Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27163 |
| ensemblid | ENSG00000138744.16 |
| hgncid | 736 |
| symbol | NAAA |
| name | N-acylethanolamine acid amidase |
| refseq_nuc | NM_014435.4 |
| refseq_prot | NP_055250.2 |
| ensembl_nuc | ENST00000286733.9 |
| ensembl_prot | ENSP00000286733.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 75913660 |
| end | 75941013 |
| strand | - |
| ver | v1.2 |
| region | chr4:75913660-75941013 |
| region5000 | chr4:75908660-75946013 |
| regionname0 | NAAA_chr4_75913660_75941013 |
| regionname5000 | NAAA_chr4_75908660_75946013 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 359 | 161 | 69 | 24 | 38 | 5 | 25 | 26 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0002 | 1/1 | 359 | 116 | 1 | 18 | 84 | 5 | 6 | 67 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0003 | 0/0 | 359 | 93 | 9 | 22 | 52 | 3 | 7 | 38 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0004 | 0/0 | 359 | 9 | 0 | 1 | 8 | 0 | 0 | 7 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0005 | 0/0 | 359 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0006 | 0/0 | 359 | 5 | 3 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0007 | 0/0 | 359 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0008 | 0/0 | 359 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0009 | 0/0 | 359 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0010 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0011 | 0/0 | 359 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| a0012 | 0/0 | 359 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | MRTAD others(354): Show |
chr4 | 75908660 | 75946013 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1077 | 156 | 64 | 24 | 38 | 5 | 25 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0001c0006 | 0/0 | 1077 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0001c0012 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0002c0002 | 1/1 | 1077 | 114 | 1 | 18 | 83 | 5 | 5 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0002c0013 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0002c0014 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0003c0003 | 0/0 | 1077 | 93 | 9 | 22 | 52 | 3 | 7 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0004c0004 | 0/0 | 1077 | 9 | 0 | 1 | 8 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0005c0007 | 0/0 | 1077 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0005c0010 | 0/0 | 1077 | 2 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0006c0005 | 0/0 | 1077 | 5 | 3 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0007c0009 | 0/0 | 1077 | 3 | 0 | 3 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0008c0008 | 0/0 | 1077 | 3 | 3 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0009c0011 | 0/0 | 1077 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0010c0016 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0011c0017 | 0/0 | 1077 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 | ||
| a0012c0015 | 0/0 | 1077 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ATGCG others(1072): Show |
chr4 | 75908660 | 75946013 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1859 | 128 | 43 | 22 | 37 | 5 | 21 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0002 | 0/0 | 1859 | 12 | 10 | 0 | 0 | 0 | 2 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0003 | 0/0 | 1859 | 10 | 9 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0005 | 0/0 | 1859 | 2 | 0 | 0 | 0 | 0 | 2 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0006 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0008 | 0/0 | 1859 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0009 | 0/0 | 1859 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0001t0010 | 0/0 | 1859 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0006t0001 | 0/0 | 1859 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0001c0012t0002 | 0/0 | 1859 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0002c0002t0001 | 1/1 | 1859 | 112 | 1 | 16 | 83 | 5 | 5 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0002c0002t0007 | 0/0 | 1859 | 2 | 0 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0002c0013t0001 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0002c0014t0001 | 0/0 | 1859 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0003c0003t0001 | 0/0 | 1859 | 91 | 9 | 22 | 50 | 3 | 7 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0003c0003t0002 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0003c0003t0006 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0004c0004t0001 | 0/0 | 1859 | 9 | 0 | 1 | 8 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0005c0007t0004 | 0/0 | 1859 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0005c0010t0002 | 0/0 | 1859 | 2 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0006c0005t0001 | 0/0 | 1859 | 5 | 3 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0007c0009t0001 | 0/0 | 1859 | 3 | 0 | 3 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0008c0008t0004 | 0/0 | 1859 | 3 | 3 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0009c0011t0001 | 0/0 | 1859 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0010c0016t0001 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0011c0017t0001 | 0/0 | 1859 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| a0012c0015t0001 | 0/0 | 1859 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | ACGGC others(1854): Show |
chr4 | 75908660 | 75946013 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 7 | 3 | 0 | 3 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0003g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0008g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0009g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0001t0010g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0006t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0006t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0001c0012t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0003 | 0/0 | 6 | 0 | 1 | 4 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0006 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0008 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0012 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0194 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0002t0007g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0013t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0002c0014t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0001 | 0/0 | 17 | 1 | 6 | 9 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0004 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0035 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0036 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0003c0003t0006g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0004c0004t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0005c0007t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0005c0007t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0005c0007t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0005c0007t0004g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0005c0010t0002g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0006c0005t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0006c0005t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0006c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0006c0005t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0006c0005t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0007c0009t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0007c0009t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0008c0008t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0008c0008t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0008c0008t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0009c0011t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0010c0016t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0011c0017t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| a0012c0015t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | GBR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | GBR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00140 | hp1 | a0003 | c0003 | t0001 | g0293 | EUR | GBR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | FIN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0272 | EUR | FIN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0152 | EUR | FIN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0277 | EUR | FIN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00544 | hp1 | a0003 | c0003 | t0001 | g0299 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00544 | hp2 | a0002 | c0013 | t0001 | g0145 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0273 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00609 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0286 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00639 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0290 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0033 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | CHS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00735 | hp1 | a0004 | c0004 | t0001 | g0289 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00735 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0223 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01069 | hp1 | a0007 | c0009 | t0001 | g0314 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01071 | hp1 | a0007 | c0009 | t0001 | g0039 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01081 | hp1 | a0003 | c0003 | t0001 | g0274 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01109 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01168 | hp1 | a0007 | c0009 | t0001 | g0039 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01168 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0251 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01175 | hp2 | a0006 | c0005 | t0001 | g0245 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01192 | hp2 | a0003 | c0003 | t0001 | g0291 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01243 | hp2 | a0006 | c0005 | t0001 | g0249 | AMR | PUR | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01256 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01346 | hp1 | a0003 | c0003 | t0001 | g0268 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01346 | hp2 | a0002 | c0002 | t0007 | g0117 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0300 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0173 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0035 | AMR | CLM | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0052 | EUR | IBS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0022 | EUR | IBS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0046 | EUR | IBS | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01884 | hp1 | a0008 | c0008 | t0004 | g0203 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01891 | hp1 | a0005 | c0007 | t0004 | g0184 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0128 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01928 | hp2 | a0003 | c0003 | t0001 | g0244 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01943 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01943 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0297 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0084 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01981 | hp1 | a0003 | c0003 | t0001 | g0004 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01981 | hp2 | a0003 | c0003 | t0001 | g0280 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02015 | hp1 | a0004 | c0004 | t0001 | g0278 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02027 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02055 | hp2 | a0001 | c0006 | t0001 | g0205 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02074 | hp2 | a0003 | c0003 | t0001 | g0085 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02083 | hp1 | a0003 | c0003 | t0006 | g0255 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02083 | hp2 | a0003 | c0003 | t0001 | g0033 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0236 | EAS | KHV | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0229 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | CDX | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0265 | EAS | CDX | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02165 | hp1 | a0003 | c0003 | t0001 | g0035 | EAS | CDX | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0238 | EAS | CDX | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02257 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02258 | hp2 | a0005 | c0010 | t0002 | g0038 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02273 | hp1 | a0003 | c0003 | t0001 | g0262 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0004 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02280 | hp2 | a0003 | c0003 | t0001 | g0304 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02293 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02300 | hp1 | a0002 | c0002 | t0007 | g0092 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02451 | hp2 | a0003 | c0003 | t0001 | g0288 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02602 | hp1 | a0002 | c0002 | t0001 | g0235 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02602 | hp2 | a0003 | c0003 | t0001 | g0266 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02615 | hp1 | a0005 | c0007 | t0004 | g0312 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02622 | hp1 | a0009 | c0011 | t0001 | g0186 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0041 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02809 | hp1 | a0006 | c0005 | t0001 | g0250 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02818 | hp1 | a0003 | c0003 | t0001 | g0248 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02886 | hp2 | a0001 | c0001 | t0009 | g0077 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02895 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0225 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0017 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02970 | hp1 | a0003 | c0003 | t0001 | g0279 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02976 | hp2 | a0003 | c0003 | t0001 | g0303 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03041 | hp2 | a0003 | c0003 | t0001 | g0307 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0195 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03130 | hp2 | a0003 | c0003 | t0001 | g0305 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03139 | hp1 | a0006 | c0005 | t0001 | g0246 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | ESN | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03209 | hp1 | a0005 | c0007 | t0004 | g0191 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0198 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03239 | hp1 | a0003 | c0003 | t0001 | g0294 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03453 | hp1 | a0001 | c0012 | t0002 | g0207 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03486 | hp2 | a0005 | c0007 | t0004 | g0311 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0189 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03540 | hp2 | a0006 | c0005 | t0001 | g0247 | AFR | GWD | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03579 | hp2 | a0001 | c0006 | t0001 | g0211 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0036 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03669 | hp1 | a0001 | c0001 | t0005 | g0056 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0001 | SAS | PJL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03927 | hp2 | a0003 | c0003 | t0001 | g0004 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0257 | SAS | BEB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0070 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0113 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04199 | hp2 | a0001 | c0001 | t0005 | g0075 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04228 | hp1 | a0002 | c0014 | t0001 | g0157 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | CHB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | CHB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | CHB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18906 | hp2 | a0008 | c0008 | t0004 | g0156 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18939 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18939 | hp2 | a0001 | c0001 | t0006 | g0208 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18940 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18944 | hp2 | a0002 | c0002 | t0001 | g0219 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18945 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18945 | hp2 | a0003 | c0003 | t0001 | g0243 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18946 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18948 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18949 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18951 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18952 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0150 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18964 | hp2 | a0003 | c0003 | t0001 | g0239 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18968 | hp2 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18974 | hp1 | a0003 | c0003 | t0001 | g0254 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18974 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18975 | hp1 | a0003 | c0003 | t0001 | g0263 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18975 | hp2 | a0010 | c0016 | t0001 | g0044 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18978 | hp1 | a0003 | c0003 | t0001 | g0241 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18981 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18981 | hp2 | a0003 | c0003 | t0001 | g0281 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18982 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18983 | hp1 | a0003 | c0003 | t0001 | g0285 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0261 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18985 | hp2 | a0003 | c0003 | t0002 | g0287 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18986 | hp1 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18987 | hp1 | a0003 | c0003 | t0001 | g0256 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18987 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18989 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18990 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18990 | hp2 | a0002 | c0002 | t0001 | g0216 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18991 | hp1 | a0003 | c0003 | t0001 | g0252 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18994 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18995 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19003 | hp2 | a0003 | c0003 | t0001 | g0302 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19005 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0213 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19007 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19012 | hp1 | a0004 | c0004 | t0001 | g0259 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19054 | hp2 | a0004 | c0004 | t0001 | g0269 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19055 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19055 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19056 | hp1 | a0004 | c0004 | t0001 | g0258 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19057 | hp2 | a0004 | c0004 | t0001 | g0296 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19060 | hp1 | a0003 | c0003 | t0001 | g0264 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19062 | hp1 | a0003 | c0003 | t0001 | g0242 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19062 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19063 | hp2 | a0004 | c0004 | t0001 | g0292 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0034 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19064 | hp2 | a0004 | c0004 | t0001 | g0270 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0313 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19066 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19068 | hp1 | a0003 | c0003 | t0001 | g0240 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19068 | hp2 | a0002 | c0002 | t0001 | g0147 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19070 | hp2 | a0011 | c0017 | t0001 | g0178 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19078 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19078 | hp2 | a0003 | c0003 | t0001 | g0253 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19079 | hp1 | a0003 | c0003 | t0001 | g0282 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0143 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0284 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0131 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0260 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19087 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19088 | hp1 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19088 | hp2 | a0004 | c0004 | t0001 | g0295 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | YRI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ASW | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20752 | hp1 | a0012 | c0015 | t0001 | g0081 | EUR | TSI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0176 | EUR | TSI | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20905 | hp2 | a0003 | c0003 | t0001 | g0267 | SAS | GIH | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02559 | hp1 | a0008 | c0008 | t0004 | g0101 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03471 | hp1 | a0005 | c0010 | t0002 | g0038 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0298 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA20300 | hp2 | a0001 | c0001 | t0010 | g0315 | AFR | USA | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | LWK | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0089 | REF | REF | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0194 | REF | REF | NAAA_chr4_75908660_75946013 | NAAA | chr4 | 75908660 | 75946013 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75914984 | A | G | 9 | a0001 a0003 a0005 others(6): Show |
274 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(271): Show |
missense_variant&splice_region_variant | MODERATE | c.1000T>C | p.Phe334Leu | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/11 | 1064/1859 | 1000/1080 | 334/359 | chr4 | 75914984 | |||
| chr4:75918784 | C | A | 1 | a0008 | 3 | HG01884.hp1 HG02559.hp1 NA18906.hp2 |
missense_variant | MODERATE | c.975G>T | p.Leu325Phe | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/11 | 1039/1859 | 975/1080 | 325/359 | chr4 | 75918784 | |||
| chr4:75920984 | G | C | 1 | a0012 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.806C>G | p.Ala269Gly | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 6/11 | 870/1859 | 806/1080 | 269/359 | chr4 | 75920984 | |||
| chr4:75921116 | C | T | 2 | a0005 a0008 |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
missense_variant | MODERATE | c.674G>A | p.Ser225Asn | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 6/11 | 738/1859 | 674/1080 | 225/359 | chr4 | 75921116 | |||
| chr4:75921122 | G | A | 2 | a0005 a0008 |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
missense_variant&splice_region_variant | MODERATE | c.668C>T | p.Thr223Ile | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 6/11 | 732/1859 | 668/1080 | 223/359 | chr4 | 75921122 | |||
| chr4:75925770 | G | A | 1 | a0010 | 1 | NA18975.hp2 | missense_variant | MODERATE | c.631C>T | p.Arg211Trp | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/11 | 695/1859 | 631/1080 | 211/359 | chr4 | 75925770 | |||
| chr4:75936149 | C | T | 1 | a0006 | 5 | HG01175.hp2 HG01243.hp2 HG02809.hp1 others(2): Show |
missense_variant | MODERATE | c.458G>A | p.Arg153His | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/11 | 522/1859 | 458/1080 | 153/359 | chr4 | 75936149 | |||
| chr4:75936156 | C | T | 2 | a0003 a0004 |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
missense_variant | MODERATE | c.451G>A | p.Val151Ile | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/11 | 515/1859 | 451/1080 | 151/359 | chr4 | 75936156 | |||
| chr4:75940046 | C | A | 1 | a0011 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.326G>T | p.Ser109Ile | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/11 | 390/1859 | 326/1080 | 109/359 | chr4 | 75940046 | |||
| chr4:75940051 | G | T | 1 | a0009 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.321C>A | p.Asn107Lys | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/11 | 385/1859 | 321/1080 | 107/359 | chr4 | 75940051 | |||
