Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1103 |
| ensemblid | ENSG00000070748.19 |
| hgncid | 1912 |
| symbol | CHAT |
| name | choline O-acetyltransferase |
| refseq_nuc | NM_020549.5 |
| refseq_prot | NP_065574.4 |
| ensembl_nuc | ENST00000337653.7 |
| ensembl_prot | ENSP00000337103.2 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 49614037 |
| end | 49667942 |
| strand | + |
| ver | v1.2 |
| region | chr10:49614037-49667942 |
| region5000 | chr10:49609037-49672942 |
| regionname0 | CHAT_chr10_49614037_49667942 |
| regionname5000 | CHAT_chr10_49609037_49672942 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 748 | 261 | 76 | 56 | 82 | 13 | 33 | 63 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0002 | 0/0 | 748 | 67 | 0 | 16 | 36 | 4 | 11 | 29 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0003 | 0/0 | 748 | 63 | 1 | 4 | 58 | 0 | 0 | 40 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0004 | 1/0 | 748 | 11 | 10 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0005 | 0/0 | 748 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0006 | 0/0 | 748 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0007 | 0/0 | 748 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0008 | 0/0 | 748 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0009 | 0/0 | 748 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0010 | 0/0 | 748 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0011 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0012 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0013 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0014 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0015 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0016 | 0/0 | 748 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| a0017 | 0/0 | 748 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | MGLRT others(743): Show |
chr10 | 49609037 | 49672942 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2244 | 172 | 50 | 40 | 45 | 10 | 26 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0003 | 0/0 | 2244 | 43 | 7 | 13 | 15 | 3 | 5 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0005 | 0/0 | 2244 | 20 | 0 | 0 | 20 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0010 | 0/0 | 2244 | 9 | 8 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0011 | 0/0 | 2244 | 4 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0013 | 0/0 | 2244 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0015 | 0/0 | 2244 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0017 | 0/0 | 2244 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0019 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0026 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0027 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0028 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0030 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0001c0035 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0002c0002 | 0/0 | 2244 | 50 | 0 | 15 | 21 | 4 | 10 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0002c0008 | 0/0 | 2244 | 13 | 0 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0002c0012 | 0/0 | 2244 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0002c0020 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0003c0004 | 0/0 | 2244 | 31 | 0 | 3 | 28 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0003c0006 | 0/0 | 2244 | 17 | 0 | 0 | 17 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0003c0007 | 0/0 | 2244 | 14 | 1 | 1 | 12 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0003c0039 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0004c0009 | 1/0 | 2244 | 9 | 8 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0004c0025 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0004c0034 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0005c0014 | 0/0 | 2244 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0006c0023 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0006c0024 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0007c0016 | 0/0 | 2244 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0008c0038 | 0/0 | 2244 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0009c0021 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0010c0018 | 0/0 | 2244 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0011c0032 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0012c0031 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0013c0036 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0014c0037 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0015c0022 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0016c0029 | 0/0 | 2244 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 | ||
| a0017c0033 | 0/0 | 2244 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | ATGGG others(2239): Show |
chr10 | 49609037 | 49672942 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5296 | 42 | 12 | 7 | 18 | 1 | 4 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0002 | 0/1 | 5296 | 30 | 1 | 8 | 12 | 2 | 6 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0003 | 0/0 | 5296 | 14 | 11 | 3 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0004 | 0/0 | 5296 | 28 | 8 | 7 | 9 | 2 | 2 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0005 | 0/0 | 5296 | 4 | 3 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0006 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0007 | 0/0 | 5296 | 19 | 1 | 5 | 4 | 3 | 6 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0008 | 0/0 | 5296 | 12 | 0 | 6 | 0 | 2 | 4 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0011 | 0/0 | 5296 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0012 | 0/0 | 5296 | 2 | 0 | 0 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0013 | 0/0 | 5296 | 4 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0014 | 0/0 | 5296 | 3 | 2 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0015 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0016 | 0/0 | 5278 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5273): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0018 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0019 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0023 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0026 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0028 | 0/0 | 5278 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5273): Show |
chr10 | 49609037 | 49672942 |
| a0001c0001t0036 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0003 | 0/0 | 5296 | 3 | 2 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0006 | 0/0 | 5296 | 23 | 1 | 11 | 9 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0008 | 0/0 | 5296 | 4 | 2 | 1 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0010 | 0/0 | 5296 | 9 | 0 | 0 | 4 | 2 | 3 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0020 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0021 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0033 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0003t0034 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0005t0005 | 0/0 | 5296 | 10 | 0 | 0 | 10 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0005t0009 | 0/0 | 5296 | 9 | 0 | 0 | 9 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0005t0030 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0010t0003 | 0/0 | 5296 | 8 | 7 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0010t0008 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0011t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0011t0022 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0011t0024 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0011t0029 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0013t0005 | 0/0 | 5296 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0013t0032 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0015t0005 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0015t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0017t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0017t0004 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0019t0002 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0026t0005 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0027t0031 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0028t0005 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0030t0004 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0001c0035t0003 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0002 | 0/0 | 5296 | 30 | 0 | 8 | 14 | 3 | 5 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0007 | 0/0 | 5296 | 11 | 0 | 2 | 7 | 1 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0008 | 0/0 | 5296 | 4 | 0 | 4 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0009 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0012 | 0/0 | 5296 | 3 | 0 | 0 | 0 | 0 | 3 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0002t0017 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0008t0008 | 0/0 | 5296 | 4 | 0 | 1 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0008t0010 | 0/0 | 5296 | 9 | 0 | 0 | 9 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0012t0009 | 0/0 | 5296 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0002c0020t0012 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0004t0001 | 0/0 | 5296 | 25 | 0 | 3 | 22 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0004t0004 | 0/0 | 5296 | 4 | 0 | 0 | 4 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0004t0013 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0004t0027 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0006t0005 | 0/0 | 5296 | 17 | 0 | 0 | 17 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0007t0003 | 0/0 | 5296 | 6 | 0 | 1 | 5 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0007t0006 | 0/0 | 5296 | 8 | 1 | 0 | 7 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0003c0039t0006 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0004c0009t0003 | 0/0 | 5296 | 3 | 3 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0004c0009t0011 | 1/0 | 5296 | 5 | 4 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0004c0009t0014 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0004c0025t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0004c0034t0015 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0005c0014t0004 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0005c0014t0007 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0006c0023t0007 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0006c0024t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0007c0016t0008 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0007c0016t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0008c0038t0004 | 0/0 | 5296 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0009c0021t0002 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0010c0018t0003 | 0/0 | 5296 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0011c0032t0025 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0012c0031t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0013c0036t0003 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0014c0037t0035 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0015c0022t0002 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0016c0029t0009 | 0/0 | 5296 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| a0017c0033t0009 | 0/0 | 5296 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | AAATG others(5291): Show |
chr10 | 49609037 | 49672942 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0002g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0004g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0005g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0006g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0001 | 0/0 | 4 | 0 | 3 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0007g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0008g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0011g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0011g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0012g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0012g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0013g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0014g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0015g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0016g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0016g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0018g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0019g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0023g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0026g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0028g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0001t0036g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0003g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0346 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0006g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0008g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0018 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0010g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0020g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0021g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0033g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0003t0034g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0009g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0005t0030g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0010t0008g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0022g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0024g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0011t0029g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0005g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0013t0032g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0015t0005g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0015t0009g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0017t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0017t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0019t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0026t0005g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0027t0031g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0028t0005g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0030t0004g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0001c0035t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0002g0373 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0366 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0369 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0007g0375 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0008g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0009g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0012g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0002t0017g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0359 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0368 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0371 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0008g0372 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0374 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0008t0010g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0365 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0012t0009g0367 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0002c0020t0012g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0004t0027g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0006t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0007t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0003c0039t0006g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0003g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0011g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0009t0014g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0025t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0004c0034t0015g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0005c0014t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0005c0014t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0006c0023t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0006c0024t0009g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0007c0016t0008g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0007c0016t0009g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0008c0038t0004g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0009c0021t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0010c0018t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0011c0032t0025g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0012c0031t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0013c0036t0003g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0014c0037t0035g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0015c0022t0002g0370 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0016c0029t0009g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| a0017c0033t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0021 | g0293 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0006 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00140 | hp2 | a0001 | c0001 | t0007 | g0040 | EUR | GBR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00280 | hp1 | a0008 | c0038 | t0004 | g0231 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0292 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0096 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0008 | EUR | FIN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00408 | hp1 | a0003 | c0006 | t0005 | g0133 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00408 | hp2 | a0003 | c0004 | t0001 | g0135 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00423 | hp1 | a0003 | c0007 | t0003 | g0148 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00423 | hp2 | a0001 | c0005 | t0005 | g0328 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00438 | hp1 | a0003 | c0006 | t0005 | g0120 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00544 | hp1 | a0001 | c0003 | t0006 | g0053 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00544 | hp2 | a0003 | c0007 | t0003 | g0127 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0343 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00597 | hp2 | a0002 | c0012 | t0009 | g0367 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00609 | hp1 | a0001 | c0005 | t0005 | g0344 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00609 | hp2 | a0003 | c0004 | t0004 | g0166 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00621 | hp1 | a0001 | c0005 | t0005 | g0065 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00621 | hp2 | a0001 | c0005 | t0005 | g0301 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0088 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00639 | hp2 | a0001 | c0035 | t0003 | g0233 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00642 | hp1 | a0002 | c0002 | t0009 | g0100 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0263 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00673 | hp1 | a0001 | c0001 | t0026 | g0064 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0108 | EAS | CHS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00733 | hp1 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0067 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00735 | hp1 | a0001 | c0001 | t0011 | g0172 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0175 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00738 | hp1 | a0002 | c0008 | t0008 | g0359 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00738 | hp2 | a0001 | c0001 | t0008 | g0037 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00741 | hp1 | a0002 | c0002 | t0008 | g0356 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG00741 | hp2 | a0001 | c0001 | t0007 | g0234 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0299 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01070 | hp1 | a0001 | c0001 | t0004 | g0349 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01070 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0326 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0348 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0294 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01081 | hp2 | a0009 | c0021 | t0002 | g0083 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01106 | hp1 | a0002 | c0002 | t0007 | g0089 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0230 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01109 | hp1 | a0001 | c0001 | t0014 | g0279 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0206 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01167 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01167 | hp2 | a0001 | c0010 | t0003 | g0255 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0237 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01169 | hp1 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01169 | hp2 | a0002 | c0002 | t0002 | g0009 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01175 | hp1 | a0001 | c0003 | t0006 | g0060 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01243 | hp1 | a0001 | c0001 | t0011 | g0173 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01255 | hp2 | a0001 | c0003 | t0006 | g0027 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01256 | hp2 | a0002 | c0002 | t0008 | g0355 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01261 | hp2 | a0001 | c0003 | t0006 | g0305 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01358 | hp1 | a0001 | c0003 | t0006 | g0027 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01358 | hp2 | a0002 | c0002 | t0008 | g0091 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01433 | hp1 | a0001 | c0001 | t0008 | g0201 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01433 | hp2 | a0002 | c0002 | t0008 | g0090 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01496 | hp2 | a0001 | c0003 | t0006 | g0360 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01515 | hp1 | a0002 | c0002 | t0002 | g0012 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01516 | hp1 | a0002 | c0002 | t0007 | g0092 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01516 | hp2 | a0001 | c0003 | t0010 | g0018 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01517 | hp1 | a0001 | c0003 | t0010 | g0018 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0012 | EUR | IBS | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01884 | hp1 | a0001 | c0013 | t0005 | g0289 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01891 | hp1 | a0001 | c0026 | t0005 | g0363 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01891 | hp2 | a0004 | c0009 | t0011 | g0044 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01928 | hp1 | a0003 | c0004 | t0001 | g0167 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01928 | hp2 | a0001 | c0003 | t0006 | g0304 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01934 | hp1 | a0002 | c0002 | t0007 | g0102 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01943 | hp1 | a0003 | c0007 | t0003 | g0114 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01943 | hp2 | a0003 | c0004 | t0001 | g0163 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01952 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01952 | hp2 | a0001 | c0003 | t0008 | g0250 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01975 | hp1 | a0001 | c0003 | t0006 | g0028 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0309 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01978 | hp2 | a0001 | c0001 | t0007 | g0001 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01981 | hp1 | a0001 | c0027 | t0031 | g0174 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01981 | hp2 | a0001 | c0003 | t0006 | g0028 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02015 | hp1 | a0003 | c0004 | t0001 | g0134 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02027 | hp1 | a0002 | c0008 | t0010 | g0071 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02055 | hp2 | a0001 | c0001 | t0013 | g0329 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02056 | hp2 | a0003 | c0004 | t0001 | g0160 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02071 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02071 | hp2 | a0003 | c0004 | t0001 | g0126 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02074 | hp1 | a0001 | c0005 | t0005 | g0066 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02074 | hp2 | a0003 | c0004 | t0027 | g0118 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02083 | hp1 | a0003 | c0007 | t0003 | g0137 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02132 | hp1 | a0001 | c0003 | t0008 | g0183 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02132 | hp2 | a0003 | c0004 | t0001 | g0121 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02135 | hp1 | a0003 | c0007 | t0003 | g0124 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02145 | hp1 | a0001 | c0028 | t0005 | g0364 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02148 | hp1 | a0001 | c0003 | t0006 | g0316 