Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 22944 |
| ensemblid | ENSG00000151657.12 |
| hgncid | 6327 |
| symbol | KIN |
| name | Kin17 DNA and RNA binding protein |
| refseq_nuc | NM_012311.4 |
| refseq_prot | NP_036443.1 |
| ensembl_nuc | ENST00000379562.9 |
| ensembl_prot | ENSP00000368881.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 7750962 |
| end | 7787993 |
| strand | - |
| ver | v1.2 |
| region | chr10:7750962-7787993 |
| region5000 | chr10:7745962-7792993 |
| regionname0 | KIN_chr10_7750962_7787993 |
| regionname5000 | KIN_chr10_7745962_7792993 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 393 | 422 | 81 | 68 | 218 | 16 | 37 | 178 | KIN_chr10_7745962_7792993 | KIN | MGKSD others(388): Show |
chr10 | 7745962 | 7792993 |
| a0002 | 0/0 | 393 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | MGKSD others(388): Show |
chr10 | 7745962 | 7792993 |
| a0003 | 0/0 | 393 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | MGKSD others(388): Show |
chr10 | 7745962 | 7792993 |
| a0004 | 0/0 | 393 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | MGKSD others(388): Show |
chr10 | 7745962 | 7792993 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1179 | 406 | 66 | 67 | 218 | 16 | 37 | KIN_chr10_7745962_7792993 | KIN | ATGGG others(1174): Show |
chr10 | 7745962 | 7792993 | ||
| a0001c0002 | 0/0 | 1179 | 16 | 15 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | ATGGG others(1174): Show |
chr10 | 7745962 | 7792993 | ||
| a0002c0003 | 0/0 | 1179 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | ATGGG others(1174): Show |
chr10 | 7745962 | 7792993 | ||
| a0003c0004 | 0/0 | 1179 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | ATGGG others(1174): Show |
chr10 | 7745962 | 7792993 | ||
| a0004c0005 | 0/0 | 1179 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | ATGGG others(1174): Show |
chr10 | 7745962 | 7792993 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6144 | 64 | 4 | 10 | 41 | 3 | 6 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0002 | 0/0 | 6144 | 56 | 7 | 21 | 22 | 2 | 4 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0003 | 0/0 | 6143 | 33 | 1 | 5 | 26 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0004 | 0/0 | 6144 | 27 | 0 | 2 | 22 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0005 | 0/0 | 6140 | 27 | 2 | 4 | 20 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0006 | 0/0 | 6144 | 19 | 0 | 2 | 17 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0007 | 0/0 | 6140 | 13 | 0 | 0 | 12 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0008 | 0/0 | 6143 | 9 | 0 | 4 | 0 | 0 | 5 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0010 | 0/0 | 6144 | 8 | 5 | 1 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0011 | 0/0 | 6360 | 8 | 0 | 1 | 3 | 0 | 4 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6355): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0012 | 0/0 | 6143 | 7 | 0 | 5 | 0 | 1 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0013 | 0/0 | 6364 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6359): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0014 | 0/0 | 6143 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0015 | 0/0 | 6140 | 6 | 0 | 2 | 0 | 2 | 2 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0016 | 0/0 | 6144 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0017 | 0/0 | 6144 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0018 | 0/0 | 6144 | 5 | 5 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0019 | 0/0 | 6144 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0020 | 0/0 | 6144 | 4 | 0 | 1 | 2 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0021 | 0/0 | 6144 | 4 | 4 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0022 | 1/0 | 6360 | 4 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6355): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0023 | 0/0 | 6144 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0024 | 0/0 | 6143 | 3 | 0 | 1 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0025 | 0/0 | 6144 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0026 | 0/0 | 6140 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0027 | 0/0 | 6144 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0028 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0029 | 0/0 | 6364 | 2 | 0 | 0 | 0 | 1 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6359): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0030 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0032 | 0/0 | 6143 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0033 | 0/0 | 6144 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0034 | 0/0 | 6144 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0035 | 0/0 | 6144 | 2 | 0 | 0 | 1 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0036 | 0/0 | 6144 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0037 | 0/0 | 6144 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0038 | 0/0 | 6140 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0039 | 0/0 | 6140 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0040 | 0/0 | 6140 | 2 | 1 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0041 | 0/0 | 6140 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0042 | 0/0 | 6361 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6356): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0043 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0044 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0045 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0046 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0047 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0049 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0050 | 0/1 | 6363 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6358): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0052 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0053 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0054 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0055 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0056 | 0/0 | 6365 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6360): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0057 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0058 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0059 | 0/0 | 6143 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0060 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0061 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0062 | 0/0 | 6143 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0063 | 0/0 | 6143 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0064 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0065 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0071 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0072 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0073 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0074 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0075 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0076 | 0/0 | 6144 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0077 | 0/0 | 6144 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0078 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0079 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6360): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0080 | 0/0 | 6143 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0081 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0082 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0083 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0084 | 0/0 | 6140 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0085 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0086 | 0/0 | 6361 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6356): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0087 | 0/0 | 6140 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0088 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0089 | 0/0 | 6361 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6356): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0090 | 0/0 | 6360 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6355): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0091 | 0/0 | 6140 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0092 | 0/0 | 6140 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6135): Show |
chr10 | 7745962 | 7792993 |
| a0001c0001t0093 | 0/0 | 6361 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6356): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0009 | 0/0 | 6144 | 10 | 10 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0051 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0066 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0067 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0068 | 0/0 | 6144 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0069 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6360): Show |
chr10 | 7745962 | 7792993 |
| a0001c0002t0070 | 0/0 | 6365 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6360): Show |
chr10 | 7745962 | 7792993 |
| a0002c0003t0031 | 0/0 | 6144 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| a0003c0004t0008 | 0/0 | 6143 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6138): Show |
chr10 | 7745962 | 7792993 |
| a0004c0005t0048 | 0/0 | 6144 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | GGTTC others(6139): Show |
chr10 | 7745962 | 7792993 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 0 | 3 | 7 | 2 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0002 | 0/0 | 9 | 2 | 5 | 1 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0018 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0004g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0005g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0008g0007 | 0/0 | 5 | 0 | 2 | 0 | 0 | 3 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0008g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0008g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0008g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0008g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0011g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0012g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0012g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0012g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0012g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0013g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0013g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0013g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0013g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0013g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0014g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0014g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0014g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0014g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0015g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0016g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0017g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0018g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0018g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0018g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0018g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0018g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0019g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0019g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0020g0042 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0020g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0020g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0021g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0021g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0022g0048 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0022g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0022g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0023g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0023g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0023g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0024g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0024g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0025g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0025g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0026g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0026g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0027g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0028g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0028g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0029g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0029g0317 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0030g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0030g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0032g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0033g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0033g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0034g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0034g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0035g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0036g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0036g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0037g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0038g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0038g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0039g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0040g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0040g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0041g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0041g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0042g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0042g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0043g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0044g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0045g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0046g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0047g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0049g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0050g0316 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0052g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0053g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0054g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0055g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0056g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0057g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0058g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0059g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0060g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0061g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0062g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0063g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0064g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0065g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0071g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0072g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0073g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0074g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0075g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0076g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0077g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0078g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0079g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0080g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0081g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0082g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0083g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0084g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0085g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0086g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0087g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0088g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0089g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0090g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0091g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0092g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0001t0093g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0009g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0051g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0066g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0067g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0068g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0069g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0001c0002t0070g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0002c0003t0031g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0002c0003t0031g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0003c0004t0008g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| a0004c0005t0048g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0015 | g0053 | EUR | GBR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00099 | hp2 | a0001 | c0001 | t0029 | g0317 | EUR | GBR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00280 | hp1 | a0001 | c0001 | t0035 | g0065 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00323 | hp1 | a0001 | c0001 | t0012 | g0276 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00323 | hp2 | a0001 | c0001 | t0064 | g0083 | EUR | FIN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00408 | hp1 | a0001 | c0001 | t0014 | g0224 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00408 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00438 | hp1 | a0002 | c0003 | t0031 | g0207 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00438 | hp2 | a0001 | c0001 | t0027 | g0031 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00558 | hp1 | a0001 | c0001 | t0007 | g0164 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00558 | hp2 | a0001 | c0001 | t0046 | g0172 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0183 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00609 | hp2 | a0001 | c0001 | t0007 | g0170 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0147 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00642 | hp2 | a0001 | c0001 | t0012 | g0277 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00673 | hp2 | a0001 | c0001 | t0024 | g0043 | EAS | CHS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00733 | hp2 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0318 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00741 | hp1 | a0001 | c0001 | t0006 | g0141 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01069 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01070 | hp1 | a0001 | c0001 | t0039 | g0049 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01070 | hp2 | a0001 | c0001 | t0059 | g0279 