Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1056 |
| ensemblid | ENSG00000170835.17 |
| hgncid | 1848 |
| symbol | CEL |
| name | carboxyl ester lipase |
| refseq_nuc | NM_001807.6 |
| refseq_prot | NP_001798.3 |
| ensembl_nuc | ENST00000372080.8 |
| ensembl_prot | ENSP00000361151.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 133061981 |
| end | 133071861 |
| strand | + |
| ver | v1.2 |
| region | chr9:133061981-133071861 |
| region5000 | chr9:133056981-133076861 |
| regionname0 | CEL_chr9_133061981_133071861 |
| regionname5000 | CEL_chr9_133056981_133076861 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 753 | 384 | 73 | 77 | 181 | 14 | 38 | 134 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0002 | 0/0 | 753 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0003 | 0/0 | 742 | 4 | 0 | 2 | 0 | 2 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(737): Show |
chr9 | 133056981 | 133076861 |
| a0004 | 0/0 | 753 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0005 | 0/0 | 753 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0006 | 0/0 | 753 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0007 | 0/0 | 753 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0008 | 0/0 | 742 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(737): Show |
chr9 | 133056981 | 133076861 |
| a0009 | 0/0 | 14 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MPAGH others(9): Show |
chr9 | 133056981 | 133076861 |
| a0010 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0011 | 0/0 | 753 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0012 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0013 | 0/0 | 621 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(616): Show |
chr9 | 133056981 | 133076861 |
| a0014 | 0/0 | 191 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(186): Show |
chr9 | 133056981 | 133076861 |
| a0015 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0016 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0017 | 0/0 | 753 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(748): Show |
chr9 | 133056981 | 133076861 |
| a0018 | 0/0 | 221 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(216): Show |
chr9 | 133056981 | 133076861 |
| a0019 | 0/1 | 674 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | MGRLQ others(669): Show |
chr9 | 133056981 | 133076861 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2259 | 287 | 56 | 46 | 141 | 10 | 33 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0002 | 0/0 | 2259 | 84 | 11 | 27 | 39 | 3 | 4 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0003 | 0/0 | 2259 | 6 | 5 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0009 | 0/0 | 2259 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0017 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0022 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0024 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0026 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0001c0027 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0002c0004 | 0/0 | 2259 | 4 | 4 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0002c0013 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0003c0006 | 0/0 | 2226 | 4 | 0 | 2 | 0 | 2 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2221): Show |
chr9 | 133056981 | 133076861 | ||
| a0004c0005 | 0/0 | 2259 | 4 | 4 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0005c0007 | 0/0 | 2259 | 3 | 3 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0006c0008 | 0/0 | 2259 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0007c0010 | 0/0 | 2259 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0008c0020 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2221): Show |
chr9 | 133056981 | 133076861 | ||
| a0009c0028 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | GTGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0010c0019 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0011c0012 | 0/0 | 2259 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0012c0021 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0013c0025 | 0/0 | 1863 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(1858): Show |
chr9 | 133056981 | 133076861 | ||
| a0014c0014 | 0/0 | 2293 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2288): Show |
chr9 | 133056981 | 133076861 | ||
| a0015c0015 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0016c0011 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0017c0018 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2254): Show |
chr9 | 133056981 | 133076861 | ||
| a0018c0023 | 0/0 | 22651 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(22646): Show |
chr9 | 133056981 | 133076861 | ||
| a0019c0016 | 0/1 | 2227 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | ATGGG others(2222): Show |
chr9 | 133056981 | 133076861 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2381 | 281 | 55 | 46 | 136 | 10 | 33 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0001t0002 | 0/0 | 2381 | 5 | 0 | 0 | 5 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0001t0003 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0002t0001 | 0/0 | 2381 | 84 | 11 | 27 | 39 | 3 | 4 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0003t0001 | 0/0 | 2381 | 6 | 5 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0009t0001 | 0/0 | 2381 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0017t0001 | 0/0 | 2381 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0022t0001 | 0/0 | 2381 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0024t0001 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0026t0001 | 0/0 | 2381 | 1 | 0 | 0 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0001c0027t0001 | 0/0 | 2381 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0002c0004t0001 | 0/0 | 2381 | 4 | 4 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0002c0013t0001 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0003c0006t0001 | 0/0 | 2348 | 4 | 0 | 2 | 0 | 2 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2343): Show |
chr9 | 133056981 | 133076861 |
| a0004c0005t0001 | 0/0 | 2381 | 4 | 4 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0005c0007t0001 | 0/0 | 2381 | 3 | 3 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0006c0008t0001 | 0/0 | 2381 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0007c0010t0001 | 0/0 | 2381 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0008c0020t0001 | 0/0 | 2348 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2343): Show |
chr9 | 133056981 | 133076861 |
| a0009c0028t0001 | 0/0 | 2381 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0010c0019t0001 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0011c0012t0001 | 0/0 | 2381 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0012c0021t0001 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0013c0025t0001 | 0/0 | 1985 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(1980): Show |
chr9 | 133056981 | 133076861 |
| a0014c0014t0001 | 0/0 | 2415 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2410): Show |
chr9 | 133056981 | 133076861 |
| a0015c0015t0001 | 0/0 | 2381 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0016c0011t0001 | 0/0 | 2381 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0017c0018t0001 | 0/0 | 2381 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2376): Show |
chr9 | 133056981 | 133076861 |
| a0018c0023t0001 | 0/0 | 22773 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(22768): Show |
chr9 | 133056981 | 133076861 |
| a0019c0016t0001 | 0/1 | 2349 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | CACCC others(2344): Show |
chr9 | 133056981 | 133076861 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 119 | 27 | 19 | 51 | 7 | 14 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0003 | 0/0 | 44 | 0 | 9 | 33 | 0 | 2 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0004 | 0/0 | 14 | 0 | 0 | 13 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0006 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0007 | 0/0 | 8 | 1 | 5 | 0 | 2 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0008 | 0/0 | 7 | 2 | 1 | 4 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0012 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0001t0003g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0002 | 0/0 | 46 | 1 | 16 | 26 | 2 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0005 | 0/0 | 9 | 4 | 4 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0011 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0021 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0003t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0003t0001g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0009t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0017t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0022t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0024t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0026t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0001c0027t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0002c0004t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0002c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0002c0004t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0002c0013t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0003c0006t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0004c0005t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0004c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0005c0007t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0005c0007t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0006c0008t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0007c0010t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0008c0020t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0009c0028t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0010c0019t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0011c0012t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0012c0021t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0013c0025t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0014c0014t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0015c0015t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0016c0011t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0017c0018t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0018c0023t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| a0019c0016t0001g0003 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00140 | hp2 | a0001 | c0026 | t0001 | g0001 | EUR | GBR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00280 | hp1 | a0003 | c0006 | t0001 | g0002 | EUR | FIN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | FIN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0026 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00733 | hp2 | a0003 | c0006 | t0001 | g0002 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00738 | hp2 | a0008 | c0020 | t0001 | g0002 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0062 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01070 | hp1 | a0006 | c0008 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01081 | hp1 | a0006 | c0008 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01099 | hp1 | a0001 | c0009 | t0001 | g0030 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01106 | hp2 | a0001 | c0022 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01168 | hp1 | a0007 | c0010 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01169 | hp1 | a0007 | c0010 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01243 | hp1 | a0001 | c0009 | t0001 | g0030 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0084 | AMR | PUR | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01255 | hp1 | a0001 | c0017 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0083 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01517 | hp2 | a0003 | c0006 | t0001 | g0002 | EUR | IBS | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01943 | hp1 | a0003 | c0006 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02080 | hp2 | a0009 | c0028 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CDX | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PEL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02451 | hp1 | a0001 | c0024 | t0001 | g0090 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02698 | hp2 | a0011 | c0012 | t0001 | g0080 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02886 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02895 | hp1 | a0004 | c0005 | t0001 | g0017 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02896 | hp1 | a0002 | c0004 | t0001 | g0022 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02897 | hp2 | a0002 | c0004 | t0001 | g0022 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02965 | hp2 | a0005 | c0007 | t0001 | g0025 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02970 | hp1 | a0005 | c0007 | t0001 | g0025 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02970 | hp2 | a0001 | c0003 | t0001 | g0054 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02976 | hp1 | a0012 | c0021 | t0001 | g0034 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03098 | hp2 | a0013 | c0025 | t0001 | g0091 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03195 | hp1 | a0004 | c0005 | t0001 | g0017 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03209 | hp1 | a0002 | c0004 | t0001 | g0037 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03486 | hp1 | a0002 | c0004 | t0001 | g0035 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03579 | hp2 | a0001 | c0003 | t0001 | g0013 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03654 | hp2 | a0001 | c0002 | t0001 | g0011 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0089 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03710 | hp2 | a0001 | c0003 | t0001 | g0005 | SAS | PJL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0061 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | BEB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04204 | hp2 | a0014 | c0014 | t0001 | g0064 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | CHB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18906 | hp2 | a0002 | c0013 | t0001 | g0036 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18952 | hp1 | a0015 | c0015 | t0001 | g0058 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18965 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18977 | hp2 | a0016 | c0011 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18987 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18990 | hp1 | a0001 | c0027 | t0001 | g0065 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19043 | hp2 | a0017 | c0018 | t0001 | g0045 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19054 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19084 | hp1 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0002 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19240 | hp1 | a0005 | c0007 | t0001 | g0001 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20129 | hp1 | a0004 | c0005 | t0001 | g0017 | AFR | ASW | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0002 | EUR | TSI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0005 | EUR | TSI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | GIH | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | GIH | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02486 | hp1 | a0010 | c0019 | t0001 | g0032 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0033 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| HG03471 | hp2 | a0004 | c0005 | t0001 | g0052 | AFR | MSL | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20300 | hp1 | a0018 | c0023 | t0001 | g0040 | AFR | USA | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| homoSapiens | chm13v2 | a0019 | c0016 | t0001 | g0003 | REF | REF | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | CEL_chr9_133056981_133076861 | CEL | chr9 | 133056981 | 133076861 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133062003 | A | G | 1 | a0009 | 1 | HG02080.hp2 | start_lost | HIGH | c.1A>G | p.Met1? | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/11 | 23/2381 | 1/2262 | 1/753 | chr9 | 133062003 | |||
| chr9:133062063 | G | A | 1 | a0016 | 1 | NA18977.hp2 | missense_variant | MODERATE | c.61G>A | p.Ala21Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/11 | 83/2381 | 61/2262 | 21/753 | chr9 | 133062063 | |||
| chr9:133064661 | T | C | 1 | a0011 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.239T>C | p.Phe80Ser | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/11 | 261/2381 | 239/2262 | 80/753 | chr9 | 133064661 | |||
| chr9:133065052 | T | G | 1 | a0002 | 5 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(2): Show |
missense_variant | MODERATE | c.353T>G | p.Leu118Arg | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/11 | 375/2381 | 353/2262 | 118/753 | chr9 | 133065052 | |||
| chr9:133065138 | G | GGCGAGGA others(27): Show |
1 | a0014 | 1 | HG04204.hp2 | frameshift_variant | HIGH | c.441_474dupCGAGGAGA others(26): Show |
p.Val159fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/11 | 497/2381 | 475/2262 | 159/753 | INFO_REALIGN_3_PRIME | chr9 | 133065138 | ||
| chr9:133067160 | C | G | 1 | a0013 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.850C>G | p.Arg284Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/11 | 872/2381 | 850/2262 | 284/753 | chr9 | 133067160 | |||
| chr9:133068741 | A | G | 1 | a0012 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.965A>G | p.Asn322Ser | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/11 | 987/2381 | 965/2262 | 322/753 | chr9 | 133068741 | |||
| chr9:133070540 | G | A | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1366G>A | p.Ala456Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1388/2381 | 1366/2262 | 456/753 | chr9 | 133070540 | |||
| chr9:133070541 | C | G | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1367C>G | p.Ala456Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1389/2381 | 1367/2262 | 456/753 | chr9 | 133070541 | |||
| chr9:133070548 | C | G | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1374C>G | p.Asp458Glu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1396/2381 | 1374/2262 | 458/753 | chr9 | 133070548 | |||
| chr9:133070558 | G | A | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1384G>A | p.Val462Ile | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1406/2381 | 1384/2262 | 462/753 | chr9 | 133070558 | |||
| chr9:133070567 | A | G | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1393A>G | p.Lys465Glu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1415/2381 | 1393/2262 | 465/753 | chr9 | 133070567 | |||
| chr9:133070585 | A | C | 1 | a0015 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.1411A>C | p.Thr471Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1433/2381 | 1411/2262 | 471/753 | chr9 | 133070585 | |||
| chr9:133070601 | A | G | 1 | a0007 | 2 | HG01168.hp1 HG01169.hp1 |
missense_variant | MODERATE | c.1427A>G | p.Gln476Arg | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1449/2381 | 1427/2262 | 476/753 | chr9 | 133070601 | |||
| chr9:133070628 | T | C | 2 | a0005 a0015 |
4 | HG02965.hp2 HG02970.hp1 NA18952.hp1 others(1): Show |
missense_variant | MODERATE | c.1454T>C | p.Ile485Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1476/2381 | 1454/2262 | 485/753 | chr9 | 133070628 | |||
| chr9:133071003 | G | C | 1 | a0006 | 2 | HG01070.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.1501G>C | p.Asp501His | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1523/2381 | 1501/2262 | 501/753 | chr9 | 133071003 | |||
| chr9:133071121 | G | A | 1 | a0004 | 4 | HG02895.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.1619G>A | p.Arg540His | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1641/2381 | 1619/2262 | 540/753 | chr9 | 133071121 | |||
| chr9:133071216 | CCCCCCAC others(389): Show |
C | 1 | a0013 | 1 | HG03098.hp2 | disruptive_inframe_deletion | MODERATE | c.1776_2171del | p.Val593_Pro724del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1798/2381 | 1776/2262 | 592/753 | INFO_REALIGN_3_PRIME | chr9 | 133071216 | ||
| chr9:133071218 | CCCCACGG others(26): Show |
C | 1 | a0001 | 1 | HG03704.hp2 | disruptive_inframe_deletion | MODERATE | c.1733_1765delAGACCG others(27): Show |
p.Glu578_Ser588del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1755/2381 | 1733/2262 | 578/753 | INFO_REALIGN_3_PRIME | chr9 | 133071218 | ||
| chr9:133071218 | CCCCACGG others(92): Show |
C | 1 | a0001 | 2 | HG03942.hp2 HG04199.hp1 |
disruptive_inframe_deletion | MODERATE | c.1733_1831delAGACCG others(93): Show |
p.Glu578_Ser610del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1755/2381 | 1733/2262 | 578/753 | INFO_REALIGN_3_PRIME | chr9 | 133071218 | ||
| chr9:133071240 | GCCCCCGT others(26): Show |
G | 4 | a0001 a0005 a0007 others(1): Show |
83 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(80): Show |
disruptive_inframe_deletion | MODERATE | c.1965_1997delGGCCCC others(27): Show |
p.Ala656_Gly666del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071240 | ||
| chr9:133071240 | GCCCCCGT others(59): Show |
G | 3 | a0001 a0005 a0009 |
38 | HG00140.hp1 HG00323.hp1 HG00741.hp1 others(35): Show |
