Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 112869 |
| ensemblid | ENSG00000176476.9 |
| hgncid | 25156 |
| symbol | SGF29 |
| name | SAGA complex associated factor 29 |
| refseq_nuc | NM_138414.3 |
| refseq_prot | NP_612423.1 |
| ensembl_nuc | ENST00000317058.8 |
| ensembl_prot | ENSP00000316114.3 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 28553920 |
| end | 28591790 |
| strand | + |
| ver | v1.2 |
| region | chr16:28553920-28591790 |
| region5000 | chr16:28548920-28596790 |
| regionname0 | SGF29_chr16_28553920_28591790 |
| regionname5000 | SGF29_chr16_28548920_28596790 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 293 | 345 | 90 | 64 | 139 | 10 | 40 | 102 | SGF29_chr16_28548920_28596790 | SGF29 | MALVS others(288): Show |
chr16 | 28548920 | 28596790 |
| a0002 | 0/0 | 293 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | MALVS others(288): Show |
chr16 | 28548920 | 28596790 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 879 | 275 | 75 | 49 | 112 | 6 | 31 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 | ||
| a0001c0002 | 0/0 | 879 | 51 | 10 | 10 | 26 | 1 | 4 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 | ||
| a0001c0003 | 0/0 | 879 | 17 | 3 | 5 | 1 | 3 | 5 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 | ||
| a0001c0005 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 | ||
| a0001c0006 | 0/0 | 879 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 | ||
| a0002c0004 | 0/0 | 879 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | ATGGC others(874): Show |
chr16 | 28548920 | 28596790 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 1159 | 184 | 45 | 22 | 85 | 3 | 28 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0002 | 0/1 | 1158 | 81 | 24 | 25 | 25 | 3 | 3 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0003 | 0/0 | 1158 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0004 | 0/0 | 1158 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0005 | 0/0 | 1158 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0006 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0007 | 0/0 | 1159 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| a0001c0001t0008 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| a0001c0002t0002 | 0/0 | 1158 | 37 | 10 | 4 | 18 | 1 | 4 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0002t0003 | 0/0 | 1158 | 13 | 0 | 6 | 7 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0002t0009 | 0/0 | 1158 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0003t0001 | 0/0 | 1159 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| a0001c0003t0002 | 0/0 | 1158 | 16 | 3 | 4 | 1 | 3 | 5 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0005t0002 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0001c0006t0002 | 0/0 | 1158 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1153): Show |
chr16 | 28548920 | 28596790 |
| a0002c0004t0001 | 0/0 | 1159 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | CCTCC others(1154): Show |
chr16 | 28548920 | 28596790 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 9 | 0 | 1 | 5 | 1 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0264 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0004g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0004g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0004g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0005g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0004 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0011 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0027 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0002t0009g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0024 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0003t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0005t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0001c0006t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| a0002c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0002 | g0027 | EUR | GBR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00609 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00642 | hp1 | a0001 | c0003 | t0002 | g0213 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00738 | hp2 | a0001 | c0003 | t0002 | g0216 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0054 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01106 | hp2 | a0001 | c0003 | t0002 | g0221 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0272 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0170 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01192 | hp1 | a0001 | c0002 | t0003 | g0032 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01258 | hp2 | a0001 | c0001 | t0003 | g0038 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01261 | hp1 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01261 | hp2 | a0001 | c0003 | t0002 | g0219 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0005 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01433 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0068 | EUR | IBS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01884 | hp1 | a0001 | c0001 | t0004 | g0290 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0084 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG01978 | hp2 | a0001 | c0002 | t0003 | g0040 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02004 | hp2 | a0001 | c0002 | t0003 | g0034 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0288 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02056 | hp2 | a0001 | c0003 | t0002 | g0220 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02071 | hp1 | a0002 | c0004 | t0001 | g0134 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02080 | hp2 | a0001 | c0002 | t0003 | g0035 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02083 | hp2 | a0001 | c0002 | t0003 | g0031 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02132 | hp1 | a0001 | c0002 | t0002 | g0037 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02148 | hp2 | a0001 | c0002 | t0003 | g0030 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0299 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | CDX | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0282 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0300 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0295 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0280 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PEL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02572 | hp2 | a0001 | c0002 | t0002 | g0274 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02602 | hp2 | a0001 | c0003 | t0002 | g0218 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02698 | hp2 | a0001 | c0002 | t0002 | g0093 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02735 | hp2 | a0001 | c0003 | t0002 | g0259 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02809 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0275 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0110 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0109 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0270 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0296 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0271 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0281 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0285 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0293 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0291 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0029 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03492 | hp2 | a0001 | c0002 | t0002 | g0028 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03540 | hp2 | a0001 | c0005 | t0002 | g0279 | AFR | GWD | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0222 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03704 | hp2 | a0001 | c0003 | t0002 | g0217 | SAS | PJL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0298 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0214 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | BEB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | STU | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0276 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18522 | hp2 | a0001 | c0003 | t0002 | g0212 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18906 | hp1 | a0001 | c0006 | t0002 | g0108 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18943 | hp1 | a0001 | c0001 | t0006 | g0244 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0052 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18947 | hp1 | a0001 | c0001 | t0008 | g0113 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18952 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18960 | hp1 | a0001 | c0002 | t0003 | g0033 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18961 | hp1 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18962 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18971 | hp1 | a0001 | c0002 | t0003 | g0005 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18975 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18980 | hp2 | a0001 | c0002 | t0003 | g0039 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18983 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18991 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19030 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19077 | hp2 | a0001 | c0002 | t0002 | g0053 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19087 | hp1 | a0001 | c0002 | t0003 | g0036 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19091 | hp2 | a0001 | c0002 | t0009 | g0044 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | ASW | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0269 | AFR | ASW | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20752 | hp1 | a0001 | c0003 | t0002 | g0215 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20752 | hp2 | a0001 | c0003 | t0002 | g0024 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0024 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0079 | EUR | TSI | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | GIH | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | GIH | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02109 | hp1 | a0001 | c0003 | t0002 | g0210 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0297 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02486 | hp2 | a0001 | c0001 | t0002 | g0286 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ACB | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG03471 | hp2 | a0001 | c0003 | t0002 | g0211 | AFR | MSL | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20300 | hp1 | a0001 | c0001 | t0004 | g0292 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0284 | AFR | USA | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0004 | AFR | LWK | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0098 | REF | REF | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0264 | REF | REF | SGF29_chr16_28548920_28596790 | SGF29 | chr16 | 28548920 | 28596790 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28585692 | G | A | 1 | a0002 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.196G>A | p.Ala66Thr | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/10 | 389/1159 | 196/882 | 66/293 | chr16 | 28585692 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28591646 | C | G | 1 | a0001c0006 | 1 | NA18906.hp1 | synonymous_variant | LOW | c.822C>G | p.Ser274Ser | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1015/1159 | 822/882 | 274/293 | chr16 | 28591646 | |||
| chr16:28591670 | A | G | 3 | a0001c0002 a0001c0003 a0001c0006 |
69 | HG00099.hp1 HG00609.hp1 HG00642.hp1 others(66): Show |
synonymous_variant | LOW | c.846A>G | p.Arg282Arg | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1039/1159 | 846/882 | 282/293 | chr16 | 28591670 | |||
| chr16:28591673 | C | T | 1 | a0001c0005 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.849C>T | p.Tyr283Tyr | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1042/1159 | 849/882 | 283/293 | chr16 | 28591673 | |||
| chr16:28591691 | A | G | 2 | a0001c0003 a0001c0006 |
18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
synonymous_variant | LOW | c.867A>G | p.Glu289Glu | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 1060/1159 | 867/882 | 289/293 | chr16 | 28591691 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28553947 | G | C | 1 | a0001c0001t0006 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27123 | chr16 | 28553947 | ||||||
| chr16:28553948 | GA | G | 10 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(7): Show |
156 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(153): Show |
5_prime_UTR_variant | MODIFIER | c.-157delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27114 | INFO_REALIGN_3_PRIME | chr16 | 28553948 | |||||
| chr16:28554004 | G | C | 1 | a0001c0001t0004 | 3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-109G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27066 | chr16 | 28554004 | ||||||
| chr16:28554006 | T | G | 2 | a0001c0001t0003 a0001c0002t0003 |
15 | HG01192.hp1 HG01258.hp2 HG01261.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-107T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/10 | 27064 | chr16 | 28554006 | ||||||
| chr16:28591710 | C | T | 1 | a0001c0002t0009 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 4 | chr16 | 28591710 | ||||||
| chr16:28591736 | C | T | 1 | a0001c0001t0008 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*30C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 30 | chr16 | 28591736 | ||||||
| chr16:28591761 | C | T | 1 | a0001c0001t0007 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*55C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 55 | chr16 | 28591761 | ||||||
| chr16:28591762 | G | A | 1 | a0001c0001t0005 | 2 | HG02896.hp2 HG02897.hp1 |
3_prime_UTR_variant | MODIFIER | c.*56G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 10/10 | 56 | chr16 | 28591762 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr16:28554124 | G | A | 32 | a0001c0001t0002g0047 a0001c0001t0003g0038 a0001c0001t0003g0046 others(29): Show |
39 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+27G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554124 | |||||||
| chr16:28554168 | G | A | 54 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(51): Show |
58 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+71G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554168 | |||||||
| chr16:28554172 | C | G | 1 | a0001c0001t0002g0107 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.-16+75C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554172 | |||||||
| chr16:28554176 | G | T | 1 | a0001c0001t0002g0300 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-16+79G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554176 | |||||||
| chr16:28554182 | G | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+85G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554182 | |||||||