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01071 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01071 | hp2 | a0001 | c0001 | t0039 | g0049 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01081 | hp1 | a0001 | c0001 | t0089 | g0114 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0007 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0263 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0285 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01175 | hp1 | a0001 | c0001 | t0020 | g0042 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0140 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01243 | hp1 | a0001 | c0002 | t0068 | g0145 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01243 | hp2 | a0001 | c0001 | t0087 | g0095 | AMR | PUR | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01255 | hp2 | a0001 | c0001 | t0008 | g0283 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01257 | hp2 | a0001 | c0001 | t0015 | g0161 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0028 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0314 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01433 | hp2 | a0001 | c0001 | t0084 | g0323 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01496 | hp2 | a0001 | c0001 | t0015 | g0162 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01515 | hp1 | a0001 | c0001 | t0037 | g0024 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0021 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01516 | hp2 | a0001 | c0001 | t0049 | g0221 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01517 | hp2 | a0001 | c0001 | t0037 | g0024 | EUR | IBS | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01884 | hp1 | a0001 | c0001 | t0079 | g0123 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01884 | hp2 | a0001 | c0001 | t0080 | g0278 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01891 | hp1 | a0001 | c0001 | t0030 | g0134 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01891 | hp2 | a0001 | c0001 | t0060 | g0282 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0301 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01981 | hp2 | a0001 | c0001 | t0011 | g0110 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01993 | hp1 | a0001 | c0001 | t0024 | g0274 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01993 | hp2 | a0001 | c0001 | t0063 | g0290 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02015 | hp1 | a0001 | c0001 | t0035 | g0064 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02015 | hp2 | a0001 | c0001 | t0091 | g0117 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02027 | hp1 | a0001 | c0001 | t0081 | g0171 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02055 | hp1 | a0001 | c0001 | t0028 | g0218 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02055 | hp2 | a0001 | c0002 | t0009 | g0098 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02056 | hp1 | a0001 | c0001 | t0090 | g0124 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02056 | hp2 | a0001 | c0001 | t0014 | g0302 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02080 | hp1 | a0001 | c0001 | t0062 | g0190 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02129 | hp2 | a0001 | c0001 | t0014 | g0289 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02132 | hp1 | a0001 | c0001 | t0007 | g0155 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02132 | hp2 | a0001 | c0001 | t0023 | g0139 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02135 | hp2 | a0002 | c0003 | t0031 | g0208 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02145 | hp1 | a0001 | c0001 | t0010 | g0150 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02145 | hp2 | a0001 | c0001 | t0002 | g0267 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02148 | hp1 | a0001 | c0001 | t0005 | g0130 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0182 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02155 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | CDX | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CDX | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02257 | hp1 | a0001 | c0001 | t0022 | g0320 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02257 | hp2 | a0001 | c0002 | t0009 | g0102 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02258 | hp1 | a0001 | c0001 | t0083 | g0166 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02280 | hp1 | a0001 | c0001 | t0042 | g0112 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02280 | hp2 | a0001 | c0001 | t0019 | g0017 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02300 | hp1 | a0001 | c0001 | t0027 | g0031 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02523 | hp1 | a0001 | c0001 | t0024 | g0043 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | KHV | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02602 | hp2 | a0001 | c0001 | t0041 | g0227 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02615 | hp1 | a0001 | c0001 | t0022 | g0048 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02615 | hp2 | a0001 | c0001 | t0034 | g0205 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02622 | hp1 | a0001 | c0002 | t0009 | g0100 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02622 | hp2 | a0001 | c0001 | t0092 | g0104 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02630 | hp1 | a0001 | c0002 | t0009 | g0099 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02630 | hp2 | a0001 | c0001 | t0093 | g0116 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02647 | hp1 | a0001 | c0001 | t0078 | g0086 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0306 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0220 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02717 | hp1 | a0001 | c0001 | t0019 | g0219 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02717 | hp2 | a0001 | c0002 | t0066 | g0103 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02723 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02723 | hp2 | a0001 | c0001 | t0042 | g0129 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02735 | hp1 | a0001 | c0001 | t0005 | g0111 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02735 | hp2 | a0001 | c0001 | t0011 | g0165 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02738 | hp1 | a0001 | c0001 | t0011 | g0120 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02809 | hp1 | a0001 | c0001 | t0085 | g0322 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02809 | hp2 | a0001 | c0001 | t0038 | g0128 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0143 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0148 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02896 | hp1 | a0001 | c0002 | t0067 | g0094 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02896 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02970 | hp1 | a0001 | c0002 | t0070 | g0146 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02970 | hp2 | a0001 | c0002 | t0051 | g0101 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02976 | hp1 | a0001 | c0001 | t0025 | g0059 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02976 | hp2 | a0001 | c0001 | t0026 | g0050 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03017 | hp1 | a0003 | c0004 | t0008 | g0307 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03017 | hp2 | a0001 | c0001 | t0029 | g0275 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0271 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03041 | hp2 | a0001 | c0002 | t0009 | g0097 | AFR | GWD | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03098 | hp2 | a0001 | c0001 | t0025 | g0019 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03130 | hp1 | a0001 | c0001 | t0058 | g0091 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03130 | hp2 | a0001 | c0001 | t0019 | g0017 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03139 | hp1 | a0001 | c0001 | t0026 | g0321 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03139 | hp2 | a0001 | c0001 | t0040 | g0115 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03209 | hp1 | a0001 | c0001 | t0038 | g0093 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03225 | hp1 | a0004 | c0005 | t0048 | g0149 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03225 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0288 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03453 | hp2 | a0001 | c0001 | t0065 | g0217 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0092 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03486 | hp2 | a0001 | c0001 | t0018 | g0270 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03490 | hp1 | a0001 | c0001 | t0008 | g0284 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03491 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03491 | hp2 | a0001 | c0001 | t0041 | g0119 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03516 | hp2 | a0001 | c0001 | t0030 | g0135 | AFR | ESN | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03669 | hp1 | a0001 | c0001 | t0076 | g0066 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03669 | hp2 | a0001 | c0001 | t0061 | g0286 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03688 | hp1 | a0001 | c0001 | t0040 | g0056 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03688 | hp2 | a0001 | c0001 | t0012 | g0273 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03704 | hp2 | a0001 | c0001 | t0015 | g0163 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03710 | hp2 | a0001 | c0001 | t0011 | g0113 | SAS | PJL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03831 | hp1 | a0001 | c0001 | t0056 | g0252 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03831 | hp2 | a0001 | c0001 | t0004 | g0090 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03834 | hp2 | a0001 | c0001 | t0015 | g0167 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03927 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03927 | hp2 | a0001 | c0001 | t0020 | g0042 | SAS | BEB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG04115 | hp2 | a0001 | c0001 | t0010 | g0153 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0151 | SAS | STU | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18522 | hp1 | a0001 | c0001 | t0019 | g0017 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18522 | hp2 | a0001 | c0002 | t0009 | g0025 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0175 | EAS | CHB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18906 | hp1 | a0001 | c0001 | t0075 | g0082 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18906 | hp2 | a0001 | c0002 | t0069 | g0052 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18939 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18939 | hp2 | a0001 | c0001 | t0007 | g0229 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18940 | hp1 | a0001 | c0001 | t0036 | g0214 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18941 | hp1 | a0001 | c0001 | t0045 | g0131 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18941 | hp2 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18943 | hp2 | a0001 | c0001 | t0016 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18944 | hp1 | a0001 | c0001 | t0006 | g0132 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18944 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18945 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18946 | hp1 | a0001 | c0001 | t0044 | g0185 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18949 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18949 | hp2 | a0001 | c0001 | t0023 | g0133 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18950 | hp1 | a0001 | c0001 | t0013 | g0241 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18951 | hp2 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18953 | hp1 | a0001 | c0001 | t0055 | g0230 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18953 | hp2 | a0001 | c0001 | t0006 | g0034 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18954 | hp2 | a0001 | c0001 | t0077 | g0068 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18956 | hp1 | a0001 | c0001 | t0005 | g0125 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18956 | hp2 | a0001 | c0001 | t0003 | g0051 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18960 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18964 | hp1 | a0001 | c0001 | t0082 | g0157 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18964 | hp2 | a0001 | c0001 | t0032 | g0044 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18966 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18967 | hp1 | a0001 | c0001 | t0013 | g0251 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0087 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18968 | hp1 | a0001 | c0001 | t0036 | g0212 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18968 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18969 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18972 | hp1 | a0001 | c0001 | t0013 | g0233 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18973 | hp1 | a0001 | c0001 | t0004 | g0174 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18975 | hp1 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18975 | hp2 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18977 | hp2 | a0001 | c0001 | t0004 | g0173 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18979 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18980 | hp1 | a0001 | c0001 | t0013 | g0039 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18981 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18984 | hp1 | a0001 | c0001 | t0017 | g0204 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18985 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18985 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0122 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18987 | hp1 | a0001 | c0001 | t0020 | g0247 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18988 | hp1 | a0001 | c0001 | t0013 | g0039 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18988 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18989 | hp1 | a0001 | c0001 | t0006 | g0184 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18989 | hp2 | a0001 | c0001 | t0013 | g0232 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18990 | hp1 | a0001 | c0001 | t0053 | g0280 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18990 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18991 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18993 | hp2 | a0001 | c0001 | t0014 | g0045 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18994 | hp1 | a0001 | c0001 | t0088 | g0158 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18994 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0188 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18998 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19000 | hp2 | a0001 | c0001 | t0010 | g0154 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19001 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19003 | hp1 | a0001 | c0001 | t0074 | g0076 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19003 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19005 | hp1 | a0001 | c0001 | t0011 | g0168 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19007 | hp1 | a0001 | c0001 | t0016 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19009 | hp2 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0269 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19030 | hp2 | a0001 | c0001 | t0034 | g0203 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19043 | hp1 | a0001 | c0002 | t0009 | g0025 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19043 | hp2 | a0001 | c0001 | t0057 | g0194 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19055 | hp1 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19057 | hp1 | a0001 | c0001 | t0016 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19058 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19059 | hp1 | a0001 | c0001 | t0006 | g0181 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19059 | hp2 | a0001 | c0001 | t0005 | g0126 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19060 | hp1 | a0001 | c0001 | t0043 | g0178 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19062 | hp2 | a0001 | c0001 | t0011 | g0029 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19063 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19064 | hp2 | a0001 | c0001 | t0007 | g0054 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19065 | hp1 | a0001 | c0001 | t0007 | g0159 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19066 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0057 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0004 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19074 | hp2 | a0001 | c0001 | t0004 | g0008 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19075 | hp2 | a0001 | c0001 | t0014 | g0305 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19076 | hp1 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19076 | hp2 | a0001 | c0001 | t0020 | g0238 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19077 | hp1 | a0001 | c0001 | t0016 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19079 | hp1 | a0001 | c0001 | t0017 | g0009 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19079 | hp2 | a0001 | c0001 | t0007 | g0228 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19080 | hp1 | a0001 | c0001 | t0047 | g0179 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19080 | hp2 | a0001 | c0001 | t0054 | g0245 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19081 | hp2 | a0001 | c0001 | t0004 | g0186 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19082 | hp2 | a0001 | c0001 | t0023 | g0138 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19083 | hp2 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0033 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19085 | hp1 | a0001 | c0001 | t0032 | g0044 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19087 | hp1 | a0001 | c0001 | t0033 | g0243 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19087 | hp2 | a0001 | c0001 | t0071 | g0296 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19088 | hp1 | a0001 | c0001 | t0004 | g0311 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19090 | hp1 | a0001 | c0001 | t0016 | g0006 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19091 | hp1 | a0001 | c0001 | t0007 | g0016 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19240 | hp1 | a0001 | c0001 | t0018 | g0268 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA19240 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | YRI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20129 | hp2 | a0001 | c0001 | t0010 | g0015 | AFR | ASW | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20752 | hp1 | a0001 | c0001 | t0072 | g0074 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20752 | hp2 | a0001 | c0001 | t0015 | g0169 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20805 | hp1 | a0001 | c0001 | t0033 | g0195 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | TSI | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | GIH | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20905 | hp2 | a0001 | c0001 | t0007 | g0160 | SAS | GIH | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01123 | hp1 | a0001 | c0001 | t0012 | g0010 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0062 | AMR | CLM | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02109 | hp1 | a0001 | c0001 | t0073 | g0058 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02109 | hp2 | a0001 | c0001 | t0021 | g0014 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02486 | hp1 | a0001 | c0001 | t0022 | g0319 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02486 | hp2 | a0001 | c0001 | t0028 | g0144 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02559 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG02559 | hp2 | a0001 | c0001 | t0021 | g0096 | AFR | ACB | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG03471 | hp2 | a0001 | c0001 | t0026 | g0050 | AFR | MSL | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG06807 | hp1 | a0001 | c0001 | t0025 | g0019 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18955 | hp1 | a0001 | c0001 | t0052 | g0193 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20300 | hp1 | a0001 | c0002 | t0009 | g0013 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA20300 | hp2 | a0001 | c0001 | t0005 | g0118 | AFR | USA | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| NA21309 | hp2 | a0001 | c0001 | t0086 | g0127 | AFR | LWK | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0050 | g0316 | REF | REF | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0022 | g0048 | REF | REF | KIN_chr10_7745962_7792993 | KIN | chr10 | 7745962 | 7792993 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:7759942 | G | A | 1 | a0002 | 2 | HG00438.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.1067C>T | p.Thr356Ile | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/13 | 1127/6360 | 1067/1182 | 356/393 | chr10 | 7759942 | |||