disruptive_inframe_deletion | MODERATE | c.1932_1997delGGCCCC others(60): Show |
p.Ala645_Gly666del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | INFO_REALIGN_3_PRIME | chr9 | 133071240 | ||
| chr9:133071240 | GCCCCCGT others(92): Show |
G | 1 | a0001 | 13 | HG01257.hp2 HG01258.hp1 HG02109.hp1 others(10): Show |
disruptive_inframe_deletion | MODERATE | c.1899_1997delGGCCCC others(93): Show |
p.Ala634_Gly666del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071240 | ||
| chr9:133071240 | GCCCCCGT others(125): Show |
G | 1 | a0001 | 3 | HG02896.hp2 NA18747.hp2 NA19240.hp2 |
disruptive_inframe_deletion | MODERATE | c.1866_1997del | p.Ala623_Gly666del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1888/2381 | 1866/2262 | 622/753 | INFO_REALIGN_3_PRIME | chr9 | 133071240 | ||
| chr9:133071240 | GCCCCCGT others(158): Show |
G | 2 | a0001 a0002 |
3 | HG01109.hp1 HG03486.hp1 HG03654.hp1 |
disruptive_inframe_deletion | MODERATE | c.1833_1997del | p.Ala612_Gly666del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1855/2381 | 1833/2262 | 611/753 | INFO_REALIGN_3_PRIME | chr9 | 133071240 | ||
| chr9:133071270 | G | GC | 2 | a0001 a0002 |
45 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(42): Show |
frameshift_variant | HIGH | c.1776dupC | p.Val593fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1799/2381 | 1777/2262 | 593/753 | INFO_REALIGN_3_PRIME | chr9 | 133071270 | ||
| chr9:133071273 | C | CCCCCCGT others(20495): Show |
1 | a0001 | 1 | NA18975.hp2 | stop_gained&conservative_inframe_insertion | HIGH | c.1875_1876insCGTGCC others(20496): Show |
p.Pro625_Val626insAr others(20500): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071273 | ||
| chr9:133071273 | C | CCCCCCGT others(20691): Show |
1 | a0001 | 1 | NA18747.hp1 | frameshift_variant&stop_gained | HIGH | c.1931_1932insCGCCCC others(20692): Show |
p.Ser654fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | INFO_REALIGN_3_PRIME | chr9 | 133071273 | ||
| chr9:133071303 | G | C | 1 | a0001 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1801G>C | p.Ala601Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1823/2381 | 1801/2262 | 601/753 | chr9 | 133071303 | |||
| chr9:133071304 | CCCCCCCC others(25): Show |
C | 1 | a0001 | 28 | HG00423.hp1 HG00438.hp2 HG00597.hp2 others(25): Show |
frameshift_variant | HIGH | c.1810_1841delGTGCCG others(26): Show |
p.Val604fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1832/2381 | 1810/2262 | 604/753 | INFO_REALIGN_3_PRIME | chr9 | 133071304 | ||
| chr9:133071304 | CCCCCCCC others(58): Show |
C | 1 | a0001 | 6 | HG00438.hp1 HG00738.hp1 HG02647.hp2 others(3): Show |
frameshift_variant | HIGH | c.1810_1874delGTGCCG others(59): Show |
p.Val604fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1832/2381 | 1810/2262 | 604/753 | INFO_REALIGN_3_PRIME | chr9 | 133071304 | ||
| chr9:133071304 | CCCCCCCC others(91): Show |
C | 2 | a0001 a0002 |
7 | HG00735.hp2 HG02165.hp2 HG02602.hp1 others(4): Show |
frameshift_variant | HIGH | c.1810_1907delGTGCCG others(92): Show |
p.Val604fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1832/2381 | 1810/2262 | 604/753 | INFO_REALIGN_3_PRIME | chr9 | 133071304 | ||
| chr9:133071306 | C | CCCCCCGT others(20382): Show |
1 | a0001 | 1 | HG00558.hp2 | frameshift_variant&stop_gained | HIGH | c.1964_1965insCGCCCC others(20383): Show |
p.Ser665fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071306 | ||
| chr9:133071330 | T | G | 1 | a0004 | 4 | HG02895.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
missense_variant | MODERATE | c.1828T>G | p.Ser610Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1850/2381 | 1828/2262 | 610/753 | chr9 | 133071330 | |||
| chr9:133071336 | G | C | 1 | a0001 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1834G>C | p.Ala612Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1856/2381 | 1834/2262 | 612/753 | chr9 | 133071336 | |||
| chr9:133071337 | CCCCCCCC others(25): Show |
C | 1 | a0001 | 20 | HG01099.hp1 HG01106.hp1 HG01433.hp1 others(17): Show |
frameshift_variant | HIGH | c.1843_1874delGTGCCG others(26): Show |
p.Val615fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | chr9 | 133071337 | ||
| chr9:133071337 | CCCCCCCC others(58): Show |
C | 2 | a0001 a0011 |
5 | HG01099.hp2 HG02055.hp2 HG02698.hp2 others(2): Show |
frameshift_variant | HIGH | c.1843_1907delGTGCCG others(59): Show |
p.Val615fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | chr9 | 133071337 | ||
| chr9:133071337 | CCCCCCCC others(91): Show |
C | 1 | a0001 | 1 | NA19072.hp1 | frameshift_variant | HIGH | c.1843_1940delGTGCCG others(92): Show |
p.Val615fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1865/2381 | 1843/2262 | 615/753 | INFO_REALIGN_3_PRIME | chr9 | 133071337 | ||
| chr9:133071339 | C | CCCCCCGT others(20288): Show |
1 | a0001 | 1 | HG03834.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.1898_1899insCGCCCC others(20289): Show |
p.Gly633_Ala634insAl others(20293): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20285): Show |
1 | a0001 | 1 | NA19004.hp2 | stop_gained&disruptive_inframe_insertion | HIGH | c.1898_1899insCGCCCC others(20286): Show |
p.Gly633_Ala634insAl others(20290): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20283): Show |
1 | a0001 | 1 | NA18947.hp1 | frameshift_variant&stop_gained | HIGH | c.1898_1899insCGCCCC others(20284): Show |
p.Ser643fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20286): Show |
1 | a0001 | 1 | NA18957.hp1 | frameshift_variant&stop_gained | HIGH | c.1898_1899insCGCCCC others(20287): Show |
p.Ser643fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20286): Show |
1 | a0018 | 1 | NA20300.hp1 | frameshift_variant&stop_gained | HIGH | c.1898_1899insCGCCCC others(20287): Show |
p.Ser643fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20286): Show |
1 | a0001 | 1 | NA19009.hp1 | frameshift_variant&stop_gained | HIGH | c.1898_1899insCGCCCC others(20287): Show |
p.Ser643fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20285): Show |
1 | a0001 | 1 | NA18959.hp1 | stop_gained&disruptive_inframe_insertion | HIGH | c.1898_1899insCGCCCC others(20286): Show |
p.Gly633_Ala634insAl others(20290): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20317): Show |
1 | a0001 | 1 | NA18943.hp1 | frameshift_variant&stop_gained | HIGH | c.1931_1932insCGCCCC others(20318): Show |
p.Ser654fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20284): Show |
1 | a0001 | 1 | NA19070.hp2 | frameshift_variant&stop_gained | HIGH | c.1931_1932insCGCCCC others(20285): Show |
p.Pro671fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071339 | C | CCCCCCGT others(20350): Show |
1 | a0001 | 1 | HG00280.hp2 | frameshift_variant&stop_gained | HIGH | c.1964_1965insCGCCCC others(20351): Show |
p.Ser665fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071339 | ||
| chr9:133071348 | C | A | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1846C>A | p.Pro616Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1868/2381 | 1846/2262 | 616/753 | chr9 | 133071348 | |||
| chr9:133071350 | G | GCCCACGG others(20251): Show |
1 | a0001 | 1 | NA19080.hp1 | frameshift_variant&stop_gained | HIGH | c.1898_1899insCGCCCC others(20252): Show |
p.Ser643fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071350 | ||
| chr9:133071363 | T | G | 3 | a0001 a0004 a0012 |
6 | HG02895.hp1 HG02976.hp1 HG03195.hp1 others(3): Show |
missense_variant | MODERATE | c.1861T>G | p.Ser621Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1883/2381 | 1861/2262 | 621/753 | chr9 | 133071363 | |||
| chr9:133071366 | GGGGCCCC others(91): Show |
G | 1 | a0001 | 1 | NA18979.hp1 | frameshift_variant | HIGH | c.1868_1965delCCCCCC others(92): Show |
p.Ala623fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1890/2381 | 1868/2262 | 623/753 | INFO_REALIGN_3_PRIME | chr9 | 133071366 | ||
| chr9:133071367 | G | A | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1865G>A | p.Gly622Glu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1887/2381 | 1865/2262 | 622/753 | chr9 | 133071367 | |||
| chr9:133071368 | GGCCCCCC others(125): Show |
G | 1 | a0001 | 1 | HG02451.hp1 | conservative_inframe_deletion | MODERATE | c.1894_2025del | p.Ser632_Asp675del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1916/2381 | 1894/2262 | 632/753 | INFO_REALIGN_3_PRIME | chr9 | 133071368 | ||
| chr9:133071369 | G | A | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1867G>A | p.Ala623Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1889/2381 | 1867/2262 | 623/753 | chr9 | 133071369 | |||
| chr9:133071369 | G | C | 2 | a0001 a0012 |
3 | HG01433.hp2 HG02976.hp1 HG03491.hp2 |
missense_variant | MODERATE | c.1867G>C | p.Ala623Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1889/2381 | 1867/2262 | 623/753 | chr9 | 133071369 | |||
| chr9:133071369 | G | GC | 2 | a0001 a0010 |
24 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(21): Show |
frameshift_variant | HIGH | c.1875dupC | p.Val626fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071369 | ||
| chr9:133071369 | G | GCCCCCCC others(20426): Show |
1 | a0001 | 1 | HG03831.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.1875_1876insCGTGCC others(20427): Show |
p.Pro625_Val626insAr others(20431): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071369 | ||
| chr9:133071369 | GCCCCCCC others(158): Show |
G | 1 | a0002 | 1 | HG02897.hp2 | disruptive_inframe_deletion | MODERATE | c.1899_2063del | p.Ala634_Gly688del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | INFO_REALIGN_3_PRIME | chr9 | 133071369 | ||
| chr9:133071370 | CCCCCCCC others(25): Show |
C | 1 | a0001 | 8 | HG00642.hp2 HG02145.hp2 NA18960.hp1 others(5): Show |
frameshift_variant | HIGH | c.1876_1907delGTGCCG others(26): Show |
p.Val626fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071370 | ||
| chr9:133071370 | CCCCCCCC others(58): Show |
C | 1 | a0001 | 2 | HG00609.hp1 HG02258.hp1 |
frameshift_variant | HIGH | c.1876_1940delGTGCCG others(59): Show |
p.Val626fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071370 | ||
| chr9:133071372 | C | G | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1870C>G | p.Pro624Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1892/2381 | 1870/2262 | 624/753 | chr9 | 133071372 | |||
| chr9:133071373 | CCCCCGTG others(256): Show |
C | 1 | a0004 | 1 | HG03195.hp1 | frameshift_variant | HIGH | c.1876_2138del | p.Val626fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1898/2381 | 1876/2262 | 626/753 | INFO_REALIGN_3_PRIME | chr9 | 133071373 | ||
| chr9:133071384 | C | G | 1 | a0001 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1882C>G | p.Pro628Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1904/2381 | 1882/2262 | 628/753 | chr9 | 133071384 | |||