| chr4:75940852 | G | A | 1 | a0007 | 3 | HG01069.hp1 HG01071.hp1 HG01168.hp1 |
missense_variant | MODERATE | c.98C>T | p.Ala33Val | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/11 | 162/1859 | 98/1080 | 33/359 | chr4 | 75940852 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75914928 | C | T | 1 | a0002c0014 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.1056G>A | p.Arg352Arg | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/11 | 1120/1859 | 1056/1080 | 352/359 | chr4 | 75914928 | |||
| chr4:75914967 | C | T | 2 | a0001c0012 a0002c0013 |
2 | HG00544.hp2 HG03453.hp1 |
synonymous_variant | LOW | c.1017G>A | p.Thr339Thr | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/11 | 1081/1859 | 1017/1080 | 339/359 | chr4 | 75914967 | |||
| chr4:75919909 | C | T | 1 | a0001c0006 | 4 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.969G>A | p.Gln323Gln | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/11 | 1033/1859 | 969/1080 | 323/359 | chr4 | 75919909 | |||
| chr4:75921004 | C | T | 2 | a0005c0007 a0008c0008 |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
synonymous_variant | LOW | c.786G>A | p.Thr262Thr | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 6/11 | 850/1859 | 786/1080 | 262/359 | chr4 | 75921004 | |||
| chr4:75936235 | C | T | 2 | a0003c0003 a0004c0004 |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
splice_region_variant&synonymous_variant | LOW | c.372G>A | p.Val124Val | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/11 | 436/1859 | 372/1080 | 124/359 | chr4 | 75936235 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75913710 | A | C | 2 | a0001c0001t0003 a0001c0001t0009 |
11 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*665T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 1194 | chr4 | 75913710 | ||||||
| chr4:75913714 | C | T | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(5): Show |
25 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*661G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 1190 | chr4 | 75913714 | ||||||
| chr4:75913745 | T | G | 2 | a0001c0001t0006 a0003c0003t0006 |
2 | HG02083.hp1 NA18939.hp2 |
3_prime_UTR_variant | MODIFIER | c.*630A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 1159 | chr4 | 75913745 | ||||||
| chr4:75913779 | G | A | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(5): Show |
25 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*596C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 1125 | chr4 | 75913779 | ||||||
| chr4:75913815 | T | C | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(5): Show |
25 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*560A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 1089 | chr4 | 75913815 | ||||||
| chr4:75914040 | G | A | 8 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0010 others(5): Show |
25 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*335C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 864 | chr4 | 75914040 | ||||||
| chr4:75914211 | C | A | 9 | a0001c0001t0002 a0001c0001t0008 a0001c0001t0009 others(6): Show |
26 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*164G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 693 | chr4 | 75914211 | ||||||
| chr4:75914224 | T | C | 1 | a0002c0002t0007 | 2 | HG01346.hp2 HG02300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*151A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 680 | chr4 | 75914224 | ||||||
| chr4:75914313 | A | G | 1 | a0001c0001t0005 | 2 | HG03669.hp1 HG04199.hp2 |
3_prime_UTR_variant | MODIFIER | c.*62T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 591 | chr4 | 75914313 | ||||||
| chr4:75914328 | T | A | 2 | a0005c0007t0004 a0008c0008t0004 |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*47A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 11/11 | 576 | chr4 | 75914328 | ||||||
| chr4:75914883 | C | G | 1 | a0001c0001t0008 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*21G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/11 | 21 | chr4 | 75914883 | ||||||
| chr4:75940974 | T | C | 1 | a0001c0001t0010 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-25A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/11 | 25 | chr4 | 75940974 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:75914358 | C | T | 22 | a0001c0001t0001g0310 a0001c0001t0002g0076 a0001c0001t0002g0113 others(19): Show |
23 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.*37-20G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914358 | |||||||
| chr4:75914364 | T | G | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.*37-26A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914364 | |||||||
| chr4:75914378 | A | AT | 6 | a0001c0001t0003g0187 a0001c0012t0002g0207 a0002c0002t0001g0138 others(3): Show |
6 | HG01175.hp2 HG03209.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.*37-41dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914378 | |||||||
| chr4:75914378 | AT | A | 9 | a0002c0002t0001g0127 a0003c0003t0001g0302 a0004c0004t0001g0296 others(6): Show |
9 | HG00597.hp1 HG01884.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.*37-41delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914378 | |||||||
| chr4:75914425 | A | G | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.*37-87T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914425 | |||||||
| chr4:75914505 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.*37-167A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914505 | |||||||
| chr4:75914757 | C | T | 1 | a0001c0012t0002g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.*36+111G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 10/10 | chr4 | 75914757 | |||||||
| chr4:75915178 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.999-193A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915178 | |||||||
| chr4:75915209 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-224A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915209 | |||||||
| chr4:75915211 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.999-226C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915211 | |||||||
| chr4:75915281 | A | G | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-296T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915281 | |||||||
| chr4:75915395 | C | A | 3 | a0002c0002t0001g0146 a0004c0004t0001g0292 a0004c0004t0001g0295 |
3 | NA19055.hp2 NA19063.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.999-410G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915395 | |||||||
| chr4:75915515 | G | C | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.999-530C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915515 | |||||||
| chr4:75915521 | T | C | 14 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(11): Show |
15 | HG00741.hp2 HG02258.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.999-536A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915521 | |||||||
| chr4:75915873 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-888A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915873 | |||||||
| chr4:75915945 | C | T | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-960G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915945 | |||||||
| chr4:75915991 | A | C | 1 | a0001c0001t0001g0053 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.999-1006T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75915991 | |||||||
| chr4:75916064 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.999-1079G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916064 | |||||||
| chr4:75916084 | C | T | 2 | a0001c0001t0001g0306 a0003c0003t0001g0279 |
2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.999-1099G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916084 | |||||||
| chr4:75916131 | C | G | 1 | a0002c0002t0001g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.999-1146G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916131 | |||||||
| chr4:75916182 | A | G | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-1197T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916182 | |||||||
| chr4:75916228 | T | C | 1 | a0003c0003t0001g0275 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.999-1243A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916228 | |||||||
| chr4:75916437 | G | A | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.999-1452C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916437 | |||||||
| chr4:75916520 | A | G | 1 | a0006c0005t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.999-1535T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916520 | |||||||
| chr4:75916713 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.999-1728A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916713 | |||||||
| chr4:75916778 | C | CT | 135 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(132): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.999-1794dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916778 | C | CTT | 26 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0060 others(23): Show |
27 | HG00642.hp2 HG00673.hp2 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.999-1795_999-1794d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916778 | CT | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(50): Show |
66 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.999-1794delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916778 | CTTTT | C | 19 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(16): Show |
20 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.999-1797_999-1794d others(6): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916778 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0187 others(3): Show |
10 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.999-1801_999-1794d others(10): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916778 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0053 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.999-1806_999-1794d others(15): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916778 | |||||||
| chr4:75916872 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.999-1887G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916872 | |||||||
| chr4:75916887 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1874A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916887 | |||||||
| chr4:75916937 | G | A | 19 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(16): Show |
20 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.998+1824C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916937 | |||||||
| chr4:75916938 | C | G | 19 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(16): Show |
20 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.998+1823G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75916938 | |||||||
| chr4:75917068 | T | C | 28 | a0001c0001t0001g0132 a0001c0001t0002g0076 a0001c0001t0002g0113 others(25): Show |
33 | HG00741.hp2 HG01109.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.998+1693A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917068 | |||||||
| chr4:75917178 | T | C | 1 | a0003c0003t0001g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.998+1583A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917178 | |||||||
| chr4:75917313 | A | C | 1 | a0001c0001t0001g0067 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.998+1448T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917313 | |||||||
| chr4:75917417 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1344A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917417 | |||||||
| chr4:75917419 | C | A | 5 | a0002c0002t0001g0029 a0002c0002t0001g0119 a0002c0002t0001g0171 others(2): Show |
6 | HG00558.hp1 HG02040.hp2 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+1342G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917419 | |||||||
| chr4:75917485 | A | G | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1276T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917485 | |||||||
| chr4:75917487 | C | CA | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1273dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917487 | |||||||
| chr4:75917581 | G | A | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1180C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917581 | |||||||
