Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23275 |
| ensemblid | ENSG00000186866.17 |
| hgncid | 14683 |
| symbol | POFUT2 |
| name | protein O-fucosyltransferase 2 |
| refseq_nuc | NM_133635.6 |
| refseq_prot | NP_598368.2 |
| ensembl_nuc | ENST00000349485.10 |
| ensembl_prot | ENSP00000339613.5 |
| mane_status | MANE Select |
| chr | chr21 |
| start | 45263935 |
| end | 45287895 |
| strand | - |
| ver | v1.2 |
| region | chr21:45263935-45287895 |
| region5000 | chr21:45258935-45292895 |
| regionname0 | POFUT2_chr21_45263935_45287895 |
| regionname5000 | POFUT2_chr21_45258935_45292895 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 429 | 412 | 82 | 75 | 195 | 16 | 42 | 156 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0002 | 0/0 | 429 | 12 | 12 | 0 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0003 | 0/0 | 429 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0004 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0005 | 0/0 | 429 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0006 | 0/0 | 429 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0007 | 0/0 | 429 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0008 | 0/0 | 429 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0009 | 0/0 | 429 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0010 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| a0011 | 0/0 | 429 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | MATLS others(424): Show |
chr21 | 45258935 | 45292895 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1287 | 341 | 80 | 60 | 156 | 13 | 31 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0001c0002 | 0/1 | 1287 | 69 | 1 | 15 | 38 | 3 | 11 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0001c0010 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0001c0011 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0002c0003 | 0/0 | 1287 | 12 | 12 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0003c0004 | 0/0 | 1287 | 3 | 3 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0003c0005 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0004c0013 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0005c0015 | 0/0 | 1287 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0006c0012 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0007c0009 | 0/0 | 1287 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0008c0014 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0009c0008 | 0/0 | 1287 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0010c0007 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 | ||
| a0011c0006 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | ATGGC others(1282): Show |
chr21 | 45258935 | 45292895 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2861 | 188 | 13 | 50 | 95 | 11 | 18 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0002 | 0/0 | 2865 | 85 | 25 | 7 | 44 | 0 | 9 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0003 | 0/0 | 2865 | 9 | 4 | 0 | 1 | 2 | 2 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0004 | 0/0 | 2861 | 8 | 0 | 0 | 8 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0005 | 0/0 | 2865 | 7 | 6 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0006 | 0/0 | 2865 | 6 | 6 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0007 | 0/0 | 2865 | 5 | 4 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0008 | 0/0 | 2862 | 5 | 5 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2857): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0009 | 0/0 | 2865 | 4 | 4 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0010 | 0/0 | 2862 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2857): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0011 | 0/0 | 2862 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2857): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0012 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0014 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0015 | 0/0 | 2865 | 2 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0016 | 0/0 | 2861 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0017 | 0/0 | 2865 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0018 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0021 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0022 | 0/0 | 2840 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2835): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0023 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0025 | 0/0 | 2861 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0026 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0027 | 0/0 | 2836 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2831): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0028 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2866): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0029 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0030 | 0/0 | 2861 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0001c0001t0032 | 0/0 | 2862 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2857): Show |
chr21 | 45258935 | 45292895 |
| a0001c0002t0002 | 0/1 | 2865 | 67 | 1 | 14 | 37 | 3 | 11 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0002t0019 | 0/0 | 2865 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0002t0020 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0010t0003 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0001c0011t0001 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0002c0003t0001 | 0/0 | 2861 | 12 | 12 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0003c0004t0012 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0003c0004t0013 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0003c0004t0031 | 0/0 | 2862 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2857): Show |
chr21 | 45258935 | 45292895 |
| a0003c0005t0013 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0004c0013t0001 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0005c0015t0002 | 0/0 | 2865 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0006c0012t0024 | 0/0 | 2865 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0007c0009t0001 | 0/0 | 2861 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0008c0014t0002 | 0/0 | 2865 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2860): Show |
chr21 | 45258935 | 45292895 |
| a0009c0008t0001 | 0/0 | 2861 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0010c0007t0001 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| a0011c0006t0001 | 0/0 | 2861 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | GGAAG others(2856): Show |
chr21 | 45258935 | 45292895 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 49 | 2 | 9 | 31 | 1 | 6 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0003 | 0/0 | 17 | 0 | 9 | 7 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0006 | 1/0 | 7 | 0 | 3 | 0 | 2 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0008 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0011 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0007 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0004g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0005g0024 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0005g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0006g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0006g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0006g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0007g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0007g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0007g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0008g0051 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0008g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0008g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0010g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0011g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0012g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0014g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0014g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0015g0048 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0016g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0017g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0017g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0018g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0021g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0022g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0023g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0025g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0026g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0027g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0028g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0029g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0030g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0001t0032g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0002 | 0/0 | 21 | 1 | 2 | 14 | 1 | 3 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0004 | 0/0 | 10 | 0 | 4 | 6 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0047 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0002g0252 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0019g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0002t0020g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0010t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0001c0011t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0002c0003t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0003c0004t0012g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0003c0004t0013g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0003c0004t0031g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0003c0005t0013g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0004c0013t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0005c0015t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0006c0012t0024g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0007c0009t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0008c0014t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0009c0008t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0010c0007t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| a0011c0006t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0099 | EUR | GBR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0244 | EUR | GBR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | FIN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0105 | EUR | FIN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | FIN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0199 | EUR | FIN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00423 | hp1 | a0004 | c0013 | t0001 | g0182 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00597 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00597 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0226 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0242 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG00741 | hp2 | a0001 | c0002 | t0020 | g0236 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01069 | hp1 | a0005 | c0015 | t0002 | g0225 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0044 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01099 | hp1 | a0001 | c0002 | t0002 | g0229 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01099 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0221 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0227 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01258 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01261 | hp1 | a0001 | c0001 | t0032 | g0253 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01361 | hp2 | a0001 | c0001 | t0015 | g0048 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01884 | hp1 | a0001 | c0001 | t0017 | g0247 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01891 | hp2 | a0003 | c0005 | t0013 | g0059 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01981 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02027 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02055 | hp1 | a0001 | c0001 | t0009 | g0111 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02055 | hp2 | a0001 | c0001 | t0022 | g0056 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | KHV | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02145 | hp2 | a0001 | c0001 | t0012 | g0187 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CDX | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | CDX | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | CDX | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0024 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02257 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02258 | hp1 | a0003 | c0004 | t0012 | g0191 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02258 | hp2 | a0001 | c0001 | t0009 | g0131 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02622 | hp2 | a0001 | c0001 | t0014 | g0193 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02630 | hp1 | a0001 | c0001 | t0010 | g0053 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0245 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02647 | hp1 | a0002 | c0003 | t0001 | g0103 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02647 | hp2 | a0002 | c0003 | t0001 | g0101 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0047 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0231 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02738 | hp1 | a0001 | c0002 | t0002 | g0219 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02809 | hp2 | a0001 | c0001 | t0018 | g0190 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02818 | hp1 | a0001 | c0001 | t0006 | g0080 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02818 | hp2 | a0007 | c0009 | t0001 | g0135 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0251 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02886 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0087 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02896 | hp2 | a0001 | c0001 | t0011 | g0027 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02897 | hp1 | a0001 | c0001 | t0011 | g0027 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0088 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02922 | hp2 | a0001 | c0001 | t0014 | g0192 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02965 | hp1 | a0001 | c0001 | t0009 | g0137 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0089 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02970 | hp2 | a0002 | c0003 | t0001 | g0016 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0256 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0249 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03041 | hp2 | a0001 | c0001 | t0027 | g0133 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03130 | hp1 | a0001 | c0001 | t0030 | g0107 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0248 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0255 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03225 | hp1 | a0001 | c0001 | t0006 | g0116 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03225 | hp2 | a0002 | c0003 | t0001 | g0029 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0197 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03453 | hp1 | a0003 | c0004 | t0031 | g0055 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0024 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03490 | hp1 | a0001 | c0001 | t0015 | g0048 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03490 | hp2 | a0001 | c0001 | t0025 | g0146 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03516 | hp2 | a0001 | c0001 | t0008 | g0254 | AFR | ESN | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0029 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03540 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03831 | hp1 | a0001 | c0002 | t0002 | g0220 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03834 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04115 | hp2 | a0008 | c0014 | t0002 | g0230 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | BEB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04199 | hp2 | a0009 | c0008 | t0001 | g0112 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | STU | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18522 | hp1 | a0001 | c0001 | t0008 | g0051 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0213 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18747 | hp1 | a0001 | c0001 | t0007 | g0052 | EAS | CHB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18747 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18941 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18948 | hp1 | a0010 | c0007 | t0001 | g0142 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0235 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18950 | hp2 | a0011 | c0006 | t0001 | g0124 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18951 | hp1 | a0001 | c0001 | t0026 | g0108 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18952 | hp1 | a0001 | c0001 | t0021 | g0067 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18960 | hp1 | a0001 | c0002 | t0002 | g0237 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18967 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18982 | hp1 | a0001 | c0011 | t0001 | g0159 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18984 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18986 | hp1 | a0001 | c0002 | t0002 | g0228 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18989 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18991 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18991 | hp2 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18994 | hp2 | a0001 | c0002 | t0002 | g0223 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19000 | hp1 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19001 | hp1 | a0001 | c0001 | t0028 | g0165 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19001 | hp2 | a0001 | c0002 | t0002 | g0218 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19006 | hp2 | a0001 | c0001 | t0016 | g0034 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19007 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19009 | hp2 | a0001 | c0001 | t0029 | g0155 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19030 | hp1 | a0002 | c0003 | t0001 | g0100 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19043 | hp1 | a0001 | c0010 | t0003 | g0189 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19043 | hp2 | a0002 | c0003 | t0001 | g0102 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19055 | hp2 | a0001 | c0001 | t0023 | g0072 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19060 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19062 | hp2 | a0001 | c0002 | t0002 | g0234 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0243 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19066 | hp2 | a0001 | c0002 | t0002 | g0004 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19080 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19085 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19086 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19088 | hp2 | a0001 | c0002 | t0019 | g0233 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19089 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0005 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | YRI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0030 | AFR | ASW | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | ASW | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0002 | EUR | TSI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | TSI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0224 | EUR | TSI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0222 | EUR | TSI | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0044 | SAS | GIH | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20905 | hp2 | a0001 | c0002 | t0002 | g0238 | SAS | GIH | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02109 | hp1 | a0006 | c0012 | t0024 | g0210 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02486 | hp1 | a0002 | c0003 | t0001 | g0016 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02486 | hp2 | a0001 | c0001 | t0006 | g0128 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0054 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG03471 | hp2 | a0001 | c0001 | t0017 | g0246 | AFR | MSL | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG06807 | hp1 | a0003 | c0004 | t0013 | g0188 | AFR | USA | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0129 | AFR | USA | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0030 | AFR | USA | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0104 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | LWK | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0252 | REF | REF | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | POFUT2_chr21_45258935_45292895 | POFUT2 | chr21 | 45258935 | 45292895 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:45263936 | T | A | 5 | a0001 a0003 a0005 others(2): Show |
172 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(169): Show |
splice_region_variant | LOW | c.*1546A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | chr21 | 45263936 | |||||||
| chr21:45265555 | G | A | 1 | a0005 | 1 | HG01069.hp1 | missense_variant | MODERATE | c.1217C>T | p.Thr406Met | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1241/2861 | 1217/1290 | 406/429 | chr21 | 45265555 | |||
| chr21:45265628 | T | C | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1144A>G | p.Ile382Val | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1168/2861 | 1144/1290 | 382/429 | chr21 | 45265628 | |||
| chr21:45265630 | A | T | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1142T>A | p.Phe381Tyr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1166/2861 | 1142/1290 | 381/429 | chr21 | 45265630 | |||
| chr21:45265631 | A | T | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1141T>A | p.Phe381Ile | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1165/2861 | 1141/1290 | 381/429 | chr21 | 45265631 | |||
| chr21:45265632 | A | T | 1 | a0007 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1140T>A | p.Phe380Leu | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1164/2861 | 1140/1290 | 380/429 | chr21 | 45265632 | |||
| chr21:45265633 | A | T | 1 | a0007 | 1 | HG02818.hp2 | missense_variant&splice_region_variant | MODERATE | c.1139T>A | p.Phe380Tyr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1163/2861 | 1139/1290 | 380/429 | chr21 | 45265633 | |||
| chr21:45265634 | A | C | 1 | a0007 | 1 | HG02818.hp2 | missense_variant&splice_region_variant | MODERATE | c.1138T>G | p.Phe380Val | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1162/2861 | 1138/1290 | 380/429 | chr21 | 45265634 | |||
| chr21:45267627 | C | T | 1 | a0003 | 4 | HG01891.hp2 HG02258.hp1 HG03453.hp1 others(1): Show |
missense_variant | MODERATE | c.1099G>A | p.Val367Ile | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/9 | 1123/2861 | 1099/1290 | 367/429 | chr21 | 45267627 | |||
| chr21:45267680 | A | G | 1 | a0009 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.1046T>C | p.Met349Thr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/9 | 1070/2861 | 1046/1290 | 349/429 | chr21 | 45267680 | |||
| chr21:45269880 | C | T | 1 | a0006 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.971G>A | p.Arg324Gln | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/9 | 995/2861 | 971/1290 | 324/429 | chr21 | 45269880 | |||
| chr21:45269898 | C | G | 1 | a0006 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.953G>C | p.Ser318Thr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/9 | 977/2861 | 953/1290 | 318/429 | chr21 | 45269898 | |||
| chr21:45269914 | C | T | 1 | a0008 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.937G>A | p.Val313Met | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/9 | 961/2861 | 937/1290 | 313/429 | chr21 | 45269914 | |||
| chr21:45270004 | C | T | 1 | a0010 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.847G>A | p.Ala283Thr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/9 | 871/2861 | 847/1290 | 283/429 | chr21 | 45270004 | |||
| chr21:45277094 | C | T | 1 | a0011 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.754G>A | p.Glu252Lys | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/9 | 778/2861 | 754/1290 | 252/429 | chr21 | 45277094 | |||
| chr21:45283495 | C | T | 1 | a0002 | 12 | HG02257.hp2 HG02486.hp1 HG02647.hp1 others(9): Show |
missense_variant | MODERATE | c.415G>A | p.Val139Ile | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/9 | 439/2861 | 415/1290 | 139/429 | chr21 | 45283495 | |||
| chr21:45285700 | G | C | 1 | a0004 | 1 | HG00423.hp1 | missense_variant | MODERATE | c.360C>G | p.Ile120Met | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/9 | 384/2861 | 360/1290 | 120/429 | chr21 | 45285700 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:45265635 | C | T | 2 | a0001c0010 a0007c0009 |
2 | HG02818.hp2 NA19043.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1137G>A | p.Arg379Arg | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1161/2861 | 1137/1290 | 379/429 | chr21 | 45265635 | |||
| chr21:45277059 | G | A | 1 | a0001c0011 | 1 | NA18982.hp1 | synonymous_variant | LOW | c.789C>T | p.Asp263Asp | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/9 | 813/2861 | 789/1290 | 263/429 | chr21 | 45277059 | |||
| chr21:45277112 | G | A | 1 | a0006c0012 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.736C>T | p.Leu246Leu | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/9 | 760/2861 | 736/1290 | 246/429 | chr21 | 45277112 | |||
| chr21:45285706 | G | A | 3 | a0001c0002 a0005c0015 a0008c0014 |
70 | HG00408.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
synonymous_variant | LOW | c.354C>T | p.Pro118Pro | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/9 | 378/2861 | 354/1290 | 118/429 | chr21 | 45285706 | |||
| chr21:45285871 | A | G | 1 | a0003c0005 | 1 | HG01891.hp2 | synonymous_variant | LOW | c.189T>C | p.Tyr63Tyr | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/9 | 213/2861 | 189/1290 | 63/429 | chr21 | 45285871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:45264020 | G | GCAACTGA others(3): Show |
1 | a0001c0001t0028 | 1 | NA19001.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1452_*1461dupTCAT others(6): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1461 | chr21 | 45264020 | ||||||
| chr21:45264093 | G | C | 1 | a0001c0001t0029 | 1 | NA19009.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1389C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1389 | chr21 | 45264093 | ||||||
| chr21:45264214 | C | CCTCA | 29 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(26): Show |
213 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*1267_*1268insTGAG | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1267 | chr21 | 45264214 | ||||||
| chr21:45264278 | G | T | 2 | a0003c0004t0013 a0003c0005t0013 |
2 | HG01891.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1204C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1204 | chr21 | 45264278 | ||||||
| chr21:45264356 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
4 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1126G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1126 | chr21 | 45264356 | ||||||
| chr21:45264462 | CGTG | C | 5 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0011 others(2): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1017_*1019delCAC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 1017 | chr21 | 45264462 | ||||||
| chr21:45264490 | G | T | 1 | a0001c0001t0016 | 2 | NA18991.hp2 NA19006.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 992 | chr21 | 45264490 | ||||||
| chr21:45264602 | C | T | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(20): Show |
188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*880G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 880 | chr21 | 45264602 | ||||||
| chr21:45264608 | T | C | 2 | a0001c0001t0005 a0001c0001t0030 |
8 | HG01167.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*874A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 874 | chr21 | 45264608 | ||||||
| chr21:45264627 | TGCCAGCC others(18): Show |
T | 1 | a0001c0001t0027 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*830_*854delCGTCCC others(19): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 830 | chr21 | 45264627 | ||||||
| chr21:45264639 | C | T | 1 | a0001c0001t0001 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*843G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 843 | chr21 | 45264639 | ||||||
| chr21:45264664 | G | A | 2 | a0001c0001t0012 a0003c0004t0012 |