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02148 | hp2 | a0003 | c0004 | t0001 | g0131 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02155 | hp1 | a0001 | c0005 | t0005 | g0030 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02155 | hp2 | a0002 | c0002 | t0007 | g0375 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02165 | hp1 | a0003 | c0004 | t0001 | g0050 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02257 | hp2 | a0001 | c0010 | t0003 | g0049 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02258 | hp2 | a0001 | c0011 | t0024 | g0280 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0325 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02273 | hp2 | a0001 | c0003 | t0006 | g0354 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02280 | hp1 | a0003 | c0007 | t0006 | g0159 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02280 | hp2 | a0004 | c0009 | t0011 | g0042 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02293 | hp1 | a0001 | c0003 | t0006 | g0303 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0097 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02300 | hp2 | a0001 | c0003 | t0003 | g0308 | AMR | PEL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0062 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02451 | hp2 | a0001 | c0010 | t0003 | g0256 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02523 | hp1 | a0003 | c0004 | t0001 | g0144 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02572 | hp1 | a0001 | c0001 | t0013 | g0225 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02572 | hp2 | a0001 | c0013 | t0032 | g0378 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0076 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02602 | hp2 | a0001 | c0019 | t0002 | g0171 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02622 | hp1 | a0001 | c0001 | t0023 | g0281 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02683 | hp1 | a0001 | c0001 | t0008 | g0207 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0055 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02698 | hp1 | a0001 | c0001 | t0008 | g0195 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02698 | hp2 | a0001 | c0030 | t0004 | g0310 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02717 | hp1 | a0011 | c0032 | t0025 | g0059 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02723 | hp2 | a0004 | c0009 | t0003 | g0272 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0179 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0008 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02738 | hp1 | a0001 | c0001 | t0008 | g0180 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02738 | hp2 | a0001 | c0003 | t0010 | g0038 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02818 | hp1 | a0001 | c0010 | t0003 | g0254 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02886 | hp1 | a0001 | c0011 | t0003 | g0214 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02886 | hp2 | a0001 | c0001 | t0036 | g0295 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02895 | hp2 | a0001 | c0003 | t0008 | g0017 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02896 | hp1 | a0001 | c0017 | t0004 | g0228 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02896 | hp2 | a0001 | c0001 | t0015 | g0023 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02897 | hp1 | a0001 | c0001 | t0015 | g0023 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02897 | hp2 | a0001 | c0003 | t0008 | g0017 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0300 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0221 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02970 | hp1 | a0012 | c0031 | t0003 | g0222 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02970 | hp2 | a0004 | c0009 | t0003 | g0377 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02976 | hp1 | a0001 | c0001 | t0016 | g0218 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02976 | hp2 | a0001 | c0001 | t0013 | g0020 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03041 | hp1 | a0001 | c0010 | t0008 | g0265 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0286 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03098 | hp1 | a0013 | c0036 | t0003 | g0331 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03098 | hp2 | a0004 | c0034 | t0015 | g0275 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03130 | hp1 | a0004 | c0009 | t0011 | g0047 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0252 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03139 | hp2 | a0001 | c0001 | t0004 | g0285 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03195 | hp1 | a0001 | c0010 | t0003 | g0048 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03195 | hp2 | a0014 | c0037 | t0035 | g0296 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03209 | hp2 | a0001 | c0010 | t0003 | g0223 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03225 | hp1 | a0001 | c0003 | t0034 | g0362 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03225 | hp2 | a0004 | c0009 | t0003 | g0273 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0232 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03453 | hp1 | a0001 | c0017 | t0003 | g0253 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03453 | hp2 | a0001 | c0010 | t0003 | g0259 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03486 | hp2 | a0001 | c0011 | t0029 | g0216 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03491 | hp2 | a0001 | c0003 | t0006 | g0346 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03492 | hp1 | a0001 | c0001 | t0019 | g0242 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0258 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0350 | AFR | ESN | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03540 | hp1 | a0001 | c0010 | t0003 | g0257 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0336 | AFR | GWD | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03654 | hp1 | a0002 | c0002 | t0002 | g0082 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03654 | hp2 | a0001 | c0003 | t0010 | g0239 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03669 | hp1 | a0001 | c0001 | t0007 | g0039 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03669 | hp2 | a0001 | c0003 | t0006 | g0317 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0085 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03688 | hp2 | a0001 | c0001 | t0007 | g0001 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03704 | hp1 | a0001 | c0001 | t0018 | g0213 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03704 | hp2 | a0002 | c0002 | t0007 | g0110 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0034 | SAS | PJL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03831 | hp2 | a0001 | c0001 | t0008 | g0211 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03834 | hp1 | a0001 | c0001 | t0012 | g0192 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0191 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03927 | hp2 | a0002 | c0020 | t0012 | g0087 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0202 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04115 | hp1 | a0002 | c0002 | t0012 | g0078 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04115 | hp2 | a0001 | c0003 | t0010 | g0170 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04184 | hp1 | a0002 | c0002 | t0012 | g0101 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04184 | hp2 | a0002 | c0002 | t0017 | g0086 | SAS | BEB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04199 | hp2 | a0002 | c0002 | t0012 | g0098 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0210 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0204 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG04228 | hp2 | a0001 | c0001 | t0012 | g0188 | SAS | STU | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0182 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18522 | hp2 | a0005 | c0014 | t0007 | g0178 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18612 | hp2 | a0003 | c0039 | t0006 | g0151 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0032 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18747 | hp2 | a0001 | c0005 | t0005 | g0030 | EAS | CHB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0036 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18939 | hp1 | a0003 | c0004 | t0001 | g0015 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18943 | hp1 | a0001 | c0001 | t0007 | g0352 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18944 | hp1 | a0001 | c0003 | t0006 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18944 | hp2 | a0003 | c0006 | t0005 | g0142 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18946 | hp1 | a0003 | c0004 | t0013 | g0153 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18946 | hp2 | a0006 | c0024 | t0009 | g0103 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18947 | hp2 | a0001 | c0005 | t0009 | g0249 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18948 | hp1 | a0007 | c0016 | t0009 | g0268 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18948 | hp2 | a0003 | c0007 | t0006 | g0165 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18949 | hp1 | a0001 | c0001 | t0007 | g0241 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18949 | hp2 | a0003 | c0004 | t0001 | g0146 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18952 | hp2 | a0002 | c0008 | t0010 | g0070 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18953 | hp1 | a0001 | c0005 | t0005 | g0320 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0361 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18954 | hp1 | a0001 | c0003 | t0010 | g0236 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18954 | hp2 | a0002 | c0002 | t0007 | g0369 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18957 | hp2 | a0003 | c0006 | t0005 | g0117 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18959 | hp1 | a0002 | c0008 | t0010 | g0011 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18959 | hp2 | a0001 | c0001 | t0004 | g0323 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18960 | hp1 | a0001 | c0005 | t0009 | g0262 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18960 | hp2 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18962 | hp1 | a0003 | c0007 | t0006 | g0150 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18962 | hp2 | a0007 | c0016 | t0008 | g0266 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18964 | hp1 | a0002 | c0008 | t0010 | g0376 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18964 | hp2 | a0002 | c0008 | t0008 | g0371 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18965 | hp1 | a0003 | c0006 | t0005 | g0149 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18965 | hp2 | a0001 | c0003 | t0006 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18966 | hp1 | a0003 | c0006 | t0005 | g0136 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18966 | hp2 | a0001 | c0001 | t0007 | g0244 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18968 | hp1 | a0002 | c0002 | t0007 | g0093 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18969 | hp1 | a0003 | c0007 | t0006 | g0162 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18969 | hp2 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18970 | hp1 | a0003 | c0004 | t0001 | g0141 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0315 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18971 | hp2 | a0002 | c0002 | t0007 | g0366 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18973 | hp1 | a0002 | c0002 | t0007 | g0072 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18973 | hp2 | a0001 | c0005 | t0030 | g0335 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18974 | hp2 | a0001 | c0003 | t0010 | g0208 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18975 | hp2 | a0002 | c0008 | t0008 | g0372 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18979 | hp1 | a0003 | c0004 | t0004 | g0128 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18979 | hp2 | a0003 | c0004 | t0001 | g0123 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18982 | hp1 | a0001 | c0003 | t0006 | g0313 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18983 | hp2 | a0003 | c0004 | t0001 | g0014 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18984 | hp1 | a0003 | c0006 | t0005 | g0125 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18984 | hp2 | a0003 | c0004 | t0004 | g0156 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18985 | hp2 | a0003 | c0004 | t0004 | g0130 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18986 | hp2 | a0001 | c0005 | t0009 | g0190 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18988 | hp1 | a0001 | c0005 | t0009 | g0248 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18988 | hp2 | a0001 | c0003 | t0010 | g0209 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18990 | hp1 | a0003 | c0007 | t0006 | g0138 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18993 | hp1 | a0001 | c0003 | t0010 | g0187 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18993 | hp2 | a0001 | c0005 | t0009 | g0240 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18994 | hp1 | a0002 | c0008 | t0010 | g0095 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18994 | hp2 | a0003 | c0006 | t0005 | g0161 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18995 | hp1 | a0001 | c0003 | t0006 | g0345 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18995 | hp2 | a0002 | c0002 | t0007 | g0104 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18997 | hp1 | a0003 | c0007 | t0006 | g0115 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18997 | hp2 | a0015 | c0022 | t0002 | g0370 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18998 | hp1 | a0002 | c0002 | t0007 | g0357 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0106 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0332 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18999 | hp2 | a0001 | c0005 | t0009 | g0269 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0307 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19000 | hp2 | a0003 | c0006 | t0005 | g0147 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19002 | hp2 | a0001 | c0005 | t0009 | g0186 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19005 | hp1 | a0003 | c0006 | t0005 | g0013 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19007 | hp1 | a0003 | c0006 | t0005 | g0157 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19007 | hp2 | a0002 | c0008 | t0010 | g0011 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0373 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19009 | hp2 | a0003 | c0007 | t0003 | g0158 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19012 | hp1 | a0001 | c0001 | t0004 | g0337 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19012 | hp2 | a0003 | c0006 | t0005 | g0013 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19030 | hp1 | a0001 | c0001 | t0014 | g0278 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19030 | hp2 | a0005 | c0014 | t0004 | g0284 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19043 | hp1 | a0004 | c0009 | t0011 | g0043 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19043 | hp2 | a0001 | c0001 | t0013 | g0020 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19054 | hp1 | a0001 | c0001 | t0004 | g0339 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19054 | hp2 | a0003 | c0006 | t0005 | g0143 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19057 | hp1 | a0003 | c0004 | t0001 | g0132 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19058 | hp1 | a0003 | c0004 | t0001 | g0139 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19058 | hp2 | a0001 | c0005 | t0009 | g0247 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19060 | hp1 | a0003 | c0006 | t0005 | g0152 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19062 | hp1 | a0001 | c0003 | t0020 | g0069 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0267 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19063 | hp1 | a0001 | c0015 | t0009 | g0245 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19063 | hp2 | a0003 | c0007 | t0006 | g0164 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19065 | hp1 | a0003 | c0007 | t0006 | g0129 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19065 | hp2 | a0002 | c0012 | t0009 | g0365 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19068 | hp1 | a0016 | c0029 | t0009 | g0246 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19068 | hp2 | a0003 | c0004 | t0001 | g0154 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19070 | hp1 | a0003 | c0004 | t0001 | g0140 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19070 | hp2 | a0001 | c0005 | t0005 | g0298 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19074 | hp2 | a0001 | c0003 | t0006 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19076 | hp2 | a0002 | c0008 | t0008 | g0368 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19078 | hp1 | a0006 | c0023 | t0007 | g0105 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19079 | hp1 | a0002 | c0002 | t0002 | g0034 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19079 | hp2 | a0003 | c0006 | t0005 | g0155 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19080 | hp1 | a0003 | c0004 | t0001 | g0016 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19080 | hp2 | a0001 | c0003 | t0006 | g0002 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19081 | hp1 | a0001 | c0005 | t0009 | g0193 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19081 | hp2 | a0001 | c0001 | t0028 | g0341 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19083 | hp1 | a0001 | c0003 | t0006 | g0322 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19083 | hp2 | a0002 | c0008 | t0010 | g0094 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19084 | hp1 | a0002 | c0012 | t0009 | g0079 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0107 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19085 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19085 | hp2 | a0003 | c0004 | t0001 | g0116 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19086 | hp1 | a0001 | c0001 | t0004 | g0321 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19087 | hp1 | a0002 | c0008 | t0010 | g0374 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19088 | hp2 | a0003 | c0006 | t0005 | g0119 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19090 | hp1 | a0003 | c0006 | t0005 | g0145 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19090 | hp2 | a0002 | c0008 | t0010 | g0358 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19091 | hp1 | a0001 | c0015 | t0005 | g0306 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19091 | hp2 | a0001 | c0003 | t0006 | g0330 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19240 | hp1 | a0001 | c0003 | t0003 | g0288 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | YRI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | ASW | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | ASW | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0238 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20752 | hp2 | a0001 | c0001 | t0007 | g0051 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20805 | hp1 | a0001 | c0001 | t0008 | g0003 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20805 | hp2 | a0001 | c0001 | t0007 | g0181 | EUR | TSI | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01123 | hp1 | a0010 | c0018 | t0003 | g0324 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | CLM | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02109 | hp2 | a0001 | c0003 | t0033 | g0046 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02486 | hp1 | a0004 | c0009 | t0014 | g0277 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02486 | hp2 | a0001 | c0001 | t0016 | g0026 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02559 | hp1 | a0001 | c0001 | t0014 | g0276 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG02559 | hp2 | a0001 | c0011 | t0022 | g0283 | AFR | ACB | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03471 | hp1 | a0001 | c0013 | t0005 | g0217 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG03471 | hp2 | a0001 | c0001 | t0005 | g0264 | AFR | MSL | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0347 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| HG06807 | hp2 | a0001 | c0001 | t0016 | g0026 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18955 | hp1 | a0001 | c0005 | t0005 | g0168 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0227 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA20300 | hp2 | a0001 | c0003 | t0006 | g0302 | AFR | USA | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA21309 | hp1 | a0004 | c0025 | t0003 | g0351 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| NA21309 | hp2 | a0017 | c0033 | t0009 | g0177 | AFR | LWK | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0199 | REF | REF | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| homoSapiens | grch38p0 | a0004 | c0009 | t0011 | g0045 | REF | REF | CHAT_chr10_49609037_49672942 | CHAT | chr10 | 49609037 | 49672942 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614245 | G | C | 1 | a0010 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.56G>C | p.Arg19Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 209/5296 | 56/2247 | 19/748 | chr10 | 49614245 | |||
| chr10:49614330 | C | G | 1 | a0003 | 63 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(60): Show |
missense_variant | MODERATE | c.141C>G | p.Asp47Glu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 294/5296 | 141/2247 | 47/748 | chr10 | 49614330 | |||
| chr10:49616573 | G | A | 4 | a0002 a0006 a0009 others(1): Show |
71 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
missense_variant | MODERATE | c.358G>A | p.Ala120Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/15 | 511/5296 | 358/2247 | 120/748 | chr10 | 49616573 | |||
| chr10:49622109 | C | G | 1 | a0006 | 2 | NA18946.hp2 NA19078.hp1 |
missense_variant | MODERATE | c.711C>G | p.Ser237Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 864/5296 | 711/2247 | 237/748 | chr10 | 49622109 | |||
| chr10:49622125 | C | T | 1 | a0008 | 1 | HG00280.hp1 | missense_variant | MODERATE | c.727C>T | p.Leu243Phe | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 880/5296 | 727/2247 | 243/748 | chr10 | 49622125 | |||
| chr10:49622138 | C | T | 1 | a0014 | 1 | HG03195.hp2 | missense_variant | MODERATE | c.740C>T | p.Ala247Val | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/15 | 893/5296 | 740/2247 | 247/748 | chr10 | 49622138 | |||
| chr10:49625616 | C | T | 2 | a0010 a0013 |
2 | HG01123.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.896C>T | p.Pro299Leu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1049/5296 | 896/2247 | 299/748 | chr10 | 49625616 | |||
| chr10:49627707 | G | A | 1 | a0016 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1186/5296 | 1033/2247 | 345/748 | chr10 | 49627707 | |||
| chr10:49627743 | G | A | 1 | a0012 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.1069G>A | p.Gly357Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1222/5296 | 1069/2247 | 357/748 | chr10 | 49627743 | |||
| chr10:49646528 | G | C | 1 | a0005 | 2 | NA18522.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.1135G>C | p.Asp379His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1288/5296 | 1135/2247 | 379/748 | chr10 | 49646528 | |||
| chr10:49648606 | G | A | 14 | a0001 a0002 a0003 others(11): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
missense_variant&splice_region_variant | MODERATE | c.1381G>A | p.Val461Met | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/15 | 1534/5296 | 1381/2247 | 461/748 | chr10 | 49648606 | |||
| chr10:49655142 | G | A | 1 | a0009 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.1682G>A | p.Arg561Gln | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1835/5296 | 1682/2247 | 561/748 | chr10 | 49655142 | |||
| chr10:49655178 | C | A | 1 | a0015 | 1 | NA18997.hp2 | missense_variant | MODERATE | c.1718C>A | p.Ala573Asp | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1871/5296 | 1718/2247 | 573/748 | chr10 | 49655178 | |||
| chr10:49655210 | G | A | 1 | a0011 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.1750G>A | p.Val584Met | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1903/5296 | 1750/2247 | 584/748 | chr10 | 49655210 | |||
| chr10:49664982 | C | T | 2 | a0007 a0016 |
3 | NA18948.hp1 NA18962.hp2 NA19068.hp1 |
missense_variant | MODERATE | c.2183C>T | p.Thr728Ile | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2336/5296 | 2183/2247 | 728/748 | chr10 | 49664982 | |||
| chr10:49665021 | G | A | 1 | a0017 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.2222G>A | p.Arg741Lys | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2375/5296 | 2222/2247 | 741/748 | chr10 | 49665021 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49616542 | G | A | 1 | a0001c0019 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.327G>A | p.Thr109Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/15 | 480/5296 | 327/2247 | 109/748 | chr10 | 49616542 | |||