| chr4:75917586 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1175A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917586 | |||||||
| chr4:75917617 | C | T | 2 | a0001c0001t0001g0306 a0002c0002t0001g0049 |
2 | HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.998+1144G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917617 | |||||||
| chr4:75917629 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1132A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917629 | |||||||
| chr4:75917635 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.998+1126A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917635 | |||||||
| chr4:75917654 | C | T | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+1107G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917654 | |||||||
| chr4:75917705 | A | T | 119 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(116): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.998+1056T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917705 | |||||||
| chr4:75917713 | G | A | 1 | a0003c0003t0001g0302 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.998+1048C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917713 | |||||||
| chr4:75917776 | T | TA | 9 | a0002c0002t0001g0090 a0005c0007t0004g0184 a0005c0007t0004g0191 others(6): Show |
10 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.998+984dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917776 | |||||||
| chr4:75917776 | TA | T | 120 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0018 others(117): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.998+984delT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917776 | |||||||
| chr4:75917935 | G | A | 1 | a0001c0001t0002g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.998+826C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917935 | |||||||
| chr4:75917940 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.998+821A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917940 | |||||||
| chr4:75917955 | C | T | 64 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(61): Show |
77 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.998+806G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75917955 | |||||||
| chr4:75918159 | G | A | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+602C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918159 | |||||||
| chr4:75918176 | G | A | 58 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(55): Show |
71 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.998+585C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918176 | |||||||
| chr4:75918192 | T | G | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+569A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918192 | |||||||
| chr4:75918416 | C | T | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.998+345G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918416 | |||||||
| chr4:75918426 | G | T | 1 | a0003c0003t0001g0272 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.998+335C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918426 | |||||||
| chr4:75918441 | C | G | 121 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(118): Show |
162 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.998+320G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918441 | |||||||
| chr4:75918576 | A | C | 52 | a0002c0002t0001g0003 a0002c0002t0001g0005 a0002c0002t0001g0006 others(49): Show |
71 | HG00099.hp1 HG00597.hp1 HG00642.hp1 others(68): Show |
intron_variant | MODIFIER | c.998+185T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918576 | |||||||
| chr4:75918700 | C | T | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.998+61G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 9/10 | chr4 | 75918700 | |||||||
| chr4:75918809 | T | A | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.970-20A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75918809 | |||||||
| chr4:75918865 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.970-76C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75918865 | |||||||
| chr4:75918895 | C | A | 1 | a0001c0001t0001g0023 | 2 | HG00738.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.970-106G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75918895 | |||||||
| chr4:75918898 | T | A | 1 | a0001c0001t0001g0060 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.970-109A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75918898 | |||||||
| chr4:75918940 | C | A | 1 | a0002c0002t0001g0159 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.970-151G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75918940 | |||||||
| chr4:75919004 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.970-215A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919004 | |||||||
| chr4:75919052 | C | CT | 107 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(104): Show |
128 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.970-264dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919052 | |||||||
| chr4:75919052 | C | CTT | 108 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(105): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.970-265_970-264dup others(2): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919052 | |||||||
| chr4:75919067 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.970-278T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919067 | |||||||
| chr4:75919158 | C | T | 1 | a0001c0001t0002g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.970-369G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919158 | |||||||
| chr4:75919182 | T | C | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.970-393A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919182 | |||||||
| chr4:75919332 | A | G | 21 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(18): Show |
22 | HG00741.hp2 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.970-543T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919332 | |||||||
| chr4:75919484 | TA | T | 5 | a0005c0007t0004g0311 a0005c0007t0004g0312 a0008c0008t0004g0101 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+424delT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919484 | |||||||
| chr4:75919485 | A | AC | 15 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(12): Show |
16 | HG00741.hp2 HG02258.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.969+423_969+424ins others(1): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919485 | |||||||
| chr4:75919486 | A | T | 15 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(12): Show |
16 | HG00741.hp2 HG02258.hp2 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.969+423T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919486 | |||||||
| chr4:75919487 | T | C | 5 | a0005c0007t0004g0311 a0005c0007t0004g0312 a0008c0008t0004g0101 others(2): Show |
5 | HG01884.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+422A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919487 | |||||||
| chr4:75919539 | C | T | 1 | a0003c0003t0001g0271 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.969+370G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919539 | |||||||
| chr4:75919545 | C | T | 20 | a0001c0001t0002g0076 a0001c0001t0002g0113 a0001c0001t0002g0120 others(17): Show |
21 | HG00741.hp2 HG01884.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.969+364G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919545 | |||||||
| chr4:75919580 | G | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0187 others(3): Show |
10 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.969+329C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919580 | |||||||
| chr4:75919602 | T | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(213): Show |
275 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.969+307A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919602 | |||||||
| chr4:75919627 | C | T | 108 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(105): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.969+282G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919627 | |||||||
| chr4:75919731 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.969+178C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919731 | |||||||
| chr4:75919755 | G | T | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.969+154C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919755 | |||||||
| chr4:75919841 | T | C | 3 | a0001c0006t0001g0017 a0001c0006t0001g0205 a0001c0006t0001g0211 |
4 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.969+68A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 8/10 | chr4 | 75919841 | |||||||
| chr4:75919978 | G | A | 3 | a0008c0008t0004g0101 a0008c0008t0004g0156 a0008c0008t0004g0203 |
3 | HG01884.hp1 HG02559.hp1 NA18906.hp2 |
splice_region_variant&intron_variant | LOW | c.903-3C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75919978 | |||||||
| chr4:75919996 | G | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.903-21C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75919996 | |||||||
| chr4:75920035 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.903-60A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920035 | |||||||
| chr4:75920263 | C | T | 11 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0037 others(8): Show |
14 | HG01255.hp1 HG01496.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.903-288G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920263 | |||||||
| chr4:75920279 | C | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.903-304G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920279 | |||||||
| chr4:75920362 | G | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.902+376C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920362 | |||||||
| chr4:75920496 | G | T | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.902+242C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920496 | |||||||
| chr4:75920499 | G | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.902+239C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920499 | |||||||
| chr4:75920595 | A | G | 217 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(214): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.902+143T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920595 | |||||||
| chr4:75920725 | C | T | 4 | a0001c0001t0001g0180 a0006c0005t0001g0245 a0006c0005t0001g0246 others(1): Show |
4 | HG01175.hp2 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.902+13G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 7/10 | chr4 | 75920725 | |||||||
| chr4:75920950 | C | T | 3 | a0001c0006t0001g0017 a0001c0006t0001g0205 a0001c0006t0001g0211 |
4 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
splice_donor_variant&intron_variant | HIGH | c.839+1G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 6/10 | chr4 | 75920950 | |||||||
| chr4:75921130 | G | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.667-7C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921130 | |||||||
| chr4:75921223 | T | C | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.667-100A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921223 | |||||||
| chr4:75921283 | A | T | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.667-160T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921283 | |||||||
| chr4:75921383 | C | G | 8 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-260G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921383 | |||||||
| chr4:75921453 | A | C | 8 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-330T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921453 | |||||||
| chr4:75921459 | G | A | 1 | a0003c0003t0001g0244 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.667-336C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921459 | |||||||
| chr4:75921525 | G | A | 1 | a0001c0001t0001g0037 | 2 | HG01496.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.667-402C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921525 | |||||||
| chr4:75921635 | A | G | 8 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.667-512T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921635 | |||||||
| chr4:75921690 | G | A | 1 | a0001c0006t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.667-567C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921690 | |||||||