2 | HG02145.hp2 HG02258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*818C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 818 | chr21 | 45264664 | ||||||
| chr21:45264665 | AGGGCGGG others(18): Show |
A | 1 | a0001c0001t0022 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*792_*816delCACCCT others(19): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 792 | chr21 | 45264665 | ||||||
| chr21:45264715 | G | T | 1 | a0006c0012t0024 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*767C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 767 | chr21 | 45264715 | ||||||
| chr21:45264750 | C | T | 1 | a0001c0002t0020 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*732G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 732 | chr21 | 45264750 | ||||||
| chr21:45264918 | C | G | 1 | a0001c0001t0026 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 564 | chr21 | 45264918 | ||||||
| chr21:45264989 | A | G | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(16): Show |
183 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*493T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 493 | chr21 | 45264989 | ||||||
| chr21:45265099 | C | T | 3 | a0001c0001t0012 a0001c0001t0018 a0003c0004t0012 |
3 | HG02145.hp2 HG02258.hp1 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*383G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 383 | chr21 | 45265099 | ||||||
| chr21:45265117 | A | G | 1 | a0001c0002t0019 | 1 | NA19088.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 365 | chr21 | 45265117 | ||||||
| chr21:45265187 | C | T | 1 | a0001c0001t0009 | 4 | HG02055.hp1 HG02258.hp2 HG02965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*295G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 295 | chr21 | 45265187 | ||||||
| chr21:45265201 | C | T | 1 | a0001c0001t0025 | 1 | HG03490.hp2 | 3_prime_UTR_variant | MODIFIER | c.*281G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 281 | chr21 | 45265201 | ||||||
| chr21:45265218 | A | G | 1 | a0001c0001t0010 | 2 | HG02559.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*264T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 264 | chr21 | 45265218 | ||||||
| chr21:45265222 | A | G | 1 | a0001c0001t0018 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*260T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 260 | chr21 | 45265222 | ||||||
| chr21:45265240 | G | A | 1 | a0006c0012t0024 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 242 | chr21 | 45265240 | ||||||
| chr21:45265260 | A | G | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0008 others(20): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*222T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 222 | chr21 | 45265260 | ||||||
| chr21:45265294 | T | C | 1 | a0001c0001t0017 | 2 | HG01884.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*188A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 188 | chr21 | 45265294 | ||||||
| chr21:45265310 | C | T | 1 | a0001c0001t0011 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*172G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 172 | chr21 | 45265310 | ||||||
| chr21:45265317 | G | A | 1 | a0001c0001t0004 | 8 | HG00597.hp2 HG02074.hp1 NA18949.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*165C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 165 | chr21 | 45265317 | ||||||
| chr21:45265336 | G | C | 3 | a0001c0001t0008 a0001c0001t0011 a0003c0004t0031 |
8 | HG02896.hp2 HG02897.hp1 HG02976.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*146C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 146 | chr21 | 45265336 | ||||||
| chr21:45265381 | C | T | 2 | a0001c0001t0010 a0001c0001t0011 |
4 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*101G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 101 | chr21 | 45265381 | ||||||
| chr21:45265441 | C | T | 1 | a0001c0001t0006 | 6 | HG02486.hp2 HG02622.hp1 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*41G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 9/9 | 41 | chr21 | 45265441 | ||||||
| chr21:45287879 | G | A | 2 | a0001c0001t0008 a0001c0001t0032 |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/9 | 8 | chr21 | 45287879 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr21:45265636 | C | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.1137-1G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265636 | |||||||
| chr21:45265638 | G | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | splice_region_variant&intron_variant | LOW | c.1137-3C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265638 | |||||||
| chr21:45265645 | A | ATCACAGA others(26): Show |
2 | a0001c0001t0001g0145 a0003c0005t0013g0059 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1137-11_1137-10ins others(33): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265645 | |||||||
| chr21:45265645 | ATCACAGA others(26): Show |
A | 100 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(97): Show |
158 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.1137-43_1137-11del others(33): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265645 | |||||||
| chr21:45265647 | C | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-12G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265647 | |||||||
| chr21:45265648 | A | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-13T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265648 | |||||||
| chr21:45265649 | C | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-14G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265649 | |||||||
| chr21:45265650 | A | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-15T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265650 | |||||||
| chr21:45265663 | T | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-28A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265663 | |||||||
| chr21:45265664 | C | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-29G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265664 | |||||||
| chr21:45265667 | G | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-32C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265667 | |||||||
| chr21:45265670 | G | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-35C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265670 | |||||||
| chr21:45265672 | A | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-37T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265672 | |||||||
| chr21:45265677 | C | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(123): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1137-42G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265677 | |||||||
| chr21:45265681 | A | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-46T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265681 | |||||||
| chr21:45265686 | G | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-51C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265686 | |||||||
| chr21:45265689 | T | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-54A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265689 | |||||||
| chr21:45265694 | A | G | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-59T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265694 | |||||||
| chr21:45265695 | G | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-60C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265695 | |||||||
| chr21:45265698 | A | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-63T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265698 | |||||||
| chr21:45265705 | A | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-70T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265705 | |||||||
| chr21:45265707 | T | A | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-72A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265707 | |||||||
| chr21:45265713 | G | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-78C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265713 | |||||||
| chr21:45265720 | T | G | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-85A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265720 | |||||||
| chr21:45265721 | G | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-86C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265721 | |||||||
| chr21:45265750 | A | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-115T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265750 | |||||||
| chr21:45265754 | A | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-119T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265754 | |||||||
| chr21:45265755 | C | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-120G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265755 | |||||||
| chr21:45265758 | G | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-123C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265758 | |||||||
| chr21:45265764 | C | G | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-129G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265764 | |||||||
| chr21:45265769 | G | A | 1 | a0001c0002t0002g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1137-134C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265769 | |||||||
| chr21:45265777 | A | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-142T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265777 | |||||||
| chr21:45265778 | C | T | 2 | a0001c0001t0012g0187 a0003c0004t0012g0191 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1137-143G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265778 | |||||||
| chr21:45265782 | C | G | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-147G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265782 | |||||||
| chr21:45265784 | G | C | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-149C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265784 | |||||||
| chr21:45265790 | C | T | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1137-155G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265790 | |||||||
| chr21:45265808 | C | T | 1 | a0001c0002t0002g0229 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1137-173G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265808 | |||||||
| chr21:45265893 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1137-258G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265893 | |||||||
| chr21:45265914 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1137-279G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265914 | |||||||
| chr21:45265972 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0127 a0001c0001t0001g0166 |
5 | HG00140.hp2 HG00738.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.1137-337G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265972 | |||||||
| chr21:45265994 | T | C | 129 | a0001c0001t0001g0148 a0001c0001t0001g0178 a0001c0001t0002g0007 others(126): Show |
191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1137-359A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45265994 | |||||||
| chr21:45266165 | G | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0215 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1137-530C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266165 | |||||||
| chr21:45266190 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1137-555G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266190 | |||||||
| chr21:45266290 | C | T | 8 | a0001c0001t0008g0254 a0001c0001t0008g0255 a0001c0001t0008g0256 others(5): Show |
9 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1137-655G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266290 | |||||||
| chr21:45266451 | G | A | 1 | a0003c0004t0013g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1137-816C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266451 | |||||||
| chr21:45266579 | T | C | 216 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(213): Show |
360 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(357): Show |
intron_variant | MODIFIER | c.1137-944A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266579 | |||||||
| chr21:45266584 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0010 others(219): Show |
367 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(364): Show |
intron_variant | MODIFIER | c.1137-949T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266584 | |||||||
| chr21:45266606 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1137-971C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266606 | |||||||
| chr21:45266626 | C | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1136+964G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266626 | |||||||
| chr21:45266627 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1136+963C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266627 | |||||||
| chr21:45266684 | C | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0023 a0001c0001t0002g0041 others(3): Show |
12 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1136+906G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266684 | |||||||
| chr21:45266704 | C | T | 111 | a0001c0001t0001g0144 a0001c0001t0002g0007 a0001c0001t0002g0013 others(108): Show |
171 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1136+886G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266704 | |||||||
| chr21:45266739 | T | C | 1 | a0001c0001t0001g0009 | 4 | NA18959.hp2 NA18962.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.1136+851A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266739 | |||||||
| chr21:45266793 | C | G | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1136+797G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266793 | |||||||
| chr21:45266811 | C | T | 108 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
168 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.1136+779G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266811 | |||||||
| chr21:45266818 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1136+772C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266818 | |||||||
| chr21:45266867 | T | G | 2 | a0003c0004t0012g0191 a0003c0005t0013g0059 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1136+723A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266867 | |||||||
| chr21:45266911 | C | T | 2 | a0001c0001t0001g0031 a0001c0001t0030g0107 |
3 | HG02109.hp2 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1136+679G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266911 | |||||||
