Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7357 |
| ensemblid | ENSG00000148154.10 |
| hgncid | 12524 |
| symbol | UGCG |
| name | UDP-glucose ceramide glucosyltransferase |
| refseq_nuc | NM_003358.3 |
| refseq_prot | NP_003349.1 |
| ensembl_nuc | ENST00000374279.4 |
| ensembl_prot | ENSP00000363397.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 111896814 |
| end | 111935369 |
| strand | + |
| ver | v1.2 |
| region | chr9:111896814-111935369 |
| region5000 | chr9:111891814-111940369 |
| regionname0 | UGCG_chr9_111896814_111935369 |
| regionname5000 | UGCG_chr9_111891814_111940369 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 394 | 423 | 90 | 76 | 197 | 18 | 40 | 149 | UGCG_chr9_111891814_111940369 | UGCG | MALLD others(389): Show |
chr9 | 111891814 | 111940369 |
| a0002 | 0/0 | 394 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | MALLD others(389): Show |
chr9 | 111891814 | 111940369 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1182 | 273 | 54 | 45 | 131 | 14 | 27 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0001c0002 | 0/0 | 1182 | 126 | 35 | 25 | 52 | 4 | 10 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0001c0003 | 0/0 | 1182 | 18 | 0 | 3 | 14 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0001c0004 | 0/0 | 1182 | 4 | 0 | 2 | 0 | 0 | 2 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0001c0006 | 0/0 | 1182 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0001c0007 | 0/0 | 1182 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 | ||
| a0002c0005 | 0/0 | 1182 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | ATGGC others(1177): Show |
chr9 | 111891814 | 111940369 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3959 | 92 | 10 | 16 | 58 | 4 | 4 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0003 | 1/1 | 3959 | 36 | 1 | 15 | 6 | 4 | 8 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0004 | 0/0 | 3956 | 24 | 0 | 0 | 21 | 2 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3951): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0005 | 0/0 | 3955 | 22 | 21 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0007 | 0/0 | 3959 | 19 | 0 | 0 | 17 | 0 | 2 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0010 | 0/0 | 3959 | 9 | 1 | 5 | 0 | 1 | 2 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0011 | 0/0 | 3968 | 8 | 0 | 0 | 6 | 0 | 2 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3963): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0013 | 0/0 | 3960 | 6 | 0 | 1 | 2 | 1 | 2 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0014 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3961): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0015 | 0/0 | 3959 | 5 | 1 | 0 | 4 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0016 | 0/0 | 3956 | 5 | 1 | 0 | 4 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3951): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0018 | 0/0 | 3969 | 4 | 0 | 0 | 3 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0019 | 0/0 | 3955 | 4 | 4 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0024 | 0/0 | 3959 | 3 | 2 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0025 | 0/0 | 3960 | 3 | 2 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0026 | 0/0 | 3959 | 3 | 2 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0027 | 0/0 | 3965 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3960): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0028 | 0/0 | 3958 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3953): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0029 | 0/0 | 3960 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0031 | 0/0 | 3965 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3960): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0038 | 0/0 | 3969 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0039 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0041 | 0/0 | 3960 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0042 | 0/0 | 3956 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3951): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0043 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0047 | 0/0 | 3955 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0048 | 0/0 | 3961 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3956): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0050 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0051 | 0/0 | 3959 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0052 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0053 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0054 | 0/0 | 3955 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0055 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0056 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0057 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0058 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0059 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0060 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0061 | 0/0 | 3959 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0062 | 0/0 | 3954 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3949): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0063 | 0/0 | 3955 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0001t0064 | 0/0 | 3956 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3951): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0002 | 0/0 | 3969 | 66 | 5 | 18 | 31 | 4 | 8 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0006 | 0/0 | 3959 | 19 | 13 | 3 | 3 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0009 | 0/0 | 3959 | 10 | 3 | 0 | 6 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0012 | 0/0 | 3979 | 7 | 7 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3974): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0017 | 0/0 | 3970 | 4 | 3 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3965): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0021 | 0/0 | 3959 | 4 | 0 | 2 | 1 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0022 | 0/0 | 3979 | 3 | 3 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3974): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0023 | 0/0 | 3969 | 3 | 0 | 0 | 3 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0030 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3965): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0032 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0033 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0034 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0035 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0036 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0037 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0040 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0045 | 0/0 | 3969 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0001c0002t0049 | 0/0 | 3959 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0003t0008 | 0/0 | 3960 | 13 | 0 | 0 | 12 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0003t0014 | 0/0 | 3966 | 3 | 0 | 3 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3961): Show |
chr9 | 111891814 | 111940369 |
| a0001c0003t0044 | 0/0 | 3959 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3954): Show |
chr9 | 111891814 | 111940369 |
| a0001c0003t0046 | 0/0 | 3960 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3955): Show |
chr9 | 111891814 | 111940369 |
| a0001c0004t0020 | 0/0 | 3958 | 4 | 0 | 2 | 0 | 0 | 2 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3953): Show |
chr9 | 111891814 | 111940369 |
| a0001c0006t0005 | 0/0 | 3955 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3950): Show |
chr9 | 111891814 | 111940369 |
| a0001c0007t0002 | 0/0 | 3969 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3964): Show |
chr9 | 111891814 | 111940369 |
| a0002c0005t0014 | 0/0 | 3966 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | AGTGC others(3961): Show |
chr9 | 111891814 | 111940369 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0002 | 0/0 | 8 | 0 | 6 | 0 | 1 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0003 | 0/0 | 7 | 0 | 0 | 5 | 1 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0004g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0007g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0353 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0010g0360 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0011g0011 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0011g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0011g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0011g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0013g0028 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0013g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0013g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0013g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0013g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0014g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0015g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0015g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0015g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0015g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0015g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0016g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0016g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0016g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0016g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0016g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0018g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0018g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0018g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0018g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0019g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0019g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0019g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0024g0364 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0024g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0024g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0025g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0025g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0025g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0026g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0026g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0026g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0027g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0027g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0028g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0028g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0029g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0029g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0031g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0038g0002 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0039g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0041g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0042g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0043g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0047g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0048g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0050g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0051g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0052g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0053g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0054g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0055g0361 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0056g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0057g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0058g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0059g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0060g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0061g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0062g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0063g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0001t0064g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0001 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0006g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0009g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0017g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0017g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0017g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0021g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0021g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0021g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0021g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0022g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0022g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0022g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0023g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0023g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0030g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0032g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0033g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0034g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0035g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0036g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0037g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0040g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0045g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0002t0049g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0014g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0014g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0014g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0044g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0003t0046g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0004t0020g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0004t0020g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0004t0020g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0004t0020g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0006t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0001c0007t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| a0002c0005t0014g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0156 | EUR | GBR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00099 | hp2 | a0001 | c0001 | t0004 | g0279 | EUR | GBR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0002 | EUR | GBR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0059 | EUR | GBR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0204 | EUR | FIN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0227 | EUR | FIN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00323 | hp1 | a0001 | c0001 | t0010 | g0353 | EUR | FIN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00323 | hp2 | a0001 | c0001 | t0013 | g0028 | EUR | FIN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00408 | hp2 | a0001 | c0001 | t0016 | g0329 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00423 | hp1 | a0001 | c0002 | t0035 | g0050 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00423 | hp2 | a0001 | c0001 | t0007 | g0260 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00438 | hp1 | a0001 | c0001 | t0007 | g0314 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00438 | hp2 | a0001 | c0001 | t0064 | g0272 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00544 | hp1 | a0001 | c0002 | t0002 | g0070 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00544 | hp2 | a0001 | c0002 | t0009 | g0187 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00558 | hp1 | a0001 | c0003 | t0008 | g0136 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0261 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00609 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00621 | hp1 | a0001 | c0002 | t0009 | g0093 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00639 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0124 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00642 | hp2 | a0001 | c0001 | t0024 | g0364 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00673 | hp1 | a0001 | c0001 | t0016 | g0189 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0011 | EAS | CHS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0029 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00733 | hp2 | a0001 | c0003 | t0014 | g0185 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00738 | hp2 | a0001 | c0003 | t0014 | g0184 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG00741 | hp2 | a0001 | c0001 | t0042 | g0144 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0150 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01069 | hp2 | a0001 | c0002 | t0002 | g0114 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01070 | hp2 | a0001 | c0002 | t0002 | g0068 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01071 | hp2 | a0001 | c0002 | t0002 | g0115 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01074 | hp2 | a0001 | c0003 | t0014 | g0186 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01081 | hp1 | a0001 | c0001 | t0005 | g0023 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01081 | hp2 | a0001 | c0001 | t0010 | g0331 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01099 | hp1 | a0001 | c0002 | t0032 | g0004 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0168 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01106 | hp1 | a0001 | c0002 | t0006 | g0354 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01106 | hp2 | a0001 | c0004 | t0020 | g0322 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01167 | hp1 | a0001 | c0002 | t0021 | g0265 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01167 | hp2 | a0001 | c0001 | t0013 | g0341 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01168 | hp1 | a0001 | c0004 | t0020 | g0319 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01168 | hp2 | a0001 | c0001 | t0010 | g0360 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01169 | hp1 | a0001 | c0001 | t0010 | g0029 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01169 | hp2 | a0001 | c0002 | t0021 | g0264 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01175 | hp1 | a0001 | c0002 | t0002 | g0121 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01192 | hp2 | a0001 | c0001 | t0043 | g0149 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01243 | hp1 | a0001 | c0001 | t0047 | g0338 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01243 | hp2 | a0001 | c0002 | t0017 | g0006 | AMR | PUR | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01255 | hp1 | a0001 | c0001 | t0039 | g0030 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0346 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01256 | hp2 | a0001 | c0001 | t0051 | g0350 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0155 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0120 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01261 | hp1 | a0001 | c0002 | t0006 | g0325 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01261 | hp2 | a0001 | c0002 | t0006 | g0345 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01361 | hp1 | a0001 | c0001 | t0025 | g0205 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0127 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01515 | hp2 | a0001 | c0001 | t0041 | g0160 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0148 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0118 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0117 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0193 | EUR | IBS | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01884 | hp1 | a0001 | c0002 | t0009 | g0170 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01928 | hp2 | a0001 | c0002 | t0002 | g0051 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0183 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01952 | hp2 | a0001 | c0002 | t0002 | g0054 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0001 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01978 | hp2 | a0001 | c0002 | t0002 | g0123 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0055 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02015 | hp1 | a0001 | c0001 | t0018 | g0037 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02015 | hp2 | a0001 | c0001 | t0026 | g0355 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02027 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02027 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02055 | hp1 | a0001 | c0001 | t0005 | g0290 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02071 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02074 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02080 | hp1 | a0001 | c0002 | t0006 | g0237 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02080 | hp2 | a0001 | c0001 | t0007 | g0316 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0060 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02129 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0166 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02132 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02135 | hp2 | a0001 | c0001 | t0007 | g0301 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02145 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02145 | hp2 | a0001 | c0002 | t0006 | g0008 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0056 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0347 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02155 | hp1 | a0001 | c0002 | t0040 | g0057 | EAS | CDX | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CDX | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | CDX | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | CDX | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02257 | hp1 | a0001 | c0001 | t0005 | g0298 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02257 | hp2 | a0001 | c0002 | t0006 | g0008 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02258 | hp1 | a0001 | c0001 | t0005 | g0289 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02258 | hp2 | a0001 | c0002 | t0012 | g0101 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02273 | hp1 | a0001 | c0007 | t0002 | g0053 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02280 | hp1 | a0001 | c0001 | t0062 | g0288 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02280 | hp2 | a0001 | c0002 | t0006 | g0327 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0085 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02300 | hp2 | a0001 | c0001 | t0010 | g0352 | AMR | PEL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02451 | hp1 | a0001 | c0002 | t0006 | g0027 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02451 | hp2 | a0001 | c0002 | t0012 | g0103 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0048 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02572 | hp2 | a0001 | c0001 | t0005 | g0291 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02602 | hp1 | a0001 | c0001 | t0059 | g0307 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0038 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02615 | hp1 | a0001 | c0002 | t0022 | g0100 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02615 | hp2 | a0001 | c0002 | t0009 | g0181 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02630 | hp1 | a0001 | c0002 | t0012 | g0099 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02630 | hp2 | a0001 | c0002 | t0006 | g0324 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02698 | hp1 | a0001 | c0001 | t0010 | g0351 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02717 | hp2 | a0001 | c0001 | t0016 | g0337 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02738 | hp1 | a0001 | c0001 | t0055 | g0361 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02738 | hp2 | a0001 | c0001 | t0003 | g0163 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02809 | hp1 | a0001 | c0002 | t0012 | g0096 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02809 | hp2 | a0001 | c0001 | t0056 | g0005 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02886 | hp1 | a0001 | c0001 | t0019 | g0175 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02886 | hp2 | a0001 | c0001 | t0029 | g0110 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02895 | hp1 | a0001 | c0001 | t0024 | g0365 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02895 | hp2 | a0001 | c0001 | t0058 | g0005 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02896 | hp1 | a0001 | c0002 | t0017 | g0004 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0292 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02897 | hp1 | a0001 | c0002 | t0017 | g0004 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02897 | hp2 | a0001 | c0001 | t0024 | g0366 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02965 | hp1 | a0001 | c0002 | t0022 | g0102 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02970 | hp1 | a0001 | c0002 | t0006 | g0362 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0026 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02976 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03017 | hp1 | a0001 | c0002 | t0009 | g0032 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03017 | hp2 | a0001 | c0002 | t0002 | g0126 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0363 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03098 | hp1 | a0001 | c0001 | t0015 | g0145 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03098 | hp2 | a0001 | c0001 | t0027 | g0001 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03130 | hp1 | a0001 | c0006 | t0005 | g0287 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03130 | hp2 | a0001 | c0001 | t0019 | g0173 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03139 | hp1 | a0001 | c0002 | t0009 | g0171 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03139 | hp2 | a0001 | c0001 | t0025 | g0367 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03209 | hp1 | a0001 | c0002 | t0017 | g0001 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03209 | hp2 | a0001 | c0002 | t0006 | g0323 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03225 | hp2 | a0001 | c0002 | t0006 | g0027 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03239 | hp1 | a0001 | c0001 | t0013 | g0028 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03239 | hp2 | a0001 | c0001 | t0011 | g0116 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03453 | hp1 | a0001 | c0002 | t0012 | g0097 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03453 | hp2 | a0001 | c0001 | t0025 | g0368 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03486 | hp1 | a0001 | c0002 | t0006 | g0008 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03490 | hp1 | a0001 | c0001 | t0050 | g0240 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03490 | hp2 | a0001 | c0001 | t0007 | g0024 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0034 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03492 | hp2 | a0001 | c0001 | t0007 | g0024 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03516 | hp1 | a0001 | c0001 | t0060 | g0286 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03516 | hp2 | a0001 | c0002 | t0012 | g0104 | AFR | ESN | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03540 | hp2 | a0001 | c0002 | t0012 | g0095 | AFR | GWD | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03579 | hp1 | a0001 | c0001 | t0010 | g0359 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03579 | hp2 | a0001 | c0002 | t0049 | g0358 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03654 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0147 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03669 | hp1 | a0001 | c0004 | t0020 | g0320 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0340 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03704 | hp1 | a0001 | c0001 | t0013 | g0196 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03704 | hp2 | a0001 | c0004 | t0020 | g0321 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03710 | hp1 | a0001 | c0002 | t0002 | g0009 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0165 | SAS | PJL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03831 | hp2 | a0001 | c0001 | t0048 | g0349 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0086 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03927 | hp2 | a0001 | c0001 | t0061 | g0271 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03942 | hp1 | a0001 | c0001 | t0011 | g0011 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0164 | SAS | BEB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04115 | hp2 | a0001 | c0003 | t0008 | g0142 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04199 | hp1 | a0001 | c0002 | t0002 | g0119 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04199 | hp2 | a0001 | c0001 | t0018 | g0128 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04204 | hp1 | a0001 | c0002 | t0021 | g0262 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0348 | SAS | STU | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18522 | hp2 | a0001 | c0002 | t0022 | g0098 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18747 | hp1 | a0001 | c0001 | t0014 | g0079 | EAS | CHB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | CHB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0294 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0082 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18940 | hp1 | a0001 | c0001 | t0004 | g0257 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18940 