Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3792 |
| ensemblid | ENSG00000197993.9 |
| hgncid | 6308 |
| symbol | KEL |
| name | Kell metallo-endopeptidase (Kell blood group) |
| refseq_nuc | NM_000420.3 |
| refseq_prot | NP_000411.1 |
| ensembl_nuc | ENST00000355265.7 |
| ensembl_prot | ENSP00000347409.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 142941114 |
| end | 142962363 |
| strand | - |
| ver | v1.2 |
| region | chr7:142941114-142962363 |
| region5000 | chr7:142936114-142967363 |
| regionname0 | KEL_chr7_142941114_142962363 |
| regionname5000 | KEL_chr7_142936114_142967363 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 732 | 231 | 80 | 55 | 54 | 13 | 28 | 39 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0002 | 0/0 | 732 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0003 | 0/0 | 732 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0004 | 0/0 | 732 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0005 | 0/0 | 732 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0006 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0007 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0008 | 0/0 | 732 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| a0009 | 0/0 | 732 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | MEGGD others(727): Show |
chr7 | 142936114 | 142967363 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2196 | 176 | 40 | 49 | 45 | 13 | 28 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0001c0002 | 0/0 | 2196 | 31 | 19 | 3 | 9 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0001c0003 | 0/0 | 2196 | 20 | 18 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0001c0005 | 0/0 | 2196 | 3 | 3 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0001c0011 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0002c0004 | 0/0 | 2196 | 12 | 12 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0003c0006 | 0/0 | 2196 | 3 | 0 | 2 | 0 | 1 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0004c0007 | 0/0 | 2196 | 2 | 0 | 0 | 2 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0005c0008 | 0/0 | 2196 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0006c0013 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0007c0012 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0008c0010 | 0/0 | 2196 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 | ||
| a0009c0009 | 0/0 | 2196 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | ATGGA others(2191): Show |
chr7 | 142936114 | 142967363 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2494 | 176 | 40 | 49 | 45 | 13 | 28 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0001c0002t0001 | 0/0 | 2494 | 31 | 19 | 3 | 9 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0001c0003t0001 | 0/0 | 2494 | 20 | 18 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0001c0005t0001 | 0/0 | 2494 | 3 | 3 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0001c0011t0001 | 0/0 | 2494 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0002c0004t0001 | 0/0 | 2494 | 12 | 12 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0003c0006t0001 | 0/0 | 2494 | 3 | 0 | 2 | 0 | 1 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0004c0007t0001 | 0/0 | 2494 | 2 | 0 | 0 | 2 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0005c0008t0001 | 0/0 | 2494 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0006c0013t0001 | 0/0 | 2494 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0007c0012t0001 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0008c0010t0001 | 0/0 | 2494 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| a0009c0009t0001 | 0/0 | 2494 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | AGTCC others(2489): Show |
chr7 | 142936114 | 142967363 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 50 | 4 | 14 | 22 | 1 | 9 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0002 | 0/0 | 35 | 9 | 9 | 11 | 2 | 4 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0005 | 0/0 | 6 | 1 | 1 | 3 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0006 | 0/0 | 6 | 1 | 2 | 0 | 2 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 0 | 0 | 3 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 1 | 0 | 2 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0011 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0078 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0004 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0005t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0005t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0001c0011t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0002c0004t0001g0003 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0002c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0002c0004t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0002c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0003c0006t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0003c0006t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0003c0006t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0004c0007t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0004c0007t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0005c0008t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0006c0013t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0007c0012t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0008c0010t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| a0009c0009t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | FIN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00642 | hp1 | a0001 | c0003 | t0001 | g0034 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00733 | hp2 | a0003 | c0006 | t0001 | g0081 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00735 | hp1 | a0001 | c0003 | t0001 | g0045 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01168 | hp1 | a0005 | c0008 | t0001 | g0044 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01175 | hp2 | a0003 | c0006 | t0001 | g0082 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01358 | hp1 | a0001 | c0011 | t0001 | g0068 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0102 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0046 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02040 | hp1 | a0006 | c0013 | t0001 | g0077 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02055 | hp2 | a0002 | c0004 | t0001 | g0029 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0105 | EAS | CDX | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02280 | hp2 | a0001 | c0005 | t0001 | g0092 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0090 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02572 | hp2 | a0007 | c0012 | t0001 | g0100 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02615 | hp1 | a0008 | c0010 | t0001 | g0032 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02615 | hp2 | a0002 | c0004 | t0001 | g0036 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02630 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02723 | hp1 | a0001 | c0005 | t0001 | g0091 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02896 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02897 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0015 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02965 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03041 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03098 | hp1 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0088 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03195 | hp2 | a0001 | c0003 | t0001 | g0097 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03209 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03225 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03453 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03453 | hp2 | a0002 | c0004 | t0001 | g0028 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03486 | hp1 | a0001 | c0003 | t0001 | g0095 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0003 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0103 | AFR | ESN | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03540 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | GWD | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03579 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18906 | hp2 | a0001 | c0003 | t0001 | g0047 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18972 | hp2 | a0004 | c0007 | t0001 | g0057 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19030 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | LWK | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19043 | hp1 | a0001 | c0003 | t0001 | g0049 | AFR | LWK | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19063 | hp1 | a0009 | c0009 | t0001 | g0059 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0012 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19088 | hp1 | a0004 | c0007 | t0001 | g0058 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19240 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | YRI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20752 | hp2 | a0003 | c0006 | t0001 | g0083 | EUR | TSI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0086 | EUR | TSI | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | GIH | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02109 | hp2 | a0001 | c0003 | t0001 | g0004 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02486 | hp1 | a0001 | c0003 | t0001 | g0096 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG02559 | hp2 | a0002 | c0004 | t0001 | g0003 | AFR | ACB | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG03471 | hp2 | a0001 | c0003 | t0001 | g0016 | AFR | MSL | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG06807 | hp1 | a0001 | c0002 | t0001 | g0038 | AFR | USA | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | USA | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0078 | REF | REF | KEL_chr7_142936114_142967363 | KEL | chr7 | 142936114 | 142967363 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142943026 | A | G | 1 | a0002 | 12 | HG02055.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
missense_variant | MODERATE | c.1790T>C | p.Leu597Pro | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 17/19 | 1947/2494 | 1790/2199 | 597/732 | chr7 | 142943026 | |||
| chr7:142943339 | C | T | 1 | a0007 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.1708G>A | p.Val570Met | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 16/19 | 1865/2494 | 1708/2199 | 570/732 | chr7 | 142943339 | |||
| chr7:142944339 | C | T | 1 | a0008 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1475G>A | p.Arg492Gln | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/19 | 1632/2494 | 1475/2199 | 492/732 | chr7 | 142944339 | |||
| chr7:142944665 | G | A | 1 | a0005 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.1391C>T | p.Thr464Ile | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 12/19 | 1548/2494 | 1391/2199 | 464/732 | chr7 | 142944665 | |||
| chr7:142953944 | C | T | 1 | a0009 | 1 | NA19063.hp1 | missense_variant | MODERATE | c.937G>A | p.Ala313Thr | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/19 | 1094/2494 | 937/2199 | 313/732 | chr7 | 142953944 | |||
| chr7:142954207 | T | C | 1 | a0006 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.901A>G | p.Met301Val | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 8/19 | 1058/2494 | 901/2199 | 301/732 | chr7 | 142954207 | |||
| chr7:142954233 | C | T | 1 | a0004 | 2 | NA18972.hp2 NA19088.hp1 |
missense_variant | MODERATE | c.875G>A | p.Arg292Gln | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 8/19 | 1032/2494 | 875/2199 | 292/732 | chr7 | 142954233 | |||
| chr7:142957921 | G | A | 1 | a0003 | 3 | HG00733.hp2 HG01175.hp2 NA20752.hp2 |
missense_variant | MODERATE | c.578C>T | p.Thr193Met | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/19 | 735/2494 | 578/2199 | 193/732 | chr7 | 142957921 | |||
| chr7:142960939 | C | T | 1 | a0005 | 1 | HG01168.hp1 | missense_variant | MODERATE | c.389G>A | p.Arg130Gln | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/19 | 546/2494 | 389/2199 | 130/732 | chr7 | 142960939 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142942917 | T | C | 2 | a0001c0003 a0002c0004 |
