Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56052 |
| ensemblid | ENSG00000033011.14 |
| hgncid | 18294 |
| symbol | ALG1 |
| name | ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase |
| refseq_nuc | NM_019109.5 |
| refseq_prot | NP_061982.3 |
| ensembl_nuc | ENST00000262374.10 |
| ensembl_prot | ENSP00000262374.5 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 5071843 |
| end | 5087379 |
| strand | + |
| ver | v1.2 |
| region | chr16:5071843-5087379 |
| region5000 | chr16:5066843-5092379 |
| regionname0 | ALG1_chr16_5071843_5087379 |
| regionname5000 | ALG1_chr16_5066843_5092379 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 464 | 315 | 78 | 50 | 136 | 11 | 38 | 97 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0002 | 0/0 | 464 | 71 | 19 | 22 | 26 | 1 | 3 | 21 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0003 | 0/0 | 464 | 51 | 1 | 13 | 35 | 0 | 2 | 29 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0004 | 0/0 | 464 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0005 | 0/0 | 464 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | MADSC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0006 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0007 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0008 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| a0009 | 0/0 | 265 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(260): Show |
chr16 | 5066843 | 5092379 |
| a0010 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | MAASC others(459): Show |
chr16 | 5066843 | 5092379 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1392 | 205 | 37 | 29 | 108 | 5 | 26 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0002 | 1/1 | 1392 | 93 | 36 | 16 | 25 | 6 | 8 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0006 | 0/0 | 1392 | 8 | 3 | 3 | 0 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0007 | 0/0 | 1392 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0009 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0011 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0012 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0013 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0019 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0001c0020 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0002c0003 | 0/0 | 1392 | 59 | 14 | 20 | 25 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0002c0005 | 0/0 | 1392 | 11 | 5 | 2 | 0 | 1 | 3 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0002c0014 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0003c0004 | 0/0 | 1392 | 51 | 1 | 13 | 35 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0004c0015 | 0/0 | 1392 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0005c0008 | 0/0 | 1392 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0006c0021 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0007c0010 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0008c0018 | 0/0 | 1392 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 | ||
| a0009c0016 | 0/0 | 1379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1374): Show |
chr16 | 5066843 | 5092379 | ||
| a0010c0017 | 0/0 | 1392 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | ATGGC others(1387): Show |
chr16 | 5066843 | 5092379 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3896 | 115 | 12 | 17 | 65 | 3 | 18 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0003 | 0/0 | 3896 | 56 | 7 | 11 | 29 | 2 | 7 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0007 | 0/0 | 3897 | 9 | 3 | 1 | 5 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3892): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0013 | 0/0 | 3896 | 5 | 5 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0014 | 0/0 | 3896 | 5 | 5 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0015 | 0/0 | 3896 | 3 | 3 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0016 | 0/0 | 3896 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0020 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0024 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0026 | 0/0 | 3899 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0029 | 0/0 | 3900 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0030 | 0/0 | 3897 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3892): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0031 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0032 | 0/0 | 3899 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0033 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0001t0034 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0001 | 0/0 | 3896 | 2 | 0 | 0 | 0 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0002 | 0/1 | 3901 | 19 | 2 | 9 | 0 | 3 | 4 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0003 | 0/0 | 3896 | 7 | 7 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0005 | 0/0 | 3901 | 41 | 9 | 6 | 23 | 1 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0006 | 0/0 | 3900 | 11 | 11 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0007 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3892): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0012 | 1/0 | 3900 | 5 | 4 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0017 | 0/0 | 3902 | 3 | 1 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3897): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0020 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0022 | 0/0 | 3901 | 2 | 0 | 0 | 0 | 2 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0002t0037 | 0/0 | 3901 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0006t0002 | 0/0 | 3901 | 5 | 3 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0006t0008 | 0/0 | 3902 | 3 | 0 | 2 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3897): Show |
chr16 | 5066843 | 5092379 |
| a0001c0007t0001 | 0/0 | 3896 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0009t0002 | 0/0 | 3901 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0011t0003 | 0/0 | 3896 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0012t0008 | 0/0 | 3902 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3897): Show |
chr16 | 5066843 | 5092379 |
| a0001c0013t0003 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0001c0019t0002 | 0/0 | 3901 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0001c0020t0001 | 0/0 | 3896 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0004 | 0/0 | 3899 | 43 | 7 | 15 | 21 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0009 | 0/0 | 3900 | 4 | 0 | 0 | 4 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0010 | 0/0 | 3900 | 6 | 5 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0018 | 0/0 | 3896 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0019 | 0/0 | 3899 | 2 | 0 | 2 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0023 | 0/0 | 3897 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3892): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0025 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0002c0003t0027 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0002c0005t0004 | 0/0 | 3899 | 4 | 0 | 1 | 0 | 1 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0002c0005t0009 | 0/0 | 3900 | 2 | 0 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0002c0005t0011 | 0/0 | 3899 | 5 | 5 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0002c0014t0004 | 0/0 | 3899 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3894): Show |
chr16 | 5066843 | 5092379 |
| a0003c0004t0002 | 0/0 | 3901 | 42 | 1 | 13 | 26 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0003c0004t0008 | 0/0 | 3902 | 5 | 0 | 0 | 5 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3897): Show |
chr16 | 5066843 | 5092379 |
| a0003c0004t0021 | 0/0 | 3901 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0003c0004t0035 | 0/0 | 3901 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3896): Show |
chr16 | 5066843 | 5092379 |
| a0003c0004t0036 | 0/0 | 3902 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3897): Show |
chr16 | 5066843 | 5092379 |
| a0004c0015t0001 | 0/0 | 3896 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0005c0008t0018 | 0/0 | 3896 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0006c0021t0003 | 0/0 | 3896 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0007c0010t0001 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| a0008c0018t0028 | 0/0 | 3900 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3895): Show |
chr16 | 5066843 | 5092379 |
| a0009c0016t0003 | 0/0 | 3883 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3878): Show |
chr16 | 5066843 | 5092379 |
| a0010c0017t0001 | 0/0 | 3896 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | AGCCA others(3891): Show |
chr16 | 5066843 | 5092379 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 71 | 7 | 11 | 37 | 3 | 13 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0008 | 0/0 | 5 | 1 | 2 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0009 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0004 | 0/0 | 29 | 5 | 6 | 16 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0008 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0011 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0024 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0007g0001 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0007g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0007g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0007g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0013g0013 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0014g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0014g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0015g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0015g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0015g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0016g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0020g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0024g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0026g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0029g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0030g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0031g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0032g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0033g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0001g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0002 | 0/1 | 13 | 1 | 5 | 0 | 2 | 4 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0003g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0003g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0003g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0005 | 0/0 | 18 | 4 | 2 | 12 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0014 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0019 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0025 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0005g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0006g0006 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0007g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0012g0022 