| chr10:49625509 | G | A | 1 | a0004c0025 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.789G>A | p.Leu263Leu | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 942/5296 | 789/2247 | 263/748 | chr10 | 49625509 | |||
| chr10:49625623 | T | C | 4 | a0001c0011 a0001c0026 a0001c0027 others(1): Show |
7 | HG01891.hp1 HG01981.hp1 HG02145.hp1 others(4): Show |
synonymous_variant | LOW | c.903T>C | p.Pro301Pro | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1056/5296 | 903/2247 | 301/748 | chr10 | 49625623 | |||
| chr10:49625629 | C | T | 1 | a0001c0035 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.909C>T | p.His303His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/15 | 1062/5296 | 909/2247 | 303/748 | chr10 | 49625629 | |||
| chr10:49627736 | G | A | 1 | a0001c0030 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.1062G>A | p.Thr354Thr | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/15 | 1215/5296 | 1062/2247 | 354/748 | chr10 | 49627736 | |||
| chr10:49646515 | C | T | 3 | a0001c0010 a0001c0017 a0001c0028 |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.1122C>T | p.Asn374Asn | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1275/5296 | 1122/2247 | 374/748 | chr10 | 49646515 | |||
| chr10:49646524 | G | A | 3 | a0001c0010 a0001c0017 a0001c0028 |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
synonymous_variant | LOW | c.1131G>A | p.Ser377Ser | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1284/5296 | 1131/2247 | 377/748 | chr10 | 49646524 | |||
| chr10:49646566 | C | T | 1 | a0001c0027 | 1 | HG01981.hp1 | synonymous_variant | LOW | c.1173C>T | p.Asp391Asp | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1326/5296 | 1173/2247 | 391/748 | chr10 | 49646566 | |||
| chr10:49646641 | C | T | 1 | a0003c0039 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.1248C>T | p.Asn416Asn | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/15 | 1401/5296 | 1248/2247 | 416/748 | chr10 | 49646641 | |||
| chr10:49649533 | C | A | 1 | a0002c0020 | 1 | HG03927.hp2 | synonymous_variant | LOW | c.1408C>A | p.Arg470Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/15 | 1561/5296 | 1408/2247 | 470/748 | chr10 | 49649533 | |||
| chr10:49655101 | T | C | 27 | a0001c0001 a0001c0005 a0001c0011 others(24): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
synonymous_variant | LOW | c.1641T>C | p.His547His | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1794/5296 | 1641/2247 | 547/748 | chr10 | 49655101 | |||
| chr10:49655134 | C | T | 4 | a0001c0010 a0001c0013 a0001c0026 others(1): Show |
14 | HG01167.hp2 HG01884.hp1 HG01891.hp1 others(11): Show |
synonymous_variant | LOW | c.1674C>T | p.Ser558Ser | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 12/15 | 1827/5296 | 1674/2247 | 558/748 | chr10 | 49655134 | |||
| chr10:49662687 | C | A | 1 | a0001c0015 | 2 | NA19063.hp1 NA19091.hp1 |
synonymous_variant | LOW | c.1882C>A | p.Arg628Arg | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/15 | 2035/5296 | 1882/2247 | 628/748 | chr10 | 49662687 | |||
| chr10:49664866 | C | T | 7 | a0001c0005 a0001c0015 a0002c0012 others(4): Show |
46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
synonymous_variant | LOW | c.2067C>T | p.Ile689Ile | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2220/5296 | 2067/2247 | 689/748 | chr10 | 49664866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614087 | C | G | 2 | a0001c0001t0036 a0014c0037t0035 |
2 | HG02886.hp2 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-103C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 103 | chr10 | 49614087 | ||||||
| chr10:49614134 | C | T | 1 | a0001c0003t0034 | 1 | HG03225.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | chr10 | 49614134 | |||||||
| chr10:49614146 | G | C | 33 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0008 others(30): Show |
167 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(164): Show |
5_prime_UTR_variant | MODIFIER | c.-44G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 44 | chr10 | 49614146 | ||||||
| chr10:49614173 | G | A | 7 | a0001c0001t0014 a0001c0001t0015 a0001c0001t0023 others(4): Show |
10 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-17G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 17 | chr10 | 49614173 | ||||||
| chr10:49614180 | T | G | 84 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(81): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
5_prime_UTR_variant | MODIFIER | c.-10T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/15 | 10 | chr10 | 49614180 | ||||||
| chr10:49665257 | T | A | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 211 | chr10 | 49665257 | ||||||
| chr10:49665439 | C | T | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 393 | chr10 | 49665439 | ||||||
| chr10:49665577 | G | A | 1 | a0011c0032t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*531G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 531 | chr10 | 49665577 | ||||||
| chr10:49665982 | T | C | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0015 others(10): Show |
136 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(133): Show |
3_prime_UTR_variant | MODIFIER | c.*936T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 936 | chr10 | 49665982 | ||||||
| chr10:49666237 | CCCAGCCC others(11): Show |
C | 2 | a0001c0001t0016 a0001c0001t0028 |
4 | HG02486.hp2 HG02976.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1233_*1250delCCCA others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1233 | INFO_REALIGN_3_PRIME | chr10 | 49666237 | |||||
| chr10:49666300 | G | A | 1 | a0001c0001t0019 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1254G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1254 | chr10 | 49666300 | ||||||
| chr10:49666327 | G | C | 1 | a0001c0001t0026 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1281G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1281 | chr10 | 49666327 | ||||||
| chr10:49666392 | C | T | 3 | a0001c0001t0012 a0002c0002t0012 a0002c0020t0012 |
6 | HG03834.hp1 HG03927.hp2 HG04115.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1346C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1346 | chr10 | 49666392 | ||||||
| chr10:49666503 | C | A | 16 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(13): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1457C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1457 | chr10 | 49666503 | ||||||
| chr10:49666514 | C | G | 16 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0013 others(13): Show |
77 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1468C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1468 | chr10 | 49666514 | ||||||
| chr10:49666752 | C | T | 1 | a0001c0027t0031 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1706C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1706 | chr10 | 49666752 | ||||||
| chr10:49666855 | G | T | 1 | a0001c0005t0030 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1809G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1809 | chr10 | 49666855 | ||||||
| chr10:49667004 | C | G | 1 | a0001c0003t0021 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1958C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1958 | chr10 | 49667004 | ||||||
| chr10:49667028 | G | A | 1 | a0001c0003t0020 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1982G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 1982 | chr10 | 49667028 | ||||||
| chr10:49667071 | T | C | 1 | a0001c0011t0022 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2025T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2025 | chr10 | 49667071 | ||||||
| chr10:49667253 | C | T | 9 | a0001c0001t0006 a0001c0003t0006 a0001c0003t0010 others(6): Show |
54 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*2207C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2207 | chr10 | 49667253 | ||||||
| chr10:49667355 | C | T | 1 | a0003c0004t0027 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2309C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2309 | chr10 | 49667355 | ||||||
| chr10:49667377 | A | G | 1 | a0001c0001t0018 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2331A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2331 | chr10 | 49667377 | ||||||
| chr10:49667456 | T | C | 33 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(30): Show |
200 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*2410T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2410 | chr10 | 49667456 | ||||||
| chr10:49667602 | C | G | 3 | a0001c0003t0034 a0001c0011t0024 a0001c0011t0029 |
3 | HG02258.hp2 HG03225.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2556C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2556 | chr10 | 49667602 | ||||||
| chr10:49667624 | G | C | 1 | a0002c0002t0017 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2578G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2578 | chr10 | 49667624 | ||||||
| chr10:49667882 | A | T | 1 | a0011c0032t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2836A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 15/15 | 2836 | chr10 | 49667882 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:49614513 | T | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.286+38T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614513 | |||||||
| chr10:49614519 | G | T | 1 | a0001c0013t0032g0378 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.286+44G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614519 | |||||||
| chr10:49614716 | C | T | 1 | a0004c0009t0003g0377 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.286+241C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614716 | |||||||
| chr10:49614734 | A | G | 13 | a0002c0002t0002g0034 a0002c0002t0002g0373 a0002c0002t0007g0366 others(10): Show |
14 | HG00597.hp2 HG02155.hp2 HG03710.hp2 others(11): Show |
intron_variant | MODIFIER | c.286+259A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614734 | |||||||
| chr10:49614889 | A | G | 3 | a0001c0003t0034g0362 a0001c0026t0005g0363 a0001c0028t0005g0364 |
3 | HG01891.hp1 HG02145.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.286+414A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614889 | |||||||
| chr10:49614939 | G | A | 5 | a0001c0001t0007g0039 a0001c0001t0007g0040 a0001c0001t0008g0003 others(2): Show |
7 | HG00140.hp2 HG00738.hp2 HG01167.hp1 others(4): Show |
intron_variant | MODIFIER | c.286+464G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614939 | |||||||
| chr10:49614992 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.286+517G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49614992 | |||||||
| chr10:49615001 | C | CACAG | 370 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(367): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.286+529_286+530ins others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr10 | 49615001 | ||||||
| chr10:49615158 | G | C | 2 | a0001c0010t0003g0048 a0001c0010t0003g0049 |
2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.286+683G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615158 | |||||||
| chr10:49615166 | G | C | 1 | a0003c0004t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.286+691G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615166 | |||||||
| chr10:49615166 | G | T | 1 | a0001c0001t0002g0361 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.286+691G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615166 | |||||||
| chr10:49615397 | G | A | 1 | a0001c0001t0007g0051 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.286+922G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615397 | |||||||
| chr10:49615465 | A | G | 1 | a0001c0001t0001g0033 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.286+990A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615465 | |||||||
| chr10:49615706 | A | G | 1 | a0001c0003t0006g0360 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.287-796A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615706 | |||||||
| chr10:49615784 | G | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(18): Show |
25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-718G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615784 | |||||||
| chr10:49615796 | C | T | 2 | a0002c0008t0008g0359 a0002c0008t0010g0358 |
2 | HG00738.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.287-706C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615796 | |||||||
| chr10:49615838 | A | G | 1 | a0002c0002t0007g0357 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.287-664A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615838 | |||||||
| chr10:49615880 | G | A | 1 | a0002c0012t0009g0365 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.287-622G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615880 | |||||||
| chr10:49615922 | C | A | 1 | a0001c0003t0020g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.287-580C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615922 | |||||||
| chr10:49615935 | C | T | 21 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(18): Show |
25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-567C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615935 | |||||||
| chr10:49615939 | A | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.287-563A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615939 | |||||||
| chr10:49615992 | C | T | 23 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(20): Show |
27 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.287-510C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49615992 | |||||||
| chr10:49616018 | C | T | 1 | a0001c0003t0006g0354 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.287-484C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616018 | |||||||
| chr10:49616060 | C | T | 1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.287-442C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616060 | |||||||
| chr10:49616071 | G | A | 64 | a0002c0002t0002g0004 a0002c0002t0002g0009 a0002c0002t0002g0010 others(61): Show |
71 | HG00323.hp1 HG00597.hp2 HG00639.hp1 others(68): Show |
intron_variant | MODIFIER | c.287-431G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616071 | |||||||
| chr10:49616198 | C | A | 21 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(18): Show |
25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.287-304C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616198 | |||||||
| chr10:49616433 | G | C | 1 | a0001c0001t0004g0111 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.287-69G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 1/14 | chr10 | 49616433 | |||||||
| chr10:49616702 | T | C | 1 | a0001c0001t0002g0112 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.387+100T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49616702 | |||||||
| chr10:49616980 | C | T | 1 | a0001c0001t0007g0352 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.387+378C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49616980 | |||||||
| chr10:49617020 | A | G | 2 | a0001c0001t0006g0350 a0004c0025t0003g0351 |
2 | HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.387+418A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617020 | |||||||
| chr10:49617055 | C | T | 2 | a0001c0001t0001g0348 a0001c0001t0004g0349 |
2 | HG01070.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.387+453C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617055 | |||||||
| chr10:49617116 | C | T | 283 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0029 others(280): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.387+514C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617116 | |||||||
| chr10:49617139 | C | G | 1 | a0001c0001t0003g0347 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.387+537C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617139 | |||||||
| chr10:49617145 | C | T | 65 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0297 others(62): Show |
74 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.387+543C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617145 | |||||||
| chr10:49617170 | TCTTCCCC | T | 4 | a0001c0001t0002g0291 a0001c0001t0008g0292 a0001c0001t0008g0294 others(1): Show |
4 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(1): Show |
intron_variant | MODIFIER | c.387+583_387+589del others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr10 | 49617170 | ||||||
| chr10:49617272 | T | C | 206 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0169 others(203): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.387+670T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617272 | |||||||
| chr10:49617607 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.387+1005G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617607 | |||||||
| chr10:49617730 | A | G | 1 | a0001c0003t0006g0346 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.387+1128A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617730 | |||||||
| chr10:49617735 | C | G | 21 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(18): Show |
25 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(22): Show |
intron_variant | MODIFIER | c.387+1133C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617735 | |||||||
| chr10:49617749 | G | T | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0017t0004g0228 |
3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.387+1147G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617749 | |||||||
| chr10:49617776 | G | T | 2 | a0001c0003t0006g0345 a0001c0005t0005g0344 |
2 | HG00609.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.387+1174G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617776 | |||||||
| chr10:49617885 | C | G | 167 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0031 others(164): Show |
185 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.387+1283C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617885 | |||||||
| chr10:49617999 | C | G | 1 | a0002c0002t0007g0110 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.387+1397C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49617999 | |||||||
| chr10:49618000 | A | C | 366 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(363): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.387+1398A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618000 | |||||||
| chr10:49618051 | A | G | 2 | a0001c0001t0002g0212 a0001c0001t0018g0213 |
2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.387+1449A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618051 | |||||||
| chr10:49618117 | A | G | 360 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0029 others(357): Show |
398 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(395): Show |
intron_variant | MODIFIER | c.387+1515A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618117 | |||||||
| chr10:49618231 | A | G | 1 | a0004c0009t0011g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388-1494A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618231 | |||||||
| chr10:49618361 | C | T | 1 | a0004c0009t0003g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.388-1364C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618361 | |||||||
| chr10:49618552 | A | G | 68 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0169 others(65): Show |
78 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.388-1173A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618552 | |||||||
| chr10:49618652 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0229 |
3 | HG02055.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.388-1073T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618652 | |||||||
| chr10:49618684 | C | G | 1 | a0001c0001t0001g0343 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.388-1041C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618684 | |||||||
| chr10:49618816 | C | G | 160 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0031 others(157): Show |
178 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.388-909C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618816 | |||||||
| chr10:49618839 | G | A | 1 | a0001c0001t0006g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.388-886G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49618839 | |||||||
| chr10:49619143 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.388-582C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619143 | |||||||
| chr10:49619144 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.388-581A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619144 | |||||||
| chr10:49619657 | G | C | 10 | a0001c0001t0001g0282 a0001c0001t0014g0276 a0001c0001t0014g0278 others(7): Show |
11 | HG01109.hp1 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.388-68G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619657 | |||||||
| chr10:49619675 | C | T | 62 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0311 others(59): Show |
71 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.388-50C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 2/14 | chr10 | 49619675 | |||||||
| chr10:49619953 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.579+37C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49619953 | |||||||
| chr10:49620018 | A | C | 22 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0054 others(19): Show |
26 | HG00140.hp1 HG00323.hp2 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.579+102A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620018 | |||||||
| chr10:49620156 | T | A | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0017t0004g0228 |
3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.579+240T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620156 | |||||||
| chr10:49620212 | G | T | 1 | a0002c0002t0002g0109 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.580-283G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620212 | |||||||
| chr10:49620247 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.580-248G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620247 | |||||||
| chr10:49620430 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.580-65T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620430 | |||||||
| chr10:49620431 | C | T | 1 | a0001c0001t0001g0068 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.580-64C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620431 | |||||||
| chr10:49620460 | G | A | 366 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(363): Show |
406 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(403): Show |
intron_variant | MODIFIER | c.580-35G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 3/14 | chr10 | 49620460 | |||||||
| chr10:49620629 | T | C | 1 | a0003c0007t0003g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.698+16T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620629 | |||||||
| chr10:49620673 | C | T | 1 | a0001c0001t0003g0067 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.698+60C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620673 | |||||||
| chr10:49620750 | C | T | 1 | a0001c0003t0033g0046 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.698+137C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620750 | |||||||
| chr10:49620809 | A | G | 2 | a0001c0001t0001g0290 a0001c0001t0016g0026 |
3 | HG02258.hp1 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.698+196A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620809 | |||||||
| chr10:49620912 | G | A | 2 | a0001c0003t0010g0170 a0001c0019t0002g0171 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.698+299G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620912 | |||||||
| chr10:49620916 | C | A | 1 | a0001c0001t0008g0003 | 3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.698+303C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49620916 | |||||||
| chr10:49621029 | G | C | 1 | a0005c0014t0004g0284 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.698+416G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621029 | |||||||
| chr10:49621068 | G | A | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.698+455G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621068 | |||||||
| chr10:49621173 | A | T | 104 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0029 others(101): Show |
117 | HG00280.hp1 HG00423.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.698+560A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621173 | |||||||
| chr10:49621201 | G | A | 1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.698+588G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621201 | |||||||
| chr10:49621218 | C | T | 43 | a0001c0001t0001g0169 a0001c0001t0001g0215 a0001c0001t0001g0297 others(40): Show |
45 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(42): Show |
intron_variant | MODIFIER | c.698+605C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621218 | |||||||
| chr10:49621256 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.698+643A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621256 | |||||||
| chr10:49621384 | T | A | 4 | a0001c0001t0001g0033 a0001c0001t0002g0175 a0001c0001t0004g0230 others(1): Show |