| chr10:7763783 | A | C | 1 | a0003 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.858T>G | p.Ile286Met | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/13 | 918/6360 | 858/1182 | 286/393 | chr10 | 7763783 | |||
| chr10:7775762 | T | A | 1 | a0004 | 1 | HG03225.hp1 | missense_variant | MODERATE | c.596A>T | p.Asp199Val | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/13 | 656/6360 | 596/1182 | 199/393 | chr10 | 7775762 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:7778871 | C | T | 1 | a0001c0002 | 16 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(13): Show |
synonymous_variant | LOW | c.525G>A | p.Glu175Glu | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/13 | 585/6360 | 525/1182 | 175/393 | chr10 | 7778871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:7751072 | A | C | 19 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0016 others(16): Show |
72 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5008T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 5008 | chr10 | 7751072 | ||||||
| chr10:7751086 | T | A | 1 | a0001c0001t0055 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4994A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4994 | chr10 | 7751086 | ||||||
| chr10:7751159 | C | T | 1 | a0001c0001t0074 | 1 | NA19003.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4921G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4921 | chr10 | 7751159 | ||||||
| chr10:7751426 | T | C | 2 | a0001c0001t0023 a0001c0001t0053 |
4 | HG02132.hp2 NA18949.hp2 NA18990.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4654A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4654 | chr10 | 7751426 | ||||||
| chr10:7751472 | G | A | 1 | a0001c0001t0073 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4608C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4608 | chr10 | 7751472 | ||||||
| chr10:7751807 | C | T | 44 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(41): Show |
216 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*4273G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4273 | chr10 | 7751807 | ||||||
| chr10:7751825 | T | TC | 88 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(85): Show |
404 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(401): Show |
3_prime_UTR_variant | MODIFIER | c.*4254_*4255insG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4254 | chr10 | 7751825 | ||||||
| chr10:7751827 | T | C | 3 | a0001c0001t0025 a0001c0001t0039 a0001c0001t0085 |
6 | HG01070.hp1 HG01071.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4253A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4253 | chr10 | 7751827 | ||||||
| chr10:7751851 | T | C | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
394 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(391): Show |
3_prime_UTR_variant | MODIFIER | c.*4229A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4229 | chr10 | 7751851 | ||||||
| chr10:7751854 | TAAAAGTA others(214): Show |
T | 80 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(77): Show |
395 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*4005_*4225del | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4005 | chr10 | 7751854 | ||||||
| chr10:7751867 | G | GTACTAAA others(127): Show |
1 | a0001c0002t0070 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4212_*4213insGAGA others(130): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4212 | chr10 | 7751867 | ||||||
| chr10:7751892 | G | A | 2 | a0001c0001t0011 a0001c0001t0042 |
2 | HG02280.hp1 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4188C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4188 | chr10 | 7751892 | ||||||
| chr10:7751895 | C | T | 1 | a0001c0001t0042 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4185G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4185 | chr10 | 7751895 | ||||||
| chr10:7751897 | C | T | 4 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0042 others(1): Show |
9 | HG01884.hp1 HG02280.hp1 HG02698.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4183G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4183 | chr10 | 7751897 | ||||||
| chr10:7751898 | G | GGTGGCTC others(128): Show |
1 | a0001c0002t0069 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4181_*4182insTACG others(131): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4181 | chr10 | 7751898 | ||||||
| chr10:7751903 | C | T | 1 | a0001c0001t0042 | 2 | HG02280.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4177G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4177 | chr10 | 7751903 | ||||||
| chr10:7751904 | G | C | 1 | a0001c0001t0029 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4176C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4176 | chr10 | 7751904 | ||||||
| chr10:7751928 | G | T | 1 | a0001c0001t0022 | 2 | HG02257.hp1 HG02486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4152C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4152 | chr10 | 7751928 | ||||||
| chr10:7751953 | T | G | 1 | a0001c0001t0011 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4127A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4127 | chr10 | 7751953 | ||||||
| chr10:7751964 | A | G | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0042 |
4 | HG00099.hp2 HG02280.hp1 HG02723.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4116T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4116 | chr10 | 7751964 | ||||||
| chr10:7752021 | G | A | 4 | a0001c0001t0079 a0001c0001t0086 a0001c0002t0069 others(1): Show |
4 | HG01884.hp1 HG02970.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4059C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4059 | chr10 | 7752021 | ||||||
| chr10:7752028 | C | T | 1 | a0001c0001t0056 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4052G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4052 | chr10 | 7752028 | ||||||
| chr10:7752041 | CA | C | 5 | a0001c0001t0011 a0001c0001t0013 a0001c0001t0056 others(2): Show |
6 | HG01884.hp1 HG01981.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4038delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4038 | chr10 | 7752041 | ||||||
| chr10:7752041 | CAA | C | 3 | a0001c0001t0011 a0001c0001t0029 a0001c0001t0089 |
7 | HG00099.hp2 HG01081.hp1 HG02698.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4037_*4038delTT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4037 | chr10 | 7752041 | ||||||
| chr10:7752041 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0042 | 2 | HG02280.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4026_*4038delTTTT others(9): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 4026 | chr10 | 7752041 | ||||||
| chr10:7752178 | C | T | 28 | a0001c0001t0010 a0001c0001t0012 a0001c0001t0018 others(25): Show |
66 | HG00323.hp1 HG00558.hp2 HG00642.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*3902G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3902 | chr10 | 7752178 | ||||||
| chr10:7752331 | A | C | 28 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(25): Show |
190 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(187): Show |
3_prime_UTR_variant | MODIFIER | c.*3749T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3749 | chr10 | 7752331 | ||||||
| chr10:7752336 | A | G | 1 | a0002c0003t0031 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3744T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3744 | chr10 | 7752336 | ||||||
| chr10:7752391 | T | G | 1 | a0001c0001t0077 | 1 | NA18954.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3689A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3689 | chr10 | 7752391 | ||||||
| chr10:7752435 | G | A | 1 | a0001c0001t0062 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3645C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3645 | chr10 | 7752435 | ||||||
| chr10:7752472 | G | A | 1 | a0001c0001t0056 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3608C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3608 | chr10 | 7752472 | ||||||
| chr10:7752572 | G | A | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*3508C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3508 | chr10 | 7752572 | ||||||
| chr10:7752685 | T | G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(26): Show |
170 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(167): Show |
3_prime_UTR_variant | MODIFIER | c.*3395A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3395 | chr10 | 7752685 | ||||||
| chr10:7752843 | G | C | 2 | a0001c0001t0038 a0001c0001t0086 |
3 | HG02809.hp2 HG03209.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3237C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3237 | chr10 | 7752843 | ||||||
| chr10:7752902 | G | A | 1 | a0001c0001t0065 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3178C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3178 | chr10 | 7752902 | ||||||
| chr10:7752965 | A | C | 3 | a0001c0001t0010 a0001c0001t0049 a0004c0005t0048 |
10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3115T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3115 | chr10 | 7752965 | ||||||
| chr10:7753046 | A | C | 1 | a0001c0001t0019 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3034T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 3034 | chr10 | 7753046 | ||||||
| chr10:7753122 | G | A | 1 | a0001c0001t0037 | 2 | HG01515.hp1 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2958C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2958 | chr10 | 7753122 | ||||||
| chr10:7753202 | A | G | 1 | a0001c0001t0058 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2878T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2878 | chr10 | 7753202 | ||||||
| chr10:7753351 | G | C | 1 | a0001c0002t0051 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2729C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2729 | chr10 | 7753351 | ||||||
| chr10:7753460 | C | A | 1 | a0001c0001t0057 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2620G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2620 | chr10 | 7753460 | ||||||
| chr10:7753476 | C | G | 1 | a0001c0001t0054 | 1 | NA19080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2604G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2604 | chr10 | 7753476 | ||||||
| chr10:7753479 | G | C | 2 | a0001c0001t0039 a0001c0001t0087 |
3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2601C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2601 | chr10 | 7753479 | ||||||
| chr10:7753498 | T | A | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2582A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2582 | chr10 | 7753498 | ||||||
| chr10:7753742 | A | G | 1 | a0001c0001t0091 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2338T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2338 | chr10 | 7753742 | ||||||
| chr10:7753860 | C | T | 1 | a0001c0001t0044 | 1 | NA18946.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2220G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2220 | chr10 | 7753860 | ||||||
| chr10:7753933 | C | T | 2 | a0001c0001t0078 a0001c0001t0079 |
2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2147G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2147 | chr10 | 7753933 | ||||||
| chr10:7753948 | A | G | 59 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(56): Show |
255 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(252): Show |
3_prime_UTR_variant | MODIFIER | c.*2132T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2132 | chr10 | 7753948 | ||||||
| chr10:7753962 | C | T | 5 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0081 others(2): Show |
22 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2118G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2118 | chr10 | 7753962 | ||||||
| chr10:7753970 | T | A | 1 | a0001c0001t0049 | 1 | HG01516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2110A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2110 | chr10 | 7753970 | ||||||
| chr10:7754065 | C | T | 1 | a0001c0001t0089 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2015G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 2015 | chr10 | 7754065 | ||||||
| chr10:7754166 | C | A | 2 | a0001c0001t0078 a0001c0001t0079 |
2 | HG01884.hp1 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1914G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1914 | chr10 | 7754166 | ||||||
| chr10:7754191 | C | A | 1 | a0001c0001t0088 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1889G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1889 | chr10 | 7754191 | ||||||
| chr10:7754360 | C | T | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*1720G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1720 | chr10 | 7754360 | ||||||
| chr10:7754502 | G | A | 1 | a0002c0003t0031 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1578C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1578 | chr10 | 7754502 | ||||||
| chr10:7754558 | G | A | 10 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0040 others(7): Show |
46 | HG00738.hp2 HG01081.hp1 HG01257.hp1 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1522C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1522 | chr10 | 7754558 | ||||||
| chr10:7754590 | A | G | 1 | a0001c0002t0067 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1490T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1490 | chr10 | 7754590 | ||||||
| chr10:7754629 | G | C | 27 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0018 others(24): Show |
112 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*1451C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1451 | chr10 | 7754629 | ||||||
| chr10:7754633 | GA | G | 17 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(14): Show |
71 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
3_prime_UTR_variant | MODIFIER | c.*1446delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1446 | chr10 | 7754633 | ||||||
| chr10:7754718 | T | C | 48 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(45): Show |
191 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1362A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1362 | chr10 | 7754718 | ||||||
| chr10:7754799 | G | A | 1 | a0001c0001t0079 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1281 | chr10 | 7754799 | ||||||
| chr10:7754928 | A | G | 5 | a0001c0001t0012 a0001c0001t0024 a0001c0001t0032 others(2): Show |
14 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1152T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1152 | chr10 | 7754928 | ||||||
| chr10:7755023 | G | A | 3 | a0001c0001t0018 a0001c0001t0078 a0001c0001t0079 |
7 | HG01884.hp1 HG02647.hp1 HG02818.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1057C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 1057 | chr10 | 7755023 | ||||||
| chr10:7755128 | G | T | 1 | a0001c0001t0019 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*952C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 952 | chr10 | 7755128 | ||||||
| chr10:7755159 | C | T | 1 | a0002c0003t0031 | 2 | HG00438.hp1 HG02135.hp2 |
3_prime_UTR_variant | MODIFIER | c.*921G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 921 | chr10 | 7755159 | ||||||
| chr10:7755262 | A | G | 1 | a0001c0001t0030 | 2 | HG01891.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*818T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 818 | chr10 | 7755262 | ||||||
| chr10:7755278 | C | T | 4 | a0001c0001t0010 a0001c0001t0049 a0001c0001t0052 others(1): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*802G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 802 | chr10 | 7755278 | ||||||
| chr10:7755402 | C | A | 1 | a0001c0001t0080 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*678G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 678 | chr10 | 7755402 | ||||||
| chr10:7755467 | A | G | 7 | a0001c0001t0010 a0001c0001t0023 a0001c0001t0028 others(4): Show |
18 | HG00099.hp2 HG00642.hp1 HG01516.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*613T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 613 | chr10 | 7755467 | ||||||
| chr10:7755561 | C | T | 1 | a0001c0001t0019 | 4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*519G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 519 | chr10 | 7755561 | ||||||
| chr10:7755910 | T | C | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*170A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 170 | chr10 | 7755910 | ||||||
| chr10:7755940 | C | CAACT | 69 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(66): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*136_*139dupAGTT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 139 | chr10 | 7755940 | ||||||
| chr10:7756070 | A | T | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*10T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 13/13 | 10 | chr10 | 7756070 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:7756187 | C | T | 52 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(49): Show |
69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1120-45G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756187 | |||||||