| chr16:28554266 | G | A | 3 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0006t0002g0108 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+169G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554266 | |||||||
| chr16:28554305 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+208C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554305 | |||||||
| chr16:28554346 | C | G | 124 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(121): Show |
140 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.-16+249C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554346 | |||||||
| chr16:28554350 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+253G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554350 | |||||||
| chr16:28554351 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-16+254A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554351 | |||||||
| chr16:28554352 | G | C | 2 | a0001c0002t0002g0028 a0001c0002t0002g0029 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-16+255G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554352 | |||||||
| chr16:28554353 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0008g0113 |
2 | HG01934.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.-16+256G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554353 | |||||||
| chr16:28554456 | C | T | 1 | a0001c0002t0002g0027 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+359C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554456 | |||||||
| chr16:28554632 | A | G | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-16+535A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554632 | |||||||
| chr16:28554658 | T | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02040.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-16+561T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554658 | |||||||
| chr16:28554687 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-16+590G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554687 | |||||||
| chr16:28554837 | G | T | 124 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(121): Show |
140 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.-16+740G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28554837 | |||||||
| chr16:28555054 | T | C | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(288): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-16+957T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555054 | |||||||
| chr16:28555171 | A | G | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16+1074A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555171 | |||||||
| chr16:28555215 | GCACTTTG others(3): Show |
G | 1 | a0001c0001t0002g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-16+1119_-16+1128d others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555215 | |||||||
| chr16:28555230 | G | A | 4 | a0001c0001t0002g0055 a0001c0001t0002g0056 a0001c0001t0002g0057 others(1): Show |
4 | HG00639.hp1 HG00642.hp2 HG01070.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+1133G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555230 | |||||||
| chr16:28555301 | T | TA | 34 | a0001c0001t0002g0047 a0001c0001t0002g0059 a0001c0001t0002g0060 others(31): Show |
41 | HG00609.hp1 HG00735.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.-16+1221dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28555301 | ||||||
| chr16:28555301 | TA | T | 15 | a0001c0001t0001g0116 a0001c0001t0001g0254 a0001c0001t0001g0255 others(12): Show |
15 | HG01099.hp1 HG01167.hp1 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+1221delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28555301 | ||||||
| chr16:28555332 | C | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0051 a0001c0002t0002g0052 others(1): Show |
6 | HG00609.hp1 NA18944.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1235C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555332 | |||||||
| chr16:28555347 | A | G | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+1250A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555347 | |||||||
| chr16:28555380 | G | T | 4 | a0001c0001t0001g0025 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
5 | NA18967.hp2 NA18970.hp2 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+1283G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555380 | |||||||
| chr16:28555477 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-16+1380A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555477 | |||||||
| chr16:28555508 | C | T | 1 | a0001c0001t0002g0296 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-16+1411C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555508 | |||||||
| chr16:28555612 | A | G | 32 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0224 others(29): Show |
33 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.-16+1515A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555612 | |||||||
| chr16:28555683 | A | G | 15 | a0001c0003t0002g0024 a0001c0003t0002g0210 a0001c0003t0002g0211 others(12): Show |
16 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+1586A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28555683 | |||||||
| chr16:28556042 | T | C | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+1945T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556042 | |||||||
| chr16:28556263 | G | A | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(3): Show |
6 | HG01891.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+2166G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556263 | |||||||
| chr16:28556339 | T | C | 1 | a0001c0002t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+2242T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556339 | |||||||
| chr16:28556368 | C | G | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-16+2271C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556368 | |||||||
| chr16:28556368 | C | T | 1 | a0001c0002t0002g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+2271C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556368 | |||||||
| chr16:28556433 | C | T | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-16+2336C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556433 | |||||||
| chr16:28556479 | C | G | 1 | a0001c0001t0001g0208 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-16+2382C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556479 | |||||||
| chr16:28556743 | A | T | 1 | a0001c0001t0002g0012 | 2 | HG00741.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-16+2646A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556743 | |||||||
| chr16:28556747 | G | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+2650G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556747 | |||||||
| chr16:28556757 | C | A | 1 | a0001c0001t0002g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-16+2660C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556757 | |||||||
| chr16:28556809 | A | G | 3 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0105 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-16+2712A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556809 | |||||||
| chr16:28556839 | G | A | 3 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0006t0002g0108 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+2742G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556839 | |||||||
| chr16:28556894 | C | T | 32 | a0001c0001t0002g0047 a0001c0001t0003g0038 a0001c0001t0003g0046 others(29): Show |
39 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+2797C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556894 | |||||||
| chr16:28556900 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-16+2803G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28556900 | |||||||
| chr16:28557010 | T | C | 3 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 |
3 | NA18939.hp1 NA19000.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.-16+2913T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557010 | |||||||
| chr16:28557046 | G | T | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+2949G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557046 | |||||||
| chr16:28557357 | C | T | 15 | a0001c0003t0002g0024 a0001c0003t0002g0210 a0001c0003t0002g0211 others(12): Show |
16 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.-16+3260C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557357 | |||||||
| chr16:28557649 | C | T | 1 | a0001c0001t0002g0295 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-16+3552C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557649 | |||||||
| chr16:28557733 | A | G | 1 | a0001c0001t0002g0012 | 2 | HG00741.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-16+3636A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557733 | |||||||
| chr16:28557824 | C | G | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+3727C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557824 | |||||||
| chr16:28557965 | G | GT | 44 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0181 others(41): Show |
47 | HG00544.hp2 HG00558.hp2 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.-16+3894dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28557965 | ||||||
| chr16:28557965 | GT | G | 62 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(59): Show |
72 | HG00609.hp1 HG00642.hp1 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.-16+3894delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28557965 | ||||||
| chr16:28557966 | T | G | 1 | a0001c0001t0002g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-16+3869T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557966 | |||||||
| chr16:28557967 | T | G | 1 | a0001c0001t0002g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-16+3870T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557967 | |||||||
| chr16:28557991 | T | C | 1 | a0001c0001t0001g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-16+3894T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557991 | |||||||
| chr16:28557992 | C | T | 1 | a0001c0002t0002g0093 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-16+3895C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28557992 | |||||||
| chr16:28558184 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0201 a0001c0001t0001g0203 others(3): Show |
7 | HG02615.hp2 HG02895.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+4087C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558184 | |||||||
| chr16:28558199 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-16+4102G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558199 | |||||||
| chr16:28558200 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+4103G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558200 | |||||||
| chr16:28558272 | A | AT | 21 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
25 | HG02080.hp1 HG02145.hp1 HG02698.hp1 others(22): Show |
intron_variant | MODIFIER | c.-16+4190dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28558272 | ||||||
| chr16:28558443 | G | C | 54 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(51): Show |
58 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+4346G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558443 | |||||||
| chr16:28558455 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+4358C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558455 | |||||||
| chr16:28558523 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-16+4426T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558523 | |||||||
| chr16:28558536 | G | A | 3 | a0001c0003t0002g0210 a0001c0003t0002g0211 a0001c0003t0002g0212 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-16+4439G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558536 | |||||||
| chr16:28558556 | G | A | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+4459G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558556 | |||||||
| chr16:28558684 | C | T | 77 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(74): Show |
82 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-16+4587C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558684 | |||||||
| chr16:28558701 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+4604A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558701 | |||||||
| chr16:28558729 | A | G | 43 | a0001c0001t0002g0047 a0001c0001t0002g0273 a0001c0001t0003g0038 others(40): Show |
53 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.-16+4632A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558729 | |||||||
| chr16:28558901 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-16+4804G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558901 | |||||||
| chr16:28558951 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0196 |
3 | HG02280.hp1 HG02615.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.-16+4854A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28558951 | |||||||
| chr16:28559000 | A | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(288): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-16+4903A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559000 | |||||||
| chr16:28559007 | T | C | 1 | a0001c0002t0002g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-16+4910T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559007 | |||||||
| chr16:28559300 | A | G | 14 | a0001c0001t0001g0025 a0001c0001t0001g0223 a0001c0001t0001g0224 others(11): Show |
15 | HG00558.hp1 HG02132.hp2 NA18939.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+5203A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559300 | |||||||
| chr16:28559318 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.-16+5221C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559318 | |||||||
| chr16:28559382 | TTTG | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-16+5300_-16+5302d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28559382 | ||||||
| chr16:28559401 | T | A | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+5304T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559401 | |||||||
| chr16:28559414 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+5317C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559414 | |||||||
| chr16:28559709 | C | A | 11 | a0001c0002t0003g0005 a0001c0002t0003g0030 a0001c0002t0003g0031 others(8): Show |
13 | HG01192.hp1 HG01261.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.-16+5612C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559709 | |||||||
| chr16:28559772 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-16+5675C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28559772 | |||||||
| chr16:28560102 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-16+6005C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560102 | |||||||
| chr16:28560235 | C | A | 6 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(3): Show |
7 | HG00099.hp1 HG02109.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+6138C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560235 | |||||||
| chr16:28560370 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+6273C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560370 | |||||||