32 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(29): Show |
synonymous_variant | LOW | c.1899A>G | p.Leu633Leu | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 17/19 | 2056/2494 | 1899/2199 | 633/732 | chr7 | 142942917 | |||
| chr7:142943328 | G | A | 1 | a0001c0011 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.1719C>T | p.Gly573Gly | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 16/19 | 1876/2494 | 1719/2199 | 573/732 | chr7 | 142943328 | |||
| chr7:142943509 | T | G | 2 | a0001c0002 a0007c0012 |
32 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(29): Show |
synonymous_variant | LOW | c.1680A>C | p.Pro560Pro | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 15/19 | 1837/2494 | 1680/2199 | 560/732 | chr7 | 142943509 | |||
| chr7:142943829 | G | T | 1 | a0001c0005 | 3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.1546C>A | p.Arg516Arg | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 14/19 | 1703/2494 | 1546/2199 | 516/732 | chr7 | 142943829 | |||
| chr7:142954262 | C | G | 1 | a0001c0005 | 3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.846G>C | p.Leu282Leu | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 8/19 | 1003/2494 | 846/2199 | 282/732 | chr7 | 142954262 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:142941470 | G | A | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2038-57C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941470 | |||||||
| chr7:142941610 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0033 others(9): Show |
13 | HG01261.hp1 HG01361.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.2038-197A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941610 | |||||||
| chr7:142941790 | ACAGT | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0101 others(2): Show |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2038-381_2038-378d others(6): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941790 | |||||||
| chr7:142941809 | C | CT | 17 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0040 others(14): Show |
22 | HG00408.hp2 HG00735.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.2038-397dupA | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941809 | |||||||
| chr7:142941894 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2038-481G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941894 | |||||||
| chr7:142941918 | C | T | 1 | a0001c0001t0001g0070 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2038-505G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941918 | |||||||
| chr7:142941957 | C | T | 3 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0002c0004t0001g0028 |
4 | HG02486.hp2 HG03130.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2037+477G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142941957 | |||||||
| chr7:142942068 | T | C | 50 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0030 others(47): Show |
79 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.2037+366A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142942068 | |||||||
| chr7:142942197 | G | C | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0101 others(2): Show |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2037+237C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142942197 | |||||||
| chr7:142942234 | C | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): Show |
183 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.2037+200G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142942234 | |||||||
| chr7:142942239 | T | C | 2 | a0001c0001t0001g0017 a0001c0001t0001g0048 |
3 | HG01361.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2037+195A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142942239 | |||||||
| chr7:142942309 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2037+125C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 18/18 | chr7 | 142942309 | |||||||
| chr7:142942552 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1942-23C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 17/18 | chr7 | 142942552 | |||||||
| chr7:142942643 | T | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0031 a0001c0001t0001g0101 others(2): Show |
6 | HG02055.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1942-114A>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 17/18 | chr7 | 142942643 | |||||||
| chr7:142942759 | C | T | 2 | a0001c0003t0001g0034 a0001c0003t0001g0095 |
2 | HG00642.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1941+116G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 17/18 | chr7 | 142942759 | |||||||
| chr7:142943190 | T | C | 10 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0031 others(7): Show |
11 | HG01261.hp1 HG01361.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1771+86A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 16/18 | chr7 | 142943190 | |||||||
| chr7:142943600 | T | A | 1 | a0001c0003t0001g0047 | 1 | NA18906.hp2 | splice_region_variant&intron_variant | LOW | c.1593-4A>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 14/18 | chr7 | 142943600 | |||||||
| chr7:142943936 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1492-53G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142943936 | |||||||
| chr7:142943952 | T | G | 1 | a0001c0001t0001g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1492-69A>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142943952 | |||||||
| chr7:142944000 | G | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1492-117C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944000 | |||||||
| chr7:142944087 | A | T | 1 | a0001c0001t0001g0062 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1492-204T>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944087 | |||||||
| chr7:142944102 | T | C | 27 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(24): Show |
47 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(44): Show |