| chr4:75921721 | G | T | 109 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(106): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.667-598C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921721 | |||||||
| chr4:75921824 | C | T | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-701G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921824 | |||||||
| chr4:75921867 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0006c0005t0001g0245 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.667-744C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921867 | |||||||
| chr4:75921873 | G | C | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-750C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921873 | |||||||
| chr4:75921879 | T | A | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-756A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921879 | |||||||
| chr4:75921947 | G | T | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-824C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75921947 | |||||||
| chr4:75922128 | G | A | 1 | a0003c0003t0001g0282 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.667-1005C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922128 | |||||||
| chr4:75922140 | G | T | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-1017C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922140 | |||||||
| chr4:75922187 | C | T | 1 | a0001c0012t0002g0207 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.667-1064G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922187 | |||||||
| chr4:75922357 | G | T | 6 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0187 others(3): Show |
10 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-1234C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922357 | |||||||
| chr4:75922377 | C | CA | 15 | a0001c0001t0001g0043 a0001c0001t0001g0180 a0001c0001t0001g0182 others(12): Show |
16 | HG01175.hp2 HG01361.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.667-1255dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922377 | |||||||
| chr4:75922377 | CA | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0019 others(39): Show |
51 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.667-1255delT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922377 | |||||||
| chr4:75922377 | CAA | C | 11 | a0001c0001t0001g0306 a0003c0003t0001g0276 a0003c0003t0001g0279 others(8): Show |
11 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1256_667-1255d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922377 | |||||||
| chr4:75922578 | A | G | 10 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1455T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922578 | |||||||
| chr4:75922733 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0052 others(4): Show |
10 | HG00140.hp2 HG00639.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.667-1610A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922733 | |||||||
| chr4:75922771 | T | C | 120 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(117): Show |
161 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.667-1648A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922771 | |||||||
| chr4:75922809 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.667-1686T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922809 | |||||||
| chr4:75922833 | A | G | 1 | a0003c0003t0001g0293 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.667-1710T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922833 | |||||||
| chr4:75922910 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.667-1787G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922910 | |||||||
| chr4:75922964 | G | GCCT | 10 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(7): Show |
11 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.667-1842_667-1841i others(5): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75922964 | |||||||
| chr4:75923017 | G | A | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-1894C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923017 | |||||||
| chr4:75923032 | C | CTT | 8 | a0003c0003t0001g0279 a0005c0007t0004g0184 a0005c0007t0004g0191 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.667-1911_667-1910d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923032 | |||||||
| chr4:75923044 | T | A | 3 | a0001c0001t0001g0155 a0003c0003t0001g0032 a0003c0003t0001g0239 |
4 | HG00423.hp2 NA18964.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.667-1921A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923044 | |||||||
| chr4:75923093 | C | T | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-1970G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923093 | |||||||
| chr4:75923290 | T | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(106): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.667-2167A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923290 | |||||||
| chr4:75923324 | G | A | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-2201C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923324 | |||||||
| chr4:75923333 | G | A | 9 | a0001c0001t0001g0306 a0003c0003t0001g0279 a0005c0007t0004g0184 others(6): Show |
9 | HG01884.hp1 HG01884.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.667-2210C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923333 | |||||||
| chr4:75923416 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.667-2293G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923416 | |||||||
| chr4:75923564 | G | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0080 others(1): Show |
4 | HG00099.hp2 HG00323.hp2 HG01099.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+2171C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923564 | |||||||
| chr4:75923588 | G | A | 5 | a0001c0001t0001g0180 a0001c0001t0001g0185 a0006c0005t0001g0245 others(2): Show |
5 | HG01175.hp2 HG01243.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.666+2147C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923588 | |||||||
| chr4:75923641 | G | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+2094C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923641 | |||||||
| chr4:75923646 | T | C | 1 | a0006c0005t0001g0250 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.666+2089A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923646 | |||||||
| chr4:75923696 | C | T | 123 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(120): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.666+2039G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923696 | |||||||
| chr4:75923702 | A | G | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+2033T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923702 | |||||||
| chr4:75923765 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.666+1970G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923765 | |||||||
| chr4:75923961 | A | G | 2 | a0002c0002t0007g0092 a0002c0002t0007g0117 |
2 | HG01346.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.666+1774T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75923961 | |||||||
| chr4:75924050 | A | T | 1 | a0001c0001t0001g0185 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.666+1685T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924050 | |||||||
| chr4:75924115 | T | C | 6 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0187 others(3): Show |
10 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.666+1620A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924115 | |||||||
| chr4:75924214 | G | C | 3 | a0001c0006t0001g0017 a0001c0006t0001g0205 a0001c0006t0001g0211 |
4 | HG02055.hp2 HG02895.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.666+1521C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924214 | |||||||
| chr4:75924484 | G | A | 109 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(106): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.666+1251C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924484 | |||||||
| chr4:75924617 | A | G | 8 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(5): Show |
9 | HG01884.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.666+1118T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924617 | |||||||
| chr4:75924689 | T | A | 7 | a0005c0007t0004g0184 a0005c0007t0004g0191 a0005c0007t0004g0311 others(4): Show |
7 | HG01884.hp1 HG01891.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.666+1046A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924689 | |||||||
| chr4:75924760 | C | T | 1 | a0003c0003t0001g0257 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.666+975G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924760 | |||||||
| chr4:75924900 | C | G | 1 | a0001c0001t0009g0077 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.666+835G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924900 | |||||||
| chr4:75924983 | G | A | 6 | a0001c0001t0003g0011 a0001c0001t0003g0030 a0001c0001t0003g0187 others(3): Show |
10 | HG01109.hp2 HG02145.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.666+752C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924983 | |||||||
| chr4:75924996 | A | AT | 142 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0016 others(139): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(181): Show |
intron_variant | MODIFIER | c.666+738dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75924996 | |||||||
| chr4:75925159 | G | C | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.666+576C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925159 | |||||||
| chr4:75925302 | T | C | 1 | a0001c0001t0002g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.666+433A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925302 | |||||||
| chr4:75925324 | T | C | 1 | a0003c0003t0001g0257 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.666+411A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925324 | |||||||
| chr4:75925436 | T | C | 2 | a0001c0001t0001g0185 a0001c0001t0003g0218 |
2 | HG01243.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.666+299A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925436 | |||||||
| chr4:75925523 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(189): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.666+212G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925523 | |||||||
| chr4:75925602 | T | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(149): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.666+133A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 5/10 | chr4 | 75925602 | |||||||
| chr4:75925953 | T | C | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.590-142A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75925953 | |||||||
| chr4:75925998 | T | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(106): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.590-187A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75925998 | |||||||
| chr4:75926052 | G | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(104): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.590-241C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926052 | |||||||
| chr4:75926062 | G | A | 106 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(103): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.590-251C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926062 | |||||||
| chr4:75926070 | CA | C | 107 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(104): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.590-260delT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926070 | |||||||
| chr4:75926211 | T | C | 1 | a0004c0004t0001g0258 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.590-400A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926211 | |||||||
| chr4:75926261 | G | A | 101 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(98): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.590-450C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926261 | |||||||
| chr4:75926286 | T | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(99): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.590-475A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926286 | |||||||
| chr4:75926288 | T | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(99): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.590-477A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926288 | |||||||
| chr4:75926335 | C | T | 1 | a0003c0003t0001g0283 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.590-524G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926335 | |||||||