| chr16:28560435 | T | A | 291 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(288): Show |
335 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.-16+6338T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560435 | |||||||
| chr16:28560480 | T | G | 2 | a0001c0001t0002g0277 a0001c0001t0002g0278 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+6383T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560480 | |||||||
| chr16:28560552 | G | A | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+6455G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560552 | |||||||
| chr16:28560565 | G | T | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+6468G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560565 | |||||||
| chr16:28560575 | C | G | 3 | a0001c0002t0002g0045 a0001c0002t0002g0050 a0001c0002t0009g0044 |
3 | NA18962.hp2 NA18977.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-16+6478C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560575 | |||||||
| chr16:28560684 | C | T | 31 | a0001c0001t0001g0123 a0001c0001t0002g0047 a0001c0002t0002g0006 others(28): Show |
38 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(35): Show |
intron_variant | MODIFIER | c.-16+6587C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560684 | |||||||
| chr16:28560700 | G | A | 33 | a0001c0001t0001g0025 a0001c0001t0001g0181 a0001c0001t0001g0223 others(30): Show |
34 | HG00280.hp1 HG00438.hp2 HG00558.hp1 others(31): Show |
intron_variant | MODIFIER | c.-16+6603G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560700 | |||||||
| chr16:28560830 | G | A | 1 | a0001c0002t0002g0037 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-16+6733G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560830 | |||||||
| chr16:28560960 | C | CA | 60 | a0001c0001t0001g0115 a0001c0001t0001g0128 a0001c0001t0001g0223 others(57): Show |
64 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-16+6879dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28560960 | ||||||
| chr16:28560974 | AAAG | A | 8 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0269 others(5): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+6878_-16+6880d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28560974 | |||||||
| chr16:28561031 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-16+6934A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561031 | |||||||
| chr16:28561162 | C | T | 2 | a0001c0001t0002g0293 a0001c0001t0002g0294 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-16+7065C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561162 | |||||||
| chr16:28561273 | G | A | 6 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0270 others(3): Show |
9 | HG01109.hp1 HG01884.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+7176G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561273 | |||||||
| chr16:28561527 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-16+7430C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561527 | |||||||
| chr16:28561652 | C | T | 2 | a0001c0003t0002g0210 a0001c0003t0002g0211 |
2 | HG02109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-16+7555C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561652 | |||||||
| chr16:28561915 | C | G | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+7818C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561915 | |||||||
| chr16:28561926 | A | G | 1 | a0001c0002t0002g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-16+7829A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28561926 | |||||||
| chr16:28562010 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+7913A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562010 | |||||||
| chr16:28562042 | G | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
10 | HG00408.hp1 NA18943.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.-16+7945G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562042 | |||||||
| chr16:28562058 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-16+7961C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562058 | |||||||
| chr16:28562237 | C | T | 1 | a0001c0002t0002g0027 | 2 | HG00099.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-16+8140C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562237 | |||||||
| chr16:28562291 | T | G | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+8194T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562291 | |||||||
| chr16:28562402 | G | A | 1 | a0001c0002t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+8305G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562402 | |||||||
| chr16:28562417 | A | T | 1 | a0001c0001t0002g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-16+8320A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562417 | |||||||
| chr16:28562642 | C | T | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+8545C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562642 | |||||||
| chr16:28562670 | A | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0204 a0001c0001t0001g0205 |
4 | HG02895.hp2 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+8573A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562670 | |||||||
| chr16:28562688 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-16+8591C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562688 | |||||||
| chr16:28562756 | T | C | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+8659T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562756 | |||||||
| chr16:28562826 | C | T | 3 | a0001c0001t0002g0088 a0001c0001t0002g0089 a0001c0001t0002g0090 |
3 | HG02015.hp1 NA18970.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.-16+8729C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28562826 | |||||||
| chr16:28562903 | C | CA | 93 | a0001c0001t0001g0112 a0001c0001t0001g0124 a0001c0001t0001g0133 others(90): Show |
102 | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(99): Show |
intron_variant | MODIFIER | c.-16+8830dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | ||||||
| chr16:28562903 | C | CAA | 22 | a0001c0001t0001g0111 a0001c0001t0001g0132 a0001c0001t0001g0231 others(19): Show |
22 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.-16+8829_-16+8830d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | ||||||
| chr16:28562903 | CA | C | 28 | a0001c0001t0001g0120 a0001c0001t0002g0026 a0001c0001t0002g0276 others(25): Show |
30 | HG00099.hp1 HG01106.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.-16+8830delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28562903 | ||||||
| chr16:28563008 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-16+8911G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563008 | |||||||
| chr16:28563033 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-16+8936A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563033 | |||||||
| chr16:28563294 | A | G | 146 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0123 others(143): Show |
163 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.-16+9197A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563294 | |||||||
| chr16:28563316 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-16+9219T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563316 | |||||||
| chr16:28563338 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-16+9241C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563338 | |||||||
| chr16:28563350 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-16+9253G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563350 | |||||||
| chr16:28563715 | C | CT | 86 | a0001c0001t0001g0019 a0001c0001t0001g0114 a0001c0001t0001g0118 others(83): Show |
92 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.-16+9641dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | ||||||
| chr16:28563715 | C | CTT | 11 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0069 others(8): Show |
11 | HG01175.hp2 HG01255.hp2 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+9640_-16+9641d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | ||||||
| chr16:28563715 | CT | C | 19 | a0001c0001t0001g0112 a0001c0001t0005g0109 a0001c0001t0005g0110 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+9641delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28563715 | ||||||
| chr16:28563781 | C | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+9684C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563781 | |||||||
| chr16:28563998 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+9901C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28563998 | |||||||
| chr16:28564023 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0002g0047 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+9926A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564023 | |||||||
| chr16:28564214 | G | C | 1 | a0001c0001t0001g0172 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-16+10117G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564214 | |||||||
| chr16:28564431 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-16+10334A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564431 | |||||||
| chr16:28564479 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-16+10382C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564479 | |||||||
| chr16:28564511 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-16+10414A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564511 | |||||||
| chr16:28564517 | ATATGTGT others(3): Show |
A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10424_-16+1043 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564517 | ||||||
| chr16:28564521 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10424G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564521 | |||||||
| chr16:28564523 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10426G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564523 | |||||||
| chr16:28564525 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10428G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564525 | |||||||
| chr16:28564526 | T | TGTATATA others(17): Show |
1 | a0001c0001t0001g0177 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-16+10442_-16+1046 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564526 | ||||||
| chr16:28564527 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10430G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564527 | |||||||
| chr16:28564529 | A | ATACGTAT others(11): Show |
2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10434_-16+1043 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564529 | ||||||
| chr16:28564529 | A | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+10432A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564529 | |||||||
| chr16:28564535 | A | G | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10438A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564535 | |||||||
| chr16:28564537 | A | G | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10440A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564537 | |||||||
| chr16:28564538 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0002g0070 others(1): Show |
4 | HG01346.hp1 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-16+10441T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564538 | |||||||
| chr16:28564538 | TGTATATA others(33): Show |
T | 1 | a0001c0001t0004g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-16+10442_-16+1048 others(44): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564538 | |||||||
| chr16:28564541 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0002g0047 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10444A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564541 | |||||||
| chr16:28564549 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+10452A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564549 | |||||||
| chr16:28564549 | ACG | A | 70 | a0001c0001t0002g0026 a0001c0001t0002g0273 a0001c0001t0002g0276 others(67): Show |
81 | HG00609.hp1 HG00642.hp1 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.-16+10453_-16+1045 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564549 | |||||||
| chr16:28564550 | C | T | 69 | a0001c0001t0001g0123 a0001c0001t0001g0190 a0001c0001t0001g0231 others(66): Show |
74 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.-16+10453C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564550 | |||||||
| chr16:28564551 | G | A | 3 | a0001c0001t0001g0123 a0001c0001t0002g0047 a0001c0001t0002g0082 |
3 | HG02257.hp2 HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10454G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564551 | |||||||
| chr16:28564551 | GTA | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(27): Show |
39 | HG00408.hp1 HG00558.hp2 HG00597.hp1 others(36): Show |
intron_variant | MODIFIER | c.-16+10467_-16+1046 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564551 | ||||||
| chr16:28564552 | T | TGTGTGTA others(21): Show |
1 | a0001c0001t0001g0190 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-16+10455_-16+1045 others(32): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564552 | |||||||
| chr16:28564553 | A | ATATATAT others(3): Show |
1 | a0001c0001t0002g0082 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-16+10464_-16+1046 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | ||||||
| chr16:28564553 | A | ATATATAT others(5): Show |
51 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(48): Show |
55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | ||||||
| chr16:28564553 | A | ATATATAT others(19): Show |
3 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0105 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(30): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564553 | ||||||
| chr16:28564553 | A | G | 73 | a0001c0001t0001g0123 a0001c0001t0001g0190 a0001c0001t0002g0026 others(70): Show |
84 | HG00544.hp2 HG00609.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-16+10456A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564553 | |||||||
| chr16:28564554 | T | TATATATA others(5): Show |
2 | a0001c0001t0002g0091 a0001c0001t0002g0102 |
2 | NA18941.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564554 | ||||||
| chr16:28564555 | A | ATATATAT others(19): Show |
3 | a0001c0001t0001g0161 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG03195.hp2 HG03516.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-16+10470_-16+1049 others(30): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564555 | ||||||
| chr16:28564555 | A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0162 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-16+10495_-16+1049 others(56): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564555 | ||||||
| chr16:28564558 | T | TATATACG others(41): Show |
1 | a0001c0001t0002g0095 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10466_-16+1046 others(52): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564558 | ||||||
