(11): Show |
17 | HG02027.hp1 HG02083.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.-12+333G>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148828 | |||||||
| chr19:55148924 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-12+237T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148924 | |||||||
| chr19:55148937 | G | A | 4 | a0001c0001t0001g0109 a0001c0001t0003g0066 a0001c0001t0003g0068 others(1): Show |
4 | HG01109.hp1 HG02897.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-12+224C>T | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148937 | |||||||
| chr19:55148945 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG02004.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-12+216G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55148945 | |||||||
| chr19:55149059 | C | G | 1 | a0001c0001t0001g0111 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-12+102G>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55149059 | |||||||
| chr19:55149079 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-12+82G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55149079 | |||||||
| chr19:55149131 | A | G | 52 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(49): Show |
57 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.-12+30T>C | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55149131 | |||||||
| chr19:55149146 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-12+15G>A | TNNT1 | ENSG00000105048.18 | transcript | ENST00000588981.6 | protein_coding | 1/13 | chr19 | 55149146 |