| chr9:133071396 | T | G | 1 | a0001 | 3 | HG00642.hp1 HG01069.hp2 HG01433.hp2 |
missense_variant | MODERATE | c.1894T>G | p.Ser632Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1916/2381 | 1894/2262 | 632/753 | chr9 | 133071396 | |||
| chr9:133071401 | GGCCCCCC others(92): Show |
G | 1 | a0001 | 1 | NA20905.hp1 | conservative_inframe_deletion | MODERATE | c.1927_2025delTCCGGG others(93): Show |
p.Ser643_Asp675del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1949/2381 | 1927/2262 | 643/753 | INFO_REALIGN_3_PRIME | chr9 | 133071401 | ||
| chr9:133071401 | GGCCCCCC others(158): Show |
G | 1 | a0001 | 2 | HG02083.hp1 HG02155.hp1 |
conservative_inframe_deletion | MODERATE | c.1945_2109del | p.Pro649_Val703del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1967/2381 | 1945/2262 | 649/753 | INFO_REALIGN_3_PRIME | chr9 | 133071401 | ||
| chr9:133071402 | G | C | 1 | a0001 | 4 | HG00642.hp1 HG01069.hp2 HG01433.hp2 others(1): Show |
missense_variant | MODERATE | c.1900G>C | p.Ala634Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1922/2381 | 1900/2262 | 634/753 | chr9 | 133071402 | |||
| chr9:133071402 | G | GC | 1 | a0001 | 28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
frameshift_variant | HIGH | c.1908dupC | p.Val637fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1931/2381 | 1909/2262 | 637/753 | INFO_REALIGN_3_PRIME | chr9 | 133071402 | ||
| chr9:133071403 | CCCCCCCC others(25): Show |
C | 3 | a0001 a0005 a0007 |
15 | HG00544.hp2 HG00558.hp1 HG01109.hp2 others(12): Show |
frameshift_variant | HIGH | c.1909_1940delGTGCCG others(26): Show |
p.Val637fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1931/2381 | 1909/2262 | 637/753 | INFO_REALIGN_3_PRIME | chr9 | 133071403 | ||
| chr9:133071403 | CCCCCCCC others(91): Show |
C | 1 | a0001 | 4 | HG02293.hp1 NA18987.hp1 NA19003.hp2 others(1): Show |
frameshift_variant | HIGH | c.1909_2006delGTGCCG others(92): Show |
p.Val637fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1931/2381 | 1909/2262 | 637/753 | INFO_REALIGN_3_PRIME | chr9 | 133071403 | ||
| chr9:133071405 | CCCCCCGT others(224): Show |
C | 1 | a0001 | 2 | HG03491.hp1 HG03492.hp2 |
disruptive_inframe_deletion | MODERATE | c.1941_2171del | p.Val648_Pro724del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1963/2381 | 1941/2262 | 647/753 | INFO_REALIGN_3_PRIME | chr9 | 133071405 | ||
| chr9:133071410 | CGTGCCGC others(257): Show |
C | 1 | a0004 | 3 | HG02895.hp1 HG03471.hp2 NA20129.hp1 |
disruptive_inframe_deletion | MODERATE | c.1914_2177del | p.Pro639_Pro726del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1936/2381 | 1914/2262 | 638/753 | INFO_REALIGN_3_PRIME | chr9 | 133071410 | ||
| chr9:133071429 | T | G | 1 | a0001 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.1927T>G | p.Ser643Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1949/2381 | 1927/2262 | 643/753 | chr9 | 133071429 | |||
| chr9:133071432 | GGGGCCCC others(91): Show |
G | 2 | a0001 a0003 |
5 | HG00280.hp1 HG00642.hp1 HG01175.hp2 others(2): Show |
frameshift_variant | HIGH | c.1942_2039delGTGCCG others(92): Show |
p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071432 | ||
| chr9:133071433 | G | GC | 1 | a0001 | 18 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(15): Show |
frameshift_variant | HIGH | c.1931_1932insC | p.Ala645fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | chr9 | 133071433 | |||
| chr9:133071435 | G | C | 1 | a0001 | 19 | HG00408.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
missense_variant | MODERATE | c.1933G>C | p.Ala645Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1955/2381 | 1933/2262 | 645/753 | chr9 | 133071435 | |||
| chr9:133071435 | G | GC | 1 | a0001 | 23 | HG00544.hp1 HG00597.hp2 HG01099.hp2 others(20): Show |
frameshift_variant | HIGH | c.1941dupC | p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | G | GCCCCCCC others(27): Show |
1 | a0001 | 1 | NA19043.hp1 | frameshift_variant&stop_gained | HIGH | c.1959_1960insGCCGGG others(28): Show |
p.Ser654fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1982/2381 | 1960/2262 | 654/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | G | GCCCCCCC others(59): Show |
1 | a0001 | 2 | HG02647.hp1 NA21309.hp1 |
disruptive_inframe_insertion | MODERATE | c.1964_1965insCGCCCC others(60): Show |
p.Gly655_Ala656insAl others(64): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | G | GCCCCCCC others(60): Show |
1 | a0001 | 2 | HG01167.hp1 HG02622.hp2 |
frameshift_variant&stop_gained | HIGH | c.1964_1965insCGCCCC others(61): Show |
p.Ser665fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | G | GCCCCCCC others(20353): Show |
1 | a0014 | 1 | HG04204.hp2 | frameshift_variant&stop_gained | HIGH | c.1964_1965insCGCCCC others(20354): Show |
p.Ser665fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | GCCCCCCC others(27): Show |
G | 1 | a0001 | 1 | HG01123.hp1 | frameshift_variant | HIGH | c.1941_1974delCGTGCC others(28): Show |
p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1963/2381 | 1941/2262 | 647/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071435 | GCCCCCCC others(92): Show |
G | 2 | a0001 a0006 |
4 | HG00140.hp2 HG01070.hp1 HG01081.hp1 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.1965_2063delGGCCCC others(93): Show |
p.Ala656_Gly688del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | INFO_REALIGN_3_PRIME | chr9 | 133071435 | ||
| chr9:133071436 | CCCCCCCC others(25): Show |
C | 1 | a0001 | 8 | HG01243.hp1 HG04115.hp2 HG04228.hp1 others(5): Show |
frameshift_variant | HIGH | c.1942_1973delGTGCCG others(26): Show |
p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071436 | ||
| chr9:133071436 | CCCCCCCC others(58): Show |
C | 2 | a0001 a0002 |
2 | NA18906.hp2 NA18954.hp1 |
frameshift_variant | HIGH | c.1942_2006delGTGCCG others(59): Show |
p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071436 | ||
| chr9:133071436 | CCCCCCCC others(90): Show |
C | 1 | a0003 | 2 | HG00733.hp2 HG01517.hp2 |
frameshift_variant | HIGH | c.1942_2038delGTGCCG others(91): Show |
p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071436 | ||
| chr9:133071436 | CCCCCCCC others(157): Show |
C | 1 | a0002 | 1 | HG02896.hp1 | frameshift_variant | HIGH | c.1942_2105del | p.Val648fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1964/2381 | 1942/2262 | 648/753 | INFO_REALIGN_3_PRIME | chr9 | 133071436 | ||
| chr9:133071443 | CGTGCCGC others(224): Show |
C | 1 | a0012 | 1 | HG02976.hp1 | disruptive_inframe_deletion | MODERATE | c.1947_2177del | p.Pro650_Pro726del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1969/2381 | 1947/2262 | 649/753 | INFO_REALIGN_3_PRIME | chr9 | 133071443 | ||
| chr9:133071447 | C | A | 1 | a0001 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1945C>A | p.Pro649Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1967/2381 | 1945/2262 | 649/753 | chr9 | 133071447 | |||
| chr9:133071462 | T | G | 3 | a0001 a0008 a0017 |
79 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(76): Show |
missense_variant | MODERATE | c.1960T>G | p.Ser654Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1982/2381 | 1960/2262 | 654/753 | chr9 | 133071462 | |||
| chr9:133071465 | GGGGCCCC others(91): Show |
G | 1 | a0001 | 2 | HG01433.hp2 HG01934.hp2 |
frameshift_variant | HIGH | c.1966_2063delGCCCCC others(92): Show |
p.Ala656fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1988/2381 | 1966/2262 | 656/753 | INFO_REALIGN_3_PRIME | chr9 | 133071465 | ||
| chr9:133071466 | G | A | 1 | a0001 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1964G>A | p.Gly655Glu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1986/2381 | 1964/2262 | 655/753 | chr9 | 133071466 | |||
| chr9:133071467 | G | GC | 3 | a0001 a0008 a0017 |
38 | HG00408.hp1 HG00558.hp1 HG00621.hp1 others(35): Show |
frameshift_variant | HIGH | c.1965_1966insC | p.Ala656fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1988/2381 | 1966/2262 | 656/753 | chr9 | 133071467 | |||
| chr9:133071467 | GGCCCCCC others(26): Show |
G | 1 | a0001 | 1 | HG03041.hp2 | conservative_inframe_deletion | MODERATE | c.1993_2025delTCCGGC others(27): Show |
p.Ser665_Asp675del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2015/2381 | 1993/2262 | 665/753 | INFO_REALIGN_3_PRIME | chr9 | 133071467 | ||
| chr9:133071467 | GGCCCCCC others(92): Show |
G | 1 | a0001 | 1 | HG01069.hp2 | disruptive_inframe_deletion | MODERATE | c.1998_2096delCGCCCC others(93): Show |
p.Ala667_Gly699del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2020/2381 | 1998/2262 | 666/753 | INFO_REALIGN_3_PRIME | chr9 | 133071467 | ||
| chr9:133071468 | G | A | 1 | a0001 | 1 | HG03491.hp2 | missense_variant | MODERATE | c.1966G>A | p.Ala656Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1988/2381 | 1966/2262 | 656/753 | chr9 | 133071468 | |||
| chr9:133071468 | G | C | 3 | a0001 a0008 a0017 |
79 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(76): Show |
missense_variant | MODERATE | c.1966G>C | p.Ala656Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1988/2381 | 1966/2262 | 656/753 | chr9 | 133071468 | |||
| chr9:133071468 | G | GC | 2 | a0001 a0005 |
23 | HG01109.hp2 HG01169.hp2 HG01175.hp1 others(20): Show |
frameshift_variant | HIGH | c.1974dupC | p.Val659fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1997/2381 | 1975/2262 | 659/753 | INFO_REALIGN_3_PRIME | chr9 | 133071468 | ||
| chr9:133071469 | CCCCCCCC others(25): Show |
C | 2 | a0001 a0016 |
11 | HG02071.hp2 HG02109.hp2 HG02280.hp1 others(8): Show |
frameshift_variant | HIGH | c.1975_2006delGTGCCG others(26): Show |
p.Val659fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1997/2381 | 1975/2262 | 659/753 | INFO_REALIGN_3_PRIME | chr9 | 133071469 | ||
| chr9:133071469 | CCCCCCCC others(91): Show |
C | 1 | a0001 | 1 | HG02055.hp1 | frameshift_variant | HIGH | c.1975_2072delGTGCCG others(92): Show |
p.Val659fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1997/2381 | 1975/2262 | 659/753 | INFO_REALIGN_3_PRIME | chr9 | 133071469 | ||
| chr9:133071495 | T | G | 2 | a0001 a0010 |
3 | HG02486.hp1 HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.1993T>G | p.Ser665Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2015/2381 | 1993/2262 | 665/753 | chr9 | 133071495 | |||
| chr9:133071500 | CGCCCCCC others(25): Show |
C | 1 | a0001 | 2 | NA19063.hp2 NA19065.hp1 |
frameshift_variant | HIGH | c.2008_2039delGTGCCG others(26): Show |
p.Val670fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2030/2381 | 2008/2262 | 670/753 | INFO_REALIGN_3_PRIME | chr9 | 133071500 | ||
| chr9:133071501 | G | C | 2 | a0001 a0010 |