| chr4:75926430 | G | A | 2 | a0001c0001t0001g0196 a0008c0008t0004g0156 |
2 | HG02922.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.590-619C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926430 | |||||||
| chr4:75926551 | ACT | A | 3 | a0002c0002t0001g0006 a0002c0002t0001g0049 a0002c0002t0001g0051 |
6 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-742_590-741del others(2): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926551 | |||||||
| chr4:75926560 | C | CA | 28 | a0001c0001t0001g0165 a0001c0001t0001g0227 a0001c0001t0002g0190 others(25): Show |
29 | HG00741.hp1 HG01175.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.590-750dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926560 | |||||||
| chr4:75926560 | C | CAA | 8 | a0001c0001t0001g0055 a0001c0001t0001g0103 a0001c0001t0005g0056 others(5): Show |
8 | HG02155.hp2 HG02615.hp1 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.590-751_590-750dup others(2): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926560 | |||||||
| chr4:75926560 | C | CAAA | 93 | a0001c0001t0001g0007 a0001c0001t0001g0021 a0001c0001t0001g0041 others(90): Show |
127 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.590-752_590-750dup others(3): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926560 | |||||||
| chr4:75926560 | CA | C | 8 | a0001c0001t0001g0065 a0001c0001t0001g0087 a0001c0001t0001g0181 others(5): Show |
8 | HG01167.hp2 HG02451.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.590-750delT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926560 | |||||||
| chr4:75926583 | C | T | 94 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(91): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.590-772G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926583 | |||||||
| chr4:75926708 | T | C | 102 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(99): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.590-897A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75926708 | |||||||
| chr4:75927078 | C | T | 102 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(99): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.590-1267G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927078 | |||||||
| chr4:75927269 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.590-1458G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927269 | |||||||
| chr4:75927399 | C | T | 6 | a0001c0001t0001g0134 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02135.hp1 NA18948.hp1 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-1588G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927399 | |||||||
| chr4:75927633 | G | GC | 29 | a0001c0001t0001g0093 a0001c0001t0001g0108 a0001c0001t0001g0124 others(26): Show |
31 | HG00408.hp2 HG00423.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.590-1823dupG | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927633 | |||||||
| chr4:75927633 | G | GCC | 25 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0130 others(22): Show |
31 | HG00323.hp1 HG00597.hp1 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.590-1824_590-1823d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927633 | |||||||
| chr4:75927633 | GC | G | 15 | a0001c0001t0001g0142 a0001c0001t0001g0164 a0001c0001t0002g0212 others(12): Show |
19 | HG01243.hp2 HG01256.hp2 HG01346.hp2 others(16): Show |
intron_variant | MODIFIER | c.590-1823delG | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927633 | |||||||
| chr4:75927633 | GCC | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(50): Show |
65 | HG00621.hp1 HG00741.hp2 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.590-1824_590-1823d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927633 | |||||||
| chr4:75927633 | GCCC | G | 48 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(45): Show |
63 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(60): Show |
intron_variant | MODIFIER | c.590-1825_590-1823d others(5): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927633 | |||||||
| chr4:75927642 | C | A | 47 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(44): Show |
59 | HG00621.hp1 HG00741.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.590-1831G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927642 | |||||||
| chr4:75927643 | C | G | 1 | a0005c0007t0004g0191 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.590-1832G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927643 | |||||||
| chr4:75927644 | C | G | 87 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(84): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.590-1833G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927644 | |||||||
| chr4:75927645 | C | G | 6 | a0001c0001t0001g0042 a0001c0001t0001g0103 a0001c0001t0001g0136 others(3): Show |
6 | HG01192.hp2 HG03942.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.590-1834G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927645 | |||||||
| chr4:75927645 | CCCG | C | 87 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(84): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.590-1837_590-1835d others(5): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927645 | |||||||
| chr4:75927646 | C | G | 2 | a0001c0001t0003g0218 a0005c0007t0004g0312 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.590-1835G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927646 | |||||||
| chr4:75927647 | C | G | 3 | a0001c0001t0001g0308 a0001c0001t0001g0310 a0002c0002t0001g0008 |
3 | HG03453.hp2 HG03688.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.590-1836G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927647 | |||||||
| chr4:75927648 | G | C | 2 | a0001c0001t0001g0308 a0001c0001t0001g0310 |
2 | HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.590-1837C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927648 | |||||||
| chr4:75927650 | C | A | 97 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(94): Show |
131 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.590-1839G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927650 | |||||||
| chr4:75927663 | T | C | 24 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0037 others(21): Show |
30 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.590-1852A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927663 | |||||||
| chr4:75927733 | A | G | 100 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(97): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.590-1922T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927733 | |||||||
| chr4:75927777 | ACT | A | 6 | a0001c0001t0002g0190 a0001c0001t0002g0192 a0001c0001t0002g0193 others(3): Show |
6 | HG02809.hp2 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.590-1968_590-1967d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927777 | |||||||
| chr4:75927794 | A | T | 100 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(97): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.590-1983T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927794 | |||||||
| chr4:75927795 | C | CA | 99 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(96): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.590-1985dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927795 | |||||||
| chr4:75927801 | A | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(36): Show |
51 | HG00621.hp1 HG00741.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.590-1990T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927801 | |||||||
| chr4:75927853 | G | T | 1 | a0003c0003t0001g0262 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.590-2042C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927853 | |||||||
| chr4:75927884 | C | A | 2 | a0001c0012t0002g0207 a0003c0003t0001g0189 |
2 | HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.590-2073G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75927884 | |||||||
| chr4:75928007 | T | G | 1 | a0003c0003t0001g0313 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.590-2196A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928007 | |||||||
| chr4:75928144 | T | A | 1 | a0002c0002t0001g0133 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.590-2333A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928144 | |||||||
| chr4:75928651 | G | T | 24 | a0001c0001t0001g0142 a0001c0001t0001g0158 a0001c0001t0001g0164 others(21): Show |
32 | HG00408.hp1 HG00544.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.589+2563C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928651 | |||||||
| chr4:75928681 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.589+2533T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928681 | |||||||
| chr4:75928784 | CT | C | 101 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0021 others(98): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.589+2429delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928784 | |||||||
| chr4:75928816 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.589+2398G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928816 | |||||||
| chr4:75928915 | C | G | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+2299G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928915 | |||||||
| chr4:75928936 | C | T | 2 | a0002c0002t0001g0135 a0003c0003t0001g0033 |
3 | HG00673.hp1 HG02083.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.589+2278G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928936 | |||||||
| chr4:75928961 | G | GT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(55): Show |
73 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.589+2252dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928961 | |||||||
| chr4:75928963 | T | TG | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+2250_589+2251i others(3): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75928963 | |||||||
| chr4:75929082 | G | A | 2 | a0001c0001t0001g0228 a0001c0001t0001g0230 |
2 | HG03130.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.589+2132C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929082 | |||||||
| chr4:75929085 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.589+2129G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929085 | |||||||
| chr4:75929370 | T | C | 6 | a0002c0002t0001g0135 a0003c0003t0001g0033 a0003c0003t0001g0034 others(3): Show |
8 | HG00673.hp1 HG02083.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.589+1844A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929370 | |||||||
| chr4:75929405 | G | A | 6 | a0005c0007t0004g0184 a0006c0005t0001g0245 a0006c0005t0001g0246 others(3): Show |
6 | HG01175.hp2 HG01243.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.589+1809C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929405 | |||||||
| chr4:75929412 | G | A | 6 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(3): Show |
6 | HG02258.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.589+1802C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929412 | |||||||
| chr4:75929488 | A | G | 1 | a0002c0002t0001g0114 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.589+1726T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929488 | |||||||
| chr4:75929589 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.589+1625G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929589 | |||||||
| chr4:75929612 | A | C | 1 | a0001c0001t0001g0310 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.589+1602T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929612 | |||||||
| chr4:75929880 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.589+1334G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75929880 | |||||||
| chr4:75930227 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.589+987C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930227 | |||||||
| chr4:75930498 | T | C | 1 | a0003c0003t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.589+716A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930498 | |||||||
| chr4:75930786 | T | C | 1 | a0001c0001t0003g0229 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.589+428A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930786 | |||||||
| chr4:75930893 | G | T | 1 | a0001c0001t0002g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.589+321C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930893 | |||||||