| chr16:28564562 | TATAC | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10466_-16+1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564562 | |||||||
| chr16:28564564 | TACGTATA others(7): Show |
T | 6 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0010 others(3): Show |
7 | HG00438.hp2 HG02165.hp2 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+10484_-16+1049 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564564 | ||||||
| chr16:28564566 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10469C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564566 | |||||||
| chr16:28564569 | A | G | 1 | a0001c0001t0002g0095 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-16+10472A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564569 | |||||||
| chr16:28564578 | C | T | 135 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0123 others(132): Show |
151 | HG00099.hp1 HG00280.hp2 HG00609.hp1 others(148): Show |
intron_variant | MODIFIER | c.-16+10481C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564578 | |||||||
| chr16:28564580 | C | CATATATA others(1): Show |
3 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0105 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-16+10483_-16+1048 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564580 | |||||||
| chr16:28564581 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10484G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564581 | |||||||
| chr16:28564582 | T | C | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10485T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564582 | |||||||
| chr16:28564583 | A | G | 3 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0105 |
3 | HG01081.hp1 HG01099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.-16+10486A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564583 | |||||||
| chr16:28564592 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+10495C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564592 | |||||||
| chr16:28564594 | CACATATA others(17): Show |
C | 1 | a0001c0001t0002g0281 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10499_-16+1052 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564594 | ||||||
| chr16:28564596 | C | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-16+10499C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564596 | |||||||
| chr16:28564597 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10500A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564597 | |||||||
| chr16:28564599 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10502A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564599 | |||||||
| chr16:28564601 | ATGTGTAT others(35): Show |
A | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10508_-16+1054 others(46): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564601 | ||||||
| chr16:28564603 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10506G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564603 | |||||||
| chr16:28564604 | TGTATATA others(55): Show |
T | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-16+10508_-16+1056 others(66): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564604 | |||||||
| chr16:28564605 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10508G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564605 | |||||||
| chr16:28564617 | A | G | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10520A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564617 | |||||||
| chr16:28564624 | C | T | 2 | a0001c0002t0002g0298 a0001c0002t0002g0299 |
2 | HG02155.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-16+10527C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564624 | |||||||
| chr16:28564626 | T | C | 2 | a0001c0001t0002g0276 a0001c0001t0002g0289 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-16+10529T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564626 | |||||||
| chr16:28564635 | G | A | 4 | a0001c0003t0002g0213 a0001c0003t0002g0215 a0001c0003t0002g0220 others(1): Show |
4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10538G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564635 | |||||||
| chr16:28564641 | A | ATG | 7 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0214 others(4): Show |
8 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+10548_-16+1054 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564641 | ||||||
| chr16:28564641 | A | G | 4 | a0001c0003t0002g0213 a0001c0003t0002g0215 a0001c0003t0002g0220 others(1): Show |
4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10544A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564641 | |||||||
| chr16:28564645 | G | A | 4 | a0001c0003t0002g0213 a0001c0003t0002g0215 a0001c0003t0002g0220 others(1): Show |
4 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10548G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564645 | |||||||
| chr16:28564645 | G | GTA | 8 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0002g0210 others(5): Show |
8 | HG02109.hp1 HG02602.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-16+10555_-16+1055 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564645 | ||||||
| chr16:28564654 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10557C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564654 | |||||||
| chr16:28564665 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG00735.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.-16+10568G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564665 | |||||||
| chr16:28564666 | C | CATATATG others(1): Show |
76 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(73): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.-16+10575_-16+1057 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564666 | ||||||
| chr16:28564666 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10569C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564666 | |||||||
| chr16:28564666 | CAT | C | 27 | a0001c0001t0002g0026 a0001c0001t0002g0071 a0001c0001t0002g0072 others(24): Show |
28 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.-16+10576_-16+1057 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564666 | ||||||
| chr16:28564667 | A | G | 1 | a0001c0001t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-16+10570A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564667 | |||||||
| chr16:28564671 | ATATGTAT others(7): Show |
A | 35 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0002g0297 others(32): Show |
43 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-16+10576_-16+1058 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564671 | ||||||
| chr16:28564675 | G | A | 2 | a0001c0001t0002g0104 a0001c0001t0002g0294 |
2 | HG01099.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10578G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564675 | |||||||
| chr16:28564677 | A | G | 2 | a0001c0001t0002g0104 a0001c0001t0002g0294 |
2 | HG01099.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10580A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564677 | |||||||
| chr16:28564683 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0182 |
3 | HG02074.hp2 HG03942.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.-16+10586A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564683 | |||||||
| chr16:28564685 | G | A | 2 | a0001c0001t0002g0106 a0001c0001t0002g0294 |
2 | HG02129.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10588G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564685 | |||||||
| chr16:28564685 | GTGTATAT others(3): Show |
G | 12 | a0001c0001t0002g0276 a0001c0001t0002g0277 a0001c0001t0002g0278 others(9): Show |
12 | HG01891.hp1 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.-16+10600_-16+1060 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564685 | ||||||
| chr16:28564685 | GTGTATAT others(41): Show |
G | 5 | a0001c0001t0002g0026 a0001c0001t0002g0285 a0001c0001t0002g0286 others(2): Show |
6 | HG01106.hp1 HG02055.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+10590_-16+1063 others(52): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564685 | ||||||
| chr16:28564687 | G | A | 63 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0047 others(60): Show |
67 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-16+10590G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564687 | |||||||
| chr16:28564687 | GTA | G | 9 | a0001c0001t0001g0123 a0001c0001t0002g0273 a0001c0002t0002g0004 others(6): Show |
12 | HG01109.hp1 HG01884.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-16+10598_-16+1059 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564687 | ||||||
| chr16:28564688 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0106 |
2 | HG02129.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-16+10591T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564688 | |||||||
| chr16:28564695 | A | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(54): Show |
61 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.-16+10598A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564695 | |||||||
| chr16:28564695 | ATGTATAT others(43): Show |
A | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+10600_-16+1064 others(54): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564695 | ||||||
| chr16:28564696 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(66): Show |
90 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.-16+10599T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564696 | |||||||
| chr16:28564697 | G | A | 66 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(63): Show |
70 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.-16+10600G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564697 | |||||||
| chr16:28564698 | T | C | 1 | a0001c0005t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+10601T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564698 | |||||||
| chr16:28564698 | TATATATA others(3): Show |
T | 3 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0006t0002g0108 |
3 | HG02896.hp2 HG02897.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-16+10610_-16+1061 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564698 | ||||||
| chr16:28564704 | TATAC | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10611_-16+1061 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564704 | ||||||
| chr16:28564705 | A | ATG | 5 | a0001c0003t0002g0212 a0001c0003t0002g0213 a0001c0003t0002g0215 others(2): Show |
5 | HG00642.hp1 HG02056.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10609_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564705 | ||||||
| chr16:28564705 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-16+10608A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564705 | |||||||
| chr16:28564706 | T | C | 4 | a0001c0001t0001g0125 a0001c0001t0001g0132 a0001c0001t0001g0145 others(1): Show |
4 | HG02717.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10609T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564706 | |||||||
| chr16:28564706 | TAC | T | 10 | a0001c0001t0002g0297 a0001c0003t0001g0170 a0001c0003t0002g0024 others(7): Show |
11 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.-16+10611_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564706 | ||||||
| chr16:28564707 | A | G | 41 | a0001c0001t0001g0184 a0001c0001t0001g0226 a0001c0001t0001g0231 others(38): Show |
48 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.-16+10610A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564707 | |||||||
| chr16:28564708 | C | CAT | 14 | a0001c0001t0001g0023 a0001c0001t0001g0111 a0001c0001t0001g0112 others(11): Show |
15 | HG01891.hp2 HG02559.hp1 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.-16+10618_-16+1061 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564708 | ||||||
| chr16:28564708 | C | T | 39 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(36): Show |
46 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.-16+10611C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564708 | |||||||
| chr16:28564709 | A | G | 45 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(42): Show |
54 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-16+10612A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564709 | |||||||
| chr16:28564710 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-16+10613T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564710 | |||||||
| chr16:28564711 | A | G | 9 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0214 others(6): Show |
10 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.-16+10614A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564711 | |||||||
| chr16:28564714 | TATGTATA others(7): Show |
T | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-16+10620_-16+1063 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564714 | ||||||
| chr16:28564716 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0126 a0001c0001t0001g0128 others(7): Show |
11 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+10619T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564716 | |||||||
| chr16:28564717 | G | GTA | 49 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(46): Show |
53 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-16+10629_-16+1063 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564717 | ||||||
| chr16:28564717 | G | GTATATAT others(27): Show |
2 | a0001c0001t0002g0064 a0001c0001t0002g0068 |
2 | HG01256.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.-16+10629_-16+1063 others(38): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564717 | ||||||
| chr16:28564721 | ATATATAC others(9): Show |
A | 1 | a0001c0001t0001g0255 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-16+10631_-16+1064 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564721 | ||||||
| chr16:28564725 | A | G | 14 | a0001c0001t0002g0063 a0001c0001t0002g0106 a0001c0001t0002g0276 others(11): Show |
14 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+10628A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564725 | |||||||
| chr16:28564728 | C | CAT | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10638_-16+1063 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564728 | ||||||
| chr16:28564728 | C | T | 14 | a0001c0001t0002g0063 a0001c0001t0002g0106 a0001c0001t0002g0276 others(11): Show |
14 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+10631C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564728 | |||||||
| chr16:28564728 | CATATATA others(11): Show |
C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(130): Show |
158 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564728 | ||||||
| chr16:28564735 | A | G | 15 | a0001c0001t0001g0205 a0001c0001t0002g0063 a0001c0001t0002g0106 others(12): Show |
15 | HG01891.hp1 HG02129.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+10638A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564735 | |||||||
| chr16:28564736 | T | C | 3 | a0001c0001t0002g0073 a0001c0001t0002g0294 a0001c0002t0002g0269 |
3 | HG02451.hp1 NA19074.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-16+10639T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564736 | |||||||