4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.1999G>C | p.Ala667Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2021/2381 | 1999/2262 | 667/753 | chr9 | 133071501 | |||
| chr9:133071501 | G | GC | 3 | a0001 a0002 a0014 |
52 | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(49): Show |
frameshift_variant | HIGH | c.2007dupC | p.Val670fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2030/2381 | 2008/2262 | 670/753 | INFO_REALIGN_3_PRIME | chr9 | 133071501 | ||
| chr9:133071501 | GCCCCCCC others(26): Show |
G | 1 | a0001 | 1 | HG03540.hp2 | conservative_inframe_deletion | MODERATE | c.2026_2058delGCCGGG others(27): Show |
p.Ala676_Asp686del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2048/2381 | 2026/2262 | 676/753 | INFO_REALIGN_3_PRIME | chr9 | 133071501 | ||
| chr9:133071504 | C | CCCCCCGT others(59): Show |
1 | a0017 | 1 | NA19043.hp2 | conservative_inframe_insertion | MODERATE | c.2025_2026insTCCGGG others(60): Show |
p.Asp675_Ala676insSe others(64): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2048/2381 | 2026/2262 | 676/753 | INFO_REALIGN_3_PRIME | chr9 | 133071504 | ||
| chr9:133071504 | CCCCCCGT others(125): Show |
C | 1 | a0001 | 1 | HG03491.hp2 | conservative_inframe_deletion | MODERATE | c.2026_2157del | p.Ala676_Asp719del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2048/2381 | 2026/2262 | 676/753 | INFO_REALIGN_3_PRIME | chr9 | 133071504 | ||
| chr9:133071505 | CCCCCGTG others(124): Show |
C | 1 | a0001 | 1 | HG01496.hp2 | frameshift_variant | HIGH | c.2008_2138del | p.Val670fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2030/2381 | 2008/2262 | 670/753 | INFO_REALIGN_3_PRIME | chr9 | 133071505 | ||
| chr9:133071528 | G | T | 3 | a0001 a0010 a0017 |
4 | HG02486.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.2026G>T | p.Ala676Ser | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2048/2381 | 2026/2262 | 676/753 | chr9 | 133071528 | |||
| chr9:133071532 | G | C | 2 | a0001 a0003 |
3 | HG00280.hp1 HG00642.hp1 HG01943.hp1 |
missense_variant | MODERATE | c.2030G>C | p.Gly677Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2052/2381 | 2030/2262 | 677/753 | chr9 | 133071532 | |||
| chr9:133071533 | G | GC | 6 | a0001 a0002 a0007 others(3): Show |
181 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(178): Show |
frameshift_variant | HIGH | c.2040dupC | p.Val681fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2063/2381 | 2041/2262 | 681/753 | INFO_REALIGN_3_PRIME | chr9 | 133071533 | ||
| chr9:133071533 | G | GCCCCCCC others(95): Show |
1 | a0001 | 1 | HG03139.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.2040_2041insCGTGCC others(96): Show |
p.Pro680_Val681insAr others(100): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2063/2381 | 2041/2262 | 681/753 | INFO_REALIGN_3_PRIME | chr9 | 133071533 | ||
| chr9:133071534 | C | G | 3 | a0001 a0010 a0017 |
3 | HG02486.hp1 NA19043.hp2 NA20905.hp1 |
missense_variant | MODERATE | c.2032C>G | p.Pro678Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2054/2381 | 2032/2262 | 678/753 | chr9 | 133071534 | |||
| chr9:133071534 | CCCCCCCC others(26): Show |
C | 1 | a0001 | 32 | HG00323.hp2 HG00558.hp1 HG00639.hp1 others(29): Show |
disruptive_inframe_deletion | MODERATE | c.2064_2096delCGCCCC others(27): Show |
p.Ala689_Gly699del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2086/2381 | 2064/2262 | 688/753 | INFO_REALIGN_3_PRIME | chr9 | 133071534 | ||
| chr9:133071535 | CCCCCCCC others(25): Show |
C | 2 | a0001 a0008 |
42 | HG00408.hp1 HG00597.hp1 HG00621.hp1 others(39): Show |
frameshift_variant | HIGH | c.2041_2072delGTGCCG others(26): Show |
p.Val681fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2063/2381 | 2041/2262 | 681/753 | INFO_REALIGN_3_PRIME | chr9 | 133071535 | ||
| chr9:133071561 | T | G | 1 | a0001 | 2 | HG00642.hp1 NA20905.hp1 |
missense_variant | MODERATE | c.2059T>G | p.Ser687Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2081/2381 | 2059/2262 | 687/753 | chr9 | 133071561 | |||
| chr9:133071564 | GGCGCCCC others(25): Show |
G | 1 | a0001 | 1 | HG01192.hp1 | frameshift_variant | HIGH | c.2064_2095delCGCCCC others(26): Show |
p.Ala689fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2086/2381 | 2064/2262 | 688/753 | INFO_REALIGN_3_PRIME | chr9 | 133071564 | ||
| chr9:133071567 | G | C | 1 | a0001 | 5 | HG00642.hp1 HG01069.hp2 HG01433.hp2 others(2): Show |
missense_variant | MODERATE | c.2065G>C | p.Ala689Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2087/2381 | 2065/2262 | 689/753 | chr9 | 133071567 | |||
| chr9:133071567 | G | GC | 3 | a0001 a0002 a0007 |
85 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(82): Show |
frameshift_variant | HIGH | c.2073dupC | p.Val692fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2096/2381 | 2074/2262 | 692/753 | INFO_REALIGN_3_PRIME | chr9 | 133071567 | ||
| chr9:133071567 | G | GCCCCCCC others(95): Show |
1 | a0001 | 1 | HG02809.hp1 | stop_gained&conservative_inframe_insertion | HIGH | c.2073_2074insCGTGCC others(96): Show |
p.Pro691_Val692insAr others(100): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2096/2381 | 2074/2262 | 692/753 | INFO_REALIGN_3_PRIME | chr9 | 133071567 | ||
| chr9:133071567 | G | GCCCCCCC others(27): Show |
1 | a0001 | 1 | NA18947.hp1 | frameshift_variant&stop_gained | HIGH | c.2091_2092insGCCGGG others(28): Show |
p.Ser698fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2114/2381 | 2092/2262 | 698/753 | INFO_REALIGN_3_PRIME | chr9 | 133071567 | ||
| chr9:133071579 | C | A | 1 | a0010 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2077C>A | p.Pro693Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2099/2381 | 2077/2262 | 693/753 | chr9 | 133071579 | |||
| chr9:133071581 | GCCCACGG others(26): Show |
G | 1 | a0001 | 1 | HG02970.hp2 | disruptive_inframe_deletion | MODERATE | c.2096_2128delGGGCCC others(27): Show |
p.Gly699_Ser709del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2118/2381 | 2096/2262 | 699/753 | INFO_REALIGN_3_PRIME | chr9 | 133071581 | ||
| chr9:133071594 | T | G | 2 | a0001 a0017 |
3 | HG00609.hp1 NA18954.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2092T>G | p.Ser698Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2114/2381 | 2092/2262 | 698/753 | chr9 | 133071594 | |||
| chr9:133071598 | G | A | 1 | a0010 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2096G>A | p.Gly699Glu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2118/2381 | 2096/2262 | 699/753 | chr9 | 133071598 | |||
| chr9:133071600 | G | A | 1 | a0010 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2098G>A | p.Ala700Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2120/2381 | 2098/2262 | 700/753 | chr9 | 133071600 | |||
| chr9:133071600 | G | C | 2 | a0001 a0017 |
4 | HG00609.hp1 HG01192.hp1 NA18954.hp1 others(1): Show |
missense_variant | MODERATE | c.2098G>C | p.Ala700Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2120/2381 | 2098/2262 | 700/753 | chr9 | 133071600 | |||
| chr9:133071600 | G | GC | 1 | a0001 | 47 | HG00423.hp2 HG00544.hp2 HG00597.hp2 others(44): Show |
frameshift_variant | HIGH | c.2106dupC | p.Val703fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2129/2381 | 2107/2262 | 703/753 | INFO_REALIGN_3_PRIME | chr9 | 133071600 | ||
| chr9:133071603 | C | G | 1 | a0010 | 1 | HG02486.hp1 | missense_variant | MODERATE | c.2101C>G | p.Pro701Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2123/2381 | 2101/2262 | 701/753 | chr9 | 133071603 | |||
| chr9:133071603 | CCCCCCGT others(26): Show |
C | 1 | a0001 | 1 | HG00609.hp1 | conservative_inframe_deletion | MODERATE | c.2110_2142delACCCCC others(27): Show |
p.Thr704_Val714del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2132/2381 | 2110/2262 | 704/753 | INFO_REALIGN_3_PRIME | chr9 | 133071603 | ||
| chr9:133071604 | CCCCCGTG others(25): Show |
C | 1 | a0001 | 1 | NA18954.hp1 | frameshift_variant | HIGH | c.2107_2138delGTGACC others(26): Show |
p.Val703fs | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2129/2381 | 2107/2262 | 703/753 | INFO_REALIGN_3_PRIME | chr9 | 133071604 | ||
| chr9:133071612 | A | C | 2 | a0010 a0017 |
2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2110A>C | p.Thr704Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2132/2381 | 2110/2262 | 704/753 | chr9 | 133071612 | |||
| chr9:133071614 | CCCCACGG others(26): Show |
C | 1 | a0003 | 4 | HG00280.hp1 HG00733.hp2 HG01517.hp2 others(1): Show |
disruptive_inframe_deletion | MODERATE | c.2129_2161delAGACCG others(27): Show |
p.Glu710_Ser720del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2151/2381 | 2129/2262 | 710/753 | INFO_REALIGN_3_PRIME | chr9 | 133071614 | ||
| chr9:133071627 | T | G | 1 | a0017 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.2125T>G | p.Ser709Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2147/2381 | 2125/2262 | 709/753 | chr9 | 133071627 | |||
| chr9:133071631 | A | G | 2 | a0010 a0017 |
2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2129A>G | p.Glu710Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2151/2381 | 2129/2262 | 710/753 | chr9 | 133071631 | |||
| chr9:133071632 | G | C | 2 | a0010 a0017 |
2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2130G>C | p.Glu710Asp | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2152/2381 | 2130/2262 | 710/753 | chr9 | 133071632 | |||
| chr9:133071633 | A | G | 2 | a0010 a0017 |
2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2131A>G | p.Thr711Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2153/2381 | 2131/2262 | 711/753 | chr9 | 133071633 | |||
| chr9:133071636 | G | C | 2 | a0010 a0017 |
2 | HG02486.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.2134G>C | p.Ala712Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2156/2381 | 2134/2262 | 712/753 | chr9 | 133071636 | |||
| chr9:133071669 | CCCCCTGT others(26): Show |
C | 1 | a0008 | 1 | HG00738.hp2 | disruptive_inframe_deletion | MODERATE | c.2184_2216delGGGTGA others(27): Show |
p.Gly729_Thr739del | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2206/2381 | 2184/2262 | 728/753 | INFO_REALIGN_3_PRIME | chr9 | 133071669 | ||
| chr9:133071678 | C | A | 2 | a0004 a0012 |
5 | HG02895.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
missense_variant | MODERATE | c.2176C>A | p.Pro726Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2198/2381 | 2176/2262 | 726/753 | chr9 | 133071678 | |||
| chr9:133071859 | C | G | 1 | a0001 | 1 | HG02055.hp2 | splice_region_variant | LOW | c.*95C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | chr9 | 133071859 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133065056 | C | T | 1 | a0001c0027 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.357C>T | p.Pro119Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/11 | 379/2381 | 357/2262 | 119/753 | chr9 | 133065056 | |||