| chr4:75930931 | G | A | 1 | a0003c0003t0001g0280 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.589+283C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930931 | |||||||
| chr4:75930975 | A | AC | 96 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0041 others(93): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.589+238dupG | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 4/10 | chr4 | 75930975 | |||||||
| chr4:75931384 | C | A | 3 | a0002c0002t0001g0027 a0002c0002t0001g0098 a0002c0002t0001g0162 |
4 | HG01070.hp2 HG01943.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-80G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931384 | |||||||
| chr4:75931432 | A | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(51): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.499-128T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931432 | |||||||
| chr4:75931686 | T | A | 91 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0041 others(88): Show |
124 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.499-382A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931686 | |||||||
| chr4:75931834 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.499-530C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931834 | |||||||
| chr4:75931857 | A | G | 2 | a0003c0003t0001g0281 a0003c0003t0001g0282 |
2 | NA18981.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.499-553T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931857 | |||||||
| chr4:75931913 | T | A | 1 | a0001c0001t0001g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.499-609A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75931913 | |||||||
| chr4:75932045 | C | T | 38 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(35): Show |
50 | HG00621.hp1 HG00741.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.499-741G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932045 | |||||||
| chr4:75932086 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499-782C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932086 | |||||||
| chr4:75932153 | C | T | 1 | a0001c0006t0001g0205 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.499-849G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932153 | |||||||
| chr4:75932178 | G | C | 6 | a0001c0001t0002g0190 a0001c0001t0002g0192 a0001c0001t0002g0193 others(3): Show |
6 | HG02809.hp2 HG03098.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.499-874C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932178 | |||||||
| chr4:75932185 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.499-881G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932185 | |||||||
| chr4:75932348 | T | C | 7 | a0003c0003t0001g0014 a0003c0003t0001g0243 a0003c0003t0001g0281 others(4): Show |
9 | HG00609.hp2 HG02027.hp1 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.499-1044A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932348 | |||||||
| chr4:75932413 | A | G | 1 | a0003c0003t0001g0252 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.499-1109T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932413 | |||||||
| chr4:75932525 | G | A | 1 | a0003c0003t0001g0285 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.499-1221C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932525 | |||||||
| chr4:75932570 | C | A | 92 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0041 others(89): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.499-1266G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932570 | |||||||
| chr4:75932637 | C | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(51): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.499-1333G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932637 | |||||||
| chr4:75932666 | A | T | 92 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0041 others(89): Show |
125 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.499-1362T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932666 | |||||||
| chr4:75932788 | G | T | 98 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0041 others(95): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.499-1484C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932788 | |||||||
| chr4:75932905 | T | C | 202 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(199): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.499-1601A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932905 | |||||||
| chr4:75932909 | C | G | 1 | a0003c0003t0001g0240 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.499-1605G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932909 | |||||||
| chr4:75932965 | A | T | 85 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0136 others(82): Show |
114 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.499-1661T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75932965 | |||||||
| chr4:75933030 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.499-1726C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933030 | |||||||
| chr4:75933076 | C | T | 1 | a0001c0001t0003g0187 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.499-1772G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933076 | |||||||
| chr4:75933114 | C | T | 4 | a0001c0001t0001g0306 a0003c0003t0001g0303 a0003c0003t0001g0304 others(1): Show |
4 | HG01884.hp2 HG02280.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-1810G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933114 | |||||||
| chr4:75933131 | T | C | 3 | a0001c0001t0001g0231 a0001c0001t0003g0030 a0001c0001t0003g0201 |
4 | HG01109.hp2 HG02280.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.499-1827A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933131 | |||||||
| chr4:75933132 | C | CA | 128 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(125): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.499-1829dupT | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933132 | |||||||
| chr4:75933132 | C | CAA | 64 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(61): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.499-1830_499-1829d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933132 | |||||||
| chr4:75933356 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(162): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.499-2052G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933356 | |||||||
| chr4:75933375 | C | T | 165 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(162): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.499-2071G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933375 | |||||||
| chr4:75933402 | A | C | 1 | a0002c0002t0001g0206 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.499-2098T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933402 | |||||||
| chr4:75933416 | C | T | 1 | a0002c0002t0001g0109 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.499-2112G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933416 | |||||||
| chr4:75933498 | C | G | 1 | a0001c0001t0001g0196 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.499-2194G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933498 | |||||||
| chr4:75933722 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.498+2387G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933722 | |||||||
| chr4:75933756 | C | A | 2 | a0001c0001t0001g0031 a0001c0001t0001g0232 |
3 | HG01081.hp2 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.498+2353G>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933756 | |||||||
| chr4:75933774 | C | T | 7 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0001g0310 others(4): Show |
8 | HG02258.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.498+2335G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933774 | |||||||
| chr4:75933806 | G | A | 2 | a0002c0002t0001g0166 a0002c0002t0001g0167 |
2 | NA18942.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.498+2303C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933806 | |||||||
| chr4:75933953 | A | C | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+2156T>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933953 | |||||||
| chr4:75933985 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.498+2124C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75933985 | |||||||
| chr4:75934009 | G | A | 3 | a0006c0005t0001g0245 a0006c0005t0001g0246 a0006c0005t0001g0247 |
3 | HG01175.hp2 HG03139.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.498+2100C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934009 | |||||||
| chr4:75934016 | C | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+2093G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934016 | |||||||
| chr4:75934017 | G | A | 46 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0031 others(43): Show |
55 | HG00741.hp2 HG01081.hp2 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.498+2092C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934017 | |||||||
| chr4:75934023 | C | T | 3 | a0003c0003t0001g0303 a0003c0003t0001g0304 a0003c0003t0001g0305 |
3 | HG02280.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.498+2086G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934023 | |||||||
| chr4:75934052 | GTAA | G | 30 | a0001c0001t0001g0096 a0001c0001t0001g0103 a0001c0001t0001g0105 others(27): Show |
34 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.498+2054_498+2056d others(5): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934052 | GTAATAA | G | 66 | a0001c0001t0001g0023 a0001c0001t0001g0091 a0001c0001t0001g0093 others(63): Show |
85 | HG00140.hp1 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.498+2051_498+2056d others(8): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934052 | GTAATAAT others(2): Show |
G | 64 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0310 others(61): Show |
87 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.498+2048_498+2056d others(11): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934052 | GTAATAAT others(5): Show |
G | 8 | a0001c0001t0001g0308 a0001c0001t0001g0309 a0001c0001t0002g0183 others(5): Show |
9 | HG02258.hp2 HG03098.hp2 HG03225.hp1 others(6): Show |
intron_variant | MODIFIER | c.498+2045_498+2056d others(14): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934052 | GTAATAAT others(8): Show |
G | 25 | a0001c0001t0001g0074 a0001c0001t0001g0087 a0001c0001t0001g0185 others(22): Show |
25 | HG00609.hp1 HG01175.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.498+2042_498+2056d others(17): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934052 | GTAATAAT others(11): Show |
G | 100 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0010 others(97): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.498+2039_498+2056d others(20): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934052 | |||||||
| chr4:75934229 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.498+1880A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934229 | |||||||
| chr4:75934355 | C | G | 1 | a0001c0001t0001g0105 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.498+1754G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934355 | |||||||
| chr4:75934472 | C | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+1637G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934472 | |||||||
| chr4:75934482 | A | AT | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(52): Show |
75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.498+1626dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934482 | |||||||
| chr4:75934482 | AT | A | 29 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(26): Show |
30 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.498+1626delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934482 | |||||||
| chr4:75934482 | ATT | A | 70 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(67): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.498+1625_498+1626d others(4): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934482 | |||||||
| chr4:75934576 | C | G | 1 | a0003c0003t0001g0256 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.498+1533G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934576 | |||||||
| chr4:75934616 | C | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+1493G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934616 | |||||||
| chr4:75934619 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.498+1490C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934619 | |||||||