| chr10:7756387 | A | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(249): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.1120-245T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756387 | |||||||
| chr10:7756637 | C | T | 1 | a0001c0001t0004g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1120-495G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756637 | |||||||
| chr10:7756682 | T | C | 2 | a0001c0001t0029g0275 a0001c0001t0029g0317 |
2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1120-540A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756682 | |||||||
| chr10:7756686 | G | A | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1120-544C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756686 | |||||||
| chr10:7756772 | C | CA | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(249): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.1120-631_1120-630i others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756772 | |||||||
| chr10:7756785 | T | C | 60 | a0001c0001t0004g0008 a0001c0001t0004g0030 a0001c0001t0004g0032 others(57): Show |
82 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.1120-643A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756785 | |||||||
| chr10:7756807 | T | C | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1120-665A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756807 | |||||||
| chr10:7756825 | T | C | 1 | a0001c0001t0092g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1120-683A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7756825 | |||||||
| chr10:7757007 | A | G | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.1120-865T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757007 | |||||||
| chr10:7757222 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1120-1080C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757222 | |||||||
| chr10:7757265 | G | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(59): Show |
85 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1120-1123C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757265 | |||||||
| chr10:7757521 | A | T | 4 | a0001c0001t0005g0027 a0001c0001t0005g0106 a0001c0001t0005g0126 others(1): Show |
5 | HG03453.hp2 NA18981.hp1 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-1379T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757521 | |||||||
| chr10:7757526 | T | A | 106 | a0001c0001t0001g0242 a0001c0001t0001g0262 a0001c0001t0002g0020 others(103): Show |
145 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.1120-1384A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757526 | |||||||
| chr10:7757531 | T | A | 93 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(90): Show |
131 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.1120-1389A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757531 | |||||||
| chr10:7757536 | A | T | 114 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(111): Show |
157 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1120-1394T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757536 | |||||||
| chr10:7757632 | C | A | 16 | a0001c0001t0003g0011 a0001c0001t0003g0046 a0001c0001t0003g0047 others(13): Show |
21 | HG02074.hp1 HG02129.hp1 NA18944.hp2 others(18): Show |
intron_variant | MODIFIER | c.1120-1490G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757632 | |||||||
| chr10:7757717 | A | G | 91 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(88): Show |
127 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1120-1575T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757717 | |||||||
| chr10:7757855 | C | G | 52 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(49): Show |
69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1120-1713G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757855 | |||||||
| chr10:7757908 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(249): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.1120-1766A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757908 | |||||||
| chr10:7757941 | C | T | 1 | a0001c0001t0075g0082 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1120-1799G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757941 | |||||||
| chr10:7757975 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG01346.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1120-1833C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7757975 | |||||||
| chr10:7758010 | A | AT | 71 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(68): Show |
91 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.1120-1869dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758010 | |||||||
| chr10:7758010 | ATTT | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0037 others(58): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1120-1871_1120-186 others(7): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758010 | |||||||
| chr10:7758078 | C | CT | 64 | a0001c0001t0001g0258 a0001c0001t0002g0002 a0001c0001t0002g0012 others(61): Show |
83 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1119+1811dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | |||||||
| chr10:7758078 | CT | C | 39 | a0001c0001t0001g0089 a0001c0001t0004g0008 a0001c0001t0004g0030 others(36): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.1119+1811delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | |||||||
| chr10:7758078 | CTT | C | 10 | a0001c0001t0004g0174 a0001c0001t0006g0180 a0001c0001t0010g0015 others(7): Show |
12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1119+1810_1119+181 others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758078 | |||||||
| chr10:7758197 | C | T | 62 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(59): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.1119+1693G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758197 | |||||||
| chr10:7758226 | C | T | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+1664G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758226 | |||||||
| chr10:7758258 | T | C | 1 | a0001c0001t0028g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1119+1632A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758258 | |||||||
| chr10:7758280 | G | A | 5 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1610C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758280 | |||||||
| chr10:7758353 | A | C | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1119+1537T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758353 | |||||||
| chr10:7758391 | G | A | 5 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1499C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758391 | |||||||
| chr10:7758435 | G | A | 1 | a0001c0001t0028g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1119+1455C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758435 | |||||||
| chr10:7758550 | T | C | 4 | a0001c0001t0010g0147 a0001c0001t0010g0153 a0001c0001t0010g0154 others(1): Show |
4 | HG00642.hp1 HG01516.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+1340A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758550 | |||||||
| chr10:7758571 | C | G | 1 | a0001c0001t0003g0288 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1119+1319G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758571 | |||||||
| chr10:7758612 | A | G | 3 | a0001c0001t0002g0061 a0001c0001t0035g0064 a0001c0001t0074g0076 |
3 | HG02015.hp1 NA18946.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.1119+1278T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758612 | |||||||
| chr10:7758675 | CA | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(178): Show |
250 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.1119+1214delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758675 | |||||||
| chr10:7758675 | CAA | C | 51 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(48): Show |
68 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1119+1213_1119+121 others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758675 | |||||||
| chr10:7758743 | T | C | 5 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+1147A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758743 | |||||||
| chr10:7758815 | T | TC | 4 | a0001c0001t0001g0040 a0001c0001t0001g0236 a0001c0001t0001g0242 others(1): Show |
5 | HG00423.hp1 HG02027.hp2 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1119+1074dupG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758815 | |||||||
| chr10:7758845 | G | A | 141 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(138): Show |
181 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(178): Show |
intron_variant | MODIFIER | c.1119+1045C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758845 | |||||||
| chr10:7758918 | T | C | 54 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(51): Show |
73 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.1119+972A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7758918 | |||||||
| chr10:7759241 | A | G | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1119+649T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759241 | |||||||
| chr10:7759425 | A | C | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1119+465T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759425 | |||||||
| chr10:7759544 | C | A | 2 | a0001c0001t0039g0049 a0001c0001t0087g0095 |
3 | HG01070.hp1 HG01071.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1119+346G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759544 | |||||||
| chr10:7759608 | T | C | 4 | a0001c0001t0003g0191 a0001c0001t0003g0225 a0001c0001t0003g0303 others(1): Show |
4 | NA18961.hp1 NA18982.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.1119+282A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759608 | |||||||
| chr10:7759615 | T | C | 5 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(2): Show |
5 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.1119+275A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759615 | |||||||
| chr10:7759709 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1119+181T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 12/12 | chr10 | 7759709 | |||||||
| chr10:7759997 | T | C | 39 | a0001c0001t0004g0008 a0001c0001t0004g0030 a0001c0001t0004g0032 others(36): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1019-7A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7759997 | |||||||
| chr10:7760155 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1019-165C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760155 | |||||||
| chr10:7760194 | C | A | 1 | a0001c0001t0003g0301 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1019-204G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760194 | |||||||
| chr10:7760285 | C | A | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-295G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760285 | |||||||
| chr10:7760380 | CAT | C | 15 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(12): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1019-392_1019-391d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760380 | |||||||
| chr10:7760521 | A | G | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.1019-531T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760521 | |||||||
| chr10:7760547 | T | C | 1 | a0001c0002t0009g0097 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1019-557A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760547 | |||||||
| chr10:7760590 | C | A | 2 | a0001c0001t0003g0293 a0001c0001t0003g0295 |
2 | NA18987.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1019-600G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760590 | |||||||
| chr10:7760649 | T | A | 59 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(56): Show |
77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1019-659A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760649 | |||||||
| chr10:7760660 | A | G | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-670T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760660 | |||||||
| chr10:7760668 | TTATTA | T | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(57): Show |
86 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.1019-683_1019-679d others(7): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760668 | |||||||
| chr10:7760750 | G | C | 59 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(56): Show |
77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.1019-760C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760750 | |||||||
| chr10:7760812 | T | C | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1019-822A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760812 | |||||||
| chr10:7760822 | G | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(115): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1019-832C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760822 | |||||||
| chr10:7760846 | G | A | 4 | a0001c0001t0004g0033 a0001c0001t0004g0057 a0001c0001t0004g0173 others(1): Show |
5 | NA18747.hp2 NA18977.hp2 NA19070.hp2 others(2): Show |
intron_variant | MODIFIER | c.1019-856C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760846 | |||||||
| chr10:7760973 | C | T | 1 | a0001c0001t0060g0282 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1019-983G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7760973 | |||||||
| chr10:7761058 | G | A | 14 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(11): Show |
17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1019-1068C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761058 | |||||||
| chr10:7761136 | A | G | 4 | a0001c0001t0005g0092 a0001c0001t0040g0115 a0001c0001t0089g0114 others(1): Show |
4 | HG01081.hp1 HG02630.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1019-1146T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761136 | |||||||
| chr10:7761142 | T | C | 3 | a0001c0001t0018g0269 a0001c0001t0018g0270 a0001c0001t0018g0271 |
3 | HG03041.hp1 HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1019-1152A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761142 | |||||||
| chr10:7761184 | A | G | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1019-1194T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761184 | |||||||
| chr10:7761200 | A | C | 1 | a0001c0001t0012g0277 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1019-1210T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761200 | |||||||
| chr10:7761256 | C | G | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1018+1201G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761256 | |||||||
| chr10:7761318 | G | C | 40 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(37): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.1018+1139C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761318 | |||||||
| chr10:7761493 | C | G | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.1018+964G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761493 | |||||||
| chr10:7761656 | T | C | 7 | a0001c0001t0007g0016 a0001c0001t0007g0156 a0001c0001t0007g0159 others(4): Show |
9 | HG00609.hp2 NA18964.hp1 NA18975.hp2 others(6): Show |
intron_variant | MODIFIER | c.1018+801A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761656 | |||||||
| chr10:7761754 | C | A | 1 | a0001c0001t0079g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1018+703G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761754 | |||||||
| chr10:7761757 | T | C | 58 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(55): Show |
79 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1018+700A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761757 | |||||||
| chr10:7761880 | T | C | 3 | a0001c0001t0002g0060 a0001c0001t0025g0019 a0001c0001t0025g0059 |
4 | HG02976.hp1 HG03098.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1018+577A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761880 | |||||||
| chr10:7761883 | T | A | 2 | a0001c0001t0002g0137 a0001c0001t0002g0267 |
2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.1018+574A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7761883 | |||||||
| chr10:7762132 | C | G | 1 | a0001c0001t0002g0036 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1018+325G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762132 | |||||||
| chr10:7762179 | A | G | 8 | a0001c0001t0010g0015 a0001c0001t0010g0147 a0001c0001t0010g0148 others(5): Show |
10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018+278T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762179 | |||||||
| chr10:7762305 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1018+152G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762305 | |||||||
| chr10:7762345 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(308): Show |
412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.1018+112G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762345 | |||||||
| chr10:7762347 | G | A | 8 | a0001c0001t0010g0015 a0001c0001t0010g0147 a0001c0001t0010g0148 others(5): Show |
10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1018+110C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 11/12 | chr10 | 7762347 | |||||||
| chr10:7762563 | T | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0196 a0001c0001t0001g0197 |
4 | HG01109.hp1 HG02647.hp2 HG03453.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.919-7A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762563 | |||||||
| chr10:7762624 | CAAATG | C | 6 | a0001c0001t0002g0067 a0001c0001t0002g0080 a0001c0001t0002g0081 others(3): Show |
6 | HG01891.hp1 HG02258.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.919-73_919-69delCA others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762624 | |||||||
| chr10:7762732 | A | C | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.919-176T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762732 | |||||||
| chr10:7762741 | C | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.919-185G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7762741 | |||||||
| chr10:7763085 | G | A | 1 | a0001c0002t0009g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.919-529C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763085 | |||||||
| chr10:7763088 | T | G | 3 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0051g0101 |
3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.919-532A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763088 | |||||||
| chr10:7763119 | G | A | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.919-563C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763119 | |||||||
| chr10:7763345 | C | G | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.918+378G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763345 | |||||||
| chr10:7763518 | C | T | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.918+205G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763518 | |||||||
| chr10:7763613 | A | C | 1 | a0001c0001t0077g0068 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.918+110T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763613 | |||||||
