Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10040 |
| ensemblid | ENSG00000141198.16 |
| hgncid | 11983 |
| symbol | TOM1L1 |
| name | target of myb1 like 1 membrane trafficking protein |
| refseq_nuc | NM_005486.3 |
| refseq_prot | NP_005477.2 |
| ensembl_nuc | ENST00000575882.6 |
| ensembl_prot | ENSP00000460823.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 54900852 |
| end | 54961956 |
| strand | + |
| ver | v1.2 |
| region | chr17:54900852-54961956 |
| region5000 | chr17:54895852-54966956 |
| regionname0 | TOM1L1_chr17_54900852_54961956 |
| regionname5000 | TOM1L1_chr17_54895852_54966956 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 476 | 388 | 89 | 70 | 179 | 12 | 36 | 141 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | MAFGK others(471): Show |
chr17 | 54895852 | 54966956 |
| a0002 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | MAFGK others(471): Show |
chr17 | 54895852 | 54966956 |
| a0003 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | MAFGK others(471): Show |
chr17 | 54895852 | 54966956 |
| a0004 | 0/0 | 476 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | MAFGK others(471): Show |
chr17 | 54895852 | 54966956 |
| a0005 | 0/0 | 476 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | MAFGK others(471): Show |
chr17 | 54895852 | 54966956 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1428 | 387 | 89 | 70 | 179 | 12 | 35 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 | ||
| a0001c0003 | 0/0 | 1428 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 | ||
| a0002c0006 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 | ||
| a0003c0004 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 | ||
| a0004c0005 | 0/0 | 1428 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 | ||
| a0005c0002 | 0/0 | 1428 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | ATGGC others(1423): Show |
chr17 | 54895852 | 54966956 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2168 | 220 | 26 | 34 | 136 | 4 | 18 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0002 | 0/0 | 2168 | 103 | 34 | 19 | 31 | 5 | 14 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0003 | 0/0 | 2168 | 39 | 5 | 16 | 12 | 3 | 3 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0004 | 0/0 | 2168 | 20 | 20 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0005 | 0/0 | 2168 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0006 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0001t0007 | 0/0 | 2168 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0001c0003t0001 | 0/0 | 2168 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0002c0006t0004 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0003c0004t0001 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0004c0005t0002 | 0/0 | 2168 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| a0005c0002t0001 | 0/0 | 2168 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | CCTCT others(2163): Show |
chr17 | 54895852 | 54966956 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 1 | 7 | 4 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0201 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0003 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0001t0007g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0001c0003t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0002c0006t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0003c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0004c0005t0002g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| a0005c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | GBR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0071 | EUR | GBR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0313 | EUR | FIN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0085 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | CHS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0309 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0301 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0082 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0075 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0069 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0074 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0249 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0083 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | IBS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0276 | EUR | IBS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0066 | EUR | IBS | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0054 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0242 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01928 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0279 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0300 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01993 | hp1 | a0001 | c0001 | t0007 | g0318 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02056 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0068 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | CDX | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CDX | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | CDX | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0003 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0039 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0265 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0284 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0271 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02723 | hp2 | a0002 | c0006 | t0004 | g0052 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0289 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0266 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0040 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0272 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0247 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0255 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0053 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0256 | AFR | ESN | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0033 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0123 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0244 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0294 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03579 | hp2 | a0001 | c0001 | t0004 | g0051 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0312 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0067 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0094 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0307 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0078 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0308 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04228 | hp1 | a0001 | c0003 | t0001 | g0117 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18612 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | CHB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0321 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0320 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18979 | hp1 | a0005 | c0002 | t0001 | g0044 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0262 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | YRI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | ASW | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0008 | EUR | TSI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | TSI | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0070 | AMR | CLM | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0264 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0173 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0032 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0246 | AFR | MSL | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG06807 | hp1 | a0004 | c0005 | t0002 | g0263 | AFR | USA | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0088 | AFR | USA | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | USA | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | USA | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0201 | REF | REF | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0150 | REF | REF | TOM1L1_chr17_54895852_54966956 | TOM1L1 | chr17 | 54895852 | 54966956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:54900887 | C | T | 1 | a0002 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.22C>T | p.Arg8Trp | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/16 | 36/2168 | 22/1431 | 8/476 | chr17 | 54900887 | |||
| chr17:54915813 | T | C | 1 | a0005 | 1 | NA18979.hp1 | missense_variant | MODERATE | c.671T>C | p.Met224Thr | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/16 | 685/2168 | 671/1431 | 224/476 | chr17 | 54915813 | |||
| chr17:54930193 | C | T | 1 | a0004 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.841C>T | p.Leu281Phe | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/16 | 855/2168 | 841/1431 | 281/476 | chr17 | 54930193 | |||
| chr17:54939020 | C | T | 1 | a0003 | 1 | HG03471.hp1 | missense_variant&splice_region_variant | MODERATE | c.1130C>T | p.Pro377Leu | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/16 | 1144/2168 | 1130/1431 | 377/476 | chr17 | 54939020 | |||
| chr17:54961954 | C | T | 2 | a0001 a0004 |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
splice_region_variant | LOW | c.*721C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | chr17 | 54961954 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:54950118 | C | G | 1 | a0001c0003 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1362C>G | p.Val454Val | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/16 | 1376/2168 | 1362/1431 | 454/476 | chr17 | 54950118 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:54961288 | C | T | 1 | a0001c0001t0007 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 662 | chr17 | 54961288 | ||||||
| chr17:54961293 | A | C | 1 | a0001c0001t0003 | 39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*60A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 667 | chr17 | 54961293 | ||||||
| chr17:54961384 | A | G | 1 | a0001c0001t0003 | 39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*151A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 758 | chr17 | 54961384 | ||||||
| chr17:54961422 | G | A | 3 | a0001c0001t0002 a0001c0001t0007 a0004c0005t0002 |
105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*189G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 796 | chr17 | 54961422 | ||||||
| chr17:54961424 | G | A | 1 | a0001c0001t0006 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*191G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 798 | chr17 | 54961424 | ||||||
| chr17:54961738 | T | C | 2 | a0001c0001t0004 a0002c0006t0004 |
21 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 16/16 | 1112 | chr17 | 54961738 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:54901098 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.58+175C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901098 | |||||||
| chr17:54901138 | A | C | 1 | a0001c0001t0001g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+215A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901138 | |||||||
| chr17:54901140 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.58+217G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901140 | |||||||
| chr17:54901152 | C | T | 12 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(9): Show |
12 | HG01109.hp2 HG02135.hp1 HG02976.hp2 others(9): Show |
intron_variant | MODIFIER | c.58+229C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901152 | |||||||
| chr17:54901313 | A | T | 71 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(68): Show |
80 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.58+390A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901313 | |||||||
| chr17:54901450 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58+527G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901450 | |||||||
| chr17:54901491 | G | A | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0002g0257 others(4): Show |
7 | HG00639.hp2 HG00673.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.58+568G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901491 | |||||||
| chr17:54901555 | C | A | 1 | a0001c0001t0001g0012 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.58+632C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901555 | |||||||
| chr17:54901698 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.58+775A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54901698 | |||||||
| chr17:54902157 | T | C | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.58+1234T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902157 | |||||||
| chr17:54902201 | G | A | 1 | a0001c0001t0003g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.58+1278G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902201 | |||||||
| chr17:54902281 | G | T | 2 | a0001c0001t0002g0254 a0001c0001t0003g0255 |
2 | HG03139.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.58+1358G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902281 | |||||||
| chr17:54902314 | T | C | 2 | a0001c0001t0002g0035 a0001c0001t0004g0036 |
2 | HG02965.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.58+1391T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902314 | |||||||
| chr17:54902394 | C | A | 5 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0005g0037 others(2): Show |
5 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.59-1314C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902394 | |||||||
| chr17:54902414 | C | T | 15 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0245 others(12): Show |
15 | HG00639.hp2 HG00673.hp2 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.59-1294C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902414 | |||||||
| chr17:54902474 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03491.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.59-1234G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902474 | |||||||
| chr17:54902537 | A | G | 1 | a0001c0001t0002g0321 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.59-1171A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902537 | |||||||
| chr17:54902624 | T | C | 78 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(75): Show |
85 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.59-1084T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902624 | |||||||
| chr17:54902638 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.59-1070C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902638 | |||||||
| chr17:54902643 | A | C | 18 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-1065A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902643 | |||||||
| chr17:54902926 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.59-782G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902926 | |||||||
| chr17:54902945 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18955.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.59-763G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902945 | |||||||
| chr17:54902984 | G | A | 1 | a0001c0001t0002g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.59-724G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54902984 | |||||||
| chr17:54903072 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.59-636G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54903072 | |||||||
| chr17:54903210 | T | TA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(4): Show |
8 | HG02040.hp1 HG02135.hp2 HG02165.hp2 others(5): Show |
intron_variant | MODIFIER | c.59-493dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr17 | 54903210 | ||||||
| chr17:54903603 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG01255.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.59-105G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54903603 | |||||||
| chr17:54903639 | G | C | 19 | a0001c0001t0001g0275 a0001c0001t0002g0022 a0001c0001t0002g0257 others(16): Show |
20 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.59-69G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 1/15 | chr17 | 54903639 | |||||||
| chr17:54903998 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.143+206T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54903998 | |||||||
| chr17:54904094 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.143+302G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904094 | |||||||
| chr17:54904142 | C | T | 1 | a0001c0001t0003g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.143+350C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904142 | |||||||
| chr17:54904155 | C | T | 3 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0093 |
3 | HG02257.hp2 HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.143+363C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904155 | |||||||
| chr17:54904219 | A | T | 70 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(67): Show |
79 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.143+427A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904219 | |||||||
| chr17:54904243 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.143+451G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904243 | |||||||
| chr17:54904299 | G | A | 1 | a0001c0001t0002g0277 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.143+507G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904299 | |||||||
| chr17:54904369 | C | CA | 14 | a0001c0001t0001g0038 a0001c0001t0001g0041 a0001c0001t0001g0119 others(11): Show |
14 | HG00621.hp1 HG01928.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.143+599dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 54904369 | ||||||
| chr17:54904369 | CA | C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(91): Show |
