Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 307 |
| ensemblid | ENSG00000196975.16 |
| hgncid | 542 |
| symbol | ANXA4 |
| name | annexin A4 |
| refseq_nuc | NM_001153.5 |
| refseq_prot | NP_001144.1 |
| ensembl_nuc | ENST00000394295.6 |
| ensembl_prot | ENSP00000377833.4 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 69742134 |
| end | 69827112 |
| strand | + |
| ver | v1.2 |
| region | chr2:69742134-69827112 |
| region5000 | chr2:69737134-69832112 |
| regionname0 | ANXA4_chr2_69742134_69827112 |
| regionname5000 | ANXA4_chr2_69737134_69832112 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 321 | 217 | 38 | 30 | 111 | 10 | 26 | 81 | ANXA4_chr2_69737134_69832112 | ANXA4 | MAMAT others(316): Show |
chr2 | 69737134 | 69832112 |
| a0002 | 0/0 | 321 | 75 | 25 | 15 | 29 | 2 | 4 | 26 | ANXA4_chr2_69737134_69832112 | ANXA4 | MAMAT others(316): Show |
chr2 | 69737134 | 69832112 |
| a0003 | 0/0 | 321 | 49 | 12 | 21 | 16 | 0 | 0 | 13 | ANXA4_chr2_69737134_69832112 | ANXA4 | MAMAT others(316): Show |
chr2 | 69737134 | 69832112 |
| a0004 | 0/0 | 321 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | MAMAT others(316): Show |
chr2 | 69737134 | 69832112 |
| a0005 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | MAMAT others(316): Show |
chr2 | 69737134 | 69832112 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 963 | 216 | 37 | 30 | 111 | 10 | 26 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 | ||
| a0001c0006 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 | ||
| a0002c0002 | 0/0 | 963 | 75 | 25 | 15 | 29 | 2 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 | ||
| a0003c0003 | 0/0 | 963 | 49 | 12 | 21 | 16 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 | ||
| a0004c0004 | 0/0 | 963 | 4 | 4 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 | ||
| a0005c0005 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | ATGGC others(958): Show |
chr2 | 69737134 | 69832112 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2651 | 79 | 3 | 14 | 47 | 5 | 9 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0002 | 0/0 | 2651 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0003 | 0/1 | 2652 | 56 | 1 | 7 | 37 | 3 | 7 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0004 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2644): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0005 | 0/0 | 2652 | 31 | 7 | 0 | 20 | 0 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0006 | 0/0 | 2650 | 18 | 17 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2645): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0007 | 0/0 | 2651 | 13 | 4 | 2 | 1 | 1 | 5 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0008 | 0/0 | 2651 | 4 | 0 | 1 | 3 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0009 | 0/0 | 2651 | 2 | 1 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0011 | 0/0 | 2650 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2645): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0012 | 0/0 | 2652 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0014 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0015 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2645): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0017 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0018 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0019 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0020 | 0/0 | 2652 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0001c0001t0021 | 0/0 | 2650 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2645): Show |
chr2 | 69737134 | 69832112 |
| a0001c0006t0006 | 0/0 | 2650 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2645): Show |
chr2 | 69737134 | 69832112 |
| a0002c0002t0001 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0002c0002t0002 | 0/0 | 2651 | 70 | 21 | 15 | 29 | 1 | 4 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0002c0002t0004 | 0/0 | 2649 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2644): Show |
chr2 | 69737134 | 69832112 |
| a0002c0002t0010 | 0/0 | 2646 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2641): Show |
chr2 | 69737134 | 69832112 |
| a0002c0002t0013 | 0/0 | 2646 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2641): Show |
chr2 | 69737134 | 69832112 |
| a0003c0003t0002 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0003c0003t0004 | 0/0 | 2649 | 46 | 10 | 21 | 15 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2644): Show |
chr2 | 69737134 | 69832112 |
| a0003c0003t0016 | 0/0 | 2649 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2644): Show |
chr2 | 69737134 | 69832112 |
| a0004c0004t0005 | 0/0 | 2652 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2647): Show |
chr2 | 69737134 | 69832112 |
| a0004c0004t0007 | 0/0 | 2651 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| a0005c0005t0007 | 0/0 | 2651 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | GTGAC others(2646): Show |
chr2 | 69737134 | 69832112 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0009g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0009g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0011g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0011g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0012g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0014g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0015g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0017g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0018g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0019g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0020g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0001t0021g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0001c0006t0006g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0002g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0010g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0002c0002t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0004g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0003c0003t0016g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0005g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0005g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0004c0004t0007g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| a0005c0005t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0007 | g0305 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0045 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0155 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0262 | EUR | GBR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00323 | hp1 | a0001 | c0001 | t0019 | g0253 | EUR | FIN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0139 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00408 | hp2 | a0003 | c0003 | t0004 | g0188 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00423 | hp1 | a0003 | c0003 | t0004 | g0087 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0173 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0027 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00558 | hp2 | a0001 | c0001 | t0005 | g0175 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00642 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00673 | hp1 | a0001 | c0001 | t0005 | g0212 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00735 | hp2 | a0003 | c0003 | t0004 | g0003 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0058 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00738 | hp2 | a0003 | c0003 | t0004 | g0001 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01069 | hp1 | a0002 | c0002 | t0002 | g0059 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01069 | hp2 | a0001 | c0001 | t0009 | g0226 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0041 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0047 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01099 | hp2 | a0003 | c0003 | t0004 | g0066 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01106 | hp2 | a0003 | c0003 | t0004 | g0001 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0307 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01167 | hp1 | a0001 | c0001 | t0021 | g0126 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01167 | hp2 | a0001 | c0001 | t0007 | g0294 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01169 | hp1 | a0001 | c0001 | t0007 | g0302 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01169 | hp2 | a0001 | c0001 | t0015 | g0280 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01175 | hp1 | a0003 | c0003 | t0004 | g0037 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01192 | hp1 | a0003 | c0003 | t0004 | g0108 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0176 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0020 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01243 | hp2 | a0002 | c0002 | t0002 | g0130 | AMR | PUR | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0046 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01256 | hp2 | a0003 | c0003 | t0004 | g0185 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01257 | hp1 | a0003 | c0003 | t0004 | g0071 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01257 | hp2 | a0002 | c0002 | t0002 | g0083 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01258 | hp1 | a0003 | c0003 | t0004 | g0068 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01261 | hp1 | a0003 | c0003 | t0004 | g0064 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01346 | hp1 | a0003 | c0003 | t0004 | g0001 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0263 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01358 | hp1 | a0003 | c0003 | t0004 | g0073 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01361 | hp1 | a0003 | c0003 | t0004 | g0040 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01433 | hp1 | a0002 | c0002 | t0002 | g0203 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01433 | hp2 | a0002 | c0002 | t0002 | g0042 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0043 | AMR | CLM | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0229 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0119 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0161 | EUR | IBS | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0026 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0296 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01891 | hp1 | a0003 | c0003 | t0004 | g0103 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01891 | hp2 | a0002 | c0002 | t0002 | g0297 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01928 | hp1 | a0003 | c0003 | t0004 | g0052 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01952 | hp2 | a0003 | c0003 | t0004 | g0039 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01975 | hp2 | a0003 | c0003 | t0004 | g0065 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01978 | hp1 | a0003 | c0003 | t0004 | g0131 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG01981 | hp2 | a0003 | c0003 | t0004 | g0072 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02004 | hp1 | a0003 | c0003 | t0004 | g0038 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02004 | hp2 | a0001 | c0001 | t0008 | g0160 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0089 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02015 | hp2 | a0001 | c0001 | t0014 | g0157 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02027 | hp2 | a0001 | c0001 | t0020 | g0198 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02132 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02135 | hp1 | a0003 | c0003 | t0004 | g0094 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02135 | hp2 | a0001 | c0001 | t0017 | g0318 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02145 | hp1 | a0002 | c0002 | t0002 | g0111 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0231 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0317 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0165 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | CDX | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0314 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0015 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02258 | hp1 | a0001 | c0001 | t0006 | g0315 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0244 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02280 | hp1 | a0003 | c0003 | t0004 | g0311 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02280 | hp2 | a0001 | c0001 | t0011 | g0208 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02300 | hp1 | a0003 | c0003 | t0004 | g0070 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | PEL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02451 | hp1 | a0002 | c0002 | t0002 | g0010 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0129 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0149 | EAS | KHV | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02615 | hp1 | a0001 | c0001 | t0005 | g0195 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02615 | hp2 | a0001 | c0001 | t0006 | g0300 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02622 | hp1 | a0001 | c0001 | t0011 | g0128 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02622 | hp2 | a0002 | c0002 | t0002 | g0335 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02630 | hp1 | a0003 | c0003 | t0004 | g0295 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02630 | hp2 | a0005 | c0005 | t0007 | g0011 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02647 | hp1 | a0001 | c0001 | t0006 | g0301 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02647 | hp2 | a0002 | c0002 | t0002 | g0219 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02683 | hp2 | a0001 | c0001 | t0005 | g0304 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02717 | hp1 | a0003 | c0003 | t0004 | g0243 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02717 | hp2 | a0003 | c0003 | t0002 | g0104 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02809 | hp1 | a0004 | c0004 | t0005 | g0202 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02818 | hp1 | a0002 | c0002 | t0010 | g0023 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02818 | hp2 | a0001 | c0001 | t0007 | g0299 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02895 | hp1 | a0002 | c0002 | t0002 | g0110 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02895 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02896 | hp1 | a0004 | c0004 | t0005 | g0199 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0124 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02897 | hp1 | a0004 | c0004 | t0007 | g0200 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02897 | hp2 | a0002 | c0002 | t0002 | g0005 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02922 | hp1 | a0001 | c0001 | t0006 | g0025 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0312 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0014 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02965 | hp2 | a0003 | c0003 | t0004 | g0019 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02970 | hp1 | a0002 | c0002 | t0002 | g0016 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02970 | hp2 | a0001 | c0006 | t0006 | g0012 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02976 | hp1 | a0003 | c0003 | t0004 | g0017 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0114 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0008 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03017 | hp2 | a0001 | c0001 | t0007 | g0271 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0100 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0303 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0192 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03098 | hp2 | a0002 | c0002 | t0010 | g0216 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0194 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0143 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03195 | hp1 | a0002 | c0002 | t0013 | g0127 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03195 | hp2 | a0002 | c0002 | t0002 | g0113 | AFR | ESN | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0207 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03209 | hp2 | a0002 | c0002 | t0002 | g0306 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03225 | hp1 | a0003 | c0003 | t0002 | g0102 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03225 | hp2 | a0003 | c0003 | t0004 | g0105 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03453 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03453 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0191 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03486 | hp2 | a0002 | c0002 | t0002 | g0334 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0309 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0255 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0217 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03540 | hp2 | a0003 | c0003 | t0004 | g0109 | AFR | GWD | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03654 | hp1 | a0001 | c0001 | t0007 | g0276 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0106 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03704 | hp1 | a0001 | c0001 | t0005 | g0332 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0272 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0132 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0310 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0133 | SAS | BEB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0189 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0115 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0048 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0308 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0057 | SAS | STU | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0146 | EAS | CHB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18747 | hp2 | a0001 | c0001 | t0005 | g0092 | EAS | CHB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0101 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0181 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18940 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18945 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18954 | hp1 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0117 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18961 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0247 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0030 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18966 | hp1 | a0003 | c0003 | t0004 | g0171 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18966 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18970 | hp1 | a0001 | c0001 | t0005 | g0327 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18971 | hp2 | a0001 | c0001 | t0005 | g0033 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0091 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18972 | hp2 | a0001 | c0001 | t0005 | g0322 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18974 | hp2 | a0003 | c0003 | t0004 | g0029 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0316 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18980 | hp1 | a0003 | c0003 | t0004 | g0331 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18980 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18990 | hp1 | a0003 | c0003 | t0004 | g0095 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18995 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0144 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19000 | hp2 | a0001 | c0001 | t0008 | g0151 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19004 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19005 | hp2 | a0003 | c0003 | t0004 | g0093 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19010 | hp1 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19010 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19011 | hp2 | a0003 | c0003 | t0004 | g0163 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19030 | hp1 | a0001 | c0001 | t0018 | g0024 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0218 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19043 | hp1 | a0002 | c0002 | t0002 | g0313 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19043 | hp2 | a0004 | c0004 | t0007 | g0201 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19055 | hp1 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19055 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19056 | hp2 | a0003 | c0003 | t0004 | g0211 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19057 | hp1 | a0001 | c0001 | t0005 | g0210 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19057 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0178 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19062 | hp2 | a0001 | c0001 | t0005 | g0174 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19063 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0097 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0156 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19068 | hp2 | a0003 | c0003 | t0004 | g0079 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19072 | hp2 | a0001 | c0001 | t0005 | g0150 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19074 | hp1 | a0003 | c0003 | t0004 | g0121 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0221 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19076 | hp2 | a0001 | c0001 | t0003 | g0320 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19078 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19078 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19080 | hp2 | a0003 | c0003 | t0004 | g0006 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19081 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19082 | hp1 | a0003 | c0003 | t0016 | g0330 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19091 | hp1 | a0003 | c0003 | t0004 | g0067 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19091 | hp2 | a0001 | c0001 | t0005 | g0284 | EAS | JPT | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19240 | hp1 | a0003 | c0003 | t0004 | g0333 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA19240 | hp2 | a0001 | c0001 | t0006 | g0336 | AFR | YRI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20129 | hp1 | a0001 | c0001 | t0007 | g0215 | AFR | ASW | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ASW | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0242 | EUR | TSI | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | GIH | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20905 | hp2 | a0001 | c0001 | t0012 | g0179 | SAS | GIH | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02486 | hp1 | a0003 | c0003 | t0004 | g0074 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0013 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| HG02559 | hp2 | a0002 | c0002 | t0002 | g0125 | AFR | ACB | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20300 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | USA | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA20300 | hp2 | a0002 | c0002 | t0002 | g0082 | AFR | USA | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0196 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0021 | AFR | LWK | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0184 | REF | REF | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0222 | REF | REF | ANXA4_chr2_69737134_69832112 | ANXA4 | chr2 | 69737134 | 69832112 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69804538 | G | C | 1 | a0004 | 4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
missense_variant | MODERATE | c.103G>C | p.Asp35His | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/13 | 191/2651 | 103/966 | 35/321 | chr2 | 69804538 | |||
| chr2:69806439 | G | A | 1 | a0005 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.247G>A | p.Val83Met | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/13 | 335/2651 | 247/966 | 83/321 | chr2 | 69806439 | |||
| chr2:69806452 | C | T | 1 | a0002 | 75 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(72): Show |
missense_variant | MODERATE | c.260C>T | p.Thr87Met | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/13 | 348/2651 | 260/966 | 87/321 | chr2 | 69806452 | |||
| chr2:69810607 | C | G | 2 | a0003 a0005 |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(47): Show |
missense_variant | MODERATE | c.411C>G | p.Ser137Arg | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/13 | 499/2651 | 411/966 | 137/321 | chr2 | 69810607 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69818633 | T | C | 1 | a0001c0006 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.663T>C | p.Asp221Asp | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/13 | 751/2651 | 663/966 | 221/321 | chr2 | 69818633 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69742148 | C | G | 1 | a0001c0001t0021 | 1 | HG01167.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/13 | 39418 | chr2 | 69742148 | ||||||
| chr2:69781553 | T | C | 1 | a0001c0001t0012 | 1 | NA20905.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/13 | chr2 | 69781553 | |||||||
| chr2:69825831 | C | G | 1 | a0001c0001t0020 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*316C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 316 | chr2 | 69825831 | ||||||
| chr2:69826001 | A | G | 1 | a0001c0001t0011 | 2 | HG02280.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*486A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 486 | chr2 | 69826001 | ||||||
| chr2:69826036 | A | G | 1 | a0001c0001t0019 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 521 | chr2 | 69826036 | ||||||
| chr2:69826290 | G | A | 1 | a0002c0002t0013 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 775 | chr2 | 69826290 | ||||||
| chr2:69826408 | T | C | 1 | a0001c0001t0014 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*893T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 893 | chr2 | 69826408 | ||||||
| chr2:69826487 | A | T | 5 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0012 others(2): Show |
62 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*972A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 972 | chr2 | 69826487 | ||||||
| chr2:69826507 | G | A | 1 | a0001c0001t0009 | 2 | HG01069.hp2 HG02145.hp2 |
3_prime_UTR_variant | MODIFIER | c.*992G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 992 | chr2 | 69826507 | ||||||
| chr2:69826536 | A | G | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(22): Show |
261 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(258): Show |
3_prime_UTR_variant | MODIFIER | c.*1021A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1021 | chr2 | 69826536 | ||||||
| chr2:69826628 | T | C | 1 | a0003c0003t0016 | 1 | NA19082.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1113T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1113 | chr2 | 69826628 | ||||||
| chr2:69826684 | T | C | 5 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0010 others(2): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*1169T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1169 | chr2 | 69826684 | ||||||
| chr2:69826780 | T | TA | 8 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0012 others(5): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*1284dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1285 | INFO_REALIGN_3_PRIME | chr2 | 69826780 | |||||
| chr2:69826780 | TA | T | 5 | a0001c0001t0004 a0001c0001t0015 a0002c0002t0004 others(2): Show |
50 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1284delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1284 | INFO_REALIGN_3_PRIME | chr2 | 69826780 | |||||
| chr2:69826923 | CAAGAT | C | 2 | a0002c0002t0010 a0002c0002t0013 |
3 | HG02818.hp1 HG03098.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1413_*1417delTAAG others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1413 | INFO_REALIGN_3_PRIME | chr2 | 69826923 | |||||
| chr2:69826931 | GA | G | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0011 others(6): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1426delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1426 | INFO_REALIGN_3_PRIME | chr2 | 69826931 | |||||
| chr2:69827104 | A | G | 1 | a0001c0001t0017 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1589A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 13/13 | 1589 | chr2 | 69827104 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:69742247 | C | T | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+72C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742247 | |||||||
| chr2:69742434 | G | A | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+259G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742434 | |||||||
| chr2:69742447 | G | A | 2 | a0002c0002t0002g0010 a0005c0005t0007g0011 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+272G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742447 | |||||||
| chr2:69742447 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-47+272G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742447 | |||||||
| chr2:69742540 | T | G | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+365T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742540 | |||||||
| chr2:69742686 | T | C | 1 | a0002c0002t0010g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-47+511T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742686 | |||||||
| chr2:69742786 | C | A | 219 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(216): Show |
228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-47+611C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742786 | |||||||
| chr2:69742877 | A | C | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+702A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742877 | |||||||
| chr2:69742988 | C | T | 261 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(258): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.-47+813C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69742988 | |||||||
| chr2:69743004 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+829C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743004 | |||||||
| chr2:69743111 | T | G | 3 | a0001c0001t0006g0025 a0001c0001t0018g0024 a0002c0002t0002g0026 |
3 | HG01884.hp1 HG02922.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+936T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743111 | |||||||
| chr2:69743178 | G | C | 79 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(76): Show |
86 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.-47+1003G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743178 | |||||||
| chr2:69743270 | C | T | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+1095C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743270 | |||||||
| chr2:69743360 | GGCGTGTG others(18): Show |
G | 6 | a0001c0001t0006g0217 a0001c0001t0007g0215 a0002c0002t0002g0218 others(3): Show |
6 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+1186_-47+1210d others(27): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743360 | |||||||
| chr2:69743432 | G | T | 5 | a0001c0001t0006g0020 a0001c0001t0006g0021 a0001c0001t0006g0336 others(2): Show |
5 | HG01243.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+1257G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743432 | |||||||
| chr2:69743517 | G | A | 17 | a0001c0001t0001g0220 a0001c0001t0006g0101 a0001c0001t0006g0107 others(14): Show |
17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+1342G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743517 | |||||||
| chr2:69743606 | G | A | 1 | a0002c0002t0002g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-47+1431G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743606 | |||||||
| chr2:69743687 | T | A | 2 | a0001c0001t0006g0020 a0001c0001t0006g0021 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-47+1512T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743687 | |||||||
| chr2:69743746 | G | A | 1 | a0002c0002t0002g0027 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-47+1571G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69743746 | |||||||
| chr2:69744099 | C | A | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1924C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744099 | |||||||
| chr2:69744100 | A | C | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1925A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744100 | |||||||
| chr2:69744102 | G | A | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+1927G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744102 | |||||||
| chr2:69744137 | G | T | 8 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(5): Show |
8 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+1962G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744137 | |||||||
| chr2:69744185 | G | A | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+2010G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744185 | |||||||
| chr2:69744213 | G | A | 1 | a0001c0001t0005g0092 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-47+2038G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744213 | |||||||
| chr2:69744282 | G | A | 10 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+2107G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744282 | |||||||
| chr2:69744297 | G | A | 219 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(216): Show |
228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-47+2122G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744297 | |||||||
| chr2:69744325 | A | C | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+2150A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744325 | |||||||
| chr2:69744332 | A | T | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+2157A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744332 | |||||||
| chr2:69744455 | T | A | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-47+2280T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744455 | |||||||
| chr2:69744511 | T | A | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+2336T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744511 | |||||||