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18941 | hp1 | a0001 | c0001 | t0053 | g0211 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18941 | hp2 | a0001 | c0001 | t0016 | g0188 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18942 | hp1 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18942 | hp2 | a0001 | c0001 | t0057 | g0259 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18943 | hp2 | a0001 | c0003 | t0008 | g0138 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18944 | hp2 | a0001 | c0003 | t0008 | g0130 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18945 | hp2 | a0001 | c0002 | t0002 | g0049 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18946 | hp2 | a0001 | c0003 | t0008 | g0129 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0330 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18950 | hp1 | a0001 | c0002 | t0002 | g0064 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18951 | hp1 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18951 | hp2 | a0001 | c0001 | t0007 | g0313 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18952 | hp1 | a0001 | c0001 | t0028 | g0172 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18953 | hp1 | a0001 | c0001 | t0004 | g0300 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18953 | hp2 | a0001 | c0003 | t0008 | g0140 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18954 | hp1 | a0001 | c0003 | t0008 | g0135 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18956 | hp1 | a0001 | c0002 | t0002 | g0047 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18959 | hp1 | a0001 | c0001 | t0007 | g0311 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18965 | hp2 | a0001 | c0002 | t0037 | g0087 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18966 | hp1 | a0001 | c0001 | t0015 | g0161 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18968 | hp1 | a0002 | c0005 | t0014 | g0065 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18968 | hp2 | a0001 | c0001 | t0054 | g0190 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18971 | hp1 | a0001 | c0001 | t0013 | g0343 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18972 | hp1 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0268 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18975 | hp2 | a0001 | c0003 | t0008 | g0141 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18977 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18977 | hp2 | a0001 | c0002 | t0036 | g0076 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18980 | hp2 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18984 | hp2 | a0001 | c0002 | t0033 | g0045 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18985 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18985 | hp2 | a0001 | c0001 | t0018 | g0035 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18986 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18987 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18990 | hp1 | a0001 | c0003 | t0008 | g0131 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18990 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18992 | hp2 | a0001 | c0002 | t0030 | g0046 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18993 | hp1 | a0001 | c0002 | t0034 | g0058 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18993 | hp2 | a0001 | c0001 | t0052 | g0019 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18995 | hp2 | a0001 | c0001 | t0011 | g0113 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18998 | hp2 | a0001 | c0003 | t0046 | g0344 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0302 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19002 | hp1 | a0001 | c0001 | t0013 | g0256 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19002 | hp2 | a0001 | c0001 | t0007 | g0312 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19003 | hp2 | a0001 | c0001 | t0007 | g0303 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19004 | hp1 | a0001 | c0002 | t0002 | g0078 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19004 | hp2 | a0001 | c0001 | t0004 | g0274 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19007 | hp1 | a0001 | c0002 | t0009 | g0091 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19009 | hp1 | a0001 | c0001 | t0018 | g0036 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19009 | hp2 | a0001 | c0003 | t0008 | g0137 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0309 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19012 | hp1 | a0001 | c0002 | t0023 | g0072 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19030 | hp2 | a0001 | c0001 | t0026 | g0357 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19043 | hp2 | a0001 | c0001 | t0019 | g0112 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19054 | hp1 | a0001 | c0002 | t0045 | g0039 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19058 | hp2 | a0001 | c0001 | t0011 | g0012 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19060 | hp1 | a0001 | c0001 | t0004 | g0275 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19060 | hp2 | a0001 | c0001 | t0007 | g0025 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19062 | hp1 | a0001 | c0001 | t0015 | g0162 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19062 | hp2 | a0001 | c0001 | t0015 | g0092 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0044 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19063 | hp2 | a0001 | c0001 | t0007 | g0304 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19064 | hp1 | a0001 | c0002 | t0006 | g0238 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19065 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19065 | hp2 | a0001 | c0003 | t0008 | g0132 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19066 | hp2 | a0001 | c0002 | t0023 | g0004 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19070 | hp1 | a0001 | c0003 | t0044 | g0139 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19070 | hp2 | a0001 | c0001 | t0015 | g0158 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19074 | hp1 | a0001 | c0002 | t0023 | g0004 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19076 | hp1 | a0001 | c0001 | t0007 | g0315 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19076 | hp2 | a0001 | c0001 | t0063 | g0266 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19078 | hp1 | a0001 | c0002 | t0009 | g0094 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19079 | hp1 | a0001 | c0002 | t0009 | g0090 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19080 | hp1 | a0001 | c0001 | t0007 | g0308 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19081 | hp1 | a0001 | c0001 | t0007 | g0310 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19081 | hp2 | a0001 | c0003 | t0008 | g0134 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0269 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19083 | hp1 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19083 | hp2 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19084 | hp2 | a0001 | c0002 | t0009 | g0089 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19088 | hp2 | a0001 | c0003 | t0008 | g0133 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19089 | hp1 | a0001 | c0001 | t0007 | g0305 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19090 | hp1 | a0001 | c0002 | t0021 | g0263 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19090 | hp2 | a0001 | c0001 | t0011 | g0013 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19091 | hp1 | a0001 | c0002 | t0006 | g0208 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19091 | hp2 | a0001 | c0001 | t0028 | g0143 | EAS | JPT | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0306 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA19240 | hp2 | a0001 | c0001 | t0027 | g0080 | AFR | YRI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20129 | hp1 | a0001 | c0001 | t0026 | g0356 | AFR | ASW | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0296 | AFR | ASW | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0151 | EUR | TSI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0003 | EUR | TSI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0122 | EUR | TSI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20805 | hp2 | a0001 | c0001 | t0038 | g0002 | EUR | TSI | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0339 | SAS | GIH | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | GIH | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0157 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0152 | AMR | CLM | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02486 | hp1 | a0001 | c0001 | t0019 | g0174 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02486 | hp2 | a0001 | c0002 | t0006 | g0326 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG02559 | hp2 | a0001 | c0001 | t0005 | g0295 | AFR | ACB | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03471 | hp1 | a0001 | c0001 | t0029 | g0111 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0083 | AFR | MSL | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG06807 | hp1 | a0001 | c0001 | t0005 | g0299 | AFR | USA | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| HG06807 | hp2 | a0001 | c0001 | t0031 | g0084 | AFR | USA | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0081 | AFR | USA | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | USA | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA21309 | hp1 | a0001 | c0001 | t0005 | g0293 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| NA21309 | hp2 | a0001 | c0002 | t0006 | g0026 | AFR | LWK | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0169 | REF | REF | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0159 | REF | REF | UGCG_chr9_111891814_111940369 | UGCG | chr9 | 111891814 | 111940369 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111922873 | G | C | 1 | a0002 | 1 | NA18968.hp1 | missense_variant | MODERATE | c.265G>C | p.Asp89His | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/9 | 667/3959 | 265/1185 | 89/394 | chr9 | 111922873 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111924781 | C | T | 1 | a0001c0003 | 18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
synonymous_variant | LOW | c.348C>T | p.Gly116Gly | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/9 | 750/3959 | 348/1185 | 116/394 | chr9 | 111924781 | |||
| chr9:111926397 | G | A | 1 | a0001c0004 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
synonymous_variant | LOW | c.459G>A | p.Thr153Thr | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/9 | 861/3959 | 459/1185 | 153/394 | chr9 | 111926397 | |||
| chr9:111932206 | A | G | 2 | a0001c0002 a0001c0007 |
127 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(124): Show |
synonymous_variant | LOW | c.861A>G | p.Thr287Thr | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/9 | 1263/3959 | 861/1185 | 287/394 | chr9 | 111932206 | |||
| chr9:111932275 | G | A | 1 | a0001c0006 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.930G>A | p.Val310Val | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/9 | 1332/3959 | 930/1185 | 310/394 | chr9 | 111932275 | |||
| chr9:111932865 | C | T | 1 | a0001c0007 | 1 | HG02273.hp1 | synonymous_variant | LOW | c.1053C>T | p.Val351Val | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1455/3959 | 1053/1185 | 351/394 | chr9 | 111932865 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111896892 | C | T | 14 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(11): Show |
79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
5_prime_UTR_variant | MODIFIER | c.-324C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 324 | chr9 | 111896892 | ||||||
| chr9:111896921 | C | T | 19 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(16): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-295C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | chr9 | 111896921 | |||||||
| chr9:111896946 | A | C | 14 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0007 others(11): Show |
82 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(79): Show |
5_prime_UTR_variant | MODIFIER | c.-270A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 270 | chr9 | 111896946 | ||||||
| chr9:111896946 | A | G | 19 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0013 others(16): Show |
152 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
5_prime_UTR_variant | MODIFIER | c.-270A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 270 | chr9 | 111896946 | ||||||
| chr9:111896983 | A | ACCCGCAG others(3): Show |
21 | a0001c0001t0011 a0001c0001t0014 a0001c0001t0018 others(18): Show |
104 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(101): Show |
5_prime_UTR_variant | MODIFIER | c.-227_-218dupAGCCGC others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 217 | INFO_REALIGN_3_PRIME | chr9 | 111896983 | |||||
| chr9:111896983 | A | ACCCGCAG others(13): Show |
2 | a0001c0002t0012 a0001c0002t0022 |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-218_-217insAGCCGC others(14): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 217 | INFO_REALIGN_3_PRIME | chr9 | 111896983 | |||||
| chr9:111896983 | A | ACCCGTAG others(3): Show |
1 | a0001c0002t0045 | 1 | NA19054.hp1 | 5_prime_UTR_variant | MODIFIER | c.-229_-228insTAGCCG others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 228 | INFO_REALIGN_3_PRIME | chr9 | 111896983 | |||||
| chr9:111897002 | C | T | 2 | a0001c0001t0026 a0001c0001t0055 |
4 | HG02015.hp2 HG02738.hp1 NA19030.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-214C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 214 | chr9 | 111897002 | ||||||
| chr9:111897079 | C | A | 1 | a0001c0003t0046 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-137C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 137 | chr9 | 111897079 | ||||||
| chr9:111897093 | C | T | 1 | a0001c0001t0064 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-123C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 123 | chr9 | 111897093 | ||||||
| chr9:111897101 | A | G | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-115A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 115 | chr9 | 111897101 | ||||||
| chr9:111897130 | C | T | 1 | a0001c0002t0040 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-86C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/9 | 86 | chr9 | 111897130 | ||||||
| chr9:111933151 | G | GA | 22 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0011 others(19): Show |
89 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*168dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 169 | INFO_REALIGN_3_PRIME | chr9 | 111933151 | |||||
| chr9:111933274 | A | T | 2 | a0001c0001t0029 a0001c0001t0039 |
3 | HG01255.hp1 HG02886.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*277A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 277 | chr9 | 111933274 | ||||||