intron_variant | MODIFIER | c.1492-219A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944102 | |||||||
| chr7:142944120 | T | C | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1491+203A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944120 | |||||||
| chr7:142944123 | G | T | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1491+200C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944123 | |||||||
| chr7:142944133 | G | C | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1491+190C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944133 | |||||||
| chr7:142944278 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1491+45C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944278 | |||||||
| chr7:142944295 | A | G | 50 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0030 others(47): Show |
79 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(76): Show |
intron_variant | MODIFIER | c.1491+28T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 13/18 | chr7 | 142944295 | |||||||
| chr7:142944464 | C | T | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1414-64G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 12/18 | chr7 | 142944464 | |||||||
| chr7:142944516 | C | CAGT | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1414-119_1414-117d others(5): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 12/18 | chr7 | 142944516 | |||||||
| chr7:142944580 | C | A | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1413+63G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 12/18 | chr7 | 142944580 | |||||||
| chr7:142944830 | G | C | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1315-89C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142944830 | |||||||
| chr7:142945011 | A | G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1315-270T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945011 | |||||||
| chr7:142945193 | A | G | 1 | a0002c0004t0001g0028 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1315-452T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945193 | |||||||
| chr7:142945284 | G | A | 10 | a0001c0003t0001g0004 a0001c0003t0001g0016 a0001c0003t0001g0034 others(7): Show |
18 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1315-543C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945284 | |||||||
| chr7:142945424 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1315-683T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945424 | |||||||
| chr7:142945509 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0098 |
6 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.1314+698T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945509 | |||||||
| chr7:142945546 | A | G | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1314+661T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945546 | |||||||
| chr7:142945632 | C | CTT | 23 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(20): Show |
35 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1314+573_1314+574d others(4): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945632 | |||||||
| chr7:142945727 | C | A | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1314+480G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945727 | |||||||
| chr7:142945737 | G | A | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1314+470C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945737 | |||||||
| chr7:142945824 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1314+383G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945824 | |||||||
| chr7:142945853 | C | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(1): Show |
4 | HG02630.hp2 HG03041.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1314+354G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945853 | |||||||
| chr7:142945895 | T | C | 10 | a0001c0003t0001g0004 a0001c0003t0001g0016 a0001c0003t0001g0034 others(7): Show |
18 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1314+312A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945895 | |||||||
| chr7:142945898 | G | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0031 a0001c0001t0001g0037 others(5): Show |
9 | HG01361.hp2 HG02109.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1314+309C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142945898 | |||||||
| chr7:142946005 | G | A | 23 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(20): Show |
35 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.1314+202C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142946005 | |||||||
| chr7:142946012 | T | C | 49 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0030 others(46): Show |
78 | HG00642.hp1 HG00735.hp1 HG01106.hp2 others(75): Show |
intron_variant | MODIFIER | c.1314+195A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142946012 | |||||||
| chr7:142946013 | G | A | 1 | a0001c0002t0001g0104 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1314+194C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142946013 | |||||||
| chr7:142946103 | C | G | 1 | a0001c0011t0001g0068 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1314+104G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 11/18 | chr7 | 142946103 | |||||||
| chr7:142946321 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01192.hp2 | splice_region_variant&intron_variant | LOW | c.1204-4A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946321 | |||||||
| chr7:142946386 | C | G | 10 | a0001c0003t0001g0004 a0001c0003t0001g0016 a0001c0003t0001g0034 others(7): Show |
18 | HG00642.hp1 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.1204-69G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946386 | |||||||
| chr7:142946409 | G | C | 1 | a0001c0002t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1204-92C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946409 | |||||||
| chr7:142946576 | T | C | 1 | a0005c0008t0001g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1204-259A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946576 | |||||||