| chr9:133065170 | C | T | 1 | a0001c0026 | 1 | HG00140.hp2 | synonymous_variant | LOW | c.471C>T | p.Ile157Ile | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/11 | 493/2381 | 471/2262 | 157/753 | chr9 | 133065170 | |||
| chr9:133065212 | C | T | 2 | a0001c0024 a0013c0025 |
2 | HG02451.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.513C>T | p.Leu171Leu | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/11 | 535/2381 | 513/2262 | 171/753 | chr9 | 133065212 | |||
| chr9:133066564 | T | C | 2 | a0001c0024 a0013c0025 |
2 | HG02451.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.573T>C | p.Ile191Ile | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 5/11 | 595/2381 | 573/2262 | 191/753 | chr9 | 133066564 | |||
| chr9:133066867 | C | T | 1 | a0001c0022 | 1 | HG01106.hp2 | synonymous_variant | LOW | c.699C>T | p.Ile233Ile | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 6/11 | 721/2381 | 699/2262 | 233/753 | chr9 | 133066867 | |||
| chr9:133068748 | C | T | 2 | a0001c0024 a0013c0025 |
2 | HG02451.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.972C>T | p.Tyr324Tyr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/11 | 994/2381 | 972/2262 | 324/753 | chr9 | 133068748 | |||
| chr9:133069137 | C | T | 8 | a0001c0002 a0001c0003 a0001c0024 others(5): Show |
99 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(96): Show |
synonymous_variant | LOW | c.1164C>T | p.Thr388Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/11 | 1186/2381 | 1164/2262 | 388/753 | chr9 | 133069137 | |||
| chr9:133070551 | T | C | 1 | a0015c0015 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1377T>C | p.Ile459Ile | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1399/2381 | 1377/2262 | 459/753 | chr9 | 133070551 | |||
| chr9:133070560 | T | C | 1 | a0015c0015 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1386T>C | p.Val462Val | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1408/2381 | 1386/2262 | 462/753 | chr9 | 133070560 | |||
| chr9:133070563 | C | T | 1 | a0015c0015 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1389C>T | p.Phe463Phe | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1411/2381 | 1389/2262 | 463/753 | chr9 | 133070563 | |||
| chr9:133070575 | C | T | 1 | a0015c0015 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1401C>T | p.Phe467Phe | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1423/2381 | 1401/2262 | 467/753 | chr9 | 133070575 | |||
| chr9:133070584 | C | T | 1 | a0015c0015 | 1 | NA18952.hp1 | synonymous_variant | LOW | c.1410C>T | p.Pro470Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/11 | 1432/2381 | 1410/2262 | 470/753 | chr9 | 133070584 | |||
| chr9:133071161 | C | G | 1 | a0012c0021 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.1659C>G | p.Thr553Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1681/2381 | 1659/2262 | 553/753 | chr9 | 133071161 | |||
| chr9:133071212 | C | T | 4 | a0001c0002 a0001c0009 a0003c0006 others(1): Show |
91 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
synonymous_variant | LOW | c.1710C>T | p.Pro570Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1732/2381 | 1710/2262 | 570/753 | chr9 | 133071212 | |||
| chr9:133071335 | G | C | 3 | a0001c0001 a0001c0002 a0012c0021 |
4 | HG00642.hp1 HG01069.hp2 HG02976.hp1 others(1): Show |
synonymous_variant | LOW | c.1833G>C | p.Gly611Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1855/2381 | 1833/2262 | 611/753 | chr9 | 133071335 | |||
| chr9:133071350 | G | C | 1 | a0001c0001 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1848G>C | p.Pro616Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1870/2381 | 1848/2262 | 616/753 | chr9 | 133071350 | |||
| chr9:133071368 | G | C | 2 | a0001c0002 a0004c0005 |
6 | HG00642.hp1 HG01069.hp2 HG02895.hp1 others(3): Show |
synonymous_variant | LOW | c.1866G>C | p.Gly622Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1888/2381 | 1866/2262 | 622/753 | chr9 | 133071368 | |||
| chr9:133071380 | G | C | 1 | a0001c0001 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1878G>C | p.Val626Val | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1900/2381 | 1878/2262 | 626/753 | chr9 | 133071380 | |||
| chr9:133071383 | G | T | 1 | a0001c0001 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1881G>T | p.Pro627Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1903/2381 | 1881/2262 | 627/753 | chr9 | 133071383 | |||
| chr9:133071386 | C | A | 1 | a0001c0001 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.1884C>A | p.Pro628Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1906/2381 | 1884/2262 | 628/753 | chr9 | 133071386 | |||
| chr9:133071401 | G | C | 4 | a0001c0001 a0001c0002 a0002c0004 others(1): Show |
9 | HG00558.hp1 HG01361.hp1 HG02293.hp1 others(6): Show |
synonymous_variant | LOW | c.1899G>C | p.Gly633Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1921/2381 | 1899/2262 | 633/753 | chr9 | 133071401 | |||
| chr9:133071434 | G | C | 8 | a0001c0001 a0001c0002 a0001c0003 others(5): Show |
67 | HG00323.hp2 HG00597.hp1 HG00733.hp2 others(64): Show |
synonymous_variant | LOW | c.1932G>C | p.Gly644Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1954/2381 | 1932/2262 | 644/753 | chr9 | 133071434 | |||
| chr9:133071443 | C | T | 1 | a0001c0001 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.1941C>T | p.Pro647Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1963/2381 | 1941/2262 | 647/753 | chr9 | 133071443 | |||
| chr9:133071449 | G | C | 1 | a0001c0001 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.1947G>C | p.Pro649Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1969/2381 | 1947/2262 | 649/753 | chr9 | 133071449 | |||
| chr9:133071467 | G | C | 4 | a0001c0001 a0001c0027 a0010c0019 others(1): Show |
15 | HG02055.hp1 HG02071.hp2 HG02109.hp2 others(12): Show |
synonymous_variant | LOW | c.1965G>C | p.Gly655Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 1987/2381 | 1965/2262 | 655/753 | chr9 | 133071467 | |||
| chr9:133071500 | C | G | 1 | a0001c0001 | 3 | HG02895.hp2 HG02897.hp1 NA18950.hp2 |
synonymous_variant | LOW | c.1998C>G | p.Gly666Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2020/2381 | 1998/2262 | 666/753 | chr9 | 133071500 | |||
| chr9:133071533 | G | C | 1 | a0010c0019 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2031G>C | p.Gly677Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2053/2381 | 2031/2262 | 677/753 | chr9 | 133071533 | |||
| chr9:133071566 | C | G | 3 | a0001c0001 a0001c0002 a0010c0019 |
3 | HG00642.hp1 HG02486.hp1 HG02809.hp1 |
synonymous_variant | LOW | c.2064C>G | p.Gly688Gly | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2086/2381 | 2064/2262 | 688/753 | chr9 | 133071566 | |||
| chr9:133071581 | G | C | 1 | a0010c0019 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2079G>C | p.Pro693Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2101/2381 | 2079/2262 | 693/753 | chr9 | 133071581 | |||
| chr9:133071602 | C | A | 1 | a0001c0001 | 1 | NA19072.hp1 | synonymous_variant | LOW | c.2100C>A | p.Ala700Ala | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2122/2381 | 2100/2262 | 700/753 | chr9 | 133071602 | |||
| chr9:133071608 | C | T | 1 | a0001c0001 | 3 | HG01109.hp1 HG03654.hp1 HG04115.hp1 |
synonymous_variant | LOW | c.2106C>T | p.Pro702Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2128/2381 | 2106/2262 | 702/753 | chr9 | 133071608 | |||
| chr9:133071614 | C | G | 2 | a0010c0019 a0017c0018 |
2 | HG02486.hp1 NA19043.hp2 |
synonymous_variant | LOW | c.2112C>G | p.Thr704Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2134/2381 | 2112/2262 | 704/753 | chr9 | 133071614 | |||
| chr9:133071653 | G | A | 1 | a0001c0017 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.2151G>A | p.Thr717Thr | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2173/2381 | 2151/2262 | 717/753 | chr9 | 133071653 | |||
| chr9:133071674 | T | C | 1 | a0004c0005 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.2172T>C | p.Pro724Pro | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 2194/2381 | 2172/2262 | 724/753 | chr9 | 133071674 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133071778 | T | C | 1 | a0001c0001t0002 | 5 | NA18974.hp1 NA18975.hp1 NA18977.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*14T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 11/11 | 14 | chr9 | 133071778 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:133062220 | A | G | 6 | a0001c0001t0001g0032 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG01346.hp1 HG01952.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+152A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062220 | |||||||
| chr9:133062339 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.66+271A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062339 | |||||||
| chr9:133062410 | A | G | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.66+342A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062410 | |||||||
| chr9:133062421 | C | G | 1 | a0001c0002t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.66+353C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062421 | |||||||
| chr9:133062455 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.66+387G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062455 | |||||||
| chr9:133062534 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.66+466C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062534 | |||||||
| chr9:133062705 | C | CACCTACC others(1): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(19): Show |
46 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(43): Show |
intron_variant | MODIFIER | c.66+641_66+642insAC others(6): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133062705 | ||||||
| chr9:133062741 | C | T | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.66+673C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062741 | |||||||
| chr9:133062780 | G | C | 4 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0095 others(1): Show |
5 | HG02486.hp2 HG04115.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+712G>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062780 | |||||||
| chr9:133062798 | G | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.66+730G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062798 | |||||||
| chr9:133062859 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(7): Show |
31 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.66+791A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062859 | |||||||