112 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.143+599delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr17 | 54904369 | ||||||
| chr17:54904466 | A | C | 1 | a0001c0001t0002g0243 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.143+674A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904466 | |||||||
| chr17:54904492 | C | T | 92 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(89): Show |
98 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.143+700C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904492 | |||||||
| chr17:54904548 | T | C | 4 | a0001c0001t0002g0009 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
6 | HG01081.hp1 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.143+756T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54904548 | |||||||
| chr17:54905046 | G | C | 2 | a0001c0001t0002g0123 a0001c0001t0002g0124 |
2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.144-443G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905046 | |||||||
| chr17:54905063 | C | T | 4 | a0001c0001t0001g0089 a0001c0001t0004g0086 a0001c0001t0004g0087 others(1): Show |
4 | HG02922.hp2 HG03579.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.144-426C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905063 | |||||||
| chr17:54905173 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0003g0085 |
2 | HG00438.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.144-316A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905173 | |||||||
| chr17:54905239 | A | G | 2 | a0001c0001t0001g0334 a0001c0001t0003g0256 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.144-250A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905239 | |||||||
| chr17:54905311 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0003g0027 others(3): Show |
6 | HG00639.hp2 HG00673.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.144-178C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905311 | |||||||
| chr17:54905352 | G | T | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0090 |
3 | HG01070.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.144-137G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905352 | |||||||
| chr17:54905464 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.144-25G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 2/15 | chr17 | 54905464 | |||||||
| chr17:54905855 | C | T | 83 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0041 others(80): Show |
90 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+288C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54905855 | |||||||
| chr17:54905936 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.222+369G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54905936 | |||||||
| chr17:54905999 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.222+432G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54905999 | |||||||
| chr17:54906062 | T | G | 1 | a0001c0001t0001g0323 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.222+495T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906062 | |||||||
| chr17:54906196 | C | T | 19 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
19 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.222+629C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906196 | |||||||
| chr17:54906213 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.222+646A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906213 | |||||||
| chr17:54906215 | T | C | 1 | a0001c0001t0001g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.222+648T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906215 | |||||||
| chr17:54906216 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.222+649C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906216 | |||||||
| chr17:54906235 | G | A | 56 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(53): Show |
63 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.222+668G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906235 | |||||||
| chr17:54906294 | C | A | 1 | a0001c0001t0001g0188 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.222+727C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906294 | |||||||
| chr17:54906330 | G | C | 1 | a0001c0001t0001g0119 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.222+763G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906330 | |||||||
| chr17:54906361 | T | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0038 a0001c0001t0001g0041 others(80): Show |
90 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+794T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906361 | |||||||
| chr17:54906418 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.222+851G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906418 | |||||||
| chr17:54906476 | C | CA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(103): Show |
123 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(120): Show |
intron_variant | MODIFIER | c.222+926dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 54906476 | ||||||
| chr17:54906476 | CA | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0043 a0001c0001t0001g0181 others(4): Show |
8 | HG02129.hp1 HG03491.hp2 NA18941.hp2 others(5): Show |
intron_variant | MODIFIER | c.222+926delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 54906476 | ||||||
| chr17:54906531 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.222+964G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906531 | |||||||
| chr17:54906588 | C | A | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.222+1021C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906588 | |||||||
| chr17:54906608 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.222+1041C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906608 | |||||||
| chr17:54906624 | TTC | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0130 |
3 | HG01168.hp2 HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.222+1058_222+1059d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906624 | |||||||
| chr17:54906843 | T | C | 4 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0001c0001t0002g0266 others(1): Show |
4 | HG02109.hp1 HG02451.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.222+1276T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906843 | |||||||
| chr17:54906880 | T | C | 3 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0002g0133 |
3 | HG01358.hp2 HG01361.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.222+1313T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906880 | |||||||
| chr17:54906933 | A | C | 1 | a0001c0001t0001g0079 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.222+1366A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906933 | |||||||
| chr17:54906939 | C | T | 2 | a0001c0001t0002g0317 a0001c0001t0004g0056 |
2 | HG01496.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.222+1372C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54906939 | |||||||
| chr17:54907074 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.222+1507G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907074 | |||||||
| chr17:54907074 | G | C | 1 | a0001c0001t0002g0035 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.222+1507G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907074 | |||||||
| chr17:54907116 | A | T | 21 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 others(18): Show |
21 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.222+1549A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907116 | |||||||
| chr17:54907153 | C | CT | 83 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(80): Show |
90 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.222+1602dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 54907153 | ||||||
| chr17:54907153 | C | CTT | 78 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(75): Show |
89 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.222+1601_222+1602d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr17 | 54907153 | ||||||
| chr17:54907191 | T | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(65): Show |
84 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.222+1624T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907191 | |||||||
| chr17:54907524 | A | G | 77 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(74): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.222+1957A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907524 | |||||||
| chr17:54907962 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(64): Show |
83 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.222+2395C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907962 | |||||||
| chr17:54907990 | G | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(53): Show |
63 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.222+2423G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54907990 | |||||||
| chr17:54908058 | A | T | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.222+2491A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908058 | |||||||
| chr17:54908245 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.222+2678C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908245 | |||||||
| chr17:54908337 | G | A | 21 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 others(18): Show |
21 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.222+2770G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908337 | |||||||
| chr17:54908359 | G | T | 1 | a0001c0001t0004g0093 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.222+2792G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908359 | |||||||
| chr17:54908530 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.222+2963G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908530 | |||||||
| chr17:54908556 | C | T | 13 | a0001c0001t0001g0227 a0001c0001t0001g0322 a0001c0001t0001g0323 others(10): Show |
13 | HG01109.hp2 HG02135.hp1 HG02976.hp2 others(10): Show |
intron_variant | MODIFIER | c.222+2989C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908556 | |||||||
| chr17:54908621 | G | A | 77 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(74): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.222+3054G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54908621 | |||||||
| chr17:54909123 | G | T | 79 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(76): Show |
90 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.223-3543G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909123 | |||||||
| chr17:54909357 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.223-3309A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909357 | |||||||
| chr17:54909364 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(244): Show |
281 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(278): Show |
intron_variant | MODIFIER | c.223-3302A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909364 | |||||||
| chr17:54909484 | T | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(53): Show |
63 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.223-3182T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909484 | |||||||
| chr17:54909547 | T | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(53): Show |
63 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.223-3119T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909547 | |||||||
| chr17:54909644 | C | T | 5 | a0001c0001t0002g0006 a0001c0001t0002g0025 a0001c0001t0002g0281 others(2): Show |
9 | NA18942.hp1 NA18946.hp1 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.223-3022C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909644 | |||||||
| chr17:54909672 | T | A | 13 | a0001c0001t0001g0030 a0001c0001t0001g0245 a0001c0001t0002g0247 others(10): Show |
13 | HG00639.hp2 HG00673.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.223-2994T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909672 | |||||||
| chr17:54909683 | G | C | 2 | a0001c0001t0001g0334 a0001c0001t0003g0256 |
2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.223-2983G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909683 | |||||||
| chr17:54909961 | T | C | 19 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
19 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.223-2705T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909961 | |||||||
| chr17:54909991 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.223-2675A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54909991 | |||||||
| chr17:54910184 | A | G | 98 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0031 others(95): Show |
105 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.223-2482A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910184 | |||||||
| chr17:54910232 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.223-2434G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910232 | |||||||
| chr17:54910277 | G | A | 3 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0004c0005t0002g0263 |
3 | HG02109.hp1 HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.223-2389G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910277 | |||||||
| chr17:54910320 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.223-2346G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910320 | |||||||
| chr17:54910586 | C | T | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.223-2080C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910586 | |||||||
| chr17:54910714 | C | G | 1 | a0001c0001t0002g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.223-1952C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910714 | |||||||
| chr17:54910871 | G | T | 55 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(52): Show |
62 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.223-1795G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54910871 | |||||||
| chr17:54911070 | G | C | 2 | a0001c0001t0004g0033 a0001c0001t0004g0086 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.223-1596G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911070 | |||||||
| chr17:54911088 | T | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.223-1578T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911088 | |||||||
| chr17:54911096 | T | G | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.223-1570T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911096 | |||||||
| chr17:54911173 | A | G | 1 | a0001c0001t0003g0034 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.223-1493A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911173 | |||||||
| chr17:54911699 | A | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(248): Show |
285 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(282): Show |
intron_variant | MODIFIER | c.223-967A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911699 | |||||||
| chr17:54911710 | A | T | 76 | a0001c0001t0001g0013 a0001c0001t0001g0045 a0001c0001t0001g0046 others(73): Show |
83 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.223-956A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911710 | |||||||
| chr17:54911782 | C | A | 2 | a0001c0001t0004g0033 a0001c0001t0004g0086 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.223-884C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911782 | |||||||
| chr17:54911787 | C | T | 2 | a0001c0001t0004g0179 a0001c0001t0004g0180 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.223-879C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911787 | |||||||
| chr17:54911946 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.223-720G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54911946 | |||||||
| chr17:54912011 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.223-655A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912011 | |||||||
| chr17:54912233 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.223-433G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912233 | |||||||
| chr17:54912237 | C | T | 60 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0045 others(57): Show |
67 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.223-429C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912237 | |||||||
| chr17:54912415 | C | G | 61 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(58): Show |
70 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.223-251C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912415 | |||||||
| chr17:54912476 | A | G | 1 | a0001c0001t0001g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.223-190A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912476 | |||||||
| chr17:54912559 | G | A | 82 | a0001c0001t0001g0275 a0001c0001t0001g0287 a0001c0001t0002g0006 others(79): Show |
93 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.223-107G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 3/15 | chr17 | 54912559 | |||||||
| chr17:54912923 | G | C | 1 | a0001c0001t0003g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.372+108G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54912923 | |||||||
| chr17:54913285 | A | G | 4 | a0001c0001t0001g0019 a0001c0001t0001g0182 a0001c0001t0001g0183 others(1): Show |
5 | HG02129.hp1 NA18941.hp2 NA18966.hp2 others(2): Show |
intron_variant | MODIFIER | c.373-463A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913285 | |||||||
| chr17:54913290 | G | T | 1 | a0001c0001t0004g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.373-458G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913290 | |||||||
| chr17:54913384 | G | A | 1 | a0001c0001t0001g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.373-364G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913384 | |||||||
| chr17:54913415 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.373-333C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913415 | |||||||