5 | HG00735.hp2 HG01106.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.699-713T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621384 | |||||||
| chr10:49621434 | G | A | 166 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0029 others(163): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.699-663G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621434 | |||||||
| chr10:49621439 | A | T | 65 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0224 others(62): Show |
72 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.699-658A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621439 | |||||||
| chr10:49621550 | G | A | 1 | a0001c0013t0032g0378 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.699-547G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621550 | |||||||
| chr10:49621567 | G | A | 33 | a0001c0001t0001g0029 a0001c0001t0001g0311 a0001c0001t0001g0312 others(30): Show |
37 | HG00609.hp2 HG00621.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.699-530G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621567 | |||||||
| chr10:49621674 | C | T | 1 | a0001c0001t0008g0211 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.699-423C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621674 | |||||||
| chr10:49621717 | G | A | 3 | a0001c0001t0001g0052 a0001c0027t0031g0174 a0001c0035t0003g0233 |
3 | HG00639.hp2 HG01981.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.699-380G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621717 | |||||||
| chr10:49621749 | T | A | 4 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0003t0034g0362 others(1): Show |
5 | HG02055.hp1 HG02818.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.699-348T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621749 | |||||||
| chr10:49621782 | A | G | 369 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(366): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.699-315A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621782 | |||||||
| chr10:49621847 | G | T | 86 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0031 others(83): Show |
97 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.699-250G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621847 | |||||||
| chr10:49621857 | GGCAAGAA others(15): Show |
G | 1 | a0001c0001t0015g0023 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.699-236_699-215del others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621857 | ||||||
| chr10:49621861 | A | AGAACCAC others(15): Show |
2 | a0002c0002t0007g0104 a0002c0002t0007g0357 |
2 | NA18995.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.699-214_699-193dup others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621861 | ||||||
| chr10:49621861 | AGAACCAC others(15): Show |
A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0220 a0001c0001t0001g0290 others(7): Show |
13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.699-214_699-193del others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621861 | ||||||
| chr10:49621907 | C | T | 6 | a0001c0003t0006g0345 a0001c0011t0003g0214 a0001c0011t0022g0283 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.699-190C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621907 | |||||||
| chr10:49621928 | G | A | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.699-169G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621928 | |||||||
| chr10:49621928 | G | T | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0017t0004g0228 |
3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.699-169G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49621928 | |||||||
| chr10:49621964 | G | GAGGGAGG others(59): Show |
324 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0029 others(321): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(355): Show |
intron_variant | MODIFIER | c.699-122_699-57dupA others(65): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | ||||||
| chr10:49621964 | G | GAGGGAGG others(125): Show |
31 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0056 others(28): Show |
34 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.699-57_699-56insAA others(130): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | ||||||
| chr10:49621964 | G | GAGGGAGG others(191): Show |
1 | a0001c0001t0002g0176 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.699-57_699-56insAA others(196): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | ||||||
| chr10:49621964 | G | GAGGGAGG others(455): Show |
1 | a0001c0001t0002g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.699-57_699-56insAA others(460): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621964 | ||||||
| chr10:49621972 | G | GAGAAGGG others(48): Show |
1 | a0002c0002t0007g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.699-112_699-58dupA others(54): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49621972 | ||||||
| chr10:49622009 | G | GGAAGGAG others(59): Show |
1 | a0001c0001t0016g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.699-57_699-56insAA others(64): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr10 | 49622009 | ||||||
| chr10:49622022 | G | GAGCGGCC others(87): Show |
1 | a0001c0001t0004g0323 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-75_699-74insAG others(92): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622022 | |||||||
| chr10:49622038 | G | C | 1 | a0001c0001t0004g0323 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-59G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622038 | |||||||
| chr10:49622039 | A | G | 1 | a0001c0001t0004g0323 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.699-58A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622039 | |||||||
| chr10:49622041 | G | T | 3 | a0001c0001t0004g0323 a0001c0005t0005g0065 a0001c0005t0005g0066 |
3 | HG00621.hp1 HG02074.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.699-56G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 4/14 | chr10 | 49622041 | |||||||
| chr10:49622205 | T | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0014g0276 others(2): Show |
6 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.752+55T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622205 | |||||||
| chr10:49622272 | T | C | 2 | a0001c0003t0006g0345 a0001c0005t0005g0344 |
2 | HG00609.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.752+122T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622272 | |||||||
| chr10:49622287 | C | T | 3 | a0002c0002t0002g0073 a0002c0002t0002g0074 a0002c0002t0002g0075 |
3 | HG02015.hp2 HG02083.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.752+137C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622287 | |||||||
| chr10:49622531 | G | A | 1 | a0001c0005t0005g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.752+381G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622531 | |||||||
| chr10:49622533 | G | C | 1 | a0002c0008t0010g0374 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.752+383G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622533 | |||||||
| chr10:49622602 | C | T | 1 | a0002c0002t0007g0375 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.752+452C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622602 | |||||||
| chr10:49622652 | C | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+502C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622652 | |||||||
| chr10:49622703 | G | T | 10 | a0001c0001t0001g0025 a0001c0001t0001g0220 a0001c0001t0001g0290 others(7): Show |
13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.752+553G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49622703 | |||||||
| chr10:49623001 | G | A | 1 | a0001c0001t0007g0234 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.752+851G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623001 | |||||||
| chr10:49623010 | C | G | 25 | a0001c0001t0001g0025 a0001c0001t0001g0220 a0001c0001t0001g0290 others(22): Show |
29 | HG00735.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.752+860C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623010 | |||||||
| chr10:49623069 | C | T | 1 | a0001c0027t0031g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.752+919C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623069 | |||||||
| chr10:49623117 | T | TTGTCTCC others(8): Show |
1 | a0003c0004t0001g0132 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.752+973_752+987dup others(15): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49623117 | ||||||
| chr10:49623155 | C | G | 1 | a0003c0007t0006g0162 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.752+1005C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623155 | |||||||
| chr10:49623156 | G | A | 1 | a0001c0001t0016g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.752+1006G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623156 | |||||||
| chr10:49623202 | C | T | 3 | a0001c0001t0001g0052 a0001c0003t0034g0362 a0001c0035t0003g0233 |
3 | HG00639.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.752+1052C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623202 | |||||||
| chr10:49623203 | G | A | 1 | a0001c0001t0008g0037 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.752+1053G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623203 | |||||||
| chr10:49623283 | C | CTT | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1133_752+1134i others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623283 | |||||||
| chr10:49623462 | C | T | 1 | a0001c0001t0016g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.752+1312C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623462 | |||||||
| chr10:49623498 | A | G | 1 | a0001c0001t0007g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.752+1348A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623498 | |||||||
| chr10:49623531 | T | C | 1 | a0002c0002t0002g0076 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.752+1381T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623531 | |||||||
| chr10:49623605 | G | A | 10 | a0001c0001t0001g0025 a0001c0001t0001g0220 a0001c0001t0001g0290 others(7): Show |
13 | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.752+1455G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623605 | |||||||
| chr10:49623632 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.752+1482C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623632 | |||||||
| chr10:49623781 | T | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1631T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623781 | |||||||
| chr10:49623798 | C | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.752+1648C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623798 | |||||||
| chr10:49623808 | T | C | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.752+1658T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623808 | |||||||
| chr10:49623865 | G | T | 2 | a0001c0001t0001g0338 a0001c0001t0004g0337 |
2 | NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.753-1608G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49623865 | |||||||
| chr10:49624020 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0016g0026 |
3 | HG02258.hp1 HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.753-1453G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624020 | |||||||
| chr10:49624050 | A | T | 2 | a0001c0005t0009g0269 a0007c0016t0009g0268 |
2 | NA18948.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.753-1423A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624050 | |||||||
| chr10:49624055 | G | A | 25 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0270 others(22): Show |
31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.753-1418G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624055 | |||||||
| chr10:49624056 | A | C | 25 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0270 others(22): Show |
31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.753-1417A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624056 | |||||||
| chr10:49624063 | C | T | 62 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0001t0001g0033 others(59): Show |
70 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.753-1410C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624063 | |||||||
| chr10:49624204 | C | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753-1269C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624204 | |||||||
| chr10:49624231 | T | C | 147 | a0001c0001t0001g0054 a0001c0001t0001g0169 a0001c0001t0001g0251 others(144): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.753-1242T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624231 | |||||||
| chr10:49624570 | T | C | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-903T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624570 | |||||||
| chr10:49624639 | C | T | 4 | a0001c0001t0007g0352 a0001c0003t0006g0002 a0001c0005t0005g0298 others(1): Show |
7 | NA18943.hp1 NA18944.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.753-834C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624639 | |||||||
| chr10:49624706 | TGGAA | T | 3 | a0001c0001t0001g0025 a0001c0001t0003g0024 a0001c0003t0003g0286 |
5 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.753-755_753-752del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624706 | ||||||
| chr10:49624718 | A | T | 7 | a0001c0001t0001g0220 a0001c0001t0001g0290 a0001c0001t0003g0287 others(4): Show |
8 | HG01884.hp1 HG02258.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.753-755A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624718 | |||||||
| chr10:49624718 | AGGATGGA others(5): Show |
A | 145 | a0001c0001t0001g0054 a0001c0001t0001g0169 a0001c0001t0001g0251 others(142): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.753-743_753-732del others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624718 | ||||||
| chr10:49624722 | TGGATGGA others(1): Show |
T | 9 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0001t0014g0278 others(6): Show |
10 | HG01109.hp1 HG02886.hp2 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.753-743_753-736del others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624722 | ||||||
| chr10:49624726 | TGGAC | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0003g0219 others(4): Show |
8 | HG01981.hp1 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.753-743_753-740del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624726 | ||||||
| chr10:49624730 | C | T | 13 | a0001c0001t0001g0025 a0001c0001t0001g0220 a0001c0001t0001g0290 others(10): Show |
16 | HG01069.hp2 HG01071.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.753-743C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624730 | |||||||
| chr10:49624730 | CGGAT | C | 3 | a0001c0001t0001g0348 a0001c0001t0004g0349 a0003c0004t0027g0118 |
3 | HG01070.hp1 HG01074.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.753-719_753-716del others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624730 | ||||||
| chr10:49624730 | CGGATGGA others(5): Show |
C | 4 | a0001c0001t0002g0270 a0001c0001t0007g0241 a0001c0003t0010g0236 others(1): Show |
4 | NA18949.hp1 NA18954.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.753-727_753-716del others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr10 | 49624730 | ||||||
| chr10:49624909 | G | T | 1 | a0001c0001t0002g0361 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.753-564G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49624909 | |||||||
| chr10:49625015 | A | G | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-458A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625015 | |||||||
| chr10:49625024 | T | C | 6 | a0001c0011t0003g0214 a0001c0011t0022g0283 a0001c0011t0024g0280 others(3): Show |
6 | HG01891.hp1 HG02145.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.753-449T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625024 | |||||||
| chr10:49625035 | C | T | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.753-438C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625035 | |||||||
| chr10:49625038 | G | A | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.753-435G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625038 | |||||||
| chr10:49625069 | A | G | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-404A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625069 | |||||||
| chr10:49625274 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.753-199G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625274 | |||||||
| chr10:49625310 | C | T | 1 | a0001c0003t0010g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.753-163C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625310 | |||||||
| chr10:49625338 | A | C | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-135A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625338 | |||||||
| chr10:49625447 | C | T | 29 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0220 others(26): Show |
34 | HG01069.hp2 HG01071.hp2 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.753-26C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625447 | |||||||
| chr10:49625457 | C | T | 1 | a0001c0028t0005g0364 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.753-16C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 5/14 | chr10 | 49625457 | |||||||
| chr10:49625793 | G | A | 25 | a0001c0001t0002g0238 a0001c0001t0002g0243 a0001c0001t0002g0270 others(22): Show |
31 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.933+140G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625793 | |||||||
| chr10:49625848 | G | A | 6 | a0001c0001t0011g0172 a0001c0001t0011g0173 a0001c0013t0005g0217 others(3): Show |
6 | HG00735.hp1 HG01243.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.933+195G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625848 | |||||||
| chr10:49625850 | G | A | 2 | a0001c0011t0024g0280 a0001c0011t0029g0216 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.933+197G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625850 | |||||||
| chr10:49625954 | C | A | 1 | a0004c0025t0003g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+301C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49625954 | |||||||
| chr10:49626010 | A | C | 1 | a0001c0005t0005g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.933+357A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626010 | |||||||
| chr10:49626011 | C | A | 3 | a0001c0001t0001g0052 a0001c0003t0034g0362 a0001c0035t0003g0233 |
3 | HG00639.hp2 HG02145.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.933+358C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626011 | |||||||
| chr10:49626065 | T | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0003g0219 others(3): Show |
7 | HG02055.hp1 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.933+412T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626065 | |||||||
| chr10:49626099 | G | T | 2 | a0001c0001t0001g0282 a0001c0001t0023g0281 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.933+446G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626099 | |||||||
| chr10:49626189 | C | T | 2 | a0001c0001t0001g0282 a0001c0001t0023g0281 |
2 | HG02622.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.933+536C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626189 | |||||||
| chr10:49626319 | C | G | 1 | a0004c0025t0003g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+666C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626319 | |||||||
| chr10:49626328 | A | G | 1 | a0004c0025t0003g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.933+675A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626328 | |||||||
| chr10:49626382 | T | C | 1 | a0001c0013t0005g0217 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.933+729T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626382 | |||||||
| chr10:49626425 | C | G | 1 | a0001c0003t0006g0305 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.933+772C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626425 | |||||||
| chr10:49626568 | G | A | 18 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0003g0035 others(15): Show |
20 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(17): Show |
intron_variant | MODIFIER | c.933+915G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626568 | |||||||
| chr10:49626600 | G | A | 3 | a0001c0011t0022g0283 a0001c0026t0005g0363 a0001c0028t0005g0364 |
3 | HG01891.hp1 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.933+947G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626600 | |||||||
| chr10:49626604 | G | A | 12 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0004g0226 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+951G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626604 | |||||||
| chr10:49626608 | C | T | 12 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0004g0226 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.933+955C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626608 | |||||||
| chr10:49626879 | C | T | 1 | a0001c0010t0008g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.934-729C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626879 | |||||||
| chr10:49626932 | A | G | 129 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0056 others(126): Show |
144 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.934-676A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626932 | |||||||
| chr10:49626990 | G | C | 1 | a0001c0001t0001g0056 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.934-618G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49626990 | |||||||
| chr10:49627194 | G | A | 2 | a0001c0001t0002g0271 a0003c0004t0004g0166 |
2 | HG00609.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.934-414G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627194 | |||||||
| chr10:49627217 | C | T | 1 | a0004c0009t0003g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.934-391C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627217 | |||||||
| chr10:49627218 | G | A | 52 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0056 others(49): Show |
62 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.934-390G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627218 | |||||||
| chr10:49627417 | T | C | 1 | a0002c0002t0002g0077 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.934-191T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627417 | |||||||
| chr10:49627427 | C | T | 1 | a0001c0001t0016g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.934-181C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627427 | |||||||
| chr10:49627452 | C | T | 1 | a0001c0001t0016g0218 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.934-156C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627452 | |||||||
| chr10:49627561 | C | T | 1 | a0002c0002t0012g0101 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.934-47C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627561 | |||||||
| chr10:49627565 | G | A | 6 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0001t0015g0023 others(3): Show |
7 | HG01243.hp2 HG01981.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.934-43G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 6/14 | chr10 | 49627565 | |||||||
| chr10:49627793 | G | A | 1 | a0001c0001t0005g0221 | 1 | HG02922.hp2 | splice_region_variant&intron_variant | LOW | c.1111+8G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627793 | |||||||
| chr10:49627830 | G | A | 17 | a0001c0001t0001g0251 a0001c0001t0003g0022 a0001c0001t0003g0041 others(14): Show |
18 | HG01167.hp2 HG01192.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1111+45G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627830 | |||||||
| chr10:49627921 | C | A | 272 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0056 others(269): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1111+136C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49627921 | |||||||
| chr10:49628044 | C | T | 2 | a0002c0002t0007g0102 a0002c0002t0007g0110 |
2 | HG01934.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1111+259C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628044 | |||||||
| chr10:49628102 | G | T | 1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+317G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628102 | |||||||
| chr10:49628126 | G | C | 2 | a0001c0003t0010g0170 a0001c0019t0002g0171 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1111+341G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628126 | |||||||
| chr10:49628350 | G | C | 1 | a0004c0009t0003g0273 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1111+565G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628350 | |||||||
| chr10:49628356 | C | G | 1 | a0002c0002t0009g0100 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1111+571C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628356 | |||||||
| chr10:49628378 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0003g0024 |
4 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+593T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628378 | |||||||
| chr10:49628420 | C | T | 269 | a0001c0001t0001g0007 a0001c0001t0001g0054 a0001c0001t0001g0056 others(266): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.1111+635C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628420 | |||||||