| chr9:133062862 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.66+794T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062862 | |||||||
| chr9:133062938 | T | C | 3 | a0001c0001t0001g0043 a0001c0002t0001g0015 a0001c0002t0001g0033 |
5 | HG02109.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+870T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062938 | |||||||
| chr9:133062984 | A | G | 2 | a0001c0002t0001g0015 a0001c0002t0001g0033 |
4 | HG02109.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+916A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062984 | |||||||
| chr9:133062994 | G | A | 1 | a0005c0007t0001g0025 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.66+926G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133062994 | |||||||
| chr9:133063052 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.66+984T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063052 | |||||||
| chr9:133063059 | C | G | 8 | a0001c0001t0001g0029 a0001c0001t0001g0031 a0001c0002t0001g0005 others(5): Show |
19 | HG00621.hp1 HG00735.hp1 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+991C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063059 | |||||||
| chr9:133063072 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(18): Show |
45 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(42): Show |
intron_variant | MODIFIER | c.66+1004C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063072 | |||||||
| chr9:133063150 | C | T | 1 | a0005c0007t0001g0025 | 2 | HG02965.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.66+1082C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063150 | |||||||
| chr9:133063171 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(7): Show |
31 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.66+1103C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063171 | |||||||
| chr9:133063206 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.66+1138C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063206 | |||||||
| chr9:133063218 | C | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0027 others(16): Show |
73 | HG00423.hp2 HG00438.hp2 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.66+1150C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063218 | |||||||
| chr9:133063498 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.67-906G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063498 | |||||||
| chr9:133063645 | G | A | 1 | a0012c0021t0001g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-759G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063645 | |||||||
| chr9:133063824 | G | A | 1 | a0017c0018t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.67-580G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133063824 | |||||||
| chr9:133064032 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0073 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.67-372C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064032 | |||||||
| chr9:133064033 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.67-371G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064033 | |||||||
| chr9:133064055 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.67-349C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064055 | |||||||
| chr9:133064177 | T | TCTAAGAT others(8): Show |
1 | a0001c0001t0002g0071 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.67-225_67-211dupTA others(13): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 133064177 | ||||||
| chr9:133064241 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.67-163A>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064241 | |||||||
| chr9:133064275 | C | T | 1 | a0012c0021t0001g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.67-129C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064275 | |||||||
| chr9:133064283 | A | C | 6 | a0001c0001t0001g0006 a0002c0004t0001g0022 a0002c0004t0001g0035 others(3): Show |
15 | HG02257.hp1 HG02258.hp1 HG02647.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-121A>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064283 | |||||||
| chr9:133064358 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.67-46C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064358 | |||||||
| chr9:133064377 | CT | C | 3 | a0001c0001t0001g0046 a0001c0024t0001g0090 a0013c0025t0001g0091 |
3 | HG02280.hp1 HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.67-26delT | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 1/10 | chr9 | 133064377 | |||||||
| chr9:133064585 | C | T | 1 | a0017c0018t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.217+31C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 2/10 | chr9 | 133064585 | |||||||
| chr9:133064768 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02683.hp1 | splice_region_variant&intron_variant | LOW | c.340+6C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/10 | chr9 | 133064768 | |||||||
| chr9:133064786 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.340+24A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/10 | chr9 | 133064786 | |||||||
| chr9:133064900 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.340+138G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/10 | chr9 | 133064900 | |||||||
| chr9:133064914 | G | A | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.341-126G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/10 | chr9 | 133064914 | |||||||
| chr9:133064992 | C | G | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.341-48C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 3/10 | chr9 | 133064992 | |||||||
| chr9:133065195 | G | GGCCCCCT others(20385): Show |
1 | a0018c0023t0001g0040 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.538+348_538+349ins others(20392): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 133065195 | ||||||
| chr9:133065335 | G | A | 1 | a0012c0021t0001g0034 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.538+98G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065335 | |||||||
| chr9:133065488 | G | A | 1 | a0001c0002t0001g0048 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.538+251G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065488 | |||||||
| chr9:133065501 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.538+264C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065501 | |||||||
| chr9:133065538 | C | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.538+301C>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065538 | |||||||
| chr9:133065572 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.538+335C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065572 | |||||||
| chr9:133065586 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0023 others(2): Show |
24 | HG02602.hp1 HG03654.hp1 HG03834.hp1 others(21): Show |
intron_variant | MODIFIER | c.538+349C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065586 | |||||||
| chr9:133065715 | G | A | 1 | a0001c0024t0001g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+478G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065715 | |||||||
| chr9:133065778 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.538+541G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065778 | |||||||
| chr9:133065795 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.538+558G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065795 | |||||||
| chr9:133065833 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.538+596T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065833 | |||||||
| chr9:133065846 | C | CA | 29 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0029 others(26): Show |
104 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.538+632dupA | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 133065846 | ||||||
| chr9:133065846 | C | CAA | 2 | a0001c0002t0001g0011 a0001c0002t0001g0083 |
7 | HG01255.hp2 HG02602.hp2 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.538+631_538+632dup others(2): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 133065846 | ||||||
| chr9:133065846 | CA | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0019 others(14): Show |
41 | HG00558.hp2 HG01257.hp1 HG01257.hp2 others(38): Show |
intron_variant | MODIFIER | c.538+632delA | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr9 | 133065846 | ||||||
| chr9:133065859 | A | C | 1 | a0001c0001t0001g0006 | 9 | HG02257.hp1 HG02258.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+622A>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065859 | |||||||
| chr9:133065869 | A | T | 1 | a0001c0002t0001g0024 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.538+632A>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065869 | |||||||
| chr9:133065870 | T | A | 1 | a0001c0001t0001g0039 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.538+633T>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065870 | |||||||
| chr9:133065871 | A | G | 1 | a0001c0002t0001g0024 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.538+634A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065871 | |||||||
| chr9:133065879 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.538+642G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065879 | |||||||
| chr9:133065967 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.539-563G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065967 | |||||||
| chr9:133065973 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.539-557G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133065973 | |||||||
| chr9:133066091 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0095 |
2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-439T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066091 | |||||||
| chr9:133066215 | C | T | 1 | a0001c0001t0002g0067 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.539-315C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066215 | |||||||
| chr9:133066249 | C | T | 1 | a0001c0002t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.539-281C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066249 | |||||||
| chr9:133066332 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.539-198C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066332 | |||||||
| chr9:133066335 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.539-195A>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066335 | |||||||
| chr9:133066344 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.539-186G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066344 | |||||||
| chr9:133066400 | G | T | 1 | a0011c0012t0001g0080 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.539-130G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066400 | |||||||