| chr17:54913493 | G | C | 1 | a0001c0001t0003g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.373-255G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913493 | |||||||
| chr17:54913507 | A | G | 2 | a0001c0001t0003g0076 a0001c0001t0003g0077 |
2 | HG01928.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.373-241A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913507 | |||||||
| chr17:54913598 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0003g0034 |
2 | HG02886.hp2 NA18940.hp2 |
intron_variant | MODIFIER | c.373-150G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | chr17 | 54913598 | |||||||
| chr17:54913665 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(86): Show |
104 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.373-63dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 54913665 | ||||||
| chr17:54913665 | C | CAA | 8 | a0001c0001t0001g0112 a0001c0001t0001g0125 a0001c0001t0001g0191 others(5): Show |
8 | HG01943.hp2 HG03209.hp1 NA18973.hp2 others(5): Show |
intron_variant | MODIFIER | c.373-64_373-63dupAA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 54913665 | ||||||
| chr17:54913665 | CAAAAAA | C | 54 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(51): Show |
60 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.373-68_373-63delAA others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr17 | 54913665 | ||||||
| chr17:54914010 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.498+137T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | chr17 | 54914010 | |||||||
| chr17:54914097 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.498+224A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | chr17 | 54914097 | |||||||
| chr17:54914275 | G | A | 242 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(239): Show |
275 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(272): Show |
intron_variant | MODIFIER | c.499-364G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | chr17 | 54914275 | |||||||
| chr17:54914370 | TA | T | 48 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0016 others(45): Show |
55 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
intron_variant | MODIFIER | c.499-253delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr17 | 54914370 | ||||||
| chr17:54914370 | TAA | T | 50 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0080 others(47): Show |
56 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.499-254_499-253del others(2): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr17 | 54914370 | ||||||
| chr17:54914414 | A | T | 4 | a0001c0001t0004g0014 a0001c0001t0004g0054 a0001c0001t0004g0055 others(1): Show |
5 | HG01884.hp1 HG02809.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.499-225A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 5/15 | chr17 | 54914414 | |||||||
| chr17:54914767 | TA | T | 73 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0059 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.603+26delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr17 | 54914767 | ||||||
| chr17:54914807 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0111 |
2 | NA18961.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.603+64A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54914807 | |||||||
| chr17:54914884 | A | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(15): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.603+141A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54914884 | |||||||
| chr17:54914907 | G | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0059 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.603+164G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54914907 | |||||||
| chr17:54914982 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.603+239G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54914982 | |||||||
| chr17:54915170 | G | A | 3 | a0001c0001t0002g0025 a0001c0001t0002g0316 a0001c0001t0002g0320 |
4 | NA18946.hp1 NA18983.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.603+427G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54915170 | |||||||
| chr17:54915174 | A | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.603+431A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54915174 | |||||||
| chr17:54915332 | A | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.604-414A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54915332 | |||||||
| chr17:54915541 | A | G | 1 | a0001c0001t0005g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.604-205A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54915541 | |||||||
| chr17:54915556 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.604-190T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 6/15 | chr17 | 54915556 | |||||||
| chr17:54915981 | T | G | 1 | a0001c0001t0001g0015 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.720+119T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54915981 | |||||||
| chr17:54915985 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(323): Show |
383 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(380): Show |
intron_variant | MODIFIER | c.720+123G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54915985 | |||||||
| chr17:54916041 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.720+179G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916041 | |||||||
| chr17:54916078 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.720+216A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916078 | |||||||
| chr17:54916473 | T | C | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.720+611T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916473 | |||||||
| chr17:54916595 | C | T | 54 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(51): Show |
60 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.720+733C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916595 | |||||||
| chr17:54916642 | A | G | 5 | a0001c0001t0001g0030 a0001c0001t0003g0027 a0001c0001t0003g0028 others(2): Show |
5 | HG00639.hp2 HG00673.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+780A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916642 | |||||||
| chr17:54916652 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.720+790G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916652 | |||||||
| chr17:54916681 | T | G | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.720+819T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916681 | |||||||
| chr17:54916683 | C | T | 2 | a0001c0001t0003g0074 a0001c0001t0003g0075 |
2 | HG01106.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.720+821C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916683 | |||||||
| chr17:54916813 | C | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0059 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.720+951C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916813 | |||||||
| chr17:54916849 | T | G | 55 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(52): Show |
61 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.720+987T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916849 | |||||||
| chr17:54916871 | T | C | 18 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(15): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+1009T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916871 | |||||||
| chr17:54916893 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.720+1031A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916893 | |||||||
| chr17:54916973 | C | T | 1 | a0001c0001t0005g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+1111C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54916973 | |||||||
| chr17:54917024 | GATTA | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(15): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+1165_720+1168d others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54917024 | ||||||
| chr17:54917278 | C | T | 18 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(15): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.720+1416C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917278 | |||||||
| chr17:54917517 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(70): Show |
89 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.720+1655T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917517 | |||||||
| chr17:54917539 | T | C | 2 | a0001c0001t0003g0060 a0001c0001t0003g0061 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.720+1677T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917539 | |||||||
| chr17:54917577 | G | T | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.720+1715G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917577 | |||||||
| chr17:54917897 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03491.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.720+2035T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917897 | |||||||
| chr17:54917919 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.720+2057C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54917919 | |||||||
| chr17:54918224 | T | G | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.720+2362T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54918224 | |||||||
| chr17:54918303 | G | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0059 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.720+2441G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54918303 | |||||||
| chr17:54918475 | G | A | 1 | a0001c0001t0005g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.720+2613G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54918475 | |||||||
| chr17:54918789 | C | T | 55 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(52): Show |
61 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.720+2927C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54918789 | |||||||
| chr17:54918867 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.720+3005C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54918867 | |||||||
| chr17:54919044 | T | C | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | NA19000.hp1 NA19002.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.720+3182T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919044 | |||||||
| chr17:54919068 | G | A | 93 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0001g0287 others(90): Show |
104 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(101): Show |
intron_variant | MODIFIER | c.720+3206G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919068 | |||||||
| chr17:54919190 | C | T | 53 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0079 others(50): Show |
59 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.720+3328C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919190 | |||||||
| chr17:54919241 | A | T | 3 | a0001c0001t0002g0280 a0001c0001t0002g0285 a0001c0001t0002g0314 |
3 | NA18960.hp1 NA19010.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.720+3379A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919241 | |||||||
| chr17:54919327 | C | T | 17 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(14): Show |
17 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.720+3465C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919327 | |||||||
| chr17:54919374 | T | G | 1 | a0001c0001t0001g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.720+3512T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919374 | |||||||
| chr17:54919405 | T | C | 19 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0095 others(16): Show |
19 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.720+3543T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919405 | |||||||
| chr17:54919618 | G | C | 2 | a0001c0001t0004g0033 a0001c0001t0004g0086 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.720+3756G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919618 | |||||||
| chr17:54919802 | AT | A | 73 | a0001c0001t0001g0030 a0001c0001t0001g0050 a0001c0001t0001g0059 others(70): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.720+3950delT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54919802 | ||||||
| chr17:54919866 | A | G | 1 | a0001c0001t0001g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.720+4004A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919866 | |||||||
| chr17:54919936 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.720+4074G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919936 | |||||||
| chr17:54919985 | G | GATTT | 46 | a0001c0001t0001g0050 a0001c0001t0001g0089 a0001c0001t0003g0003 others(43): Show |
52 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.720+4144_720+4147d others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54919985 | ||||||
| chr17:54919985 | G | GATTTATT others(1): Show |
4 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0093 others(1): Show |
4 | HG02257.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.720+4140_720+4147d others(10): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54919985 | ||||||
| chr17:54919985 | G | T | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+4123G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919985 | |||||||
| chr17:54919989 | T | G | 95 | a0001c0001t0001g0245 a0001c0001t0001g0252 a0001c0001t0001g0275 others(92): Show |
106 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.720+4127T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919989 | |||||||
| chr17:54919993 | T | G | 91 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0001g0287 others(88): Show |
102 | HG00408.hp1 HG00621.hp1 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.720+4131T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919993 | |||||||
| chr17:54919997 | T | G | 40 | a0001c0001t0001g0245 a0001c0001t0001g0287 a0001c0001t0002g0006 others(37): Show |
46 | HG00621.hp1 HG01081.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.720+4135T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54919997 | |||||||
| chr17:54920001 | T | G | 13 | a0001c0001t0001g0245 a0001c0001t0001g0287 a0001c0001t0002g0173 others(10): Show |
13 | HG01243.hp1 HG02280.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.720+4139T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920001 | |||||||
| chr17:54920005 | T | G | 6 | a0001c0001t0001g0245 a0001c0001t0001g0287 a0001c0001t0002g0251 others(3): Show |
6 | HG02486.hp2 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.720+4143T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920005 | |||||||
| chr17:54920007 | T | TTTTA | 17 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0097 others(14): Show |
17 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.720+4152_720+4155d others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54920007 | ||||||
| chr17:54920010 | T | A | 94 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0001g0287 others(91): Show |
105 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.720+4148T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920010 | |||||||
| chr17:54920011 | A | T | 94 | a0001c0001t0001g0245 a0001c0001t0001g0275 a0001c0001t0001g0287 others(91): Show |
105 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(102): Show |
intron_variant | MODIFIER | c.720+4149A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920011 | |||||||
| chr17:54920077 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.720+4215C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920077 | |||||||
| chr17:54920448 | A | T | 1 | a0001c0001t0001g0125 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.720+4586A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920448 | |||||||
| chr17:54920454 | C | A | 1 | a0001c0001t0002g0295 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.720+4592C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920454 | |||||||
| chr17:54920514 | C | G | 48 | a0001c0001t0001g0050 a0001c0001t0001g0079 a0001c0001t0001g0089 others(45): Show |
54 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(51): Show |
intron_variant | MODIFIER | c.720+4652C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920514 | |||||||
| chr17:54920591 | G | T | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720+4729G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920591 | |||||||
| chr17:54920800 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.720+4938A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920800 | |||||||
| chr17:54920807 | G | T | 63 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0079 others(60): Show |
69 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.720+4945G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920807 | |||||||
| chr17:54920956 | G | GAC | 71 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0079 others(68): Show |
77 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.720+5096_720+5097d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54920956 | ||||||
| chr17:54920979 | G | A | 59 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0022 others(56): Show |
68 | HG00280.hp2 HG00408.hp1 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.720+5117G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54920979 | |||||||
| chr17:54921057 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.720+5195A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921057 | |||||||
| chr17:54921181 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.720+5319T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921181 | |||||||
| chr17:54921186 | C | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720+5324C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921186 | |||||||
| chr17:54921200 | T | G | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.720+5338T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921200 | |||||||
| chr17:54921201 | G | C | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.720+5339G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921201 | |||||||