| chr4:75934723 | A | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+1386T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934723 | |||||||
| chr4:75934837 | C | T | 1 | a0003c0003t0006g0255 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.498+1272G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934837 | |||||||
| chr4:75934945 | AT | A | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+1163delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75934945 | |||||||
| chr4:75935004 | ATAT | A | 44 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(41): Show |
56 | HG00741.hp2 HG01081.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.498+1102_498+1104d others(5): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935004 | |||||||
| chr4:75935086 | C | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+1023G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935086 | |||||||
| chr4:75935202 | T | C | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+907A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935202 | |||||||
| chr4:75935287 | T | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(54): Show |
78 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.498+822A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935287 | |||||||
| chr4:75935307 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.498+802A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935307 | |||||||
| chr4:75935325 | C | G | 1 | a0008c0008t0004g0101 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.498+784G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935325 | |||||||
| chr4:75935372 | G | C | 1 | a0001c0001t0001g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.498+737C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935372 | |||||||
| chr4:75935453 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.498+656C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935453 | |||||||
| chr4:75935482 | G | A | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+627C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935482 | |||||||
| chr4:75935583 | T | C | 2 | a0001c0001t0001g0188 a0001c0001t0003g0187 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.498+526A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935583 | |||||||
| chr4:75935614 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0003g0187 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.498+495C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935614 | |||||||
| chr4:75935837 | A | G | 45 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(42): Show |
57 | HG00741.hp2 HG01081.hp2 HG01109.hp2 others(54): Show |
intron_variant | MODIFIER | c.498+272T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935837 | |||||||
| chr4:75935911 | G | C | 79 | a0001c0001t0001g0021 a0001c0001t0001g0052 a0003c0003t0001g0001 others(76): Show |
109 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.498+198C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935911 | |||||||
| chr4:75935992 | G | T | 1 | a0002c0002t0001g0204 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.498+117C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935992 | |||||||
| chr4:75935995 | AT | A | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+113delA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935995 | |||||||
| chr4:75935997 | T | C | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+112A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75935997 | |||||||
| chr4:75936011 | C | T | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.498+98G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 3/10 | chr4 | 75936011 | |||||||
| chr4:75936242 | A | G | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
splice_region_variant&intron_variant | LOW | c.372-7T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936242 | |||||||
| chr4:75936385 | A | G | 2 | a0002c0002t0001g0099 a0002c0002t0001g0100 |
2 | NA18974.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.372-150T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936385 | |||||||
| chr4:75936524 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.372-289A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936524 | |||||||
| chr4:75936796 | A | G | 5 | a0003c0003t0001g0033 a0003c0003t0001g0034 a0003c0003t0001g0252 others(2): Show |
7 | HG00673.hp1 HG02083.hp2 NA18962.hp2 others(4): Show |
intron_variant | MODIFIER | c.372-561T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936796 | |||||||
| chr4:75936847 | G | A | 74 | a0003c0003t0001g0001 a0003c0003t0001g0004 a0003c0003t0001g0014 others(71): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(99): Show |
intron_variant | MODIFIER | c.372-612C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936847 | |||||||
| chr4:75936929 | G | A | 77 | a0001c0001t0001g0237 a0001c0001t0002g0195 a0002c0002t0001g0238 others(74): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.372-694C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936929 | |||||||
| chr4:75936960 | G | T | 1 | a0006c0005t0001g0245 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.372-725C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75936960 | |||||||
| chr4:75937060 | C | T | 77 | a0001c0001t0001g0237 a0001c0001t0002g0195 a0002c0002t0001g0238 others(74): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.372-825G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937060 | |||||||
| chr4:75937118 | T | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(219): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.372-883A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937118 | |||||||
| chr4:75937248 | A | G | 76 | a0001c0001t0001g0237 a0002c0002t0001g0238 a0003c0003t0001g0001 others(73): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.372-1013T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937248 | |||||||
| chr4:75937288 | G | A | 3 | a0003c0003t0001g0303 a0003c0003t0001g0304 a0003c0003t0001g0305 |
3 | HG02280.hp2 HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.372-1053C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937288 | |||||||
| chr4:75937479 | G | A | 110 | a0001c0001t0001g0023 a0001c0001t0001g0087 a0001c0001t0001g0091 others(107): Show |
133 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.372-1244C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937479 | |||||||
| chr4:75937486 | GTTAT | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0013 others(219): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.372-1255_372-1252d others(6): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937486 | |||||||
| chr4:75937621 | G | T | 1 | a0003c0003t0001g0251 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.372-1386C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75937621 | |||||||
| chr4:75938462 | A | T | 54 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(51): Show |
72 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.371+1539T>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938462 | |||||||
| chr4:75938509 | TCTTTTCT others(4): Show |
T | 1 | a0001c0001t0001g0199 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.371+1481_371+1491d others(13): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938509 | |||||||
| chr4:75938552 | C | G | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(52): Show |
75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.371+1449G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938552 | |||||||
| chr4:75938887 | G | A | 56 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(53): Show |
76 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(73): Show |
intron_variant | MODIFIER | c.371+1114C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938887 | |||||||
| chr4:75938895 | T | A | 1 | a0002c0002t0001g0170 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.371+1106A>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938895 | |||||||
| chr4:75938998 | C | T | 3 | a0001c0001t0002g0190 a0001c0001t0002g0192 a0001c0001t0002g0193 |
3 | HG02809.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.371+1003G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75938998 | |||||||
| chr4:75939099 | C | T | 5 | a0006c0005t0001g0245 a0006c0005t0001g0246 a0006c0005t0001g0247 others(2): Show |
5 | HG01175.hp2 HG01243.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.371+902G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939099 | |||||||
| chr4:75939209 | G | C | 1 | a0001c0001t0002g0193 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.371+792C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939209 | |||||||
| chr4:75939295 | T | G | 2 | a0006c0005t0001g0249 a0006c0005t0001g0250 |
2 | HG01243.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.371+706A>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939295 | |||||||
| chr4:75939317 | C | T | 71 | a0001c0001t0001g0037 a0001c0001t0001g0237 a0001c0001t0001g0301 others(68): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.371+684G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939317 | |||||||
| chr4:75939414 | A | AT | 125 | a0001c0001t0001g0023 a0001c0001t0001g0040 a0001c0001t0001g0041 others(122): Show |
151 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.371+586dupA | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939414 | |||||||
| chr4:75939414 | A | ATT | 18 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0093 others(15): Show |
19 | HG00609.hp1 HG00738.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.371+585_371+586dup others(2): Show |
NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939414 | |||||||
| chr4:75939498 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.371+503G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939498 | |||||||
| chr4:75939567 | C | G | 1 | a0003c0003t0001g0189 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.371+434G>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939567 | |||||||
| chr4:75939755 | A | G | 2 | a0001c0001t0001g0188 a0001c0001t0003g0187 |
2 | HG03209.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.371+246T>C | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939755 | |||||||
| chr4:75939768 | G | A | 2 | a0002c0002t0001g0176 a0002c0002t0001g0177 |
2 | HG01167.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.371+233C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939768 | |||||||
| chr4:75939782 | G | A | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(50): Show |
66 | HG00741.hp2 HG01081.hp2 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.371+219C>T | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939782 | |||||||
| chr4:75939877 | G | T | 1 | a0002c0002t0001g0083 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.371+124C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939877 | |||||||
| chr4:75939885 | T | C | 53 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0028 others(50): Show |
66 | HG00741.hp2 HG01081.hp2 HG01109.hp2 others(63): Show |
intron_variant | MODIFIER | c.371+116A>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939885 | |||||||
| chr4:75939984 | G | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(247): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.371+17C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 2/10 | chr4 | 75939984 | |||||||
| chr4:75940338 | G | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.207-173C>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/10 | chr4 | 75940338 | |||||||
| chr4:75940564 | C | T | 106 | a0001c0001t0001g0023 a0001c0001t0001g0087 a0001c0001t0001g0091 others(103): Show |
129 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.206+180G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/10 | chr4 | 75940564 | |||||||
| chr4:75940592 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.206+152G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/10 | chr4 | 75940592 | |||||||
| chr4:75940682 | G | C | 1 | a0003c0003t0001g0313 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.206+62C>G | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/10 | chr4 | 75940682 | |||||||
| chr4:75940706 | C | T | 55 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0015 others(52): Show |
75 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(72): Show |
intron_variant | MODIFIER | c.206+38G>A | NAAA | ENSG00000138744.16 | transcript | ENST00000286733.9 | protein_coding | 1/10 | chr4 | 75940706 |