| chr9:111933320 | G | A | 2 | a0001c0001t0011 a0001c0001t0028 |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*323G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 323 | chr9 | 111933320 | ||||||
| chr9:111933479 | C | T | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*482C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 482 | chr9 | 111933479 | ||||||
| chr9:111933546 | T | C | 21 | a0001c0001t0026 a0001c0001t0050 a0001c0002t0002 others(18): Show |
131 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(128): Show |
3_prime_UTR_variant | MODIFIER | c.*549T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 549 | chr9 | 111933546 | ||||||
| chr9:111933649 | T | G | 1 | a0001c0002t0032 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 652 | chr9 | 111933649 | ||||||
| chr9:111933741 | T | C | 1 | a0001c0001t0059 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*744T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 744 | chr9 | 111933741 | ||||||
| chr9:111934079 | TGA | T | 2 | a0001c0001t0011 a0001c0001t0028 |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1084_*1085delAG | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1084 | INFO_REALIGN_3_PRIME | chr9 | 111934079 | |||||
| chr9:111934128 | G | GT | 16 | a0001c0001t0004 a0001c0001t0014 a0001c0001t0016 others(13): Show |
63 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*1143dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1144 | INFO_REALIGN_3_PRIME | chr9 | 111934128 | |||||
| chr9:111934135 | T | G | 1 | a0001c0002t0033 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1138T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1138 | chr9 | 111934135 | ||||||
| chr9:111934137 | T | G | 1 | a0001c0002t0034 | 1 | NA18993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1140T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1140 | chr9 | 111934137 | ||||||
| chr9:111934140 | TG | T | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1144delG | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1144 | chr9 | 111934140 | ||||||
| chr9:111934143 | T | G | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1146T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1146 | chr9 | 111934143 | ||||||
| chr9:111934192 | T | C | 1 | a0001c0002t0049 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1195T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1195 | chr9 | 111934192 | ||||||
| chr9:111934208 | A | C | 61 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(58): Show |
374 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(371): Show |
3_prime_UTR_variant | MODIFIER | c.*1211A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1211 | chr9 | 111934208 | ||||||
| chr9:111934320 | G | A | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1323G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1323 | chr9 | 111934320 | ||||||
| chr9:111934340 | C | T | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1343C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1343 | chr9 | 111934340 | ||||||
| chr9:111934359 | T | A | 3 | a0001c0001t0029 a0001c0001t0051 a0001c0001t0052 |
4 | HG01256.hp2 HG02886.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1362T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1362 | chr9 | 111934359 | ||||||
| chr9:111934360 | A | T | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1363A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1363 | chr9 | 111934360 | ||||||
| chr9:111934372 | C | A | 1 | a0001c0002t0023 | 3 | NA19012.hp1 NA19066.hp2 NA19074.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1375C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1375 | chr9 | 111934372 | ||||||
| chr9:111934379 | G | C | 1 | a0001c0001t0024 | 3 | HG00642.hp2 HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1382G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1382 | chr9 | 111934379 | ||||||
| chr9:111934533 | C | T | 1 | a0001c0002t0037 | 1 | NA18965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1536 | chr9 | 111934533 | ||||||
| chr9:111934620 | A | G | 1 | a0001c0002t0036 | 1 | NA18977.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1623A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1623 | chr9 | 111934620 | ||||||
| chr9:111934719 | CTTTCT | C | 18 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0014 others(15): Show |
72 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1726_*1730delCTTT others(1): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1726 | INFO_REALIGN_3_PRIME | chr9 | 111934719 | |||||
| chr9:111934723 | CT | C | 41 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0011 others(38): Show |
285 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(282): Show |
3_prime_UTR_variant | MODIFIER | c.*1741delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1741 | INFO_REALIGN_3_PRIME | chr9 | 111934723 | |||||
| chr9:111934753 | T | C | 6 | a0001c0001t0011 a0001c0001t0028 a0001c0001t0053 others(3): Show |
26 | HG00558.hp1 HG00609.hp2 HG00673.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1756T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1756 | chr9 | 111934753 | ||||||
| chr9:111934828 | C | A | 4 | a0001c0001t0053 a0001c0003t0008 a0001c0003t0044 others(1): Show |
16 | HG00558.hp1 HG04115.hp2 NA18941.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1831C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1831 | chr9 | 111934828 | ||||||
| chr9:111934879 | G | A | 1 | a0001c0001t0058 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1882G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 1882 | chr9 | 111934879 | ||||||
| chr9:111935041 | A | G | 1 | a0001c0001t0027 | 2 | HG03098.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2044A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2044 | chr9 | 111935041 | ||||||
| chr9:111935088 | A | G | 2 | a0001c0001t0026 a0001c0001t0050 |
4 | HG02015.hp2 HG03490.hp1 NA19030.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2091A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2091 | chr9 | 111935088 | ||||||
| chr9:111935123 | G | A | 1 | a0001c0002t0022 | 3 | HG02615.hp1 HG02965.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2126G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2126 | chr9 | 111935123 | ||||||
| chr9:111935206 | A | T | 1 | a0001c0002t0035 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2209A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2209 | chr9 | 111935206 | ||||||
| chr9:111935280 | C | A | 1 | a0001c0004t0020 | 4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2283C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2283 | chr9 | 111935280 | ||||||
| chr9:111935327 | T | A | 2 | a0001c0001t0043 a0001c0001t0060 |
2 | HG01192.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2330T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 9/9 | 2330 | chr9 | 111935327 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:111897363 | A | G | 125 | a0001c0001t0001g0317 a0001c0001t0001g0318 a0001c0001t0001g0328 others(122): Show |
142 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.98+50A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897363 | |||||||
| chr9:111897381 | A | T | 129 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(126): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.98+68A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897381 | |||||||
| chr9:111897390 | G | T | 1 | a0001c0001t0013g0256 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.98+77G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897390 | |||||||
| chr9:111897418 | G | T | 1 | a0001c0002t0009g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.98+105G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897418 | |||||||
| chr9:111897587 | G | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+274G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897587 | |||||||
| chr9:111897645 | G | A | 68 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(65): Show |
79 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.98+332G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897645 | |||||||
| chr9:111897670 | G | A | 83 | a0001c0001t0014g0079 a0001c0001t0015g0092 a0001c0001t0018g0035 others(80): Show |
96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+357G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897670 | |||||||
| chr9:111897727 | C | G | 151 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(148): Show |
175 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(172): Show |
intron_variant | MODIFIER | c.98+414C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897727 | |||||||
| chr9:111897730 | A | G | 1 | a0001c0001t0007g0316 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.98+417A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897730 | |||||||
| chr9:111897948 | G | C | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+635G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111897948 | |||||||
| chr9:111898024 | G | T | 7 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
7 | NA18947.hp2 NA18965.hp1 NA18992.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+711G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898024 | |||||||
| chr9:111898172 | T | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(128): Show |
143 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.98+859T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898172 | |||||||
| chr9:111898184 | C | T | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98+871C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898184 | |||||||
| chr9:111898255 | A | G | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.98+942A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898255 | |||||||
| chr9:111898385 | A | C | 3 | a0001c0003t0014g0184 a0001c0003t0014g0185 a0001c0003t0014g0186 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.98+1072A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898385 | |||||||
| chr9:111898394 | G | GT | 30 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(27): Show |
32 | HG00438.hp1 HG00642.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.98+1093dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111898394 | ||||||
| chr9:111898395 | T | G | 53 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(50): Show |
62 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.98+1082T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898395 | |||||||
| chr9:111898436 | G | C | 1 | a0001c0001t0039g0030 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98+1123G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898436 | |||||||
| chr9:111898506 | C | T | 1 | a0001c0001t0005g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.98+1193C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898506 | |||||||
| chr9:111898702 | A | G | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+1389A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898702 | |||||||
| chr9:111898735 | T | C | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.98+1422T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898735 | |||||||
| chr9:111898883 | A | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+1570A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898883 | |||||||
| chr9:111898986 | T | G | 129 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(126): Show |
145 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(142): Show |
intron_variant | MODIFIER | c.98+1673T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111898986 | |||||||
| chr9:111899093 | GATTT | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+1788_98+1791del others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111899093 | ||||||
| chr9:111899134 | A | G | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG00735.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.98+1821A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899134 | |||||||
| chr9:111899309 | T | C | 31 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(28): Show |
38 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.98+1996T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899309 | |||||||
| chr9:111899331 | T | G | 119 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(116): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.98+2018T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899331 | |||||||
| chr9:111899544 | C | T | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98+2231C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899544 | |||||||
| chr9:111899574 | A | G | 1 | a0001c0001t0004g0279 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.98+2261A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899574 | |||||||
| chr9:111899633 | C | T | 18 | a0001c0001t0005g0306 a0001c0001t0007g0024 a0001c0001t0007g0025 others(15): Show |
20 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.98+2320C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899633 | |||||||
| chr9:111899645 | A | G | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0244 others(1): Show |
4 | HG02040.hp2 NA19007.hp2 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+2332A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899645 | |||||||
| chr9:111899813 | T | C | 83 | a0001c0001t0014g0079 a0001c0001t0015g0092 a0001c0001t0018g0035 others(80): Show |
96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+2500T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111899813 | |||||||
| chr9:111900076 | C | A | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+2763C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900076 | |||||||
| chr9:111900078 | A | T | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+2765A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900078 | |||||||
| chr9:111900096 | A | G | 70 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(67): Show |
81 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.98+2783A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900096 | |||||||
| chr9:111900120 | A | AT | 55 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0258 others(52): Show |
64 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.98+2824dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900120 | ||||||
| chr9:111900120 | AT | A | 192 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(189): Show |
216 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.98+2824delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900120 | ||||||
| chr9:111900120 | ATT | A | 51 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(48): Show |
53 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.98+2823_98+2824del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900120 | ||||||