| chr17:54921362 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.720+5500T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921362 | |||||||
| chr17:54921381 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.720+5519T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921381 | |||||||
| chr17:54921462 | C | T | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.720+5600C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921462 | |||||||
| chr17:54921479 | T | C | 171 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0059 others(168): Show |
191 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.720+5617T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921479 | |||||||
| chr17:54921538 | G | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0228 |
2 | NA19009.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.720+5676G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921538 | |||||||
| chr17:54921644 | A | T | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.720+5782A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921644 | |||||||
| chr17:54921706 | C | G | 282 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(279): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.720+5844C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54921706 | |||||||
| chr17:54922068 | G | A | 1 | a0001c0001t0002g0247 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.720+6206G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922068 | |||||||
| chr17:54922518 | G | A | 1 | a0001c0001t0003g0028 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.720+6656G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922518 | |||||||
| chr17:54922535 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.720+6673C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922535 | |||||||
| chr17:54922595 | G | A | 170 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0059 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.720+6733G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922595 | |||||||
| chr17:54922633 | T | A | 3 | a0001c0001t0001g0089 a0001c0001t0004g0087 a0001c0001t0004g0088 |
3 | HG02922.hp2 HG03579.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.720+6771T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922633 | |||||||
| chr17:54922703 | T | G | 1 | a0001c0001t0001g0326 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.720+6841T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922703 | |||||||
| chr17:54922854 | A | C | 5 | a0001c0001t0001g0245 a0001c0001t0005g0037 a0001c0001t0005g0039 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.720+6992A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922854 | |||||||
| chr17:54922952 | G | T | 1 | a0001c0001t0001g0047 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.720+7090G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54922952 | |||||||
| chr17:54923107 | G | A | 21 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(18): Show |
22 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(19): Show |
intron_variant | MODIFIER | c.721-6966G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923107 | |||||||
| chr17:54923118 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.721-6955G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923118 | |||||||
| chr17:54923346 | C | T | 76 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(73): Show |
88 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.721-6727C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923346 | |||||||
| chr17:54923360 | A | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(13): Show |
17 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.721-6713A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923360 | |||||||
| chr17:54923504 | G | C | 8 | a0001c0001t0002g0257 a0001c0001t0002g0267 a0001c0001t0002g0268 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.721-6569G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923504 | |||||||
| chr17:54923521 | T | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(324): Show |
384 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(381): Show |
intron_variant | MODIFIER | c.721-6552T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923521 | |||||||
| chr17:54923551 | T | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.721-6522T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923551 | |||||||
| chr17:54923556 | A | T | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.721-6517A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923556 | |||||||
| chr17:54923631 | T | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(280): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.721-6442T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923631 | |||||||
| chr17:54923670 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721-6403G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923670 | |||||||
| chr17:54923686 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(245): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.721-6387T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923686 | |||||||
| chr17:54923736 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(69): Show |
87 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.721-6337G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923736 | |||||||
| chr17:54923759 | T | C | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.721-6314T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923759 | |||||||
| chr17:54923806 | A | G | 1 | a0001c0001t0003g0255 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.721-6267A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54923806 | |||||||
| chr17:54924095 | T | C | 170 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0059 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.721-5978T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924095 | |||||||
| chr17:54924115 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.721-5958C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924115 | |||||||
| chr17:54924259 | T | C | 4 | a0001c0001t0001g0030 a0001c0001t0003g0027 a0001c0001t0003g0028 others(1): Show |
4 | HG00639.hp2 HG00673.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5814T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924259 | |||||||
| chr17:54924277 | T | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.721-5796T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924277 | |||||||
| chr17:54924283 | C | CT | 69 | a0001c0001t0001g0030 a0001c0001t0001g0079 a0001c0001t0001g0111 others(66): Show |
76 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.721-5776dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54924283 | ||||||
| chr17:54924283 | C | CTT | 19 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(16): Show |
20 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.721-5777_721-5776d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54924283 | ||||||
| chr17:54924365 | C | T | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.721-5708C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924365 | |||||||
| chr17:54924713 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | NA19000.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.721-5360C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924713 | |||||||
| chr17:54924750 | T | TAA | 249 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(246): Show |
284 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.721-5321_721-5320d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54924750 | ||||||
| chr17:54924830 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.721-5243G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924830 | |||||||
| chr17:54924971 | AGAGGCTA others(5): Show |
A | 1 | a0001c0001t0002g0286 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.721-5088_721-5077d others(14): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54924971 | ||||||
| chr17:54924984 | G | A | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.721-5089G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924984 | |||||||
| chr17:54924990 | A | G | 4 | a0001c0001t0001g0030 a0001c0001t0003g0027 a0001c0001t0003g0028 others(1): Show |
4 | HG00639.hp2 HG00673.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-5083A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54924990 | |||||||
| chr17:54925075 | T | C | 5 | a0001c0001t0001g0245 a0001c0001t0005g0037 a0001c0001t0005g0039 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-4998T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925075 | |||||||
| chr17:54925114 | T | C | 2 | a0001c0001t0005g0039 a0001c0001t0005g0040 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.721-4959T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925114 | |||||||
| chr17:54925243 | A | G | 2 | a0001c0001t0001g0080 a0001c0001t0001g0334 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.721-4830A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925243 | |||||||
| chr17:54925496 | G | A | 9 | a0001c0001t0002g0254 a0001c0001t0002g0257 a0001c0001t0002g0267 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.721-4577G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925496 | |||||||
| chr17:54925733 | G | A | 1 | a0001c0001t0002g0288 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.721-4340G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925733 | |||||||
| chr17:54925910 | A | AAACAAC | 191 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0031 others(188): Show |
211 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.721-4157_721-4152d others(8): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54925910 | ||||||
| chr17:54925922 | A | C | 77 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0059 others(74): Show |
84 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.721-4151A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54925922 | |||||||
| chr17:54926041 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.721-4032C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54926041 | |||||||
| chr17:54926130 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.721-3943C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54926130 | |||||||
| chr17:54926456 | TTTTG | T | 20 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0106 others(17): Show |
20 | HG01109.hp2 HG02135.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.721-3597_721-3594d others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54926456 | ||||||
| chr17:54926611 | A | T | 1 | a0001c0001t0003g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.721-3462A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54926611 | |||||||
| chr17:54926641 | G | GA | 120 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0089 others(117): Show |
132 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.721-3418dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54926641 | ||||||
| chr17:54926641 | G | GAA | 6 | a0001c0001t0002g0288 a0001c0001t0002g0296 a0001c0001t0004g0091 others(3): Show |
6 | HG01175.hp2 HG02257.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.721-3419_721-3418d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54926641 | ||||||
| chr17:54926783 | T | A | 190 | a0001c0001t0001g0012 a0001c0001t0001g0030 a0001c0001t0001g0031 others(187): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.721-3290T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54926783 | |||||||
| chr17:54926944 | G | A | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.721-3129G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54926944 | |||||||
| chr17:54927289 | G | A | 1 | a0001c0001t0001g0322 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.721-2784G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54927289 | |||||||
| chr17:54927467 | A | G | 16 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(13): Show |
17 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.721-2606A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54927467 | |||||||
| chr17:54927827 | A | G | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.721-2246A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54927827 | |||||||
| chr17:54927905 | A | G | 5 | a0001c0001t0001g0245 a0001c0001t0005g0037 a0001c0001t0005g0039 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-2168A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54927905 | |||||||
| chr17:54927967 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.721-2106C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54927967 | |||||||
| chr17:54928122 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.721-1951G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928122 | |||||||
| chr17:54928225 | C | T | 190 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(187): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.721-1848C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928225 | |||||||
| chr17:54928323 | C | T | 1 | a0001c0001t0003g0072 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.721-1750C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928323 | |||||||
| chr17:54928355 | A | G | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.721-1718A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928355 | |||||||
| chr17:54928367 | C | CA | 57 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0079 others(54): Show |
63 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.721-1697dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54928367 | ||||||
| chr17:54928367 | C | CAA | 17 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(14): Show |
18 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.721-1698_721-1697d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54928367 | ||||||
| chr17:54928367 | C | CAAA | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.721-1699_721-1697d others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54928367 | ||||||
| chr17:54928436 | A | G | 2 | a0001c0001t0005g0039 a0001c0001t0005g0040 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.721-1637A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928436 | |||||||
| chr17:54928482 | G | T | 1 | a0001c0001t0001g0275 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.721-1591G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928482 | |||||||
| chr17:54928640 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.721-1433T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928640 | |||||||
| chr17:54928682 | T | C | 92 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(89): Show |
105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.721-1391T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928682 | |||||||
| chr17:54928761 | G | T | 1 | a0001c0001t0002g0315 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.721-1312G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928761 | |||||||
| chr17:54928963 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.721-1110A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928963 | |||||||
| chr17:54928978 | G | A | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.721-1095G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54928978 | |||||||
| chr17:54929046 | G | A | 4 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(1): Show |
4 | NA18972.hp2 NA18977.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.721-1027G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929046 | |||||||
| chr17:54929067 | A | G | 1 | a0001c0001t0002g0311 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.721-1006A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929067 | |||||||
| chr17:54929166 | T | C | 5 | a0001c0001t0001g0245 a0001c0001t0005g0037 a0001c0001t0005g0039 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.721-907T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929166 | |||||||
| chr17:54929293 | T | C | 35 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(32): Show |
40 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.721-780T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929293 | |||||||
| chr17:54929374 | G | GA | 22 | a0001c0001t0001g0202 a0001c0001t0001g0245 a0001c0001t0002g0247 others(19): Show |
22 | HG00408.hp2 HG01243.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.721-686dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929374 | ||||||
| chr17:54929445 | GGTATTCA others(6): Show |
G | 1 | a0001c0001t0001g0043 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.721-625_721-613del others(13): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929445 | ||||||
| chr17:54929529 | G | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.721-544G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929529 | |||||||
| chr17:54929741 | G | GT | 101 | a0001c0001t0001g0041 a0001c0001t0001g0136 a0001c0001t0001g0168 others(98): Show |
114 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.721-317dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929741 | ||||||
| chr17:54929741 | G | GTT | 11 | a0001c0001t0002g0124 a0001c0001t0002g0133 a0001c0001t0002g0156 others(8): Show |
11 | HG00733.hp2 HG01074.hp1 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.721-318_721-317dup others(2): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929741 | ||||||
| chr17:54929741 | G | GTTT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(11): Show |
15 | HG00673.hp1 HG02027.hp1 HG02080.hp1 others(12): Show |
intron_variant | MODIFIER | c.721-319_721-317dup others(3): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929741 | ||||||
| chr17:54929741 | G | GTTTTT | 31 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(28): Show |
36 | HG00140.hp2 HG00438.hp2 HG00558.hp2 others(33): Show |