| chr10:7763662 | T | G | 1 | a0001c0001t0002g0021 | 2 | HG00738.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.918+61A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 10/12 | chr10 | 7763662 | |||||||
| chr10:7763838 | G | A | 8 | a0001c0001t0010g0015 a0001c0001t0010g0147 a0001c0001t0010g0148 others(5): Show |
10 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-47C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763838 | |||||||
| chr10:7763865 | C | G | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-74G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763865 | |||||||
| chr10:7763905 | C | T | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-114G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763905 | |||||||
| chr10:7763964 | A | T | 5 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-173T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7763964 | |||||||
| chr10:7764011 | G | GA | 8 | a0001c0001t0004g0030 a0001c0001t0004g0033 a0001c0001t0004g0057 others(5): Show |
10 | HG00597.hp1 NA18747.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-221dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764011 | |||||||
| chr10:7764237 | G | A | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.850-446C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764237 | |||||||
| chr10:7764239 | A | G | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.850-448T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764239 | |||||||
| chr10:7764435 | G | A | 5 | a0001c0001t0001g0235 a0001c0001t0001g0244 a0001c0001t0001g0250 others(2): Show |
5 | HG00673.hp1 NA18940.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.850-644C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764435 | |||||||
| chr10:7764607 | T | C | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.850-816A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764607 | |||||||
| chr10:7764632 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0246 a0001c0001t0001g0249 others(4): Show |
8 | NA18747.hp1 NA18953.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.850-841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764632 | |||||||
| chr10:7764752 | C | T | 15 | a0001c0001t0010g0015 a0001c0001t0010g0147 a0001c0001t0010g0148 others(12): Show |
19 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.850-961G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764752 | |||||||
| chr10:7764886 | G | A | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.850-1095C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764886 | |||||||
| chr10:7764989 | G | A | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+1064C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7764989 | |||||||
| chr10:7765114 | G | A | 1 | a0001c0001t0002g0213 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.849+939C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765114 | |||||||
| chr10:7765159 | C | CA | 69 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(66): Show |
91 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.849+893dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765159 | |||||||
| chr10:7765159 | CA | C | 25 | a0001c0001t0001g0231 a0001c0001t0001g0259 a0001c0001t0003g0295 others(22): Show |
28 | HG00323.hp1 HG01069.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.849+893delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765159 | |||||||
| chr10:7765368 | G | A | 40 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(37): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.849+685C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765368 | |||||||
| chr10:7765375 | G | A | 1 | a0001c0001t0034g0203 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.849+678C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765375 | |||||||
| chr10:7765405 | G | A | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(116): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.849+648C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765405 | |||||||
| chr10:7765439 | T | TA | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.849+613dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765439 | |||||||
| chr10:7765650 | A | G | 5 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.849+403T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765650 | |||||||
| chr10:7765696 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(308): Show |
412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.849+357G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765696 | |||||||
| chr10:7765901 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(55): Show |
84 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.849+152G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 9/12 | chr10 | 7765901 | |||||||
| chr10:7766123 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(116): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.799-20A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766123 | |||||||
| chr10:7766726 | T | C | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.799-623A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766726 | |||||||
| chr10:7766727 | C | T | 1 | a0001c0001t0005g0318 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.799-624G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766727 | |||||||
| chr10:7766799 | G | A | 4 | a0001c0001t0021g0014 a0001c0001t0021g0096 a0001c0001t0034g0203 others(1): Show |
6 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799-696C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766799 | |||||||
| chr10:7766810 | T | C | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.799-707A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766810 | |||||||
| chr10:7766849 | G | A | 1 | a0001c0001t0025g0059 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.799-746C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766849 | |||||||
| chr10:7766954 | C | T | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.799-851G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7766954 | |||||||
| chr10:7767001 | C | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(116): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.799-898G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767001 | |||||||
| chr10:7767022 | C | CA | 28 | a0001c0001t0006g0181 a0001c0001t0006g0184 a0001c0001t0007g0016 others(25): Show |
32 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.799-920dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767022 | |||||||
| chr10:7767032 | A | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.799-929T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767032 | |||||||
| chr10:7767035 | AAAACCTC others(14): Show |
A | 1 | a0001c0001t0001g0259 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.799-953_799-933del others(21): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767035 | |||||||
| chr10:7767036 | AAACCTCA others(13): Show |
A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(50): Show |
75 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.799-953_799-934del others(20): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767036 | |||||||
| chr10:7767037 | AACCTCAT others(12): Show |
A | 9 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0040 others(6): Show |
9 | HG02027.hp2 HG02738.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-953_799-935del others(19): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767037 | |||||||
| chr10:7767105 | A | G | 1 | a0001c0001t0038g0093 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799-1002T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767105 | |||||||
| chr10:7767112 | G | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.799-1009C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767112 | |||||||
| chr10:7767248 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.799-1145C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767248 | |||||||
| chr10:7767335 | G | A | 1 | a0001c0001t0003g0294 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.799-1232C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767335 | |||||||
| chr10:7767405 | G | A | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.799-1302C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767405 | |||||||
| chr10:7767585 | G | A | 1 | a0001c0001t0007g0159 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.799-1482C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767585 | |||||||
| chr10:7767699 | A | T | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.798+1517T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767699 | |||||||
| chr10:7767736 | G | A | 11 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(8): Show |
14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+1480C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767736 | |||||||
| chr10:7767769 | G | C | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+1447C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767769 | |||||||
| chr10:7767786 | G | A | 8 | a0001c0001t0004g0030 a0001c0001t0004g0033 a0001c0001t0004g0057 others(5): Show |
10 | HG00597.hp1 NA18747.hp2 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.798+1430C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767786 | |||||||
| chr10:7767842 | G | C | 3 | a0001c0001t0021g0014 a0001c0001t0021g0096 a0001c0002t0066g0103 |
5 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+1374C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767842 | |||||||
| chr10:7767865 | C | CA | 28 | a0001c0001t0002g0264 a0001c0001t0003g0295 a0001c0001t0007g0156 others(25): Show |
34 | HG01070.hp1 HG01071.hp2 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.798+1350dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767865 | |||||||
| chr10:7767865 | CA | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(102): Show |
150 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.798+1350delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767865 | |||||||
| chr10:7767997 | C | T | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.798+1219G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7767997 | |||||||
| chr10:7768054 | A | G | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.798+1162T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768054 | |||||||
| chr10:7768108 | C | T | 88 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(85): Show |
113 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.798+1108G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768108 | |||||||
| chr10:7768163 | T | C | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.798+1053A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768163 | |||||||
| chr10:7768281 | A | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(112): Show |
160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.798+935T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768281 | |||||||
| chr10:7768431 | G | C | 2 | a0001c0001t0021g0014 a0001c0001t0021g0096 |
4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.798+785C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768431 | |||||||
| chr10:7768469 | C | G | 3 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0051g0101 |
3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.798+747G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768469 | |||||||
| chr10:7768541 | C | CA | 56 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(53): Show |
74 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.798+674dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768541 | |||||||
| chr10:7768575 | G | A | 5 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(2): Show |
5 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+641C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768575 | |||||||
| chr10:7768576 | C | T | 15 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(12): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.798+640G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768576 | |||||||
| chr10:7768600 | A | G | 9 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(6): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.798+616T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768600 | |||||||
| chr10:7768643 | G | C | 1 | a0001c0001t0001g0255 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.798+573C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768643 | |||||||
| chr10:7768845 | C | T | 1 | a0001c0001t0075g0082 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798+371G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768845 | |||||||
| chr10:7768912 | G | T | 3 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0051g0101 |
3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.798+304C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7768912 | |||||||
| chr10:7769185 | A | C | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.798+31T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 8/12 | chr10 | 7769185 | |||||||
| chr10:7769365 | T | C | 1 | a0001c0001t0023g0139 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.669-20A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769365 | |||||||
| chr10:7769415 | T | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-70A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769415 | |||||||
| chr10:7769444 | G | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
76 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.669-99C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769444 | |||||||
| chr10:7769582 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-237C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769582 | |||||||
| chr10:7769692 | GT | G | 9 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(6): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-348delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769692 | |||||||
| chr10:7769700 | C | CTA | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-357_669-356dup others(2): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769700 | |||||||
| chr10:7769786 | T | C | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.669-441A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769786 | |||||||
| chr10:7769815 | T | C | 2 | a0001c0002t0068g0145 a0001c0002t0069g0052 |
2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.669-470A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769815 | |||||||
| chr10:7769827 | C | T | 3 | a0001c0001t0015g0053 a0001c0001t0015g0161 a0001c0001t0015g0162 |
3 | HG00099.hp1 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.669-482G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769827 | |||||||
| chr10:7769851 | T | C | 16 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(13): Show |
20 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.669-506A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769851 | |||||||
| chr10:7769886 | G | A | 11 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(8): Show |
14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.669-541C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769886 | |||||||
| chr10:7769940 | C | G | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.669-595G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769940 | |||||||
| chr10:7769969 | C | T | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.669-624G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769969 | |||||||
| chr10:7769992 | G | A | 14 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(11): Show |
17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.669-647C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7769992 | |||||||
| chr10:7770017 | G | A | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.669-672C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770017 | |||||||
| chr10:7770040 | C | T | 52 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(49): Show |
69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.669-695G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770040 | |||||||
| chr10:7770045 | C | T | 2 | a0001c0001t0005g0026 a0001c0001t0005g0122 |
3 | NA18986.hp2 NA19011.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.669-700G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770045 | |||||||
| chr10:7770128 | G | A | 2 | a0001c0001t0007g0156 a0001c0001t0007g0159 |
2 | NA19001.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.669-783C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770128 | |||||||
| chr10:7770238 | T | C | 3 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0051g0101 |
3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.669-893A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770238 | |||||||
| chr10:7770379 | G | C | 2 | a0001c0001t0021g0014 a0001c0001t0021g0096 |
4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.669-1034C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770379 | |||||||
| chr10:7770483 | C | T | 1 | a0001c0001t0026g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.669-1138G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770483 | |||||||
| chr10:7770577 | TAGGG | T | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.669-1236_669-1233d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770577 | |||||||
| chr10:7770578 | A | G | 40 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(37): Show |
59 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(56): Show |
intron_variant | MODIFIER | c.669-1233T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770578 | |||||||
| chr10:7770923 | T | C | 9 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(6): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-1578A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770923 | |||||||
| chr10:7770950 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(112): Show |
160 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.669-1605A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770950 | |||||||
| chr10:7770974 | C | G | 5 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(2): Show |
5 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.669-1629G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7770974 | |||||||
| chr10:7771014 | C | T | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.669-1669G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771014 | |||||||
| chr10:7771016 | C | T | 17 | a0001c0001t0019g0017 a0001c0001t0019g0219 a0001c0001t0028g0144 others(14): Show |
22 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.669-1671G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771016 | |||||||
| chr10:7771145 | T | TA | 208 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(205): Show |
278 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(275): Show |
intron_variant | MODIFIER | c.669-1801dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771145 | |||||||
| chr10:7771161 | A | G | 56 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(53): Show |
75 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.669-1816T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771161 | |||||||