| chr9:111900476 | A | ATG | 5 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0003g0179 others(2): Show |
5 | HG01074.hp1 HG02027.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+3185_98+3186dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900476 | ||||||
| chr9:111900476 | ATG | A | 298 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(295): Show |
335 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(332): Show |
intron_variant | MODIFIER | c.98+3185_98+3186del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900476 | ||||||
| chr9:111900478 | G | GTA | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+3166_98+3167ins others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900478 | ||||||
| chr9:111900478 | G | GTATA | 3 | a0001c0001t0024g0364 a0001c0001t0024g0365 a0001c0001t0024g0366 |
3 | HG00642.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.98+3166_98+3167ins others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111900478 | ||||||
| chr9:111900480 | G | A | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+3167G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900480 | |||||||
| chr9:111900503 | C | T | 87 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(84): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+3190C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900503 | |||||||
| chr9:111900513 | T | G | 87 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(84): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+3200T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900513 | |||||||
| chr9:111900578 | C | T | 1 | a0001c0002t0006g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.98+3265C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900578 | |||||||
| chr9:111900651 | G | A | 1 | a0001c0002t0002g0031 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.98+3338G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900651 | |||||||
| chr9:111900792 | C | A | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98+3479C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900792 | |||||||
| chr9:111900807 | T | A | 1 | a0001c0001t0010g0331 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.98+3494T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900807 | |||||||
| chr9:111900844 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0250 |
2 | NA19001.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.98+3531G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900844 | |||||||
| chr9:111900919 | C | T | 78 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(75): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.98+3606C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900919 | |||||||
| chr9:111900927 | G | T | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98+3614G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900927 | |||||||
| chr9:111900980 | G | A | 78 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(75): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.98+3667G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111900980 | |||||||
| chr9:111901101 | C | G | 21 | a0001c0001t0001g0328 a0001c0001t0001g0339 a0001c0001t0001g0342 others(18): Show |
23 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.98+3788C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901101 | |||||||
| chr9:111901206 | C | T | 1 | a0001c0002t0009g0187 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.98+3893C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901206 | |||||||
| chr9:111901319 | A | G | 87 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(84): Show |
100 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.98+4006A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901319 | |||||||
| chr9:111901514 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG01884.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.98+4201G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901514 | |||||||
| chr9:111901579 | A | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+4266A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901579 | |||||||
| chr9:111901581 | T | C | 2 | a0001c0001t0001g0339 a0001c0001t0010g0340 |
2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.98+4268T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901581 | |||||||
| chr9:111901689 | A | C | 77 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(74): Show |
85 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.98+4376A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901689 | |||||||
| chr9:111901799 | A | G | 6 | a0001c0001t0010g0029 a0001c0001t0010g0351 a0001c0001t0010g0352 others(3): Show |
7 | HG00323.hp1 HG00733.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.98+4486A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901799 | |||||||
| chr9:111901874 | C | T | 76 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(73): Show |
84 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.98+4561C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111901874 | |||||||
| chr9:111902279 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.98+4966C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902279 | |||||||
| chr9:111902491 | T | C | 3 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 |
3 | HG02015.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.98+5178T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902491 | |||||||
| chr9:111902681 | C | T | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+5368C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902681 | |||||||
| chr9:111902719 | A | T | 5 | a0001c0001t0010g0359 a0001c0002t0006g0008 a0001c0002t0006g0362 others(2): Show |
7 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.98+5406A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902719 | |||||||
| chr9:111902721 | G | A | 8 | a0001c0001t0010g0359 a0001c0001t0026g0355 a0001c0001t0026g0356 others(5): Show |
10 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+5408G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902721 | |||||||
| chr9:111902735 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.98+5422C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902735 | |||||||
| chr9:111902782 | C | CTT | 77 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(74): Show |
90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.98+5481_98+5482dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111902782 | ||||||
| chr9:111902814 | G | C | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+5501G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902814 | |||||||
| chr9:111902934 | C | T | 5 | a0001c0001t0001g0346 a0001c0001t0001g0347 a0001c0001t0001g0348 others(2): Show |
5 | HG01255.hp2 HG02148.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.98+5621C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902934 | |||||||
| chr9:111902993 | G | T | 3 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 |
3 | HG02015.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.98+5680G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111902993 | |||||||
| chr9:111903102 | G | T | 1 | a0001c0001t0005g0299 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.98+5789G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903102 | |||||||
| chr9:111903129 | G | A | 1 | a0001c0001t0005g0306 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98+5816G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903129 | |||||||
| chr9:111903142 | G | A | 56 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(53): Show |
65 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.98+5829G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903142 | |||||||
| chr9:111903195 | AG | A | 3 | a0001c0001t0005g0296 a0001c0001t0005g0297 a0001c0001t0005g0298 |
3 | HG01891.hp2 HG02257.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.98+5883delG | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903195 | |||||||
| chr9:111903381 | G | A | 59 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(56): Show |
68 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.98+6068G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903381 | |||||||
| chr9:111903442 | GT | G | 75 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(72): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.98+6130delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903442 | |||||||
| chr9:111903480 | G | A | 25 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0280 others(22): Show |
27 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.98+6167G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903480 | |||||||
| chr9:111903626 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.98+6313C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903626 | |||||||
| chr9:111903706 | C | T | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+6393C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903706 | |||||||
| chr9:111903782 | G | A | 75 | a0001c0001t0014g0079 a0001c0001t0015g0092 a0001c0001t0018g0035 others(72): Show |
86 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.98+6469G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903782 | |||||||
| chr9:111903801 | G | A | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+6488G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903801 | |||||||
| chr9:111903863 | T | C | 1 | a0001c0001t0004g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.98+6550T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903863 | |||||||
| chr9:111903892 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+6579C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903892 | |||||||
| chr9:111903933 | A | G | 8 | a0001c0001t0010g0359 a0001c0001t0026g0355 a0001c0001t0026g0356 others(5): Show |
10 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+6620A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111903933 | |||||||
| chr9:111903948 | CA | C | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+6637delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111903948 | ||||||
| chr9:111904079 | G | GC | 170 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(167): Show |
188 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.98+6770dupC | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111904079 | ||||||
| chr9:111904197 | C | A | 1 | a0001c0001t0005g0280 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.98+6884C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904197 | |||||||
| chr9:111904213 | C | A | 19 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(16): Show |
22 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+6900C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904213 | |||||||
| chr9:111904321 | G | A | 5 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0283 others(2): Show |
5 | HG02145.hp1 HG02559.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.98+7008G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904321 | |||||||
| chr9:111904356 | C | A | 1 | a0001c0001t0001g0203 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.98+7043C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904356 | |||||||
| chr9:111904689 | C | T | 39 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(36): Show |
41 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.98+7376C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904689 | |||||||
| chr9:111904697 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98+7384C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904697 | |||||||
| chr9:111904755 | C | T | 3 | a0001c0001t0024g0364 a0001c0001t0024g0365 a0001c0001t0024g0366 |
3 | HG00642.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.98+7442C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904755 | |||||||
| chr9:111904756 | G | A | 2 | a0001c0001t0010g0359 a0001c0002t0049g0358 |
2 | HG03579.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.98+7443G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904756 | |||||||
| chr9:111904814 | G | A | 2 | a0001c0002t0002g0033 a0001c0002t0002g0034 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.98+7501G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904814 | |||||||
| chr9:111904828 | C | T | 14 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(11): Show |
14 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+7515C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904828 | |||||||
| chr9:111904834 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+7521C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904834 | |||||||
| chr9:111904838 | G | A | 10 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(7): Show |
10 | HG00642.hp2 HG01884.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.98+7525G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111904838 | |||||||
| chr9:111905031 | C | T | 29 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(26): Show |
31 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.98+7718C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905031 | |||||||
| chr9:111905089 | C | T | 3 | a0001c0002t0006g0027 a0001c0002t0006g0325 a0001c0002t0006g0326 |
4 | HG01261.hp1 HG02451.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.98+7776C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905089 | |||||||
| chr9:111905221 | C | T | 19 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(16): Show |
22 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.98+7908C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905221 | |||||||
| chr9:111905239 | C | G | 1 | a0001c0002t0009g0181 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.98+7926C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905239 | |||||||
| chr9:111905276 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.98+7963T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905276 | |||||||
| chr9:111905282 | C | G | 3 | a0001c0001t0005g0294 a0001c0001t0005g0295 a0001c0001t0005g0299 |
3 | HG02559.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.98+7969C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905282 | |||||||
| chr9:111905453 | A | G | 83 | a0001c0001t0014g0079 a0001c0001t0015g0092 a0001c0001t0018g0035 others(80): Show |
96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+8140A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905453 | |||||||
| chr9:111905459 | C | CT | 27 | a0001c0001t0004g0278 a0001c0001t0010g0359 a0001c0001t0011g0011 others(24): Show |
32 | HG00597.hp1 HG00609.hp2 HG00639.hp1 others(29): Show |
intron_variant | MODIFIER | c.98+8159dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111905459 | ||||||
| chr9:111905459 | CT | C | 19 | a0001c0001t0001g0339 a0001c0001t0005g0306 a0001c0001t0007g0024 others(16): Show |
21 | HG01361.hp1 HG02080.hp2 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.98+8159delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111905459 | ||||||