| chr2:69744744 | C | T | 1 | a0001c0001t0003g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-47+2569C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744744 | |||||||
| chr2:69744745 | GAAAGCTT others(2): Show |
G | 6 | a0001c0001t0006g0217 a0001c0001t0007g0215 a0002c0002t0002g0218 others(3): Show |
6 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+2572_-47+2580d others(11): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69744745 | ||||||
| chr2:69744852 | C | T | 7 | a0001c0001t0001g0209 a0001c0001t0003g0213 a0001c0001t0005g0207 others(4): Show |
7 | HG00673.hp1 HG02132.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-47+2677C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744852 | |||||||
| chr2:69744912 | A | G | 1 | a0001c0001t0001g0293 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-47+2737A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744912 | |||||||
| chr2:69744971 | T | C | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-47+2796T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69744971 | |||||||
| chr2:69745206 | C | A | 17 | a0001c0001t0001g0220 a0001c0001t0006g0101 a0001c0001t0006g0107 others(14): Show |
17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+3031C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745206 | |||||||
| chr2:69745276 | A | G | 1 | a0002c0002t0002g0099 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+3101A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745276 | |||||||
| chr2:69745285 | G | A | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+3110G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745285 | |||||||
| chr2:69745572 | T | C | 219 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(216): Show |
228 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.-47+3397T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745572 | |||||||
| chr2:69745633 | C | T | 2 | a0001c0001t0003g0205 a0001c0001t0003g0206 |
2 | NA18987.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-47+3458C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745633 | |||||||
| chr2:69745773 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-47+3598C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745773 | |||||||
| chr2:69745821 | AC | A | 6 | a0001c0001t0007g0204 a0002c0002t0002g0203 a0004c0004t0005g0199 others(3): Show |
6 | HG01433.hp1 HG02809.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+3647delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69745821 | |||||||
| chr2:69746070 | C | T | 1 | a0001c0001t0020g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-47+3895C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746070 | |||||||
| chr2:69746261 | C | T | 8 | a0001c0001t0001g0209 a0001c0001t0003g0213 a0001c0001t0005g0207 others(5): Show |
8 | HG00673.hp1 HG02132.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-47+4086C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746261 | |||||||
| chr2:69746605 | G | A | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+4430G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746605 | |||||||
| chr2:69746619 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+4444C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746619 | |||||||
| chr2:69746782 | G | C | 1 | a0002c0002t0004g0100 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-47+4607G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746782 | |||||||
| chr2:69746827 | GA | G | 327 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0034 others(324): Show |
337 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(334): Show |
intron_variant | MODIFIER | c.-47+4664delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69746827 | ||||||
| chr2:69746944 | G | A | 5 | a0001c0001t0005g0304 a0001c0001t0006g0336 a0001c0001t0007g0305 others(2): Show |
5 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+4769G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746944 | |||||||
| chr2:69746946 | C | A | 17 | a0001c0001t0001g0220 a0001c0001t0006g0101 a0001c0001t0006g0107 others(14): Show |
17 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+4771C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69746946 | |||||||
| chr2:69747229 | G | A | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-47+5054G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747229 | |||||||
| chr2:69747273 | G | A | 1 | a0001c0001t0003g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-47+5098G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747273 | |||||||
| chr2:69747293 | C | T | 1 | a0001c0001t0001g0291 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.-47+5118C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747293 | |||||||
| chr2:69747396 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-47+5221A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747396 | |||||||
| chr2:69747396 | A | T | 1 | a0001c0001t0003g0224 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-47+5221A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747396 | |||||||
| chr2:69747587 | C | T | 3 | a0002c0002t0002g0334 a0002c0002t0002g0335 a0003c0003t0004g0333 |
3 | HG02622.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+5412C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747587 | |||||||
| chr2:69747588 | G | A | 4 | a0001c0001t0005g0304 a0001c0001t0007g0305 a0002c0002t0002g0010 others(1): Show |
4 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+5413G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747588 | |||||||
| chr2:69747689 | C | T | 17 | a0001c0001t0001g0319 a0001c0001t0001g0321 a0001c0001t0001g0323 others(14): Show |
17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+5514C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747689 | |||||||
| chr2:69747741 | C | A | 223 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(220): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.-47+5566C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747741 | |||||||
| chr2:69747805 | C | T | 1 | a0001c0001t0005g0197 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-47+5630C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747805 | |||||||
| chr2:69747821 | G | T | 17 | a0001c0001t0006g0101 a0001c0001t0006g0107 a0001c0001t0006g0112 others(14): Show |
17 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+5646G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747821 | |||||||
| chr2:69747868 | C | T | 223 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(220): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.-47+5693C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747868 | |||||||
| chr2:69747957 | G | A | 1 | a0003c0003t0004g0029 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-47+5782G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69747957 | |||||||
| chr2:69748146 | C | T | 10 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+5971C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748146 | |||||||
| chr2:69748166 | G | C | 11 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(8): Show |
11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+5991G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748166 | |||||||
| chr2:69748210 | C | G | 4 | a0001c0001t0005g0304 a0001c0001t0007g0305 a0002c0002t0002g0010 others(1): Show |
4 | HG00099.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+6035C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748210 | |||||||
| chr2:69748377 | C | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-47+6202C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748377 | |||||||
| chr2:69748390 | G | GA | 9 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(6): Show |
9 | HG00099.hp1 HG01243.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+6226dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748390 | ||||||
| chr2:69748422 | C | T | 2 | a0002c0002t0002g0218 a0002c0002t0002g0219 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-47+6247C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748422 | |||||||
| chr2:69748491 | T | C | 11 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(8): Show |
11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+6316T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748491 | |||||||
| chr2:69748550 | C | T | 11 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(8): Show |
11 | HG00099.hp1 HG01243.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+6375C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748550 | |||||||
| chr2:69748687 | G | A | 194 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(191): Show |
203 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-47+6512G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748687 | |||||||
| chr2:69748710 | C | CT | 103 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(100): Show |
110 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.-47+6552dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748710 | ||||||
| chr2:69748710 | CT | C | 17 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(14): Show |
17 | HG00099.hp1 HG00544.hp2 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.-47+6552delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69748710 | ||||||
| chr2:69748796 | G | T | 18 | a0001c0001t0001g0220 a0001c0001t0006g0101 a0001c0001t0006g0107 others(15): Show |
18 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+6621G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748796 | |||||||
| chr2:69748893 | TG | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(9): Show |
12 | HG03704.hp1 NA18961.hp2 NA18965.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+6719delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748893 | |||||||
| chr2:69748894 | G | T | 5 | a0001c0001t0001g0319 a0001c0001t0003g0320 a0001c0001t0005g0316 others(2): Show |
5 | HG02135.hp2 HG02155.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+6719G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748894 | |||||||
| chr2:69748905 | G | A | 6 | a0001c0001t0001g0190 a0001c0001t0001g0209 a0001c0001t0003g0213 others(3): Show |
6 | HG00673.hp1 HG02132.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+6730G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69748905 | |||||||
| chr2:69749013 | T | C | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG00558.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.-47+6838T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749013 | |||||||
| chr2:69749020 | T | A | 2 | a0001c0001t0009g0226 a0001c0001t0009g0231 |
2 | HG01069.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-47+6845T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749020 | |||||||
| chr2:69749044 | A | G | 256 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(253): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.-47+6869A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749044 | |||||||
| chr2:69749074 | A | G | 5 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+6899A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749074 | |||||||
| chr2:69749167 | A | G | 1 | a0002c0002t0002g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-47+6992A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749167 | |||||||
| chr2:69749192 | G | A | 5 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(2): Show |
5 | HG02257.hp2 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+7017G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749192 | |||||||
| chr2:69749252 | G | T | 192 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(189): Show |
201 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-47+7077G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749252 | |||||||
| chr2:69749292 | C | T | 78 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(75): Show |
80 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-47+7117C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749292 | |||||||
| chr2:69749351 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-47+7176T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749351 | |||||||
| chr2:69749415 | G | T | 2 | a0001c0001t0006g0020 a0001c0001t0006g0021 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-47+7240G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749415 | |||||||
| chr2:69749460 | T | C | 78 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(75): Show |
85 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.-47+7285T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749460 | |||||||
| chr2:69749487 | A | G | 4 | a0001c0001t0004g0129 a0001c0001t0011g0128 a0002c0002t0002g0130 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+7312A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749487 | |||||||
| chr2:69749529 | T | C | 4 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(1): Show |
4 | HG01106.hp1 HG01517.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+7354T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749529 | |||||||
| chr2:69749717 | A | T | 10 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(7): Show |
10 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+7542A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749717 | |||||||
| chr2:69749763 | T | TA | 14 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(11): Show |
14 | HG01243.hp1 HG02257.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+7601dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69749763 | ||||||
| chr2:69749789 | G | A | 9 | a0001c0001t0005g0304 a0001c0001t0006g0013 a0001c0001t0006g0014 others(6): Show |
9 | HG00099.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-47+7614G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69749789 | |||||||
| chr2:69749922 | C | CAA | 84 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(81): Show |
86 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.-47+7758_-47+7759d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69749922 | ||||||
| chr2:69750119 | A | T | 82 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(79): Show |
84 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(81): Show |
intron_variant | MODIFIER | c.-47+7944A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750119 | |||||||
| chr2:69750212 | A | AT | 250 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(247): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-47+8040dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69750212 | ||||||
| chr2:69750236 | C | T | 1 | a0001c0001t0021g0126 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+8061C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750236 | |||||||
| chr2:69750297 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-47+8122A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750297 | |||||||
| chr2:69750406 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+8231G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750406 | |||||||
| chr2:69750565 | G | A | 108 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(105): Show |
115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+8390G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750565 | |||||||
| chr2:69750631 | T | G | 5 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(2): Show |
5 | NA18963.hp1 NA18971.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+8456T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69750631 | |||||||
| chr2:69750956 | CCT | C | 18 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(15): Show |
18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+8788_-47+8789d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69750956 | ||||||
| chr2:69751011 | C | T | 18 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(15): Show |
18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+8836C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751011 | |||||||
| chr2:69751158 | T | G | 244 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(241): Show |
253 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.-47+8983T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751158 | |||||||
| chr2:69751189 | ACT | A | 108 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(105): Show |
110 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-47+9017_-47+9018d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751189 | ||||||
| chr2:69751251 | C | T | 3 | a0001c0001t0006g0112 a0002c0002t0002g0113 a0002c0002t0002g0114 |
3 | HG02976.hp2 HG03195.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-47+9076C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751251 | |||||||
| chr2:69751362 | G | T | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+9187G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751362 | |||||||
| chr2:69751461 | T | C | 1 | a0001c0001t0007g0305 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47+9286T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751461 | |||||||
| chr2:69751507 | C | CA | 95 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(92): Show |
102 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(99): Show |
intron_variant | MODIFIER | c.-47+9353dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | ||||||
| chr2:69751507 | C | CAA | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0005g0031 others(9): Show |
12 | HG00438.hp1 HG00735.hp1 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.-47+9352_-47+9353d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | ||||||
| chr2:69751507 | CA | C | 104 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(101): Show |
106 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.-47+9353delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | ||||||
| chr2:69751507 | CAA | C | 42 | a0001c0001t0001g0287 a0001c0001t0003g0022 a0001c0001t0003g0186 others(39): Show |
42 | HG00099.hp1 HG00741.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.-47+9352_-47+9353d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69751507 | ||||||
| chr2:69751703 | A | C | 9 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+9528A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751703 | |||||||
| chr2:69751813 | G | A | 108 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(105): Show |
110 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.-47+9638G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69751813 | |||||||
| chr2:69752158 | C | A | 108 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(105): Show |
115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+9983C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752158 | |||||||
| chr2:69752263 | A | T | 84 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(81): Show |
86 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.-47+10088A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752263 | |||||||
| chr2:69752509 | G | A | 2 | a0001c0001t0018g0024 a0002c0002t0002g0026 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+10334G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752509 | |||||||
| chr2:69752581 | G | A | 3 | a0002c0002t0002g0334 a0002c0002t0002g0335 a0003c0003t0004g0333 |
3 | HG02622.hp2 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+10406G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752581 | |||||||
| chr2:69752682 | T | C | 9 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+10507T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752682 | |||||||
| chr2:69752735 | A | G | 2 | a0002c0002t0002g0306 a0002c0002t0002g0307 |
2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+10560A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752735 | |||||||
| chr2:69752745 | A | C | 3 | a0001c0001t0006g0315 a0002c0002t0002g0313 a0002c0002t0002g0314 |
3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+10570A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752745 | |||||||
| chr2:69752779 | T | A | 1 | a0001c0001t0001g0209 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-47+10604T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752779 | |||||||
| chr2:69752833 | T | G | 1 | a0001c0001t0003g0241 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-47+10658T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752833 | |||||||
| chr2:69752854 | G | C | 108 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(105): Show |
115 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.-47+10679G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69752854 | |||||||
| chr2:69753031 | A | G | 6 | a0001c0001t0006g0018 a0001c0001t0007g0196 a0001c0001t0007g0204 others(3): Show |
6 | HG01433.hp1 HG02965.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.-47+10856A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753031 | |||||||
| chr2:69753042 | T | G | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+10867T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753042 | |||||||
| chr2:69753061 | C | T | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+10886C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753061 | |||||||
| chr2:69753062 | C | T | 1 | a0001c0001t0020g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-47+10887C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753062 | |||||||
| chr2:69753072 | A | G | 34 | a0001c0001t0001g0287 a0001c0001t0006g0020 a0001c0001t0006g0021 others(31): Show |
34 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.-47+10897A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753072 | |||||||
| chr2:69753143 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.-47+10968C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753143 | |||||||
| chr2:69753164 | C | G | 1 | a0001c0001t0003g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-47+10989C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753164 | |||||||
| chr2:69753205 | T | C | 5 | a0001c0001t0006g0217 a0002c0002t0002g0218 a0002c0002t0002g0219 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11030T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753205 | |||||||
| chr2:69753284 | A | C | 1 | a0002c0002t0002g0099 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.-47+11109A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753284 | |||||||
| chr2:69753287 | C | G | 98 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(95): Show |
100 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-47+11112C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753287 | |||||||
| chr2:69753294 | C | G | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+11119C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753294 | |||||||
| chr2:69753295 | A | G | 235 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(232): Show |
244 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.-47+11120A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753295 | |||||||
| chr2:69753377 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0034 |
2 | NA18963.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+11202G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753377 | |||||||
| chr2:69753384 | C | T | 7 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(4): Show |
7 | HG02257.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+11209C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753384 | |||||||
| chr2:69753412 | C | T | 3 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0006t0006g0012 |
3 | HG02559.hp1 HG02965.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-47+11237C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753412 | |||||||
| chr2:69753474 | T | C | 4 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0043 others(1): Show |
4 | HG01074.hp1 HG01433.hp2 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+11299T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753474 | |||||||
| chr2:69753636 | G | A | 5 | a0001c0001t0006g0020 a0001c0001t0006g0021 a0002c0002t0002g0334 others(2): Show |
5 | HG01243.hp1 HG02622.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11461G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753636 | |||||||
| chr2:69753657 | T | C | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-47+11482T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753657 | |||||||
| chr2:69753677 | G | T | 3 | a0001c0001t0006g0315 a0002c0002t0002g0313 a0002c0002t0002g0314 |
3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+11502G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753677 | |||||||
| chr2:69753754 | G | GCTA | 19 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(16): Show |
19 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.-47+11580_-47+1158 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69753754 | ||||||
| chr2:69753778 | C | T | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+11603C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753778 | |||||||
| chr2:69753894 | A | G | 98 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(95): Show |
100 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.-47+11719A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753894 | |||||||
| chr2:69753934 | G | C | 5 | a0001c0001t0006g0217 a0002c0002t0002g0218 a0002c0002t0002g0219 others(2): Show |
5 | HG02647.hp2 HG02818.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+11759G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753934 | |||||||
| chr2:69753970 | T | C | 17 | a0001c0001t0001g0319 a0001c0001t0001g0321 a0001c0001t0001g0323 others(14): Show |
17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+11795T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753970 | |||||||
| chr2:69753981 | C | G | 1 | a0002c0002t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-47+11806C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753981 | |||||||
| chr2:69753983 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0003g0242 |
2 | HG01255.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.-47+11808G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69753983 | |||||||
| chr2:69754163 | G | A | 206 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(203): Show |
215 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.-47+11988G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754163 | |||||||
| chr2:69754376 | C | A | 2 | a0002c0002t0002g0306 a0002c0002t0002g0307 |
2 | HG01109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-47+12201C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754376 | |||||||
| chr2:69754426 | T | G | 17 | a0001c0001t0001g0319 a0001c0001t0001g0321 a0001c0001t0001g0323 others(14): Show |
17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+12251T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754426 | |||||||
| chr2:69754434 | TTTATTTT others(23): Show |
T | 1 | a0001c0001t0005g0031 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+12263_-47+1229 others(34): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69754434 | ||||||
| chr2:69754653 | A | G | 3 | a0001c0001t0006g0315 a0002c0002t0002g0313 a0002c0002t0002g0314 |
3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+12478A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754653 | |||||||
| chr2:69754760 | G | T | 3 | a0001c0001t0006g0336 a0002c0002t0002g0306 a0002c0002t0002g0307 |
3 | HG01109.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+12585G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754760 | |||||||
| chr2:69754777 | T | A | 5 | a0001c0001t0006g0018 a0001c0001t0007g0204 a0002c0002t0002g0203 others(2): Show |
5 | HG01433.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+12602T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754777 | |||||||
| chr2:69754796 | T | C | 3 | a0001c0001t0006g0336 a0002c0002t0002g0306 a0002c0002t0002g0307 |
3 | HG01109.hp1 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+12621T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754796 | |||||||
| chr2:69754959 | G | A | 97 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0137 others(94): Show |
99 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-47+12784G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69754959 | |||||||
| chr2:69755001 | T | G | 6 | a0001c0001t0001g0220 a0001c0001t0006g0020 a0001c0001t0006g0021 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+12826T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755001 | |||||||
| chr2:69755021 | T | G | 17 | a0001c0001t0001g0319 a0001c0001t0001g0321 a0001c0001t0001g0323 others(14): Show |
17 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+12846T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755021 | |||||||
| chr2:69755110 | T | A | 1 | a0001c0001t0021g0126 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+12935T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755110 | |||||||
| chr2:69755216 | C | T | 2 | a0001c0001t0018g0024 a0002c0002t0002g0026 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-47+13041C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755216 | |||||||
| chr2:69755223 | G | A | 2 | a0001c0001t0003g0116 a0001c0001t0003g0136 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-47+13048G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755223 | |||||||
| chr2:69755378 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-47+13203G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755378 | |||||||
| chr2:69755389 | G | A | 1 | a0001c0001t0007g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-47+13214G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755389 | |||||||
| chr2:69755472 | A | C | 2 | a0003c0003t0004g0006 a0003c0003t0004g0093 |
3 | NA18954.hp1 NA19005.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.-47+13297A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755472 | |||||||
| chr2:69755577 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0277 |
2 | HG01109.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.-47+13402C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755577 | |||||||
| chr2:69755618 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0137 |
2 | HG03654.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+13443T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755618 | |||||||
| chr2:69755640 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13465A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755640 | |||||||
| chr2:69755646 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13471T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755646 | |||||||
| chr2:69755655 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13480T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755655 | |||||||
| chr2:69755679 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13504A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755679 | |||||||
| chr2:69755682 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13507C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755682 | |||||||
| chr2:69755693 | T | G | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13518T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755693 | |||||||
| chr2:69755695 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13520T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755695 | |||||||
| chr2:69755696 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13521T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755696 | |||||||
| chr2:69755697 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13522C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755697 | |||||||
| chr2:69755699 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13524T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755699 | |||||||
| chr2:69755700 | C | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13525C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755700 | |||||||
| chr2:69755702 | A | C | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13527A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755702 | |||||||
| chr2:69755706 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13531C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755706 | |||||||
| chr2:69755707 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13532C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755707 | |||||||
| chr2:69755708 | C | G | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13533C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755708 | |||||||
| chr2:69755709 | A | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13534A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755709 | |||||||
| chr2:69755710 | G | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13535G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755710 | |||||||
| chr2:69755712 | G | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-47+13537G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755712 | |||||||
| chr2:69755801 | C | T | 5 | a0001c0001t0005g0304 a0001c0001t0006g0315 a0001c0001t0007g0305 others(2): Show |
5 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+13626C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69755801 | |||||||
| chr2:69756265 | C | A | 2 | a0001c0001t0005g0138 a0001c0001t0005g0139 |
2 | HG00408.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.-47+14090C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756265 | |||||||
| chr2:69756274 | G | A | 5 | a0001c0001t0005g0304 a0001c0001t0006g0315 a0001c0001t0007g0305 others(2): Show |
5 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+14099G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756274 | |||||||
| chr2:69756531 | G | C | 227 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(224): Show |
236 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(233): Show |
intron_variant | MODIFIER | c.-47+14356G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756531 | |||||||
| chr2:69756575 | A | G | 1 | a0001c0001t0007g0276 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-47+14400A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756575 | |||||||
| chr2:69756709 | C | G | 2 | a0001c0001t0006g0015 a0002c0002t0002g0016 |
2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-47+14534C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756709 | |||||||
| chr2:69756711 | A | G | 2 | a0001c0001t0006g0013 a0001c0001t0006g0014 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-47+14536A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756711 | |||||||