| chr21:45266994 | G | A | 1 | a0001c0001t0016g0034 | 2 | NA18991.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.1136+596C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266994 | |||||||
| chr21:45266995 | C | CAGGGCCC others(52): Show |
2 | a0003c0004t0012g0191 a0003c0005t0013g0059 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1136+594_1136+595i others(61): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45266995 | |||||||
| chr21:45267017 | TGGGACGC others(52): Show |
T | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1136+514_1136+572d others(61): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267017 | |||||||
| chr21:45267039 | C | T | 2 | a0003c0004t0012g0191 a0003c0005t0013g0059 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1136+551G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267039 | |||||||
| chr21:45267064 | G | A | 1 | a0001c0001t0006g0033 | 2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1136+526C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267064 | |||||||
| chr21:45267141 | G | A | 3 | a0003c0004t0012g0191 a0003c0004t0013g0188 a0003c0005t0013g0059 |
3 | HG01891.hp2 HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1136+449C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267141 | |||||||
| chr21:45267146 | T | C | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1136+444A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267146 | |||||||
| chr21:45267157 | C | A | 2 | a0003c0004t0012g0191 a0003c0005t0013g0059 |
2 | HG01891.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1136+433G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267157 | |||||||
| chr21:45267194 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1136+396C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267194 | |||||||
| chr21:45267195 | G | A | 2 | a0002c0003t0001g0030 a0002c0003t0001g0104 |
3 | NA20129.hp1 NA20300.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1136+395C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267195 | |||||||
| chr21:45267412 | TCAGCCCA others(4): Show |
T | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1136+167_1136+177d others(13): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267412 | |||||||
| chr21:45267498 | C | G | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1136+92G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267498 | |||||||
| chr21:45267550 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1136+40T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267550 | |||||||
| chr21:45267554 | G | A | 2 | a0001c0001t0003g0184 a0001c0001t0003g0196 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1136+36C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 8/8 | chr21 | 45267554 | |||||||
| chr21:45267734 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1013-21G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267734 | |||||||
| chr21:45267794 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0181 |
3 | NA18960.hp2 NA18973.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1013-81G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267794 | |||||||
| chr21:45267842 | GAC | G | 2 | a0001c0001t0002g0039 a0001c0001t0002g0209 |
3 | NA18949.hp2 NA18965.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1013-131_1013-130d others(4): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267842 | |||||||
| chr21:45267909 | G | A | 1 | a0001c0001t0002g0070 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1013-196C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267909 | |||||||
| chr21:45267917 | C | G | 1 | a0001c0001t0001g0161 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1013-204G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267917 | |||||||
| chr21:45267938 | C | G | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1013-225G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267938 | |||||||
| chr21:45267984 | T | TTCTCCC | 12 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0049 others(9): Show |
22 | HG00558.hp1 HG00597.hp2 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.1013-277_1013-272d others(8): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267984 | |||||||
| chr21:45267995 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1013-282G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267995 | |||||||
| chr21:45267997 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1013-284A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45267997 | |||||||
| chr21:45268006 | G | A | 2 | a0001c0002t0002g0226 a0001c0002t0002g0237 |
2 | HG00621.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.1013-293C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268006 | |||||||
| chr21:45268118 | C | A | 1 | a0001c0001t0002g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1013-405G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268118 | |||||||
| chr21:45268120 | A | T | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1013-407T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268120 | |||||||
| chr21:45268121 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1013-408C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268121 | |||||||
| chr21:45268122 | T | A | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1013-409A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268122 | |||||||
| chr21:45268129 | G | A | 1 | a0001c0001t0022g0056 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1013-416C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268129 | |||||||
| chr21:45268217 | G | A | 10 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(7): Show |
12 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1013-504C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268217 | |||||||
| chr21:45268273 | G | A | 3 | a0003c0004t0012g0191 a0003c0004t0013g0188 a0003c0005t0013g0059 |
3 | HG01891.hp2 HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1013-560C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268273 | |||||||
| chr21:45268324 | G | A | 4 | a0001c0001t0002g0081 a0001c0001t0002g0083 a0001c0001t0002g0087 others(1): Show |
4 | HG02559.hp2 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-611C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268324 | |||||||
| chr21:45268329 | G | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1013-616C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268329 | |||||||
| chr21:45268400 | G | A | 99 | a0001c0001t0001g0154 a0001c0001t0002g0007 a0001c0001t0002g0013 others(96): Show |
157 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1013-687C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268400 | |||||||
| chr21:45268440 | G | A | 3 | a0003c0004t0012g0191 a0003c0004t0013g0188 a0003c0005t0013g0059 |
3 | HG01891.hp2 HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1013-727C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268440 | |||||||
| chr21:45268507 | C | T | 1 | a0001c0002t0020g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1013-794G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268507 | |||||||
| chr21:45268511 | C | T | 1 | a0001c0001t0002g0071 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1013-798G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268511 | |||||||
| chr21:45268551 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1013-838G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268551 | |||||||
| chr21:45268555 | C | T | 4 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0244 others(1): Show |
5 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1013-842G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268555 | |||||||
| chr21:45268561 | C | T | 2 | a0001c0001t0002g0208 a0001c0001t0002g0215 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1013-848G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268561 | |||||||
| chr21:45268578 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1013-865C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268578 | |||||||
| chr21:45268583 | T | A | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1013-870A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268583 | |||||||
| chr21:45268657 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1013-944G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268657 | |||||||
| chr21:45268711 | C | T | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1013-998G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268711 | |||||||
| chr21:45268740 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1013-1027G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268740 | |||||||
| chr21:45268745 | G | A | 1 | a0001c0001t0002g0212 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1013-1032C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268745 | |||||||
| chr21:45268775 | G | A | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1013-1062C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268775 | |||||||
| chr21:45268792 | ACCCCGTC others(42): Show |
A | 1 | a0001c0001t0029g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1012+998_1012+1046 others(52): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268792 | |||||||
| chr21:45268792 | ACCCCGTC others(91): Show |
A | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG01884.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1012+949_1012+1046 others(101): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268792 | |||||||
| chr21:45268811 | TGGGGGGG others(41): Show |
T | 1 | a0001c0001t0002g0022 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1012+980_1012+1027 others(51): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268811 | |||||||
| chr21:45268812 | GGGGGGGT others(41): Show |
G | 4 | a0001c0001t0002g0014 a0001c0001t0002g0065 a0001c0001t0002g0073 others(1): Show |
4 | HG02056.hp1 HG02056.hp2 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+979_1012+1026 others(51): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268812 | |||||||
| chr21:45268826 | T | C | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(245): Show |
425 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(422): Show |
intron_variant | MODIFIER | c.1012+1013A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268826 | |||||||
| chr21:45268828 | C | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1012+1011G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268828 | |||||||
| chr21:45268829 | G | A | 12 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(9): Show |
14 | HG01261.hp1 HG01891.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1012+1010C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268829 | |||||||
| chr21:45268831 | CCGGCCAG others(42): Show |
C | 99 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(96): Show |
157 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1012+959_1012+1007 others(52): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268831 | |||||||
| chr21:45268840 | C | T | 6 | a0001c0001t0002g0076 a0001c0001t0002g0078 a0003c0004t0012g0191 others(3): Show |
6 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1012+999G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268840 | |||||||
| chr21:45268849 | CGGGAGGG others(169): Show |
C | 1 | a0001c0001t0002g0076 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1012+814_1012+989d others(2): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268849 | |||||||
| chr21:45268871 | GCACCCCG others(43): Show |
G | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1012+918_1012+967d others(52): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268871 | |||||||
| chr21:45268873 | A | C | 5 | a0001c0001t0002g0014 a0001c0001t0002g0022 a0001c0001t0002g0065 others(2): Show |
5 | HG02056.hp1 HG02056.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012+966T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268873 | |||||||
| chr21:45268879 | G | C | 5 | a0001c0001t0002g0014 a0001c0001t0002g0022 a0001c0001t0002g0065 others(2): Show |
5 | HG02056.hp1 HG02056.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.1012+960C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268879 | |||||||
| chr21:45268879 | G | GCCGGCCA others(169): Show |
1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1012+959_1012+960i others(178): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268879 | |||||||
| chr21:45268879 | GGCGGCCA others(120): Show |
G | 1 | a0001c0001t0001g0169 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1012+833_1012+959d others(2): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268879 | |||||||
| chr21:45268880 | G | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(149): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.1012+959C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268880 | |||||||
| chr21:45268889 | C | T | 93 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(90): Show |
151 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.1012+950G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268889 | |||||||
| chr21:45268895 | G | A | 3 | a0001c0001t0010g0053 a0001c0001t0010g0054 a0001c0001t0011g0027 |
4 | HG02559.hp1 HG02630.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1012+944C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268895 | |||||||
| chr21:45268899 | G | A | 1 | a0001c0002t0002g0238 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1012+940C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268899 | |||||||
| chr21:45268922 | C | A | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1012+917G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268922 | |||||||
| chr21:45268926 | CGCCTGGC others(71): Show |
C | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1012+835_1012+912d others(80): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268926 | |||||||
| chr21:45268936 | G | T | 1 | a0001c0001t0001g0001 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1012+903C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268936 | |||||||
| chr21:45268938 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1012+901G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268938 | |||||||
| chr21:45268944 | G | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0017 a0001c0001t0001g0149 others(1): Show |
9 | HG01928.hp2 HG01934.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+895C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268944 | |||||||