| chr16:28564737 | G | A | 20 | a0001c0001t0001g0205 a0001c0001t0002g0026 a0001c0001t0002g0063 others(17): Show |
21 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-16+10640G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564737 | |||||||
| chr16:28564745 | G | A | 79 | a0001c0001t0001g0123 a0001c0001t0001g0199 a0001c0001t0001g0205 others(76): Show |
88 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.-16+10648G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564745 | |||||||
| chr16:28564746 | T | C | 24 | a0001c0001t0001g0205 a0001c0001t0001g0255 a0001c0001t0002g0026 others(21): Show |
25 | HG01106.hp1 HG01515.hp2 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.-16+10649T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564746 | |||||||
| chr16:28564746 | T | TAC | 52 | a0001c0001t0001g0123 a0001c0001t0001g0199 a0001c0001t0001g0231 others(49): Show |
60 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.-16+10650_-16+1065 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | ||||||
| chr16:28564746 | T | TATAC | 5 | a0001c0001t0002g0065 a0001c0001t0002g0074 a0001c0001t0002g0091 others(2): Show |
5 | HG02135.hp1 HG02523.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10652_-16+1065 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | ||||||
| chr16:28564746 | T | TATATATA others(15): Show |
6 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0270 others(3): Show |
9 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.-16+10665_-16+1066 others(26): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | ||||||
| chr16:28564746 | T | TATATATA others(55): Show |
1 | a0001c0002t0002g0271 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-16+10665_-16+1066 others(66): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564746 | ||||||
| chr16:28564754 | T | C | 1 | a0001c0001t0002g0280 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-16+10657T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564754 | |||||||
| chr16:28564754 | T | TGTATATA others(15): Show |
1 | a0001c0002t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-16+10665_-16+1066 others(26): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564754 | ||||||
| chr16:28564755 | G | A | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10658G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564755 | |||||||
| chr16:28564755 | GTATATAT others(13): Show |
G | 6 | a0001c0001t0001g0013 a0001c0001t0001g0121 a0001c0001t0001g0132 others(3): Show |
7 | HG01243.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(24): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564755 | ||||||
| chr16:28564756 | T | C | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10659T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564756 | |||||||
| chr16:28564757 | ATATATGT others(9): Show |
A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0139 a0001c0001t0001g0152 others(2): Show |
6 | HG01192.hp2 HG02486.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1068 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564757 | ||||||
| chr16:28564759 | ATATGTAT others(7): Show |
A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10666_-16+1067 others(18): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564759 | ||||||
| chr16:28564762 | T | C | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-16+10665T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564762 | |||||||
| chr16:28564763 | G | A | 54 | a0001c0001t0001g0192 a0001c0001t0002g0003 a0001c0001t0002g0012 others(51): Show |
58 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.-16+10666G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564763 | |||||||
| chr16:28564763 | GTATATAT others(11): Show |
G | 1 | a0001c0001t0001g0229 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-16+10673_-16+1069 others(22): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564763 | ||||||
| chr16:28564765 | A | ACATATAT others(3): Show |
1 | a0001c0005t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-16+10668_-16+1066 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564765 | |||||||
| chr16:28564765 | A | ACATATAT others(3): Show |
49 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(46): Show |
53 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-16+10668_-16+1066 others(14): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564765 | |||||||
| chr16:28564768 | TATATGTA others(17): Show |
T | 1 | a0001c0001t0001g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-16+10673_-16+1069 others(28): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564768 | ||||||
| chr16:28564773 | GTA | G | 51 | a0001c0001t0001g0123 a0001c0001t0001g0231 a0001c0001t0001g0234 others(48): Show |
59 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.-16+10689_-16+1069 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564773 | ||||||
| chr16:28564773 | GTATA | G | 21 | a0001c0001t0002g0026 a0001c0001t0002g0106 a0001c0001t0002g0276 others(18): Show |
22 | HG01106.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-16+10687_-16+1069 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564773 | ||||||
| chr16:28564775 | A | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-16+10678A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564775 | |||||||
| chr16:28564777 | A | ATATATAC others(27): Show |
6 | a0001c0001t0002g0063 a0001c0001t0002g0065 a0001c0001t0002g0074 others(3): Show |
6 | HG02135.hp1 HG02523.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.-16+10686_-16+1068 others(38): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | ||||||
| chr16:28564777 | A | ATATATG | 49 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(46): Show |
53 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.-16+10685_-16+1068 others(10): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | ||||||
| chr16:28564777 | A | ATATGTAT others(45): Show |
2 | a0001c0001t0002g0069 a0001c0001t0002g0082 |
2 | HG01255.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.-16+10683_-16+1068 others(56): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28564777 | ||||||
| chr16:28564777 | A | G | 1 | a0001c0002t0002g0042 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-16+10680A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564777 | |||||||
| chr16:28564782 | T | C | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10685T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564782 | |||||||
| chr16:28564783 | A | G | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10686A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564783 | |||||||
| chr16:28564784 | T | C | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+10687T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564784 | |||||||
| chr16:28564786 | T | C | 24 | a0001c0001t0001g0020 a0001c0001t0001g0115 a0001c0001t0001g0118 others(21): Show |
29 | HG00099.hp1 HG00738.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.-16+10689T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564786 | |||||||
| chr16:28564788 | C | T | 2 | a0001c0001t0001g0151 a0001c0001t0002g0294 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-16+10691C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564788 | |||||||
| chr16:28564790 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10693C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564790 | |||||||
| chr16:28564792 | C | T | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-16+10695C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564792 | |||||||
| chr16:28564806 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10709C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564806 | |||||||
| chr16:28564807 | A | C | 1 | a0001c0001t0001g0131 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-16+10710A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564807 | |||||||
| chr16:28564808 | A | C | 1 | a0001c0001t0002g0281 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-16+10711A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564808 | |||||||
| chr16:28564824 | T | C | 3 | a0001c0001t0002g0277 a0001c0001t0002g0278 a0001c0001t0002g0282 |
3 | HG02257.hp1 HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-16+10727T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564824 | |||||||
| chr16:28564880 | T | C | 8 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0269 others(5): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+10783T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564880 | |||||||
| chr16:28564921 | T | C | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-16+10824T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28564921 | |||||||
| chr16:28565048 | G | A | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-16+10951G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565048 | |||||||
| chr16:28565099 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+11002A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565099 | |||||||
| chr16:28565116 | C | T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0176 |
2 | HG01496.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-16+11019C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565116 | |||||||
| chr16:28565186 | C | T | 16 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0117 others(13): Show |
18 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.-16+11089C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565186 | |||||||
| chr16:28565260 | C | A | 1 | a0001c0001t0002g0026 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-16+11163C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565260 | |||||||
| chr16:28565397 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-16+11300G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565397 | |||||||
| chr16:28565575 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-16+11478G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565575 | |||||||
| chr16:28565585 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-16+11488C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565585 | |||||||
| chr16:28565733 | C | T | 4 | a0001c0001t0002g0297 a0001c0002t0002g0027 a0001c0002t0002g0298 others(1): Show |
5 | HG00099.hp1 HG02155.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-16+11636C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565733 | |||||||
| chr16:28565769 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.-16+11672G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565769 | |||||||
| chr16:28565995 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-16+11898C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28565995 | |||||||
| chr16:28566089 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0245 |
2 | HG00558.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-16+11992C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566089 | |||||||
| chr16:28566149 | C | T | 1 | a0001c0001t0002g0287 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-16+12052C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566149 | |||||||
| chr16:28566158 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-16+12061C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566158 | |||||||
| chr16:28566273 | C | CA | 6 | a0001c0001t0001g0242 a0001c0001t0001g0245 a0001c0001t0002g0297 others(3): Show |
7 | HG00099.hp1 HG00558.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.-16+12187dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28566273 | ||||||
| chr16:28566279 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-16+12182A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566279 | |||||||
| chr16:28566610 | T | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(76): Show |
101 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.-16+12513T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566610 | |||||||
| chr16:28566641 | C | T | 8 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0269 others(5): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-16+12544C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566641 | |||||||
| chr16:28566813 | G | A | 1 | a0001c0003t0002g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-16+12716G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566813 | |||||||
| chr16:28566959 | C | T | 1 | a0001c0001t0001g0206 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-16+12862C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566959 | |||||||
| chr16:28566999 | T | G | 18 | a0001c0001t0002g0026 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16+12902T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28566999 | |||||||
| chr16:28567510 | CT | C | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-16+13414delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28567510 | |||||||
| chr16:28567761 | A | C | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-13294A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28567761 | |||||||
| chr16:28568146 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15-12909C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568146 | |||||||
| chr16:28568186 | G | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-12869G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568186 | |||||||
| chr16:28568313 | C | CA | 142 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0023 others(139): Show |
160 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-15-12718dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | ||||||
| chr16:28568313 | C | CAA | 7 | a0001c0001t0001g0123 a0001c0001t0001g0166 a0001c0001t0002g0059 others(4): Show |
7 | HG01099.hp1 HG02135.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.-15-12719_-15-1271 others(6): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | ||||||
| chr16:28568313 | CA | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0130 a0001c0001t0001g0135 others(4): Show |
8 | HG01167.hp1 HG01243.hp1 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-12718delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568313 | ||||||
| chr16:28568515 | AT | A | 16 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(13): Show |
17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-12538delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568515 | ||||||
| chr16:28568594 | GT | G | 94 | a0001c0001t0001g0142 a0001c0001t0002g0003 a0001c0001t0002g0012 others(91): Show |
101 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.-15-12459delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568594 | ||||||
| chr16:28568596 | T | G | 51 | a0001c0001t0001g0123 a0001c0001t0001g0231 a0001c0001t0001g0234 others(48): Show |
61 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-15-12459T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568596 | |||||||
| chr16:28568597 | G | C | 8 | a0001c0001t0002g0273 a0001c0002t0002g0004 a0001c0002t0002g0269 others(5): Show |
11 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.-15-12458G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568597 | |||||||