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0012g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0017g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0017g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0017g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0020g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0022g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0002t0037g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0006t0002g0021 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0006t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0006t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0006t0008g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0006t0008g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0007t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0009t0002g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0011t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0012t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0013t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0019t0002g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0001c0020t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0003 | 0/0 | 32 | 0 | 14 | 18 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0009g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0009g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0010g0010 | 0/0 | 6 | 5 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0018g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0019g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0023g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0025g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0003t0027g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0004g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0004g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0009g0037 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0011g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0005t0011g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0002c0014t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0002 | 0/0 | 30 | 1 | 9 | 19 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0008g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0008g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0008g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0021g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0021g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0035g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0003c0004t0036g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0004c0015t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0005c0008t0018g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0006c0021t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0007c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0008c0018t0028g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0009c0016t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| a0010c0017t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00280 | hp1 | a0001 | c0002 | t0005 | g0019 | EUR | FIN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00323 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | FIN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0090 | EUR | FIN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00408 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00558 | hp2 | a0001 | c0001 | t0016 | g0007 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00597 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00597 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00621 | hp1 | a0001 | c0001 | t0034 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0076 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0044 | EAS | CHS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00735 | hp1 | a0001 | c0002 | t0005 | g0025 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00738 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00741 | hp1 | a0001 | c0009 | t0002 | g0002 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01069 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01069 | hp2 | a0001 | c0006 | t0008 | g0031 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01070 | hp1 | a0001 | c0002 | t0002 | g0015 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01070 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01071 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01071 | hp2 | a0001 | c0006 | t0008 | g0031 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01081 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01099 | hp2 | a0002 | c0003 | t0010 | g0010 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01167 | hp1 | a0004 | c0015 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01167 | hp2 | a0002 | c0003 | t0019 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01169 | hp1 | a0002 | c0003 | t0019 | g0003 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01175 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01192 | hp2 | a0003 | c0004 | t0002 | g0064 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01243 | hp1 | a0001 | c0006 | t0002 | g0021 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01255 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01256 | hp2 | a0003 | c0004 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01257 | hp2 | a0002 | c0003 | t0023 | g0033 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01258 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01258 | hp2 | a0002 | c0003 | t0018 | g0033 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01261 | hp2 | a0003 | c0004 | t0002 | g0002 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0011 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01361 | hp1 | a0001 | c0002 | t0005 | g0005 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01433 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01496 | hp2 | a0001 | c0002 | t0005 | g0005 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01515 | hp2 | a0001 | c0002 | t0022 | g0002 | EUR | IBS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0067 | EUR | IBS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01517 | hp2 | a0001 | c0002 | t0022 | g0002 | EUR | IBS | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01884 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01891 | hp1 | a0001 | c0006 | t0002 | g0070 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01891 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01928 | hp1 | a0003 | c0004 | t0002 | g0058 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01928 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01934 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01934 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01943 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01952 | hp1 | a0002 | c0005 | t0004 | g0101 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01975 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01975 | hp2 | a0001 | c0011 | t0003 | g0011 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01978 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01978 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01981 | hp1 | a0003 | c0004 | t0002 | g0061 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01981 | hp2 | a0001 | c0002 | t0007 | g0049 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01993 | hp1 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01993 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02004 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02004 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02015 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02015 | hp2 | a0001 | c0002 | t0005 | g0012 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02027 | hp1 | a0003 | c0004 | t0008 | g0002 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02027 | hp2 | a0001 | c0001 | t0016 | g0007 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02040 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02071 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02071 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02074 | hp2 | a0001 | c0001 | t0024 | g0094 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02080 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02083 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02083 | hp2 | a0001 | c0001 | t0031 | g0001 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02129 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02135 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02135 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02145 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02145 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02148 | hp1 | a0003 | c0004 | t0002 | g0069 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02148 | hp2 | a0003 | c0004 | t0002 | g0002 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | CDX | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02165 | hp2 | a0002 | c0003 | t0004 | g0074 | EAS | CDX | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02257 | hp1 | a0001 | c0002 | t0005 | g0005 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02258 | hp1 | a0002 | c0003 | t0025 | g0010 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02258 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02273 | hp1 | a0003 | c0004 | t0002 | g0002 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02273 | hp2 | a0003 | c0004 | t0002 | g0002 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0004 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02280 | hp2 | a0001 | c0002 | t0020 | g0004 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02293 | hp1 | a0002 | c0003 | t0004 | g0072 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02300 | hp1 | a0001 | c0002 | t0005 | g0025 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02300 | hp2 | a0002 | c0003 | t0004 | g0003 | AMR | PEL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02451 | hp2 | a0002 | c0003 | t0004 | g0075 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02523 | hp2 | a0001 | c0002 | t0005 | g0050 | EAS | KHV | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02572 | hp1 | a0001 | c0002 | t0012 | g0022 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02572 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02602 | hp2 | a0001 | c0006 | t0008 | g0080 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02615 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02630 | hp2 | a0001 | c0001 | t0015 | g0115 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02647 | hp1 | a0002 | c0003 | t0010 | g0010 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02698 | hp2 | a0002 | c0005 | t0004 | g0077 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02717 | hp1 | a0001 | c0002 | t0006 | g0084 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02717 | hp2 | a0002 | c0003 | t0004 | g0055 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02723 | hp1 