| chr21:45268950 | G | A | 3 | a0001c0001t0014g0192 a0001c0001t0014g0193 a0001c0001t0018g0190 |
3 | HG02622.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1012+889C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268950 | |||||||
| chr21:45268962 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0174 |
2 | NA18939.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1012+877C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268962 | |||||||
| chr21:45268971 | C | T | 97 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(94): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1012+868G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268971 | |||||||
| chr21:45268991 | C | T | 110 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(107): Show |
170 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(167): Show |
intron_variant | MODIFIER | c.1012+848G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268991 | |||||||
| chr21:45268992 | A | G | 123 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(120): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1012+847T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45268992 | |||||||
| chr21:45269006 | C | G | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1012+833G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269006 | |||||||
| chr21:45269020 | C | A | 1 | a0001c0002t0002g0241 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1012+819G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269020 | |||||||
| chr21:45269025 | T | C | 2 | a0001c0001t0001g0169 a0001c0001t0012g0187 |
2 | HG02145.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1012+814A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269025 | |||||||
| chr21:45269036 | TG | T | 10 | a0001c0001t0003g0038 a0001c0001t0003g0184 a0001c0001t0003g0185 others(7): Show |
12 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012+802delC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269036 | |||||||
| chr21:45269057 | T | C | 123 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(120): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1012+782A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269057 | |||||||
| chr21:45269070 | C | T | 10 | a0001c0001t0003g0038 a0001c0001t0003g0184 a0001c0001t0003g0185 others(7): Show |
12 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.1012+769G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269070 | |||||||
| chr21:45269074 | C | T | 1 | a0002c0003t0001g0101 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1012+765G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269074 | |||||||
| chr21:45269103 | G | A | 1 | a0003c0004t0013g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1012+736C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269103 | |||||||
| chr21:45269118 | T | C | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1012+721A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269118 | |||||||
| chr21:45269180 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0001g0149 |
2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1012+659G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269180 | |||||||
| chr21:45269182 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1012+657G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269182 | |||||||
| chr21:45269193 | G | A | 1 | a0001c0001t0002g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1012+646C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269193 | |||||||
| chr21:45269198 | G | A | 8 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(5): Show |
9 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1012+641C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269198 | |||||||
| chr21:45269215 | C | T | 1 | a0001c0001t0007g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1012+624G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269215 | |||||||
| chr21:45269216 | G | A | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1012+623C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269216 | |||||||
| chr21:45269225 | C | T | 97 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(94): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.1012+614G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269225 | |||||||
| chr21:45269229 | C | T | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1012+610G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269229 | |||||||
| chr21:45269272 | C | G | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1012+567G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269272 | |||||||
| chr21:45269327 | C | T | 1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1012+512G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269327 | |||||||
| chr21:45269348 | C | G | 2 | a0001c0001t0003g0244 a0001c0001t0011g0027 |
3 | HG00099.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1012+491G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269348 | |||||||
| chr21:45269436 | T | C | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1012+403A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269436 | |||||||
| chr21:45269577 | C | T | 13 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(10): Show |
15 | HG01261.hp1 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1012+262G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269577 | |||||||
| chr21:45269614 | A | C | 1 | a0001c0002t0002g0045 | 2 | NA18971.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1012+225T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269614 | |||||||
| chr21:45269631 | A | C | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1012+208T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269631 | |||||||
| chr21:45269632 | T | C | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.1012+207A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269632 | |||||||
| chr21:45269672 | C | T | 1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1012+167G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269672 | |||||||
| chr21:45269817 | C | T | 1 | a0001c0001t0018g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1012+22G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 7/8 | chr21 | 45269817 | |||||||
| chr21:45270084 | G | A | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.832-65C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270084 | |||||||
| chr21:45270099 | C | T | 1 | a0001c0001t0018g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.832-80G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270099 | |||||||
| chr21:45270392 | C | G | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-373G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270392 | |||||||
| chr21:45270710 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.832-691C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270710 | |||||||
| chr21:45270718 | G | T | 125 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(122): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.832-699C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270718 | |||||||
| chr21:45270770 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.832-751G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270770 | |||||||
| chr21:45270921 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.832-902G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270921 | |||||||
| chr21:45270990 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.832-971T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45270990 | |||||||
| chr21:45271053 | C | G | 125 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(122): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.832-1034G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271053 | |||||||
| chr21:45271074 | C | T | 1 | a0001c0002t0002g0224 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.832-1055G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271074 | |||||||
| chr21:45271077 | A | G | 1 | a0001c0001t0006g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.832-1058T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271077 | |||||||
| chr21:45271147 | A | C | 2 | a0001c0001t0002g0064 a0001c0001t0002g0075 |
2 | NA18972.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.832-1128T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271147 | |||||||
| chr21:45271328 | T | G | 1 | a0001c0001t0002g0057 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.832-1309A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271328 | |||||||
| chr21:45271470 | C | T | 2 | a0001c0002t0002g0223 a0001c0002t0002g0235 |
2 | NA18950.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.832-1451G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271470 | |||||||
| chr21:45271985 | T | C | 1 | a0001c0001t0006g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.832-1966A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45271985 | |||||||
| chr21:45272052 | C | T | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-2033G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272052 | |||||||
| chr21:45272103 | A | G | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.832-2084T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272103 | |||||||
| chr21:45272372 | C | T | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.832-2353G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272372 | |||||||
| chr21:45272468 | A | G | 1 | a0001c0001t0016g0034 | 2 | NA18991.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.832-2449T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272468 | |||||||
| chr21:45272588 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.832-2569G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272588 | |||||||
| chr21:45272802 | T | C | 1 | a0001c0001t0001g0134 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.832-2783A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45272802 | |||||||
| chr21:45273028 | C | A | 107 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(104): Show |
167 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.832-3009G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273028 | |||||||
| chr21:45273057 | T | C | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.832-3038A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273057 | |||||||
| chr21:45273096 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.832-3077T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273096 | |||||||
| chr21:45273140 | A | G | 7 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0003g0196 others(4): Show |
8 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.832-3121T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273140 | |||||||
| chr21:45273197 | C | T | 1 | a0001c0001t0006g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.832-3178G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273197 | |||||||
| chr21:45273213 | C | T | 96 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(93): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.832-3194G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273213 | |||||||
| chr21:45273310 | C | G | 1 | a0003c0005t0013g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.832-3291G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273310 | |||||||
| chr21:45273324 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.832-3305T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273324 | |||||||
| chr21:45273342 | T | C | 3 | a0001c0001t0014g0192 a0001c0001t0014g0193 a0001c0001t0018g0190 |
3 | HG02622.hp2 HG02809.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.832-3323A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273342 | |||||||
| chr21:45273376 | T | C | 1 | a0001c0001t0029g0155 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.832-3357A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273376 | |||||||
| chr21:45273380 | G | A | 96 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(93): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.832-3361C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273380 | |||||||
| chr21:45273547 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0003g0185 a0001c0001t0003g0186 |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3470A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273547 | |||||||
| chr21:45273614 | A | G | 1 | a0002c0003t0001g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.831+3403T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273614 | |||||||
| chr21:45273702 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.831+3315T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273702 | |||||||
| chr21:45273866 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0175 a0001c0011t0001g0159 |
4 | HG04184.hp2 NA18979.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+3151C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273866 | |||||||
| chr21:45273940 | A | G | 1 | a0001c0001t0002g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.831+3077T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273940 | |||||||
| chr21:45273952 | A | G | 1 | a0002c0003t0001g0102 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.831+3065T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45273952 | |||||||
| chr21:45274135 | A | G | 1 | a0007c0009t0001g0135 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.831+2882T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274135 | |||||||
| chr21:45274216 | C | T | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+2801G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274216 | |||||||
| chr21:45274240 | A | G | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.831+2777T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274240 | |||||||
| chr21:45274599 | C | T | 117 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(114): Show |
179 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.831+2418G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274599 | |||||||
| chr21:45274604 | T | C | 1 | a0001c0001t0011g0027 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.831+2413A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274604 | |||||||
| chr21:45274687 | G | T | 1 | a0001c0001t0002g0213 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.831+2330C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274687 | |||||||