intron_variant | MODIFIER | c.721-321_721-317dup others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr17 | 54929741 | ||||||
| chr17:54929787 | A | T | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG00673.hp2 HG01433.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.721-286A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929787 | |||||||
| chr17:54929932 | G | C | 3 | a0001c0001t0002g0264 a0001c0001t0002g0265 a0004c0005t0002g0263 |
3 | HG02109.hp1 HG02451.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.721-141G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54929932 | |||||||
| chr17:54930064 | C | T | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.721-9C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 7/15 | chr17 | 54930064 | |||||||
| chr17:54930294 | T | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(162): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.854+88T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930294 | |||||||
| chr17:54930382 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.854+176G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930382 | |||||||
| chr17:54930496 | G | A | 3 | a0001c0001t0002g0009 a0001c0001t0002g0186 a0001c0001t0002g0243 |
5 | HG01081.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.854+290G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930496 | |||||||
| chr17:54930526 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.854+320A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930526 | |||||||
| chr17:54930708 | C | T | 1 | a0001c0001t0002g0307 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.854+502C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930708 | |||||||
| chr17:54930710 | C | T | 32 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(29): Show |
37 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.854+504C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930710 | |||||||
| chr17:54930711 | G | A | 1 | a0001c0001t0002g0316 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.854+505G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930711 | |||||||
| chr17:54930791 | A | G | 248 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(245): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.854+585A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930791 | |||||||
| chr17:54930877 | T | TA | 9 | a0001c0001t0001g0089 a0001c0001t0004g0051 a0001c0001t0004g0053 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.854+679dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54930877 | ||||||
| chr17:54930885 | A | T | 1 | a0001c0001t0001g0181 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.854+679A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54930885 | |||||||
| chr17:54931126 | AGTGACCG others(5): Show |
A | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.854+921_854+932del others(12): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931126 | |||||||
| chr17:54931406 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.854+1200C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931406 | |||||||
| chr17:54931492 | A | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.854+1286A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931492 | |||||||
| chr17:54931512 | T | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(162): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.854+1306T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931512 | |||||||
| chr17:54931757 | C | T | 1 | a0001c0001t0002g0310 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.854+1551C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931757 | |||||||
| chr17:54931908 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.854+1702G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931908 | |||||||
| chr17:54931919 | G | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.854+1713G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931919 | |||||||
| chr17:54931923 | T | G | 3 | a0001c0001t0001g0175 a0001c0001t0001g0188 a0001c0001t0001g0200 |
3 | NA18957.hp1 NA19072.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.854+1717T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931923 | |||||||
| chr17:54931949 | G | GT | 22 | a0001c0001t0001g0017 a0001c0001t0001g0137 a0001c0001t0001g0138 others(19): Show |
25 | HG01081.hp1 HG02055.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.854+1753dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54931949 | ||||||
| chr17:54931949 | G | GTT | 10 | a0001c0001t0002g0174 a0001c0001t0002g0185 a0001c0001t0002g0247 others(7): Show |
10 | HG01243.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.854+1752_854+1753d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54931949 | ||||||
| chr17:54931949 | G | GTTT | 62 | a0001c0001t0001g0080 a0001c0001t0002g0006 a0001c0001t0002g0008 others(59): Show |
73 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.854+1751_854+1753d others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54931949 | ||||||
| chr17:54931956 | T | TTTG | 75 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(72): Show |
90 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.854+1752_854+1753i others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54931956 | ||||||
| chr17:54931957 | TTTGTTTG | T | 72 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(69): Show |
79 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.854+1754_854+1760d others(9): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54931957 | ||||||
| chr17:54931960 | G | T | 44 | a0001c0001t0002g0009 a0001c0001t0002g0022 a0001c0001t0002g0023 others(41): Show |
48 | HG01081.hp1 HG01175.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.854+1754G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931960 | |||||||
| chr17:54931964 | G | T | 23 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(20): Show |
25 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.854+1758G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54931964 | |||||||
| chr17:54932250 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.854+2044G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932250 | |||||||
| chr17:54932263 | C | G | 9 | a0001c0001t0002g0254 a0001c0001t0002g0257 a0001c0001t0002g0267 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.854+2057C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932263 | |||||||
| chr17:54932365 | C | CT | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG00673.hp2 HG01433.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.854+2160dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54932365 | ||||||
| chr17:54932610 | G | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.854+2404G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932610 | |||||||
| chr17:54932651 | C | T | 1 | a0001c0001t0002g0313 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.854+2445C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932651 | |||||||
| chr17:54932713 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(74): Show |
92 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.854+2507G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932713 | |||||||
| chr17:54932737 | T | C | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.854+2531T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932737 | |||||||
| chr17:54932900 | C | T | 1 | a0001c0001t0003g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.854+2694C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932900 | |||||||
| chr17:54932935 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.854+2729A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54932935 | |||||||
| chr17:54933020 | T | G | 92 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(89): Show |
105 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.854+2814T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933020 | |||||||
| chr17:54933115 | T | C | 1 | a0001c0001t0004g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.854+2909T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933115 | |||||||
| chr17:54933119 | T | A | 1 | a0001c0001t0003g0065 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.854+2913T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933119 | |||||||
| chr17:54933309 | C | T | 35 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(32): Show |
40 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.854+3103C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933309 | |||||||
| chr17:54933394 | A | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.854+3188A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933394 | |||||||
| chr17:54933668 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.855-2981G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933668 | |||||||
| chr17:54933679 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.855-2970C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933679 | |||||||
| chr17:54933811 | A | G | 165 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(162): Show |
185 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.855-2838A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54933811 | |||||||
| chr17:54934050 | G | A | 19 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0106 others(16): Show |
19 | HG01109.hp2 HG02135.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.855-2599G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934050 | |||||||
| chr17:54934090 | A | C | 21 | a0001c0001t0001g0089 a0001c0001t0004g0014 a0001c0001t0004g0033 others(18): Show |
22 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.855-2559A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934090 | |||||||
| chr17:54934438 | G | T | 1 | a0001c0001t0001g0047 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.855-2211G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934438 | |||||||
| chr17:54934696 | G | A | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.855-1953G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934696 | |||||||
| chr17:54934696 | G | C | 3 | a0001c0001t0001g0158 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG01106.hp1 HG02148.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.855-1953G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934696 | |||||||
| chr17:54934713 | AT | A | 7 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0168 others(4): Show |
7 | HG01952.hp2 HG02683.hp1 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.855-1921delT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54934713 | ||||||
| chr17:54934713 | ATT | A | 163 | a0001c0001t0001g0031 a0001c0001t0001g0079 a0001c0001t0001g0080 others(160): Show |
182 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.855-1922_855-1921d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54934713 | ||||||
| chr17:54934713 | ATTT | A | 8 | a0001c0001t0001g0245 a0001c0001t0002g0315 a0001c0001t0003g0255 others(5): Show |
8 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.855-1923_855-1921d others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54934713 | ||||||
| chr17:54934728 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.855-1921T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934728 | |||||||
| chr17:54934798 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0334 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.855-1851A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54934798 | |||||||
| chr17:54935018 | G | T | 170 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(167): Show |
190 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(187): Show |
intron_variant | MODIFIER | c.855-1631G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935018 | |||||||
| chr17:54935084 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.855-1565C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935084 | |||||||
| chr17:54935129 | G | T | 2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.855-1520G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935129 | |||||||
| chr17:54935152 | G | C | 1 | a0001c0001t0001g0287 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.855-1497G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935152 | |||||||
| chr17:54935258 | AGGGCAG | A | 5 | a0001c0001t0001g0245 a0001c0001t0005g0037 a0001c0001t0005g0039 others(2): Show |
5 | HG02280.hp2 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-1383_855-1378d others(8): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr17 | 54935258 | ||||||
| chr17:54935566 | C | G | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.855-1083C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935566 | |||||||
| chr17:54935737 | G | A | 4 | a0001c0001t0002g0023 a0001c0001t0002g0297 a0001c0001t0002g0298 others(1): Show |
5 | NA18955.hp1 NA18962.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.855-912G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935737 | |||||||
| chr17:54935789 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.855-860G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935789 | |||||||
| chr17:54935882 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.855-767G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935882 | |||||||
| chr17:54935906 | T | A | 1 | a0001c0001t0005g0040 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.855-743T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935906 | |||||||
| chr17:54935928 | G | T | 73 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(70): Show |
80 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.855-721G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935928 | |||||||
| chr17:54935974 | T | C | 1 | a0005c0002t0001g0044 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.855-675T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935974 | |||||||
| chr17:54935996 | G | A | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.855-653G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54935996 | |||||||
| chr17:54936006 | C | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.855-643C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54936006 | |||||||
| chr17:54936031 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.855-618G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54936031 | |||||||
| chr17:54936076 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | NA18941.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.855-573T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54936076 | |||||||
| chr17:54936234 | G | T | 52 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0079 others(49): Show |
58 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.855-415G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54936234 | |||||||
| chr17:54936619 | A | G | 35 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(32): Show |
40 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(37): Show |
intron_variant | MODIFIER | c.855-30A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 8/15 | chr17 | 54936619 | |||||||
| chr17:54936776 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.915+67C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 9/15 | chr17 | 54936776 | |||||||
| chr17:54936825 | G | A | 16 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(13): Show |
17 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.915+116G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 9/15 | chr17 | 54936825 | |||||||
| chr17:54936871 | A | ATTAAG | 190 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(187): Show |
210 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.915+166_915+167ins others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 54936871 | ||||||
| chr17:54937081 | C | CT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.916-14dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 54937081 | ||||||
| chr17:54937081 | CT | C | 17 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.916-14delT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr17 | 54937081 | ||||||
| chr17:54937594 | G | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(58): Show |
76 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1033+368G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937594 | |||||||
| chr17:54937665 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1033+439A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937665 | |||||||
| chr17:54937774 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1033+548G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937774 | |||||||
| chr17:54937803 | TTTATAAA others(4): Show |
T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(12): Show |
16 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1033+578_1033+588d others(13): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937803 | |||||||
| chr17:54937816 | T | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(12): Show |
16 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1033+590T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937816 | |||||||
| chr17:54937817 | T | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0095 others(12): Show |
16 | HG00673.hp1 HG02027.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1033+591T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937817 | |||||||
| chr17:54937856 | A | G | 1 | a0001c0001t0002g0250 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1033+630A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54937856 | |||||||
| chr17:54938310 | A | G | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1034-614A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54938310 | |||||||
| chr17:54938493 | C | CA | 65 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0010 others(62): Show |
82 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1034-409dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 54938493 | ||||||