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02723 | hp2 | a0002 | c0003 | t0004 | g0020 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02738 | hp1 | a0002 | c0005 | t0009 | g0037 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02738 | hp2 | a0002 | c0005 | t0004 | g0032 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0008 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02809 | hp2 | a0002 | c0005 | t0011 | g0016 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02818 | hp1 | a0002 | c0003 | t0027 | g0054 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02818 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02886 | hp2 | a0001 | c0001 | t0015 | g0100 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02895 | hp1 | a0002 | c0005 | t0011 | g0016 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02895 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02896 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02896 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02897 | hp1 | a0001 | c0002 | t0005 | g0014 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02897 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02922 | hp1 | a0002 | c0003 | t0004 | g0057 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02922 | hp2 | a0001 | c0002 | t0012 | g0022 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02965 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02970 | hp1 | a0001 | c0002 | t0012 | g0034 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02970 | hp2 | a0002 | c0005 | t0011 | g0085 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02976 | hp2 | a0001 | c0001 | t0020 | g0097 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03041 | hp2 | a0001 | c0002 | t0006 | g0083 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03098 | hp1 | a0001 | c0013 | t0003 | g0092 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03098 | hp2 | a0001 | c0002 | t0003 | g0004 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03130 | hp1 | a0001 | c0002 | t0012 | g0034 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03130 | hp2 | a0001 | c0001 | t0007 | g0041 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03139 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03139 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03195 | hp1 | a0001 | c0001 | t0007 | g0041 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03195 | hp2 | a0001 | c0002 | t0003 | g0035 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03209 | hp1 | a0001 | c0012 | t0008 | g0047 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03225 | hp1 | a0001 | c0001 | t0014 | g0106 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03486 | hp1 | a0001 | c0002 | t0003 | g0035 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03490 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0028 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03516 | hp1 | a0001 | c0002 | t0006 | g0006 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03516 | hp2 | a0001 | c0002 | t0005 | g0014 | AFR | ESN | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03540 | hp1 | a0001 | c0002 | t0017 | g0046 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03540 | hp2 | a0002 | c0003 | t0010 | g0010 | AFR | GWD | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03579 | hp1 | a0001 | c0001 | t0026 | g0079 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03579 | hp2 | a0001 | c0002 | t0006 | g0006 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03654 | hp1 | a0003 | c0004 | t0002 | g0002 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03688 | hp1 | a0001 | c0002 | t0005 | g0019 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03688 | hp2 | a0005 | c0008 | t0018 | g0081 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03710 | hp2 | a0001 | c0019 | t0002 | g0002 | SAS | PJL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03834 | hp1 | a0001 | c0002 | t0005 | g0019 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03942 | hp1 | a0001 | c0001 | t0029 | g0001 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03942 | hp2 | a0003 | c0004 | t0002 | g0088 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04115 | hp1 | a0001 | c0006 | t0002 | g0021 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04184 | hp2 | a0001 | c0020 | t0001 | g0001 | SAS | BEB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0095 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18612 | hp2 | a0001 | c0002 | t0005 | g0005 | EAS | CHB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18747 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | CHB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18906 | hp1 | a0001 | c0006 | t0002 | g0021 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18906 | hp2 | a0006 | c0021 | t0003 | g0087 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18941 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18943 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18946 | hp2 | a0001 | c0002 | t0005 | g0012 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18947 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18948 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18948 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18949 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18949 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18950 | hp1 | a0003 | c0004 | t0008 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18950 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18952 | hp2 | a0001 | c0001 | t0016 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18953 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18953 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18956 | hp1 | a0003 | c0004 | t0035 | g0043 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18956 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18959 | hp1 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18960 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18961 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18961 | hp2 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18963 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18963 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18964 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18965 | hp1 | a0001 | c0002 | t0005 | g0053 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18965 | hp2 | a0003 | c0004 | t0008 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18970 | hp1 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18973 | hp1 | a0001 | c0002 | t0005 | g0012 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18974 | hp2 | a0001 | c0002 | t0005 | g0052 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18975 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18979 | hp2 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18980 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18980 | hp2 | a0002 | c0003 | t0009 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18981 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18981 | hp2 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18982 | hp2 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18983 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18984 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18985 | hp1 | a0001 | c0001 | t0033 | g0111 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18990 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18990 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18993 | hp2 | a0003 | c0004 | t0021 | g0082 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18994 | hp1 | a0002 | c0003 | t0009 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18994 | hp2 | a0001 | c0002 | t0017 | g0051 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18997 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18997 | hp2 | a0002 | c0003 | t0009 | g0078 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18998 | hp2 | a0002 | c0003 | t0004 | g0119 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18999 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19000 | hp2 | a0003 | c0004 | t0036 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19001 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19002 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19002 | hp2 | a0002 | c0003 | t0009 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19003 | hp1 | a0003 | c0004 | t0008 | g0059 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19003 | hp2 | a0003 | c0004 | t0002 | g0065 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19007 | hp2 | a0002 | c0003 | t0004 | g0073 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19009 | hp1 | a0002 | c0014 | t0004 | g0118 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19010 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19011 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19030 | hp1 | a0001 | c0002 | t0006 | g0102 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19030 | hp2 | a0001 | c0006 | t0002 | g0071 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19043 | hp1 | a0001 | c0002 | t0003 | g0105 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19043 | hp2 | a0008 | c0018 | t0028 | g0089 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19058 | hp1 | a0003 | c0004 | t0002 | g0045 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19058 | hp2 | a0001 | c0001 | t0007 | g0026 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19062 | hp1 | a0001 | c0002 | t0005 | g0048 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19062 | hp2 | a0003 | c0004 | t0002 | g0062 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19063 | hp1 | a0009 | c0016 | t0003 | g0096 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19064 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19066 | hp1 | a0001 | c0002 | t0005 | g0012 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19067 | hp1 | a0010 | c0017 | t0001 | g0027 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19067 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19068 | hp1 | a0001 | c0001 | t0007 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19068 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19070 | hp1 | a0001 | c0002 | t0005 | g0012 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19074 | hp1 | a0003 | c0004 | t0002 | g0030 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19076 | hp1 | a0003 | c0004 | t0008 | g0043 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19079 | hp1 | a0003 | c0004 | t0002 | g0066 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19079 | hp2 | a0001 | c0002 | t0017 | g0012 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19080 | hp1 | a0001 | c0002 | t0005 | g0005 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19080 | hp2 | a0003 | c0004 | t0021 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19081 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19082 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19084 | hp2 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19085 