| chr2:69756927 | A | AATT | 3 | a0001c0001t0001g0035 a0001c0001t0020g0198 a0001c0001t0021g0126 |
3 | HG00735.hp1 HG01167.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.-47+14759_-47+1476 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756927 | ||||||
| chr2:69756933 | TA | T | 17 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 others(14): Show |
17 | HG01106.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+14759delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756933 | |||||||
| chr2:69756934 | A | ATT | 107 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(104): Show |
114 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.-47+14770_-47+1477 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756934 | ||||||
| chr2:69756934 | A | ATTT | 116 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0001g0123 others(113): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-47+14769_-47+1477 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69756934 | ||||||
| chr2:69756934 | A | T | 2 | a0001c0001t0001g0220 a0001c0001t0006g0101 |
2 | HG01109.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-47+14759A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756934 | |||||||
| chr2:69756978 | C | T | 1 | a0001c0001t0006g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47+14803C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69756978 | |||||||
| chr2:69757073 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+14898C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757073 | |||||||
| chr2:69757176 | G | A | 2 | a0001c0001t0001g0321 a0001c0001t0001g0323 |
2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-47+15001G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757176 | |||||||
| chr2:69757213 | G | C | 194 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(191): Show |
203 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(200): Show |
intron_variant | MODIFIER | c.-47+15038G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757213 | |||||||
| chr2:69757222 | C | G | 1 | a0001c0001t0004g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-47+15047C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757222 | |||||||
| chr2:69757238 | T | TTATATAT others(7): Show |
1 | a0003c0003t0004g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-47+15079_-47+1509 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757238 | ||||||
| chr2:69757238 | T | TTTTTTAT others(23): Show |
1 | a0001c0001t0005g0304 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-47+15064_-47+1506 others(34): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757238 | ||||||
| chr2:69757240 | A | T | 8 | a0001c0001t0006g0112 a0001c0001t0006g0315 a0001c0001t0006g0336 others(5): Show |
8 | HG00099.hp1 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+15065A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757240 | |||||||
| chr2:69757256 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0001g0034 a0002c0002t0002g0044 |
2 | HG02258.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.-47+15083_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | ||||||
| chr2:69757256 | ATATATAT others(5): Show |
A | 69 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0036 others(66): Show |
75 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-47+15083_-47+1509 others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | ||||||
| chr2:69757256 | ATATATAT others(6): Show |
A | 1 | a0001c0001t0001g0051 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-47+15083_-47+1509 others(17): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | ||||||
| chr2:69757256 | ATATATAT others(11): Show |
A | 1 | a0001c0001t0021g0126 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-47+15083_-47+1510 others(22): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757256 | ||||||
| chr2:69757258 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0005g0033 a0001c0001t0007g0048 a0004c0004t0005g0199 |
3 | HG02896.hp1 HG04204.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | ||||||
| chr2:69757258 | ATATATAT others(4): Show |
A | 2 | a0002c0002t0002g0049 a0002c0002t0002g0050 |
2 | NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | ||||||
| chr2:69757258 | ATATATAT others(5): Show |
A | 2 | a0002c0002t0002g0047 a0003c0003t0004g0006 |
3 | HG01074.hp2 NA18954.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1509 others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | ||||||
| chr2:69757258 | ATATATAT others(10): Show |
A | 2 | a0002c0002t0002g0010 a0005c0005t0007g0011 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+15085_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757258 | ||||||
| chr2:69757260 | ATATATAT others(4): Show |
A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+15087_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | ||||||
| chr2:69757260 | ATATATAT others(8): Show |
A | 9 | a0001c0001t0006g0296 a0001c0001t0006g0298 a0001c0001t0006g0300 others(6): Show |
9 | HG01167.hp2 HG01169.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | ||||||
| chr2:69757260 | ATATATAT others(9): Show |
A | 4 | a0001c0001t0004g0129 a0001c0001t0011g0128 a0002c0002t0002g0203 others(1): Show |
4 | HG01433.hp1 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | ||||||
| chr2:69757260 | ATATATAT others(13): Show |
A | 9 | a0001c0001t0005g0207 a0001c0001t0005g0312 a0001c0001t0006g0013 others(6): Show |
9 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15087_-47+1510 others(24): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757260 | ||||||
| chr2:69757261 | TATA | T | 3 | a0001c0001t0006g0315 a0002c0002t0002g0313 a0002c0002t0002g0314 |
3 | HG02257.hp1 HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-47+15087_-47+1508 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757261 | |||||||
| chr2:69757262 | ATATATTT others(1): Show |
A | 55 | a0001c0001t0001g0045 a0001c0001t0001g0122 a0001c0001t0001g0123 others(52): Show |
57 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.-47+15089_-47+1509 others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | ||||||
| chr2:69757262 | ATATATTT others(7): Show |
A | 1 | a0001c0001t0005g0193 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-47+15089_-47+1510 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | ||||||
| chr2:69757262 | ATATATTT others(8): Show |
A | 3 | a0001c0001t0006g0015 a0001c0001t0007g0196 a0002c0002t0002g0016 |
3 | HG02257.hp2 HG02970.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-47+15089_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | ||||||
| chr2:69757262 | ATATATTT others(9): Show |
A | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+15089_-47+1510 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | ||||||
| chr2:69757262 | ATATATTT others(10): Show |
A | 4 | a0001c0001t0006g0020 a0001c0001t0007g0204 a0003c0003t0004g0017 others(1): Show |
4 | HG01243.hp1 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15089_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757262 | ||||||
| chr2:69757264 | A | AT | 4 | a0001c0001t0001g0278 a0001c0001t0001g0288 a0001c0001t0001g0293 others(1): Show |
4 | HG00741.hp2 HG03654.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15090dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | A | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0261 a0001c0001t0001g0291 |
3 | HG00597.hp2 HG02486.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.-47+15089A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757264 | |||||||
| chr2:69757264 | ATATTTT | A | 10 | a0001c0001t0001g0237 a0001c0001t0003g0046 a0001c0001t0003g0133 others(7): Show |
10 | HG01255.hp2 HG01496.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | ATATTTTT | A | 9 | a0001c0001t0003g0120 a0001c0001t0003g0177 a0001c0001t0003g0205 others(6): Show |
9 | HG00673.hp1 NA18939.hp1 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(11): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | ATATTTTT others(1): Show |
A | 16 | a0001c0001t0001g0137 a0001c0001t0001g0321 a0001c0001t0001g0323 others(13): Show |
16 | HG00423.hp2 HG03654.hp2 NA18940.hp2 others(13): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1509 others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | ATATTTTT others(7): Show |
A | 4 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0194 others(1): Show |
4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15091_-47+1510 others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | ATATTTTT others(8): Show |
A | 1 | a0001c0001t0006g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-47+15091_-47+1510 others(19): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757264 | ATATTTTT others(10): Show |
A | 1 | a0001c0001t0006g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-47+15091_-47+1510 others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757264 | ||||||
| chr2:69757265 | TA | T | 5 | a0001c0001t0001g0229 a0001c0001t0001g0239 a0001c0001t0001g0250 others(2): Show |
5 | HG01070.hp2 HG01515.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+15091delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757265 | |||||||
| chr2:69757266 | A | ATATATAT others(24): Show |
1 | a0001c0001t0007g0305 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-47+15092_-47+1509 others(35): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | ||||||
| chr2:69757266 | A | T | 49 | a0001c0001t0001g0009 a0001c0001t0001g0187 a0001c0001t0001g0234 others(46): Show |
50 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.-47+15091A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757266 | |||||||
| chr2:69757266 | ATTTTTT | A | 10 | a0001c0001t0001g0287 a0001c0001t0003g0168 a0001c0001t0006g0107 others(7): Show |
10 | HG01192.hp1 HG02559.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.-47+15109_-47+1511 others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | ||||||
| chr2:69757266 | ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15104_-47+1511 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757266 | ||||||
| chr2:69757267 | T | TATATATA others(4): Show |
2 | a0002c0002t0002g0334 a0002c0002t0002g0335 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+15092_-47+1509 others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757267 | |||||||
| chr2:69757268 | T | A | 3 | a0001c0001t0001g0220 a0001c0001t0001g0256 a0003c0003t0004g0333 |
3 | HG01109.hp2 HG02132.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+15093T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757268 | |||||||
| chr2:69757269 | T | A | 3 | a0002c0002t0002g0334 a0002c0002t0002g0335 a0003c0003t0004g0103 |
3 | HG01891.hp1 HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-47+15094T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757269 | |||||||
| chr2:69757270 | T | A | 3 | a0001c0001t0001g0220 a0003c0003t0002g0104 a0003c0003t0004g0333 |
3 | HG01109.hp2 HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-47+15095T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757270 | |||||||
| chr2:69757271 | T | A | 4 | a0002c0002t0002g0334 a0002c0002t0002g0335 a0003c0003t0004g0103 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-47+15096T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757271 | |||||||
| chr2:69757272 | T | A | 4 | a0001c0001t0001g0220 a0001c0001t0006g0336 a0002c0002t0002g0106 others(1): Show |
4 | HG01109.hp2 HG02717.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.-47+15097T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757272 | |||||||
| chr2:69757273 | T | A | 2 | a0003c0003t0004g0103 a0003c0003t0004g0105 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-47+15098T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757273 | |||||||
| chr2:69757274 | T | A | 13 | a0001c0001t0001g0220 a0001c0001t0001g0287 a0001c0001t0006g0107 others(10): Show |
13 | HG01109.hp2 HG01192.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-47+15099T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757274 | |||||||
| chr2:69757276 | T | A | 2 | a0001c0001t0001g0220 a0001c0001t0006g0336 |
2 | HG01109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-47+15101T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757276 | |||||||
| chr2:69757278 | T | A | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+15103T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757278 | |||||||
| chr2:69757279 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15104T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757279 | |||||||
| chr2:69757281 | T | A | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+15106T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757281 | |||||||
| chr2:69757363 | C | T | 1 | a0002c0002t0002g0335 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-47+15188C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757363 | |||||||
| chr2:69757366 | G | A | 2 | a0001c0001t0003g0140 a0001c0001t0003g0141 |
2 | HG00544.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.-47+15191G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757366 | |||||||
| chr2:69757440 | G | GT | 35 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0003g0096 others(32): Show |
35 | HG00609.hp2 HG00735.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.-47+15279dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757440 | ||||||
| chr2:69757440 | G | T | 17 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(14): Show |
17 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-47+15265G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757440 | |||||||
| chr2:69757447 | T | G | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+15272T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757447 | |||||||
| chr2:69757508 | C | T | 14 | a0001c0001t0001g0035 a0001c0001t0005g0191 a0001c0001t0005g0192 others(11): Show |
14 | HG00735.hp1 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+15333C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757508 | |||||||
| chr2:69757570 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+15395G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757570 | |||||||
| chr2:69757624 | G | A | 1 | a0002c0002t0002g0244 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-47+15449G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757624 | |||||||
| chr2:69757681 | G | A | 9 | a0001c0001t0005g0207 a0001c0001t0005g0312 a0001c0001t0006g0013 others(6): Show |
9 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+15506G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757681 | |||||||
| chr2:69757746 | C | T | 2 | a0001c0001t0005g0310 a0001c0001t0007g0309 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.-47+15571C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757746 | |||||||
| chr2:69757958 | CA | C | 161 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0045 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.-47+15804delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757958 | ||||||
| chr2:69757958 | CAA | C | 93 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(90): Show |
100 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.-47+15803_-47+1580 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69757958 | ||||||
| chr2:69757979 | A | T | 1 | a0001c0001t0005g0192 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-47+15804A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69757979 | |||||||
| chr2:69758298 | C | G | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-47+16123C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758298 | |||||||
| chr2:69758303 | G | A | 216 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(213): Show |
225 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.-47+16128G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758303 | |||||||
| chr2:69758357 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-47+16182C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758357 | |||||||
| chr2:69758398 | G | A | 1 | a0003c0003t0002g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-47+16223G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758398 | |||||||
| chr2:69758512 | C | T | 78 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(75): Show |
85 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.-47+16337C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758512 | |||||||
| chr2:69758526 | A | T | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-47+16351A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758526 | |||||||
| chr2:69758606 | A | G | 1 | a0001c0001t0005g0033 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-47+16431A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758606 | |||||||
| chr2:69758710 | A | G | 10 | a0001c0001t0005g0207 a0001c0001t0005g0312 a0001c0001t0006g0013 others(7): Show |
10 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+16535A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758710 | |||||||
| chr2:69758737 | C | T | 10 | a0001c0001t0005g0207 a0001c0001t0005g0312 a0001c0001t0006g0013 others(7): Show |
10 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.-47+16562C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758737 | |||||||
| chr2:69758814 | G | T | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+16639G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758814 | |||||||
| chr2:69758868 | C | T | 1 | a0001c0001t0005g0212 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-47+16693C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758868 | |||||||
| chr2:69758887 | C | T | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-47+16712C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758887 | |||||||
| chr2:69758905 | C | G | 224 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47+16730C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758905 | |||||||
| chr2:69758964 | T | G | 18 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(15): Show |
18 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-47+16789T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69758964 | |||||||
| chr2:69759004 | C | T | 225 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(222): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+16829C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759004 | |||||||
| chr2:69759060 | C | T | 2 | a0002c0002t0002g0010 a0005c0005t0007g0011 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-47+16885C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759060 | |||||||
| chr2:69759067 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+16892C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759067 | |||||||
| chr2:69759080 | G | A | 1 | a0003c0003t0004g0052 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-47+16905G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759080 | |||||||
| chr2:69759124 | T | C | 224 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47+16949T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759124 | |||||||
| chr2:69759129 | CA | C | 20 | a0001c0001t0001g0220 a0001c0001t0001g0287 a0001c0001t0005g0031 others(17): Show |
20 | HG01109.hp2 HG01192.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.-47+16973delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | ||||||
| chr2:69759129 | CAAA | C | 215 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(212): Show |
224 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.-47+16971_-47+1697 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | ||||||
| chr2:69759129 | CAAAA | C | 7 | a0001c0001t0003g0180 a0001c0001t0006g0018 a0001c0001t0006g0020 others(4): Show |
7 | HG01243.hp1 HG02965.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.-47+16970_-47+1697 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69759129 | ||||||
| chr2:69759131 | A | C | 1 | a0001c0001t0005g0031 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+16956A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759131 | |||||||
| chr2:69759151 | T | C | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-47+16976T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759151 | |||||||
| chr2:69759315 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-47+17140C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759315 | |||||||
| chr2:69759344 | A | G | 1 | a0001c0001t0012g0179 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-47+17169A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759344 | |||||||
| chr2:69759439 | G | A | 5 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(2): Show |
5 | NA18747.hp1 NA18945.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.-47+17264G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759439 | |||||||
| chr2:69759539 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+17364C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759539 | |||||||
| chr2:69759618 | A | G | 2 | a0001c0001t0003g0223 a0001c0001t0003g0224 |
2 | HG02129.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-47+17443A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759618 | |||||||
| chr2:69759665 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+17490G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759665 | |||||||
| chr2:69759679 | G | C | 14 | a0001c0001t0001g0035 a0001c0001t0005g0191 a0001c0001t0005g0192 others(11): Show |
14 | HG00735.hp1 HG01243.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-47+17504G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759679 | |||||||
| chr2:69759856 | G | A | 1 | a0001c0001t0003g0148 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-47+17681G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759856 | |||||||
| chr2:69759869 | A | G | 226 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(223): Show |
235 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(232): Show |
intron_variant | MODIFIER | c.-47+17694A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759869 | |||||||
| chr2:69759960 | G | A | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-47+17785G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69759960 | |||||||
| chr2:69760056 | T | C | 1 | a0001c0001t0001g0009 | 2 | HG00597.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.-47+17881T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760056 | |||||||
| chr2:69760074 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-47+17899C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760074 | |||||||
| chr2:69760128 | G | A | 1 | a0001c0001t0006g0296 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-47+17953G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760128 | |||||||
| chr2:69760247 | T | C | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+18072T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760247 | |||||||
| chr2:69760252 | A | G | 225 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(222): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+18077A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760252 | |||||||
| chr2:69760575 | T | C | 1 | a0001c0001t0005g0031 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-47+18400T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760575 | |||||||
| chr2:69760608 | G | A | 8 | a0001c0001t0006g0124 a0003c0003t0002g0102 a0003c0003t0004g0185 others(5): Show |
8 | HG01256.hp2 HG02717.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18433G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760608 | |||||||
| chr2:69760680 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-47+18505G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760680 | |||||||
| chr2:69760991 | G | A | 1 | a0001c0001t0006g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-47+18816G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69760991 | |||||||
| chr2:69760998 | T | TTAAA | 225 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(222): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.-47+18825_-47+1882 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69760998 | ||||||
| chr2:69761000 | A | AAATT | 8 | a0001c0001t0005g0312 a0001c0001t0006g0013 a0001c0001t0006g0014 others(5): Show |
8 | HG01109.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-47+18848_-47+1885 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761000 | ||||||
| chr2:69761004 | T | A | 224 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(221): Show |
233 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(230): Show |
intron_variant | MODIFIER | c.-47+18829T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761004 | |||||||
| chr2:69761008 | T | A | 122 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(119): Show |
127 | HG00423.hp1 HG00438.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.-47+18833T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761008 | |||||||
| chr2:69761012 | T | A | 18 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(15): Show |
18 | HG02155.hp1 HG02451.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.-47+18837T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761012 | |||||||
| chr2:69761016 | T | A | 11 | a0001c0001t0001g0321 a0001c0001t0001g0323 a0001c0001t0001g0324 others(8): Show |
11 | NA18961.hp2 NA18965.hp1 NA18966.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+18841T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761016 | |||||||
| chr2:69761101 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-47+18926A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761101 | |||||||
| chr2:69761220 | G | A | 2 | a0001c0001t0006g0015 a0002c0002t0002g0016 |
2 | HG02257.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-47+19045G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761220 | |||||||
| chr2:69761519 | T | TAAGTA | 262 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(259): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-47+19346_-47+1934 others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761519 | ||||||
| chr2:69761541 | A | G | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-47+19366A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761541 | |||||||
| chr2:69761572 | G | A | 3 | a0001c0001t0003g0230 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | NA18943.hp2 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-47+19397G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761572 | |||||||
| chr2:69761585 | T | C | 253 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(250): Show |
262 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-47+19410T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761585 | |||||||
| chr2:69761715 | G | C | 1 | a0001c0001t0005g0210 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-47+19540G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761715 | |||||||
| chr2:69761738 | T | C | 1 | a0001c0001t0006g0124 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-47+19563T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761738 | |||||||
| chr2:69761746 | C | T | 11 | a0001c0001t0004g0129 a0001c0001t0006g0298 a0001c0001t0006g0300 others(8): Show |
11 | HG01167.hp2 HG01169.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-47+19571C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761746 | |||||||
| chr2:69761749 | C | T | 6 | a0001c0001t0003g0120 a0001c0001t0003g0177 a0001c0001t0003g0205 others(3): Show |
6 | NA18939.hp1 NA18969.hp2 NA18987.hp2 others(3): Show |
intron_variant | MODIFIER | c.-47+19574C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761749 | |||||||
| chr2:69761776 | T | TA | 14 | a0001c0001t0001g0232 a0001c0001t0005g0207 a0001c0001t0005g0312 others(11): Show |
14 | HG01109.hp1 HG02280.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-47+19620dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | ||||||
| chr2:69761776 | T | TAA | 15 | a0001c0001t0001g0287 a0001c0001t0006g0107 a0001c0001t0006g0112 others(12): Show |
15 | HG01192.hp1 HG01891.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-47+19619_-47+1962 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | ||||||
| chr2:69761776 | TA | T | 208 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(205): Show |
217 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.-47+19620delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | ||||||
| chr2:69761776 | TAA | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0283 a0001c0001t0001g0323 others(6): Show |
9 | HG00735.hp1 HG01496.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.-47+19619_-47+1962 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69761776 | ||||||
| chr2:69761854 | A | T | 1 | a0003c0003t0004g0087 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-46-19666A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761854 | |||||||
| chr2:69761927 | A | G | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-19593A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761927 | |||||||
| chr2:69761946 | T | C | 1 | a0001c0001t0006g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-46-19574T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69761946 | |||||||
| chr2:69762156 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-19364T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762156 | |||||||
| chr2:69762195 | A | G | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-19325A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762195 | |||||||
| chr2:69762264 | G | A | 2 | a0001c0001t0004g0129 a0001c0001t0011g0128 |
2 | HG02451.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-46-19256G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762264 | |||||||
| chr2:69762288 | G | A | 2 | a0001c0001t0003g0152 a0001c0001t0008g0151 |
2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.-46-19232G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762288 | |||||||
| chr2:69762306 | A | G | 4 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18957.hp1 NA19056.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-19214A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762306 | |||||||
| chr2:69762325 | G | A | 2 | a0001c0001t0005g0304 a0001c0001t0007g0305 |
2 | HG00099.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.-46-19195G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762325 | |||||||
| chr2:69762389 | GA | G | 27 | a0001c0001t0001g0287 a0001c0001t0005g0207 a0001c0001t0005g0312 others(24): Show |
27 | HG01109.hp1 HG01192.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.-46-19116delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762389 | ||||||
| chr2:69762390 | A | G | 1 | a0003c0003t0004g0333 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-46-19130A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762390 | |||||||
| chr2:69762446 | T | G | 2 | a0002c0002t0002g0113 a0002c0002t0002g0114 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-46-19074T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762446 | |||||||
| chr2:69762484 | G | A | 1 | a0001c0001t0003g0153 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-46-19036G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762484 | |||||||
| chr2:69762645 | G | A | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-18875G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762645 | |||||||
| chr2:69762663 | T | C | 4 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | NA18957.hp1 NA19056.hp1 NA19077.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-18857T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762663 | |||||||
| chr2:69762669 | C | G | 117 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0122 others(114): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.-46-18851C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762669 | |||||||
| chr2:69762697 | C | T | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-46-18823C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762697 | |||||||
| chr2:69762777 | G | A | 1 | a0001c0001t0007g0305 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-46-18743G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69762777 | |||||||
| chr2:69762855 | ACACT | A | 3 | a0001c0001t0005g0304 a0001c0001t0007g0305 a0001c0001t0009g0231 |
3 | HG00099.hp1 HG02145.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.-46-18657_-46-1865 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762855 | ||||||
| chr2:69762863 | T | TCA | 241 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(238): Show |
250 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.-46-18651_-46-1865 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69762863 | ||||||
| chr2:69763158 | T | G | 131 | a0001c0001t0001g0035 a0001c0001t0001g0045 a0001c0001t0001g0055 others(128): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.-46-18362T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763158 | |||||||
| chr2:69763172 | A | G | 3 | a0002c0002t0002g0130 a0003c0003t0004g0185 a0003c0003t0004g0243 |
3 | HG01243.hp2 HG01256.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.-46-18348A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763172 | |||||||
| chr2:69763277 | C | T | 3 | a0001c0001t0004g0129 a0001c0001t0011g0128 a0002c0002t0013g0127 |
3 | HG02451.hp2 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-18243C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763277 | |||||||
| chr2:69763295 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-18225C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763295 | |||||||
| chr2:69763309 | G | A | 1 | a0001c0001t0005g0031 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-46-18211G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763309 | |||||||
| chr2:69763310 | T | G | 1 | a0001c0001t0005g0031 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-46-18210T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763310 | |||||||
| chr2:69763449 | GT | G | 3 | a0001c0001t0006g0018 a0003c0003t0004g0017 a0003c0003t0004g0019 |
3 | HG02965.hp2 HG02976.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-46-18069delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763449 | ||||||
| chr2:69763496 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0268 |
2 | HG01109.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.-46-18024A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763496 | |||||||