| chr17:54938493 | C | CAA | 7 | a0001c0001t0001g0021 a0001c0001t0001g0121 a0001c0001t0001g0194 others(4): Show |
8 | HG00733.hp1 HG01071.hp1 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.1034-410_1034-409d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 54938493 | ||||||
| chr17:54938493 | CA | C | 42 | a0001c0001t0001g0079 a0001c0001t0001g0104 a0001c0001t0001g0138 others(39): Show |
47 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(44): Show |
intron_variant | MODIFIER | c.1034-409delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 54938493 | ||||||
| chr17:54938692 | A | T | 113 | a0001c0001t0001g0089 a0001c0001t0002g0006 a0001c0001t0002g0008 others(110): Show |
127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.1034-232A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54938692 | |||||||
| chr17:54938758 | A | G | 1 | a0001c0001t0001g0218 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1034-166A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54938758 | |||||||
| chr17:54938769 | G | T | 36 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(33): Show |
41 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1034-155G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | chr17 | 54938769 | |||||||
| chr17:54938794 | CTT | C | 36 | a0001c0001t0001g0079 a0001c0001t0003g0003 a0001c0001t0003g0007 others(33): Show |
41 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(38): Show |
intron_variant | MODIFIER | c.1034-127_1034-126d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr17 | 54938794 | ||||||
| chr17:54939058 | A | C | 1 | a0001c0001t0005g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1130+38A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939058 | |||||||
| chr17:54939060 | A | G | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1130+40A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939060 | |||||||
| chr17:54939124 | A | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0275 |
2 | HG02280.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1130+104A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939124 | |||||||
| chr17:54939134 | G | A | 2 | a0001c0001t0003g0074 a0001c0001t0003g0075 |
2 | HG01106.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1130+114G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939134 | |||||||
| chr17:54939163 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0334 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1130+143C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939163 | |||||||
| chr17:54939400 | A | T | 3 | a0001c0001t0002g0123 a0001c0001t0002g0124 a0001c0001t0002g0173 |
3 | HG02559.hp1 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1130+380A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939400 | |||||||
| chr17:54939413 | CAG | C | 20 | a0001c0001t0001g0031 a0001c0001t0001g0080 a0001c0001t0001g0106 others(17): Show |
20 | HG01109.hp2 HG02135.hp1 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1130+394_1130+395d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54939413 | |||||||
| chr17:54940126 | G | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(6): Show |
11 | HG01081.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1130+1106G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54940126 | |||||||
| chr17:54940181 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1130+1161G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54940181 | |||||||
| chr17:54940386 | A | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1130+1366A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54940386 | |||||||
| chr17:54940635 | G | A | 1 | a0001c0001t0004g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1130+1615G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54940635 | |||||||
| chr17:54940797 | G | GA | 24 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(21): Show |
26 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1130+1783dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54940797 | ||||||
| chr17:54940920 | T | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1130+1900T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54940920 | |||||||
| chr17:54941184 | T | G | 1 | a0001c0001t0001g0189 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1130+2164T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941184 | |||||||
| chr17:54941191 | A | G | 36 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(33): Show |
37 | HG00673.hp1 HG01109.hp2 HG02027.hp1 others(34): Show |
intron_variant | MODIFIER | c.1130+2171A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941191 | |||||||
| chr17:54941328 | A | T | 35 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(32): Show |
36 | HG00673.hp1 HG01109.hp2 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.1130+2308A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941328 | |||||||
| chr17:54941408 | A | G | 1 | a0001c0001t0004g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1130+2388A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941408 | |||||||
| chr17:54941463 | C | T | 189 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(186): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1130+2443C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941463 | |||||||
| chr17:54941464 | T | G | 189 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(186): Show |
209 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.1130+2444T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941464 | |||||||
| chr17:54941931 | T | G | 1 | a0001c0001t0003g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1130+2911T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54941931 | |||||||
| chr17:54942200 | G | A | 1 | a0001c0001t0004g0054 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1130+3180G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942200 | |||||||
| chr17:54942263 | A | AT | 124 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0059 others(121): Show |
138 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.1130+3258dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54942263 | ||||||
| chr17:54942263 | A | ATT | 13 | a0001c0001t0001g0095 a0001c0001t0001g0098 a0001c0001t0001g0101 others(10): Show |
13 | HG00673.hp1 HG01993.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1130+3257_1130+325 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54942263 | ||||||
| chr17:54942263 | A | ATTT | 54 | a0001c0001t0001g0089 a0001c0001t0003g0003 a0001c0001t0003g0007 others(51): Show |
60 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.1130+3256_1130+325 others(7): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54942263 | ||||||
| chr17:54942339 | C | A | 2 | a0001c0001t0003g0058 a0001c0001t0003g0067 |
2 | HG01081.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1130+3319C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942339 | |||||||
| chr17:54942347 | G | A | 1 | a0001c0001t0003g0029 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1130+3327G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942347 | |||||||
| chr17:54942351 | T | C | 153 | a0001c0001t0001g0089 a0001c0001t0001g0245 a0001c0001t0002g0006 others(150): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1130+3331T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942351 | |||||||
| chr17:54942742 | A | G | 1 | a0001c0001t0003g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1130+3722A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942742 | |||||||
| chr17:54942784 | A | C | 1 | a0001c0001t0004g0180 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1130+3764A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942784 | |||||||
| chr17:54942791 | C | A | 15 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1130+3771C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942791 | |||||||
| chr17:54942856 | A | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1130+3836A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942856 | |||||||
| chr17:54942935 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(280): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1130+3915A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54942935 | |||||||
| chr17:54943169 | G | T | 9 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(6): Show |
11 | HG01081.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1131-4092G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943169 | |||||||
| chr17:54943213 | C | T | 1 | a0001c0001t0001g0012 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.1131-4048C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943213 | |||||||
| chr17:54943238 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0239 |
2 | HG02145.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1131-4023A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943238 | |||||||
| chr17:54943441 | G | GGT | 62 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(59): Show |
69 | HG00558.hp2 HG01106.hp1 HG01109.hp2 others(66): Show |
intron_variant | MODIFIER | c.1131-3782_1131-378 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGT | 79 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0015 others(76): Show |
96 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.1131-3784_1131-378 others(8): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGT | 21 | a0001c0001t0001g0005 a0001c0001t0001g0030 a0001c0001t0001g0118 others(18): Show |
24 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(21): Show |
intron_variant | MODIFIER | c.1131-3786_1131-378 others(10): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGTG others(1): Show |
16 | a0001c0001t0001g0115 a0001c0001t0001g0192 a0001c0001t0001g0214 others(13): Show |
16 | HG00673.hp2 HG01081.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.1131-3788_1131-378 others(12): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGTG others(3): Show |
9 | a0001c0001t0001g0116 a0001c0001t0001g0166 a0001c0001t0001g0202 others(6): Show |
9 | HG01884.hp2 HG02717.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1131-3790_1131-378 others(14): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGTG others(5): Show |
4 | a0001c0001t0001g0127 a0001c0001t0002g0009 a0001c0001t0003g0058 others(1): Show |
6 | HG01081.hp2 HG02257.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131-3792_1131-378 others(16): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGTG others(7): Show |
1 | a0001c0001t0004g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1131-3794_1131-378 others(18): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | G | GGTGTGTG others(11): Show |
1 | a0001c0001t0004g0092 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1131-3798_1131-378 others(22): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | GGT | G | 13 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(10): Show |
13 | HG00673.hp1 HG01175.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.1131-3782_1131-378 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943441 | GGTGTGTG others(3): Show |
G | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1131-3790_1131-378 others(14): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943441 | ||||||
| chr17:54943443 | T | C | 1 | a0001c0001t0002g0295 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1131-3818T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943443 | |||||||
| chr17:54943479 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1131-3781_1131-378 others(16): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54943479 | ||||||
| chr17:54943759 | A | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0335 |
3 | HG02615.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1131-3502A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943759 | |||||||
| chr17:54943795 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1131-3466G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943795 | |||||||
| chr17:54943796 | G | T | 1 | a0001c0001t0001g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1131-3465G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943796 | |||||||
| chr17:54943886 | G | A | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1131-3375G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943886 | |||||||
| chr17:54943923 | G | A | 2 | a0001c0001t0001g0323 a0001c0001t0001g0327 |
2 | NA18972.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1131-3338G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943923 | |||||||
| chr17:54943926 | G | A | 15 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1131-3335G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54943926 | |||||||
| chr17:54944011 | AAAGG | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-3246_1131-324 others(8): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54944011 | ||||||
| chr17:54944169 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1131-3092C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944169 | |||||||
| chr17:54944254 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1131-3007C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944254 | |||||||
| chr17:54944340 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1131-2921C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944340 | |||||||
| chr17:54944363 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(110): Show |
130 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.1131-2898T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944363 | |||||||
| chr17:54944415 | A | C | 9 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(6): Show |
11 | HG01081.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1131-2846A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944415 | |||||||
| chr17:54944428 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1131-2833C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944428 | |||||||
| chr17:54944429 | G | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-2832G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944429 | |||||||
| chr17:54944449 | C | CA | 10 | a0001c0001t0001g0046 a0001c0001t0001g0118 a0001c0001t0001g0203 others(7): Show |
10 | HG02135.hp1 HG02486.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1131-2797dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54944449 | ||||||
| chr17:54944449 | C | CAA | 88 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(85): Show |
101 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1131-2798_1131-279 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54944449 | ||||||
| chr17:54944449 | CA | C | 8 | a0001c0001t0001g0130 a0001c0001t0001g0138 a0001c0001t0001g0145 others(5): Show |
8 | HG01168.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1131-2797delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54944449 | ||||||
| chr17:54944449 | CAA | C | 33 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(30): Show |
38 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1131-2798_1131-279 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54944449 | ||||||
| chr17:54944562 | T | C | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1131-2699T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944562 | |||||||
| chr17:54944594 | A | G | 129 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(126): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1131-2667A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944594 | |||||||
| chr17:54944679 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0335 |
3 | HG02615.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1131-2582T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944679 | |||||||
| chr17:54944688 | T | C | 131 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(128): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1131-2573T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944688 | |||||||
| chr17:54944731 | T | G | 24 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(21): Show |
26 | HG01081.hp1 HG01243.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1131-2530T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944731 | |||||||
| chr17:54944794 | A | G | 1 | a0001c0001t0002g0321 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1131-2467A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54944794 | |||||||
| chr17:54945240 | C | G | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-2021C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945240 | |||||||
| chr17:54945279 | G | A | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1131-1982G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945279 | |||||||
| chr17:54945344 | G | A | 1 | a0001c0001t0002g0307 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1131-1917G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945344 | |||||||
| chr17:54945353 | A | T | 132 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(129): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1131-1908A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945353 | |||||||
| chr17:54945488 | A | G | 10 | a0001c0001t0004g0014 a0001c0001t0004g0033 a0001c0001t0004g0054 others(7): Show |
11 | HG01884.hp1 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1131-1773A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945488 | |||||||
| chr17:54945505 | G | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-1756G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945505 | |||||||
| chr17:54945530 | G | T | 6 | a0001c0001t0002g0035 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG02559.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131-1731G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945530 | |||||||
| chr17:54945564 | T | G | 1 | a0001c0001t0002g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1131-1697T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945564 | |||||||