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19086 | hp1 | a0003 | c0004 | t0002 | g0002 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19087 | hp1 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19088 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19089 | hp1 | a0001 | c0001 | t0030 | g0036 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19089 | hp2 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19090 | hp1 | a0002 | c0003 | t0004 | g0003 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19091 | hp2 | a0001 | c0001 | t0032 | g0024 | EAS | JPT | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19240 | hp1 | a0001 | c0002 | t0003 | g0023 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA19240 | hp2 | a0002 | c0005 | t0011 | g0016 | AFR | YRI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ASW | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20129 | hp2 | a0001 | c0001 | t0015 | g0098 | AFR | ASW | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20752 | hp1 | a0002 | c0005 | t0004 | g0032 | EUR | TSI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0011 | EUR | TSI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | GIH | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01123 | hp1 | a0002 | c0005 | t0009 | g0037 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG01123 | hp2 | a0001 | c0002 | t0005 | g0025 | AMR | CLM | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0086 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02109 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02486 | hp1 | a0002 | c0003 | t0004 | g0020 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02486 | hp2 | a0002 | c0003 | t0004 | g0056 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02559 | hp1 | a0003 | c0004 | t0002 | g0002 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG02559 | hp2 | a0001 | c0002 | t0003 | g0023 | AFR | ACB | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03471 | hp1 | a0002 | c0003 | t0004 | g0020 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG06807 | hp1 | a0001 | c0001 | t0014 | g0018 | AFR | USA | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| HG06807 | hp2 | a0002 | c0005 | t0011 | g0016 | AFR | USA | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20300 | hp1 | a0001 | c0001 | t0013 | g0013 | AFR | USA | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA21309 | hp1 | a0001 | c0002 | t0037 | g0030 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| NA21309 | hp2 | a0001 | c0002 | t0005 | g0005 | AFR | LWK | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0002 | REF | REF | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0012 | g0022 | REF | REF | ALG1_chr16_5066843_5092379 | ALG1 | chr16 | 5066843 | 5092379 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5071857 | C | A | 1 | a0005 | 1 | HG03688.hp2 | missense_variant | MODERATE | c.8C>A | p.Ala3Asp | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 15/3900 | 8/1395 | 3/464 | chr16 | 5071857 | |||
| chr16:5071911 | G | A | 1 | a0007 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.62G>A | p.Gly21Glu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 69/3900 | 62/1395 | 21/464 | chr16 | 5071911 | |||
| chr16:5073200 | A | C | 1 | a0008 | 1 | NA19043.hp2 | missense_variant | MODERATE | c.334A>C | p.Met112Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/13 | 341/3900 | 334/1395 | 112/464 | chr16 | 5073200 | |||
| chr16:5077459 | T | G | 2 | a0006 a0008 |
2 | NA18906.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.554T>G | p.Phe185Cys | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/13 | 561/3900 | 554/1395 | 185/464 | chr16 | 5077459 | |||
| chr16:5078005 | C | T | 1 | a0010 | 1 | NA19067.hp1 | missense_variant | MODERATE | c.728C>T | p.Pro243Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/13 | 735/3900 | 728/1395 | 243/464 | chr16 | 5078005 | |||
| chr16:5078734 | AGGCTTTT others(28): Show |
A | 1 | a0009 | 1 | NA19063.hp1 | frameshift_variant&splice_acceptor_variant&splice_region_variant&intron_variant | HIGH | c.741-21_754delGCTTT others(30): Show |
p.Ser248fs | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/13 | 741/1395 | 247/464 | INFO_REALIGN_3_PRIME | chr16 | 5078734 | |||
| chr16:5078816 | G | A | 1 | a0003 | 51 | HG00597.hp1 HG01192.hp2 HG01255.hp1 others(48): Show |
missense_variant | MODERATE | c.800G>A | p.Ser267Asn | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/13 | 807/3900 | 800/1395 | 267/464 | chr16 | 5078816 | |||
| chr16:5079073 | A | G | 1 | a0004 | 1 | HG01167.hp1 | missense_variant | MODERATE | c.872A>G | p.Asp291Gly | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/13 | 879/3900 | 872/1395 | 291/464 | chr16 | 5079073 | |||
| chr16:5084773 | T | A | 2 | a0002 a0005 |
72 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(69): Show |
missense_variant | MODERATE | c.1287T>A | p.Asp429Glu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1294/3900 | 1287/1395 | 429/464 | chr16 | 5084773 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5071870 | C | T | 1 | a0006c0021 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.21C>T | p.Val7Val | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 28/3900 | 21/1395 | 7/464 | chr16 | 5071870 | |||
| chr16:5071871 | C | T | 1 | a0001c0020 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.22C>T | p.Leu8Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 29/3900 | 22/1395 | 8/464 | chr16 | 5071871 | |||
| chr16:5071885 | T | C | 1 | a0001c0009 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.36T>C | p.Cys12Cys | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 43/3900 | 36/1395 | 12/464 | chr16 | 5071885 | |||
| chr16:5071904 | C | T | 1 | a0001c0019 | 1 | HG03710.hp2 | synonymous_variant | LOW | c.55C>T | p.Leu19Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/13 | 62/3900 | 55/1395 | 19/464 | chr16 | 5071904 | |||
| chr16:5073250 | T | C | 1 | a0001c0007 | 3 | NA18961.hp2 NA18970.hp1 NA18981.hp2 |
synonymous_variant | LOW | c.384T>C | p.Phe128Phe | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/13 | 391/3900 | 384/1395 | 128/464 | chr16 | 5073250 | |||
| chr16:5077517 | G | A | 1 | a0001c0011 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.612G>A | p.Ala204Ala | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/13 | 619/3900 | 612/1395 | 204/464 | chr16 | 5077517 | |||
| chr16:5078000 | C | T | 2 | a0002c0003 a0005c0008 |
60 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(57): Show |
synonymous_variant | LOW | c.723C>T | p.His241His | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/13 | 730/3900 | 723/1395 | 241/464 | chr16 | 5078000 | |||
| chr16:5078856 | G | C | 1 | a0001c0006 | 8 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(5): Show |
synonymous_variant | LOW | c.840G>C | p.Leu280Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/13 | 847/3900 | 840/1395 | 280/464 | chr16 | 5078856 | |||
| chr16:5082575 | T | G | 1 | a0001c0012 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.1089T>G | p.Gly363Gly | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/13 | 1096/3900 | 1089/1395 | 363/464 | chr16 | 5082575 | |||
| chr16:5082635 | C | T | 10 | a0001c0001 a0001c0007 a0001c0011 others(7): Show |
216 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(213): Show |
synonymous_variant | LOW | c.1149C>T | p.Phe383Phe | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/13 | 1156/3900 | 1149/1395 | 383/464 | chr16 | 5082635 | |||
| chr16:5083716 | C | T | 1 | a0001c0013 | 1 | HG03098.hp1 | synonymous_variant | LOW | c.1222C>T | p.Leu408Leu | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/13 | 1229/3900 | 1222/1395 | 408/464 | chr16 | 5083716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5084897 | C | CTA | 15 | a0001c0002t0002 a0001c0002t0005 a0001c0002t0017 others(12): Show |
127 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*17_*18dupTA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 19 | INFO_REALIGN_3_PRIME | chr16 | 5084897 | |||||
| chr16:5084909 | G | A | 4 | a0002c0003t0018 a0002c0003t0023 a0002c0005t0011 others(1): Show |
8 | HG01257.hp2 HG01258.hp2 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*28G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 28 | chr16 | 5084909 | ||||||
| chr16:5084934 | T | G | 2 | a0001c0001t0024 a0003c0004t0035 |
2 | HG02074.hp2 NA18956.hp1 |
3_prime_UTR_variant | MODIFIER | c.*53T>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 53 | chr16 | 5084934 | ||||||
| chr16:5085156 | G | T | 1 | a0001c0001t0014 | 5 | HG02109.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*275G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 275 | chr16 | 5085156 | ||||||
| chr16:5085267 | C | T | 1 | a0001c0001t0003 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 386 | chr16 | 5085267 | ||||||
| chr16:5085379 | A | G | 30 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(27): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(225): Show |
3_prime_UTR_variant | MODIFIER | c.*498A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 498 | chr16 | 5085379 | ||||||
| chr16:5085547 | A | C | 4 | a0002c0003t0018 a0002c0003t0023 a0002c0005t0011 others(1): Show |
8 | HG01257.hp2 HG01258.hp2 HG02809.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*666A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 666 | chr16 | 5085547 | ||||||
| chr16:5085656 | C | T | 1 | a0001c0001t0034 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 775 | chr16 | 5085656 | ||||||
| chr16:5085722 | C | T | 1 | a0001c0001t0033 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 841 | chr16 | 5085722 | ||||||
| chr16:5085869 | G | A | 1 | a0001c0002t0006 | 11 | HG01891.hp2 HG02257.hp2 HG02717.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*988G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 988 | chr16 | 5085869 | ||||||
| chr16:5085946 | C | G | 29 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(26): Show |
227 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(224): Show |
3_prime_UTR_variant | MODIFIER | c.*1065C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1065 | chr16 | 5085946 | ||||||
| chr16:5085955 | G | T | 16 | a0001c0001t0026 a0001c0002t0002 a0001c0002t0005 others(13): Show |
128 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1074G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1074 | chr16 | 5085955 | ||||||
| chr16:5085978 | T | C | 59 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(56): Show |
438 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(435): Show |
3_prime_UTR_variant | MODIFIER | c.*1097T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1097 | chr16 | 5085978 | ||||||
| chr16:5086000 | G | A | 1 | a0003c0004t0021 | 2 | NA18993.hp2 NA19080.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1119G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1119 | chr16 | 5086000 | ||||||
| chr16:5086084 | C | A | 14 | a0001c0001t0026 a0001c0002t0002 a0001c0002t0022 others(11): Show |