| chr21:45274786 | C | A | 1 | a0001c0002t0002g0232 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.831+2231G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274786 | |||||||
| chr21:45274867 | C | T | 123 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(120): Show |
185 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.831+2150G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274867 | |||||||
| chr21:45274920 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.831+2097G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274920 | |||||||
| chr21:45274985 | G | A | 5 | a0001c0001t0002g0013 a0001c0001t0002g0023 a0001c0001t0002g0041 others(2): Show |
11 | HG01081.hp1 HG01109.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+2032C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45274985 | |||||||
| chr21:45275014 | T | C | 3 | a0001c0001t0003g0038 a0001c0001t0003g0185 a0001c0001t0003g0186 |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.831+2003A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275014 | |||||||
| chr21:45275020 | C | T | 1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.831+1997G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275020 | |||||||
| chr21:45275051 | A | G | 1 | a0001c0001t0002g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.831+1966T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275051 | |||||||
| chr21:45275078 | A | G | 1 | a0001c0001t0008g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.831+1939T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275078 | |||||||
| chr21:45275091 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.831+1926A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275091 | |||||||
| chr21:45275124 | T | G | 98 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(95): Show |
156 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(153): Show |
intron_variant | MODIFIER | c.831+1893A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275124 | |||||||
| chr21:45275159 | C | T | 1 | a0003c0005t0013g0059 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.831+1858G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275159 | |||||||
| chr21:45275229 | T | C | 9 | a0001c0001t0002g0015 a0001c0001t0002g0063 a0001c0001t0002g0064 others(6): Show |
11 | HG00408.hp1 NA18944.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+1788A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275229 | |||||||
| chr21:45275230 | T | C | 2 | a0001c0001t0002g0208 a0001c0001t0002g0215 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.831+1787A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275230 | |||||||
| chr21:45275280 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.831+1737C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275280 | |||||||
| chr21:45275285 | G | C | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.831+1732C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275285 | |||||||
| chr21:45275353 | CAG | C | 5 | a0001c0001t0012g0187 a0001c0001t0014g0192 a0001c0001t0014g0193 others(2): Show |
5 | HG02145.hp2 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.831+1662_831+1663d others(4): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275353 | |||||||
| chr21:45275375 | G | A | 108 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.831+1642C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275375 | |||||||
| chr21:45275608 | A | T | 1 | a0001c0002t0002g0222 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.831+1409T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275608 | |||||||
| chr21:45275647 | G | A | 1 | a0001c0001t0002g0206 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.831+1370C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275647 | |||||||
| chr21:45275691 | T | C | 96 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(93): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.831+1326A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275691 | |||||||
| chr21:45275787 | G | A | 2 | a0001c0001t0002g0208 a0001c0001t0002g0215 |
2 | NA18995.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.831+1230C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275787 | |||||||
| chr21:45275859 | C | A | 1 | a0001c0001t0005g0249 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.831+1158G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275859 | |||||||
| chr21:45275884 | T | TA | 109 | a0001c0001t0001g0171 a0001c0001t0002g0007 a0001c0001t0002g0013 others(106): Show |
169 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.831+1132dupT | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275884 | |||||||
| chr21:45275960 | G | A | 1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.831+1057C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45275960 | |||||||
| chr21:45276052 | G | C | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+965C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276052 | |||||||
| chr21:45276194 | G | A | 108 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(105): Show |
168 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.831+823C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276194 | |||||||
| chr21:45276245 | TA | T | 97 | a0001c0001t0001g0122 a0001c0001t0002g0007 a0001c0001t0002g0013 others(94): Show |
155 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.831+771delT | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276245 | |||||||
| chr21:45276245 | TAA | T | 9 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(6): Show |
11 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.831+770_831+771del others(2): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276245 | |||||||
| chr21:45276260 | G | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG01884.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.831+757C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276260 | |||||||
| chr21:45276638 | T | G | 1 | a0001c0001t0002g0079 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.831+379A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276638 | |||||||
| chr21:45276776 | G | A | 1 | a0001c0001t0032g0253 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.831+241C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 6/8 | chr21 | 45276776 | |||||||
| chr21:45277185 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.706-43G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277185 | |||||||
| chr21:45277290 | G | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.706-148C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277290 | |||||||
| chr21:45277351 | C | G | 1 | a0001c0001t0011g0027 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.706-209G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277351 | |||||||
| chr21:45277362 | G | A | 1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.706-220C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277362 | |||||||
| chr21:45277417 | G | A | 2 | a0001c0001t0005g0025 a0001c0001t0005g0249 |
4 | HG02145.hp1 HG02572.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.706-275C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277417 | |||||||
| chr21:45277465 | T | C | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.706-323A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277465 | |||||||
| chr21:45277471 | A | G | 1 | a0001c0002t0002g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.706-329T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277471 | |||||||
| chr21:45277656 | G | A | 1 | a0001c0001t0014g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.705+447C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277656 | |||||||
| chr21:45277727 | C | T | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.705+376G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277727 | |||||||
| chr21:45277733 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.705+370G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277733 | |||||||
| chr21:45277905 | G | T | 96 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(93): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.705+198C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277905 | |||||||
| chr21:45277945 | G | A | 1 | a0001c0001t0007g0248 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.705+158C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45277945 | |||||||
| chr21:45278082 | C | T | 1 | a0006c0012t0024g0210 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.705+21G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 5/8 | chr21 | 45278082 | |||||||
| chr21:45278184 | C | A | 1 | a0001c0001t0009g0137 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.639-15G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278184 | |||||||
| chr21:45278261 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.639-92G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278261 | |||||||
| chr21:45278303 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.639-134G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278303 | |||||||
| chr21:45278341 | T | C | 132 | a0001c0001t0001g0115 a0001c0001t0001g0136 a0001c0001t0001g0140 others(129): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.639-172A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278341 | |||||||
| chr21:45278383 | T | G | 100 | a0001c0001t0001g0140 a0001c0001t0001g0174 a0001c0001t0002g0007 others(97): Show |
158 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.639-214A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278383 | |||||||
| chr21:45278384 | A | G | 63 | a0001c0001t0001g0140 a0001c0001t0001g0174 a0001c0001t0002g0021 others(60): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.639-215T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278384 | |||||||
| chr21:45278530 | G | C | 96 | a0001c0001t0002g0007 a0001c0001t0002g0013 a0001c0001t0002g0014 others(93): Show |
154 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(151): Show |
intron_variant | MODIFIER | c.639-361C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278530 | |||||||
| chr21:45278619 | G | A | 1 | a0001c0002t0002g0239 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.639-450C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278619 | |||||||
| chr21:45278670 | G | A | 1 | a0001c0001t0011g0027 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639-501C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278670 | |||||||
| chr21:45278690 | C | T | 4 | a0001c0001t0002g0206 a0001c0001t0014g0192 a0001c0001t0014g0193 others(1): Show |
4 | HG02622.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.639-521G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278690 | |||||||
| chr21:45278729 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0119 a0001c0001t0001g0156 others(2): Show |
10 | HG02071.hp2 NA18941.hp2 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.639-560C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278729 | |||||||
| chr21:45278765 | C | T | 1 | a0001c0002t0002g0234 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.639-596G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278765 | |||||||
| chr21:45278919 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.639-750G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278919 | |||||||
| chr21:45278959 | G | A | 1 | a0001c0001t0007g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.639-790C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45278959 | |||||||
| chr21:45279021 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.639-852G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279021 | |||||||
| chr21:45279073 | G | A | 1 | a0001c0001t0008g0254 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.639-904C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279073 | |||||||
| chr21:45279119 | C | G | 4 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0244 others(1): Show |
5 | HG00099.hp2 HG00323.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-950G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279119 | |||||||
| chr21:45279158 | A | G | 97 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(94): Show |
171 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.639-989T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279158 | |||||||
| chr21:45279162 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.639-993A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279162 | |||||||
| chr21:45279180 | A | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(63): Show |
134 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.639-1011T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279180 | |||||||
| chr21:45279183 | A | C | 36 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0058 others(33): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.639-1014T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279183 | |||||||
| chr21:45279184 | G | A | 36 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0058 others(33): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.639-1015C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279184 | |||||||
| chr21:45279187 | C | T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0058 others(33): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.639-1018G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279187 | |||||||
| chr21:45279190 | GAC | G | 36 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0058 others(33): Show |
44 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.639-1023_639-1022d others(4): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279190 | |||||||
| chr21:45279198 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0011 others(142): Show |
265 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.639-1029A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279198 | |||||||
| chr21:45279205 | G | C | 175 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(172): Show |
301 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(298): Show |
intron_variant | MODIFIER | c.639-1036C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279205 | |||||||
| chr21:45279205 | G | T | 21 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 others(18): Show |
28 | HG01167.hp1 HG01261.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.639-1036C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279205 | |||||||