| chr17:54945673 | G | GT | 88 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(85): Show |
101 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1131-1578dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54945673 | ||||||
| chr17:54945673 | G | GTT | 6 | a0001c0001t0002g0035 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG02559.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1131-1579_1131-157 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr17 | 54945673 | ||||||
| chr17:54945673 | G | T | 1 | a0001c0001t0002g0276 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1131-1588G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945673 | |||||||
| chr17:54945932 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1131-1329A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54945932 | |||||||
| chr17:54946024 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-1237C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946024 | |||||||
| chr17:54946128 | A | G | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-1133A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946128 | |||||||
| chr17:54946186 | C | T | 1 | a0001c0001t0004g0088 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1131-1075C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946186 | |||||||
| chr17:54946285 | T | A | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1131-976T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946285 | |||||||
| chr17:54946530 | C | T | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1131-731C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946530 | |||||||
| chr17:54946668 | C | G | 299 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0010 others(296): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.1131-593C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946668 | |||||||
| chr17:54946879 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(90): Show |
109 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.1131-382T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946879 | |||||||
| chr17:54946918 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1131-343A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946918 | |||||||
| chr17:54946955 | T | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | NA18955.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.1131-306T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54946955 | |||||||
| chr17:54947049 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1131-212C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54947049 | |||||||
| chr17:54947254 | A | G | 1 | a0001c0001t0003g0256 | 1 | HG03195.hp2 | splice_region_variant&intron_variant | LOW | c.1131-7A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 11/15 | chr17 | 54947254 | |||||||
| chr17:54947381 | T | C | 1 | a0001c0001t0004g0244 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1182+69T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54947381 | |||||||
| chr17:54947492 | T | C | 9 | a0001c0001t0002g0254 a0001c0001t0002g0257 a0001c0001t0002g0267 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1182+180T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54947492 | |||||||
| chr17:54947762 | T | C | 20 | a0001c0001t0004g0014 a0001c0001t0004g0033 a0001c0001t0004g0036 others(17): Show |
21 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1182+450T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54947762 | |||||||
| chr17:54947981 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1182+669C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54947981 | |||||||
| chr17:54948056 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1182+744A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948056 | |||||||
| chr17:54948059 | G | A | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1182+747G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948059 | |||||||
| chr17:54948114 | A | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1182+802A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948114 | |||||||
| chr17:54948119 | T | C | 131 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(128): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1182+807T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948119 | |||||||
| chr17:54948233 | C | A | 3 | a0001c0001t0003g0027 a0001c0001t0003g0028 a0001c0001t0003g0029 |
3 | HG00673.hp2 HG01433.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.1182+921C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948233 | |||||||
| chr17:54948328 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1182+1016C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948328 | |||||||
| chr17:54948380 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1182+1068C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948380 | |||||||
| chr17:54948416 | T | C | 1 | a0001c0001t0003g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1183-1102T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948416 | |||||||
| chr17:54948452 | C | A | 1 | a0001c0001t0002g0254 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1183-1066C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948452 | |||||||
| chr17:54948569 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1183-949C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948569 | |||||||
| chr17:54948971 | G | GT | 36 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0080 others(33): Show |
37 | HG00140.hp1 HG00673.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.1183-538dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54948971 | ||||||
| chr17:54948972 | T | G | 3 | a0001c0001t0002g0009 a0001c0001t0002g0186 a0001c0001t0002g0243 |
5 | HG01081.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-546T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948972 | |||||||
| chr17:54948992 | T | C | 6 | a0001c0001t0001g0095 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG00673.hp1 NA18951.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.1183-526T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54948992 | |||||||
| chr17:54949081 | A | G | 12 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0045 others(9): Show |
14 | HG02040.hp1 HG02129.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1183-437A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949081 | |||||||
| chr17:54949110 | A | T | 3 | a0001c0001t0003g0082 a0001c0001t0003g0083 a0001c0001t0003g0090 |
3 | HG01070.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1183-408A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949110 | |||||||
| chr17:54949203 | A | ATTTT | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1183-302_1183-299d others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949203 | A | ATTTTTTT others(1): Show |
69 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(66): Show |
81 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.1183-306_1183-299d others(10): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949203 | A | ATTTTTTT others(2): Show |
18 | a0001c0001t0002g0022 a0001c0001t0002g0131 a0001c0001t0002g0259 others(15): Show |
19 | HG01074.hp1 HG01175.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.1183-307_1183-299d others(11): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949203 | A | ATTTTTTT others(3): Show |
5 | a0001c0001t0002g0123 a0001c0001t0002g0260 a0001c0001t0002g0264 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.1183-308_1183-299d others(12): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949203 | A | ATTTTTTT others(4): Show |
2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1183-309_1183-299d others(13): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949203 | AT | A | 37 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0080 others(34): Show |
38 | HG00140.hp1 HG00639.hp2 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.1183-299delT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949203 | ||||||
| chr17:54949207 | T | A | 1 | a0001c0001t0001g0165 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1183-311T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949207 | |||||||
| chr17:54949226 | T | C | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1183-292T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949226 | |||||||
| chr17:54949286 | C | T | 1 | a0001c0001t0003g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1183-232C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949286 | |||||||
| chr17:54949375 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1183-143A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | chr17 | 54949375 | |||||||
| chr17:54949462 | TAAAAG | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1183-50_1183-46del others(5): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr17 | 54949462 | ||||||
| chr17:54949890 | A | AT | 15 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(12): Show |
15 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1289-152dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr17 | 54949890 | ||||||
| chr17:54950200 | T | A | 20 | a0001c0001t0002g0008 a0001c0001t0002g0011 a0001c0001t0002g0132 others(17): Show |
24 | HG00099.hp1 HG00408.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1370+74T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54950200 | |||||||
| chr17:54950304 | C | T | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1370+178C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54950304 | |||||||
| chr17:54950681 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1370+555A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54950681 | |||||||
| chr17:54950682 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+556C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54950682 | |||||||
| chr17:54950873 | A | G | 1 | a0001c0001t0001g0189 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1370+747A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54950873 | |||||||
| chr17:54951053 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+927G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951053 | |||||||
| chr17:54951254 | C | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1370+1128C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951254 | |||||||
| chr17:54951322 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1370+1196C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951322 | |||||||
| chr17:54951620 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1370+1494G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951620 | |||||||
| chr17:54951681 | G | C | 1 | a0001c0001t0001g0331 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1370+1555G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951681 | |||||||
| chr17:54951907 | A | C | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1370+1781A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951907 | |||||||
| chr17:54951925 | A | T | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+1799A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951925 | |||||||
| chr17:54951967 | G | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1370+1841G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54951967 | |||||||
| chr17:54952015 | T | C | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1370+1889T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952015 | |||||||
| chr17:54952022 | G | C | 4 | a0001c0001t0004g0091 a0001c0001t0004g0092 a0001c0001t0004g0093 others(1): Show |
4 | HG02257.hp2 HG02717.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370+1896G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952022 | |||||||
| chr17:54952111 | A | C | 2 | a0001c0001t0001g0080 a0001c0001t0001g0334 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1370+1985A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952111 | |||||||
| chr17:54952253 | A | G | 129 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(126): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1370+2127A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952253 | |||||||
| chr17:54952264 | G | A | 2 | a0001c0001t0005g0039 a0001c0001t0005g0040 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1370+2138G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952264 | |||||||
| chr17:54952329 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(244): Show |
282 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.1370+2203A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952329 | |||||||
| chr17:54952417 | C | T | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+2291C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952417 | |||||||
| chr17:54952486 | G | A | 1 | a0001c0001t0003g0256 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1370+2360G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952486 | |||||||
| chr17:54952500 | T | A | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1370+2374T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952500 | |||||||
| chr17:54952502 | G | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+2376G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952502 | |||||||
| chr17:54952515 | T | C | 97 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(94): Show |
110 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.1370+2389T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952515 | |||||||
| chr17:54952546 | C | CA | 155 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0018 others(152): Show |
176 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.1370+2442dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54952546 | ||||||
| chr17:54952546 | C | CAA | 72 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0020 others(69): Show |
87 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.1370+2441_1370+244 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54952546 | ||||||
| chr17:54952546 | C | CAAA | 10 | a0001c0001t0001g0125 a0001c0001t0001g0192 a0001c0001t0001g0207 others(7): Show |
10 | HG01978.hp1 NA18972.hp1 NA18972.hp2 others(7): Show |
intron_variant | MODIFIER | c.1370+2440_1370+244 others(7): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54952546 | ||||||
| chr17:54952546 | CA | C | 8 | a0001c0001t0001g0139 a0001c0001t0001g0164 a0001c0001t0001g0172 others(5): Show |
8 | HG02486.hp2 HG02897.hp1 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1370+2442delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54952546 | ||||||
| chr17:54952567 | A | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0186 a0001c0001t0002g0243 |
5 | HG01081.hp1 HG02257.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370+2441A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952567 | |||||||
| chr17:54952582 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1370+2456T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952582 | |||||||
| chr17:54952690 | T | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0237 |
2 | HG00544.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1370+2564T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952690 | |||||||
| chr17:54952744 | A | AC | 4 | a0001c0001t0001g0099 a0001c0001t0001g0148 a0001c0001t0002g0154 others(1): Show |
4 | HG01952.hp1 HG02717.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1370+2620dupC | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54952744 | ||||||
| chr17:54952842 | C | T | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1370+2716C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952842 | |||||||
| chr17:54952865 | G | A | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1370+2739G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54952865 | |||||||
| chr17:54953100 | C | T | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1370+2974C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953100 | |||||||
| chr17:54953108 | G | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(6): Show |
11 | HG01081.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1370+2982G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953108 | |||||||
| chr17:54953223 | C | A | 33 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0080 others(30): Show |
34 | HG00673.hp1 HG01109.hp2 HG02027.hp1 others(31): Show |
intron_variant | MODIFIER | c.1370+3097C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953223 | |||||||
| chr17:54953223 | C | CA | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1370+3104dupA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54953223 | ||||||
| chr17:54953260 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0162 |
2 | HG00738.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1370+3134T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953260 | |||||||
| chr17:54953307 | G | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1370+3181G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953307 | |||||||
| chr17:54953312 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1370+3186T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953312 | |||||||
| chr17:54953381 | A | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0335 |
3 | HG02615.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1370+3255A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953381 | |||||||
| chr17:54953542 | C | T | 1 | a0001c0001t0001g0335 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1370+3416C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953542 | |||||||
| chr17:54953629 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1370+3503T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953629 | |||||||
| chr17:54953709 | G | A | 1 | a0001c0001t0002g0283 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1370+3583G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953709 | |||||||