84 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1203C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1203 | chr16 | 5086084 | ||||||
| chr16:5086185 | A | G | 1 | a0001c0001t0016 | 3 | HG00558.hp2 HG02027.hp2 NA18952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1304A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1304 | chr16 | 5086185 | ||||||
| chr16:5086199 | A | G | 1 | a0001c0002t0022 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1318A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1318 | chr16 | 5086199 | ||||||
| chr16:5086293 | C | T | 13 | a0001c0001t0032 a0002c0003t0004 a0002c0003t0009 others(10): Show |
68 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1412C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1412 | chr16 | 5086293 | ||||||
| chr16:5086319 | G | A | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(55): Show |
427 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*1438G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1438 | chr16 | 5086319 | ||||||
| chr16:5086334 | CA | C | 19 | a0001c0001t0026 a0001c0001t0032 a0001c0002t0002 others(16): Show |
173 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*1471delA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1471 | INFO_REALIGN_3_PRIME | chr16 | 5086334 | |||||
| chr16:5086334 | CAAA | C | 3 | a0001c0001t0007 a0001c0001t0030 a0001c0002t0007 |
11 | HG00438.hp1 HG01175.hp1 HG01981.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1469_*1471delAAA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1469 | INFO_REALIGN_3_PRIME | chr16 | 5086334 | |||||
| chr16:5086334 | CAAAA | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0013 others(20): Show |
213 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*1468_*1471delAAAA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1468 | INFO_REALIGN_3_PRIME | chr16 | 5086334 | |||||
| chr16:5086352 | A | G | 1 | a0001c0002t0037 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1471A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1471 | chr16 | 5086352 | ||||||
| chr16:5086353 | C | A | 1 | a0003c0004t0036 | 1 | NA19000.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1472C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1472 | chr16 | 5086353 | ||||||
| chr16:5086419 | C | G | 1 | a0001c0001t0015 | 3 | HG02630.hp2 HG02886.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1538C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1538 | chr16 | 5086419 | ||||||
| chr16:5086752 | C | T | 1 | a0002c0003t0019 | 2 | HG01167.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1871C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1871 | chr16 | 5086752 | ||||||
| chr16:5086754 | C | T | 1 | a0001c0001t0031 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1873C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1873 | chr16 | 5086754 | ||||||
| chr16:5086878 | G | T | 1 | a0002c0003t0025 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1997G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 1997 | chr16 | 5086878 | ||||||
| chr16:5086899 | C | A | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(55): Show |
427 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*2018C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2018 | chr16 | 5086899 | ||||||
| chr16:5086900 | C | G | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(55): Show |
427 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*2019C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2019 | chr16 | 5086900 | ||||||
| chr16:5087068 | C | G | 14 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0014 others(11): Show |
143 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(140): Show |
3_prime_UTR_variant | MODIFIER | c.*2187C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2187 | chr16 | 5087068 | ||||||
| chr16:5087150 | GGAA | G | 3 | a0002c0003t0018 a0002c0003t0023 a0005c0008t0018 |
3 | HG01257.hp2 HG01258.hp2 HG03688.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2279_*2281delGAA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2279 | INFO_REALIGN_3_PRIME | chr16 | 5087150 | |||||
| chr16:5087242 | C | T | 2 | a0002c0003t0010 a0002c0003t0025 |
7 | HG01099.hp2 HG02258.hp1 HG02258.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2361C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2361 | chr16 | 5087242 | ||||||
| chr16:5087272 | C | T | 1 | a0001c0001t0013 | 5 | HG02145.hp1 HG02615.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2391C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2391 | chr16 | 5087272 | ||||||
| chr16:5087284 | A | G | 58 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0007 others(55): Show |
427 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(424): Show |
3_prime_UTR_variant | MODIFIER | c.*2403A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2403 | chr16 | 5087284 | ||||||
| chr16:5087312 | C | G | 3 | a0002c0003t0010 a0002c0003t0025 a0002c0003t0027 |
8 | HG01099.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2431C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2431 | chr16 | 5087312 | ||||||
| chr16:5087372 | G | C | 4 | a0001c0001t0013 a0001c0001t0020 a0001c0001t0026 others(1): Show |
8 | HG02145.hp1 HG02280.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2491G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 13/13 | 2491 | chr16 | 5087372 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:5072071 | G | GGTCT | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
239 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.208+16_208+19dupTC others(2): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 5072071 | ||||||
| chr16:5072190 | C | CG | 150 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(147): Show |
421 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(418): Show |
intron_variant | MODIFIER | c.208+135dupG | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr16 | 5072190 | ||||||
| chr16:5072225 | G | A | 1 | a0003c0004t0002g0045 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.208+168G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072225 | |||||||
| chr16:5072267 | A | C | 1 | a0003c0004t0021g0082 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.208+210A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072267 | |||||||
| chr16:5072358 | C | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(148): Show |
422 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(419): Show |
intron_variant | MODIFIER | c.208+301C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072358 | |||||||
| chr16:5072502 | C | T | 3 | a0002c0003t0018g0033 a0002c0003t0023g0033 a0005c0008t0018g0081 |
3 | HG01257.hp2 HG01258.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.208+445C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072502 | |||||||
| chr16:5072551 | A | G | 4 | a0001c0001t0001g0009 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
10 | HG00438.hp2 HG00544.hp1 NA18939.hp2 others(7): Show |
intron_variant | MODIFIER | c.209-400A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072551 | |||||||
| chr16:5072589 | A | T | 1 | a0001c0001t0003g0044 | 2 | HG00544.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.209-362A>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072589 | |||||||
| chr16:5072609 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.209-342A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072609 | |||||||
| chr16:5072612 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.209-339C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072612 | |||||||
| chr16:5072639 | C | A | 1 | a0003c0004t0008g0059 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.209-312C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072639 | |||||||
| chr16:5072645 | G | T | 1 | a0001c0006t0008g0080 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.209-306G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072645 | |||||||
| chr16:5072680 | C | G | 83 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(80): Show |
239 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(236): Show |
intron_variant | MODIFIER | c.209-271C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072680 | |||||||
| chr16:5072767 | T | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(81): Show |
240 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(237): Show |
intron_variant | MODIFIER | c.209-184T>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072767 | |||||||
| chr16:5072783 | C | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(51): Show |
159 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(156): Show |
intron_variant | MODIFIER | c.209-168C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072783 | |||||||
| chr16:5072878 | G | T | 16 | a0001c0002t0005g0012 a0001c0002t0005g0076 a0001c0002t0017g0012 others(13): Show |
55 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-73G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072878 | |||||||
| chr16:5072879 | C | T | 16 | a0001c0002t0005g0012 a0001c0002t0005g0076 a0001c0002t0017g0012 others(13): Show |
55 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.209-72C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 1/12 | chr16 | 5072879 | |||||||
| chr16:5073269 | C | A | 1 | a0001c0002t0005g0014 | 5 | HG02630.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.390+13C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073269 | |||||||
| chr16:5073269 | C | T | 32 | a0001c0001t0001g0063 a0001c0002t0002g0002 a0001c0002t0002g0015 others(29): Show |
80 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.390+13C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073269 | |||||||
| chr16:5073302 | T | A | 1 | a0008c0018t0028g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+46T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073302 | |||||||
| chr16:5073431 | G | T | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+175G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073431 | |||||||
| chr16:5073463 | C | G | 1 | a0008c0018t0028g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.390+207C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073463 | |||||||
| chr16:5073473 | A | G | 23 | a0001c0002t0005g0012 a0001c0002t0005g0076 a0001c0002t0017g0012 others(20): Show |
69 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.390+217A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073473 | |||||||
| chr16:5073615 | A | G | 1 | a0001c0006t0002g0071 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.390+359A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073615 | |||||||
| chr16:5073617 | C | T | 1 | a0001c0001t0015g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.390+361C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073617 | |||||||
| chr16:5073703 | C | T | 1 | a0001c0001t0003g0099 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.390+447C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073703 | |||||||
| chr16:5073711 | C | G | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
235 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.390+455C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073711 | |||||||