| chr16:28568619 | A | C | 1 | a0001c0001t0002g0080 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-15-12436A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568619 | |||||||
| chr16:28568710 | C | T | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-12345C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568710 | |||||||
| chr16:28568919 | G | GA | 43 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0002g0063 others(40): Show |
54 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-15-12124dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28568919 | ||||||
| chr16:28568949 | G | A | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-15-12106G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568949 | |||||||
| chr16:28568956 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-12099C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28568956 | |||||||
| chr16:28569012 | T | C | 142 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0231 others(139): Show |
159 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(156): Show |
intron_variant | MODIFIER | c.-15-12043T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569012 | |||||||
| chr16:28569123 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0058 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-15-11932T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569123 | |||||||
| chr16:28569247 | T | C | 1 | a0001c0001t0002g0076 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-15-11808T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569247 | |||||||
| chr16:28569277 | A | G | 5 | a0001c0001t0001g0181 a0001c0001t0001g0240 a0001c0001t0001g0241 others(2): Show |
5 | NA18961.hp2 NA18971.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-11778A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569277 | |||||||
| chr16:28569364 | A | G | 56 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(53): Show |
60 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-15-11691A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569364 | |||||||
| chr16:28569393 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-11662C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569393 | |||||||
| chr16:28569428 | G | A | 1 | a0001c0002t0002g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-15-11627G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569428 | |||||||
| chr16:28569508 | C | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-15-11547C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569508 | |||||||
| chr16:28569562 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-15-11493G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569562 | |||||||
| chr16:28569652 | A | G | 1 | a0001c0001t0002g0069 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-15-11403A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569652 | |||||||
| chr16:28569717 | G | C | 56 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(53): Show |
60 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-15-11338G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569717 | |||||||
| chr16:28569751 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-15-11304A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569751 | |||||||
| chr16:28569917 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-15-11138C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28569917 | |||||||
| chr16:28570390 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0133 a0001c0001t0001g0141 others(1): Show |
5 | NA18966.hp1 NA18991.hp1 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-10665T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570390 | |||||||
| chr16:28570406 | A | G | 3 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0257 |
5 | HG01074.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-15-10649A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570406 | |||||||
| chr16:28570419 | C | T | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-10636C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570419 | |||||||
| chr16:28570544 | T | TTTTA | 53 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0021 others(50): Show |
64 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15-10466_-15-1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | T | TTTTATTT others(1): Show |
17 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0157 others(14): Show |
17 | HG00408.hp1 HG01081.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-10470_-15-1046 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | TTTTA | T | 85 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0023 others(82): Show |
91 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.-15-10466_-15-1046 others(8): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | TTTTATTT others(1): Show |
T | 8 | a0001c0001t0001g0124 a0001c0001t0001g0137 a0001c0001t0001g0152 others(5): Show |
8 | HG02129.hp2 NA18906.hp1 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-10470_-15-1046 others(12): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | TTTTATTT others(5): Show |
T | 18 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(15): Show |
19 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.-15-10474_-15-1046 others(16): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | TTTTATTT others(9): Show |
T | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-15-10478_-15-1046 others(20): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570544 | TTTTATTT others(13): Show |
T | 33 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0231 others(30): Show |
40 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.-15-10482_-15-1046 others(24): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28570544 | ||||||
| chr16:28570780 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-15-10275G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570780 | |||||||
| chr16:28570821 | G | T | 125 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(122): Show |
151 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.-15-10234G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28570821 | |||||||
| chr16:28571216 | C | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-9839C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571216 | |||||||
| chr16:28571528 | A | G | 143 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0132 others(140): Show |
160 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(157): Show |
intron_variant | MODIFIER | c.-15-9527A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571528 | |||||||
| chr16:28571591 | T | TA | 32 | a0001c0001t0001g0124 a0001c0001t0001g0128 a0001c0001t0001g0153 others(29): Show |
33 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.-15-9446dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | ||||||
| chr16:28571591 | T | TAA | 56 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(53): Show |
64 | HG00099.hp1 HG00642.hp2 HG00741.hp1 others(61): Show |
intron_variant | MODIFIER | c.-15-9447_-15-9446d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | ||||||
| chr16:28571591 | T | TAAA | 40 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0001t0002g0063 others(37): Show |
47 | HG00280.hp2 HG00438.hp2 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-15-9448_-15-9446d others(5): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28571591 | ||||||
| chr16:28571620 | C | A | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-9435C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571620 | |||||||
| chr16:28571685 | C | T | 1 | a0001c0001t0002g0065 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-15-9370C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571685 | |||||||
| chr16:28571817 | T | C | 1 | a0001c0002t0003g0036 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-15-9238T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571817 | |||||||
| chr16:28571894 | G | A | 19 | a0001c0001t0005g0109 a0001c0001t0005g0110 a0001c0003t0001g0170 others(16): Show |
20 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.-15-9161G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571894 | |||||||
| chr16:28571926 | A | C | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-9129A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28571926 | |||||||
| chr16:28572041 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-9014A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572041 | |||||||
| chr16:28572268 | G | A | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-8787G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572268 | |||||||
| chr16:28572289 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-8766C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572289 | |||||||
| chr16:28572377 | C | A | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-15-8678C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572377 | |||||||
| chr16:28572377 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-15-8678C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572377 | |||||||
| chr16:28572416 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0002g0047 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-15-8639C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572416 | |||||||
| chr16:28572520 | C | T | 1 | a0001c0003t0002g0220 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-15-8535C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572520 | |||||||
| chr16:28572544 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-8511C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572544 | |||||||
| chr16:28572547 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-15-8508G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572547 | |||||||
| chr16:28572561 | G | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-8494G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572561 | |||||||
| chr16:28572665 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-15-8390G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572665 | |||||||
| chr16:28572779 | G | A | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-8276G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572779 | |||||||
| chr16:28572824 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-15-8231G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572824 | |||||||
| chr16:28572827 | G | T | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-8228G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572827 | |||||||
| chr16:28572869 | T | C | 1 | a0001c0001t0002g0106 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-15-8186T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572869 | |||||||
| chr16:28572870 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-8185T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572870 | |||||||
| chr16:28572891 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15-8164A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572891 | |||||||
| chr16:28572912 | C | T | 8 | a0001c0001t0002g0062 a0001c0001t0002g0067 a0001c0001t0002g0077 others(5): Show |
8 | HG02015.hp1 HG02129.hp2 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.-15-8143C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28572912 | |||||||
| chr16:28573057 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0122 |
3 | HG01891.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-15-7998A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573057 | |||||||
| chr16:28573212 | G | A | 1 | a0001c0001t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-15-7843G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573212 | |||||||
| chr16:28573241 | C | G | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-7814C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573241 | |||||||
| chr16:28573357 | G | A | 1 | a0001c0001t0004g0290 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-15-7698G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573357 | |||||||
| chr16:28573616 | G | A | 17 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(14): Show |
18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.-15-7439G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573616 | |||||||
| chr16:28573724 | A | G | 3 | a0001c0001t0002g0283 a0001c0001t0002g0296 a0001c0001t0002g0300 |
3 | HG02258.hp1 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-15-7331A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573724 | |||||||
| chr16:28573898 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-7157C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28573898 | |||||||
| chr16:28574300 | T | C | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-6755T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574300 | |||||||
| chr16:28574315 | C | T | 78 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(75): Show |
83 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.-15-6740C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574315 | |||||||
| chr16:28574376 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-15-6679G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574376 | |||||||
| chr16:28574474 | G | A | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-15-6581G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574474 | |||||||
| chr16:28574500 | A | G | 3 | a0001c0003t0002g0210 a0001c0003t0002g0211 a0001c0003t0002g0212 |
3 | HG02109.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-15-6555A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574500 | |||||||
| chr16:28574611 | T | C | 8 | a0001c0001t0002g0297 a0001c0002t0002g0004 a0001c0002t0002g0269 others(5): Show |
11 | HG01109.hp1 HG01884.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-6444T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574611 | |||||||
| chr16:28574683 | G | A | 1 | a0001c0002t0003g0040 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-15-6372G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574683 | |||||||
| chr16:28574735 | T | G | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-6320T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574735 | |||||||
| chr16:28574784 | G | C | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-6271G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574784 | |||||||
| chr16:28574806 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-6249T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28574806 | |||||||
| chr16:28575546 | T | C | 2 | a0001c0001t0002g0276 a0001c0001t0002g0289 |
2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-15-5509T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575546 | |||||||
| chr16:28575652 | T | C | 1 | a0001c0002t0002g0042 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-15-5403T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575652 | |||||||
| chr16:28575844 | C | T | 3 | a0001c0001t0002g0079 a0001c0001t0002g0086 a0001c0001t0002g0101 |
3 | HG01168.hp1 HG01169.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-15-5211C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575844 | |||||||