| chr21:45279207 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.639-1038G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279207 | |||||||
| chr21:45279243 | T | A | 7 | a0001c0001t0006g0033 a0001c0001t0006g0116 a0001c0001t0006g0128 others(4): Show |
8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-1074A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279243 | |||||||
| chr21:45279255 | G | A | 1 | a0001c0001t0003g0196 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.639-1086C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279255 | |||||||
| chr21:45279271 | A | G | 1 | a0001c0001t0002g0084 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.639-1102T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279271 | |||||||
| chr21:45279276 | C | A | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-1107G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279276 | |||||||
| chr21:45279372 | G | A | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.639-1203C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279372 | |||||||
| chr21:45279540 | C | T | 7 | a0001c0001t0006g0033 a0001c0001t0006g0116 a0001c0001t0006g0128 others(4): Show |
8 | HG02055.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-1371G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279540 | |||||||
| chr21:45279623 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.639-1454G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279623 | |||||||
| chr21:45279638 | C | T | 3 | a0001c0001t0002g0068 a0001c0001t0002g0069 a0001c0001t0002g0076 |
3 | HG01943.hp2 HG01978.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.639-1469G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279638 | |||||||
| chr21:45279707 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.639-1538G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279707 | |||||||
| chr21:45279862 | A | G | 69 | a0001c0001t0002g0013 a0001c0001t0002g0021 a0001c0001t0002g0022 others(66): Show |
117 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(114): Show |
intron_variant | MODIFIER | c.639-1693T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279862 | |||||||
| chr21:45279888 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.639-1719C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279888 | |||||||
| chr21:45279934 | C | T | 2 | a0001c0001t0001g0138 a0003c0004t0031g0055 |
2 | HG03453.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.639-1765G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45279934 | |||||||
| chr21:45280072 | G | A | 1 | a0001c0001t0006g0116 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.639-1903C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280072 | |||||||
| chr21:45280092 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.639-1923C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280092 | |||||||
| chr21:45280101 | T | C | 1 | a0001c0002t0002g0240 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.639-1932A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280101 | |||||||
| chr21:45280143 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
132 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.639-1974C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280143 | |||||||
| chr21:45280210 | C | T | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.639-2041G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280210 | |||||||
| chr21:45280240 | C | T | 1 | a0001c0001t0002g0208 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.639-2071G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280240 | |||||||
| chr21:45280273 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.638+2076T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280273 | |||||||
| chr21:45280274 | T | C | 8 | a0001c0001t0001g0120 a0001c0001t0002g0028 a0001c0001t0002g0084 others(5): Show |
9 | HG01884.hp2 HG02886.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.638+2075A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280274 | |||||||
| chr21:45280424 | G | A | 4 | a0001c0001t0001g0035 a0001c0001t0001g0158 a0001c0001t0001g0175 others(1): Show |
5 | HG04184.hp2 NA18979.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.638+1925C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280424 | |||||||
| chr21:45280438 | C | T | 4 | a0001c0001t0012g0187 a0001c0001t0014g0192 a0001c0001t0014g0193 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+1911G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280438 | |||||||
| chr21:45280471 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0001g0181 |
3 | NA18960.hp2 NA18973.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.638+1878G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280471 | |||||||
| chr21:45280480 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.638+1869C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280480 | |||||||
| chr21:45280528 | C | G | 1 | a0001c0001t0007g0245 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638+1821G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280528 | |||||||
| chr21:45280594 | G | A | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+1755C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280594 | |||||||
| chr21:45280658 | ACCTCACC others(64): Show |
A | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.638+1620_638+1690d others(73): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280658 | |||||||
| chr21:45280692 | AGTTTCGT others(64): Show |
A | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+1586_638+1656d others(73): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280692 | |||||||
| chr21:45280710 | C | T | 1 | a0003c0004t0012g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.638+1639G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280710 | |||||||
| chr21:45280718 | G | A | 1 | a0002c0003t0001g0016 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.638+1631C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280718 | |||||||
| chr21:45280763 | G | GGTTTCGT others(64): Show |
1 | a0001c0010t0003g0189 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.638+1515_638+1585d others(73): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280763 | |||||||
| chr21:45280883 | C | T | 3 | a0001c0001t0003g0038 a0001c0001t0003g0185 a0001c0001t0003g0186 |
4 | HG02280.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.638+1466G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280883 | |||||||
| chr21:45280995 | T | C | 8 | a0001c0001t0001g0120 a0001c0001t0002g0028 a0001c0001t0002g0084 others(5): Show |
9 | HG01884.hp2 HG02886.hp1 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.638+1354A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45280995 | |||||||
| chr21:45281106 | G | C | 1 | a0001c0001t0002g0026 | 2 | HG00733.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.638+1243C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281106 | |||||||
| chr21:45281153 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.638+1196C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281153 | |||||||
| chr21:45281207 | G | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.638+1142C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281207 | |||||||
| chr21:45281324 | A | T | 1 | a0001c0001t0002g0026 | 2 | HG00733.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.638+1025T>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281324 | |||||||
| chr21:45281387 | C | CAATTCAG others(14): Show |
1 | a0001c0002t0002g0228 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.638+941_638+961dup others(21): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281387 | |||||||
| chr21:45281458 | C | G | 2 | a0001c0001t0002g0063 a0001c0001t0021g0067 |
2 | NA18952.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.638+891G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281458 | |||||||
| chr21:45281460 | C | T | 1 | a0001c0001t0012g0187 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.638+889G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281460 | |||||||
| chr21:45281522 | C | T | 2 | a0001c0001t0022g0056 a0003c0005t0013g0059 |
2 | HG01891.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.638+827G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281522 | |||||||
| chr21:45281523 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0020 others(7): Show |
18 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.638+826C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281523 | |||||||
| chr21:45281529 | C | A | 1 | a0003c0004t0012g0191 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.638+820G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281529 | |||||||
| chr21:45281630 | G | A | 4 | a0001c0001t0012g0187 a0001c0001t0014g0192 a0001c0001t0014g0193 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.638+719C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281630 | |||||||
| chr21:45281666 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.638+683C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281666 | |||||||
| chr21:45281892 | G | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.638+457C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281892 | |||||||
| chr21:45281948 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.638+401G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281948 | |||||||
| chr21:45281983 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.638+366C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281983 | |||||||
| chr21:45281987 | G | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0074 |
2 | HG02056.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.638+362C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281987 | |||||||
| chr21:45281994 | G | C | 75 | a0001c0001t0001g0183 a0001c0001t0002g0013 a0001c0001t0002g0021 others(72): Show |
123 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(120): Show |
intron_variant | MODIFIER | c.638+355C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45281994 | |||||||
| chr21:45282107 | C | G | 1 | a0001c0001t0002g0205 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.638+242G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45282107 | |||||||
| chr21:45282144 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.638+205C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45282144 | |||||||
| chr21:45282259 | C | T | 3 | a0001c0001t0002g0084 a0001c0001t0002g0085 a0001c0001t0002g0086 |
3 | HG01884.hp2 HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.638+90G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45282259 | |||||||
| chr21:45282296 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.638+53G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45282296 | |||||||
| chr21:45282305 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.638+44G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 4/8 | chr21 | 45282305 | |||||||
| chr21:45282591 | C | T | 69 | a0001c0001t0001g0183 a0001c0001t0002g0013 a0001c0001t0002g0021 others(66): Show |
117 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.528-132G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282591 | |||||||
| chr21:45282638 | T | C | 129 | a0001c0001t0001g0110 a0001c0001t0001g0183 a0001c0001t0002g0007 others(126): Show |
191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.528-179A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282638 | |||||||
| chr21:45282639 | G | A | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.528-180C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282639 | |||||||
| chr21:45282871 | A | G | 1 | a0003c0004t0013g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.528-412T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282871 | |||||||
| chr21:45282907 | A | G | 55 | a0001c0001t0001g0018 a0001c0001t0001g0127 a0001c0001t0001g0166 others(52): Show |
71 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.528-448T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282907 | |||||||
| chr21:45282978 | G | A | 12 | a0001c0001t0003g0038 a0001c0001t0003g0185 a0001c0001t0003g0199 others(9): Show |
13 | HG00099.hp2 HG00323.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.527+405C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45282978 | |||||||
| chr21:45283064 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0003g0184 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.527+319G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283064 | |||||||
| chr21:45283084 | G | A | 32 | a0001c0001t0002g0007 a0001c0001t0002g0015 a0001c0001t0002g0026 others(29): Show |
42 | HG00408.hp1 HG00733.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.527+299C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283084 | |||||||
| chr21:45283102 | G | A | 14 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(11): Show |
17 | HG01261.hp1 HG02559.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.527+281C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283102 | |||||||
| chr21:45283183 | G | C | 5 | a0001c0001t0008g0255 a0001c0001t0012g0187 a0001c0001t0014g0192 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.527+200C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283183 | |||||||
| chr21:45283201 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0028g0165 |
3 | NA18961.hp2 NA19001.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.527+182C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283201 | |||||||
| chr21:45283205 | G | A | 4 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0256 others(1): Show |
5 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+178C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283205 | |||||||
| chr21:45283251 | A | AG | 24 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0092 others(21): Show |
25 | HG00597.hp1 HG00642.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.527+131dupC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283251 | |||||||
| chr21:45283259 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0173 |
2 | HG00741.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.527+124G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283259 | |||||||
| chr21:45283259 | C | T | 1 | a0001c0002t0002g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.527+124G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283259 | |||||||
| chr21:45283272 | C | T | 67 | a0001c0001t0001g0110 a0001c0001t0001g0123 a0001c0001t0001g0125 others(64): Show |