| chr16:5073743 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.390+487T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073743 | |||||||
| chr16:5073813 | C | G | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390+557C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073813 | |||||||
| chr16:5073863 | C | T | 13 | a0001c0002t0005g0012 a0001c0002t0005g0076 a0001c0002t0017g0012 others(10): Show |
52 | HG00597.hp2 HG00639.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.390+607C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073863 | |||||||
| chr16:5073897 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.390+641T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073897 | |||||||
| chr16:5073967 | G | A | 1 | a0001c0001t0001g0038 | 2 | HG00609.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.390+711G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073967 | |||||||
| chr16:5073999 | G | A | 32 | a0001c0001t0001g0063 a0001c0002t0002g0002 a0001c0002t0002g0015 others(29): Show |
80 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.390+743G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5073999 | |||||||
| chr16:5074065 | TTTTC | T | 4 | a0002c0003t0004g0020 a0002c0003t0004g0055 a0002c0003t0004g0056 others(1): Show |
6 | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.390+817_390+820del others(4): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr16 | 5074065 | ||||||
| chr16:5074078 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
419 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(416): Show |
intron_variant | MODIFIER | c.390+822C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074078 | |||||||
| chr16:5074105 | T | A | 1 | a0003c0004t0002g0058 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.390+849T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074105 | |||||||
| chr16:5074106 | T | A | 29 | a0001c0001t0001g0063 a0001c0002t0002g0002 a0001c0002t0002g0015 others(26): Show |
74 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.390+850T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074106 | |||||||
| chr16:5074113 | A | G | 1 | a0003c0004t0002g0069 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.390+857A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074113 | |||||||
| chr16:5074238 | C | T | 1 | a0001c0002t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.390+982C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074238 | |||||||
| chr16:5074402 | G | T | 2 | a0001c0001t0015g0098 a0001c0001t0015g0100 |
2 | HG02886.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.391-986G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074402 | |||||||
| chr16:5074468 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.391-920C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074468 | |||||||
| chr16:5074485 | A | G | 3 | a0002c0003t0004g0020 a0002c0003t0004g0056 a0002c0003t0004g0057 |
5 | HG02486.hp1 HG02486.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.391-903A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074485 | |||||||
| chr16:5074513 | G | A | 1 | a0001c0002t0003g0035 | 2 | HG03195.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.391-875G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074513 | |||||||
| chr16:5074629 | G | T | 1 | a0008c0018t0028g0089 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.391-759G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074629 | |||||||
| chr16:5074739 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.391-649G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074739 | |||||||
| chr16:5074942 | G | A | 1 | a0001c0002t0005g0019 | 3 | HG00280.hp1 HG03688.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.391-446G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074942 | |||||||
| chr16:5074992 | C | T | 1 | a0001c0002t0002g0068 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.391-396C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5074992 | |||||||
| chr16:5075039 | G | A | 32 | a0001c0001t0001g0063 a0001c0002t0002g0002 a0001c0002t0002g0015 others(29): Show |
80 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.391-349G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5075039 | |||||||
| chr16:5075321 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.391-67A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5075321 | |||||||
| chr16:5075348 | G | C | 3 | a0002c0003t0010g0010 a0002c0003t0025g0010 a0002c0003t0027g0054 |
8 | HG01099.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.391-40G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5075348 | |||||||
| chr16:5075364 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
420 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(417): Show |
intron_variant | MODIFIER | c.391-24C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5075364 | |||||||
| chr16:5075373 | C | G | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391-15C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 3/12 | chr16 | 5075373 | |||||||
| chr16:5075552 | G | A | 1 | a0001c0001t0026g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.539+16G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075552 | |||||||
| chr16:5075603 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.539+67C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075603 | |||||||
| chr16:5075605 | A | G | 4 | a0002c0003t0004g0020 a0002c0003t0004g0055 a0002c0003t0004g0056 others(1): Show |
6 | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.539+69A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075605 | |||||||
| chr16:5075618 | G | A | 1 | a0002c0003t0004g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.539+82G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075618 | |||||||
| chr16:5075675 | G | T | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+139G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075675 | |||||||
| chr16:5075714 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.539+178G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075714 | |||||||
| chr16:5075731 | C | T | 1 | a0001c0002t0002g0067 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.539+195C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075731 | |||||||
| chr16:5075767 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.539+231C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075767 | |||||||
| chr16:5075878 | G | C | 4 | a0001c0001t0003g0011 a0001c0001t0003g0090 a0001c0001t0003g0091 others(1): Show |
9 | HG00323.hp2 HG01074.hp1 HG01346.hp1 others(6): Show |
intron_variant | MODIFIER | c.539+342G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5075878 | |||||||
| chr16:5076141 | T | C | 14 | a0001c0002t0001g0028 a0001c0002t0005g0005 a0001c0002t0005g0012 others(11): Show |
41 | HG00280.hp1 HG00408.hp1 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.539+605T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076141 | |||||||
| chr16:5076152 | C | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(144): Show |
418 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(415): Show |
intron_variant | MODIFIER | c.539+616C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076152 | |||||||
| chr16:5076221 | C | T | 1 | a0003c0004t0002g0045 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.539+685C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076221 | |||||||
| chr16:5076232 | C | G | 2 | a0001c0002t0005g0012 a0001c0002t0017g0012 |
6 | HG02015.hp2 NA18946.hp2 NA18973.hp1 others(3): Show |
intron_variant | MODIFIER | c.539+696C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076232 | |||||||
| chr16:5076296 | T | C | 2 | a0001c0001t0003g0036 a0001c0001t0030g0036 |
2 | NA18940.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.539+760T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076296 | |||||||
| chr16:5076430 | A | G | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.539+894A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076430 | |||||||
| chr16:5076480 | A | G | 1 | a0003c0004t0002g0066 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.539+944A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076480 | |||||||
| chr16:5076530 | A | G | 1 | a0002c0003t0004g0055 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.540-915A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076530 | |||||||
| chr16:5076533 | C | G | 1 | a0001c0001t0003g0091 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.540-912C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076533 | |||||||
| chr16:5076596 | T | C | 1 | a0001c0006t0002g0070 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.540-849T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076596 | |||||||
| chr16:5076626 | C | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
233 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.540-819C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076626 | |||||||
| chr16:5076632 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.540-813C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076632 | |||||||
| chr16:5076739 | G | C | 1 | a0001c0012t0008g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.540-706G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076739 | |||||||
| chr16:5076792 | CT | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0063 a0001c0001t0003g0004 others(56): Show |
160 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.540-631delT | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 5076792 | ||||||
| chr16:5076792 | CTT | C | 16 | a0001c0001t0001g0093 a0001c0002t0001g0028 a0001c0002t0002g0015 others(13): Show |
42 | HG00280.hp1 HG00408.hp1 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-632_540-631del others(2): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr16 | 5076792 | ||||||
| chr16:5076851 | A | G | 1 | a0001c0001t0015g0100 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.540-594A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076851 | |||||||
| chr16:5076971 | T | A | 1 | a0002c0003t0004g0072 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.540-474T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5076971 | |||||||
| chr16:5077007 | C | G | 1 | a0001c0001t0001g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.540-438C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077007 | |||||||
| chr16:5077014 | C | T | 1 | a0002c0003t0009g0078 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.540-431C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077014 | |||||||
| chr16:5077030 | A | T | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.540-415A>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077030 | |||||||
| chr16:5077051 | C | G | 3 | a0001c0002t0005g0076 a0002c0005t0004g0032 a0002c0005t0004g0077 |
4 | HG00639.hp2 HG02698.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.540-394C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077051 | |||||||