| chr2:69763662 | C | CT | 17 | a0001c0001t0001g0036 a0001c0001t0001g0209 a0001c0001t0001g0220 others(14): Show |
17 | HG01109.hp2 HG02523.hp2 HG04115.hp1 others(14): Show |
intron_variant | MODIFIER | c.-46-17840dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763662 | ||||||
| chr2:69763662 | C | CTT | 17 | a0001c0001t0002g0267 a0001c0001t0003g0230 a0001c0001t0003g0285 others(14): Show |
17 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-17841_-46-1784 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69763662 | ||||||
| chr2:69763736 | C | G | 83 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(80): Show |
87 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.-46-17784C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763736 | |||||||
| chr2:69763820 | G | A | 15 | a0001c0001t0002g0267 a0001c0001t0005g0092 a0001c0001t0005g0138 others(12): Show |
15 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.-46-17700G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763820 | |||||||
| chr2:69763951 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-17569G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763951 | |||||||
| chr2:69763999 | A | G | 1 | a0001c0001t0011g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-46-17521A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69763999 | |||||||
| chr2:69764128 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0007g0299 |
2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-17392A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764128 | |||||||
| chr2:69764364 | T | C | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-17156T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764364 | |||||||
| chr2:69764397 | TTAAA | T | 3 | a0003c0003t0004g0006 a0003c0003t0004g0079 a0003c0003t0004g0093 |
4 | NA18954.hp1 NA19005.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-17119_-46-1711 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69764397 | ||||||
| chr2:69764470 | T | A | 1 | a0001c0001t0003g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-46-17050T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764470 | |||||||
| chr2:69764573 | C | A | 2 | a0002c0002t0002g0218 a0002c0002t0002g0219 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-46-16947C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764573 | |||||||
| chr2:69764644 | T | G | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-16876T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764644 | |||||||
| chr2:69764696 | C | T | 96 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(93): Show |
98 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-46-16824C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764696 | |||||||
| chr2:69764825 | T | C | 6 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0001c0001t0021g0126 others(3): Show |
6 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-16695T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764825 | |||||||
| chr2:69764941 | T | A | 1 | a0001c0001t0003g0320 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.-46-16579T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764941 | |||||||
| chr2:69764953 | T | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-16567T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69764953 | |||||||
| chr2:69764964 | ACTTAG | A | 84 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(81): Show |
85 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.-46-16550_-46-1654 others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69764964 | ||||||
| chr2:69765075 | T | TAC | 21 | a0001c0001t0001g0239 a0001c0001t0001g0248 a0001c0001t0001g0249 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.-46-16422_-46-1642 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | ||||||
| chr2:69765075 | T | TACAC | 4 | a0001c0001t0001g0220 a0001c0001t0006g0315 a0001c0001t0007g0299 others(1): Show |
4 | HG01109.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-16424_-46-1642 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | ||||||
| chr2:69765075 | TAC | T | 91 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(88): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-46-16422_-46-1642 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69765075 | ||||||
| chr2:69765220 | G | A | 1 | a0001c0001t0014g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-46-16300G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765220 | |||||||
| chr2:69765302 | A | G | 10 | a0002c0002t0002g0007 a0002c0002t0002g0097 a0002c0002t0002g0106 others(7): Show |
11 | HG03688.hp1 HG04115.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.-46-16218A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765302 | |||||||
| chr2:69765310 | T | C | 1 | a0001c0001t0001g0250 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-46-16210T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765310 | |||||||
| chr2:69765379 | A | G | 4 | a0001c0001t0011g0208 a0002c0002t0002g0005 a0002c0002t0002g0334 others(1): Show |
5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-16141A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765379 | |||||||
| chr2:69765414 | A | G | 98 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(95): Show |
100 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-46-16106A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765414 | |||||||
| chr2:69765474 | C | T | 1 | a0001c0001t0006g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-46-16046C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765474 | |||||||
| chr2:69765620 | T | C | 91 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(88): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-46-15900T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765620 | |||||||
| chr2:69765635 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15885C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765635 | |||||||
| chr2:69765657 | A | G | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-15863A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765657 | |||||||
| chr2:69765763 | C | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0137 a0001c0001t0002g0267 others(30): Show |
33 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.-46-15757C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765763 | |||||||
| chr2:69765858 | C | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-15662C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765858 | |||||||
| chr2:69765985 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15535C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69765985 | |||||||
| chr2:69766052 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15468A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766052 | |||||||
| chr2:69766123 | A | G | 2 | a0002c0002t0002g0218 a0002c0002t0002g0219 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-46-15397A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766123 | |||||||
| chr2:69766140 | A | G | 4 | a0001c0001t0011g0208 a0002c0002t0002g0005 a0002c0002t0002g0334 others(1): Show |
5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-15380A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766140 | |||||||
| chr2:69766446 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-15074C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766446 | |||||||
| chr2:69766514 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 |
3 | NA18963.hp1 NA18986.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.-46-15006G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766514 | |||||||
| chr2:69766850 | T | A | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-14670T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766850 | |||||||
| chr2:69766942 | C | G | 2 | a0001c0001t0001g0220 a0001c0001t0007g0299 |
2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-14578C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69766942 | |||||||
| chr2:69767050 | T | C | 3 | a0001c0001t0001g0137 a0001c0001t0005g0308 a0001c0001t0007g0048 |
3 | HG03654.hp2 HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-46-14470T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767050 | |||||||
| chr2:69767142 | T | C | 3 | a0001c0001t0005g0316 a0001c0001t0005g0317 a0001c0001t0017g0318 |
3 | HG02135.hp2 HG02155.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.-46-14378T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767142 | |||||||
| chr2:69767347 | C | G | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-14173C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767347 | |||||||
| chr2:69767386 | A | G | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-14134A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767386 | |||||||
| chr2:69767411 | T | G | 31 | a0001c0001t0001g0035 a0001c0001t0001g0137 a0001c0001t0002g0267 others(28): Show |
31 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-14109T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767411 | |||||||
| chr2:69767616 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-46-13904G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767616 | |||||||
| chr2:69767659 | G | C | 40 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(37): Show |
44 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-46-13861G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767659 | |||||||
| chr2:69767835 | T | C | 2 | a0001c0001t0007g0271 a0001c0001t0007g0272 |
2 | HG03017.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-46-13685T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767835 | |||||||
| chr2:69767905 | C | T | 1 | a0001c0001t0001g0325 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-46-13615C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767905 | |||||||
| chr2:69767929 | A | G | 2 | a0001c0001t0001g0321 a0001c0001t0001g0323 |
2 | NA19004.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-46-13591A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69767929 | |||||||
| chr2:69768328 | C | T | 3 | a0002c0002t0002g0297 a0002c0002t0002g0306 a0002c0002t0002g0307 |
3 | HG01109.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-46-13192C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768328 | |||||||
| chr2:69768380 | C | T | 4 | a0001c0001t0011g0208 a0002c0002t0002g0005 a0002c0002t0002g0334 others(1): Show |
5 | HG02280.hp2 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-13140C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768380 | |||||||
| chr2:69768412 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-46-13108G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768412 | |||||||
| chr2:69768434 | C | T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-13086C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768434 | |||||||
| chr2:69768435 | G | T | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-13085G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768435 | |||||||
| chr2:69768447 | C | T | 3 | a0001c0001t0004g0129 a0001c0001t0006g0025 a0001c0001t0006g0217 |
3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-13073C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768447 | |||||||
| chr2:69768448 | A | G | 265 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0053 others(262): Show |
274 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.-46-13072A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768448 | |||||||
| chr2:69768474 | T | C | 141 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0055 others(138): Show |
147 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(144): Show |
intron_variant | MODIFIER | c.-46-13046T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768474 | |||||||
| chr2:69768722 | CT | C | 13 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0207 others(10): Show |
13 | HG02135.hp2 HG02155.hp1 HG03209.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46-12796delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69768722 | ||||||
| chr2:69768962 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0007g0299 |
2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-12558C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69768962 | |||||||
| chr2:69769022 | A | G | 91 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(88): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-46-12498A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769022 | |||||||
| chr2:69769148 | C | T | 7 | a0001c0001t0006g0015 a0001c0001t0006g0112 a0001c0001t0006g0296 others(4): Show |
7 | HG01167.hp1 HG01884.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.-46-12372C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769148 | |||||||
| chr2:69769181 | C | T | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-12339C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769181 | |||||||
| chr2:69769237 | C | T | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-12283C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769237 | |||||||
| chr2:69769250 | G | A | 91 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(88): Show |
93 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-46-12270G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769250 | |||||||
| chr2:69769266 | ATCAT | A | 89 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(86): Show |
91 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-46-12252_-46-1224 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69769266 | ||||||
| chr2:69769284 | A | C | 1 | a0001c0001t0005g0150 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-46-12236A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769284 | |||||||
| chr2:69769652 | T | G | 1 | a0001c0001t0006g0336 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-46-11868T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769652 | |||||||
| chr2:69769725 | G | A | 31 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0002c0002t0002g0069 others(28): Show |
35 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.-46-11795G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769725 | |||||||
| chr2:69769785 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-46-11735C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769785 | |||||||
| chr2:69769810 | G | A | 65 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-46-11710G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769810 | |||||||
| chr2:69769874 | G | C | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-11646G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769874 | |||||||
| chr2:69769979 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0007g0299 |
2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-46-11541T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769979 | |||||||
| chr2:69769981 | A | T | 1 | a0001c0001t0005g0150 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-46-11539A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69769981 | |||||||
| chr2:69770054 | G | T | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-11466G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770054 | |||||||
| chr2:69770210 | C | T | 2 | a0001c0001t0005g0191 a0001c0001t0005g0192 |
2 | HG03098.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-46-11310C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770210 | |||||||
| chr2:69770234 | A | C | 3 | a0001c0001t0004g0129 a0001c0001t0006g0025 a0001c0001t0006g0217 |
3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-11286A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770234 | |||||||
| chr2:69770305 | A | G | 3 | a0003c0003t0004g0006 a0003c0003t0004g0079 a0003c0003t0004g0093 |
4 | NA18954.hp1 NA19005.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-11215A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770305 | |||||||
| chr2:69770491 | C | A | 15 | a0001c0001t0001g0035 a0001c0001t0006g0013 a0001c0001t0006g0014 others(12): Show |
15 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.-46-11029C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770491 | |||||||
| chr2:69770644 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-46-10876A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770644 | |||||||
| chr2:69770659 | ACTCT | A | 5 | a0003c0003t0002g0104 a0003c0003t0004g0103 a0003c0003t0004g0105 others(2): Show |
5 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-10855_-46-1085 others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770659 | ||||||
| chr2:69770736 | AACACACA others(9): Show |
A | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-10760_-46-1074 others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770736 | ||||||
| chr2:69770745 | G | A | 2 | a0001c0001t0018g0024 a0002c0002t0002g0026 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-10775G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770745 | |||||||
| chr2:69770761 | G | A | 1 | a0002c0002t0002g0125 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-46-10759G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770761 | |||||||
| chr2:69770828 | A | G | 2 | a0001c0001t0003g0008 a0001c0001t0003g0189 |
3 | HG03017.hp1 HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-46-10692A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770828 | |||||||
| chr2:69770863 | A | G | 185 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0053 others(182): Show |
191 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.-46-10657A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770863 | |||||||
| chr2:69770865 | G | A | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-10655G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770865 | |||||||
| chr2:69770930 | T | A | 1 | a0001c0001t0003g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-46-10590T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69770930 | |||||||
| chr2:69770930 | T | TAA | 9 | a0001c0001t0003g0046 a0001c0001t0003g0084 a0001c0001t0003g0116 others(6): Show |
9 | HG01255.hp2 HG01975.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-10577_-46-1057 others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770930 | ||||||
| chr2:69770930 | T | TAAA | 73 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(70): Show |
75 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.-46-10578_-46-1057 others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69770930 | ||||||
| chr2:69771094 | C | CA | 47 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0075 others(44): Show |
51 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.-46-10412dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771094 | ||||||
| chr2:69771105 | A | G | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-10415A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771105 | |||||||
| chr2:69771109 | G | A | 3 | a0001c0001t0001g0220 a0001c0001t0011g0128 a0002c0002t0013g0127 |
3 | HG01109.hp2 HG02622.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-46-10411G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771109 | |||||||
| chr2:69771109 | G | GA | 16 | a0001c0001t0001g0258 a0001c0001t0005g0192 a0001c0001t0006g0013 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.-46-10395dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771109 | ||||||
| chr2:69771109 | GA | G | 113 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(110): Show |
115 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-46-10395delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69771109 | ||||||
| chr2:69771110 | A | G | 4 | a0001c0001t0005g0316 a0001c0001t0005g0317 a0001c0001t0011g0128 others(1): Show |
4 | HG02155.hp1 HG02622.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-46-10410A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771110 | |||||||
| chr2:69771159 | A | G | 1 | a0001c0001t0007g0215 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-46-10361A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771159 | |||||||
| chr2:69771208 | T | C | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-10312T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771208 | |||||||
| chr2:69771231 | A | G | 1 | a0002c0002t0010g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-46-10289A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771231 | |||||||
| chr2:69771305 | C | A | 15 | a0001c0001t0001g0009 a0001c0001t0001g0122 a0001c0001t0001g0227 others(12): Show |
16 | HG00544.hp2 HG00597.hp2 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-10215C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771305 | |||||||
| chr2:69771556 | G | T | 19 | a0001c0001t0001g0035 a0001c0001t0001g0220 a0001c0001t0006g0013 others(16): Show |
19 | HG00735.hp1 HG01109.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-9964G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771556 | |||||||
| chr2:69771651 | C | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-9869C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69771651 | |||||||
| chr2:69772001 | G | A | 1 | a0001c0001t0014g0157 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-46-9519G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772001 | |||||||
| chr2:69772121 | G | A | 1 | a0001c0001t0007g0271 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-46-9399G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772121 | |||||||
| chr2:69772218 | G | T | 1 | a0001c0001t0012g0179 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-46-9302G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772218 | |||||||
| chr2:69772304 | A | G | 48 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0204 others(45): Show |
53 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.-46-9216A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772304 | |||||||
| chr2:69772328 | A | C | 1 | a0001c0001t0001g0098 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-46-9192A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772328 | |||||||
| chr2:69772366 | T | A | 17 | a0001c0001t0001g0035 a0001c0001t0006g0013 a0001c0001t0006g0014 others(14): Show |
17 | HG00735.hp1 HG01167.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-46-9154T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772366 | |||||||
| chr2:69772369 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-46-9151C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772369 | |||||||
| chr2:69772441 | A | G | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-46-9079A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772441 | |||||||
| chr2:69772490 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-9030G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772490 | |||||||
| chr2:69772501 | CCTTAGCA others(14): Show |
C | 177 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0123 others(174): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-46-9016_-46-8996d others(23): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69772501 | ||||||
| chr2:69772525 | G | A | 177 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0123 others(174): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-46-8995G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772525 | |||||||
| chr2:69772526 | T | C | 177 | a0001c0001t0001g0035 a0001c0001t0001g0055 a0001c0001t0001g0123 others(174): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-46-8994T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772526 | |||||||
| chr2:69772542 | G | A | 5 | a0001c0001t0002g0159 a0001c0001t0003g0046 a0001c0001t0003g0158 others(2): Show |
5 | HG01255.hp2 HG01978.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-8978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772542 | |||||||
| chr2:69772542 | G | T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-8978G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772542 | |||||||
| chr2:69772585 | C | T | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-8935C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772585 | |||||||
| chr2:69772595 | T | C | 99 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-46-8925T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772595 | |||||||
| chr2:69772596 | T | A | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-8924T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772596 | |||||||
| chr2:69772617 | G | C | 1 | a0002c0002t0002g0078 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-46-8903G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772617 | |||||||
| chr2:69772632 | G | A | 1 | a0001c0001t0001g0325 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-46-8888G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772632 | |||||||
| chr2:69772699 | G | A | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-8821G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772699 | |||||||
| chr2:69772804 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-46-8716G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772804 | |||||||
| chr2:69772922 | C | T | 2 | a0001c0001t0003g0146 a0001c0001t0003g0147 |
2 | NA18747.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.-46-8598C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772922 | |||||||
| chr2:69772965 | C | G | 2 | a0001c0001t0005g0312 a0003c0003t0004g0311 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-46-8555C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69772965 | |||||||
| chr2:69773020 | AAAAG | A | 45 | a0001c0001t0006g0101 a0001c0001t0006g0336 a0001c0001t0007g0215 others(42): Show |
50 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.-46-8480_-46-8477d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773020 | ||||||
| chr2:69773077 | A | G | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-8443A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773077 | |||||||
| chr2:69773293 | C | G | 1 | a0001c0001t0007g0272 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-46-8227C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773293 | |||||||
| chr2:69773614 | T | C | 3 | a0001c0001t0007g0204 a0001c0001t0007g0294 a0001c0001t0007g0302 |
3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-7906T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773614 | |||||||
| chr2:69773621 | C | CT | 29 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0077 others(26): Show |
30 | HG01175.hp2 HG01257.hp2 HG01346.hp2 others(27): Show |
intron_variant | MODIFIER | c.-46-7875dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | ||||||
| chr2:69773621 | C | CTT | 5 | a0002c0002t0002g0005 a0002c0002t0002g0027 a0002c0002t0002g0030 others(2): Show |
6 | HG00438.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-7876_-46-7875d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | ||||||
| chr2:69773621 | CT | C | 118 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(115): Show |
119 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.-46-7875delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | ||||||
| chr2:69773621 | CTT | C | 34 | a0001c0001t0003g0141 a0001c0001t0006g0018 a0001c0001t0006g0298 others(31): Show |
35 | HG00423.hp1 HG01256.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.-46-7876_-46-7875d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | ||||||
| chr2:69773621 | CTTT | C | 9 | a0003c0003t0004g0001 a0003c0003t0004g0003 a0003c0003t0004g0029 others(6): Show |
12 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(9): Show |
intron_variant | MODIFIER | c.-46-7877_-46-7875d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69773621 | ||||||
| chr2:69773646 | G | T | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-7874G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773646 | |||||||
| chr2:69773681 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-46-7839G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773681 | |||||||
| chr2:69773866 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-7654G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773866 | |||||||
| chr2:69773881 | C | T | 1 | a0002c0002t0002g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46-7639C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773881 | |||||||
| chr2:69773974 | A | G | 32 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0011g0128 others(29): Show |
36 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46-7546A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69773974 | |||||||
| chr2:69774042 | C | T | 1 | a0001c0001t0005g0033 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-46-7478C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774042 | |||||||
| chr2:69774043 | G | A | 1 | a0003c0003t0004g0185 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-46-7477G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774043 | |||||||
| chr2:69774112 | C | G | 19 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0076 others(16): Show |
19 | HG02040.hp1 HG02135.hp2 HG02155.hp1 others(16): Show |
intron_variant | MODIFIER | c.-46-7408C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774112 | |||||||
| chr2:69774139 | A | G | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-7381A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774139 | |||||||
| chr2:69774155 | C | T | 1 | a0003c0003t0016g0330 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-46-7365C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774155 | |||||||
| chr2:69774157 | T | TCTGTGCC others(3): Show |
1 | a0003c0003t0016g0330 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-46-7363_-46-7362i others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774157 | |||||||
| chr2:69774310 | G | T | 3 | a0001c0001t0004g0129 a0001c0001t0006g0025 a0001c0001t0006g0217 |
3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-7210G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774310 | |||||||
| chr2:69774327 | G | C | 37 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0002c0002t0002g0069 others(34): Show |
41 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.-46-7193G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774327 | |||||||
| chr2:69774327 | GC | G | 60 | a0001c0001t0001g0028 a0001c0001t0001g0077 a0001c0001t0001g0137 others(57): Show |
61 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(58): Show |
intron_variant | MODIFIER | c.-46-7180delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774327 | ||||||
| chr2:69774327 | GCC | G | 99 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0075 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-46-7181_-46-7180d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774327 | ||||||
| chr2:69774337 | C | CT | 6 | a0003c0003t0004g0029 a0003c0003t0004g0037 a0003c0003t0004g0039 others(3): Show |
6 | HG01175.hp1 HG01256.hp2 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-7183_-46-7182i others(3): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774337 | |||||||
| chr2:69774337 | C | T | 32 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(29): Show |
36 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.-46-7183C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774337 | |||||||
| chr2:69774338 | C | G | 1 | a0001c0001t0005g0175 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-46-7182C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774338 | |||||||
| chr2:69774338 | C | T | 38 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(35): Show |
42 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.-46-7182C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774338 | |||||||
| chr2:69774339 | C | T | 47 | a0001c0001t0005g0207 a0001c0001t0006g0018 a0001c0001t0006g0336 others(44): Show |
52 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-46-7181C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774339 | |||||||
| chr2:69774340 | C | CT | 24 | a0001c0001t0001g0045 a0001c0001t0001g0233 a0001c0001t0001g0254 others(21): Show |
24 | HG00099.hp1 HG00099.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.-46-7165dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69774340 | ||||||
| chr2:69774340 | C | T | 287 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0032 others(284): Show |
297 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(294): Show |
intron_variant | MODIFIER | c.-46-7180C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774340 | |||||||
| chr2:69774354 | T | C | 1 | a0002c0002t0002g0082 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-46-7166T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774354 | |||||||
| chr2:69774368 | C | T | 65 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-46-7152C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774368 | |||||||
| chr2:69774399 | C | T | 1 | a0001c0001t0005g0308 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-46-7121C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774399 | |||||||
| chr2:69774425 | G | A | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-7095G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69774425 | |||||||
| chr2:69775122 | A | G | 1 | a0002c0002t0002g0115 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-46-6398A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775122 | |||||||
| chr2:69775248 | C | T | 1 | a0001c0001t0007g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-46-6272C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775248 | |||||||
| chr2:69775343 | C | T | 100 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(97): Show |
101 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.-46-6177C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775343 | |||||||
| chr2:69775601 | G | A | 2 | a0001c0001t0006g0101 a0001c0001t0007g0299 |
2 | HG02818.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-46-5919G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775601 | |||||||
| chr2:69775878 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-46-5642A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775878 | |||||||
| chr2:69775920 | G | T | 2 | a0002c0002t0002g0313 a0002c0002t0002g0314 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-46-5600G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775920 | |||||||
| chr2:69775939 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-46-5581C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775939 | |||||||