| chr7:142946589 | C | T | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1204-272G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946589 | |||||||
| chr7:142946687 | G | A | 25 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(22): Show |
37 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.1204-370C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946687 | |||||||
| chr7:142946717 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1204-400C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946717 | |||||||
| chr7:142946758 | C | T | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1204-441G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946758 | |||||||
| chr7:142946783 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0067 |
6 | HG01433.hp2 HG02738.hp1 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-466G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142946783 | |||||||
| chr7:142947010 | T | A | 1 | a0008c0010t0001g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1204-693A>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947010 | |||||||
| chr7:142947021 | A | G | 4 | a0001c0003t0001g0004 a0001c0003t0001g0016 a0001c0003t0001g0045 others(1): Show |
12 | HG00735.hp1 HG02109.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1204-704T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947021 | |||||||
| chr7:142947065 | T | C | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1204-748A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947065 | |||||||
| chr7:142947137 | C | T | 4 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 others(1): Show |
4 | HG00733.hp2 HG02280.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-820G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947137 | |||||||
| chr7:142947173 | C | T | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1204-856G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947173 | |||||||
| chr7:142947280 | G | T | 5 | a0001c0001t0001g0014 a0001c0005t0001g0090 a0001c0005t0001g0091 others(2): Show |
6 | HG02280.hp2 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204-963C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947280 | |||||||
| chr7:142947387 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(100): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.1204-1070T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947387 | |||||||
| chr7:142947397 | A | G | 2 | a0001c0001t0001g0017 a0001c0001t0001g0048 |
3 | HG01361.hp2 HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1204-1080T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947397 | |||||||
| chr7:142947434 | T | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(92): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1204-1117A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947434 | |||||||
| chr7:142947478 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1204-1161A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947478 | |||||||
| chr7:142947597 | C | T | 5 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 others(2): Show |
5 | HG02055.hp2 HG02280.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1204-1280G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947597 | |||||||
| chr7:142947602 | G | A | 1 | a0001c0001t0001g0065 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1204-1285C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947602 | |||||||
| chr7:142947813 | G | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0101 others(16): Show |
31 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1204-1496C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142947813 | |||||||
| chr7:142948511 | G | A | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1204-2194C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948511 | |||||||
| chr7:142948527 | C | T | 19 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0101 others(16): Show |
31 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.1204-2210G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948527 | |||||||
| chr7:142948668 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1204-2351T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948668 | |||||||
| chr7:142948692 | CT | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0073 |
3 | HG01167.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1204-2376delA | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948692 | |||||||
| chr7:142948738 | T | C | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1204-2421A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948738 | |||||||
| chr7:142948772 | G | A | 1 | a0001c0002t0001g0089 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1204-2455C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948772 | |||||||
| chr7:142948843 | C | T | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1204-2526G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948843 | |||||||
| chr7:142948857 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1204-2540A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948857 | |||||||
| chr7:142948899 | G | GAC | 6 | a0001c0001t0001g0017 a0001c0001t0001g0020 a0001c0001t0001g0048 others(3): Show |
9 | HG01361.hp2 HG02257.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1204-2584_1204-258 others(6): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACAC | 13 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0012 others(10): Show |
20 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1204-2586_1204-258 others(8): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACACAC | 4 | a0001c0002t0001g0009 a0001c0002t0001g0084 a0001c0002t0001g0088 others(1): Show |
8 | HG02572.hp2 HG02647.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.1204-2588_1204-258 others(10): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACACACA others(3): Show |
1 | a0001c0001t0001g0014 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1204-2592_1204-258 others(14): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACACACA others(5): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0041 others(5): Show |