| chr10:49628572 | T | C | 12 | a0001c0001t0001g0224 a0001c0001t0003g0347 a0001c0001t0013g0020 others(9): Show |
13 | HG01891.hp1 HG01981.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111+787T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628572 | |||||||
| chr10:49628686 | G | C | 136 | a0001c0001t0001g0007 a0001c0001t0001g0056 a0001c0001t0001g0058 others(133): Show |
152 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1111+901G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628686 | |||||||
| chr10:49628728 | G | A | 1 | a0002c0002t0012g0078 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1111+943G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628728 | |||||||
| chr10:49628778 | G | T | 2 | a0001c0001t0002g0204 a0001c0001t0002g0205 |
2 | HG04204.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1111+993G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628778 | |||||||
| chr10:49628788 | C | G | 19 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0224 others(16): Show |
23 | HG01243.hp2 HG01981.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1111+1003C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628788 | |||||||
| chr10:49628868 | T | C | 372 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(369): Show |
412 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(409): Show |
intron_variant | MODIFIER | c.1111+1083T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628868 | |||||||
| chr10:49628896 | G | A | 1 | a0003c0004t0004g0156 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1111+1111G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628896 | |||||||
| chr10:49628945 | C | G | 1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+1160C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628945 | |||||||
| chr10:49628987 | C | T | 9 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0002g0235 others(6): Show |
10 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+1202C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628987 | |||||||
| chr10:49628988 | G | A | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1111+1203G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49628988 | |||||||
| chr10:49629043 | C | T | 1 | a0001c0013t0005g0289 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1111+1258C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629043 | |||||||
| chr10:49629125 | A | C | 1 | a0003c0004t0013g0153 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1111+1340A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629125 | |||||||
| chr10:49629150 | C | G | 1 | a0002c0002t0002g0373 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+1365C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629150 | |||||||
| chr10:49629363 | G | C | 1 | a0002c0012t0009g0365 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1111+1578G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629363 | |||||||
| chr10:49629533 | T | C | 4 | a0001c0001t0001g0311 a0001c0005t0005g0301 a0003c0004t0004g0156 others(1): Show |
4 | HG00621.hp2 NA18984.hp2 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.1111+1748T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629533 | |||||||
| chr10:49629711 | C | T | 1 | a0001c0001t0013g0225 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1111+1926C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629711 | |||||||
| chr10:49629733 | G | T | 1 | a0004c0009t0003g0272 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1111+1948G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629733 | |||||||
| chr10:49629795 | G | T | 1 | a0001c0001t0008g0003 | 3 | HG01167.hp1 HG01169.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1111+2010G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629795 | |||||||
| chr10:49629826 | A | C | 1 | a0001c0010t0003g0259 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1111+2041A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629826 | |||||||
| chr10:49629829 | G | A | 1 | a0001c0001t0003g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1111+2044G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629829 | |||||||
| chr10:49629946 | C | G | 40 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0001c0001t0001g0224 others(37): Show |
45 | HG01167.hp2 HG01192.hp1 HG01243.hp2 others(42): Show |
intron_variant | MODIFIER | c.1111+2161C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629946 | |||||||
| chr10:49629949 | C | T | 1 | a0001c0001t0007g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1111+2164C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629949 | |||||||
| chr10:49629956 | A | G | 3 | a0001c0001t0004g0226 a0001c0001t0004g0227 a0001c0017t0004g0228 |
3 | HG02896.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1111+2171A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629956 | |||||||
| chr10:49629995 | C | A | 3 | a0002c0002t0002g0004 a0002c0002t0002g0106 a0002c0012t0009g0079 |
5 | NA18955.hp2 NA18983.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+2210C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49629995 | |||||||
| chr10:49630040 | G | A | 3 | a0001c0001t0004g0285 a0001c0001t0007g0182 a0005c0014t0007g0178 |
3 | HG03139.hp2 NA18522.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1111+2255G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630040 | |||||||
| chr10:49630106 | G | C | 2 | a0001c0001t0001g0025 a0001c0001t0003g0024 |
4 | HG01069.hp2 HG01071.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+2321G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630106 | |||||||
| chr10:49630155 | TCAGTA | T | 3 | a0001c0001t0001g0251 a0001c0001t0003g0035 a0001c0001t0003g0036 |
3 | HG01243.hp2 HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1111+2374_1111+237 others(9): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49630155 | ||||||
| chr10:49630212 | G | A | 2 | a0001c0003t0034g0362 a0001c0035t0003g0233 |
2 | HG00639.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1111+2427G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630212 | |||||||
| chr10:49630583 | C | T | 369 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(366): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1111+2798C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630583 | |||||||
| chr10:49630828 | A | G | 242 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0029 others(239): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.1111+3043A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49630828 | |||||||
| chr10:49631138 | T | C | 5 | a0001c0001t0001g0348 a0001c0001t0004g0349 a0001c0001t0007g0039 others(2): Show |
5 | HG00140.hp2 HG01070.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1111+3353T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631138 | |||||||
| chr10:49631166 | A | T | 1 | a0001c0003t0006g0322 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1111+3381A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631166 | |||||||
| chr10:49631357 | G | A | 92 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0312 others(89): Show |
107 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.1111+3572G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631357 | |||||||
| chr10:49631521 | C | T | 64 | a0001c0001t0001g0312 a0001c0001t0002g0019 a0001c0001t0002g0260 others(61): Show |
70 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.1111+3736C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631521 | |||||||
| chr10:49631598 | G | C | 2 | a0001c0010t0003g0259 a0001c0010t0008g0265 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1111+3813G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631598 | |||||||
| chr10:49631600 | G | T | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+3815G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631600 | |||||||
| chr10:49631836 | G | A | 2 | a0001c0001t0003g0219 a0004c0025t0003g0351 |
2 | HG02615.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1111+4051G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631836 | |||||||
| chr10:49631851 | A | G | 1 | a0004c0025t0003g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1111+4066A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49631851 | |||||||
| chr10:49632044 | T | C | 1 | a0002c0002t0007g0375 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1111+4259T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632044 | |||||||
| chr10:49632151 | C | T | 4 | a0001c0001t0003g0347 a0001c0001t0004g0226 a0001c0001t0004g0227 others(1): Show |
4 | HG01109.hp1 HG06807.hp1 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+4366C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632151 | |||||||
| chr10:49632292 | G | A | 2 | a0001c0026t0005g0363 a0001c0028t0005g0364 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1111+4507G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632292 | |||||||
| chr10:49632615 | A | C | 369 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(366): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1111+4830A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632615 | |||||||
| chr10:49632640 | C | T | 1 | a0001c0001t0014g0279 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1111+4855C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632640 | |||||||
| chr10:49632641 | G | A | 3 | a0002c0002t0002g0081 a0002c0002t0002g0108 a0003c0004t0001g0134 |
3 | HG00673.hp2 HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1111+4856G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632641 | |||||||
| chr10:49632652 | T | C | 9 | a0001c0001t0001g0215 a0001c0001t0001g0224 a0001c0001t0001g0290 others(6): Show |
10 | HG01884.hp1 HG01981.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+4867T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632652 | |||||||
| chr10:49632690 | G | A | 265 | a0001c0001t0001g0007 a0001c0001t0001g0025 a0001c0001t0001g0029 others(262): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.1111+4905G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632690 | |||||||
| chr10:49632740 | T | C | 369 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(366): Show |
409 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(406): Show |
intron_variant | MODIFIER | c.1111+4955T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632740 | |||||||
| chr10:49632851 | G | C | 1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1111+5066G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632851 | |||||||
| chr10:49632868 | C | T | 344 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(341): Show |
381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.1111+5083C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49632868 | |||||||
| chr10:49633420 | G | A | 1 | a0001c0001t0001g0251 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1111+5635G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633420 | |||||||
| chr10:49633530 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1111+5745C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633530 | |||||||
| chr10:49633604 | T | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0290 a0001c0001t0003g0219 others(3): Show |
6 | HG02258.hp1 HG02559.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1111+5819T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633604 | |||||||
| chr10:49633658 | C | T | 284 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(281): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.1111+5873C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633658 | |||||||
| chr10:49633681 | A | G | 1 | a0002c0002t0002g0373 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1111+5896A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633681 | |||||||
| chr10:49633685 | C | T | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1111+5900C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633685 | |||||||
| chr10:49633745 | GC | G | 9 | a0001c0001t0004g0005 a0001c0001t0004g0055 a0001c0001t0005g0264 others(6): Show |
10 | HG01884.hp1 HG01884.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1111+5966delC | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49633745 | ||||||
| chr10:49633978 | C | T | 190 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(187): Show |
211 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.1111+6193C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49633978 | |||||||
| chr10:49634139 | A | C | 38 | a0001c0001t0001g0061 a0001c0001t0001g0348 a0001c0001t0002g0194 others(35): Show |
43 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(40): Show |
intron_variant | MODIFIER | c.1111+6354A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634139 | |||||||
| chr10:49634218 | A | G | 47 | a0001c0001t0001g0169 a0001c0001t0001g0340 a0001c0001t0002g0176 others(44): Show |
50 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.1111+6433A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634218 | |||||||
| chr10:49634270 | G | T | 1 | a0001c0010t0003g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1111+6485G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634270 | |||||||
| chr10:49634288 | G | A | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1111+6503G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634288 | |||||||
| chr10:49634298 | A | G | 1 | a0003c0004t0001g0015 | 2 | NA18612.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1111+6513A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634298 | |||||||
| chr10:49634310 | G | A | 5 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0259 others(2): Show |
5 | HG02257.hp2 HG03041.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1111+6525G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634310 | |||||||
| chr10:49634329 | C | T | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1111+6544C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634329 | |||||||
| chr10:49634391 | G | T | 3 | a0001c0001t0003g0347 a0001c0001t0014g0279 a0001c0027t0031g0174 |
3 | HG01109.hp1 HG01981.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1111+6606G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634391 | |||||||
| chr10:49634462 | T | C | 9 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(6): Show |
11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+6677T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634462 | |||||||
| chr10:49634537 | T | C | 124 | a0001c0001t0001g0029 a0001c0001t0001g0312 a0001c0001t0001g0340 others(121): Show |
136 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1111+6752T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634537 | |||||||
| chr10:49634538 | G | C | 123 | a0001c0001t0001g0029 a0001c0001t0001g0312 a0001c0001t0001g0340 others(120): Show |
135 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.1111+6753G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634538 | |||||||
| chr10:49634610 | T | C | 2 | a0001c0010t0003g0223 a0001c0028t0005g0364 |
2 | HG02145.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1111+6825T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634610 | |||||||
| chr10:49634657 | T | G | 2 | a0001c0001t0006g0350 a0001c0011t0022g0283 |
2 | HG02559.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1111+6872T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634657 | |||||||
| chr10:49634766 | C | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+6981C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634766 | |||||||
| chr10:49634842 | A | G | 365 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(362): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
intron_variant | MODIFIER | c.1111+7057A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634842 | |||||||
| chr10:49634990 | C | T | 108 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(105): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1111+7205C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634990 | |||||||
| chr10:49634995 | T | C | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+7210T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49634995 | |||||||
| chr10:49635062 | T | A | 128 | a0001c0001t0001g0029 a0001c0001t0001g0312 a0001c0001t0001g0340 others(125): Show |
140 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(137): Show |
intron_variant | MODIFIER | c.1111+7277T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635062 | |||||||
| chr10:49635080 | C | T | 1 | a0001c0001t0007g0232 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1111+7295C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635080 | |||||||
| chr10:49635133 | A | G | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+7348A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635133 | |||||||
| chr10:49635221 | T | G | 1 | a0003c0007t0006g0164 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1111+7436T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635221 | |||||||
| chr10:49635543 | G | A | 44 | a0001c0001t0001g0340 a0001c0001t0002g0176 a0001c0001t0002g0184 others(41): Show |
46 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1111+7758G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635543 | |||||||
| chr10:49635598 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+7813G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635598 | |||||||
| chr10:49635683 | G | A | 96 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(93): Show |
109 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1111+7898G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635683 | |||||||
| chr10:49635730 | C | G | 12 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(9): Show |
13 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.1111+7945C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635730 | |||||||
| chr10:49635811 | T | C | 98 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(95): Show |
111 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.1111+8026T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49635811 | |||||||
| chr10:49636093 | C | T | 9 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(6): Show |
11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+8308C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636093 | |||||||
| chr10:49636106 | A | G | 1 | a0001c0026t0005g0363 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1111+8321A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636106 | |||||||
| chr10:49636119 | G | A | 1 | a0003c0006t0005g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1111+8334G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636119 | |||||||
| chr10:49636161 | C | T | 3 | a0001c0001t0007g0051 a0001c0003t0010g0018 a0001c0003t0010g0239 |
4 | HG01516.hp2 HG01517.hp1 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+8376C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636161 | |||||||
| chr10:49636310 | A | G | 1 | a0001c0001t0005g0221 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1111+8525A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636310 | |||||||
| chr10:49636372 | G | A | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+8587G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636372 | |||||||
| chr10:49636519 | G | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+8734G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636519 | |||||||
| chr10:49636560 | C | G | 10 | a0001c0001t0001g0224 a0001c0001t0003g0024 a0001c0001t0004g0005 others(7): Show |
12 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1111+8775C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636560 | |||||||
| chr10:49636582 | G | A | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+8797G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636582 | |||||||
| chr10:49636662 | T | C | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1111+8877T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636662 | |||||||
| chr10:49636692 | C | G | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1111+8907C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636692 | |||||||
| chr10:49636729 | C | T | 1 | a0001c0030t0004g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1111+8944C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636729 | |||||||
| chr10:49636942 | T | C | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1111+9157T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636942 | |||||||
| chr10:49636957 | CTTA | C | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1111+9177_1111+917 others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49636957 | ||||||
| chr10:49636974 | G | A | 1 | a0003c0006t0005g0152 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1111+9189G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636974 | |||||||
| chr10:49636981 | G | T | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1111+9196G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49636981 | |||||||
| chr10:49637011 | G | A | 108 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(105): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1111+9226G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637011 | |||||||
| chr10:49637040 | C | CT | 29 | a0001c0001t0001g0021 a0001c0001t0001g0229 a0001c0001t0001g0312 others(26): Show |
33 | HG00735.hp1 HG00738.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1111+9266dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49637040 | ||||||
| chr10:49637071 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1111+9286T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637071 | |||||||
| chr10:49637094 | C | T | 9 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(6): Show |
11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1111+9309C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637094 | |||||||
| chr10:49637153 | A | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-9352A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637153 | |||||||
| chr10:49637250 | C | A | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-9255C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637250 | |||||||
| chr10:49637291 | A | G | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-9214A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637291 | |||||||
| chr10:49637371 | T | A | 8 | a0001c0003t0006g0002 a0001c0003t0006g0330 a0001c0003t0006g0345 others(5): Show |
11 | NA18944.hp1 NA18952.hp2 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-9134T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637371 | |||||||
| chr10:49637549 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0002g0261 |
3 | HG02615.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1112-8956C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49637549 | |||||||
| chr10:49638149 | GTCT | G | 4 | a0001c0001t0007g0181 a0001c0001t0008g0294 a0001c0030t0004g0310 others(1): Show |
4 | HG01081.hp1 HG01358.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-8351_1112-834 others(7): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49638149 | ||||||
| chr10:49638221 | A | C | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-8284A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638221 | |||||||
| chr10:49638226 | G | A | 1 | a0001c0005t0005g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1112-8279G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638226 | |||||||
| chr10:49638230 | T | C | 8 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(5): Show |
8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-8275T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638230 | |||||||
| chr10:49638291 | T | G | 1 | a0003c0007t0006g0165 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1112-8214T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638291 | |||||||
| chr10:49638520 | C | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7985C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638520 | |||||||
| chr10:49638836 | A | C | 62 | a0001c0001t0001g0029 a0001c0001t0003g0219 a0001c0001t0004g0055 others(59): Show |
70 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(67): Show |
intron_variant | MODIFIER | c.1112-7669A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638836 | |||||||
| chr10:49638935 | T | TA | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1112-7562dupA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49638935 | ||||||
| chr10:49638953 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7552G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638953 | |||||||
| chr10:49638990 | C | T | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-7515C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638990 | |||||||
| chr10:49638996 | G | A | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-7509G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49638996 | |||||||
| chr10:49639016 | G | A | 108 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(105): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-7489G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639016 | |||||||
| chr10:49639096 | G | A | 1 | a0010c0018t0003g0324 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1112-7409G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639096 | |||||||