| chr2:69775960 | AT | A | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-5556delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775960 | ||||||
| chr2:69775961 | T | TTTA | 5 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0020 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTATTTA | 13 | a0001c0001t0006g0107 a0001c0001t0006g0112 a0001c0001t0006g0124 others(10): Show |
13 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTATTTA others(4): Show |
3 | a0001c0001t0001g0220 a0001c0001t0006g0015 a0001c0001t0006g0301 |
3 | HG01109.hp2 HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-46-5557_-46-5556i others(13): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTA | 3 | a0001c0001t0001g0261 a0002c0002t0002g0297 a0003c0003t0004g0001 |
3 | HG01346.hp1 HG01891.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-46-5532_-46-5529d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTATTT others(1): Show |
7 | a0001c0001t0007g0215 a0003c0003t0002g0104 a0003c0003t0004g0074 others(4): Show |
7 | HG01891.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-5536_-46-5529d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTATTT others(9): Show |
1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-46-5544_-46-5529d others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTATTT others(13): Show |
28 | a0002c0002t0002g0069 a0003c0003t0004g0001 a0003c0003t0004g0003 others(25): Show |
31 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.-46-5548_-46-5529d others(22): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTATTT others(17): Show |
2 | a0001c0001t0006g0336 a0002c0002t0013g0127 |
2 | HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-46-5552_-46-5529d others(26): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775961 | T | TTTTATTT others(21): Show |
1 | a0001c0001t0006g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-46-5556_-46-5529d others(30): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69775961 | ||||||
| chr2:69775991 | T | TTATTTAT others(14): Show |
1 | a0003c0003t0004g0029 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-5529_-46-5528i others(23): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775991 | |||||||
| chr2:69775992 | G | A | 1 | a0003c0003t0004g0029 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-5528G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69775992 | |||||||
| chr2:69776032 | G | A | 141 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(138): Show |
146 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-46-5488G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776032 | |||||||
| chr2:69776066 | G | A | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-5454G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776066 | |||||||
| chr2:69776070 | G | T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-5450G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776070 | |||||||
| chr2:69776164 | T | G | 1 | a0001c0001t0021g0126 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-46-5356T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776164 | |||||||
| chr2:69776212 | G | A | 3 | a0001c0001t0004g0129 a0001c0001t0006g0025 a0001c0001t0006g0217 |
3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-5308G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776212 | |||||||
| chr2:69776220 | C | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-5300C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776220 | |||||||
| chr2:69776433 | A | T | 2 | a0001c0001t0018g0024 a0002c0002t0002g0026 |
2 | HG01884.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-46-5087A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776433 | |||||||
| chr2:69776530 | T | C | 3 | a0001c0001t0004g0129 a0001c0001t0006g0025 a0001c0001t0006g0217 |
3 | HG02451.hp2 HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-4990T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776530 | |||||||
| chr2:69776560 | GT | G | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-4958delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69776560 | ||||||
| chr2:69776706 | C | A | 3 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0044 |
3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.-46-4814C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776706 | |||||||
| chr2:69776892 | A | G | 150 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(147): Show |
156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-46-4628A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69776892 | |||||||
| chr2:69777050 | A | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-4470A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777050 | |||||||
| chr2:69777094 | A | T | 1 | a0001c0001t0003g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-46-4426A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777094 | |||||||
| chr2:69777133 | G | A | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-46-4387G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777133 | |||||||
| chr2:69777146 | G | T | 150 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(147): Show |
156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-46-4374G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777146 | |||||||
| chr2:69777149 | C | T | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-4371C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777149 | |||||||
| chr2:69777158 | A | C | 2 | a0002c0002t0002g0303 a0002c0002t0004g0100 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.-46-4362A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777158 | |||||||
| chr2:69777170 | T | C | 150 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(147): Show |
156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-46-4350T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777170 | |||||||
| chr2:69777196 | C | A | 177 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(174): Show |
183 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.-46-4324C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777196 | |||||||
| chr2:69777236 | T | C | 150 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(147): Show |
156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.-46-4284T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777236 | |||||||
| chr2:69777269 | A | G | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-46-4251A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777269 | |||||||
| chr2:69777351 | C | G | 5 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0020 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-4169C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777351 | |||||||
| chr2:69777400 | G | C | 1 | a0001c0001t0003g0120 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-46-4120G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777400 | |||||||
| chr2:69777457 | C | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-46-4063C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777457 | |||||||
| chr2:69777636 | C | T | 1 | a0002c0002t0002g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-46-3884C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777636 | |||||||
| chr2:69777650 | C | T | 8 | a0002c0002t0002g0007 a0002c0002t0002g0097 a0002c0002t0002g0156 others(5): Show |
9 | NA18939.hp2 NA18954.hp2 NA18963.hp2 others(6): Show |
intron_variant | MODIFIER | c.-46-3870C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777650 | |||||||
| chr2:69777756 | G | A | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-46-3764G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777756 | |||||||
| chr2:69777818 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-46-3702C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777818 | |||||||
| chr2:69777974 | A | G | 1 | a0001c0001t0007g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-46-3546A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777974 | |||||||
| chr2:69777988 | C | G | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-46-3532C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69777988 | |||||||
| chr2:69778041 | T | G | 65 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(62): Show |
66 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.-46-3479T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778041 | |||||||
| chr2:69778057 | A | G | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-3463A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778057 | |||||||
| chr2:69778074 | T | G | 3 | a0002c0002t0002g0297 a0002c0002t0002g0306 a0002c0002t0002g0307 |
3 | HG01109.hp1 HG01891.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-46-3446T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778074 | |||||||
| chr2:69778269 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-46-3251G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778269 | |||||||
| chr2:69778337 | G | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0259 a0001c0001t0001g0292 |
3 | HG00323.hp2 HG02683.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.-46-3183G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778337 | |||||||
| chr2:69778412 | T | C | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-3108T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778412 | |||||||
| chr2:69778563 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-46-2957G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778563 | |||||||
| chr2:69778584 | T | C | 2 | a0001c0001t0003g0116 a0001c0001t0003g0136 |
2 | HG01928.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-46-2936T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778584 | |||||||
| chr2:69778623 | A | C | 102 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(99): Show |
103 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.-46-2897A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778623 | |||||||
| chr2:69778668 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-2852G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778668 | |||||||
| chr2:69778698 | C | T | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-2822C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778698 | |||||||
| chr2:69778707 | G | A | 147 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(144): Show |
153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-46-2813G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778707 | |||||||
| chr2:69778730 | G | A | 1 | a0001c0001t0003g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-46-2790G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778730 | |||||||
| chr2:69778757 | G | A | 147 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(144): Show |
153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-46-2763G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778757 | |||||||
| chr2:69778775 | C | CA | 22 | a0001c0001t0001g0036 a0001c0001t0001g0252 a0001c0001t0001g0264 others(19): Show |
22 | HG00323.hp1 HG01099.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.-46-2717dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CA | C | 16 | a0001c0001t0001g0028 a0001c0001t0001g0229 a0001c0001t0001g0236 others(13): Show |
16 | HG01361.hp1 HG01515.hp1 HG01517.hp1 others(13): Show |
intron_variant | MODIFIER | c.-46-2717delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAA | C | 7 | a0001c0001t0001g0323 a0001c0001t0005g0322 a0001c0001t0006g0315 others(4): Show |
7 | HG02027.hp2 HG02258.hp1 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-46-2718_-46-2717d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAAA | C | 88 | a0001c0001t0001g0055 a0001c0001t0001g0137 a0001c0001t0001g0220 others(85): Show |
90 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.-46-2719_-46-2717d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAAAA | C | 13 | a0001c0001t0001g0123 a0001c0001t0003g0183 a0001c0001t0006g0013 others(10): Show |
13 | HG00558.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-46-2720_-46-2717d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAAAAAAA others(3): Show |
C | 4 | a0001c0001t0003g0169 a0001c0001t0003g0230 a0001c0001t0003g0285 others(1): Show |
4 | HG00597.hp1 NA18943.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-2726_-46-2717d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0007g0204 a0001c0001t0007g0294 a0001c0001t0007g0302 |
3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-2727_-46-2717d others(13): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778775 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-46-2728_-46-2717d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69778775 | ||||||
| chr2:69778806 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-46-2714G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778806 | |||||||
| chr2:69778917 | G | A | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-2603G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69778917 | |||||||
| chr2:69779068 | G | A | 6 | a0001c0001t0003g0177 a0001c0001t0003g0205 a0001c0001t0003g0206 others(3): Show |
6 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(3): Show |
intron_variant | MODIFIER | c.-46-2452G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779068 | |||||||
| chr2:69779107 | C | CA | 26 | a0001c0001t0001g0034 a0001c0001t0001g0051 a0001c0001t0001g0075 others(23): Show |
26 | HG00323.hp2 HG00673.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.-46-2387dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | ||||||
| chr2:69779107 | CA | C | 24 | a0001c0001t0001g0137 a0001c0001t0001g0232 a0001c0001t0001g0250 others(21): Show |
25 | HG01070.hp2 HG01261.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-46-2387delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | ||||||
| chr2:69779107 | CAA | C | 49 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0003g0158 others(46): Show |
54 | HG00423.hp1 HG00597.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-46-2388_-46-2387d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | ||||||
| chr2:69779107 | CAAA | C | 82 | a0001c0001t0001g0123 a0001c0001t0002g0159 a0001c0001t0003g0008 others(79): Show |
83 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.-46-2389_-46-2387d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779107 | ||||||
| chr2:69779123 | A | G | 5 | a0001c0001t0006g0315 a0003c0003t0002g0102 a0003c0003t0004g0017 others(2): Show |
5 | HG02258.hp1 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-2397A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779123 | |||||||
| chr2:69779157 | C | CT | 6 | a0001c0001t0001g0220 a0001c0001t0006g0013 a0001c0001t0006g0014 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.-46-2353dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779157 | ||||||
| chr2:69779167 | T | A | 2 | a0001c0001t0001g0270 a0005c0005t0007g0011 |
2 | HG02630.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.-46-2353T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779167 | |||||||
| chr2:69779231 | A | T | 147 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(144): Show |
153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-46-2289A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779231 | |||||||
| chr2:69779677 | CAAAA | C | 3 | a0001c0001t0007g0204 a0001c0001t0007g0294 a0001c0001t0007g0302 |
3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-46-1840_-46-1837d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69779677 | ||||||
| chr2:69779736 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0258 |
2 | HG02040.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-46-1784C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779736 | |||||||
| chr2:69779866 | C | T | 47 | a0001c0001t0006g0018 a0001c0001t0006g0315 a0001c0001t0006g0336 others(44): Show |
52 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.-46-1654C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779866 | |||||||
| chr2:69779891 | T | C | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-1629T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779891 | |||||||
| chr2:69779922 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-1598T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779922 | |||||||
| chr2:69779927 | C | G | 14 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-46-1593C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779927 | |||||||
| chr2:69779983 | C | T | 147 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(144): Show |
153 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.-46-1537C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69779983 | |||||||
| chr2:69780002 | T | C | 1 | a0001c0001t0001g0209 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-46-1518T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780002 | |||||||
| chr2:69780128 | TG | T | 39 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(36): Show |
43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-1388delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 69780128 | ||||||
| chr2:69780225 | C | T | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.-46-1295C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780225 | |||||||
| chr2:69780263 | T | C | 44 | a0001c0001t0006g0018 a0001c0001t0006g0315 a0001c0001t0006g0336 others(41): Show |
48 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.-46-1257T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780263 | |||||||
| chr2:69780266 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-46-1254C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780266 | |||||||
| chr2:69780338 | G | A | 1 | a0002c0002t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-46-1182G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780338 | |||||||
| chr2:69780364 | T | G | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-46-1156T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780364 | |||||||
| chr2:69780384 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-46-1136T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780384 | |||||||
| chr2:69780407 | G | C | 1 | a0001c0001t0003g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-46-1113G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780407 | |||||||
| chr2:69780424 | G | C | 5 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0020 others(2): Show |
5 | HG01243.hp1 HG02559.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.-46-1096G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780424 | |||||||
| chr2:69780455 | T | C | 144 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(141): Show |
149 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.-46-1065T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780455 | |||||||
| chr2:69780563 | A | G | 2 | a0001c0001t0006g0025 a0001c0001t0006g0217 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-46-957A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780563 | |||||||
| chr2:69780612 | C | T | 39 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(36): Show |
43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-908C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780612 | |||||||
| chr2:69780656 | C | T | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-46-864C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780656 | |||||||
| chr2:69780708 | C | T | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-46-812C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69780708 | |||||||
| chr2:69781307 | A | C | 1 | a0003c0003t0004g0029 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-46-213A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781307 | |||||||
| chr2:69781354 | A | G | 5 | a0001c0001t0003g0177 a0001c0001t0003g0205 a0001c0001t0003g0206 others(2): Show |
5 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.-46-166A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781354 | |||||||
| chr2:69781360 | C | G | 17 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(14): Show |
17 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.-46-160C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781360 | |||||||
| chr2:69781429 | C | T | 39 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(36): Show |
43 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.-46-91C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781429 | |||||||
| chr2:69781475 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0283 |
2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.-46-45G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 1/12 | chr2 | 69781475 | |||||||
| chr2:69781903 | G | T | 103 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(100): Show |
104 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.9+329G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69781903 | |||||||
| chr2:69781926 | C | A | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+352C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69781926 | |||||||
| chr2:69782050 | T | C | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+476T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782050 | |||||||
| chr2:69782337 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.9+763C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782337 | |||||||
| chr2:69782356 | A | T | 1 | a0001c0001t0006g0021 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.9+782A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782356 | |||||||
| chr2:69782508 | A | T | 176 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(173): Show |
182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.9+934A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782508 | |||||||
| chr2:69782509 | A | T | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.9+935A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782509 | |||||||
| chr2:69782702 | T | G | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1128T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782702 | |||||||
| chr2:69782740 | C | T | 1 | a0002c0002t0002g0297 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.9+1166C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782740 | |||||||
| chr2:69782819 | C | T | 105 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(102): Show |
106 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.9+1245C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782819 | |||||||
| chr2:69782890 | T | TA | 176 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(173): Show |
182 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(179): Show |
intron_variant | MODIFIER | c.9+1316_9+1317insA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782890 | |||||||
| chr2:69782935 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1361G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69782935 | |||||||
| chr2:69783110 | T | C | 1 | a0001c0001t0006g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+1536T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783110 | |||||||
| chr2:69783215 | A | G | 1 | a0001c0001t0007g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.9+1641A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783215 | |||||||
| chr2:69783219 | T | C | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.9+1645T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783219 | |||||||
| chr2:69783260 | C | A | 1 | a0002c0002t0002g0041 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.9+1686C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783260 | |||||||
| chr2:69783304 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.9+1730G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783304 | |||||||
| chr2:69783321 | T | C | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+1747T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783321 | |||||||
| chr2:69783494 | C | T | 71 | a0001c0001t0001g0137 a0001c0001t0002g0267 a0001c0001t0003g0177 others(68): Show |
76 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.9+1920C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783494 | |||||||
| chr2:69783984 | G | T | 2 | a0002c0002t0002g0303 a0002c0002t0004g0100 |
2 | HG03041.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.9+2410G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69783984 | |||||||
| chr2:69784184 | T | C | 175 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0137 others(172): Show |
181 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.9+2610T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784184 | |||||||
| chr2:69784208 | T | C | 5 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(2): Show |
5 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.9+2634T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784208 | |||||||
| chr2:69784290 | TA | T | 29 | a0001c0001t0001g0137 a0001c0001t0002g0267 a0001c0001t0003g0177 others(26): Show |
29 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.9+2719delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69784290 | ||||||
| chr2:69784294 | C | T | 4 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0180 others(1): Show |
4 | NA18945.hp1 NA18998.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.9+2720C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784294 | |||||||
| chr2:69784314 | C | A | 2 | a0001c0001t0006g0315 a0003c0003t0002g0102 |
2 | HG02258.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.9+2740C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784314 | |||||||
| chr2:69784377 | G | A | 21 | a0001c0001t0002g0267 a0001c0001t0003g0177 a0001c0001t0003g0205 others(18): Show |
21 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(18): Show |
intron_variant | MODIFIER | c.9+2803G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784377 | |||||||
| chr2:69784566 | G | A | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.9+2992G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784566 | |||||||
| chr2:69784653 | G | T | 20 | a0001c0001t0002g0267 a0001c0001t0003g0177 a0001c0001t0003g0205 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.9+3079G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784653 | |||||||
| chr2:69784707 | G | A | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.9+3133G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784707 | |||||||
| chr2:69784726 | A | G | 1 | a0002c0002t0002g0060 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.9+3152A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784726 | |||||||
| chr2:69784744 | G | C | 1 | a0001c0001t0003g0118 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.9+3170G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784744 | |||||||
| chr2:69784744 | G | T | 70 | a0001c0001t0001g0137 a0001c0001t0002g0267 a0001c0001t0003g0177 others(67): Show |
75 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.9+3170G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784744 | |||||||
| chr2:69784820 | G | C | 81 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(78): Show |
82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.10-3234G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784820 | |||||||
| chr2:69784838 | C | A | 3 | a0001c0001t0007g0204 a0001c0001t0007g0294 a0001c0001t0007g0302 |
3 | HG01167.hp2 HG01169.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.10-3216C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784838 | |||||||
| chr2:69784864 | G | C | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-3190G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784864 | |||||||
| chr2:69784913 | G | A | 2 | a0001c0001t0007g0204 a0003c0003t0004g0074 |
2 | HG02486.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.10-3141G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69784913 | |||||||
| chr2:69785047 | G | A | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.10-3007G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785047 | |||||||
| chr2:69785119 | A | T | 99 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(96): Show |
100 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.10-2935A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785119 | |||||||
| chr2:69785197 | C | T | 1 | a0001c0001t0003g0149 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.10-2857C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785197 | |||||||
| chr2:69785217 | A | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.10-2837A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785217 | |||||||
| chr2:69785297 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.10-2757G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785297 | |||||||
| chr2:69785551 | T | TTGATGAT others(2): Show |
29 | a0001c0001t0003g0008 a0001c0001t0003g0135 a0001c0001t0003g0148 others(26): Show |
31 | HG00642.hp1 HG01167.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.10-2482_10-2474dup others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | ||||||
| chr2:69785551 | T | TTGATGAT others(5): Show |
84 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(81): Show |
84 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.10-2485_10-2474dup others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | ||||||
| chr2:69785551 | T | TTGATGAT others(8): Show |
28 | a0001c0001t0003g0119 a0001c0001t0003g0161 a0001c0001t0006g0018 others(25): Show |
32 | HG00642.hp2 HG00735.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.10-2488_10-2474dup others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | ||||||
| chr2:69785551 | T | TTGATGAT others(11): Show |
26 | a0001c0001t0001g0137 a0001c0001t0002g0267 a0001c0001t0003g0177 others(23): Show |
26 | HG00408.hp1 HG00558.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.10-2491_10-2474dup others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | ||||||
| chr2:69785551 | T | TTGATGAT others(14): Show |
3 | a0001c0001t0005g0173 a0001c0001t0011g0128 a0001c0001t0011g0208 |
3 | HG00423.hp2 HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.10-2494_10-2474dup others(21): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69785551 | ||||||
| chr2:69785634 | A | C | 1 | a0001c0001t0001g0220 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.10-2420A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785634 | |||||||
| chr2:69785801 | C | A | 80 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0002g0159 others(77): Show |
81 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.10-2253C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69785801 | |||||||
| chr2:69786041 | T | C | 3 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0298 |
3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.10-2013T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786041 | |||||||
| chr2:69786045 | G | A | 2 | a0002c0002t0002g0027 a0002c0002t0002g0132 |
2 | HG00438.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.10-2009G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786045 | |||||||
| chr2:69786059 | C | A | 77 | a0001c0001t0001g0137 a0001c0001t0002g0267 a0001c0001t0003g0177 others(74): Show |
82 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.10-1995C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786059 | |||||||
| chr2:69786145 | C | T | 1 | a0001c0001t0003g0170 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.10-1909C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786145 | |||||||
| chr2:69786538 | T | C | 1 | a0002c0002t0002g0010 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.10-1516T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786538 | |||||||
| chr2:69786543 | A | G | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-1511A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786543 | |||||||
| chr2:69786601 | A | G | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-1453A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786601 | |||||||
| chr2:69786744 | C | T | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.10-1310C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786744 | |||||||
| chr2:69786761 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.10-1293G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786761 | |||||||
| chr2:69786861 | A | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-1193A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69786861 | |||||||
| chr2:69787001 | T | C | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-1053T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787001 | |||||||
| chr2:69787031 | T | C | 2 | a0002c0002t0002g0106 a0002c0002t0002g0115 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.10-1023T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787031 | |||||||
| chr2:69787120 | A | G | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.10-934A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787120 | |||||||
| chr2:69787168 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.10-886T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787168 | |||||||
| chr2:69787169 | A | G | 1 | a0002c0002t0002g0062 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.10-885A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787169 | |||||||
| chr2:69787195 | G | A | 1 | a0001c0001t0003g0022 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.10-859G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787195 | |||||||
| chr2:69787356 | ATC | A | 174 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(171): Show |
178 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.10-688_10-687delCT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 69787356 | ||||||
| chr2:69787429 | G | C | 96 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(93): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.10-625G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787429 | |||||||
| chr2:69787578 | G | A | 75 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(72): Show |
76 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.10-476G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787578 | |||||||
| chr2:69787597 | C | G | 3 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0298 |
3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.10-457C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787597 | |||||||
| chr2:69787824 | A | G | 2 | a0001c0001t0003g0152 a0001c0001t0008g0151 |