16 | HG02055.hp2 HG02109.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.1204-2594_1204-258 others(16): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACACACA others(7): Show |
4 | a0001c0001t0001g0037 a0001c0005t0001g0090 a0001c0005t0001g0091 others(1): Show |
4 | HG02280.hp2 HG02572.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204-2596_1204-258 others(18): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948899 | G | GACACACA others(11): Show |
1 | a0001c0001t0001g0042 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1204-2600_1204-258 others(22): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948899 | |||||||
| chr7:142948901 | C | A | 3 | a0001c0003t0001g0034 a0001c0003t0001g0095 a0001c0003t0001g0096 |
3 | HG00642.hp1 HG02486.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1204-2584G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948901 | |||||||
| chr7:142948911 | C | T | 1 | a0006c0013t0001g0077 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1204-2594G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948911 | |||||||
| chr7:142948914 | A | ACACACAC others(12): Show |
1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1204-2598_1204-259 others(23): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948914 | |||||||
| chr7:142948994 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1204-2677A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142948994 | |||||||
| chr7:142949392 | C | T | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1204-3075G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142949392 | |||||||
| chr7:142949730 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1203+2779C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142949730 | |||||||
| chr7:142949735 | C | CT | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1203+2773dupA | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142949735 | |||||||
| chr7:142949801 | T | C | 1 | a0005c0008t0001g0044 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1203+2708A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142949801 | |||||||
| chr7:142949908 | A | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+2601T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142949908 | |||||||
| chr7:142950042 | G | A | 1 | a0001c0002t0001g0103 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1203+2467C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950042 | |||||||
| chr7:142950341 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+2168G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950341 | |||||||
| chr7:142950374 | C | T | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1203+2135G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950374 | |||||||
| chr7:142950477 | C | T | 4 | a0001c0001t0001g0010 a0001c0003t0001g0034 a0001c0003t0001g0095 others(1): Show |
7 | HG00642.hp1 HG00642.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+2032G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950477 | |||||||
| chr7:142950491 | G | A | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1203+2018C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950491 | |||||||
| chr7:142950633 | C | A | 33 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0030 others(30): Show |
53 | HG01106.hp2 HG01256.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.1203+1876G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950633 | |||||||
| chr7:142950706 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1203+1803A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950706 | |||||||
| chr7:142950743 | G | A | 1 | a0007c0012t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203+1766C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142950743 | |||||||
| chr7:142951065 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1203+1444T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142951065 | |||||||
| chr7:142951101 | G | A | 1 | a0001c0001t0001g0011 | 4 | HG01074.hp1 HG02895.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1203+1408C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142951101 | |||||||
| chr7:142951186 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+1323A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142951186 | |||||||
| chr7:142951503 | C | A | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1203+1006G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142951503 | |||||||
| chr7:142951715 | T | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1203+794A>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142951715 | |||||||
| chr7:142952094 | T | C | 5 | a0001c0002t0001g0023 a0001c0002t0001g0038 a0001c0002t0001g0039 others(2): Show |
6 | HG01952.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203+415A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142952094 | |||||||
| chr7:142952205 | A | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+304T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142952205 | |||||||
| chr7:142952264 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1203+245G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142952264 | |||||||
| chr7:142952477 | A | G | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1203+32T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 10/18 | chr7 | 142952477 | |||||||
| chr7:142952759 | A | G | 1 | a0001c0001t0001g0060 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1074-121T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142952759 | |||||||
| chr7:142953071 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1074-433G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953071 | |||||||
| chr7:142953388 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(82): Show |
180 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.1073+420C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953388 | |||||||
| chr7:142953578 | G | A | 1 | a0001c0001t0001g0013 | 3 | HG00639.hp2 HG01192.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.1073+230C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953578 | |||||||