| chr10:7771190 | G | A | 89 | a0001c0001t0001g0239 a0001c0001t0002g0002 a0001c0001t0002g0012 others(86): Show |
114 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.669-1845C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771190 | |||||||
| chr10:7771192 | T | C | 1 | a0001c0001t0010g0148 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.669-1847A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771192 | |||||||
| chr10:7771421 | A | C | 1 | a0001c0001t0018g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.669-2076T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771421 | |||||||
| chr10:7771535 | G | C | 3 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0051g0101 |
3 | HG02055.hp1 HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.669-2190C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771535 | |||||||
| chr10:7771643 | G | A | 9 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(6): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.669-2298C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771643 | |||||||
| chr10:7771665 | G | A | 7 | a0001c0001t0005g0004 a0001c0001t0005g0027 a0001c0001t0005g0106 others(4): Show |
13 | NA18949.hp1 NA18956.hp1 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.669-2320C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771665 | |||||||
| chr10:7771666 | G | A | 2 | a0001c0001t0001g0259 a0001c0001t0020g0238 |
2 | NA19072.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.669-2321C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771666 | |||||||
| chr10:7771801 | A | C | 4 | a0001c0001t0010g0015 a0001c0001t0010g0148 a0001c0001t0010g0150 others(1): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.669-2456T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771801 | |||||||
| chr10:7771860 | G | A | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.669-2515C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771860 | |||||||
| chr10:7771874 | A | G | 1 | a0001c0001t0004g0312 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.669-2529T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771874 | |||||||
| chr10:7771895 | CA | C | 92 | a0001c0001t0001g0239 a0001c0001t0001g0259 a0001c0001t0002g0002 others(89): Show |
117 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.669-2551delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771895 | |||||||
| chr10:7771908 | A | G | 1 | a0001c0001t0003g0298 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.669-2563T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7771908 | |||||||
| chr10:7772048 | T | C | 1 | a0001c0001t0057g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.669-2703A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772048 | |||||||
| chr10:7772138 | G | A | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.668+2693C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772138 | |||||||
| chr10:7772206 | G | C | 1 | a0001c0001t0003g0046 | 2 | NA18944.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.668+2625C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772206 | |||||||
| chr10:7772227 | C | T | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.668+2604G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772227 | |||||||
| chr10:7772307 | G | A | 9 | a0001c0001t0001g0239 a0001c0001t0010g0015 a0001c0001t0010g0147 others(6): Show |
11 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.668+2524C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772307 | |||||||
| chr10:7772363 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.668+2468A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772363 | |||||||
| chr10:7772366 | A | G | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.668+2465T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772366 | |||||||
| chr10:7772421 | C | T | 2 | a0001c0001t0042g0112 a0001c0001t0042g0129 |
2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.668+2410G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772421 | |||||||
| chr10:7772620 | T | A | 15 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(12): Show |
18 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.668+2211A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772620 | |||||||
| chr10:7772763 | AAATT | A | 4 | a0001c0001t0010g0015 a0001c0001t0010g0148 a0001c0001t0010g0150 others(1): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.668+2064_668+2067d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772763 | |||||||
| chr10:7772782 | A | G | 1 | a0001c0001t0001g0240 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.668+2049T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772782 | |||||||
| chr10:7772995 | T | C | 1 | a0001c0001t0011g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.668+1836A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7772995 | |||||||
| chr10:7773028 | C | T | 1 | a0001c0001t0019g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.668+1803G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773028 | |||||||
| chr10:7773140 | G | A | 11 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(8): Show |
14 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.668+1691C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773140 | |||||||
| chr10:7773218 | G | T | 89 | a0001c0001t0001g0239 a0001c0001t0002g0002 a0001c0001t0002g0012 others(86): Show |
114 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.668+1613C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773218 | |||||||
| chr10:7773331 | C | T | 1 | a0001c0001t0007g0160 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.668+1500G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773331 | |||||||
| chr10:7773343 | A | G | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.668+1488T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773343 | |||||||
| chr10:7773466 | G | A | 3 | a0001c0001t0021g0014 a0001c0001t0021g0096 a0001c0002t0066g0103 |
5 | HG02109.hp2 HG02559.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+1365C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773466 | |||||||
| chr10:7773482 | T | G | 1 | a0001c0001t0077g0068 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.668+1349A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773482 | |||||||
| chr10:7773761 | G | C | 1 | a0001c0001t0028g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.668+1070C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773761 | |||||||
| chr10:7773767 | T | C | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.668+1064A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773767 | |||||||
| chr10:7773809 | T | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(58): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.668+1022A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773809 | |||||||
| chr10:7773829 | T | G | 1 | a0001c0002t0009g0099 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.668+1002A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773829 | |||||||
| chr10:7773988 | C | T | 1 | a0001c0001t0011g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.668+843G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7773988 | |||||||
| chr10:7774019 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.668+812G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774019 | |||||||
| chr10:7774112 | A | G | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.668+719T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774112 | |||||||
| chr10:7774182 | T | C | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.668+649A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774182 | |||||||
| chr10:7774183 | T | C | 1 | a0001c0001t0003g0310 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.668+648A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774183 | |||||||
| chr10:7774271 | G | A | 4 | a0001c0001t0001g0037 a0001c0001t0001g0192 a0001c0001t0001g0200 others(1): Show |
5 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+560C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774271 | |||||||
| chr10:7774338 | G | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(308): Show |
412 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(409): Show |
intron_variant | MODIFIER | c.668+493C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774338 | |||||||
| chr10:7774397 | T | C | 45 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(42): Show |
64 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.668+434A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774397 | |||||||
| chr10:7774399 | T | C | 4 | a0001c0001t0010g0015 a0001c0001t0010g0148 a0001c0001t0010g0150 others(1): Show |
6 | HG02145.hp1 HG02818.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.668+432A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774399 | |||||||
| chr10:7774501 | T | A | 1 | a0001c0001t0005g0106 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.668+330A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774501 | |||||||
| chr10:7774557 | G | A | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.668+274C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774557 | |||||||
| chr10:7774578 | G | C | 5 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(2): Show |
5 | HG00099.hp2 HG02132.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.668+253C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774578 | |||||||
| chr10:7774634 | C | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG01109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.668+197G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774634 | |||||||
| chr10:7774699 | G | A | 52 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(49): Show |
69 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.668+132C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774699 | |||||||
| chr10:7774812 | C | T | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.668+19G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774812 | |||||||
| chr10:7774813 | G | A | 2 | a0001c0001t0029g0275 a0001c0001t0029g0317 |
2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.668+18C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 7/12 | chr10 | 7774813 | |||||||
| chr10:7775028 | G | A | 1 | a0001c0001t0028g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.608-137C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775028 | |||||||
| chr10:7775052 | G | A | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.608-161C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775052 | |||||||
| chr10:7775066 | G | A | 1 | a0001c0001t0059g0279 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.608-175C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775066 | |||||||
| chr10:7775085 | T | C | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.608-194A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775085 | |||||||
| chr10:7775101 | C | T | 1 | a0001c0001t0003g0291 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.608-210G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775101 | |||||||
| chr10:7775372 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(249): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.607+379A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775372 | |||||||
| chr10:7775594 | A | G | 1 | a0001c0001t0003g0287 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.607+157T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 6/12 | chr10 | 7775594 | |||||||
| chr10:7775906 | C | T | 6 | a0001c0001t0005g0026 a0001c0001t0005g0105 a0001c0001t0005g0107 others(3): Show |
7 | NA18942.hp1 NA18947.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-107G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7775906 | |||||||
| chr10:7775955 | G | A | 22 | a0001c0001t0003g0011 a0001c0001t0003g0046 a0001c0001t0003g0047 others(19): Show |
28 | HG00408.hp1 HG02056.hp2 HG02074.hp1 others(25): Show |
intron_variant | MODIFIER | c.559-156C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7775955 | |||||||
| chr10:7776025 | G | A | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-226C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776025 | |||||||
| chr10:7776087 | G | A | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-288C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776087 | |||||||
| chr10:7776093 | G | A | 1 | a0001c0002t0068g0145 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.559-294C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776093 | |||||||
| chr10:7776127 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.559-328C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776127 | |||||||
| chr10:7776177 | C | T | 120 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(117): Show |
166 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.559-378G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776177 | |||||||
| chr10:7776229 | CA | C | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(123): Show |
177 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.559-431delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776229 | |||||||
| chr10:7776248 | T | C | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-449A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776248 | |||||||
| chr10:7776293 | C | G | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-494G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776293 | |||||||
| chr10:7776300 | C | T | 13 | a0001c0001t0004g0008 a0001c0001t0004g0030 a0001c0001t0004g0033 others(10): Show |
18 | HG00597.hp1 NA18747.hp2 NA18946.hp1 others(15): Show |
intron_variant | MODIFIER | c.559-501G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776300 | |||||||
| chr10:7776357 | G | A | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.559-558C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776357 | |||||||
| chr10:7776440 | G | T | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.559-641C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776440 | |||||||
| chr10:7776498 | T | G | 1 | a0001c0001t0004g0182 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.559-699A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776498 | |||||||
| chr10:7776546 | C | T | 57 | a0001c0001t0005g0004 a0001c0001t0005g0026 a0001c0001t0005g0027 others(54): Show |
68 | HG00099.hp1 HG00558.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.559-747G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776546 | |||||||
| chr10:7776560 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.559-761C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776560 | |||||||
| chr10:7776588 | C | T | 1 | a0001c0001t0092g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.559-789G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776588 | |||||||
| chr10:7776589 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(114): Show |
163 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.559-790C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776589 | |||||||
| chr10:7776603 | C | T | 1 | a0001c0001t0028g0144 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.559-804G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776603 | |||||||
| chr10:7776604 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.559-805C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776604 | |||||||
| chr10:7776663 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.559-864C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776663 | |||||||
| chr10:7776677 | G | A | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.559-878C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776677 | |||||||
| chr10:7776688 | G | A | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.559-889C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776688 | |||||||
| chr10:7776716 | G | A | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.559-917C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776716 | |||||||
| chr10:7776732 | C | CA | 66 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(63): Show |
86 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.559-934dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776732 | |||||||
| chr10:7776747 | AG | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(126): Show |
177 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.559-949delC | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776747 | |||||||
| chr10:7776748 | G | A | 65 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(62): Show |
89 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.559-949C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776748 | |||||||
| chr10:7776815 | C | T | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.559-1016G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776815 | |||||||
| chr10:7776895 | TA | T | 6 | a0001c0001t0002g0070 a0001c0001t0002g0216 a0001c0001t0004g0187 others(3): Show |
6 | HG02809.hp2 HG03209.hp1 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-1097delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7776895 | |||||||
| chr10:7777053 | C | CA | 47 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(44): Show |
63 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.559-1255dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777053 | C | CAA | 7 | a0001c0001t0002g0022 a0001c0001t0002g0071 a0001c0001t0002g0075 others(4): Show |
8 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.559-1256_559-1255d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777053 | CA | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(119): Show |
170 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.559-1255delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777053 | CAA | C | 23 | a0001c0001t0001g0196 a0001c0001t0001g0259 a0001c0001t0004g0151 others(20): Show |
25 | HG00438.hp1 HG00642.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.559-1256_559-1255d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777053 | CAAA | C | 6 | a0001c0001t0018g0268 a0001c0001t0018g0269 a0001c0001t0018g0270 others(3): Show |
8 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.559-1257_559-1255d others(5): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777053 | CAAAAAAA others(6): Show |
C | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.559-1267_559-1255d others(15): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777053 | |||||||
| chr10:7777246 | C | CT | 60 | a0001c0001t0001g0237 a0001c0001t0002g0002 a0001c0001t0002g0012 others(57): Show |
77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.559-1448dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777246 | |||||||
| chr10:7777246 | CT | C | 56 | a0001c0001t0001g0177 a0001c0001t0001g0259 a0001c0001t0004g0008 others(53): Show |
78 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.559-1448delA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777246 | |||||||
| chr10:7777318 | T | C | 14 | a0001c0001t0028g0144 a0001c0001t0028g0218 a0001c0002t0009g0013 others(11): Show |