| chr16:5077075 | G | A | 2 | a0001c0001t0001g0104 a0001c0002t0006g0083 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.540-370G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077075 | |||||||
| chr16:5077080 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
419 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(416): Show |
intron_variant | MODIFIER | c.540-365T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077080 | |||||||
| chr16:5077080 | T | G | 1 | a0001c0002t0005g0053 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.540-365T>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077080 | |||||||
| chr16:5077334 | T | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(145): Show |
419 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(416): Show |
intron_variant | MODIFIER | c.540-111T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077334 | |||||||
| chr16:5077386 | G | A | 1 | a0001c0002t0002g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.540-59G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 4/12 | chr16 | 5077386 | |||||||
| chr16:5077578 | C | T | 1 | a0002c0003t0027g0054 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.629+44C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/12 | chr16 | 5077578 | |||||||
| chr16:5077700 | G | A | 1 | a0002c0005t0004g0032 | 2 | HG02738.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.629+166G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/12 | chr16 | 5077700 | |||||||
| chr16:5077720 | G | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(96): Show |
293 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(290): Show |
intron_variant | MODIFIER | c.629+186G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/12 | chr16 | 5077720 | |||||||
| chr16:5077852 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(146): Show |
420 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(417): Show |
intron_variant | MODIFIER | c.630-55G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 5/12 | chr16 | 5077852 | |||||||
| chr16:5078046 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.740+29C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078046 | |||||||
| chr16:5078174 | C | T | 1 | a0001c0001t0015g0115 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.740+157C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078174 | |||||||
| chr16:5078208 | C | T | 2 | a0002c0005t0011g0016 a0002c0005t0011g0085 |
5 | HG02809.hp2 HG02895.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.740+191C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078208 | |||||||
| chr16:5078329 | C | G | 1 | a0001c0001t0001g0042 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.740+312C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078329 | |||||||
| chr16:5078436 | T | A | 1 | a0003c0004t0008g0059 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.741-321T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078436 | |||||||
| chr16:5078449 | G | A | 1 | a0002c0003t0004g0073 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.741-308G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078449 | |||||||
| chr16:5078646 | T | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(151): Show |
432 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(429): Show |
intron_variant | MODIFIER | c.741-111T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078646 | |||||||
| chr16:5078668 | C | A | 4 | a0002c0003t0004g0020 a0002c0003t0004g0055 a0002c0003t0004g0056 others(1): Show |
6 | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.741-89C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 6/12 | chr16 | 5078668 | |||||||
| chr16:5078901 | T | C | 52 | a0001c0001t0001g0063 a0001c0002t0001g0028 a0001c0002t0002g0002 others(49): Show |
131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.862+23T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/12 | chr16 | 5078901 | |||||||
| chr16:5078978 | A | G | 1 | a0006c0021t0003g0087 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.863-86A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/12 | chr16 | 5078978 | |||||||
| chr16:5078980 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.863-84G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/12 | chr16 | 5078980 | |||||||
| chr16:5078994 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.863-70C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 7/12 | chr16 | 5078994 | |||||||
| chr16:5079148 | A | C | 3 | a0002c0003t0018g0033 a0002c0003t0023g0033 a0005c0008t0018g0081 |
3 | HG01257.hp2 HG01258.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.901+46A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079148 | |||||||
| chr16:5079173 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.901+71C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079173 | |||||||
| chr16:5079348 | G | C | 16 | a0001c0002t0001g0028 a0001c0002t0005g0005 a0001c0002t0005g0012 others(13): Show |
47 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.901+246G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079348 | |||||||
| chr16:5079386 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.901+284G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079386 | |||||||
| chr16:5079399 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(70): Show |
222 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(219): Show |
intron_variant | MODIFIER | c.901+297T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079399 | |||||||
| chr16:5079522 | C | G | 1 | a0002c0003t0004g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.902-226C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079522 | |||||||
| chr16:5079573 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.902-175C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079573 | |||||||
| chr16:5079645 | C | T | 1 | a0001c0001t0007g0041 | 2 | HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.902-103C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079645 | |||||||
| chr16:5079728 | G | A | 5 | a0001c0001t0003g0007 a0001c0001t0003g0036 a0001c0001t0016g0007 others(2): Show |
11 | HG00558.hp2 HG02027.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.902-20G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 8/12 | chr16 | 5079728 | |||||||
| chr16:5079850 | C | T | 1 | a0001c0002t0005g0050 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.961+43C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5079850 | |||||||
| chr16:5079891 | T | C | 76 | a0001c0001t0001g0063 a0001c0002t0001g0028 a0001c0002t0002g0002 others(73): Show |
198 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.961+84T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5079891 | |||||||
| chr16:5079931 | G | T | 1 | a0002c0003t0004g0074 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.961+124G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5079931 | |||||||
| chr16:5079978 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(95): Show |
290 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(287): Show |
intron_variant | MODIFIER | c.961+171C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5079978 | |||||||
| chr16:5080048 | TTTG | T | 2 | a0001c0001t0014g0018 a0001c0001t0014g0106 |
5 | HG02109.hp2 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.961+250_961+252del others(3): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 5080048 | ||||||
| chr16:5080073 | C | CT | 47 | a0001c0001t0001g0063 a0001c0002t0001g0028 a0001c0002t0002g0002 others(44): Show |
126 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.961+282dupT | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 5080073 | ||||||
| chr16:5080076 | T | C | 5 | a0001c0001t0003g0007 a0001c0001t0003g0036 a0001c0001t0016g0007 others(2): Show |
11 | HG00558.hp2 HG02027.hp2 NA18940.hp2 others(8): Show |
intron_variant | MODIFIER | c.961+269T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080076 | |||||||
| chr16:5080130 | C | T | 1 | a0003c0004t0002g0064 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.961+323C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080130 | |||||||
| chr16:5080203 | G | A | 1 | a0001c0013t0003g0092 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.961+396G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080203 | |||||||
| chr16:5080216 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.961+409C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080216 | |||||||
| chr16:5080309 | C | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
223 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.961+502C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080309 | |||||||
| chr16:5080347 | A | G | 151 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(148): Show |
422 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(419): Show |
intron_variant | MODIFIER | c.961+540A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080347 | |||||||
| chr16:5080360 | C | T | 4 | a0001c0002t0006g0006 a0001c0002t0006g0083 a0001c0002t0006g0084 others(1): Show |
11 | HG01891.hp2 HG02257.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.961+553C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080360 | |||||||
| chr16:5080363 | C | T | 1 | a0001c0006t0008g0031 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.961+556C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080363 | |||||||
| chr16:5080376 | G | T | 1 | a0009c0016t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.961+569G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080376 | |||||||
| chr16:5080377 | C | A | 1 | a0009c0016t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.962-569C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080377 | |||||||
| chr16:5080381 | A | AATACCTT others(26): Show |
1 | a0009c0016t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.962-564_962-563ins others(33): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 5080381 | ||||||
| chr16:5080383 | C | A | 1 | a0009c0016t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.962-563C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080383 | |||||||
| chr16:5080407 | G | T | 3 | a0001c0001t0001g0027 a0001c0001t0001g0108 a0010c0017t0001g0027 |
4 | NA18612.hp1 NA18985.hp2 NA19004.hp2 others(1): Show |
intron_variant | MODIFIER | c.962-539G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080407 | |||||||
| chr16:5080413 | C | G | 1 | a0009c0016t0003g0096 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.962-533C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080413 | |||||||
| chr16:5080480 | A | G | 1 | a0005c0008t0018g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.962-466A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080480 | |||||||
| chr16:5080547 | A | G | 52 | a0001c0001t0001g0063 a0001c0002t0001g0028 a0001c0002t0002g0002 others(49): Show |
131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.962-399A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080547 | |||||||
| chr16:5080591 | GCTGTGCC others(25): Show |
G | 1 | a0002c0003t0004g0056 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.962-348_962-317del others(32): Show |
ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr16 | 5080591 | ||||||
| chr16:5080709 | C | T | 1 | a0001c0001t0001g0042 | 2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.962-237C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080709 | |||||||
| chr16:5080872 | G | A | 4 | a0002c0003t0004g0020 a0002c0003t0004g0055 a0002c0003t0004g0056 others(1): Show |
6 | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.962-74G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 9/12 | chr16 | 5080872 | |||||||
| chr16:5081098 | C | G | 12 | a0002c0003t0004g0003 a0002c0003t0004g0072 a0002c0003t0004g0073 others(9): Show |
48 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1072+42C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081098 | |||||||
| chr16:5081154 | C | T | 3 | a0001c0002t0005g0029 a0001c0002t0005g0050 a0001c0002t0005g0053 |
4 | HG02523.hp2 NA18965.hp1 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.1072+98C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081154 | |||||||
| chr16:5081183 | G | C | 20 | a0002c0003t0004g0003 a0002c0003t0004g0020 a0002c0003t0004g0055 others(17): Show |
58 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.1072+127G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081183 | |||||||
| chr16:5081185 | G | A | 2 | a0001c0001t0003g0017 a0001c0001t0024g0094 |
5 | HG00423.hp1 HG02074.hp2 NA18969.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+129G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081185 | |||||||
| chr16:5081380 | C | T | 1 | a0001c0001t0003g0095 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1072+324C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081380 | |||||||
| chr16:5081439 | G | A | 2 | a0001c0001t0001g0026 a0001c0001t0007g0026 |
3 | HG02040.hp2 NA18971.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1072+383G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081439 | |||||||
| chr16:5081486 | C | T | 3 | a0002c0003t0018g0033 a0002c0003t0023g0033 a0005c0008t0018g0081 |
3 | HG01257.hp2 HG01258.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.1072+430C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081486 | |||||||
| chr16:5081596 | C | T | 13 | a0001c0002t0001g0028 a0001c0002t0005g0005 a0001c0002t0005g0014 others(10): Show |
40 | HG00280.hp1 HG00408.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.1072+540C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081596 | |||||||
| chr16:5081633 | C | A | 1 | a0001c0012t0008g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1072+577C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081633 | |||||||
| chr16:5081814 | G | C | 1 | a0002c0003t0004g0057 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1073-745G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081814 | |||||||
| chr16:5081819 | T | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(148): Show |
422 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(419): Show |
intron_variant | MODIFIER | c.1073-740T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081819 | |||||||
| chr16:5081836 | C | G | 1 | a0001c0012t0008g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1073-723C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081836 | |||||||
| chr16:5081887 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1073-672C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081887 | |||||||
| chr16:5081958 | T | A | 1 | a0003c0004t0002g0065 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1073-601T>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5081958 | |||||||
| chr16:5082099 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(152): Show |
433 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(430): Show |
intron_variant | MODIFIER | c.1073-460T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5082099 | |||||||
| chr16:5082146 | T | C | 25 | a0001c0002t0005g0012 a0001c0002t0017g0012 a0002c0003t0004g0003 others(22): Show |
72 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(69): Show |
intron_variant | MODIFIER | c.1073-413T>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5082146 | |||||||
| chr16:5082191 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1073-368C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5082191 | |||||||
| chr16:5082333 | C | CA | 52 | a0001c0001t0001g0126 a0001c0002t0001g0028 a0001c0002t0002g0002 others(49): Show |
131 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1073-219dupA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr16 | 5082333 | ||||||
| chr16:5082471 | C | T | 35 | a0001c0002t0002g0002 a0001c0002t0002g0015 a0001c0002t0002g0060 others(32): Show |
83 | HG00323.hp1 HG00597.hp1 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.1073-88C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5082471 | |||||||
| chr16:5082475 | G | T | 3 | a0002c0003t0010g0010 a0002c0003t0025g0010 a0002c0003t0027g0054 |
8 | HG01099.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1073-84G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 10/12 | chr16 | 5082475 | |||||||
| chr16:5082717 | C | A | 1 | a0001c0001t0003g0090 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1187+44C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5082717 | |||||||
| chr16:5082784 | G | A | 71 | a0001c0002t0002g0002 a0001c0002t0002g0015 a0001c0002t0002g0060 others(68): Show |
192 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1187+111G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5082784 | |||||||
| chr16:5082877 | A | G | 3 | a0001c0001t0013g0013 a0001c0001t0020g0097 a0001c0001t0026g0079 |
7 | HG02145.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1187+204A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5082877 | |||||||
| chr16:5082963 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1187+290G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5082963 | |||||||
| chr16:5082967 | C | T | 1 | a0001c0001t0024g0094 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1187+294C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5082967 | |||||||
| chr16:5083031 | A | C | 1 | a0003c0004t0002g0062 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1187+358A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5083031 | |||||||
| chr16:5083223 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1188-459C>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5083223 | |||||||
| chr16:5083545 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0001g0117 |
3 | HG01168.hp1 HG01169.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1188-137G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5083545 | |||||||
| chr16:5083605 | G | T | 78 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(75): Show |
228 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(225): Show |
intron_variant | MODIFIER | c.1188-77G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5083605 | |||||||
| chr16:5083678 | G | A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0121 |
3 | NA18944.hp2 NA18951.hp2 NA18982.hp1 |
splice_region_variant&intron_variant | LOW | c.1188-4G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 11/12 | chr16 | 5083678 | |||||||
| chr16:5083882 | G | A | 3 | a0002c0003t0010g0010 a0002c0003t0025g0010 a0002c0003t0027g0054 |
8 | HG01099.hp2 HG02258.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1263+125G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5083882 | |||||||
| chr16:5083964 | C | CA | 4 | a0002c0003t0004g0020 a0002c0003t0004g0055 a0002c0003t0004g0056 others(1): Show |
6 | HG02486.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1263+208dupA | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr16 | 5083964 | ||||||
| chr16:5084025 | G | A | 2 | a0001c0001t0013g0013 a0001c0001t0026g0079 |
6 | HG02145.hp1 HG02615.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1263+268G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084025 | |||||||
| chr16:5084045 | A | G | 1 | a0001c0002t0006g0084 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1263+288A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084045 | |||||||
| chr16:5084048 | A | G | 1 | a0003c0004t0002g0061 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1263+291A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084048 | |||||||
| chr16:5084138 | C | G | 1 | a0001c0001t0033g0111 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1263+381C>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084138 | |||||||
| chr16:5084210 | G | A | 152 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(149): Show |
426 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(423): Show |
intron_variant | MODIFIER | c.1263+453G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084210 | |||||||
| chr16:5084297 | G | T | 12 | a0002c0003t0004g0003 a0002c0003t0004g0072 a0002c0003t0004g0073 others(9): Show |
48 | HG00597.hp2 HG00738.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1264-453G>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084297 | |||||||
| chr16:5084313 | A | T | 1 | a0001c0001t0001g0125 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1264-437A>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084313 | |||||||
| chr16:5084333 | A | C | 1 | a0002c0003t0004g0075 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1264-417A>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084333 | |||||||
| chr16:5084445 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(155): Show |
440 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(437): Show |
intron_variant | MODIFIER | c.1264-305A>G | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084445 | |||||||
| chr16:5084456 | G | A | 1 | a0002c0005t0011g0085 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1264-294G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084456 | |||||||
| chr16:5084499 | C | T | 6 | a0001c0002t0002g0086 a0001c0006t0002g0021 a0001c0006t0002g0070 others(3): Show |
9 | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1264-251C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084499 | |||||||
| chr16:5084500 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1264-250G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084500 | |||||||
| chr16:5084551 | C | T | 3 | a0001c0001t0013g0013 a0001c0001t0020g0097 a0001c0001t0026g0079 |
7 | HG02145.hp1 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.1264-199C>T | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084551 | |||||||
| chr16:5084552 | G | A | 1 | a0005c0008t0018g0081 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1264-198G>A | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084552 | |||||||
| chr16:5084590 | G | C | 1 | a0001c0002t0002g0060 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1264-160G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084590 | |||||||
| chr16:5084598 | G | C | 1 | a0002c0005t0011g0016 | 4 | HG02809.hp2 HG02895.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1264-152G>C | ALG1 | ENSG00000033011.14 | transcript | ENST00000262374.10 | protein_coding | 12/12 | chr16 | 5084598 |