| chr7:142953655 | C | T | 1 | a0001c0001t0001g0014 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1073+153G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953655 | |||||||
| chr7:142953787 | C | G | 1 | a0001c0001t0001g0018 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1073+21G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953787 | |||||||
| chr7:142953792 | C | G | 2 | a0001c0002t0001g0012 a0001c0002t0001g0106 |
5 | HG02040.hp2 NA18945.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073+16G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953792 | |||||||
| chr7:142953801 | G | A | 2 | a0001c0001t0001g0021 a0001c0001t0001g0076 |
3 | HG01168.hp2 HG01169.hp1 HG03688.hp2 |
splice_region_variant&intron_variant | LOW | c.1073+7C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 9/18 | chr7 | 142953801 | |||||||
| chr7:142954568 | G | A | 2 | a0001c0001t0001g0017 a0001c0002t0001g0027 |
4 | HG01361.hp2 HG02976.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-41C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142954568 | |||||||
| chr7:142954660 | A | G | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.673-133T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142954660 | |||||||
| chr7:142954781 | G | A | 33 | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0030 others(30): Show |
53 | HG01106.hp2 HG01256.hp1 HG01261.hp1 others(50): Show |
intron_variant | MODIFIER | c.673-254C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142954781 | |||||||
| chr7:142955100 | G | A | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.673-573C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142955100 | |||||||
| chr7:142955291 | A | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-764T>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142955291 | |||||||
| chr7:142955763 | T | C | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.673-1236A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142955763 | |||||||
| chr7:142955996 | C | G | 1 | a0007c0012t0001g0100 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.673-1469G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142955996 | |||||||
| chr7:142956007 | T | C | 1 | a0001c0005t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.673-1480A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956007 | |||||||
| chr7:142956027 | C | G | 1 | a0001c0002t0001g0105 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.673-1500G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956027 | |||||||
| chr7:142956100 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.673-1573G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956100 | |||||||
| chr7:142956210 | C | G | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.672+1617G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956210 | |||||||
| chr7:142956337 | A | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(14): Show |
28 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.672+1490T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956337 | |||||||
| chr7:142956373 | C | T | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.672+1454G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956373 | |||||||
| chr7:142956391 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.672+1436G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956391 | |||||||
| chr7:142956646 | A | G | 1 | a0001c0001t0001g0055 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.672+1181T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956646 | |||||||
| chr7:142956651 | C | T | 1 | a0001c0001t0001g0030 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.672+1176G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956651 | |||||||
| chr7:142956944 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.672+883T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956944 | |||||||
| chr7:142956980 | C | A | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.672+847G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142956980 | |||||||
| chr7:142957099 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.672+728G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957099 | |||||||
| chr7:142957134 | C | T | 4 | a0002c0004t0001g0003 a0002c0004t0001g0028 a0002c0004t0001g0029 others(1): Show |
12 | HG02055.hp2 HG02559.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.672+693G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957134 | |||||||
| chr7:142957248 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0085 |
7 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+579C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957248 | |||||||
| chr7:142957287 | C | A | 2 | a0001c0001t0001g0014 a0008c0010t0001g0032 |
3 | HG02615.hp1 HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.672+540G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957287 | |||||||
| chr7:142957409 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.672+418A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957409 | |||||||
| chr7:142957422 | C | T | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.672+405G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957422 | |||||||
| chr7:142957470 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.672+357G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957470 | |||||||
| chr7:142957568 | G | C | 1 | a0001c0001t0001g0035 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.672+259C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957568 | |||||||
| chr7:142957611 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.672+216A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 6/18 | chr7 | 142957611 | |||||||
| chr7:142957991 | G | A | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-18C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142957991 | |||||||
| chr7:142958010 | C | T | 14 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0037 others(11): Show |