| chr10:49639182 | C | A | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-7323C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639182 | |||||||
| chr10:49639282 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-7223G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639282 | |||||||
| chr10:49639475 | GA | G | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1112-7020delA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639475 | ||||||
| chr10:49639538 | TATAC | T | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-6965_1112-696 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639538 | ||||||
| chr10:49639540 | TAC | T | 3 | a0001c0001t0001g0052 a0001c0001t0013g0225 a0002c0008t0010g0094 |
3 | HG02145.hp2 HG02572.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1112-6937_1112-693 others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | ||||||
| chr10:49639540 | TACAC | T | 73 | a0001c0001t0001g0029 a0001c0001t0001g0282 a0001c0001t0001g0290 others(70): Show |
82 | HG00099.hp1 HG00544.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.1112-6939_1112-693 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | ||||||
| chr10:49639540 | TACACAC | T | 196 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(193): Show |
217 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1112-6941_1112-693 others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | ||||||
| chr10:49639540 | TACACACA others(1): Show |
T | 80 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(77): Show |
90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1112-6943_1112-693 others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49639540 | ||||||
| chr10:49639542 | C | T | 8 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(5): Show |
8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-6963C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639542 | |||||||
| chr10:49639546 | C | T | 3 | a0001c0001t0003g0347 a0001c0001t0014g0279 a0001c0003t0034g0362 |
3 | HG01109.hp1 HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1112-6959C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639546 | |||||||
| chr10:49639565 | ACACATAT others(3): Show |
A | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-6939_1112-693 others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639565 | |||||||
| chr10:49639578 | T | G | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-6927T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639578 | |||||||
| chr10:49639790 | T | G | 8 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(5): Show |
8 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1112-6715T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639790 | |||||||
| chr10:49639855 | C | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-6650C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639855 | |||||||
| chr10:49639906 | C | A | 5 | a0001c0001t0001g0311 a0003c0004t0001g0139 a0003c0004t0001g0140 others(2): Show |
5 | NA18970.hp1 NA18985.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.1112-6599C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639906 | |||||||
| chr10:49639951 | C | T | 108 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(105): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-6554C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639951 | |||||||
| chr10:49639980 | C | T | 2 | a0001c0003t0008g0017 a0003c0004t0004g0130 |
3 | HG02895.hp2 HG02897.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.1112-6525C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49639980 | |||||||
| chr10:49640017 | C | A | 33 | a0001c0001t0001g0061 a0001c0001t0001g0348 a0001c0001t0002g0194 others(30): Show |
38 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.1112-6488C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640017 | |||||||
| chr10:49640334 | T | A | 9 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(6): Show |
11 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1112-6171T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640334 | |||||||
| chr10:49640468 | C | A | 1 | a0002c0008t0010g0376 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1112-6037C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640468 | |||||||
| chr10:49640501 | T | TG | 84 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(81): Show |
94 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.1112-5998dupG | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49640501 | ||||||
| chr10:49640708 | G | A | 3 | a0001c0001t0004g0258 a0001c0001t0004g0285 a0001c0001t0007g0182 |
3 | HG03139.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1112-5797G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640708 | |||||||
| chr10:49640709 | G | T | 1 | a0014c0037t0035g0296 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1112-5796G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640709 | |||||||
| chr10:49640719 | A | C | 3 | a0001c0011t0024g0280 a0001c0011t0029g0216 a0001c0027t0031g0174 |
3 | HG01981.hp1 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1112-5786A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640719 | |||||||
| chr10:49640808 | T | G | 1 | a0001c0001t0003g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1112-5697T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640808 | |||||||
| chr10:49640822 | G | A | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-5683G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49640822 | |||||||
| chr10:49641007 | AACAG | A | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-5494_1112-549 others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49641007 | ||||||
| chr10:49641153 | G | C | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-5352G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641153 | |||||||
| chr10:49641204 | G | T | 1 | a0001c0026t0005g0363 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1112-5301G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641204 | |||||||
| chr10:49641296 | T | G | 96 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(93): Show |
109 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(106): Show |
intron_variant | MODIFIER | c.1112-5209T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641296 | |||||||
| chr10:49641341 | CCTTCCTC others(7): Show |
C | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1112-5160_1112-514 others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49641341 | ||||||
| chr10:49641355 | T | C | 6 | a0001c0005t0009g0247 a0001c0005t0009g0248 a0001c0005t0030g0335 others(3): Show |
6 | HG00408.hp1 NA18973.hp2 NA18988.hp1 others(3): Show |
intron_variant | MODIFIER | c.1112-5150T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641355 | |||||||
| chr10:49641488 | A | G | 10 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(7): Show |
12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-5017A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641488 | |||||||
| chr10:49641503 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1112-5002T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641503 | |||||||
| chr10:49641559 | A | T | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-4946A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641559 | |||||||
| chr10:49641574 | C | A | 1 | a0001c0010t0003g0254 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1112-4931C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641574 | |||||||
| chr10:49641667 | G | A | 1 | a0001c0001t0001g0348 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1112-4838G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641667 | |||||||
| chr10:49641950 | T | C | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-4555T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49641950 | |||||||
| chr10:49642004 | G | A | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-4501G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642004 | |||||||
| chr10:49642008 | C | T | 3 | a0001c0001t0004g0258 a0001c0001t0004g0285 a0001c0001t0007g0182 |
3 | HG03139.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1112-4497C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642008 | |||||||
| chr10:49642024 | A | G | 1 | a0001c0001t0018g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1112-4481A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642024 | |||||||
| chr10:49642117 | G | A | 95 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(92): Show |
108 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.1112-4388G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642117 | |||||||
| chr10:49642194 | T | C | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-4311T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642194 | |||||||
| chr10:49642228 | A | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-4277A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642228 | |||||||
| chr10:49642299 | T | C | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1112-4206T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642299 | |||||||
| chr10:49642306 | C | T | 1 | a0001c0003t0006g0304 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1112-4199C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642306 | |||||||
| chr10:49642332 | C | T | 10 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(7): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-4173C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642332 | |||||||
| chr10:49642481 | G | T | 1 | a0001c0001t0002g0238 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1112-4024G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642481 | |||||||
| chr10:49642598 | C | T | 1 | a0001c0001t0001g0314 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1112-3907C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642598 | |||||||
| chr10:49642673 | G | C | 10 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(7): Show |
12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-3832G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642673 | |||||||
| chr10:49642708 | C | A | 114 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(111): Show |
124 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1112-3797C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642708 | |||||||
| chr10:49642735 | G | A | 107 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(104): Show |
117 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1112-3770G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642735 | |||||||
| chr10:49642768 | C | T | 1 | a0001c0001t0004g0055 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1112-3737C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642768 | |||||||
| chr10:49642814 | T | C | 7 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0007g0179 others(4): Show |
7 | HG00642.hp1 HG01069.hp1 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-3691T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642814 | |||||||
| chr10:49642875 | A | G | 24 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0003g0057 others(21): Show |
27 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.1112-3630A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49642875 | |||||||
| chr10:49643058 | T | C | 10 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(7): Show |
12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-3447T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643058 | |||||||
| chr10:49643098 | G | A | 3 | a0001c0011t0024g0280 a0001c0011t0029g0216 a0001c0027t0031g0174 |
3 | HG01981.hp1 HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1112-3407G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643098 | |||||||
| chr10:49643100 | C | G | 1 | a0001c0005t0005g0344 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1112-3405C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643100 | |||||||
| chr10:49643228 | A | G | 1 | a0012c0031t0003g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1112-3277A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643228 | |||||||
| chr10:49643304 | G | A | 1 | a0003c0004t0001g0144 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1112-3201G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643304 | |||||||
| chr10:49643562 | C | T | 1 | a0001c0003t0006g0317 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1112-2943C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643562 | |||||||
| chr10:49643601 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-2904G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643601 | |||||||
| chr10:49643712 | C | G | 1 | a0001c0003t0010g0236 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1112-2793C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643712 | |||||||
| chr10:49643788 | T | C | 370 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(367): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1112-2717T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643788 | |||||||
| chr10:49643865 | C | A | 61 | a0001c0001t0001g0029 a0001c0001t0003g0219 a0001c0001t0004g0055 others(58): Show |
69 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(66): Show |
intron_variant | MODIFIER | c.1112-2640C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643865 | |||||||
| chr10:49643947 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2558G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49643947 | |||||||
| chr10:49644009 | G | A | 1 | a0001c0003t0006g0317 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1112-2496G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644009 | |||||||
| chr10:49644082 | A | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2423A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644082 | |||||||
| chr10:49644103 | A | T | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1112-2402A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644103 | |||||||
| chr10:49644106 | G | A | 3 | a0001c0010t0003g0259 a0001c0010t0008g0265 a0001c0017t0003g0253 |
3 | HG03041.hp1 HG03453.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1112-2399G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644106 | |||||||
| chr10:49644137 | C | T | 117 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(114): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.1112-2368C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644137 | |||||||
| chr10:49644211 | C | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-2294C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644211 | |||||||
| chr10:49644215 | G | A | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1112-2290G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644215 | |||||||
| chr10:49644278 | C | G | 44 | a0001c0001t0001g0340 a0001c0001t0002g0176 a0001c0001t0002g0184 others(41): Show |
46 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1112-2227C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644278 | |||||||
| chr10:49644280 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0002g0261 |
3 | HG02615.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1112-2225C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644280 | |||||||
| chr10:49644481 | G | C | 37 | a0001c0001t0001g0061 a0001c0001t0001g0348 a0001c0001t0002g0194 others(34): Show |
42 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(39): Show |
intron_variant | MODIFIER | c.1112-2024G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644481 | |||||||
| chr10:49644499 | T | G | 1 | a0001c0001t0004g0325 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1112-2006T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644499 | |||||||
| chr10:49644548 | G | A | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1112-1957G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644548 | |||||||
| chr10:49644573 | G | C | 24 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(21): Show |
25 | HG00738.hp1 HG01109.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.1112-1932G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644573 | |||||||
| chr10:49644660 | CAGAGT | C | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-1841_1112-183 others(9): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49644660 | ||||||
| chr10:49644707 | C | T | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-1798C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644707 | |||||||
| chr10:49644718 | G | A | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1112-1787G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644718 | |||||||
| chr10:49644736 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-1769G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644736 | |||||||
| chr10:49644786 | C | T | 364 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(361): Show |
404 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(401): Show |
intron_variant | MODIFIER | c.1112-1719C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644786 | |||||||
| chr10:49644954 | T | C | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1551T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49644954 | |||||||
| chr10:49645039 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-1466G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645039 | |||||||
| chr10:49645087 | C | T | 1 | a0002c0002t0002g0080 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1112-1418C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645087 | |||||||
| chr10:49645144 | T | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1361T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645144 | |||||||
| chr10:49645146 | T | C | 108 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(105): Show |
118 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1112-1359T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645146 | |||||||
| chr10:49645297 | C | T | 83 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(80): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.1112-1208C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645297 | |||||||
| chr10:49645304 | C | T | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1201C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645304 | |||||||
| chr10:49645348 | C | T | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1157C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645348 | |||||||
| chr10:49645352 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1153G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645352 | |||||||
| chr10:49645458 | T | G | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-1047T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645458 | |||||||
| chr10:49645480 | T | C | 257 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(254): Show |
287 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(284): Show |
intron_variant | MODIFIER | c.1112-1025T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645480 | |||||||
| chr10:49645500 | G | A | 2 | a0010c0018t0003g0324 a0013c0036t0003g0331 |
2 | HG01123.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1112-1005G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645500 | |||||||
| chr10:49645539 | C | T | 13 | a0001c0001t0004g0309 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG01978.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1112-966C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645539 | |||||||
| chr10:49645579 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1112-926G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645579 | |||||||
| chr10:49645775 | C | T | 2 | a0001c0001t0002g0260 a0001c0005t0009g0249 |
2 | NA18943.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1112-730C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49645775 | |||||||
| chr10:49646041 | A | AT | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-462dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr10 | 49646041 | ||||||
| chr10:49646087 | T | C | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1112-418T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646087 | |||||||
| chr10:49646136 | G | A | 1 | a0004c0034t0015g0275 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1112-369G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646136 | |||||||
| chr10:49646151 | G | A | 110 | a0001c0001t0001g0029 a0001c0001t0001g0340 a0001c0001t0002g0176 others(107): Show |
120 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.1112-354G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646151 | |||||||
| chr10:49646155 | C | G | 1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1112-350C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646155 | |||||||
| chr10:49646347 | C | T | 1 | a0001c0030t0004g0310 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1112-158C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646347 | |||||||
| chr10:49646395 | C | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0068 others(41): Show |
49 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.1112-110C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646395 | |||||||
| chr10:49646422 | G | T | 10 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0004g0258 others(7): Show |
12 | HG00639.hp2 HG01884.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1112-83G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646422 | |||||||
| chr10:49646437 | G | A | 60 | a0001c0001t0001g0029 a0001c0001t0002g0204 a0001c0001t0003g0219 others(57): Show |
67 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(64): Show |
intron_variant | MODIFIER | c.1112-68G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646437 | |||||||
| chr10:49646451 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1112-54G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 7/14 | chr10 | 49646451 | |||||||
| chr10:49646690 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+16G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646690 | |||||||
| chr10:49646721 | G | A | 43 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0068 others(40): Show |
48 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.1281+47G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646721 | |||||||
| chr10:49646756 | C | T | 1 | a0001c0001t0004g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1281+82C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646756 | |||||||
| chr10:49646761 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+87G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646761 | |||||||
| chr10:49646765 | G | A | 5 | a0001c0003t0010g0208 a0001c0003t0010g0209 a0003c0007t0006g0115 others(2): Show |
5 | NA18974.hp2 NA18988.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.1281+91G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646765 | |||||||
| chr10:49646856 | T | A | 1 | a0001c0001t0004g0230 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1281+182T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49646856 | |||||||
| chr10:49647016 | G | C | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1281+342G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647016 | |||||||
| chr10:49647021 | C | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1281+347C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647021 | |||||||
| chr10:49647104 | A | G | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+430A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647104 | |||||||
| chr10:49647115 | T | G | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1281+441T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647115 | |||||||
| chr10:49647321 | C | T | 1 | a0001c0001t0001g0348 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1281+647C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647321 | |||||||
| chr10:49647322 | C | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0061 a0001c0001t0001g0063 others(112): Show |
129 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1281+648C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647322 | |||||||
| chr10:49647366 | C | G | 1 | a0002c0002t0002g0010 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1281+692C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647366 | |||||||
| chr10:49647453 | A | G | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1281+779A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647453 | |||||||
| chr10:49647593 | C | T | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1282-914C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647593 | |||||||
| chr10:49647622 | A | G | 1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1282-885A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647622 | |||||||
| chr10:49647734 | C | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1282-773C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647734 | |||||||
| chr10:49647738 | GCTTTCCT others(14): Show |
G | 1 | a0001c0005t0005g0301 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1282-765_1282-745d others(23): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647738 | ||||||
| chr10:49647740 | T | TTTCC | 10 | a0001c0001t0003g0022 a0001c0003t0003g0308 a0001c0003t0006g0322 others(7): Show |