2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.10-230A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787824 | |||||||
| chr2:69787854 | T | C | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.10-200T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787854 | |||||||
| chr2:69787888 | C | T | 1 | a0001c0001t0007g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.10-166C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787888 | |||||||
| chr2:69787894 | C | T | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.10-160C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787894 | |||||||
| chr2:69787976 | A | G | 11 | a0002c0002t0001g0262 a0002c0002t0002g0041 a0002c0002t0002g0042 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.10-78A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787976 | |||||||
| chr2:69787981 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.10-73T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69787981 | |||||||
| chr2:69788049 | C | T | 94 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(91): Show |
95 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(92): Show |
splice_region_variant&intron_variant | LOW | c.10-5C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 2/12 | chr2 | 69788049 | |||||||
| chr2:69788311 | G | A | 1 | a0001c0001t0007g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.97+170G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788311 | |||||||
| chr2:69788359 | A | G | 175 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.97+218A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788359 | |||||||
| chr2:69788497 | G | A | 96 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(93): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.97+356G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788497 | |||||||
| chr2:69788565 | C | T | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+424C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788565 | |||||||
| chr2:69788649 | A | G | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+508A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788649 | |||||||
| chr2:69788653 | C | T | 41 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(38): Show |
45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+512C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788653 | |||||||
| chr2:69788699 | G | A | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+558G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788699 | |||||||
| chr2:69788707 | G | A | 94 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(91): Show |
95 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.97+566G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788707 | |||||||
| chr2:69788755 | G | A | 1 | a0001c0001t0008g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.97+614G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788755 | |||||||
| chr2:69788810 | G | C | 2 | a0001c0001t0005g0310 a0001c0001t0007g0309 |
2 | HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.97+669G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788810 | |||||||
| chr2:69788837 | C | CA | 8 | a0001c0001t0006g0101 a0003c0003t0004g0017 a0003c0003t0004g0019 others(5): Show |
8 | HG01891.hp1 HG02630.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.97+713dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69788837 | ||||||
| chr2:69788837 | CA | C | 171 | a0001c0001t0001g0055 a0001c0001t0001g0123 a0001c0001t0001g0220 others(168): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.97+713delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69788837 | ||||||
| chr2:69788896 | G | A | 41 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(38): Show |
45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+755G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788896 | |||||||
| chr2:69788921 | C | T | 94 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(91): Show |
95 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.97+780C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69788921 | |||||||
| chr2:69789067 | C | T | 1 | a0003c0003t0004g0121 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.97+926C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789067 | |||||||
| chr2:69789339 | G | C | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+1198G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789339 | |||||||
| chr2:69789341 | G | T | 1 | a0001c0001t0007g0221 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.97+1200G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789341 | |||||||
| chr2:69789392 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97+1251G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789392 | |||||||
| chr2:69789587 | C | T | 1 | a0001c0001t0006g0315 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.97+1446C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789587 | |||||||
| chr2:69789779 | A | T | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+1638A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789779 | |||||||
| chr2:69789809 | C | T | 1 | a0001c0001t0003g0225 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.97+1668C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789809 | |||||||
| chr2:69789838 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+1697G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789838 | |||||||
| chr2:69789890 | A | G | 175 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(172): Show |
179 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.97+1749A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789890 | |||||||
| chr2:69789925 | G | A | 20 | a0001c0001t0002g0267 a0001c0001t0003g0177 a0001c0001t0003g0205 others(17): Show |
20 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+1784G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789925 | |||||||
| chr2:69789971 | G | T | 96 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(93): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.97+1830G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789971 | |||||||
| chr2:69789972 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0283 |
2 | NA18950.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.97+1831G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69789972 | |||||||
| chr2:69790106 | T | G | 1 | a0001c0001t0004g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+1965T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790106 | |||||||
| chr2:69790106 | TTTGAACT others(5): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.97+1966_97+1977del others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790106 | |||||||
| chr2:69790211 | A | C | 1 | a0001c0001t0007g0204 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.97+2070A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790211 | |||||||
| chr2:69790260 | A | G | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+2119A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790260 | |||||||
| chr2:69790262 | A | T | 2 | a0002c0002t0002g0218 a0002c0002t0002g0219 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97+2121A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790262 | |||||||
| chr2:69790289 | G | A | 1 | a0001c0001t0006g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2148G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790289 | |||||||
| chr2:69790303 | A | G | 75 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(72): Show |
76 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.97+2162A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790303 | |||||||
| chr2:69790389 | G | A | 1 | a0002c0002t0002g0083 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.97+2248G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790389 | |||||||
| chr2:69790531 | C | T | 96 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(93): Show |
97 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.97+2390C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790531 | |||||||
| chr2:69790662 | C | T | 1 | a0002c0002t0002g0090 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.97+2521C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790662 | |||||||
| chr2:69790785 | T | C | 1 | a0002c0002t0002g0041 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.97+2644T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790785 | |||||||
| chr2:69790809 | T | C | 1 | a0001c0001t0006g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2668T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790809 | |||||||
| chr2:69790907 | G | C | 1 | a0001c0001t0006g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.97+2766G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790907 | |||||||
| chr2:69790910 | C | T | 1 | a0002c0002t0002g0155 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.97+2769C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69790910 | |||||||
| chr2:69791140 | A | C | 79 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0193 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.97+2999A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791140 | |||||||
| chr2:69791180 | T | A | 1 | a0001c0001t0001g0034 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.97+3039T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791180 | |||||||
| chr2:69791261 | A | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+3120A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791261 | |||||||
| chr2:69791262 | G | A | 1 | a0002c0002t0010g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.97+3121G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791262 | |||||||
| chr2:69791275 | G | A | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+3134G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791275 | |||||||
| chr2:69791330 | T | C | 223 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.97+3189T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791330 | |||||||
| chr2:69791364 | A | G | 231 | a0001c0001t0001g0055 a0001c0001t0001g0137 a0001c0001t0001g0220 others(228): Show |
240 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.97+3223A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791364 | |||||||
| chr2:69791505 | G | A | 3 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0044 |
3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.97+3364G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791505 | |||||||
| chr2:69791711 | T | C | 3 | a0002c0002t0002g0016 a0002c0002t0002g0113 a0002c0002t0002g0114 |
3 | HG02970.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.97+3570T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791711 | |||||||
| chr2:69791995 | G | A | 223 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(220): Show |
232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.97+3854G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69791995 | |||||||
| chr2:69792035 | A | G | 1 | a0001c0001t0005g0310 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97+3894A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792035 | |||||||
| chr2:69792237 | G | T | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+4096G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792237 | |||||||
| chr2:69792585 | GT | G | 149 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(146): Show |
155 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.97+4453delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69792585 | ||||||
| chr2:69792609 | G | GT | 11 | a0001c0001t0001g0036 a0002c0002t0002g0007 a0002c0002t0002g0097 others(8): Show |
12 | HG03688.hp1 HG04115.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+4477dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69792609 | ||||||
| chr2:69792619 | A | T | 73 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(70): Show |
74 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.97+4478A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792619 | |||||||
| chr2:69792620 | C | A | 73 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(70): Show |
74 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.97+4479C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792620 | |||||||
| chr2:69792735 | T | C | 3 | a0003c0003t0002g0104 a0003c0003t0004g0103 a0003c0003t0004g0105 |
3 | HG01891.hp1 HG02717.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.97+4594T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792735 | |||||||
| chr2:69792736 | C | G | 150 | a0001c0001t0001g0055 a0001c0001t0001g0220 a0001c0001t0002g0159 others(147): Show |
156 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.97+4595C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792736 | |||||||
| chr2:69792752 | T | C | 1 | a0003c0003t0002g0104 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.97+4611T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792752 | |||||||
| chr2:69792999 | A | G | 4 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0194 others(1): Show |
4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+4858A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69792999 | |||||||
| chr2:69793020 | A | G | 1 | a0003c0003t0004g0093 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.97+4879A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793020 | |||||||
| chr2:69793041 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.97+4900C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793041 | |||||||
| chr2:69793044 | G | C | 1 | a0001c0001t0005g0174 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.97+4903G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793044 | |||||||
| chr2:69793064 | C | T | 44 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(41): Show |
48 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.97+4923C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793064 | |||||||
| chr2:69793069 | T | C | 42 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.97+4928T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793069 | |||||||
| chr2:69793078 | C | T | 42 | a0001c0001t0006g0018 a0001c0001t0006g0336 a0001c0001t0007g0215 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.97+4937C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793078 | |||||||
| chr2:69793080 | C | T | 1 | a0001c0001t0005g0173 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.97+4939C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793080 | |||||||
| chr2:69793122 | C | T | 2 | a0002c0002t0002g0313 a0002c0002t0002g0314 |
2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.97+4981C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793122 | |||||||
| chr2:69793156 | A | G | 1 | a0002c0002t0002g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.97+5015A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793156 | |||||||
| chr2:69793201 | A | G | 148 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(145): Show |
154 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.97+5060A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793201 | |||||||
| chr2:69793229 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.97+5088C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793229 | |||||||
| chr2:69793250 | C | CAAAAAAA | 13 | a0001c0001t0003g0133 a0001c0001t0003g0230 a0001c0001t0005g0031 others(10): Show |
13 | HG01167.hp1 HG02486.hp1 HG02965.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+5115_97+5121dup others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | ||||||
| chr2:69793250 | C | CAAAAAAA others(1): Show |
128 | a0001c0001t0001g0055 a0001c0001t0002g0159 a0001c0001t0003g0008 others(125): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.97+5114_97+5121dup others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | ||||||
| chr2:69793250 | C | CAAAAAAA others(2): Show |
9 | a0001c0001t0003g0165 a0001c0001t0005g0316 a0001c0001t0005g0317 others(6): Show |
9 | HG01891.hp1 HG02155.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.97+5113_97+5121dup others(9): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | ||||||
| chr2:69793250 | C | CAAAAAAA others(3): Show |
3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.97+5112_97+5121dup others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793250 | ||||||
| chr2:69793262 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.97+5121A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793262 | |||||||
| chr2:69793357 | A | G | 13 | a0001c0001t0004g0129 a0001c0001t0006g0015 a0001c0001t0006g0020 others(10): Show |
13 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5216A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793357 | |||||||
| chr2:69793400 | T | C | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.97+5259T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793400 | |||||||
| chr2:69793539 | A | G | 2 | a0001c0001t0003g0162 a0001c0001t0008g0117 |
2 | NA18957.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.97+5398A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793539 | |||||||
| chr2:69793552 | A | G | 4 | a0001c0001t0007g0299 a0003c0003t0004g0017 a0003c0003t0004g0019 others(1): Show |
4 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+5411A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793552 | |||||||
| chr2:69793593 | T | C | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+5452T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793593 | |||||||
| chr2:69793596 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.97+5455G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793596 | |||||||
| chr2:69793637 | G | T | 5 | a0001c0001t0006g0124 a0002c0002t0002g0026 a0002c0002t0002g0297 others(2): Show |
5 | HG01109.hp1 HG01884.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+5496G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793637 | |||||||
| chr2:69793638 | C | T | 152 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(149): Show |
158 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.97+5497C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793638 | |||||||
| chr2:69793645 | G | C | 54 | a0001c0001t0005g0312 a0001c0001t0006g0018 a0001c0001t0006g0336 others(51): Show |
59 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.97+5504G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793645 | |||||||
| chr2:69793708 | A | G | 12 | a0001c0001t0005g0312 a0001c0001t0007g0204 a0001c0001t0007g0294 others(9): Show |
13 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5567A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793708 | |||||||
| chr2:69793760 | C | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.97+5619C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793760 | |||||||
| chr2:69793794 | G | A | 2 | a0001c0001t0003g0170 a0001c0001t0012g0179 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.97+5653G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793794 | |||||||
| chr2:69793833 | TA | T | 12 | a0001c0001t0005g0312 a0001c0001t0007g0204 a0001c0001t0007g0294 others(9): Show |
13 | HG01167.hp2 HG01169.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.97+5703delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69793833 | ||||||
| chr2:69793870 | A | AC | 250 | a0001c0001t0001g0053 a0001c0001t0001g0137 a0001c0001t0002g0159 others(247): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.97+5729_97+5730ins others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793870 | |||||||
| chr2:69793893 | A | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+5752A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69793893 | |||||||
| chr2:69794157 | G | T | 1 | a0001c0001t0005g0312 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.97+6016G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794157 | |||||||
| chr2:69794493 | GTATGTTA others(8): Show |
G | 45 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0003g0141 others(42): Show |
45 | HG00544.hp1 HG00741.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.97+6381_97+6395del others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | ||||||
| chr2:69794493 | GTATGTTA others(23): Show |
G | 1 | a0001c0001t0006g0298 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.97+6366_97+6395del others(30): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | ||||||
| chr2:69794493 | GTATGTTA others(28): Show |
G | 2 | a0001c0001t0006g0013 a0001c0001t0006g0014 |
2 | HG02559.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.97+6366_97+6400del others(35): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794493 | ||||||
| chr2:69794497 | GTTATGTT others(3): Show |
G | 24 | a0001c0001t0003g0119 a0001c0001t0003g0133 a0001c0001t0003g0136 others(21): Show |
24 | HG00673.hp2 HG01243.hp1 HG01515.hp2 others(21): Show |
intron_variant | MODIFIER | c.97+6366_97+6375del others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794497 | ||||||
| chr2:69794497 | GTTATGTT others(18): Show |
G | 3 | a0001c0001t0003g0169 a0001c0001t0003g0241 a0001c0001t0011g0208 |
3 | HG00597.hp1 HG02280.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.97+6366_97+6390del others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794497 | ||||||
| chr2:69794502 | GTTATA | G | 17 | a0001c0001t0002g0159 a0001c0001t0003g0022 a0001c0001t0003g0046 others(14): Show |
17 | HG00438.hp2 HG00642.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.97+6366_97+6370del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794502 | ||||||
| chr2:69794502 | GTTATATT others(13): Show |
G | 14 | a0001c0001t0003g0008 a0001c0001t0003g0143 a0001c0001t0003g0152 others(11): Show |
15 | HG02135.hp2 HG02300.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.97+6366_97+6385del others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794502 | ||||||
| chr2:69794507 | A | G | 7 | a0001c0001t0003g0096 a0001c0001t0003g0120 a0001c0001t0003g0146 others(4): Show |
7 | HG00609.hp2 HG02155.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.97+6366A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794507 | |||||||
| chr2:69794507 | ATTATGTT others(13): Show |
A | 2 | a0001c0001t0006g0018 a0003c0003t0004g0243 |
2 | HG02717.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.97+6381_97+6400del others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794507 | ||||||
| chr2:69794512 | GTTATGTT others(3): Show |
G | 14 | a0001c0001t0001g0281 a0001c0001t0007g0215 a0003c0003t0002g0102 others(11): Show |
16 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6381_97+6390del others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794512 | ||||||
| chr2:69794517 | GTTATA | G | 21 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 others(18): Show |
24 | HG00738.hp2 HG01106.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.97+6381_97+6385del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794517 | ||||||
| chr2:69794522 | A | ATTATG | 54 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0045 others(51): Show |
54 | HG00099.hp2 HG00597.hp2 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.97+6431_97+6435dup others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | A | ATTATGTT others(3): Show |
57 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0034 others(54): Show |
57 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.97+6426_97+6435dup others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | A | ATTATGTT others(8): Show |
25 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0077 others(22): Show |
25 | HG00544.hp2 HG01070.hp2 HG01358.hp2 others(22): Show |
intron_variant | MODIFIER | c.97+6421_97+6435dup others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | A | ATTATGTT others(13): Show |
3 | a0001c0001t0001g0325 a0001c0001t0005g0150 a0001c0001t0007g0196 |
3 | NA19005.hp1 NA19072.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.97+6416_97+6435dup others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | A | ATTATGTT others(18): Show |
1 | a0001c0001t0001g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.97+6411_97+6435dup others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | A | G | 83 | a0001c0001t0002g0159 a0001c0001t0003g0022 a0001c0001t0003g0046 others(80): Show |
83 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.97+6381A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794522 | |||||||
| chr2:69794522 | ATTATG | A | 15 | a0001c0001t0005g0092 a0002c0002t0002g0002 a0002c0002t0002g0026 others(12): Show |
16 | HG00438.hp1 HG00609.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+6431_97+6435del others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | ATTATGTT others(8): Show |
A | 1 | a0002c0002t0002g0057 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+6421_97+6435del others(15): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794522 | ATTATGTT others(18): Show |
A | 11 | a0002c0002t0001g0262 a0002c0002t0002g0041 a0002c0002t0002g0042 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+6411_97+6435del others(25): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69794522 | ||||||
| chr2:69794601 | C | T | 5 | a0001c0001t0007g0299 a0003c0003t0002g0102 a0003c0003t0004g0017 others(2): Show |
5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6460C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794601 | |||||||
| chr2:69794656 | G | T | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+6515G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794656 | |||||||
| chr2:69794705 | G | A | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97+6564G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794705 | |||||||
| chr2:69794831 | A | G | 5 | a0001c0001t0007g0299 a0003c0003t0002g0102 a0003c0003t0004g0017 others(2): Show |
5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+6690A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794831 | |||||||
| chr2:69794835 | G | A | 1 | a0001c0001t0007g0215 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.97+6694G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794835 | |||||||
| chr2:69794945 | C | T | 75 | a0001c0001t0004g0129 a0001c0001t0005g0312 a0001c0001t0006g0013 others(72): Show |
80 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.97+6804C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69794945 | |||||||
| chr2:69795119 | G | A | 1 | a0001c0001t0004g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.97+6978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795119 | |||||||
| chr2:69795314 | T | C | 116 | a0001c0001t0002g0159 a0001c0001t0006g0018 a0001c0001t0006g0112 others(113): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.97+7173T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795314 | |||||||
| chr2:69795348 | G | C | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.97+7207G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795348 | |||||||
| chr2:69795525 | A | G | 11 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0107 others(8): Show |
11 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+7384A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795525 | |||||||
| chr2:69795654 | G | A | 5 | a0001c0001t0007g0299 a0003c0003t0002g0102 a0003c0003t0004g0017 others(2): Show |
5 | HG02818.hp2 HG02965.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+7513G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795654 | |||||||
| chr2:69795684 | C | T | 1 | a0001c0001t0006g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97+7543C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795684 | |||||||
| chr2:69795772 | C | G | 1 | a0005c0005t0007g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.97+7631C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795772 | |||||||
| chr2:69795774 | T | C | 41 | a0001c0001t0007g0215 a0002c0002t0013g0127 a0003c0003t0002g0104 others(38): Show |
45 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.97+7633T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795774 | |||||||
| chr2:69795786 | T | C | 1 | a0001c0001t0005g0310 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.97+7645T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69795786 | |||||||
| chr2:69796081 | G | C | 4 | a0001c0001t0006g0315 a0002c0002t0002g0026 a0002c0002t0002g0306 others(1): Show |
4 | HG01109.hp1 HG01884.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+7940G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796081 | |||||||
| chr2:69796111 | A | G | 1 | a0001c0001t0008g0117 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.97+7970A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796111 | |||||||
| chr2:69796337 | T | C | 88 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(85): Show |
89 | HG00140.hp1 HG00140.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.97+8196T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796337 | |||||||
| chr2:69796346 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.98-8187G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796346 | |||||||
| chr2:69796364 | T | A | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-8169T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796364 | |||||||
| chr2:69796411 | A | G | 1 | a0002c0002t0010g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.98-8122A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796411 | |||||||
| chr2:69796534 | A | G | 1 | a0003c0003t0004g0295 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.98-7999A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796534 | |||||||
| chr2:69796923 | G | A | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7610G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796923 | |||||||
| chr2:69796924 | C | T | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.98-7609C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69796924 | |||||||
| chr2:69797001 | TA | T | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-7530delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69797001 | ||||||
| chr2:69797015 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.98-7518A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797015 | |||||||
| chr2:69797128 | C | T | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7405C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797128 | |||||||
| chr2:69797159 | C | T | 1 | a0001c0001t0003g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.98-7374C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797159 | |||||||
| chr2:69797282 | T | G | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-7251T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797282 | |||||||
| chr2:69797490 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-7043G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797490 | |||||||
| chr2:69797533 | A | G | 150 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(147): Show |
155 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.98-7000A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797533 | |||||||
| chr2:69797626 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.98-6907C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797626 | |||||||
| chr2:69797691 | G | T | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-6842G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797691 | |||||||
| chr2:69797966 | T | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-6567T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69797966 | |||||||
| chr2:69798007 | T | C | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-6526T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798007 | |||||||
| chr2:69798033 | C | A | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-6500C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798033 | |||||||
| chr2:69798086 | G | A | 1 | a0001c0001t0020g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.98-6447G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798086 | |||||||
| chr2:69798093 | C | A | 1 | a0001c0001t0001g0256 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.98-6440C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798093 | |||||||
| chr2:69798141 | G | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-6392G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798141 | |||||||
| chr2:69798189 | A | T | 1 | a0002c0002t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-6344A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798189 | |||||||
| chr2:69798325 | A | G | 150 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(147): Show |
155 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.98-6208A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798325 | |||||||
| chr2:69798457 | G | T | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-6076G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798457 | |||||||
| chr2:69798495 | AG | A | 4 | a0004c0004t0005g0199 a0004c0004t0005g0202 a0004c0004t0007g0200 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.98-6035delG | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69798495 | ||||||
| chr2:69798576 | G | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-5957G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798576 | |||||||
| chr2:69798605 | C | T | 76 | a0002c0002t0001g0262 a0002c0002t0002g0002 a0002c0002t0002g0004 others(73): Show |
80 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.98-5928C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798605 | |||||||
| chr2:69798606 | G | A | 1 | a0001c0001t0003g0183 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.98-5927G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798606 | |||||||
| chr2:69798677 | G | C | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-5856G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798677 | |||||||
| chr2:69798856 | G | A | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-5677G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69798856 | |||||||
| chr2:69799184 | CTG | C | 42 | a0001c0001t0007g0215 a0003c0003t0002g0102 a0003c0003t0002g0104 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-5345_98-5344del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69799184 | ||||||
| chr2:69799224 | T | C | 1 | a0001c0001t0007g0196 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-5309T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799224 | |||||||