22 | HG01261.hp1 HG02055.hp2 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.526-37G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142958010 | |||||||
| chr7:142958026 | C | G | 17 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(14): Show |
28 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.526-53G>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142958026 | |||||||
| chr7:142958052 | C | A | 1 | a0001c0003t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.526-79G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142958052 | |||||||
| chr7:142958190 | T | C | 1 | a0001c0002t0001g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.525+114A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142958190 | |||||||
| chr7:142958246 | C | T | 3 | a0001c0005t0001g0090 a0001c0005t0001g0091 a0001c0005t0001g0092 |
3 | HG02280.hp2 HG02572.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.525+58G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 5/18 | chr7 | 142958246 | |||||||
| chr7:142958602 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0031 others(3): Show |
7 | HG01261.hp1 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-174G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142958602 | |||||||
| chr7:142958630 | T | C | 21 | a0001c0001t0001g0025 a0001c0001t0001g0101 a0001c0002t0001g0009 others(18): Show |
33 | HG01106.hp2 HG01256.hp1 HG01884.hp2 others(30): Show |
intron_variant | MODIFIER | c.401-202A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142958630 | |||||||
| chr7:142958691 | A | G | 14 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0031 others(11): Show |
23 | HG01261.hp1 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.401-263T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142958691 | |||||||
| chr7:142958814 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.401-386C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142958814 | |||||||
| chr7:142959015 | A | C | 3 | a0001c0002t0001g0087 a0002c0004t0001g0028 a0002c0004t0001g0029 |
3 | HG02055.hp2 HG02257.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.401-587T>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959015 | |||||||
| chr7:142959020 | TTTGA | T | 2 | a0002c0004t0001g0003 a0002c0004t0001g0036 |
10 | HG02559.hp2 HG02615.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.401-596_401-593del others(4): Show |
KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959020 | |||||||
| chr7:142959223 | A | G | 11 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0033 others(8): Show |
11 | HG00642.hp1 HG01109.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-795T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959223 | |||||||
| chr7:142959240 | G | T | 1 | a0001c0002t0001g0023 | 2 | HG02258.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.401-812C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959240 | |||||||
| chr7:142959397 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0048 others(7): Show |
21 | HG00735.hp1 HG01361.hp2 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.401-969T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959397 | |||||||
| chr7:142959439 | C | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0088 |
6 | HG02647.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.401-1011G>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959439 | |||||||
| chr7:142959696 | A | G | 1 | a0001c0002t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400+1232T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959696 | |||||||
| chr7:142959743 | T | G | 1 | a0001c0001t0001g0085 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.400+1185A>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142959743 | |||||||
| chr7:142960393 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.400+535C>T | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142960393 | |||||||
| chr7:142960465 | G | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0088 |
6 | HG02647.hp1 HG02818.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.400+463C>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142960465 | |||||||
| chr7:142960510 | A | G | 1 | a0001c0002t0001g0087 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.400+418T>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142960510 | |||||||
| chr7:142960688 | C | T | 42 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0030 others(39): Show |
60 | HG00642.hp1 HG00738.hp1 HG01256.hp2 others(57): Show |
intron_variant | MODIFIER | c.400+240G>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142960688 | |||||||
| chr7:142960828 | T | C | 46 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0030 others(43): Show |
66 | HG00642.hp1 HG00738.hp1 HG01256.hp2 others(63): Show |
intron_variant | MODIFIER | c.400+100A>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 4/18 | chr7 | 142960828 | |||||||
| chr7:142961180 | A | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0030 a0001c0001t0001g0031 others(21): Show |
36 | HG00642.hp1 HG01261.hp1 HG02040.hp2 others(33): Show |
intron_variant | MODIFIER | c.224-76T>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 3/18 | chr7 | 142961180 | |||||||
| chr7:142961261 | A | T | 2 | a0002c0004t0001g0028 a0002c0004t0001g0029 |
2 | HG02055.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.223+99T>A | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 3/18 | chr7 | 142961261 | |||||||
| chr7:142961527 | G | C | 5 | a0001c0002t0001g0012 a0001c0002t0001g0105 a0001c0002t0001g0106 others(2): Show |
8 | HG02040.hp2 HG02155.hp1 NA18945.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-26C>G | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 2/18 | chr7 | 142961527 | |||||||
| chr7:142962082 | T | G | 6 | a0001c0002t0001g0012 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
9 | HG02040.hp2 HG02155.hp1 NA18943.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+122A>C | KEL | ENSG00000197993.9 | transcript | ENST00000355265.7 | protein_coding | 1/18 | chr7 | 142962082 |