| chr17:54953791 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1370+3665G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953791 | |||||||
| chr17:54953942 | G | A | 1 | a0001c0001t0002g0258 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1370+3816G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54953942 | |||||||
| chr17:54954062 | T | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+3936T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954062 | |||||||
| chr17:54954125 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0335 |
2 | HG02615.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1370+3999C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954125 | |||||||
| chr17:54954282 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1370+4156C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954282 | |||||||
| chr17:54954283 | G | C | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1370+4157G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954283 | |||||||
| chr17:54954466 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0335 |
3 | HG02615.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1370+4340G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954466 | |||||||
| chr17:54954478 | G | C | 4 | a0001c0001t0003g0062 a0001c0001t0003g0084 a0001c0001t0003g0085 others(1): Show |
4 | HG00438.hp2 HG02155.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1370+4352G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954478 | |||||||
| chr17:54954528 | G | C | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1370+4402G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954528 | |||||||
| chr17:54954644 | T | C | 2 | a0001c0001t0004g0179 a0001c0001t0004g0180 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1370+4518T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954644 | |||||||
| chr17:54954649 | G | A | 2 | a0001c0001t0002g0132 a0001c0001t0002g0133 |
2 | HG01361.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.1370+4523G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954649 | |||||||
| chr17:54954866 | A | G | 1 | a0001c0001t0004g0055 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1370+4740A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954866 | |||||||
| chr17:54954869 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1370+4743T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54954869 | |||||||
| chr17:54955064 | G | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1370+4938G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955064 | |||||||
| chr17:54955095 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1370+4969G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955095 | |||||||
| chr17:54955129 | A | G | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1370+5003A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955129 | |||||||
| chr17:54955283 | A | G | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1370+5157A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955283 | |||||||
| chr17:54955396 | T | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1371-5170T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955396 | |||||||
| chr17:54955601 | A | T | 2 | a0001c0001t0005g0039 a0001c0001t0005g0040 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1371-4965A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955601 | |||||||
| chr17:54955646 | T | G | 132 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(129): Show |
150 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1371-4920T>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955646 | |||||||
| chr17:54955839 | G | A | 68 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(65): Show |
79 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.1371-4727G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54955839 | |||||||
| chr17:54956214 | G | A | 9 | a0001c0001t0002g0009 a0001c0001t0002g0035 a0001c0001t0002g0123 others(6): Show |
11 | HG01081.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.1371-4352G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956214 | |||||||
| chr17:54956285 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0130 |
3 | HG01168.hp2 HG01346.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1371-4281T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956285 | |||||||
| chr17:54956293 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(245): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1371-4273T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956293 | |||||||
| chr17:54956301 | T | C | 1 | a0001c0001t0004g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1371-4265T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956301 | |||||||
| chr17:54956353 | G | C | 1 | a0001c0001t0004g0179 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1371-4213G>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956353 | |||||||
| chr17:54956484 | A | T | 248 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(245): Show |
283 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1371-4082A>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956484 | |||||||
| chr17:54956577 | G | A | 8 | a0001c0001t0002g0279 a0001c0001t0002g0283 a0001c0001t0002g0300 others(5): Show |
8 | HG00733.hp2 HG01074.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1371-3989G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956577 | |||||||
| chr17:54956638 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1371-3928G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956638 | |||||||
| chr17:54956795 | C | A | 1 | a0001c0001t0001g0209 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1371-3771C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956795 | |||||||
| chr17:54956843 | TGATA | T | 20 | a0001c0001t0004g0014 a0001c0001t0004g0033 a0001c0001t0004g0036 others(17): Show |
21 | HG01884.hp1 HG01884.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1371-3720_1371-371 others(8): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54956843 | ||||||
| chr17:54956905 | G | T | 1 | a0001c0001t0002g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1371-3661G>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956905 | |||||||
| chr17:54956975 | C | G | 1 | a0001c0001t0001g0211 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1371-3591C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54956975 | |||||||
| chr17:54957034 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1371-3532T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957034 | |||||||
| chr17:54957267 | T | A | 31 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0034 others(28): Show |
36 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(33): Show |
intron_variant | MODIFIER | c.1371-3299T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957267 | |||||||
| chr17:54957291 | T | C | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1371-3275T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957291 | |||||||
| chr17:54957501 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1371-3065G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957501 | |||||||
| chr17:54957619 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1371-2947T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957619 | |||||||
| chr17:54957634 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1371-2932A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957634 | |||||||
| chr17:54957957 | T | C | 9 | a0001c0001t0002g0022 a0001c0001t0002g0259 a0001c0001t0002g0260 others(6): Show |
10 | HG02109.hp1 HG02145.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1371-2609T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54957957 | |||||||
| chr17:54958020 | CTGAGGCC others(5): Show |
C | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1371-2544_1371-253 others(16): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54958020 | ||||||
| chr17:54958067 | T | C | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1371-2499T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958067 | |||||||
| chr17:54958133 | GA | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1371-2430delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54958133 | ||||||
| chr17:54958216 | C | T | 1 | a0001c0001t0004g0033 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1371-2350C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958216 | |||||||
| chr17:54958241 | C | T | 129 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(126): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.1371-2325C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958241 | |||||||
| chr17:54958383 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1371-2183T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958383 | |||||||
| chr17:54958435 | G | A | 5 | a0001c0001t0002g0292 a0001c0001t0002g0296 a0001c0001t0002g0302 others(2): Show |
5 | HG02602.hp2 HG02738.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1371-2131G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958435 | |||||||
| chr17:54958453 | G | A | 1 | a0001c0001t0002g0301 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1371-2113G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958453 | |||||||
| chr17:54958595 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1371-1971G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958595 | |||||||
| chr17:54958645 | G | A | 1 | a0001c0001t0002g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1371-1921G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958645 | |||||||
| chr17:54958667 | C | T | 131 | a0001c0001t0001g0245 a0001c0001t0002g0006 a0001c0001t0002g0008 others(128): Show |
149 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.1371-1899C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958667 | |||||||
| chr17:54958700 | A | C | 1 | a0001c0001t0001g0334 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1371-1866A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958700 | |||||||
| chr17:54958717 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1371-1849T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958717 | |||||||
| chr17:54958726 | A | G | 1 | a0001c0001t0002g0281 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1371-1840A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958726 | |||||||
| chr17:54958730 | CA | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(106): Show |
126 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1371-1818delA | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54958730 | ||||||
| chr17:54958730 | CAA | C | 6 | a0001c0001t0001g0116 a0001c0001t0001g0188 a0001c0001t0001g0206 others(3): Show |
6 | HG01934.hp2 HG02809.hp1 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1371-1819_1371-181 others(6): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54958730 | ||||||
| chr17:54958748 | A | AAAAAAAA others(5): Show |
5 | a0001c0001t0003g0067 a0001c0001t0003g0069 a0001c0001t0003g0070 others(2): Show |
5 | HG00438.hp2 HG01109.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(16): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | AAAAAAAA others(4): Show |
27 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(24): Show |
32 | HG00140.hp2 HG00408.hp2 HG00558.hp2 others(29): Show |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(15): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | AAAAAAAA others(3): Show |
2 | a0001c0001t0003g0061 a0001c0001t0003g0090 |
2 | HG01070.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(14): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | AAAAAAAG | 6 | a0001c0001t0002g0035 a0001c0001t0002g0123 a0001c0001t0002g0124 others(3): Show |
6 | HG02559.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(11): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | AAAAAAG | 17 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(14): Show |
17 | HG01243.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(10): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | AAAAAGG | 65 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0011 others(62): Show |
76 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.1371-1818_1371-181 others(10): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958748 | A | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0059 a0001c0003t0001g0117 |
3 | HG04228.hp1 NA18953.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1371-1818A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958748 | |||||||
| chr17:54958779 | C | T | 1 | a0001c0001t0002g0284 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1371-1787C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958779 | |||||||
| chr17:54958858 | G | A | 3 | a0001c0001t0001g0031 a0001c0001t0001g0089 a0001c0001t0001g0335 |
3 | HG02615.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1371-1708G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54958858 | |||||||
| chr17:54959123 | G | A | 1 | a0001c0001t0004g0242 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1371-1443G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959123 | |||||||
| chr17:54959140 | T | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1371-1426T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959140 | |||||||
| chr17:54959168 | C | G | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1371-1398C>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959168 | |||||||
| chr17:54959182 | T | A | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1371-1384T>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959182 | |||||||
| chr17:54959616 | A | AT | 9 | a0001c0001t0001g0107 a0001c0001t0001g0143 a0001c0001t0001g0189 others(6): Show |
9 | HG02630.hp1 HG02897.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.1371-932dupT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54959616 | ||||||
| chr17:54959616 | A | ATT | 88 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(85): Show |
101 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1371-933_1371-932d others(4): Show |
TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54959616 | ||||||
| chr17:54959616 | AT | A | 61 | a0001c0001t0001g0026 a0001c0001t0001g0050 a0001c0001t0001g0127 others(58): Show |
67 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.1371-932delT | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr17 | 54959616 | ||||||
| chr17:54959704 | G | A | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1371-862G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959704 | |||||||
| chr17:54959748 | C | T | 3 | a0001c0001t0005g0037 a0001c0001t0005g0039 a0001c0001t0005g0040 |
3 | HG02280.hp2 HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1371-818C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959748 | |||||||
| chr17:54959787 | T | C | 2 | a0001c0001t0004g0033 a0001c0001t0004g0086 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1371-779T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959787 | |||||||
| chr17:54959872 | C | T | 1 | a0003c0004t0001g0032 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1371-694C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959872 | |||||||
| chr17:54959897 | G | A | 3 | a0001c0001t0001g0010 a0001c0001t0001g0202 a0001c0001t0001g0216 |
5 | NA18948.hp2 NA18975.hp2 NA19067.hp2 others(2): Show |
intron_variant | MODIFIER | c.1371-669G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959897 | |||||||
| chr17:54959998 | T | C | 34 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0027 others(31): Show |
39 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.1371-568T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54959998 | |||||||
| chr17:54960063 | T | C | 1 | a0001c0003t0001g0117 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1371-503T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960063 | |||||||
| chr17:54960128 | C | T | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1371-438C>T | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960128 | |||||||
| chr17:54960134 | G | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1371-432G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960134 | |||||||
| chr17:54960226 | A | G | 246 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(243): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.1371-340A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960226 | |||||||
| chr17:54960248 | C | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.1371-318C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960248 | |||||||
| chr17:54960344 | A | C | 1 | a0001c0001t0003g0078 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1371-222A>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 14/15 | chr17 | 54960344 | |||||||
| chr17:54960721 | G | A | 95 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(92): Show |
108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.*1+94G>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 15/15 | chr17 | 54960721 | |||||||
| chr17:54960840 | T | C | 2 | a0001c0001t0003g0058 a0001c0001t0003g0067 |
2 | HG01081.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.*1+213T>C | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 15/15 | chr17 | 54960840 | |||||||
| chr17:54961069 | A | G | 129 | a0001c0001t0002g0006 a0001c0001t0002g0008 a0001c0001t0002g0009 others(126): Show |
147 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.*2-166A>G | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 15/15 | chr17 | 54961069 | |||||||
| chr17:54961070 | C | A | 2 | a0001c0001t0001g0245 a0001c0001t0006g0246 |
2 | HG02486.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.*2-165C>A | TOM1L1 | ENSG00000141198.16 | transcript | ENST00000575882.6 | protein_coding | 15/15 | chr17 | 54961070 |