| chr16:28575994 | T | C | 3 | a0001c0001t0001g0144 a0001c0001t0001g0187 a0001c0001t0001g0197 |
3 | HG01070.hp1 HG01109.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-15-5061T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28575994 | |||||||
| chr16:28576068 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-4987T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576068 | |||||||
| chr16:28576070 | G | A | 1 | a0001c0001t0002g0273 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-15-4985G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576070 | |||||||
| chr16:28576163 | TA | T | 18 | a0001c0001t0002g0026 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-4884delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28576163 | ||||||
| chr16:28576276 | G | T | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-4779G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576276 | |||||||
| chr16:28576277 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-4778C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576277 | |||||||
| chr16:28576327 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-15-4728A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576327 | |||||||
| chr16:28576346 | A | T | 18 | a0001c0001t0002g0026 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.-15-4709A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576346 | |||||||
| chr16:28576470 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-15-4585G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576470 | |||||||
| chr16:28576728 | A | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-4327A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576728 | |||||||
| chr16:28576738 | C | G | 10 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(7): Show |
13 | HG02698.hp1 HG02738.hp1 HG03017.hp1 others(10): Show |
intron_variant | MODIFIER | c.-15-4317C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576738 | |||||||
| chr16:28576795 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0002g0047 |
2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-15-4260C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576795 | |||||||
| chr16:28576995 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0195 |
2 | HG06807.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-15-4060G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28576995 | |||||||
| chr16:28577073 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15-3982C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577073 | |||||||
| chr16:28577074 | A | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-15-3981A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577074 | |||||||
| chr16:28577107 | G | A | 5 | a0001c0001t0001g0023 a0001c0001t0001g0203 a0001c0001t0001g0204 others(2): Show |
6 | HG02895.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.-15-3948G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577107 | |||||||
| chr16:28577122 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-3933C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577122 | |||||||
| chr16:28577350 | C | CA | 9 | a0001c0001t0002g0062 a0001c0001t0002g0067 a0001c0001t0002g0077 others(6): Show |
9 | HG02015.hp1 HG02055.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.-15-3693dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28577350 | ||||||
| chr16:28577414 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-15-3641C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577414 | |||||||
| chr16:28577662 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-15-3393A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577662 | |||||||
| chr16:28577759 | A | C | 1 | a0001c0001t0001g0164 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-15-3296A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577759 | |||||||
| chr16:28577846 | T | G | 1 | a0001c0001t0002g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-15-3209T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28577846 | |||||||
| chr16:28578052 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-15-3003G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578052 | |||||||
| chr16:28578078 | C | A | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-15-2977C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578078 | |||||||
| chr16:28578134 | G | A | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.-15-2921G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578134 | |||||||
| chr16:28578331 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0156 a0001c0001t0001g0179 |
4 | HG02698.hp1 HG03017.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-2724C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578331 | |||||||
| chr16:28578398 | A | G | 16 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(13): Show |
17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.-15-2657A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578398 | |||||||
| chr16:28578637 | G | A | 1 | a0001c0002t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-15-2418G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578637 | |||||||
| chr16:28578684 | TA | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(270): Show |
317 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.-15-2353delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28578684 | ||||||
| chr16:28578684 | TAA | T | 16 | a0001c0001t0001g0116 a0001c0001t0001g0127 a0001c0001t0001g0150 others(13): Show |
16 | HG01070.hp2 HG01168.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-2354_-15-2353d others(4): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28578684 | ||||||
| chr16:28578688 | A | G | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.-15-2367A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578688 | |||||||
| chr16:28578709 | G | A | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-2346G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578709 | |||||||
| chr16:28578786 | C | G | 2 | a0001c0002t0002g0037 a0001c0002t0002g0043 |
2 | HG02132.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-15-2269C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578786 | |||||||
| chr16:28578836 | G | A | 3 | a0001c0003t0002g0213 a0001c0003t0002g0215 a0001c0003t0002g0222 |
3 | HG00642.hp1 HG03669.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-15-2219G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28578836 | |||||||
| chr16:28579087 | T | A | 1 | a0001c0002t0003g0031 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-15-1968T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579087 | |||||||
| chr16:28579197 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-15-1858C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579197 | |||||||
| chr16:28579257 | C | CT | 11 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0001t0001g0192 others(8): Show |
11 | HG01175.hp2 HG01978.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-15-1779dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28579257 | ||||||
| chr16:28579257 | CT | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0145 a0001c0001t0001g0250 others(4): Show |
8 | HG00741.hp2 HG01081.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.-15-1779delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28579257 | ||||||
| chr16:28579259 | T | C | 1 | a0001c0005t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15-1796T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579259 | |||||||
| chr16:28579272 | T | G | 1 | a0001c0005t0002g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-15-1783T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579272 | |||||||
| chr16:28579281 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-15-1774C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579281 | |||||||
| chr16:28579508 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-15-1547G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579508 | |||||||
| chr16:28579541 | C | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.-15-1514C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579541 | |||||||
| chr16:28579657 | G | A | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-1398G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579657 | |||||||
| chr16:28579668 | C | T | 56 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0055 others(53): Show |
60 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.-15-1387C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579668 | |||||||
| chr16:28579887 | C | T | 6 | a0001c0001t0002g0065 a0001c0001t0002g0074 a0001c0001t0002g0091 others(3): Show |
6 | HG02135.hp1 HG02523.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.-15-1168C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28579887 | |||||||
| chr16:28580091 | A | G | 1 | a0001c0002t0002g0272 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-15-964A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580091 | |||||||
| chr16:28580119 | G | A | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15-936G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580119 | |||||||
| chr16:28580209 | G | A | 55 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0004 others(52): Show |
66 | HG00438.hp2 HG00609.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.-15-846G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580209 | |||||||
| chr16:28580258 | G | A | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-797G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580258 | |||||||
| chr16:28580425 | C | G | 1 | a0001c0001t0002g0294 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-15-630C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580425 | |||||||
| chr16:28580434 | G | A | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-621G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580434 | |||||||
| chr16:28580438 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0007g0202 |
2 | HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-15-617G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580438 | |||||||
| chr16:28580446 | G | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.-15-609G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580446 | |||||||
| chr16:28580510 | T | TC | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.-15-543dupC | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr16 | 28580510 | ||||||
| chr16:28580523 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-15-532G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580523 | |||||||
| chr16:28580664 | A | G | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-15-391A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580664 | |||||||
| chr16:28580785 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-15-270G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580785 | |||||||
| chr16:28580806 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-15-249C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 1/9 | chr16 | 28580806 | |||||||
| chr16:28581386 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.75+242A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581386 | |||||||
| chr16:28581388 | C | T | 2 | a0001c0001t0001g0117 a0001c0001t0001g0166 |
2 | HG00544.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.75+244C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581388 | |||||||
| chr16:28581523 | C | G | 1 | a0001c0001t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.75+379C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581523 | |||||||
| chr16:28581568 | C | T | 7 | a0001c0001t0001g0230 a0001c0001t0001g0233 a0001c0001t0001g0237 others(4): Show |
7 | HG01358.hp2 HG02074.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.75+424C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581568 | |||||||
| chr16:28581599 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.75+455G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581599 | |||||||
| chr16:28581626 | C | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0208 |
3 | NA18942.hp2 NA18955.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.75+482C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581626 | |||||||
| chr16:28581630 | G | T | 1 | a0001c0001t0001g0123 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.75+486G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581630 | |||||||
| chr16:28581810 | T | G | 31 | a0001c0001t0001g0231 a0001c0001t0001g0234 a0001c0002t0002g0006 others(28): Show |
38 | HG00438.hp2 HG00609.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.75+666T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581810 | |||||||
| chr16:28581876 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.75+732G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581876 | |||||||
| chr16:28581918 | C | CA | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
86 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.75+787dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28581918 | ||||||
| chr16:28581995 | T | C | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.75+851T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28581995 | |||||||
| chr16:28582026 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.75+882T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582026 | |||||||
| chr16:28582027 | G | A | 18 | a0001c0001t0002g0026 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.75+883G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582027 | |||||||
| chr16:28582172 | A | G | 3 | a0001c0001t0001g0137 a0001c0001t0001g0158 a0001c0001t0001g0208 |
3 | NA18942.hp2 NA18955.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.75+1028A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582172 | |||||||
| chr16:28582276 | G | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(77): Show |
85 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.75+1132G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582276 | |||||||
| chr16:28582295 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.75+1151C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582295 | |||||||
| chr16:28582373 | C | T | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.75+1229C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582373 | |||||||
| chr16:28582376 | T | C | 1 | a0001c0001t0001g0124 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.75+1232T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582376 | |||||||
| chr16:28582379 | T | TG | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.75+1241dupG | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28582379 | ||||||
| chr16:28582380 | G | T | 2 | a0001c0001t0001g0261 a0001c0001t0001g0262 |
2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.75+1236G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582380 | |||||||
| chr16:28582681 | T | C | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.75+1537T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582681 | |||||||