| chr9:111905471 | T | G | 83 | a0001c0001t0014g0079 a0001c0001t0015g0092 a0001c0001t0018g0035 others(80): Show |
96 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.98+8158T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905471 | |||||||
| chr9:111905599 | G | A | 60 | a0001c0001t0014g0079 a0001c0001t0018g0035 a0001c0001t0018g0036 others(57): Show |
70 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.98+8286G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905599 | |||||||
| chr9:111905601 | G | A | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.98+8288G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905601 | |||||||
| chr9:111905707 | G | A | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+8394G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905707 | |||||||
| chr9:111905742 | C | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.98+8429C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905742 | |||||||
| chr9:111905837 | T | C | 1 | a0001c0001t0027g0080 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.98+8524T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905837 | |||||||
| chr9:111905849 | G | A | 1 | a0001c0004t0020g0320 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.98+8536G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905849 | |||||||
| chr9:111905880 | C | T | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.98+8567C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905880 | |||||||
| chr9:111905884 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.98+8571C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905884 | |||||||
| chr9:111905913 | T | C | 60 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(57): Show |
65 | HG00323.hp1 HG00323.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.98+8600T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905913 | |||||||
| chr9:111905914 | A | G | 13 | a0001c0001t0007g0025 a0001c0001t0007g0301 a0001c0001t0007g0302 others(10): Show |
14 | HG02080.hp2 HG02135.hp2 NA18951.hp2 others(11): Show |
intron_variant | MODIFIER | c.98+8601A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111905914 | |||||||
| chr9:111906097 | G | A | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-8508G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906097 | |||||||
| chr9:111906184 | GA | G | 7 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(4): Show |
7 | HG01192.hp1 HG01243.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-8420delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906184 | |||||||
| chr9:111906228 | T | G | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-8377T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906228 | |||||||
| chr9:111906353 | G | A | 29 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(26): Show |
31 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.99-8252G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906353 | |||||||
| chr9:111906353 | G | C | 1 | a0001c0001t0015g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.99-8252G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906353 | |||||||
| chr9:111906359 | C | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(77): Show |
88 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.99-8246C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906359 | |||||||
| chr9:111906423 | G | GTGTTT | 7 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(4): Show |
9 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-8159_99-8155dup others(5): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111906423 | ||||||
| chr9:111906461 | G | A | 2 | a0001c0001t0027g0080 a0001c0002t0002g0081 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.99-8144G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906461 | |||||||
| chr9:111906469 | G | A | 8 | a0001c0001t0039g0030 a0001c0002t0006g0026 a0001c0002t0006g0027 others(5): Show |
10 | HG01255.hp1 HG01261.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-8136G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906469 | |||||||
| chr9:111906493 | G | A | 80 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(77): Show |
88 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.99-8112G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906493 | |||||||
| chr9:111906528 | C | G | 1 | a0001c0001t0007g0316 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.99-8077C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906528 | |||||||
| chr9:111906546 | C | T | 1 | a0001c0001t0007g0316 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.99-8059C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906546 | |||||||
| chr9:111906578 | C | T | 2 | a0001c0001t0001g0200 a0001c0001t0001g0201 |
2 | HG00408.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.99-8027C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906578 | |||||||
| chr9:111906726 | C | T | 1 | a0001c0001t0018g0128 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99-7879C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906726 | |||||||
| chr9:111906727 | A | G | 19 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(16): Show |
22 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-7878A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906727 | |||||||
| chr9:111906793 | A | G | 1 | a0001c0003t0008g0141 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.99-7812A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906793 | |||||||
| chr9:111906862 | G | A | 25 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0280 others(22): Show |
27 | HG01081.hp1 HG01891.hp2 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.99-7743G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906862 | |||||||
| chr9:111906984 | G | C | 1 | a0001c0002t0006g0208 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.99-7621G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111906984 | |||||||
| chr9:111907063 | G | T | 1 | a0001c0001t0003g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.99-7542G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907063 | |||||||
| chr9:111907224 | G | A | 3 | a0001c0001t0007g0308 a0001c0001t0007g0309 a0001c0001t0007g0310 |
3 | NA19010.hp1 NA19080.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.99-7381G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907224 | |||||||
| chr9:111907290 | G | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.99-7315G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907290 | |||||||
| chr9:111907309 | C | T | 19 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(16): Show |
22 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-7296C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907309 | |||||||
| chr9:111907508 | T | C | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-7097T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907508 | |||||||
| chr9:111907578 | G | A | 2 | a0001c0002t0002g0114 a0001c0002t0002g0115 |
2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.99-7027G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907578 | |||||||
| chr9:111907628 | C | CT | 169 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(166): Show |
193 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.99-6963dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111907628 | ||||||
| chr9:111907628 | C | CTT | 50 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(47): Show |
52 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.99-6964_99-6963dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111907628 | ||||||
| chr9:111907665 | C | T | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-6940C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907665 | |||||||
| chr9:111907709 | C | A | 17 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(14): Show |
17 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.99-6896C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907709 | |||||||
| chr9:111907749 | C | T | 19 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(16): Show |
22 | HG00609.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.99-6856C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907749 | |||||||
| chr9:111907909 | G | A | 334 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(331): Show |
373 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(370): Show |
intron_variant | MODIFIER | c.99-6696G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111907909 | |||||||
| chr9:111908095 | G | T | 56 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(53): Show |
65 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.99-6510G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908095 | |||||||
| chr9:111908283 | C | T | 1 | a0001c0001t0029g0111 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.99-6322C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908283 | |||||||
| chr9:111908312 | C | A | 1 | a0001c0001t0013g0341 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.99-6293C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908312 | |||||||
| chr9:111908619 | C | G | 63 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(60): Show |
72 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.99-5986C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908619 | |||||||
| chr9:111908630 | A | G | 6 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(3): Show |
8 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-5975A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908630 | |||||||
| chr9:111908665 | A | G | 6 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(3): Show |
8 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-5940A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908665 | |||||||
| chr9:111908686 | G | A | 5 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(2): Show |
8 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-5919G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908686 | |||||||
| chr9:111908765 | T | C | 5 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(2): Show |
5 | NA18944.hp2 NA18946.hp2 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-5840T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908765 | |||||||
| chr9:111908779 | T | C | 7 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(4): Show |
9 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-5826T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908779 | |||||||
| chr9:111908826 | C | G | 3 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 |
3 | HG02015.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.99-5779C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908826 | |||||||
| chr9:111908853 | G | A | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-5752G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908853 | |||||||
| chr9:111908918 | A | G | 3 | a0001c0003t0014g0184 a0001c0003t0014g0185 a0001c0003t0014g0186 |
3 | HG00733.hp2 HG00738.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.99-5687A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908918 | |||||||
| chr9:111908987 | C | T | 71 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(68): Show |
83 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.99-5618C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908987 | |||||||
| chr9:111908992 | C | T | 1 | a0001c0002t0002g0078 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.99-5613C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111908992 | |||||||
| chr9:111909035 | C | G | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-5570C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909035 | |||||||
| chr9:111909059 | T | G | 1 | a0001c0001t0019g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99-5546T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909059 | |||||||
| chr9:111909187 | T | C | 1 | a0001c0001t0051g0350 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.99-5418T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909187 | |||||||
| chr9:111909197 | A | G | 77 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(74): Show |
91 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.99-5408A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909197 | |||||||
| chr9:111909230 | T | A | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-5375T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909230 | |||||||
| chr9:111909455 | A | G | 77 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(74): Show |
91 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.99-5150A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909455 | |||||||
| chr9:111909465 | C | T | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-5140C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909465 | |||||||
| chr9:111909476 | A | C | 1 | a0001c0001t0059g0307 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99-5129A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909476 | |||||||
| chr9:111909738 | T | C | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-4867T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909738 | |||||||
| chr9:111909739 | G | C | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-4866G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909739 | |||||||
| chr9:111909817 | A | G | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-4788A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909817 | |||||||
| chr9:111909880 | G | A | 1 | a0001c0001t0055g0361 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.99-4725G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111909880 | |||||||
| chr9:111910045 | A | G | 223 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(220): Show |
252 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(249): Show |
intron_variant | MODIFIER | c.99-4560A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910045 | |||||||
| chr9:111910414 | A | G | 1 | a0001c0001t0001g0239 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.99-4191A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910414 | |||||||
| chr9:111910501 | C | A | 1 | a0001c0001t0063g0266 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.99-4104C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910501 | |||||||
| chr9:111910511 | G | A | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-4094G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910511 | |||||||
| chr9:111910575 | A | G | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-4030A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910575 | |||||||
| chr9:111910585 | C | T | 77 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(74): Show |
91 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.99-4020C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910585 | |||||||