| chr2:69799350 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.98-5183G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799350 | |||||||
| chr2:69799555 | G | A | 3 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0298 |
3 | HG02559.hp1 HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-4978G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799555 | |||||||
| chr2:69799676 | G | A | 42 | a0001c0001t0007g0215 a0003c0003t0002g0102 a0003c0003t0002g0104 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4857G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799676 | |||||||
| chr2:69799857 | T | G | 1 | a0001c0001t0006g0018 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.98-4676T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69799857 | |||||||
| chr2:69800061 | CTATT | C | 42 | a0001c0001t0007g0215 a0003c0003t0002g0102 a0003c0003t0002g0104 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4471_98-4468del others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800061 | |||||||
| chr2:69800067 | A | C | 42 | a0001c0001t0007g0215 a0003c0003t0002g0102 a0003c0003t0002g0104 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4466A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800067 | |||||||
| chr2:69800068 | G | T | 42 | a0001c0001t0007g0215 a0003c0003t0002g0102 a0003c0003t0002g0104 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-4465G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800068 | |||||||
| chr2:69800089 | A | G | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-4444A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800089 | |||||||
| chr2:69800297 | G | A | 7 | a0002c0002t0002g0110 a0002c0002t0002g0111 a0002c0002t0002g0125 others(4): Show |
7 | HG01192.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4236G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800297 | |||||||
| chr2:69800297 | G | GGTAT | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-4234_98-4233ins others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69800297 | ||||||
| chr2:69800319 | A | C | 1 | a0002c0002t0001g0262 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98-4214A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800319 | |||||||
| chr2:69800354 | A | G | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.98-4179A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800354 | |||||||
| chr2:69800664 | A | G | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.98-3869A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800664 | |||||||
| chr2:69800670 | T | C | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-3863T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800670 | |||||||
| chr2:69800777 | G | C | 8 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0248 others(5): Show |
9 | HG00597.hp2 HG02523.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.98-3756G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800777 | |||||||
| chr2:69800787 | C | T | 11 | a0001c0001t0003g0142 a0002c0002t0001g0262 a0002c0002t0002g0041 others(8): Show |
11 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-3746C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800787 | |||||||
| chr2:69800864 | A | G | 1 | a0002c0002t0001g0262 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.98-3669A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800864 | |||||||
| chr2:69800963 | G | T | 1 | a0002c0002t0002g0058 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.98-3570G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69800963 | |||||||
| chr2:69801119 | C | T | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.98-3414C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801119 | |||||||
| chr2:69801321 | A | G | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.98-3212A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801321 | |||||||
| chr2:69801403 | G | GT | 124 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(121): Show |
129 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.98-3120dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69801403 | ||||||
| chr2:69801450 | T | A | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.98-3083T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801450 | |||||||
| chr2:69801498 | G | A | 1 | a0003c0003t0004g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.98-3035G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801498 | |||||||
| chr2:69801726 | A | C | 15 | a0001c0001t0006g0015 a0001c0001t0006g0018 a0001c0001t0006g0020 others(12): Show |
15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.98-2807A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801726 | |||||||
| chr2:69801751 | C | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-2782C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801751 | |||||||
| chr2:69801772 | A | G | 150 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(147): Show |
155 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.98-2761A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801772 | |||||||
| chr2:69801844 | A | G | 81 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(78): Show |
82 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.98-2689A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801844 | |||||||
| chr2:69801943 | C | T | 1 | a0002c0002t0010g0023 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98-2590C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801943 | |||||||
| chr2:69801994 | C | A | 1 | a0002c0002t0002g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.98-2539C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69801994 | |||||||
| chr2:69802178 | A | G | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-2355A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802178 | |||||||
| chr2:69802495 | A | G | 220 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(217): Show |
229 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.98-2038A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802495 | |||||||
| chr2:69802571 | C | T | 2 | a0001c0001t0001g0232 a0001c0001t0001g0258 |
2 | HG02040.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.98-1962C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802571 | |||||||
| chr2:69802680 | C | T | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-1853C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802680 | |||||||
| chr2:69802709 | C | CA | 16 | a0001c0001t0001g0036 a0001c0001t0001g0266 a0001c0001t0006g0013 others(13): Show |
16 | HG02280.hp2 HG02559.hp1 HG02622.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-1807dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | ||||||
| chr2:69802709 | C | CAA | 62 | a0002c0002t0002g0002 a0002c0002t0002g0004 a0002c0002t0002g0005 others(59): Show |
66 | HG00438.hp1 HG00609.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.98-1808_98-1807dup others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | ||||||
| chr2:69802709 | CA | C | 7 | a0001c0001t0001g0098 a0001c0001t0001g0249 a0001c0001t0001g0268 others(4): Show |
7 | HG01070.hp1 HG01167.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.98-1807delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | ||||||
| chr2:69802709 | CAA | C | 123 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(120): Show |
128 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.98-1808_98-1807del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69802709 | ||||||
| chr2:69802830 | T | C | 220 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(217): Show |
229 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.98-1703T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802830 | |||||||
| chr2:69802841 | C | T | 2 | a0001c0001t0003g0162 a0001c0001t0008g0117 |
2 | NA18957.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.98-1692C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802841 | |||||||
| chr2:69802977 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.98-1556G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69802977 | |||||||
| chr2:69803070 | A | G | 220 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(217): Show |
229 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.98-1463A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803070 | |||||||
| chr2:69803137 | G | A | 25 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.98-1396G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803137 | |||||||
| chr2:69803230 | A | G | 1 | a0003c0003t0004g0331 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.98-1303A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803230 | |||||||
| chr2:69803321 | G | A | 2 | a0003c0003t0004g0103 a0003c0003t0004g0105 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.98-1212G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803321 | |||||||
| chr2:69803337 | C | G | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-1196C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803337 | |||||||
| chr2:69803402 | C | T | 6 | a0001c0001t0005g0322 a0001c0001t0005g0326 a0001c0001t0005g0327 others(3): Show |
6 | NA18961.hp2 NA18965.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-1131C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803402 | |||||||
| chr2:69803695 | C | T | 220 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(217): Show |
229 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(226): Show |
intron_variant | MODIFIER | c.98-838C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803695 | |||||||
| chr2:69803717 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.98-816A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803717 | |||||||
| chr2:69803773 | A | G | 125 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(122): Show |
130 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.98-760A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803773 | |||||||
| chr2:69803855 | T | A | 1 | a0001c0001t0001g0249 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.98-678T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803855 | |||||||
| chr2:69803864 | G | A | 25 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.98-669G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803864 | |||||||
| chr2:69803878 | A | G | 285 | a0001c0001t0001g0028 a0001c0001t0001g0032 a0001c0001t0001g0034 others(282): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.98-655A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803878 | |||||||
| chr2:69803904 | G | A | 1 | a0001c0001t0003g0242 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-629G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803904 | |||||||
| chr2:69803921 | T | A | 1 | a0001c0001t0003g0213 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.98-612T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69803921 | |||||||
| chr2:69804093 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0315 |
2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.98-440G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804093 | |||||||
| chr2:69804137 | C | CA | 62 | a0001c0001t0001g0249 a0001c0001t0001g0268 a0001c0001t0007g0221 others(59): Show |
66 | HG00438.hp1 HG00609.hp1 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.98-374dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | ||||||
| chr2:69804137 | CA | C | 7 | a0001c0001t0001g0032 a0001c0001t0001g0172 a0001c0001t0001g0237 others(4): Show |
7 | HG03834.hp2 HG03927.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-374delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | ||||||
| chr2:69804137 | CAA | C | 77 | a0001c0001t0002g0159 a0001c0001t0003g0008 a0001c0001t0003g0022 others(74): Show |
78 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.98-375_98-374delAA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | ||||||
| chr2:69804137 | CAAA | C | 6 | a0001c0001t0003g0118 a0001c0001t0003g0183 a0001c0001t0003g0238 others(3): Show |
6 | HG02922.hp2 HG03209.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-376_98-374delAA others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | ||||||
| chr2:69804137 | CAAAA | C | 42 | a0001c0001t0007g0215 a0001c0001t0007g0299 a0003c0003t0002g0102 others(39): Show |
46 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.98-377_98-374delAA others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 69804137 | ||||||
| chr2:69804159 | A | AAAAC | 10 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(7): Show |
10 | HG01243.hp1 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.98-374_98-373insAA others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | |||||||
| chr2:69804159 | A | AAAC | 13 | a0001c0001t0006g0015 a0001c0001t0006g0018 a0001c0001t0006g0025 others(10): Show |
13 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.98-374_98-373insAA others(1): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | |||||||
| chr2:69804159 | A | C | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.98-374A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804159 | |||||||
| chr2:69804257 | G | A | 2 | a0003c0003t0004g0068 a0003c0003t0004g0071 |
2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.98-276G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 3/12 | chr2 | 69804257 | |||||||
| chr2:69804637 | A | G | 1 | a0001c0001t0003g0165 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.192+10A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804637 | |||||||
| chr2:69804665 | C | G | 244 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(241): Show |
253 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.192+38C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804665 | |||||||
| chr2:69804809 | A | G | 244 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(241): Show |
253 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.192+182A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69804809 | |||||||
| chr2:69805013 | C | T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+386C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805013 | |||||||
| chr2:69805046 | C | CA | 48 | a0001c0001t0001g0077 a0001c0001t0001g0229 a0001c0001t0001g0260 others(45): Show |
52 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.192+445dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | ||||||
| chr2:69805046 | C | CAA | 15 | a0001c0001t0003g0084 a0001c0001t0003g0140 a0001c0001t0003g0141 others(12): Show |
15 | HG00544.hp1 HG01074.hp1 HG01361.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+444_192+445dup others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | ||||||
| chr2:69805046 | C | CAAA | 143 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(140): Show |
147 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.192+443_192+445dup others(3): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | ||||||
| chr2:69805046 | C | CAAAA | 22 | a0001c0001t0003g0120 a0001c0001t0003g0142 a0001c0001t0003g0149 others(19): Show |
23 | HG00673.hp2 HG01433.hp1 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+442_192+445dup others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | ||||||
| chr2:69805046 | CAAAAAAA | C | 9 | a0001c0001t0006g0020 a0001c0001t0006g0107 a0001c0001t0006g0112 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.192+439_192+445del others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805046 | ||||||
| chr2:69805049 | A | G | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+422A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805049 | |||||||
| chr2:69805128 | TCTGACCC others(10): Show |
T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+502_192+518del others(17): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805128 | |||||||
| chr2:69805146 | G | A | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+519G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805146 | |||||||
| chr2:69805184 | C | T | 98 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(95): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.192+557C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805184 | |||||||
| chr2:69805353 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192+726T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805353 | |||||||
| chr2:69805420 | A | G | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.192+793A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805420 | |||||||
| chr2:69805475 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.192+848G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805475 | |||||||
| chr2:69805478 | C | T | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+851C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805478 | |||||||
| chr2:69805480 | C | G | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+853C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805480 | |||||||
| chr2:69805481 | C | T | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.192+854C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805481 | |||||||
| chr2:69805503 | G | A | 25 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+876G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805503 | |||||||
| chr2:69805521 | G | A | 25 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(22): Show |
25 | HG01167.hp1 HG01167.hp2 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.193-864G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805521 | |||||||
| chr2:69805528 | T | C | 2 | a0001c0001t0004g0129 a0001c0001t0006g0101 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-857T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805528 | |||||||
| chr2:69805570 | C | T | 98 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(95): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.193-815C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805570 | |||||||
| chr2:69805579 | C | G | 1 | a0001c0001t0003g0162 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.193-806C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805579 | |||||||
| chr2:69805604 | T | TA | 69 | a0001c0001t0003g0142 a0001c0001t0004g0129 a0001c0001t0006g0013 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.193-765dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr2 | 69805604 | ||||||
| chr2:69805621 | G | A | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.193-764G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805621 | |||||||
| chr2:69805622 | A | G | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.193-763A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805622 | |||||||
| chr2:69805709 | A | G | 1 | a0001c0001t0003g0206 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.193-676A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805709 | |||||||
| chr2:69805735 | A | G | 99 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(96): Show |
100 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.193-650A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805735 | |||||||
| chr2:69805909 | C | T | 1 | a0002c0002t0010g0216 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.193-476C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 4/12 | chr2 | 69805909 | |||||||
| chr2:69806517 | G | A | 97 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(94): Show |
101 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.306+19G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806517 | |||||||
| chr2:69806579 | G | C | 148 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(145): Show |
153 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.306+81G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806579 | |||||||
| chr2:69806663 | A | T | 97 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(94): Show |
101 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.306+165A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806663 | |||||||
| chr2:69806870 | T | A | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.306+372T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806870 | |||||||
| chr2:69806877 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.306+379A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806877 | |||||||
| chr2:69806948 | A | T | 1 | a0002c0002t0002g0214 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.306+450A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69806948 | |||||||
| chr2:69807251 | T | C | 1 | a0001c0001t0003g0154 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.307-655T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807251 | |||||||
| chr2:69807311 | T | C | 5 | a0001c0001t0003g0177 a0001c0001t0003g0205 a0001c0001t0003g0206 others(2): Show |
5 | NA18939.hp1 NA18987.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.307-595T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807311 | |||||||
| chr2:69807333 | G | C | 96 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(93): Show |
100 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.307-573G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807333 | |||||||
| chr2:69807358 | C | T | 2 | a0001c0001t0006g0025 a0001c0001t0006g0217 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.307-548C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807358 | |||||||
| chr2:69807661 | A | G | 241 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(238): Show |
250 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(247): Show |
intron_variant | MODIFIER | c.307-245A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807661 | |||||||
| chr2:69807818 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.307-88A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807818 | |||||||
| chr2:69807882 | C | T | 2 | a0002c0002t0002g0218 a0002c0002t0002g0219 |
2 | HG02647.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.307-24C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 5/12 | chr2 | 69807882 | |||||||
| chr2:69808020 | T | C | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+24T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808020 | |||||||
| chr2:69808042 | A | G | 2 | a0001c0001t0004g0129 a0001c0001t0006g0101 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.397+46A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808042 | |||||||
| chr2:69808061 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.397+65G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808061 | |||||||
| chr2:69808153 | C | G | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.397+157C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808153 | |||||||
| chr2:69808350 | C | G | 73 | a0001c0001t0001g0051 a0001c0001t0001g0085 a0001c0001t0001g0123 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.397+354C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808350 | |||||||
| chr2:69808406 | G | A | 3 | a0002c0002t0002g0041 a0002c0002t0002g0042 a0002c0002t0002g0044 |
3 | HG01074.hp1 HG01433.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.397+410G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808406 | |||||||
| chr2:69808486 | C | T | 1 | a0002c0002t0002g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.397+490C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808486 | |||||||
| chr2:69808670 | C | CT | 9 | a0003c0003t0002g0102 a0003c0003t0002g0104 a0003c0003t0004g0074 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.397+683dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr2 | 69808670 | ||||||
| chr2:69808912 | T | C | 11 | a0001c0001t0005g0031 a0001c0001t0005g0033 a0001c0001t0005g0316 others(8): Show |
11 | HG02135.hp2 HG02155.hp1 HG03704.hp1 others(8): Show |
intron_variant | MODIFIER | c.397+916T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69808912 | |||||||
| chr2:69809081 | T | G | 3 | a0002c0002t0002g0005 a0002c0002t0002g0334 a0002c0002t0002g0335 |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+1085T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809081 | |||||||
| chr2:69809156 | T | C | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.397+1160T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809156 | |||||||
| chr2:69809311 | A | G | 1 | a0001c0001t0018g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.398-1283A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809311 | |||||||
| chr2:69809418 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.398-1176G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809418 | |||||||
| chr2:69809579 | A | G | 240 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(237): Show |
249 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.398-1015A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809579 | |||||||
| chr2:69809906 | C | T | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.398-688C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809906 | |||||||
| chr2:69809992 | C | T | 1 | a0001c0001t0001g0268 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.398-602C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69809992 | |||||||
| chr2:69810002 | G | C | 2 | a0001c0001t0005g0312 a0001c0001t0007g0204 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.398-592G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810002 | |||||||
| chr2:69810065 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.398-529C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810065 | |||||||
| chr2:69810359 | G | T | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.398-235G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810359 | |||||||
| chr2:69810534 | G | A | 1 | a0003c0003t0004g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.398-60G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 6/12 | chr2 | 69810534 | |||||||
| chr2:69810708 | T | G | 1 | a0002c0002t0002g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.477+35T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69810708 | |||||||
| chr2:69811046 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.477+373G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811046 | |||||||
| chr2:69811066 | A | G | 47 | a0001c0001t0017g0318 a0003c0003t0002g0102 a0003c0003t0002g0104 others(44): Show |
51 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.477+393A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811066 | |||||||
| chr2:69811100 | C | G | 242 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(239): Show |
251 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.477+427C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811100 | |||||||
| chr2:69811179 | A | C | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.477+506A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811179 | |||||||
| chr2:69811256 | G | A | 8 | a0001c0001t0001g0053 a0001c0001t0001g0075 a0001c0001t0001g0076 others(5): Show |
8 | HG02040.hp1 NA18950.hp1 NA18951.hp1 others(5): Show |
intron_variant | MODIFIER | c.477+583G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811256 | |||||||
| chr2:69811275 | G | A | 1 | a0001c0001t0011g0208 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.477+602G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811275 | |||||||
| chr2:69811660 | A | C | 215 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(212): Show |
224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.477+987A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811660 | |||||||
| chr2:69811733 | A | T | 5 | a0001c0001t0003g0046 a0001c0001t0003g0116 a0001c0001t0003g0136 others(2): Show |
5 | HG01255.hp2 HG01928.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-920A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811733 | |||||||
| chr2:69811794 | C | T | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.478-859C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69811794 | |||||||
| chr2:69812092 | C | T | 243 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(240): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.478-561C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812092 | |||||||
| chr2:69812094 | A | T | 7 | a0003c0003t0002g0102 a0003c0003t0004g0074 a0003c0003t0004g0103 others(4): Show |
7 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-559A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812094 | |||||||
| chr2:69812121 | CT | C | 71 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(68): Show |
75 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.478-514delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 69812121 | ||||||
| chr2:69812131 | T | G | 97 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.478-522T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812131 | |||||||
| chr2:69812223 | G | C | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.478-430G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812223 | |||||||
| chr2:69812272 | G | A | 4 | a0004c0004t0005g0199 a0004c0004t0005g0202 a0004c0004t0007g0200 others(1): Show |
4 | HG02809.hp1 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.478-381G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812272 | |||||||
| chr2:69812277 | C | A | 14 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0025 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.478-376C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812277 | |||||||
| chr2:69812277 | C | G | 1 | a0002c0002t0002g0081 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.478-376C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812277 | |||||||
| chr2:69812496 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.478-157G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812496 | |||||||
| chr2:69812496 | G | C | 1 | a0005c0005t0007g0011 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.478-157G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812496 | |||||||
| chr2:69812545 | A | C | 243 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(240): Show |
252 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.478-108A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812545 | |||||||
| chr2:69812643 | T | C | 1 | a0001c0001t0017g0318 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.478-10T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 7/12 | chr2 | 69812643 | |||||||
| chr2:69812902 | T | A | 1 | a0002c0002t0002g0176 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.534+193T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69812902 | |||||||
| chr2:69813012 | C | T | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.534+303C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813012 | |||||||
| chr2:69813015 | T | C | 102 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(99): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.534+306T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813015 | |||||||
| chr2:69813162 | A | G | 2 | a0003c0003t0004g0103 a0003c0003t0004g0105 |
2 | HG01891.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.534+453A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813162 | |||||||
| chr2:69813191 | C | T | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.534+482C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813191 | |||||||
| chr2:69813249 | AT | A | 72 | a0001c0001t0001g0172 a0001c0001t0001g0229 a0001c0001t0001g0291 others(69): Show |
76 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.534+556delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813249 | ||||||
| chr2:69813410 | G | A | 176 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(173): Show |
181 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.534+701G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813410 | |||||||
| chr2:69813508 | C | G | 2 | a0001c0001t0006g0018 a0001c0001t0006g0336 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.534+799C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813508 | |||||||
| chr2:69813662 | A | G | 1 | a0002c0002t0013g0127 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.534+953A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813662 | |||||||
| chr2:69813738 | TTCTC | T | 13 | a0001c0001t0001g0045 a0001c0001t0001g0233 a0001c0001t0001g0234 others(10): Show |
13 | HG00099.hp2 HG01070.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.534+1047_534+1050d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813738 | ||||||
| chr2:69813754 | CTCTCT | C | 92 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(89): Show |
93 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.534+1047_534+1051d others(7): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813754 | ||||||
| chr2:69813757 | TC | T | 8 | a0001c0001t0006g0124 a0002c0002t0002g0083 a0002c0002t0002g0113 others(5): Show |
8 | HG01257.hp1 HG01257.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.534+1049delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813757 | |||||||
| chr2:69813758 | C | T | 133 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0004g0129 others(130): Show |
141 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(138): Show |
intron_variant | MODIFIER | c.534+1049C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813758 | |||||||
| chr2:69813758 | CT | C | 7 | a0001c0001t0001g0028 a0001c0001t0001g0229 a0001c0001t0001g0273 others(4): Show |
7 | HG01515.hp1 HG03017.hp2 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+1068delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69813758 | ||||||
| chr2:69813872 | C | T | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.534+1163C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813872 | |||||||
| chr2:69813901 | G | A | 175 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(172): Show |
180 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.534+1192G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69813901 | |||||||
| chr2:69814049 | C | T | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.534+1340C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814049 | |||||||
| chr2:69814145 | C | CA | 7 | a0002c0002t0002g0214 a0003c0003t0004g0074 a0003c0003t0004g0103 others(4): Show |
7 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.534+1445dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814145 | ||||||
| chr2:69814308 | G | A | 141 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0004g0129 others(138): Show |
149 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.534+1599G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814308 | |||||||