| chr16:28582900 | A | C | 1 | a0001c0001t0002g0293 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.75+1756A>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582900 | |||||||
| chr16:28582914 | G | A | 3 | a0001c0001t0001g0144 a0001c0001t0001g0187 a0001c0001t0001g0197 |
3 | HG01070.hp1 HG01109.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.75+1770G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582914 | |||||||
| chr16:28582916 | CAA | C | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0122 |
3 | HG01891.hp2 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.75+1773_75+1774del others(2): Show |
SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28582916 | |||||||
| chr16:28583023 | A | G | 7 | a0001c0001t0001g0018 a0001c0001t0001g0117 a0001c0001t0001g0138 others(4): Show |
8 | HG00438.hp1 HG00544.hp1 HG00597.hp2 others(5): Show |
intron_variant | MODIFIER | c.75+1879A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583023 | |||||||
| chr16:28583107 | C | T | 2 | a0001c0001t0002g0283 a0001c0001t0002g0300 |
2 | HG02258.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.76-1806C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583107 | |||||||
| chr16:28583228 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.76-1685A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583228 | |||||||
| chr16:28583362 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.76-1551G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583362 | |||||||
| chr16:28583390 | C | G | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-1523C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583390 | |||||||
| chr16:28583390 | C | T | 16 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(13): Show |
17 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.76-1523C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583390 | |||||||
| chr16:28583443 | A | G | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.76-1470A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28583443 | |||||||
| chr16:28584028 | C | CT | 7 | a0001c0002t0002g0004 a0001c0002t0002g0270 a0001c0002t0002g0271 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-869dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584028 | ||||||
| chr16:28584028 | CT | C | 10 | a0001c0001t0001g0133 a0001c0001t0001g0152 a0001c0001t0001g0174 others(7): Show |
10 | HG01169.hp1 HG01515.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-869delT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584028 | ||||||
| chr16:28584101 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.76-812C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584101 | |||||||
| chr16:28584133 | C | T | 1 | a0001c0002t0003g0034 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.76-780C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584133 | |||||||
| chr16:28584188 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.76-725A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584188 | |||||||
| chr16:28584379 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.76-534A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584379 | |||||||
| chr16:28584382 | C | T | 1 | a0001c0003t0002g0212 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.76-531C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584382 | |||||||
| chr16:28584489 | C | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.76-424C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584489 | |||||||
| chr16:28584515 | C | T | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.76-398C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584515 | |||||||
| chr16:28584616 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.76-297C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584616 | |||||||
| chr16:28584621 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.76-292C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584621 | |||||||
| chr16:28584668 | A | G | 4 | a0001c0001t0001g0125 a0001c0001t0001g0146 a0001c0001t0001g0168 others(1): Show |
4 | HG02602.hp1 HG02683.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-245A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | chr16 | 28584668 | |||||||
| chr16:28584788 | CA | C | 51 | a0001c0001t0001g0205 a0001c0001t0001g0228 a0001c0001t0002g0003 others(48): Show |
55 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.76-106delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584788 | ||||||
| chr16:28584788 | CAA | C | 29 | a0001c0001t0002g0026 a0001c0001t0002g0058 a0001c0001t0002g0062 others(26): Show |
30 | HG01070.hp2 HG01106.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.76-107_76-106delAA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr16 | 28584788 | ||||||
| chr16:28585053 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.151+65G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585053 | |||||||
| chr16:28585383 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.152-265G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585383 | |||||||
| chr16:28585409 | A | T | 5 | a0001c0002t0002g0004 a0001c0002t0002g0270 a0001c0002t0002g0271 others(2): Show |
8 | HG01109.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.152-239A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585409 | |||||||
| chr16:28585563 | G | A | 17 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(14): Show |
18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.152-85G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 3/9 | chr16 | 28585563 | |||||||
| chr16:28585765 | G | A | 1 | a0001c0001t0002g0055 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.224+45G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585765 | |||||||
| chr16:28585775 | T | G | 1 | a0001c0001t0002g0071 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.224+55T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585775 | |||||||
| chr16:28585847 | T | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0195 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+127T>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585847 | |||||||
| chr16:28585848 | C | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0195 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.224+128C>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585848 | |||||||
| chr16:28585944 | A | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(2): Show |
5 | HG01891.hp2 HG03225.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.224+224A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28585944 | |||||||
| chr16:28586506 | C | CA | 6 | a0001c0001t0001g0140 a0001c0001t0001g0223 a0001c0001t0001g0235 others(3): Show |
6 | HG02056.hp1 NA18950.hp2 NA18967.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+802dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28586506 | ||||||
| chr16:28586506 | CA | C | 32 | a0001c0001t0001g0188 a0001c0002t0002g0006 a0001c0002t0002g0009 others(29): Show |
40 | HG00099.hp1 HG00609.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.224+802delA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28586506 | ||||||
| chr16:28586618 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.224+898C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28586618 | |||||||
| chr16:28586653 | T | G | 1 | a0001c0002t0002g0269 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.224+933T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28586653 | |||||||
| chr16:28587011 | T | G | 1 | a0001c0002t0002g0299 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.224+1291T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587011 | |||||||
| chr16:28587083 | C | G | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.224+1363C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587083 | |||||||
| chr16:28587657 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.225-1443T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587657 | |||||||
| chr16:28587749 | C | T | 3 | a0001c0001t0004g0290 a0001c0001t0004g0291 a0001c0001t0004g0292 |
3 | HG01884.hp1 HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.225-1351C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587749 | |||||||
| chr16:28587799 | G | A | 2 | a0001c0001t0005g0109 a0001c0001t0005g0110 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.225-1301G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587799 | |||||||
| chr16:28587878 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.225-1222C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587878 | |||||||
| chr16:28587949 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.225-1151G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28587949 | |||||||
| chr16:28588090 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(80): Show |
89 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.225-1010A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588090 | |||||||
| chr16:28588639 | A | G | 1 | a0001c0001t0002g0084 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.225-461A>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588639 | |||||||
| chr16:28588681 | C | CA | 37 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(34): Show |
47 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.225-418dupA | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28588681 | ||||||
| chr16:28588695 | G | C | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-405G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588695 | |||||||
| chr16:28588700 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0168 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.225-400G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588700 | |||||||
| chr16:28588720 | G | A | 7 | a0001c0002t0002g0004 a0001c0002t0002g0269 a0001c0002t0002g0270 others(4): Show |
10 | HG01109.hp1 HG01884.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.225-380G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588720 | |||||||
| chr16:28588770 | C | T | 79 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(76): Show |
84 | HG00280.hp2 HG00639.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.225-330C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588770 | |||||||
| chr16:28588880 | G | GT | 82 | a0001c0001t0002g0003 a0001c0001t0002g0012 a0001c0001t0002g0026 others(79): Show |
88 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.225-217dupT | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr16 | 28588880 | ||||||
| chr16:28588956 | C | T | 37 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(34): Show |
47 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.225-144C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588956 | |||||||
| chr16:28588961 | G | T | 9 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0214 others(6): Show |
10 | HG00738.hp2 HG01106.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.225-139G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28588961 | |||||||
| chr16:28589060 | C | T | 18 | a0001c0001t0002g0026 a0001c0001t0002g0276 a0001c0001t0002g0277 others(15): Show |
19 | HG01106.hp1 HG01891.hp1 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.225-40C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589060 | |||||||
| chr16:28589061 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.225-39G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589061 | |||||||
| chr16:28589067 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.225-33C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 4/9 | chr16 | 28589067 | |||||||
| chr16:28589194 | C | G | 1 | a0001c0002t0003g0033 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.289+30C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589194 | |||||||
| chr16:28589222 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.289+58C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589222 | |||||||
| chr16:28589351 | G | A | 1 | a0001c0002t0002g0274 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.289+187G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589351 | |||||||
| chr16:28589436 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG02717.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.289+272C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589436 | |||||||
| chr16:28589483 | T | C | 1 | a0001c0002t0002g0051 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.289+319T>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589483 | |||||||
| chr16:28589699 | G | T | 1 | a0001c0001t0002g0297 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.290-397G>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589699 | |||||||
| chr16:28589865 | G | C | 17 | a0001c0003t0001g0170 a0001c0003t0002g0024 a0001c0003t0002g0210 others(14): Show |
18 | HG00642.hp1 HG00738.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.290-231G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589865 | |||||||
| chr16:28589935 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.290-161G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 5/9 | chr16 | 28589935 | |||||||
| chr16:28590242 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.419+17C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 6/9 | chr16 | 28590242 | |||||||
| chr16:28590278 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.420-18C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 6/9 | chr16 | 28590278 | |||||||
| chr16:28590481 | G | A | 36 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0009 others(33): Show |
46 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.566+39G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 7/9 | chr16 | 28590481 | |||||||
| chr16:28590491 | G | A | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.566+49G>A | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 7/9 | chr16 | 28590491 | |||||||
| chr16:28591128 | T | G | 30 | a0001c0002t0002g0006 a0001c0002t0002g0009 a0001c0002t0002g0010 others(27): Show |
37 | HG00609.hp1 HG00735.hp1 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.765+193T>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591128 | |||||||
| chr16:28591162 | G | C | 3 | a0001c0002t0002g0027 a0001c0002t0002g0298 a0001c0002t0002g0299 |
4 | HG00099.hp1 HG02155.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.765+227G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591162 | |||||||
| chr16:28591366 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.766-224C>G | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591366 | |||||||
| chr16:28591367 | C | T | 1 | a0001c0006t0002g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.766-223C>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591367 | |||||||
| chr16:28591429 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.766-161A>T | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591429 | |||||||
| chr16:28591518 | G | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02559.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.766-72G>C | SGF29 | ENSG00000176476.9 | transcript | ENST00000317058.8 | protein_coding | 9/9 | chr16 | 28591518 |