17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.559-1519A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777318 | |||||||
| chr10:7777323 | A | T | 4 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(1): Show |
4 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+1515T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777323 | |||||||
| chr10:7777329 | G | C | 57 | a0001c0001t0003g0011 a0001c0001t0003g0018 a0001c0001t0003g0046 others(54): Show |
76 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.558+1509C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777329 | |||||||
| chr10:7777353 | C | G | 1 | a0001c0001t0079g0123 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.558+1485G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777353 | |||||||
| chr10:7777420 | G | A | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.558+1418C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777420 | |||||||
| chr10:7777446 | G | A | 1 | a0001c0001t0005g0028 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.558+1392C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777446 | |||||||
| chr10:7777452 | T | C | 1 | a0001c0001t0019g0219 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.558+1386A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777452 | |||||||
| chr10:7777624 | G | A | 1 | a0001c0001t0002g0069 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.558+1214C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777624 | |||||||
| chr10:7777640 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.558+1198C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777640 | |||||||
| chr10:7777691 | A | C | 2 | a0001c0001t0002g0075 a0001c0001t0072g0074 |
2 | HG01433.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.558+1147T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777691 | |||||||
| chr10:7777788 | A | G | 4 | a0001c0001t0018g0268 a0001c0001t0018g0269 a0001c0001t0018g0270 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1050T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777788 | |||||||
| chr10:7777807 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0064g0083 |
2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.558+1031C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777807 | |||||||
| chr10:7777831 | G | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(53): Show |
73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.558+1007C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777831 | |||||||
| chr10:7777871 | C | T | 1 | a0001c0001t0029g0317 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.558+967G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777871 | |||||||
| chr10:7777895 | TC | T | 68 | a0001c0001t0001g0177 a0001c0001t0001g0236 a0001c0001t0004g0008 others(65): Show |
92 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.558+942delG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777895 | |||||||
| chr10:7777902 | C | CA | 4 | a0001c0001t0002g0073 a0001c0001t0002g0078 a0001c0001t0019g0017 others(1): Show |
6 | HG01175.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.558+935_558+936ins others(1): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777902 | |||||||
| chr10:7777903 | C | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
77 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.558+935G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777903 | |||||||
| chr10:7777903 | C | CA | 8 | a0001c0001t0001g0235 a0001c0001t0001g0249 a0001c0001t0001g0250 others(5): Show |
8 | HG00673.hp1 NA18940.hp2 NA18949.hp1 others(5): Show |
intron_variant | MODIFIER | c.558+934_558+935ins others(1): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777903 | |||||||
| chr10:7777904 | C | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(270): Show |
354 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.558+934G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777904 | |||||||
| chr10:7777995 | C | T | 10 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(7): Show |
12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+843G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7777995 | |||||||
| chr10:7778012 | A | G | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.558+826T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778012 | |||||||
| chr10:7778178 | A | G | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+660T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778178 | |||||||
| chr10:7778266 | G | A | 2 | a0001c0001t0078g0086 a0001c0001t0079g0123 |
2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.558+572C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778266 | |||||||
| chr10:7778407 | G | C | 10 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(7): Show |
12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.558+431C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778407 | |||||||
| chr10:7778449 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(249): Show |
341 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(338): Show |
intron_variant | MODIFIER | c.558+389C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778449 | |||||||
| chr10:7778462 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.558+376A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778462 | |||||||
| chr10:7778478 | C | T | 12 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+360G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778478 | |||||||
| chr10:7778479 | G | C | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.558+359C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778479 | |||||||
| chr10:7778696 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG00639.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.558+142C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778696 | |||||||
| chr10:7778741 | A | AAACAAC | 165 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(162): Show |
230 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.558+91_558+96dupGT others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778741 | |||||||
| chr10:7778759 | A | C | 12 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(9): Show |
14 | HG00438.hp1 HG00642.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.558+79T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 5/12 | chr10 | 7778759 | |||||||
| chr10:7779044 | A | T | 4 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(1): Show |
4 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.377-25T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779044 | |||||||
| chr10:7779118 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(190): Show |
259 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.377-99T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779118 | |||||||
| chr10:7779118 | A | T | 58 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(55): Show |
81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.377-99T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779118 | |||||||
| chr10:7779162 | C | T | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.377-143G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779162 | |||||||
| chr10:7779220 | C | T | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.377-201G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779220 | |||||||
| chr10:7779225 | T | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(115): Show |
164 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.377-206A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779225 | |||||||
| chr10:7779230 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(208): Show |
281 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.377-211T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779230 | |||||||
| chr10:7779366 | C | T | 1 | a0001c0001t0011g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.377-347G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779366 | |||||||
| chr10:7779393 | G | A | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.377-374C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779393 | |||||||
| chr10:7779534 | G | A | 1 | a0001c0001t0075g0082 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.377-515C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779534 | |||||||
| chr10:7779632 | T | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(165): Show |
236 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.376+424A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779632 | |||||||
| chr10:7779656 | A | C | 56 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(53): Show |
73 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.376+400T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779656 | |||||||
| chr10:7779675 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(57): Show |
87 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.376+381C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779675 | |||||||
| chr10:7779756 | G | A | 9 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(6): Show |
12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.376+300C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779756 | |||||||
| chr10:7779761 | T | C | 1 | a0001c0001t0073g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.376+295A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779761 | |||||||
| chr10:7779783 | G | C | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.376+273C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779783 | |||||||
| chr10:7779806 | C | T | 4 | a0001c0001t0021g0014 a0001c0001t0021g0096 a0001c0001t0034g0203 others(1): Show |
6 | HG02109.hp2 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.376+250G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779806 | |||||||
| chr10:7779831 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(184): Show |
259 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.376+225G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779831 | |||||||
| chr10:7779847 | T | C | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376+209A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7779847 | |||||||
| chr10:7780052 | T | G | 10 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0099 others(7): Show |
13 | HG01243.hp1 HG02257.hp2 HG02559.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.376+4A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 4/12 | chr10 | 7780052 | |||||||
| chr10:7780319 | A | C | 2 | a0001c0001t0028g0144 a0001c0001t0028g0218 |
2 | HG02055.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.210-12T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780319 | |||||||
| chr10:7780383 | T | C | 1 | a0001c0001t0057g0194 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.210-76A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780383 | |||||||
| chr10:7780424 | C | T | 1 | a0001c0001t0011g0110 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.210-117G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780424 | |||||||
| chr10:7780430 | C | T | 2 | a0001c0001t0002g0061 a0001c0001t0033g0195 |
2 | NA18946.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.210-123G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780430 | |||||||
| chr10:7780455 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(247): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.210-148A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780455 | |||||||
| chr10:7780482 | C | T | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.210-175G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780482 | |||||||
| chr10:7780571 | G | A | 8 | a0001c0001t0010g0150 a0001c0001t0018g0143 a0001c0001t0018g0268 others(5): Show |
10 | HG02145.hp1 HG02280.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.210-264C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780571 | |||||||
| chr10:7780579 | C | T | 9 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(6): Show |
12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.210-272G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780579 | |||||||
| chr10:7780711 | T | C | 1 | a0001c0001t0004g0033 | 2 | NA19083.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.210-404A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780711 | |||||||
| chr10:7780746 | G | C | 1 | a0001c0002t0051g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.210-439C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780746 | |||||||
| chr10:7780803 | C | T | 2 | a0001c0001t0034g0203 a0001c0001t0034g0205 |
2 | HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.210-496G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7780803 | |||||||
| chr10:7781015 | G | C | 233 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(230): Show |
320 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(317): Show |
intron_variant | MODIFIER | c.210-708C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781015 | |||||||
| chr10:7781016 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(57): Show |
87 | HG00280.hp2 HG00423.hp1 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.210-709C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781016 | |||||||
| chr10:7781022 | C | T | 16 | a0001c0001t0003g0287 a0001c0001t0012g0010 a0001c0001t0012g0273 others(13): Show |
23 | HG00323.hp1 HG00642.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.210-715G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781022 | |||||||
| chr10:7781112 | G | A | 1 | a0001c0001t0015g0169 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.210-805C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781112 | |||||||
| chr10:7781319 | G | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(55): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.210-1012C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781319 | |||||||
| chr10:7781534 | C | T | 1 | a0001c0001t0004g0151 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.210-1227G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781534 | |||||||
| chr10:7781587 | T | TAC | 11 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(8): Show |
13 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.210-1282_210-1281d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACAC | 5 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(2): Show |
5 | HG00099.hp2 HG00558.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.210-1284_210-1281d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(1): Show |
196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(193): Show |
274 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(271): Show |
intron_variant | MODIFIER | c.210-1288_210-1281d others(10): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(3): Show |
23 | a0001c0001t0001g0037 a0001c0001t0001g0200 a0001c0001t0002g0012 others(20): Show |
29 | HG00639.hp2 HG00733.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.210-1290_210-1281d others(12): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(5): Show |
2 | a0001c0001t0037g0024 a0001c0002t0069g0052 |
3 | HG01515.hp1 HG01517.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.210-1292_210-1281d others(14): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0192 a0001c0001t0001g0201 a0001c0001t0002g0075 others(1): Show |
4 | HG01433.hp1 HG02738.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.210-1294_210-1281d others(16): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(25): Show |
1 | a0002c0003t0031g0207 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(34): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TACACACA others(27): Show |
1 | a0002c0003t0031g0208 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.210-1281_210-1280i others(36): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TCTACACA others(13): Show |
1 | a0001c0001t0018g0268 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(22): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TCTACACA others(15): Show |
1 | a0001c0001t0018g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.210-1281_210-1280i others(24): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TCTACACA others(21): Show |
2 | a0001c0001t0018g0269 a0001c0001t0018g0270 |
2 | HG03486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.210-1281_210-1280i others(30): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781587 | T | TCTACACA others(23): Show |
3 | a0001c0001t0018g0271 a0001c0001t0019g0017 a0001c0001t0019g0219 |
5 | HG02280.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.210-1281_210-1280i others(32): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781587 | |||||||
| chr10:7781645 | C | G | 1 | a0001c0001t0018g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.210-1338G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781645 | |||||||
| chr10:7781687 | C | T | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.210-1380G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781687 | |||||||
| chr10:7781688 | G | A | 7 | a0001c0001t0018g0143 a0001c0001t0018g0268 a0001c0001t0018g0269 others(4): Show |
9 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.210-1381C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781688 | |||||||
| chr10:7781750 | C | CA | 85 | a0001c0001t0001g0177 a0001c0001t0002g0023 a0001c0001t0002g0060 others(82): Show |
111 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.209+1330dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | |||||||
| chr10:7781750 | C | CAA | 46 | a0001c0001t0002g0297 a0001c0001t0003g0011 a0001c0001t0003g0018 others(43): Show |
59 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.209+1329_209+1330d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | |||||||
| chr10:7781750 | C | CAAA | 53 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0037 others(50): Show |
72 | HG00280.hp2 HG00423.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.209+1328_209+1330d others(5): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | |||||||
| chr10:7781750 | C | CAAAA | 22 | a0001c0001t0001g0005 a0001c0001t0001g0192 a0001c0001t0001g0202 others(19): Show |
33 | HG00544.hp2 HG00597.hp2 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.209+1327_209+1330d others(6): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781750 | |||||||
| chr10:7781875 | G | A | 2 | a0001c0001t0021g0014 a0001c0001t0021g0096 |
4 | HG02109.hp2 HG02559.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.209+1206C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781875 | |||||||
| chr10:7781920 | T | C | 1 | a0001c0001t0038g0128 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.209+1161A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781920 | |||||||
| chr10:7781971 | T | C | 1 | a0001c0001t0008g0306 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.209+1110A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7781971 | |||||||
| chr10:7782044 | G | A | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.209+1037C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782044 | |||||||
| chr10:7782080 | A | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(242): Show |