11 | HG01192.hp1 HG02083.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1282-700_1282-697d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | T | TTTCCTTC others(5): Show |
1 | a0003c0007t0003g0114 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1282-708_1282-697d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCC | T | 25 | a0001c0001t0001g0312 a0001c0001t0003g0024 a0001c0001t0004g0315 others(22): Show |
27 | HG00639.hp2 HG01123.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1282-700_1282-697d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(1): Show |
T | 34 | a0001c0001t0001g0025 a0001c0001t0001g0029 a0001c0001t0001g0215 others(31): Show |
38 | HG00544.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1282-704_1282-697d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(5): Show |
T | 23 | a0001c0001t0001g0220 a0001c0001t0003g0035 a0001c0001t0003g0036 others(20): Show |
25 | HG01243.hp2 HG01978.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1282-708_1282-697d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(9): Show |
T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0169 others(27): Show |
30 | HG00099.hp1 HG00621.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.1282-712_1282-697d others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(13): Show |
T | 125 | a0001c0001t0001g0021 a0001c0001t0001g0031 a0001c0001t0001g0033 others(122): Show |
137 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.1282-716_1282-697d others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(17): Show |
T | 61 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0061 others(58): Show |
68 | HG00280.hp1 HG00544.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1282-720_1282-697d others(26): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(21): Show |
T | 38 | a0001c0001t0001g0340 a0001c0001t0001g0348 a0001c0001t0002g0176 others(35): Show |
42 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1282-724_1282-697d others(30): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(25): Show |
T | 7 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0013g0020 others(4): Show |
8 | HG02055.hp2 HG02258.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1282-728_1282-697d others(34): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647740 | TTTCCTTC others(33): Show |
T | 1 | a0001c0001t0023g0281 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1282-736_1282-697d others(42): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr10 | 49647740 | ||||||
| chr10:49647787 | C | T | 2 | a0001c0003t0006g0060 a0001c0003t0010g0038 |
2 | HG01175.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.1282-720C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647787 | |||||||
| chr10:49647787 | CCTTCCTT others(17): Show |
C | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-719_1282-696d others(26): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647787 | |||||||
| chr10:49647799 | C | G | 1 | a0001c0003t0006g0302 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1282-708C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647799 | |||||||
| chr10:49647877 | G | T | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-630G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647877 | |||||||
| chr10:49647968 | T | G | 1 | a0001c0003t0008g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1282-539T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49647968 | |||||||
| chr10:49648092 | G | T | 94 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0031 others(91): Show |
106 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1282-415G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648092 | |||||||
| chr10:49648145 | G | A | 2 | a0005c0014t0004g0284 a0005c0014t0007g0178 |
2 | NA18522.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1282-362G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648145 | |||||||
| chr10:49648185 | C | G | 1 | a0001c0001t0002g0175 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1282-322C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648185 | |||||||
| chr10:49648482 | G | A | 12 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(9): Show |
12 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1282-25G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 8/14 | chr10 | 49648482 | |||||||
| chr10:49648709 | G | GA | 6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+109dupA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648709 | ||||||
| chr10:49648726 | T | TAC | 5 | a0002c0002t0002g0010 a0004c0009t0003g0272 a0004c0009t0011g0042 others(2): Show |
6 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1382+150_1382+151d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACAC | 45 | a0001c0001t0002g0176 a0001c0001t0002g0184 a0001c0001t0002g0185 others(42): Show |
49 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(46): Show |
intron_variant | MODIFIER | c.1382+148_1382+151d others(6): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACAC | 5 | a0001c0001t0016g0218 a0001c0003t0034g0362 a0003c0004t0001g0050 others(2): Show |
5 | HG02165.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1382+146_1382+151d others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACACA others(3): Show |
1 | a0001c0001t0014g0278 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1382+142_1382+151d others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACACA others(5): Show |
2 | a0001c0001t0003g0274 a0011c0032t0025g0059 |
2 | HG02717.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.1382+140_1382+151d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACACA others(9): Show |
6 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(3): Show |
7 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1382+136_1382+151d others(18): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACACA others(11): Show |
1 | a0001c0011t0003g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1382+134_1382+151d others(20): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | T | TACACACA others(13): Show |
1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1382+132_1382+151d others(22): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | TAC | T | 252 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0029 others(249): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.1382+150_1382+151d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | TACACAC | T | 14 | a0001c0003t0003g0286 a0001c0003t0003g0288 a0001c0010t0003g0048 others(11): Show |
14 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1382+146_1382+151d others(8): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648726 | TACACACA others(1): Show |
T | 11 | a0001c0001t0001g0312 a0001c0001t0003g0347 a0001c0001t0004g0111 others(8): Show |
12 | HG00738.hp1 HG01109.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.1382+144_1382+151d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648726 | ||||||
| chr10:49648856 | A | AGGAATTC others(4): Show |
1 | a0003c0006t0005g0149 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1382+251_1382+261d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr10 | 49648856 | ||||||
| chr10:49649033 | G | A | 1 | a0003c0004t0001g0050 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1382+426G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649033 | |||||||
| chr10:49649034 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1382+427C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649034 | |||||||
| chr10:49649036 | C | T | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1382+429C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649036 | |||||||
| chr10:49649060 | T | C | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383-448T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649060 | |||||||
| chr10:49649068 | A | G | 10 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(7): Show |
12 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.1383-440A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649068 | |||||||
| chr10:49649256 | C | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1383-252C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649256 | |||||||
| chr10:49649303 | G | A | 13 | a0001c0003t0034g0362 a0001c0010t0003g0048 a0001c0010t0003g0049 others(10): Show |
13 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.1383-205G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649303 | |||||||
| chr10:49649422 | C | T | 1 | a0014c0037t0035g0296 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1383-86C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649422 | |||||||
| chr10:49649466 | G | C | 24 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0215 others(21): Show |
28 | HG01069.hp2 HG01071.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1383-42G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 9/14 | chr10 | 49649466 | |||||||
| chr10:49649789 | T | C | 113 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(110): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1511+153T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649789 | |||||||
| chr10:49649803 | C | T | 307 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(304): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.1511+167C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649803 | |||||||
| chr10:49649822 | T | C | 2 | a0001c0001t0003g0035 a0001c0001t0003g0036 |
2 | HG01243.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1511+186T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649822 | |||||||
| chr10:49649844 | T | C | 370 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(367): Show |
410 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(407): Show |
intron_variant | MODIFIER | c.1511+208T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649844 | |||||||
| chr10:49649866 | AT | A | 55 | a0001c0001t0001g0282 a0001c0001t0001g0290 a0001c0001t0003g0057 others(52): Show |
61 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.1511+258delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649866 | ATT | A | 131 | a0001c0001t0001g0029 a0001c0001t0001g0169 a0001c0001t0001g0224 others(128): Show |
143 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1511+257_1511+258d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649866 | ATTT | A | 49 | a0001c0001t0003g0347 a0001c0001t0004g0006 a0001c0001t0004g0008 others(46): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1511+256_1511+258d others(5): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649866 | ATTTTTTT others(4): Show |
A | 11 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(8): Show |
11 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511+248_1511+258d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649866 | ATTTTTTT others(5): Show |
A | 6 | a0001c0001t0001g0343 a0001c0001t0014g0276 a0001c0005t0005g0344 others(3): Show |
6 | HG00597.hp1 HG00597.hp2 HG00609.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+247_1511+258d others(14): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649866 | ATTTTTTT others(6): Show |
A | 106 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(103): Show |
121 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.1511+246_1511+258d others(15): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649866 | ||||||
| chr10:49649873 | T | A | 13 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(10): Show |
15 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1511+237T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649873 | |||||||
| chr10:49649880 | T | A | 13 | a0001c0001t0003g0057 a0001c0001t0003g0067 a0001c0001t0008g0003 others(10): Show |
15 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.1511+244T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649880 | |||||||
| chr10:49649894 | T | C | 1 | a0001c0001t0011g0173 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1511+258T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649894 | |||||||
| chr10:49649926 | G | A | 1 | a0003c0007t0003g0127 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1511+290G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649926 | |||||||
| chr10:49649931 | A | G | 112 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(109): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1511+295A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649931 | |||||||
| chr10:49649946 | A | AG | 112 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(109): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1511+315dupG | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr10 | 49649946 | ||||||
| chr10:49649999 | A | C | 112 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(109): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1511+363A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49649999 | |||||||
| chr10:49650000 | A | C | 112 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(109): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1511+364A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650000 | |||||||
| chr10:49650012 | T | C | 3 | a0001c0003t0003g0286 a0001c0003t0003g0288 a0017c0033t0009g0177 |
3 | HG03041.hp2 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1511+376T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650012 | |||||||
| chr10:49650076 | G | T | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1511+440G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650076 | |||||||
| chr10:49650140 | C | T | 107 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(104): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1511+504C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650140 | |||||||
| chr10:49650185 | G | T | 1 | a0001c0001t0001g0025 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1511+549G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650185 | |||||||
| chr10:49650288 | T | C | 1 | a0001c0001t0001g0025 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1511+652T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650288 | |||||||
| chr10:49650300 | T | C | 108 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(105): Show |
123 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.1511+664T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650300 | |||||||
| chr10:49650345 | A | G | 359 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(356): Show |
397 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(394): Show |
intron_variant | MODIFIER | c.1511+709A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650345 | |||||||
| chr10:49650383 | C | T | 4 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0005g0264 others(1): Show |
6 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+747C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650383 | |||||||
| chr10:49650459 | G | C | 4 | a0001c0001t0001g0340 a0002c0002t0007g0072 a0007c0016t0009g0268 others(1): Show |
4 | NA18948.hp1 NA18973.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511+823G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650459 | |||||||
| chr10:49650487 | T | G | 2 | a0001c0001t0004g0337 a0006c0023t0007g0105 |
2 | NA19012.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.1511+851T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650487 | |||||||
| chr10:49650494 | A | G | 11 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(8): Show |
11 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511+858A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650494 | |||||||
| chr10:49650593 | G | T | 5 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0252 others(2): Show |
6 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.1511+957G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650593 | |||||||
| chr10:49650641 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG00140.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1511+1005C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650641 | |||||||
| chr10:49650658 | C | A | 1 | a0001c0003t0008g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1511+1022C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650658 | |||||||
| chr10:49650808 | T | G | 363 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(360): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1512-1076T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650808 | |||||||
| chr10:49650931 | G | A | 1 | a0001c0001t0001g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1512-953G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49650931 | |||||||
| chr10:49651000 | C | A | 5 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0005g0264 others(2): Show |
7 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512-884C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651000 | |||||||
| chr10:49651057 | A | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(104): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1512-827A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651057 | |||||||
| chr10:49651084 | G | A | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1512-800G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651084 | |||||||
| chr10:49651100 | G | A | 1 | a0001c0017t0004g0228 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1512-784G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651100 | |||||||
| chr10:49651110 | G | A | 2 | a0001c0001t0003g0274 a0001c0001t0014g0278 |
2 | HG02809.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1512-774G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651110 | |||||||
| chr10:49651199 | A | G | 118 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(115): Show |
133 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1512-685A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651199 | |||||||
| chr10:49651203 | A | G | 107 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(104): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1512-681A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651203 | |||||||
| chr10:49651227 | C | T | 1 | a0001c0027t0031g0174 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1512-657C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651227 | |||||||
| chr10:49651361 | G | T | 1 | a0001c0003t0006g0346 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1512-523G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651361 | |||||||
| chr10:49651379 | C | T | 5 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0005g0264 others(2): Show |
7 | HG00639.hp2 HG01884.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1512-505C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651379 | |||||||
| chr10:49651438 | T | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(104): Show |
122 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.1512-446T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651438 | |||||||
| chr10:49651447 | A | G | 2 | a0001c0001t0003g0347 a0001c0001t0014g0279 |
2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1512-437A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651447 | |||||||
| chr10:49651560 | G | A | 2 | a0001c0001t0001g0332 a0001c0001t0016g0026 |
3 | HG02486.hp2 HG06807.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.1512-324G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651560 | |||||||
| chr10:49651583 | T | G | 245 | a0001c0001t0001g0029 a0001c0001t0001g0169 a0001c0001t0001g0224 others(242): Show |
270 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(267): Show |
intron_variant | MODIFIER | c.1512-301T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651583 | |||||||
| chr10:49651816 | G | A | 1 | a0003c0006t0005g0125 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1512-68G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 10/14 | chr10 | 49651816 | |||||||
| chr10:49652183 | C | G | 141 | a0001c0001t0001g0029 a0001c0001t0001g0169 a0001c0001t0001g0282 others(138): Show |
152 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1634+177C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652183 | |||||||
| chr10:49652189 | A | G | 125 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(122): Show |
143 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.1634+183A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652189 | |||||||
| chr10:49652337 | T | C | 363 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(360): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.1634+331T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652337 | |||||||
| chr10:49652579 | G | T | 1 | a0001c0001t0003g0036 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1634+573G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652579 | |||||||
| chr10:49652584 | C | T | 1 | a0002c0002t0002g0081 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1634+578C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652584 | |||||||
| chr10:49652647 | C | CT | 15 | a0001c0001t0003g0024 a0001c0001t0004g0005 a0001c0001t0005g0221 others(12): Show |
17 | HG00639.hp2 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1634+644dupT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49652647 | ||||||
| chr10:49652698 | C | T | 105 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(102): Show |
121 | HG00099.hp2 HG00323.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1634+692C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652698 | |||||||
| chr10:49652758 | C | A | 11 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0297 others(8): Show |
14 | HG00438.hp2 HG02015.hp2 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1634+752C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652758 | |||||||
| chr10:49652857 | G | A | 4 | a0001c0001t0005g0221 a0001c0013t0005g0217 a0001c0013t0005g0289 others(1): Show |
4 | HG01884.hp1 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1634+851G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652857 | |||||||
| chr10:49652865 | C | T | 1 | a0001c0001t0007g0352 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1634+859C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652865 | |||||||
| chr10:49652913 | C | G | 1 | a0001c0003t0006g0303 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1634+907C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49652913 | |||||||
| chr10:49653007 | A | G | 1 | a0001c0003t0010g0236 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1634+1001A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653007 | |||||||
| chr10:49653062 | A | G | 11 | a0001c0001t0001g0282 a0001c0001t0004g0062 a0001c0001t0004g0226 others(8): Show |
12 | HG02055.hp2 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1634+1056A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653062 | |||||||
| chr10:49653076 | C | T | 1 | a0001c0003t0008g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1634+1070C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653076 | |||||||
| chr10:49653212 | C | G | 1 | a0001c0001t0019g0242 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1634+1206C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653212 | |||||||
| chr10:49653307 | G | A | 1 | a0001c0005t0009g0186 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1634+1301G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653307 | |||||||
| chr10:49653408 | G | A | 1 | a0004c0009t0011g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1634+1402G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653408 | |||||||
| chr10:49653427 | AC | A | 116 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(113): Show |
133 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.1634+1423delC | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49653427 | ||||||
| chr10:49653437 | A | G | 1 | a0002c0002t0002g0012 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1634+1431A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653437 | |||||||
| chr10:49653520 | C | T | 7 | a0001c0001t0003g0022 a0001c0001t0003g0041 a0001c0001t0003g0219 others(4): Show |
9 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1634+1514C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653520 | |||||||
| chr10:49653544 | C | T | 2 | a0002c0002t0002g0081 a0003c0004t0001g0134 |
2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1634+1538C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653544 | |||||||
| chr10:49653550 | C | T | 3 | a0001c0001t0001g0052 a0001c0001t0001g0251 a0004c0034t0015g0275 |
3 | HG02145.hp2 HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.1634+1544C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653550 | |||||||
| chr10:49653664 | T | G | 1 | a0003c0007t0003g0124 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1635-1431T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653664 | |||||||
| chr10:49653704 | G | A | 3 | a0001c0001t0003g0024 a0001c0001t0036g0295 a0001c0035t0003g0233 |
4 | HG00639.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-1391G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653704 | |||||||
| chr10:49653798 | C | T | 2 | a0001c0001t0001g0061 a0001c0001t0002g0194 |
2 | HG01515.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.1635-1297C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653798 | |||||||
| chr10:49653889 | C | T | 5 | a0001c0005t0009g0249 a0001c0005t0009g0269 a0007c0016t0008g0266 others(2): Show |