| chr9:133066455 | T | C | 3 | a0001c0001t0001g0041 a0001c0001t0001g0092 a0001c0001t0001g0095 |
3 | HG03654.hp1 HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.539-75T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066455 | |||||||
| chr9:133066515 | C | T | 1 | a0001c0027t0001g0065 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.539-15C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 4/10 | chr9 | 133066515 | |||||||
| chr9:133066715 | C | T | 1 | a0001c0002t0001g0084 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.669+55C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 5/10 | chr9 | 133066715 | |||||||
| chr9:133066722 | G | T | 1 | a0002c0004t0001g0037 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.669+62G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 5/10 | chr9 | 133066722 | |||||||
| chr9:133067068 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.778-20G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 6/10 | chr9 | 133067068 | |||||||
| chr9:133067075 | G | C | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.778-13G>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 6/10 | chr9 | 133067075 | |||||||
| chr9:133067219 | C | T | 1 | a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.895+14C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067219 | |||||||
| chr9:133067307 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.895+102G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067307 | |||||||
| chr9:133067448 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.895+243A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067448 | |||||||
| chr9:133067459 | C | T | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.895+254C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067459 | |||||||
| chr9:133067653 | G | A | 3 | a0001c0001t0001g0042 a0002c0004t0001g0035 a0012c0021t0001g0034 |
3 | HG02896.hp2 HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.895+448G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067653 | |||||||
| chr9:133067747 | C | T | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.895+542C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067747 | |||||||
| chr9:133067792 | A | T | 1 | a0014c0014t0001g0064 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.895+587A>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067792 | |||||||
| chr9:133067835 | G | A | 1 | a0017c0018t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.895+630G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067835 | |||||||
| chr9:133067895 | C | T | 3 | a0001c0003t0001g0013 a0001c0003t0001g0054 a0002c0013t0001g0036 |
6 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.895+690C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067895 | |||||||
| chr9:133067920 | C | T | 2 | a0001c0024t0001g0090 a0013c0025t0001g0091 |
2 | HG02451.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.895+715C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133067920 | |||||||
| chr9:133068071 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.896-601G>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068071 | |||||||
| chr9:133068122 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0014 others(40): Show |
141 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.896-550A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068122 | |||||||
| chr9:133068224 | C | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0016 others(9): Show |
33 | HG00558.hp2 HG01257.hp2 HG01258.hp1 others(30): Show |
intron_variant | MODIFIER | c.896-448C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068224 | |||||||
| chr9:133068393 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.896-279G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068393 | |||||||
| chr9:133068394 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0070 |
2 | HG02683.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.896-278A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068394 | |||||||
| chr9:133068487 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0092 |
3 | HG01109.hp1 HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.896-185C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068487 | |||||||
| chr9:133068614 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0029 |
10 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.896-58G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068614 | |||||||
| chr9:133068623 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0095 |
2 | HG03139.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.896-49G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068623 | |||||||
| chr9:133068631 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0095 |
2 | HG03139.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.896-41G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 7/10 | chr9 | 133068631 | |||||||
| chr9:133068899 | A | G | 1 | a0001c0002t0001g0089 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1082+41A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/10 | chr9 | 133068899 | |||||||
| chr9:133068947 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1082+89G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/10 | chr9 | 133068947 | |||||||
| chr9:133069009 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0042 others(8): Show |
16 | HG02055.hp1 HG02647.hp1 HG02895.hp1 others(13): Show |
intron_variant | MODIFIER | c.1083-47T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/10 | chr9 | 133069009 | |||||||
| chr9:133069023 | G | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0092 |
3 | HG01109.hp1 HG03491.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1083-33G>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 8/10 | chr9 | 133069023 | |||||||
| chr9:133069404 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1286+145A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069404 | |||||||
| chr9:133069421 | C | A | 1 | a0001c0002t0001g0053 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1286+162C>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069421 | |||||||
| chr9:133069532 | GAGCTACC others(11): Show |
G | 1 | a0001c0001t0002g0071 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1286+275_1286+292d others(20): Show |
CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 133069532 | ||||||
| chr9:133069583 | A | G | 2 | a0001c0001t0001g0042 a0002c0004t0001g0035 |
2 | HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1286+324A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069583 | |||||||
| chr9:133069717 | T | C | 1 | a0017c0018t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1286+458T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069717 | |||||||
| chr9:133069821 | A | G | 26 | a0001c0001t0001g0042 a0001c0002t0001g0002 a0001c0002t0001g0005 others(23): Show |
98 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1286+562A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069821 | |||||||
| chr9:133069906 | G | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0073 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1287-555G>A | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069906 | |||||||
| chr9:133069927 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1287-534C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133069927 | |||||||
| chr9:133070019 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1287-442C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070019 | |||||||
| chr9:133070084 | A | T | 2 | a0004c0005t0001g0017 a0004c0005t0001g0052 |
4 | HG02895.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1287-377A>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070084 | |||||||
| chr9:133070116 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1287-345A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070116 | |||||||
| chr9:133070174 | C | G | 1 | a0001c0001t0001g0060 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1287-287C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070174 | |||||||
| chr9:133070372 | A | G | 7 | a0001c0001t0001g0031 a0001c0001t0001g0041 a0001c0001t0001g0092 others(4): Show |
11 | HG01109.hp1 HG02486.hp2 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1287-89A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070372 | |||||||
| chr9:133070413 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0029 |
10 | HG00099.hp2 HG00280.hp2 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1287-48C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 9/10 | chr9 | 133070413 | |||||||
| chr9:133070734 | T | C | 1 | a0015c0015t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1484+76T>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070734 | |||||||
| chr9:133070829 | G | T | 1 | a0015c0015t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1485-158G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070829 | |||||||
| chr9:133070833 | A | G | 1 | a0015c0015t0001g0058 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1485-154A>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070833 | |||||||
| chr9:133070876 | G | T | 1 | a0001c0001t0001g0063 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1485-111G>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070876 | |||||||
| chr9:133070899 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0073 |
10 | HG01167.hp1 HG02145.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1485-88C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070899 | |||||||
| chr9:133070914 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1485-73C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070914 | |||||||
| chr9:133070924 | G | C | 1 | a0001c0024t0001g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1485-63G>C | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070924 | |||||||
| chr9:133070929 | C | T | 3 | a0001c0003t0001g0013 a0001c0003t0001g0054 a0002c0013t0001g0036 |
6 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1485-58C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070929 | |||||||
| chr9:133070934 | C | G | 1 | a0001c0003t0001g0013 | 4 | HG02717.hp2 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1485-53C>G | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070934 | |||||||
| chr9:133070979 | C | T | 2 | a0004c0005t0001g0017 a0004c0005t0001g0052 |
4 | HG02895.hp1 HG03195.hp1 HG03471.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1485-8C>T | CEL | ENSG00000170835.17 | transcript | ENST00000372080.8 | protein_coding | 10/10 | chr9 | 133070979 |