| chr9:111910677 | C | A | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-3928C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910677 | |||||||
| chr9:111910742 | TTTTTTG | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-3849_99-3844del others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111910742 | ||||||
| chr9:111910807 | G | A | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-3798G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910807 | |||||||
| chr9:111910979 | T | C | 1 | a0001c0002t0006g0327 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99-3626T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910979 | |||||||
| chr9:111910986 | A | G | 1 | a0001c0002t0002g0077 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99-3619A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111910986 | |||||||
| chr9:111911027 | A | G | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-3578A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911027 | |||||||
| chr9:111911068 | A | G | 113 | a0001c0001t0015g0092 a0001c0001t0027g0001 a0001c0001t0027g0080 others(110): Show |
126 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.99-3537A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911068 | |||||||
| chr9:111911104 | C | T | 10 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(7): Show |
13 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(10): Show |
intron_variant | MODIFIER | c.99-3501C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911104 | |||||||
| chr9:111911192 | A | G | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-3413A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911192 | |||||||
| chr9:111911211 | C | T | 2 | a0001c0002t0002g0075 a0001c0002t0036g0076 |
2 | NA18977.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.99-3394C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911211 | |||||||
| chr9:111911244 | G | A | 1 | a0001c0002t0002g0081 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99-3361G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911244 | |||||||
| chr9:111911249 | G | T | 4 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(1): Show |
4 | HG02015.hp2 HG03490.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-3356G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911249 | |||||||
| chr9:111911567 | C | T | 4 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(1): Show |
4 | HG02015.hp2 HG03490.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-3038C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911567 | |||||||
| chr9:111911624 | G | A | 1 | a0001c0002t0002g0038 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.99-2981G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911624 | |||||||
| chr9:111911676 | T | C | 113 | a0001c0001t0015g0092 a0001c0001t0027g0001 a0001c0001t0027g0080 others(110): Show |
126 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.99-2929T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911676 | |||||||
| chr9:111911742 | T | A | 8 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(5): Show |
10 | HG00673.hp2 HG03239.hp2 HG03942.hp1 others(7): Show |
intron_variant | MODIFIER | c.99-2863T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911742 | |||||||
| chr9:111911743 | A | T | 1 | a0001c0001t0063g0266 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.99-2862A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911743 | |||||||
| chr9:111911758 | G | T | 8 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(5): Show |
10 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-2847G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911758 | |||||||
| chr9:111911763 | G | A | 3 | a0001c0001t0024g0364 a0001c0001t0024g0365 a0001c0001t0024g0366 |
3 | HG00642.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.99-2842G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911763 | |||||||
| chr9:111911791 | G | GGGGAGGC others(25): Show |
1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99-2808_99-2777dup others(32): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911791 | ||||||
| chr9:111911902 | CAGGATAT others(38): Show |
C | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-2701_99-2657del others(45): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911902 | ||||||
| chr9:111911905 | GAT | G | 5 | a0001c0001t0001g0333 a0001c0001t0001g0336 a0001c0001t0003g0002 others(2): Show |
6 | HG00140.hp1 HG00323.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-2649_99-2648del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATAT | G | 6 | a0001c0001t0001g0332 a0001c0001t0003g0014 a0001c0001t0003g0168 others(3): Show |
6 | HG01074.hp1 HG01099.hp2 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.99-2651_99-2648del others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATAT | G | 11 | a0001c0001t0001g0105 a0001c0001t0001g0335 a0001c0001t0001g0339 others(8): Show |
11 | HG01192.hp1 HG01255.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.99-2653_99-2648del others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(1): Show |
G | 13 | a0001c0001t0003g0002 a0001c0001t0003g0156 a0001c0001t0003g0165 others(10): Show |
13 | HG00099.hp1 HG00733.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-2655_99-2648del others(8): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(3): Show |
G | 30 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0328 others(27): Show |
31 | HG00323.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.99-2657_99-2648del others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(5): Show |
G | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0003g0154 others(6): Show |
9 | HG01192.hp2 HG02109.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.99-2659_99-2648del others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(9): Show |
G | 3 | a0001c0001t0003g0002 a0001c0001t0003g0176 a0001c0001t0024g0364 |
4 | HG00642.hp2 HG01070.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.99-2663_99-2648del others(16): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(13): Show |
G | 2 | a0001c0002t0006g0362 a0001c0002t0006g0363 |
2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.99-2667_99-2648del others(20): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(15): Show |
G | 2 | a0001c0001t0005g0306 a0001c0001t0015g0145 |
2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.99-2669_99-2648del others(22): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(17): Show |
G | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.99-2671_99-2648del others(24): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(21): Show |
G | 1 | a0001c0001t0050g0240 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.99-2675_99-2648del others(28): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(23): Show |
G | 13 | a0001c0001t0004g0258 a0001c0001t0004g0275 a0001c0001t0004g0276 others(10): Show |
13 | HG00673.hp1 HG02040.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.99-2677_99-2648del others(30): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(25): Show |
G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0019 others(39): Show |
46 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.99-2679_99-2648del others(32): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(29): Show |
G | 1 | a0001c0001t0003g0177 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.99-2683_99-2648del others(36): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911905 | GATATATA others(50): Show |
G | 111 | a0001c0001t0015g0092 a0001c0001t0027g0001 a0001c0001t0027g0080 others(108): Show |
124 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.99-2698_99-2642del others(57): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911905 | ||||||
| chr9:111911906 | ATATATAT others(30): Show |
A | 2 | a0001c0001t0039g0030 a0001c0002t0009g0170 |
2 | HG01255.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.99-2698_99-2662del others(37): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911906 | |||||||
| chr9:111911921 | TATATATA others(8): Show |
T | 1 | a0001c0001t0059g0307 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.99-2683_99-2669del others(15): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911921 | |||||||
| chr9:111911923 | T | TATATATA others(21): Show |
1 | a0001c0001t0011g0113 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99-2662_99-2661ins others(28): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911923 | ||||||
| chr9:111911923 | TATATATA others(59): Show |
T | 1 | a0001c0004t0020g0320 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.99-2671_99-2606del others(66): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911923 | ||||||
| chr9:111911925 | TATATATA others(4): Show |
T | 31 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(28): Show |
34 | HG00280.hp1 HG00558.hp2 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.99-2679_99-2669del others(11): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911925 | |||||||
| chr9:111911927 | T | TATATATA others(19): Show |
1 | a0001c0001t0011g0011 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.99-2660_99-2659ins others(26): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911927 | ||||||
| chr9:111911927 | T | TATATATA others(17): Show |
2 | a0001c0001t0011g0011 a0001c0001t0011g0012 |
2 | HG00609.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.99-2662_99-2661ins others(24): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911927 | ||||||
| chr9:111911927 | TATATATA others(2): Show |
T | 44 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(41): Show |
52 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.99-2677_99-2669del others(9): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911927 | |||||||
| chr9:111911929 | T | TATATATA others(17): Show |
1 | a0001c0001t0011g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99-2660_99-2659ins others(24): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911929 | ||||||
| chr9:111911929 | T | TATATATA others(13): Show |
3 | a0001c0001t0011g0013 a0001c0001t0028g0143 a0001c0001t0028g0172 |
4 | NA18952.hp1 NA19083.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.99-2664_99-2663ins others(20): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911929 | ||||||
| chr9:111911929 | TATATATA | T | 5 | a0001c0001t0004g0003 a0001c0001t0005g0296 a0001c0001t0026g0355 others(2): Show |
5 | HG02015.hp2 HG02165.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.99-2675_99-2669del others(7): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911929 | |||||||
| chr9:111911930 | A | C | 1 | a0001c0001t0025g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99-2675A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911930 | |||||||
| chr9:111911931 | T | A | 1 | a0001c0001t0025g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99-2674T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911931 | |||||||
| chr9:111911933 | T | C | 1 | a0001c0001t0025g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99-2672T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911933 | |||||||
| chr9:111911933 | T | TATATATA others(9): Show |
1 | a0001c0001t0011g0012 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99-2664_99-2663ins others(16): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911933 | ||||||
| chr9:111911933 | TATA | T | 15 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(12): Show |
16 | HG00438.hp1 HG02300.hp1 NA18951.hp2 others(13): Show |
intron_variant | MODIFIER | c.99-2671_99-2669del others(3): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911933 | |||||||
| chr9:111911934 | A | C | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-2671A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911934 | |||||||
| chr9:111911935 | T | A | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-2670T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911935 | |||||||
| chr9:111911935 | TA | T | 3 | a0001c0001t0001g0021 a0001c0001t0007g0315 a0001c0001t0007g0316 |
3 | HG02080.hp2 NA18945.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.99-2669delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911935 | |||||||
| chr9:111911936 | A | G | 1 | a0001c0001t0025g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99-2669A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911936 | |||||||
| chr9:111911937 | T | C | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-2668T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911937 | |||||||
| chr9:111911937 | T | G | 1 | a0001c0001t0025g0205 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.99-2668T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911937 | |||||||
| chr9:111911938 | A | C | 97 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(94): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.99-2667A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911938 | |||||||
| chr9:111911938 | A | T | 1 | a0001c0001t0007g0024 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.99-2667A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911938 | |||||||
| chr9:111911939 | T | A | 97 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(94): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.99-2666T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911939 | |||||||
| chr9:111911939 | T | C | 1 | a0001c0001t0007g0024 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.99-2666T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911939 | |||||||
| chr9:111911940 | A | G | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-2665A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911940 | |||||||
| chr9:111911941 | T | A | 2 | a0001c0001t0007g0024 a0001c0001t0007g0301 |
3 | HG02135.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.99-2664T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911941 | |||||||
| chr9:111911941 | T | C | 97 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(94): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.99-2664T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911941 | |||||||
| chr9:111911941 | T | G | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-2664T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911941 | |||||||
| chr9:111911942 | A | C | 2 | a0001c0001t0007g0024 a0001c0001t0007g0301 |
3 | HG02135.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.99-2663A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911942 | |||||||
| chr9:111911942 | AT | A | 97 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(94): Show |
111 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.99-2662delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911942 | |||||||
| chr9:111911943 | T | A | 2 | a0001c0001t0007g0024 a0001c0001t0007g0301 |
3 | HG02135.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.99-2662T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911943 | |||||||