5 | NA18947.hp2 NA18948.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.1635-1206C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653889 | |||||||
| chr10:49653974 | C | T | 1 | a0001c0001t0006g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1635-1121C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653974 | |||||||
| chr10:49653986 | G | A | 1 | a0001c0011t0029g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1635-1109G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49653986 | |||||||
| chr10:49654219 | T | C | 12 | a0001c0001t0003g0347 a0001c0001t0014g0279 a0001c0010t0003g0048 others(9): Show |
12 | HG01109.hp1 HG01167.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1635-876T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654219 | |||||||
| chr10:49654289 | G | C | 201 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(198): Show |
221 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1635-806G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654289 | |||||||
| chr10:49654358 | T | C | 201 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(198): Show |
221 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(218): Show |
intron_variant | MODIFIER | c.1635-737T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654358 | |||||||
| chr10:49654407 | A | G | 11 | a0001c0003t0003g0308 a0001c0003t0008g0183 a0001c0003t0008g0250 others(8): Show |
11 | HG00423.hp1 HG00544.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1635-688A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654407 | |||||||
| chr10:49654724 | G | T | 197 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(194): Show |
217 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.1635-371G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654724 | |||||||
| chr10:49654824 | AT | A | 288 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(285): Show |
320 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.1635-263delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr10 | 49654824 | ||||||
| chr10:49654907 | C | T | 4 | a0001c0013t0005g0217 a0001c0013t0005g0289 a0001c0013t0032g0378 others(1): Show |
4 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.1635-188C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49654907 | |||||||
| chr10:49655037 | A | C | 182 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(179): Show |
202 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.1635-58A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49655037 | |||||||
| chr10:49655065 | C | T | 1 | a0003c0004t0001g0122 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1635-30C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 11/14 | chr10 | 49655065 | |||||||
| chr10:49655511 | G | C | 1 | a0002c0008t0010g0094 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1839+63G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655511 | |||||||
| chr10:49655519 | C | T | 291 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(288): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1839+71C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655519 | |||||||
| chr10:49655540 | G | A | 1 | a0001c0003t0006g0313 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1839+92G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655540 | |||||||
| chr10:49655577 | A | G | 116 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0035 others(113): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1839+129A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655577 | |||||||
| chr10:49655997 | T | A | 291 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(288): Show |
323 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(320): Show |
intron_variant | MODIFIER | c.1839+549T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49655997 | |||||||
| chr10:49656002 | T | C | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1839+554T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656002 | |||||||
| chr10:49656060 | C | G | 2 | a0001c0001t0003g0347 a0001c0001t0014g0279 |
2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1839+612C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656060 | |||||||
| chr10:49656198 | C | T | 2 | a0001c0001t0002g0198 a0002c0002t0002g0010 |
3 | HG01255.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1839+750C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656198 | |||||||
| chr10:49656242 | C | T | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+794C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656242 | |||||||
| chr10:49656283 | GT | G | 34 | a0001c0003t0003g0286 a0001c0003t0003g0288 a0001c0003t0003g0308 others(31): Show |
35 | HG00423.hp1 HG00544.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.1839+862delT | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTT | G | 35 | a0001c0003t0006g0002 a0001c0003t0006g0027 a0001c0003t0006g0028 others(32): Show |
42 | HG00099.hp1 HG01167.hp2 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.1839+861_1839+862d others(4): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTTTTTTT others(1): Show |
G | 13 | a0001c0001t0001g0314 a0001c0001t0002g0185 a0001c0001t0002g0198 others(10): Show |
14 | HG01255.hp1 HG01257.hp1 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1839+855_1839+862d others(10): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTTTTTTT others(2): Show |
G | 123 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(120): Show |
140 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1839+854_1839+862d others(11): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTTTTTTT others(3): Show |
G | 141 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0035 others(138): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.1839+853_1839+862d others(12): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTTTTTTT others(4): Show |
G | 14 | a0001c0001t0004g0005 a0001c0001t0004g0258 a0001c0001t0004g0285 others(11): Show |
15 | HG00741.hp2 HG01168.hp1 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.1839+852_1839+862d others(13): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656283 | GTTTTTTT others(8): Show |
G | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+848_1839+862d others(17): Show |
CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49656283 | ||||||
| chr10:49656421 | C | T | 1 | a0001c0010t0003g0256 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1839+973C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656421 | |||||||
| chr10:49656441 | T | C | 3 | a0001c0001t0013g0020 a0001c0001t0013g0225 a0001c0001t0013g0329 |
4 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1839+993T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656441 | |||||||
| chr10:49656646 | G | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(183): Show |
206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1839+1198G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656646 | |||||||
| chr10:49656857 | G | A | 185 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(182): Show |
205 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1839+1409G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656857 | |||||||
| chr10:49656869 | A | C | 1 | a0001c0005t0009g0248 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1839+1421A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49656869 | |||||||
| chr10:49657115 | A | T | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1839+1667A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657115 | |||||||
| chr10:49657181 | G | T | 114 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0035 others(111): Show |
126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.1839+1733G>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657181 | |||||||
| chr10:49657185 | A | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(184): Show |
207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1839+1737A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657185 | |||||||
| chr10:49657187 | T | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+1739T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657187 | |||||||
| chr10:49657305 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1839+1857T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657305 | |||||||
| chr10:49657379 | C | G | 4 | a0001c0001t0016g0026 a0001c0001t0016g0218 a0001c0011t0024g0280 others(1): Show |
5 | HG02258.hp2 HG02486.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1839+1931C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657379 | |||||||
| chr10:49657411 | T | C | 10 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(7): Show |
10 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1839+1963T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657411 | |||||||
| chr10:49657427 | C | A | 1 | a0001c0003t0006g0313 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1839+1979C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657427 | |||||||
| chr10:49657525 | A | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(184): Show |
207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1839+2077A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657525 | |||||||
| chr10:49657627 | A | C | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+2179A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657627 | |||||||
| chr10:49657704 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1839+2256G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657704 | |||||||
| chr10:49657766 | T | C | 1 | a0002c0002t0007g0375 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1839+2318T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657766 | |||||||
| chr10:49657929 | G | A | 26 | a0001c0001t0003g0024 a0001c0001t0003g0035 a0001c0001t0003g0036 others(23): Show |
29 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.1839+2481G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49657929 | |||||||
| chr10:49658018 | T | C | 1 | a0001c0003t0008g0017 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1839+2570T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658018 | |||||||
| chr10:49658263 | C | A | 2 | a0001c0003t0006g0322 a0002c0008t0010g0376 |
2 | NA18964.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1839+2815C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658263 | |||||||
| chr10:49658296 | A | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1839+2848A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658296 | |||||||
| chr10:49658378 | G | A | 2 | a0003c0006t0005g0149 a0011c0032t0025g0059 |
2 | HG02717.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.1839+2930G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658378 | |||||||
| chr10:49658385 | C | T | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1839+2937C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658385 | |||||||
| chr10:49658386 | A | G | 352 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(349): Show |
392 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(389): Show |
intron_variant | MODIFIER | c.1839+2938A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658386 | |||||||
| chr10:49658443 | G | A | 2 | a0001c0011t0024g0280 a0001c0011t0029g0216 |
2 | HG02258.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1839+2995G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658443 | |||||||
| chr10:49658551 | C | A | 374 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(371): Show |
414 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(411): Show |
intron_variant | MODIFIER | c.1839+3103C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658551 | |||||||
| chr10:49658577 | C | T | 1 | a0001c0001t0002g0205 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1839+3129C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658577 | |||||||
| chr10:49658640 | C | T | 9 | a0001c0001t0005g0299 a0001c0001t0005g0300 a0001c0001t0012g0188 others(6): Show |
9 | HG00642.hp1 HG01069.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.1839+3192C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658640 | |||||||
| chr10:49658649 | C | T | 1 | a0001c0001t0003g0057 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1839+3201C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658649 | |||||||
| chr10:49658755 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1839+3307A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49658755 | |||||||
| chr10:49659162 | G | A | 1 | a0001c0001t0012g0188 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1840-3483G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659162 | |||||||
| chr10:49659398 | A | C | 188 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(185): Show |
208 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1840-3247A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659398 | |||||||
| chr10:49659436 | C | T | 10 | a0001c0010t0003g0048 a0001c0010t0003g0049 a0001c0010t0003g0223 others(7): Show |
10 | HG01167.hp2 HG02145.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.1840-3209C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659436 | |||||||
| chr10:49659519 | G | A | 49 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0032 others(46): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1840-3126G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659519 | |||||||
| chr10:49659779 | A | T | 303 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(300): Show |
335 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(332): Show |
intron_variant | MODIFIER | c.1840-2866A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659779 | |||||||
| chr10:49659811 | G | A | 49 | a0001c0001t0004g0006 a0001c0001t0004g0008 a0001c0001t0004g0032 others(46): Show |
55 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(52): Show |
intron_variant | MODIFIER | c.1840-2834G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49659811 | |||||||
| chr10:49660076 | C | T | 1 | a0001c0011t0029g0216 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1840-2569C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660076 | |||||||
| chr10:49660137 | G | A | 1 | a0001c0001t0001g0353 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1840-2508G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660137 | |||||||
| chr10:49660157 | T | A | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1840-2488T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660157 | |||||||
| chr10:49660396 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1840-2249C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660396 | |||||||
| chr10:49660397 | G | A | 24 | a0001c0001t0003g0024 a0001c0001t0003g0035 a0001c0001t0003g0036 others(21): Show |
27 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1840-2248G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660397 | |||||||
| chr10:49660398 | C | T | 9 | a0001c0001t0004g0005 a0001c0001t0004g0258 a0001c0001t0004g0285 others(6): Show |
10 | HG00741.hp2 HG01168.hp1 HG01516.hp1 others(7): Show |
intron_variant | MODIFIER | c.1840-2247C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660398 | |||||||
| chr10:49660399 | G | A | 1 | a0001c0001t0016g0026 | 2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1840-2246G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660399 | |||||||
| chr10:49660443 | GA | G | 276 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(273): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1840-2189delA | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr10 | 49660443 | ||||||
| chr10:49660460 | C | G | 1 | a0001c0001t0003g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1840-2185C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660460 | |||||||
| chr10:49660612 | G | A | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-2033G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660612 | |||||||
| chr10:49660615 | C | T | 1 | a0001c0001t0026g0064 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1840-2030C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660615 | |||||||
| chr10:49660679 | A | C | 24 | a0001c0001t0003g0024 a0001c0001t0003g0035 a0001c0001t0003g0036 others(21): Show |
27 | HG00280.hp2 HG00639.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.1840-1966A>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660679 | |||||||
| chr10:49660686 | T | G | 2 | a0001c0001t0003g0347 a0001c0001t0014g0279 |
2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1840-1959T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660686 | |||||||
| chr10:49660865 | G | A | 44 | a0001c0005t0005g0030 a0001c0005t0005g0065 a0001c0005t0005g0066 others(41): Show |
46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1840-1780G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49660865 | |||||||
| chr10:49661114 | C | T | 1 | a0001c0001t0005g0264 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1840-1531C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661114 | |||||||
| chr10:49661116 | C | T | 46 | a0001c0003t0006g0002 a0001c0003t0006g0027 a0001c0003t0006g0028 others(43): Show |
53 | HG00099.hp1 HG00544.hp1 HG01175.hp1 others(50): Show |
intron_variant | MODIFIER | c.1840-1529C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661116 | |||||||
| chr10:49661381 | T | C | 1 | a0001c0001t0001g0332 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1840-1264T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661381 | |||||||
| chr10:49661402 | C | T | 2 | a0001c0001t0003g0347 a0001c0001t0014g0279 |
2 | HG01109.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1840-1243C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661402 | |||||||
| chr10:49661479 | G | A | 44 | a0001c0005t0005g0030 a0001c0005t0005g0065 a0001c0005t0005g0066 others(41): Show |
46 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(43): Show |
intron_variant | MODIFIER | c.1840-1166G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661479 | |||||||
| chr10:49661537 | C | A | 186 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(183): Show |
206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1840-1108C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661537 | |||||||
| chr10:49661827 | A | T | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-818A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661827 | |||||||
| chr10:49661830 | C | T | 1 | a0001c0005t0005g0065 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1840-815C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49661830 | |||||||
| chr10:49662025 | A | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(184): Show |
207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1840-620A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662025 | |||||||
| chr10:49662054 | T | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-591T>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662054 | |||||||
| chr10:49662297 | G | A | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1840-348G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662297 | |||||||
| chr10:49662339 | C | A | 2 | a0001c0027t0031g0174 a0011c0032t0025g0059 |
2 | HG01981.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1840-306C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662339 | |||||||
| chr10:49662453 | C | G | 1 | a0001c0003t0034g0362 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1840-192C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662453 | |||||||
| chr10:49662453 | C | T | 1 | a0001c0011t0022g0283 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1840-192C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662453 | |||||||
| chr10:49662454 | G | A | 104 | a0001c0001t0003g0022 a0001c0001t0003g0024 a0001c0001t0003g0035 others(101): Show |
116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.1840-191G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662454 | |||||||
| chr10:49662473 | T | C | 186 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(183): Show |
206 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1840-172T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662473 | |||||||
| chr10:49662487 | C | T | 3 | a0001c0001t0003g0035 a0001c0001t0003g0036 a0001c0011t0003g0214 |
3 | HG01243.hp2 HG02886.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1840-158C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 13/14 | chr10 | 49662487 | |||||||
| chr10:49662839 | A | T | 2 | a0001c0001t0001g0340 a0002c0002t0002g0109 |
2 | NA18952.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.1977+57A>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49662839 | |||||||
| chr10:49662881 | G | A | 1 | a0001c0001t0002g0189 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1977+99G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49662881 | |||||||
| chr10:49663011 | T | C | 1 | a0001c0001t0018g0213 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1977+229T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663011 | |||||||
| chr10:49663101 | G | A | 28 | a0001c0001t0001g0007 a0001c0001t0001g0068 a0001c0001t0001g0297 others(25): Show |
32 | HG00438.hp2 HG02015.hp2 HG02027.hp2 others(29): Show |
intron_variant | MODIFIER | c.1977+319G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663101 | |||||||
| chr10:49663143 | T | C | 187 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(184): Show |
207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1977+361T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663143 | |||||||
| chr10:49663420 | T | A | 120 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(117): Show |
137 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1977+638T>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663420 | |||||||
| chr10:49663420 | T | C | 1 | a0001c0003t0008g0183 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1977+638T>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663420 | |||||||
| chr10:49663475 | A | G | 1 | a0001c0001t0002g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1977+693A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663475 | |||||||
| chr10:49663500 | A | G | 5 | a0001c0001t0002g0200 a0001c0001t0002g0361 a0003c0004t0001g0014 others(2): Show |
6 | HG02071.hp2 NA18953.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.1977+718A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663500 | |||||||
| chr10:49663578 | G | A | 1 | a0003c0004t0001g0121 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1977+796G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663578 | |||||||
| chr10:49663635 | C | T | 1 | a0001c0010t0003g0255 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1977+853C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663635 | |||||||
| chr10:49663670 | A | G | 28 | a0001c0001t0004g0032 a0001c0001t0004g0111 a0001c0001t0004g0307 others(25): Show |
29 | HG00609.hp2 HG01074.hp1 HG01952.hp1 others(26): Show |
intron_variant | MODIFIER | c.1977+888A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663670 | |||||||
| chr10:49663795 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1978-982C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49663795 | |||||||
| chr10:49664200 | A | G | 302 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(299): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1978-577A>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664200 | |||||||
| chr10:49664306 | G | C | 2 | a0001c0001t0001g0353 a0009c0021t0002g0083 |
2 | HG01081.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1978-471G>C | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664306 | |||||||
| chr10:49664356 | C | G | 187 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0025 others(184): Show |
207 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.1978-421C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664356 | |||||||
| chr10:49664365 | G | A | 1 | a0002c0002t0002g0096 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1978-412G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664365 | |||||||
| chr10:49664401 | G | A | 1 | a0011c0032t0025g0059 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1978-376G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664401 | |||||||
| chr10:49664450 | C | T | 1 | a0001c0001t0002g0235 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1978-327C>T | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664450 | |||||||
| chr10:49664526 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1978-251G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664526 | |||||||
| chr10:49664615 | G | A | 2 | a0001c0027t0031g0174 a0011c0032t0025g0059 |
2 | HG01981.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1978-162G>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664615 | |||||||
| chr10:49664753 | C | G | 2 | a0001c0003t0003g0286 a0001c0003t0003g0288 |
2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1978-24C>G | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664753 | |||||||
| chr10:49664755 | C | A | 1 | a0017c0033t0009g0177 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1978-22C>A | CHAT | ENSG00000070748.19 | transcript | ENST00000337653.7 | protein_coding | 14/14 | chr10 | 49664755 |