| chr2:69814342 | C | CT | 50 | a0001c0001t0001g0075 a0001c0001t0001g0137 a0001c0001t0001g0172 others(47): Show |
54 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.534+1654dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | ||||||
| chr2:69814342 | C | CTT | 71 | a0001c0001t0003g0084 a0001c0001t0003g0144 a0001c0001t0003g0146 others(68): Show |
71 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.534+1653_534+1654d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | ||||||
| chr2:69814342 | C | CTTT | 116 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(113): Show |
121 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.534+1652_534+1654d others(5): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | ||||||
| chr2:69814342 | C | CTTTT | 6 | a0001c0001t0003g0116 a0001c0001t0003g0136 a0001c0001t0018g0024 others(3): Show |
6 | HG01928.hp2 HG01975.hp1 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.534+1651_534+1654d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | ||||||
| chr2:69814342 | CT | C | 9 | a0001c0001t0001g0282 a0001c0001t0001g0291 a0001c0001t0001g0321 others(6): Show |
9 | HG01069.hp2 HG01169.hp2 HG03239.hp1 others(6): Show |
intron_variant | MODIFIER | c.534+1654delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814342 | ||||||
| chr2:69814370 | G | A | 1 | a0003c0003t0004g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.534+1661G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814370 | |||||||
| chr2:69814415 | G | A | 2 | a0001c0001t0001g0075 a0001c0001t0001g0077 |
2 | HG02040.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.535-1686G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814415 | |||||||
| chr2:69814597 | C | T | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1504C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814597 | |||||||
| chr2:69814637 | C | T | 1 | a0001c0006t0006g0012 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.535-1464C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814637 | |||||||
| chr2:69814652 | A | T | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1449A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814652 | |||||||
| chr2:69814697 | A | G | 3 | a0002c0002t0002g0313 a0002c0002t0002g0314 a0003c0003t0002g0104 |
3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.535-1404A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814697 | |||||||
| chr2:69814726 | C | A | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1375C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814726 | |||||||
| chr2:69814733 | G | C | 2 | a0001c0001t0006g0018 a0001c0001t0006g0336 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.535-1368G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814733 | |||||||
| chr2:69814743 | G | GGT | 14 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0258 others(11): Show |
14 | HG00323.hp1 HG00597.hp2 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-1308_535-1307d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | ||||||
| chr2:69814743 | G | GGTGT | 9 | a0001c0001t0001g0034 a0001c0001t0001g0055 a0001c0001t0001g0232 others(6): Show |
9 | HG01070.hp2 HG01361.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.535-1310_535-1307d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | ||||||
| chr2:69814743 | G | T | 2 | a0001c0001t0001g0292 a0001c0001t0007g0309 |
2 | HG00323.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.535-1358G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814743 | |||||||
| chr2:69814743 | GGT | G | 19 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0187 others(16): Show |
19 | HG01175.hp2 HG01255.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.535-1308_535-1307d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | ||||||
| chr2:69814743 | GGTGT | G | 18 | a0001c0001t0001g0028 a0001c0001t0001g0035 a0001c0001t0001g0053 others(15): Show |
18 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.535-1310_535-1307d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | ||||||
| chr2:69814743 | GGTGTGT | G | 14 | a0001c0001t0001g0045 a0001c0001t0001g0075 a0001c0001t0001g0077 others(11): Show |
14 | HG00099.hp2 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-1312_535-1307d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814743 | ||||||
| chr2:69814745 | T | G | 2 | a0001c0001t0005g0322 a0001c0006t0006g0012 |
2 | HG02970.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.535-1356T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814745 | |||||||
| chr2:69814746 | G | A | 1 | a0001c0001t0005g0312 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.535-1355G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814746 | |||||||
| chr2:69814777 | TGTGTGTG others(17): Show |
T | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.535-1322_535-1299d others(26): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814777 | ||||||
| chr2:69814781 | TGTGTGTG others(7): Show |
T | 2 | a0001c0001t0003g0152 a0001c0001t0008g0151 |
2 | NA19000.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.535-1318_535-1305d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814781 | ||||||
| chr2:69814782 | GTGTGTGT others(11): Show |
G | 6 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0003c0003t0004g0103 others(3): Show |
6 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.535-1318_535-1301d others(20): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814782 | |||||||
| chr2:69814783 | TGTGTGTG others(5): Show |
T | 3 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0180 |
3 | NA18945.hp1 NA18998.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.535-1316_535-1305d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814783 | ||||||
| chr2:69814783 | TGTGTGTG others(7): Show |
T | 2 | a0002c0002t0002g0334 a0002c0002t0002g0335 |
2 | HG02622.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.535-1316_535-1303d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814783 | ||||||
| chr2:69814784 | GTGTGTGT others(9): Show |
G | 15 | a0001c0001t0006g0015 a0001c0001t0006g0018 a0001c0001t0006g0020 others(12): Show |
15 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-1316_535-1301d others(18): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814784 | |||||||
| chr2:69814785 | TGTGTGTG others(3): Show |
T | 25 | a0001c0001t0003g0008 a0001c0001t0003g0046 a0001c0001t0003g0096 others(22): Show |
26 | HG00438.hp2 HG00597.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.535-1314_535-1305d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814785 | ||||||
| chr2:69814785 | TGTGTGTG others(5): Show |
T | 2 | a0002c0002t0002g0005 a0003c0003t0002g0102 |
2 | HG02897.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.535-1314_535-1303d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814785 | ||||||
| chr2:69814786 | GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0006g0025 a0001c0001t0006g0217 a0001c0001t0006g0298 others(1): Show |
4 | HG02922.hp1 HG02970.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.535-1314_535-1301d others(16): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814786 | |||||||
| chr2:69814787 | TGTGTGTG others(1): Show |
T | 28 | a0001c0001t0003g0022 a0001c0001t0003g0135 a0001c0001t0003g0142 others(25): Show |
28 | HG00642.hp1 HG00741.hp1 HG02129.hp2 others(25): Show |
intron_variant | MODIFIER | c.535-1312_535-1305d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814787 | ||||||
| chr2:69814787 | TGTGTGTG others(3): Show |
T | 17 | a0002c0002t0002g0005 a0002c0002t0002g0007 a0002c0002t0002g0016 others(14): Show |
18 | HG01070.hp1 HG01243.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.535-1312_535-1303d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814787 | ||||||
| chr2:69814788 | GTGTGTGA others(5): Show |
G | 13 | a0001c0001t0011g0128 a0003c0003t0004g0039 a0003c0003t0004g0040 others(10): Show |
13 | HG00423.hp1 HG01257.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.535-1312_535-1301d others(14): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814788 | |||||||
| chr2:69814789 | TGTGTGA | T | 11 | a0001c0001t0003g0084 a0001c0001t0003g0119 a0001c0001t0003g0120 others(8): Show |
11 | HG00673.hp2 HG01496.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.535-1310_535-1305d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814789 | ||||||
| chr2:69814789 | TGTGTGAG others(1): Show |
T | 14 | a0002c0002t0002g0004 a0002c0002t0002g0054 a0002c0002t0002g0088 others(11): Show |
15 | HG02257.hp1 HG02559.hp2 HG02717.hp2 others(12): Show |
intron_variant | MODIFIER | c.535-1310_535-1303d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814789 | ||||||
| chr2:69814790 | GTGTGAGA others(3): Show |
G | 15 | a0003c0003t0004g0001 a0003c0003t0004g0003 a0003c0003t0004g0006 others(12): Show |
18 | HG00408.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.535-1310_535-1301d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814790 | |||||||
| chr2:69814791 | TGTGA | T | 16 | a0001c0001t0003g0143 a0001c0001t0003g0164 a0001c0001t0005g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp2 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.535-1308_535-1305d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | ||||||
| chr2:69814791 | TGTGAGA | T | 26 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0027 others(23): Show |
26 | HG00438.hp1 HG01074.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.535-1308_535-1303d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | ||||||
| chr2:69814791 | TGTGAGAG others(3): Show |
T | 1 | a0001c0001t0006g0101 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.535-1308_535-1299d others(12): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814791 | ||||||
| chr2:69814792 | GTGAGAGA others(1): Show |
G | 4 | a0001c0001t0006g0021 a0003c0003t0004g0006 a0003c0003t0004g0037 others(1): Show |
4 | HG01175.hp1 NA18954.hp1 NA19056.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1308_535-1301d others(10): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814792 | |||||||
| chr2:69814793 | T | A | 2 | a0001c0001t0001g0028 a0002c0002t0001g0262 |
2 | HG00140.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.535-1308T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814793 | |||||||
| chr2:69814793 | TGA | T | 7 | a0001c0001t0005g0207 a0001c0001t0005g0284 a0001c0001t0007g0294 others(4): Show |
7 | HG00140.hp1 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.535-1303_535-1302d others(4): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814793 | ||||||
| chr2:69814793 | TGAGA | T | 9 | a0002c0002t0002g0002 a0002c0002t0002g0010 a0002c0002t0002g0026 others(6): Show |
10 | HG00609.hp1 HG01069.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.535-1305_535-1302d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814793 | ||||||
| chr2:69814794 | GAGAGAA | G | 6 | a0001c0001t0011g0208 a0003c0003t0004g0066 a0003c0003t0004g0108 others(3): Show |
6 | HG01099.hp2 HG01192.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.535-1301_535-1296d others(8): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 69814794 | ||||||
| chr2:69814795 | A | T | 17 | a0001c0001t0003g0133 a0001c0001t0003g0140 a0001c0001t0003g0230 others(14): Show |
17 | HG00544.hp1 HG01192.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.535-1306A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814795 | |||||||
| chr2:69814797 | A | T | 4 | a0002c0002t0002g0058 a0002c0002t0002g0078 a0002c0002t0002g0155 others(1): Show |
4 | HG00140.hp1 HG00738.hp1 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.535-1304A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814797 | |||||||
| chr2:69814802 | G | A | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1299G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814802 | |||||||
| chr2:69814847 | A | G | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1254A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69814847 | |||||||
| chr2:69815086 | C | G | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-1015C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815086 | |||||||
| chr2:69815193 | C | T | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-908C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815193 | |||||||
| chr2:69815200 | A | G | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.535-901A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815200 | |||||||
| chr2:69815213 | T | G | 1 | a0001c0001t0001g0287 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.535-888T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815213 | |||||||
| chr2:69815286 | A | G | 1 | a0002c0002t0002g0130 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.535-815A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815286 | |||||||
| chr2:69815344 | G | A | 3 | a0001c0001t0003g0230 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | NA18943.hp2 NA18982.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.535-757G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815344 | |||||||
| chr2:69815461 | A | G | 14 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0025 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.535-640A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815461 | |||||||
| chr2:69815481 | A | G | 1 | a0001c0001t0003g0186 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.535-620A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815481 | |||||||
| chr2:69815639 | G | A | 43 | a0003c0003t0004g0001 a0003c0003t0004g0003 a0003c0003t0004g0006 others(40): Show |
47 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.535-462G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815639 | |||||||
| chr2:69815647 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.535-454G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815647 | |||||||
| chr2:69815688 | C | T | 72 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(69): Show |
76 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(73): Show |
intron_variant | MODIFIER | c.535-413C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815688 | |||||||
| chr2:69815702 | C | T | 2 | a0001c0001t0004g0129 a0001c0001t0006g0101 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.535-399C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815702 | |||||||
| chr2:69815783 | C | A | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.535-318C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815783 | |||||||
| chr2:69815865 | T | A | 1 | a0001c0001t0006g0025 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.535-236T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815865 | |||||||
| chr2:69815908 | G | A | 3 | a0003c0003t0004g0017 a0003c0003t0004g0019 a0003c0003t0004g0333 |
3 | HG02965.hp2 HG02976.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.535-193G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69815908 | |||||||
| chr2:69816013 | G | A | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.535-88G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69816013 | |||||||
| chr2:69816083 | T | C | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.535-18T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 8/12 | chr2 | 69816083 | |||||||
| chr2:69816255 | C | T | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+61C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816255 | |||||||
| chr2:69816388 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.628+194T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816388 | |||||||
| chr2:69816466 | C | A | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+272C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816466 | |||||||
| chr2:69816551 | G | T | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG01358.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.628+357G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816551 | |||||||
| chr2:69816643 | A | T | 73 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(70): Show |
77 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.628+449A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816643 | |||||||
| chr2:69816795 | A | T | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+601A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816795 | |||||||
| chr2:69816820 | C | T | 2 | a0003c0003t0004g0064 a0003c0003t0004g0066 |
2 | HG01099.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.628+626C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816820 | |||||||
| chr2:69816883 | C | T | 1 | a0001c0001t0001g0324 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.628+689C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69816883 | |||||||
| chr2:69817027 | C | G | 97 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.628+833C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817027 | |||||||
| chr2:69817076 | C | A | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+882C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817076 | |||||||
| chr2:69817234 | G | A | 69 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(66): Show |
73 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(70): Show |
intron_variant | MODIFIER | c.628+1040G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817234 | |||||||
| chr2:69817246 | CTGTT | C | 102 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(99): Show |
103 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.628+1056_628+1059d others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 69817246 | ||||||
| chr2:69817368 | G | A | 1 | a0003c0003t0002g0102 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.628+1174G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817368 | |||||||
| chr2:69817418 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.629-1181C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817418 | |||||||
| chr2:69817478 | G | T | 1 | a0001c0001t0003g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.629-1121G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817478 | |||||||
| chr2:69817576 | A | C | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.629-1023A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817576 | |||||||
| chr2:69817793 | G | T | 3 | a0003c0003t0004g0103 a0003c0003t0004g0105 a0003c0003t0004g0295 |
3 | HG01891.hp1 HG02630.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.629-806G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817793 | |||||||
| chr2:69817881 | T | A | 44 | a0001c0001t0017g0318 a0003c0003t0004g0001 a0003c0003t0004g0003 others(41): Show |
48 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.629-718T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817881 | |||||||
| chr2:69817931 | G | A | 76 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0007g0294 others(73): Show |
80 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.629-668G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817931 | |||||||
| chr2:69817948 | A | G | 6 | a0001c0001t0003g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | NA18747.hp1 NA18945.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.629-651A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69817948 | |||||||
| chr2:69818013 | A | G | 14 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0025 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-586A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818013 | |||||||
| chr2:69818014 | A | C | 14 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0025 others(11): Show |
14 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.629-585A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818014 | |||||||
| chr2:69818118 | A | AAACAAC | 66 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(63): Show |
70 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.629-475_629-470dup others(6): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr2 | 69818118 | ||||||
| chr2:69818118 | A | C | 1 | a0003c0003t0004g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.629-481A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818118 | |||||||
| chr2:69818134 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.629-465A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818134 | |||||||
| chr2:69818353 | G | T | 2 | a0001c0001t0001g0281 a0001c0001t0015g0280 |
2 | HG01169.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.629-246G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818353 | |||||||
| chr2:69818371 | G | C | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.629-228G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818371 | |||||||
| chr2:69818390 | A | C | 2 | a0001c0001t0004g0129 a0001c0001t0006g0101 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.629-209A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818390 | |||||||
| chr2:69818544 | T | G | 1 | a0002c0002t0002g0030 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.629-55T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 9/12 | chr2 | 69818544 | |||||||
| chr2:69818770 | A | T | 1 | a0002c0002t0002g0002 | 2 | HG00609.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.724+76A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818770 | |||||||
| chr2:69818771 | T | C | 2 | a0001c0001t0001g0282 a0001c0001t0003g0320 |
2 | HG03239.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.724+77T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818771 | |||||||
| chr2:69818829 | A | T | 1 | a0003c0003t0004g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.724+135A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818829 | |||||||
| chr2:69818905 | C | G | 2 | a0001c0001t0003g0118 a0001c0001t0003g0167 |
2 | NA18942.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.724+211C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818905 | |||||||
| chr2:69818933 | A | G | 3 | a0001c0001t0001g0229 a0001c0001t0001g0260 a0001c0001t0001g0261 |
3 | HG01175.hp2 HG01515.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.724+239A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818933 | |||||||
| chr2:69818938 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.724+244G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69818938 | |||||||
| chr2:69819028 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.725-252T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819028 | |||||||
| chr2:69819080 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.725-200T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819080 | |||||||
| chr2:69819123 | G | C | 97 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.725-157G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819123 | |||||||
| chr2:69819130 | G | A | 61 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(58): Show |
62 | HG00438.hp2 HG00544.hp1 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.725-150G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 10/12 | chr2 | 69819130 | |||||||
| chr2:69819728 | T | A | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+390T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819728 | |||||||
| chr2:69819729 | C | G | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+391C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819729 | |||||||
| chr2:69819801 | C | T | 2 | a0001c0001t0004g0129 a0001c0001t0006g0101 |
2 | HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.783+463C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819801 | |||||||
| chr2:69819805 | C | T | 1 | a0002c0002t0002g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+467C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819805 | |||||||
| chr2:69819832 | C | A | 77 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0007g0294 others(74): Show |
81 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.783+494C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819832 | |||||||
| chr2:69819898 | G | A | 4 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0315 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.783+560G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819898 | |||||||
| chr2:69819932 | G | C | 68 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(65): Show |
72 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.783+594G>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69819932 | |||||||
| chr2:69820074 | GA | G | 65 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0002c0002t0002g0002 others(62): Show |
69 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.784-612delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820074 | ||||||
| chr2:69820236 | G | GT | 97 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.784-450dupT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820236 | ||||||
| chr2:69820236 | GT | G | 75 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0007g0294 others(72): Show |
79 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.784-450delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 69820236 | ||||||
| chr2:69820238 | T | G | 3 | a0002c0002t0002g0313 a0002c0002t0002g0314 a0003c0003t0002g0104 |
3 | HG02257.hp1 HG02717.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.784-461T>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820238 | |||||||
| chr2:69820483 | G | A | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.784-216G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820483 | |||||||
| chr2:69820512 | G | A | 76 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0007g0294 others(73): Show |
80 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.784-187G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820512 | |||||||
| chr2:69820581 | T | C | 2 | a0002c0002t0002g0106 a0002c0002t0002g0115 |
2 | HG03688.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.784-118T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 11/12 | chr2 | 69820581 | |||||||
| chr2:69821097 | G | A | 4 | a0001c0001t0005g0191 a0001c0001t0005g0192 a0001c0001t0005g0194 others(1): Show |
4 | HG02615.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+276G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821097 | |||||||
| chr2:69821124 | C | A | 1 | a0001c0001t0006g0107 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.906+303C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821124 | |||||||
| chr2:69821309 | T | A | 2 | a0003c0003t0004g0095 a0003c0003t0004g0171 |
2 | NA18966.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.906+488T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821309 | |||||||
| chr2:69821402 | C | T | 99 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(96): Show |
100 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.906+581C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821402 | |||||||
| chr2:69821477 | AT | A | 16 | a0001c0001t0006g0015 a0001c0001t0006g0018 a0001c0001t0006g0020 others(13): Show |
16 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.906+667delT | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69821477 | ||||||
| chr2:69821636 | G | T | 4 | a0001c0001t0006g0015 a0001c0001t0006g0020 a0001c0001t0006g0315 others(1): Show |
4 | HG01243.hp1 HG02257.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+815G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821636 | |||||||
| chr2:69821644 | G | A | 1 | a0001c0001t0005g0332 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.906+823G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69821644 | |||||||
| chr2:69822045 | T | A | 8 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+1224T>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822045 | |||||||
| chr2:69822090 | G | A | 77 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0007g0294 others(74): Show |
81 | HG00140.hp1 HG00438.hp1 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.906+1269G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822090 | |||||||
| chr2:69822110 | C | G | 24 | a0001c0001t0004g0129 a0001c0001t0006g0013 a0001c0001t0006g0014 others(21): Show |
24 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.906+1289C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822110 | |||||||
| chr2:69822151 | G | A | 7 | a0001c0001t0003g0084 a0001c0001t0003g0120 a0001c0001t0003g0140 others(4): Show |
7 | HG00544.hp1 HG02523.hp2 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+1330G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822151 | |||||||
| chr2:69822225 | G | A | 2 | a0001c0001t0006g0018 a0001c0001t0006g0336 |
2 | HG03579.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.906+1404G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822225 | |||||||
| chr2:69822362 | A | G | 1 | a0002c0002t0002g0313 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.906+1541A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822362 | |||||||
| chr2:69822384 | T | C | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.906+1563T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822384 | |||||||
| chr2:69822583 | C | T | 97 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(94): Show |
98 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.906+1762C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822583 | |||||||
| chr2:69822644 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.906+1823C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822644 | |||||||
| chr2:69822844 | A | C | 2 | a0001c0001t0011g0128 a0001c0001t0011g0208 |
2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.906+2023A>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69822844 | |||||||
| chr2:69823366 | A | T | 2 | a0001c0001t0007g0294 a0001c0001t0007g0302 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.907-2090A>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823366 | |||||||
| chr2:69823509 | T | C | 98 | a0001c0001t0003g0008 a0001c0001t0003g0022 a0001c0001t0003g0046 others(95): Show |
99 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.907-1947T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823509 | |||||||
| chr2:69823593 | G | A | 244 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(241): Show |
253 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(250): Show |
intron_variant | MODIFIER | c.907-1863G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823593 | |||||||
| chr2:69823626 | C | G | 2 | a0001c0001t0005g0312 a0001c0001t0007g0204 |
2 | HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-1830C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823626 | |||||||
| chr2:69823636 | T | C | 1 | a0003c0003t0004g0094 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.907-1820T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69823636 | |||||||
| chr2:69824011 | C | T | 1 | a0001c0001t0001g0289 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.907-1445C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824011 | |||||||
| chr2:69824054 | G | T | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1402G>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824054 | |||||||
| chr2:69824177 | C | T | 2 | a0001c0001t0006g0025 a0001c0001t0006g0217 |
2 | HG02922.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.907-1279C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824177 | |||||||
| chr2:69824251 | C | G | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1205C>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824251 | |||||||
| chr2:69824435 | G | A | 3 | a0001c0001t0007g0294 a0001c0001t0007g0302 a0005c0005t0007g0011 |
3 | HG01167.hp2 HG01169.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.907-1021G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824435 | |||||||
| chr2:69824456 | T | C | 1 | a0001c0001t0005g0316 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.907-1000T>C | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824456 | |||||||
| chr2:69824490 | G | A | 40 | a0003c0003t0004g0001 a0003c0003t0004g0003 a0003c0003t0004g0006 others(37): Show |
44 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.907-966G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824490 | |||||||
| chr2:69824504 | G | GA | 101 | a0001c0001t0001g0051 a0001c0001t0003g0008 a0001c0001t0003g0022 others(98): Show |
102 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.907-935dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69824504 | ||||||
| chr2:69824510 | A | G | 1 | a0001c0001t0007g0299 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.907-946A>G | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824510 | |||||||
| chr2:69824970 | C | T | 1 | a0002c0002t0002g0047 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.907-486C>T | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824970 | |||||||
| chr2:69824992 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.907-464G>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69824992 | |||||||
| chr2:69825066 | C | CA | 55 | a0001c0001t0001g0028 a0001c0001t0001g0051 a0001c0001t0001g0077 others(52): Show |
55 | HG01106.hp1 HG01109.hp2 HG01175.hp2 others(52): Show |
intron_variant | MODIFIER | c.907-366dupA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | ||||||
| chr2:69825066 | CA | C | 13 | a0001c0001t0006g0013 a0001c0001t0006g0014 a0001c0001t0006g0015 others(10): Show |
13 | HG01175.hp1 HG01261.hp1 HG01978.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-366delA | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | ||||||
| chr2:69825066 | CAA | C | 55 | a0001c0001t0004g0129 a0001c0001t0006g0018 a0001c0001t0006g0020 others(52): Show |
59 | HG00408.hp2 HG00423.hp1 HG00642.hp2 others(56): Show |
intron_variant | MODIFIER | c.907-367_907-366del others(2): Show |
ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825066 | ||||||
| chr2:69825090 | AC | A | 12 | a0001c0001t0003g0118 a0001c0001t0003g0166 a0001c0001t0003g0230 others(9): Show |
13 | HG00673.hp2 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-364delC | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 69825090 | ||||||
| chr2:69825091 | C | A | 164 | a0001c0001t0002g0159 a0001c0001t0002g0267 a0001c0001t0003g0008 others(161): Show |
168 | HG00140.hp1 HG00408.hp1 HG00423.hp2 others(165): Show |
intron_variant | MODIFIER | c.907-365C>A | ANXA4 | ENSG00000196975.16 | transcript | ENST00000394295.6 | protein_coding | 12/12 | chr2 | 69825091 |