334 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(331): Show |
intron_variant | MODIFIER | c.209+1001T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782080 | |||||||
| chr10:7782096 | T | G | 1 | a0001c0001t0026g0321 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209+985A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782096 | |||||||
| chr10:7782101 | T | A | 17 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(14): Show |
21 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.209+980A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782101 | |||||||
| chr10:7782212 | T | C | 1 | a0001c0001t0018g0271 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.209+869A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782212 | |||||||
| chr10:7782250 | G | T | 1 | a0001c0001t0060g0282 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.209+831C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782250 | |||||||
| chr10:7782252 | A | G | 125 | a0001c0001t0001g0177 a0001c0001t0002g0002 a0001c0001t0002g0012 others(122): Show |
168 | HG00280.hp1 HG00323.hp2 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.209+829T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782252 | |||||||
| chr10:7782400 | C | T | 4 | a0001c0001t0018g0268 a0001c0001t0018g0269 a0001c0001t0018g0270 others(1): Show |
4 | HG03041.hp1 HG03486.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.209+681G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782400 | |||||||
| chr10:7782401 | A | AT | 126 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(123): Show |
172 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.209+679dupA | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782401 | |||||||
| chr10:7782401 | A | T | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.209+680T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782401 | |||||||
| chr10:7782492 | C | G | 10 | a0001c0001t0002g0060 a0001c0001t0002g0080 a0001c0001t0002g0081 others(7): Show |
11 | HG01891.hp1 HG02109.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.209+589G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782492 | |||||||
| chr10:7782522 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.209+559G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782522 | |||||||
| chr10:7782529 | G | A | 10 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(7): Show |
12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.209+552C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782529 | |||||||
| chr10:7782666 | G | C | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.209+415C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782666 | |||||||
| chr10:7782864 | T | A | 1 | a0003c0004t0008g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.209+217A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782864 | |||||||
| chr10:7782909 | G | T | 54 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(51): Show |
71 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.209+172C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782909 | |||||||
| chr10:7782939 | AAAG | A | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0030g0134 others(2): Show |
5 | HG01891.hp1 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.209+139_209+141del others(3): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 2/12 | chr10 | 7782939 | |||||||
| chr10:7783231 | A | C | 1 | a0001c0001t0001g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.115-56T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783231 | |||||||
| chr10:7783237 | A | C | 1 | a0001c0001t0073g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.115-62T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783237 | |||||||
| chr10:7783308 | A | G | 1 | a0001c0001t0003g0281 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.115-133T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783308 | |||||||
| chr10:7783334 | A | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(239): Show |
331 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(328): Show |
intron_variant | MODIFIER | c.115-159T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783334 | |||||||
| chr10:7783352 | T | G | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.115-177A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783352 | |||||||
| chr10:7783567 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(248): Show |
340 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(337): Show |
intron_variant | MODIFIER | c.115-392A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783567 | |||||||
| chr10:7783586 | C | T | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-411G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783586 | |||||||
| chr10:7783601 | A | G | 2 | a0001c0001t0013g0232 a0001c0001t0013g0233 |
2 | NA18972.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.115-426T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783601 | |||||||
| chr10:7783753 | T | C | 2 | a0001c0001t0003g0308 a0001c0001t0003g0309 |
2 | NA18982.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.115-578A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783753 | |||||||
| chr10:7783827 | C | T | 1 | a0001c0001t0007g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.115-652G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7783827 | |||||||
| chr10:7784169 | G | C | 57 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(54): Show |
74 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.115-994C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784169 | |||||||
| chr10:7784242 | A | G | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-1067T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784242 | |||||||
| chr10:7784277 | C | T | 1 | a0001c0001t0018g0143 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.115-1102G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784277 | |||||||
| chr10:7784286 | T | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(315): Show |
420 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(417): Show |
intron_variant | MODIFIER | c.115-1111A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784286 | |||||||
| chr10:7784341 | G | C | 1 | a0001c0001t0037g0024 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.115-1166C>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784341 | |||||||
| chr10:7784351 | G | A | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.115-1176C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784351 | |||||||
| chr10:7784414 | T | G | 44 | a0001c0001t0002g0297 a0001c0001t0003g0011 a0001c0001t0003g0018 others(41): Show |
56 | HG00408.hp1 HG00741.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.115-1239A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784414 | |||||||
| chr10:7784450 | G | A | 38 | a0001c0001t0001g0177 a0001c0001t0004g0008 a0001c0001t0004g0030 others(35): Show |
57 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.115-1275C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784450 | |||||||
| chr10:7784498 | G | A | 1 | a0001c0001t0003g0226 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.115-1323C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784498 | |||||||
| chr10:7784551 | G | A | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-1376C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784551 | |||||||
| chr10:7784580 | T | C | 2 | a0002c0003t0031g0207 a0002c0003t0031g0208 |
2 | HG00438.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.115-1405A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784580 | |||||||
| chr10:7784643 | G | T | 1 | a0001c0001t0003g0272 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.115-1468C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784643 | |||||||
| chr10:7784814 | C | T | 1 | a0001c0001t0004g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.115-1639G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784814 | |||||||
| chr10:7784969 | G | A | 10 | a0001c0001t0004g0151 a0001c0001t0004g0152 a0001c0001t0010g0015 others(7): Show |
12 | HG00642.hp1 HG01516.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-1794C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7784969 | |||||||
| chr10:7785016 | G | A | 4 | a0001c0001t0023g0133 a0001c0001t0023g0138 a0001c0001t0023g0139 others(1): Show |
4 | HG00099.hp2 HG02132.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.115-1841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785016 | |||||||
| chr10:7785070 | G | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(247): Show |
339 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(336): Show |
intron_variant | MODIFIER | c.115-1895C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785070 | |||||||
| chr10:7785171 | G | A | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.115-1996C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785171 | |||||||
| chr10:7785202 | T | C | 9 | a0001c0002t0009g0013 a0001c0002t0009g0025 a0001c0002t0009g0097 others(6): Show |
12 | HG02055.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.115-2027A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785202 | |||||||
| chr10:7785233 | C | T | 1 | a0001c0001t0065g0217 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.115-2058G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785233 | |||||||
| chr10:7785251 | C | CA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(79): Show |
114 | HG00280.hp2 HG00423.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.115-2077dupT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785251 | |||||||
| chr10:7785251 | C | CAA | 44 | a0001c0001t0001g0177 a0001c0001t0001g0206 a0001c0001t0001g0261 others(41): Show |
63 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(60): Show |
intron_variant | MODIFIER | c.115-2078_115-2077d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785251 | |||||||
| chr10:7785510 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(191): Show |
260 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.114+2310G>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785510 | |||||||
| chr10:7785583 | G | A | 4 | a0001c0002t0009g0025 a0001c0002t0066g0103 a0002c0003t0031g0207 others(1): Show |
5 | HG00438.hp1 HG02135.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+2237C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785583 | |||||||
| chr10:7785795 | C | T | 22 | a0001c0001t0018g0143 a0001c0001t0019g0219 a0001c0001t0021g0096 others(19): Show |
25 | HG00099.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.114+2025G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785795 | |||||||
| chr10:7785813 | G | T | 53 | a0001c0001t0002g0297 a0001c0001t0003g0011 a0001c0001t0003g0018 others(50): Show |
70 | HG00323.hp1 HG00408.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.114+2007C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | |||||||
| chr10:7785813 | GA | G | 8 | a0001c0001t0002g0216 a0001c0001t0018g0268 a0001c0001t0018g0269 others(5): Show |
8 | HG02647.hp1 HG02896.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.114+2006delT | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | |||||||
| chr10:7785813 | GAA | G | 52 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(49): Show |
69 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.114+2005_114+2006d others(4): Show |
KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785813 | |||||||
| chr10:7785872 | T | C | 5 | a0001c0001t0002g0080 a0001c0001t0002g0081 a0001c0001t0030g0134 others(2): Show |
5 | HG01891.hp1 HG02258.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.114+1948A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785872 | |||||||
| chr10:7785891 | G | A | 56 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(53): Show |
73 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.114+1929C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785891 | |||||||
| chr10:7785979 | G | A | 2 | a0001c0001t0065g0217 a0001c0001t0078g0086 |
2 | HG02647.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.114+1841C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785979 | |||||||
| chr10:7785996 | T | C | 1 | a0001c0001t0028g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.114+1824A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7785996 | |||||||
| chr10:7786066 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0064g0083 |
2 | HG00323.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.114+1754A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786066 | |||||||
| chr10:7786152 | A | G | 3 | a0001c0001t0023g0138 a0001c0001t0023g0139 a0001c0001t0029g0317 |
3 | HG00099.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1668T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786152 | |||||||
| chr10:7786154 | G | A | 3 | a0001c0001t0023g0138 a0001c0001t0023g0139 a0001c0001t0029g0317 |
3 | HG00099.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1666C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786154 | |||||||
| chr10:7786169 | C | G | 2 | a0001c0001t0005g0092 a0001c0001t0038g0093 |
2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.114+1651G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786169 | |||||||
| chr10:7786245 | T | C | 1 | a0001c0001t0019g0017 | 3 | HG02280.hp2 HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.114+1575A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786245 | |||||||
| chr10:7786257 | T | C | 2 | a0001c0001t0019g0017 a0001c0001t0019g0219 |
4 | HG02280.hp2 HG02717.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.114+1563A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786257 | |||||||
| chr10:7786268 | T | G | 2 | a0001c0001t0023g0138 a0001c0001t0023g0139 |
2 | HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1552A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786268 | |||||||
| chr10:7786270 | C | T | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+1550G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786270 | |||||||
| chr10:7786279 | G | T | 4 | a0001c0001t0019g0017 a0001c0001t0019g0219 a0001c0001t0023g0138 others(1): Show |
6 | HG02132.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1541C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786279 | |||||||
| chr10:7786281 | G | A | 4 | a0001c0001t0019g0017 a0001c0001t0019g0219 a0001c0001t0023g0138 others(1): Show |
6 | HG02132.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.114+1539C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786281 | |||||||
| chr10:7786553 | G | T | 1 | a0001c0001t0004g0142 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.114+1267C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786553 | |||||||
| chr10:7786710 | G | A | 1 | a0001c0001t0011g0220 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.114+1110C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786710 | |||||||
| chr10:7786767 | T | C | 1 | a0001c0001t0005g0136 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.114+1053A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786767 | |||||||
| chr10:7786777 | C | T | 2 | a0001c0001t0006g0140 a0001c0001t0006g0141 |
2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.114+1043G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786777 | |||||||
| chr10:7786786 | T | A | 3 | a0001c0001t0002g0137 a0001c0001t0023g0138 a0001c0001t0023g0139 |
3 | HG01192.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1034A>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786786 | |||||||
| chr10:7786787 | A | C | 3 | a0001c0001t0002g0137 a0001c0001t0023g0138 a0001c0001t0023g0139 |
3 | HG01192.hp2 HG02132.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.114+1033T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786787 | |||||||
| chr10:7786789 | T | C | 96 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(93): Show |
125 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.114+1031A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786789 | |||||||
| chr10:7786838 | T | C | 1 | a0001c0001t0049g0221 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.114+982A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786838 | |||||||
| chr10:7786894 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.114+926G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7786894 | |||||||
| chr10:7787004 | T | G | 1 | a0001c0001t0001g0222 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.114+816A>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787004 | |||||||
| chr10:7787055 | G | A | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0040 others(48): Show |
72 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.114+765C>T | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787055 | |||||||
| chr10:7787074 | T | C | 60 | a0001c0001t0002g0267 a0001c0001t0002g0297 a0001c0001t0002g0315 others(57): Show |
77 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(74): Show |
intron_variant | MODIFIER | c.114+746A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787074 | |||||||
| chr10:7787081 | GC | G | 95 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(92): Show |
124 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.114+738delG | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787081 | |||||||
| chr10:7787147 | A | G | 1 | a0001c0001t0058g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.114+673T>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787147 | |||||||
| chr10:7787368 | T | C | 1 | a0001c0001t0005g0318 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.114+452A>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787368 | |||||||
| chr10:7787468 | G | T | 1 | a0001c0001t0004g0090 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.114+352C>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787468 | |||||||
| chr10:7787475 | A | C | 314 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0035 others(311): Show |
414 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(411): Show |
intron_variant | MODIFIER | c.114+345T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787475 | |||||||
| chr10:7787521 | A | T | 1 | a0001c0001t0001g0089 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.114+299T>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787521 | |||||||
| chr10:7787565 | A | C | 1 | a0001c0001t0001g0088 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.114+255T>G | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787565 | |||||||
| chr10:7787585 | C | T | 1 | a0001c0001t0006g0087 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.114+235G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787585 | |||||||
| chr10:7787761 | C | G | 1 | a0001c0001t0078g0086 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.114+59G>C | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787761 | |||||||
| chr10:7787796 | C | T | 43 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0020 others(40): Show |
59 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.114+24G>A | KIN | ENSG00000151657.12 | transcript | ENST00000379562.9 | protein_coding | 1/12 | chr10 | 7787796 |