115 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(112): Show |
intron_variant | MODIFIER | c.527+111G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283272 | |||||||
| chr21:45283273 | G | A | 2 | a0001c0001t0003g0199 a0001c0001t0003g0244 |
2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.527+110C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283273 | |||||||
| chr21:45283292 | C | CG | 9 | a0001c0001t0001g0122 a0001c0001t0001g0176 a0001c0001t0002g0066 others(6): Show |
10 | HG01099.hp1 HG01346.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.527+90dupC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283292 | |||||||
| chr21:45283308 | C | CG | 128 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(125): Show |
244 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.527+74dupC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283308 | |||||||
| chr21:45283308 | C | CGG | 68 | a0001c0001t0001g0017 a0001c0001t0001g0092 a0001c0001t0001g0110 others(65): Show |
106 | HG00323.hp2 HG00408.hp2 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.527+73_527+74dupCC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283308 | |||||||
| chr21:45283308 | C | CGGG | 31 | a0001c0001t0001g0105 a0001c0001t0001g0183 a0001c0001t0002g0021 others(28): Show |
43 | HG00280.hp2 HG00597.hp1 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.527+72_527+74dupCC others(1): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283308 | |||||||
| chr21:45283321 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.527+62T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283321 | |||||||
| chr21:45283325 | A | ATGCGGCA others(20): Show |
3 | a0001c0001t0001g0183 a0001c0001t0003g0184 a0001c0001t0003g0196 |
3 | HG03017.hp2 HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.527+31_527+57dupGG others(25): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283325 | |||||||
| chr21:45283341 | T | TG | 13 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0001g0174 others(10): Show |
14 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(11): Show |
intron_variant | MODIFIER | c.527+41dupC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283341 | |||||||
| chr21:45283341 | TG | T | 51 | a0001c0001t0001g0031 a0001c0001t0001g0105 a0001c0001t0001g0106 others(48): Show |
64 | HG00280.hp2 HG00408.hp1 HG00733.hp1 others(61): Show |
intron_variant | MODIFIER | c.527+41delC | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 3/8 | chr21 | 45283341 | |||||||
| chr21:45283740 | T | A | 1 | a0001c0001t0002g0216 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.383-213A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45283740 | |||||||
| chr21:45283750 | A | C | 57 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(54): Show |
71 | HG00408.hp1 HG00733.hp1 HG01192.hp1 others(68): Show |
intron_variant | MODIFIER | c.383-223T>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45283750 | |||||||
| chr21:45283795 | T | C | 7 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(4): Show |
8 | HG01261.hp1 HG02559.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.383-268A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45283795 | |||||||
| chr21:45283824 | G | A | 69 | a0001c0001t0001g0183 a0001c0001t0002g0013 a0001c0001t0002g0021 others(66): Show |
117 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.383-297C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45283824 | |||||||
| chr21:45283934 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0008g0051 a0001c0001t0022g0056 |
4 | HG00099.hp1 HG02055.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.383-407G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45283934 | |||||||
| chr21:45284108 | TAAAGCGG others(38): Show |
T | 1 | a0001c0001t0001g0098 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.383-626_383-582del others(45): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284108 | |||||||
| chr21:45284127 | G | A | 2 | a0001c0001t0001g0119 a0001c0002t0002g0004 |
2 | NA19066.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.383-600C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284127 | |||||||
| chr21:45284158 | C | T | 9 | a0001c0001t0001g0097 a0001c0001t0003g0038 a0001c0001t0003g0185 others(6): Show |
10 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.383-631G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284158 | |||||||
| chr21:45284159 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.383-632C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284159 | |||||||
| chr21:45284216 | C | T | 2 | a0001c0001t0002g0062 a0001c0002t0002g0217 |
2 | HG01099.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.383-689G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284216 | |||||||
| chr21:45284249 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.383-722C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284249 | |||||||
| chr21:45284264 | G | A | 38 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(35): Show |
50 | HG00408.hp1 HG00733.hp1 HG01192.hp1 others(47): Show |
intron_variant | MODIFIER | c.383-737C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284264 | |||||||
| chr21:45284308 | G | A | 3 | a0001c0001t0014g0192 a0001c0001t0014g0193 a0003c0004t0012g0191 |
3 | HG02258.hp1 HG02622.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.383-781C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284308 | |||||||
| chr21:45284348 | C | G | 5 | a0001c0001t0014g0192 a0001c0001t0014g0193 a0001c0001t0018g0190 others(2): Show |
5 | HG02258.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.383-821G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284348 | |||||||
| chr21:45284399 | C | T | 8 | a0001c0001t0003g0038 a0001c0001t0003g0185 a0001c0001t0003g0186 others(5): Show |
9 | HG01891.hp2 HG02055.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.383-872G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284399 | |||||||
| chr21:45284450 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.383-923G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284450 | |||||||
| chr21:45284533 | G | T | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.383-1006C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284533 | |||||||
| chr21:45284743 | C | G | 1 | a0001c0001t0002g0202 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.382+935G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284743 | |||||||
| chr21:45284805 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.382+873T>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284805 | |||||||
| chr21:45284807 | G | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.382+871C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284807 | |||||||
| chr21:45284881 | T | C | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.382+797A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45284881 | |||||||
| chr21:45285039 | T | A | 1 | a0001c0001t0002g0078 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.382+639A>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285039 | |||||||
| chr21:45285047 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.382+631C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285047 | |||||||
| chr21:45285240 | T | G | 72 | a0001c0001t0001g0037 a0001c0001t0001g0183 a0001c0001t0002g0013 others(69): Show |
121 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.382+438A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285240 | |||||||
| chr21:45285259 | C | T | 29 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(26): Show |
40 | HG00408.hp1 HG00733.hp1 HG01192.hp1 others(37): Show |
intron_variant | MODIFIER | c.382+419G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285259 | |||||||
| chr21:45285297 | C | G | 1 | a0001c0001t0002g0061 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.382+381G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285297 | |||||||
| chr21:45285364 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.382+314C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285364 | |||||||
| chr21:45285381 | C | A | 1 | a0001c0001t0001g0180 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.382+297G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285381 | |||||||
| chr21:45285430 | G | A | 60 | a0001c0001t0001g0181 a0001c0001t0002g0013 a0001c0001t0002g0021 others(57): Show |
107 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.382+248C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285430 | |||||||
| chr21:45285439 | C | T | 21 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(18): Show |
30 | HG00408.hp1 HG01192.hp1 HG01943.hp2 others(27): Show |
intron_variant | MODIFIER | c.382+239G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285439 | |||||||
| chr21:45285456 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.382+222G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 2/8 | chr21 | 45285456 | |||||||
| chr21:45285979 | C | A | 2 | a0001c0001t0003g0244 a0001c0001t0015g0048 |
3 | HG00099.hp2 HG01361.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.132-51G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45285979 | |||||||
| chr21:45285988 | C | T | 2 | a0001c0001t0001g0183 a0001c0001t0003g0184 |
2 | HG03654.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.132-60G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45285988 | |||||||
| chr21:45286130 | C | T | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132-202G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286130 | |||||||
| chr21:45286227 | T | C | 129 | a0001c0001t0001g0183 a0001c0001t0002g0007 a0001c0001t0002g0013 others(126): Show |
191 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.132-299A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286227 | |||||||
| chr21:45286262 | G | A | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.132-334C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286262 | |||||||
| chr21:45286286 | T | G | 1 | a0001c0001t0001g0049 | 2 | NA18984.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.132-358A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286286 | |||||||
| chr21:45286420 | G | C | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132-492C>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286420 | |||||||
| chr21:45286485 | T | C | 2 | a0001c0001t0002g0057 a0001c0001t0022g0056 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.132-557A>G | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286485 | |||||||
| chr21:45286734 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.132-806G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286734 | |||||||
| chr21:45286772 | C | G | 1 | a0001c0001t0002g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.132-844G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286772 | |||||||
| chr21:45286817 | C | A | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.132-889G>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286817 | |||||||
| chr21:45286817 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.132-889G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45286817 | |||||||
| chr21:45287004 | G | A | 8 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0249 others(5): Show |
13 | HG01167.hp1 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.131+737C>T | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287004 | |||||||
| chr21:45287189 | C | CGGCCCT | 3 | a0001c0001t0002g0057 a0001c0001t0022g0056 a0003c0005t0013g0059 |
3 | HG01891.hp2 HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.131+551_131+552ins others(6): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287189 | |||||||
| chr21:45287196 | G | GGCCCCT | 39 | a0001c0001t0002g0007 a0001c0001t0002g0014 a0001c0001t0002g0015 others(36): Show |
51 | HG00408.hp1 HG00733.hp1 HG01192.hp1 others(48): Show |
intron_variant | MODIFIER | c.131+539_131+544dup others(6): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287196 | |||||||
| chr21:45287196 | G | T | 3 | a0001c0001t0002g0057 a0001c0001t0022g0056 a0003c0005t0013g0059 |
3 | HG01891.hp2 HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.131+545C>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287196 | |||||||
| chr21:45287196 | GGCCCCT | G | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+539_131+544del others(6): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287196 | |||||||
| chr21:45287216 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.131+525G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287216 | |||||||
| chr21:45287238 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.131+503A>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287238 | |||||||
| chr21:45287327 | AGCCCCTG others(29): Show |
A | 1 | a0001c0001t0002g0251 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.131+378_131+413del others(36): Show |
POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287327 | |||||||
| chr21:45287354 | C | T | 2 | a0001c0001t0002g0028 a0001c0001t0002g0090 |
3 | HG02922.hp1 HG03453.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.131+387G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287354 | |||||||
| chr21:45287374 | C | T | 2 | a0001c0001t0002g0057 a0001c0001t0022g0056 |
2 | HG02055.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.131+367G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287374 | |||||||
| chr21:45287466 | C | G | 1 | a0003c0004t0031g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.131+275G>C | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287466 | |||||||
| chr21:45287485 | C | T | 1 | a0001c0001t0007g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.131+256G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287485 | |||||||
| chr21:45287556 | C | T | 2 | a0001c0001t0010g0053 a0001c0001t0010g0054 |
2 | HG02559.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.131+185G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287556 | |||||||
| chr21:45287562 | C | T | 1 | a0001c0001t0007g0052 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.131+179G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287562 | |||||||
| chr21:45287639 | C | T | 5 | a0001c0001t0008g0051 a0001c0001t0008g0254 a0001c0001t0008g0255 others(2): Show |
6 | HG01261.hp1 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.131+102G>A | POFUT2 | ENSG00000186866.17 | transcript | ENST00000349485.10 | protein_coding | 1/8 | chr21 | 45287639 |