| chr9:111911944 | A | G | 101 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.99-2661A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911944 | |||||||
| chr9:111911945 | T | G | 101 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(98): Show |
116 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.99-2660T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111911945 | |||||||
| chr9:111911945 | T | TATATTCA others(5): Show |
1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99-2656_99-2655ins others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911945 | ||||||
| chr9:111911945 | T | TATTCAAC others(3): Show |
1 | a0001c0001t0010g0351 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.99-2658_99-2657ins others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911945 | ||||||
| chr9:111911967 | T | TAC | 102 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(99): Show |
117 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.99-2637_99-2636ins others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911967 | ||||||
| chr9:111911969 | TATATATA others(53): Show |
T | 1 | a0001c0004t0020g0319 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.99-2627_99-2568del others(60): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911969 | ||||||
| chr9:111911971 | TATATATT others(51): Show |
T | 1 | a0001c0004t0020g0322 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.99-2627_99-2570del others(58): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911971 | ||||||
| chr9:111911975 | TATTCAAC others(47): Show |
T | 1 | a0001c0004t0020g0321 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.99-2627_99-2574del others(54): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111911975 | ||||||
| chr9:111912011 | C | T | 103 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(100): Show |
118 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.99-2594C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912011 | |||||||
| chr9:111912017 | TATATTCA others(5): Show |
T | 2 | a0001c0001t0007g0024 a0001c0004t0020g0320 |
3 | HG03490.hp2 HG03492.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.99-2583_99-2572del others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912017 | ||||||
| chr9:111912019 | TATTCAAC others(3): Show |
T | 16 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(13): Show |
18 | HG01255.hp1 HG02135.hp2 HG02300.hp1 others(15): Show |
intron_variant | MODIFIER | c.99-2583_99-2574del others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912019 | ||||||
| chr9:111912021 | TTC | T | 15 | a0001c0001t0001g0251 a0001c0001t0004g0003 a0001c0001t0004g0270 others(12): Show |
15 | HG00438.hp1 HG01081.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2583_99-2582del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912021 | |||||||
| chr9:111912021 | TTCAACA | T | 17 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
18 | HG00597.hp1 HG00621.hp2 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-2583_99-2578del others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912021 | |||||||
| chr9:111912021 | TTCAACAG others(1): Show |
T | 30 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0193 others(27): Show |
30 | HG00099.hp2 HG00280.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.99-2583_99-2576del others(8): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912021 | |||||||
| chr9:111912022 | T | A | 30 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0213 others(27): Show |
33 | HG00408.hp2 HG00438.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.99-2583T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912022 | |||||||
| chr9:111912023 | C | A | 1 | a0001c0001t0005g0290 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99-2582C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912023 | |||||||
| chr9:111912023 | C | T | 30 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0213 others(27): Show |
33 | HG00408.hp2 HG00438.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.99-2582C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912023 | |||||||
| chr9:111912024 | A | T | 1 | a0001c0001t0005g0290 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99-2581A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912024 | |||||||
| chr9:111912024 | AACAG | A | 25 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0213 others(22): Show |
28 | HG00408.hp2 HG00438.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.99-2580_99-2577del others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912024 | |||||||
| chr9:111912025 | A | T | 20 | a0001c0001t0001g0218 a0001c0001t0001g0251 a0001c0001t0004g0003 others(17): Show |
20 | HG00438.hp1 HG01081.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.99-2580A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912025 | |||||||
| chr9:111912026 | C | A | 20 | a0001c0001t0001g0218 a0001c0001t0001g0251 a0001c0001t0004g0003 others(17): Show |
20 | HG00438.hp1 HG01081.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.99-2579C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912026 | |||||||
| chr9:111912026 | C | T | 1 | a0001c0001t0005g0290 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.99-2579C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912026 | |||||||
| chr9:111912027 | A | T | 20 | a0001c0001t0001g0218 a0001c0001t0001g0251 a0001c0001t0004g0003 others(17): Show |
20 | HG00438.hp1 HG01081.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.99-2578A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912027 | |||||||
| chr9:111912028 | G | A | 35 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(32): Show |
39 | HG00438.hp1 HG00597.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.99-2577G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912028 | |||||||
| chr9:111912029 | G | GAT | 21 | a0001c0001t0003g0002 a0001c0001t0003g0148 a0001c0001t0003g0151 others(18): Show |
22 | HG00642.hp2 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.99-2553_99-2552dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATACATA others(3): Show |
6 | a0001c0003t0008g0134 a0001c0003t0008g0135 a0001c0003t0008g0137 others(3): Show |
6 | NA18943.hp2 NA18953.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-2573_99-2572ins others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATACATA others(5): Show |
8 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(5): Show |
8 | HG00558.hp1 NA18944.hp2 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2573_99-2572ins others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATAT | 65 | a0001c0001t0001g0105 a0001c0001t0001g0108 a0001c0001t0001g0109 others(62): Show |
71 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.99-2555_99-2552dup others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATAT | 32 | a0001c0001t0001g0106 a0001c0001t0003g0166 a0001c0001t0015g0092 others(29): Show |
35 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.99-2557_99-2552dup others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(1): Show |
32 | a0001c0001t0001g0007 a0001c0001t0001g0203 a0001c0001t0001g0206 others(29): Show |
33 | HG00673.hp2 HG01255.hp2 HG01261.hp1 others(30): Show |
intron_variant | MODIFIER | c.99-2559_99-2552dup others(8): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(3): Show |
35 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0020 others(32): Show |
38 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.99-2561_99-2552dup others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(5): Show |
40 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0197 others(37): Show |
40 | HG00280.hp2 HG00423.hp2 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.99-2563_99-2552dup others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(7): Show |
6 | a0001c0001t0001g0334 a0001c0001t0001g0335 a0001c0001t0001g0339 others(3): Show |
7 | HG01192.hp1 HG01891.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.99-2565_99-2552dup others(14): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(9): Show |
3 | a0001c0001t0010g0352 a0001c0001t0028g0143 a0001c0002t0006g0008 |
3 | HG02257.hp2 HG02300.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.99-2567_99-2552dup others(16): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | GATATATA others(11): Show |
2 | a0001c0001t0001g0332 a0001c0001t0001g0336 |
2 | HG03486.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.99-2569_99-2552dup others(18): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912029 | G | T | 58 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(55): Show |
67 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.99-2576G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912029 | |||||||
| chr9:111912029 | GAT | G | 6 | a0001c0001t0003g0152 a0001c0001t0003g0157 a0001c0001t0029g0110 others(3): Show |
6 | HG01123.hp1 HG01123.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.99-2553_99-2552del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912029 | ||||||
| chr9:111912050 | A | G | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2555A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912050 | |||||||
| chr9:111912196 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-2409A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912196 | |||||||
| chr9:111912198 | C | T | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2407C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912198 | |||||||
| chr9:111912294 | C | G | 1 | a0001c0001t0001g0220 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.99-2311C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912294 | |||||||
| chr9:111912348 | C | T | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.99-2257C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912348 | |||||||
| chr9:111912376 | G | A | 24 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(21): Show |
26 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.99-2229G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912376 | |||||||
| chr9:111912585 | T | TA | 9 | a0001c0001t0003g0146 a0001c0001t0055g0361 a0001c0003t0014g0184 others(6): Show |
9 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-2007dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912585 | ||||||
| chr9:111912585 | TA | T | 6 | a0001c0001t0001g0195 a0001c0002t0006g0008 a0001c0002t0006g0327 others(3): Show |
8 | HG01515.hp1 HG02145.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.99-2007delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912585 | ||||||
| chr9:111912873 | T | C | 1 | a0001c0001t0004g0267 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.99-1732T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111912873 | |||||||
| chr9:111912888 | G | GGT | 60 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(57): Show |
69 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.99-1701_99-1700dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912888 | ||||||
| chr9:111912888 | GGTGTGT | G | 8 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(5): Show |
10 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-1705_99-1700del others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111912888 | ||||||
| chr9:111913311 | A | G | 1 | a0001c0002t0009g0093 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.99-1294A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913311 | |||||||
| chr9:111913460 | G | C | 1 | a0001c0002t0012g0095 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99-1145G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913460 | |||||||
| chr9:111913514 | A | G | 1 | a0001c0002t0023g0072 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.99-1091A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913514 | |||||||
| chr9:111913521 | C | T | 1 | a0001c0001t0004g0300 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.99-1084C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913521 | |||||||
| chr9:111913599 | A | AT | 12 | a0001c0001t0004g0279 a0001c0001t0005g0285 a0001c0001t0005g0291 others(9): Show |
12 | HG00099.hp2 HG01106.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.99-986dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111913599 | ||||||
| chr9:111913599 | A | ATT | 6 | a0001c0001t0011g0012 a0001c0001t0011g0013 a0001c0001t0011g0113 others(3): Show |
8 | HG00609.hp2 HG03239.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.99-987_99-986dupTT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111913599 | ||||||
| chr9:111913599 | AT | A | 212 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(209): Show |
234 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.99-986delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111913599 | ||||||
| chr9:111913599 | ATT | A | 29 | a0001c0001t0001g0021 a0001c0001t0001g0195 a0001c0001t0001g0221 others(26): Show |
32 | HG00438.hp1 HG01256.hp2 HG01515.hp1 others(29): Show |
intron_variant | MODIFIER | c.99-987_99-986delTT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr9 | 111913599 | ||||||
| chr9:111913691 | C | G | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.99-914C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913691 | |||||||
| chr9:111913693 | G | A | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.99-912G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913693 | |||||||
| chr9:111913731 | C | T | 8 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(5): Show |
10 | HG02015.hp2 HG02145.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.99-874C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913731 | |||||||
| chr9:111913732 | A | G | 77 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(74): Show |
91 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.99-873A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913732 | |||||||
| chr9:111913766 | C | T | 2 | a0001c0001t0005g0295 a0001c0001t0005g0299 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.99-839C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913766 | |||||||
| chr9:111913815 | C | T | 58 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(55): Show |
67 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.99-790C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913815 | |||||||
| chr9:111913833 | A | T | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99-772A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111913833 | |||||||
| chr9:111914028 | C | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0222 |
3 | HG01952.hp1 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.99-577C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914028 | |||||||
| chr9:111914138 | A | G | 1 | a0001c0001t0004g0274 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99-467A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914138 | |||||||
| chr9:111914191 | A | C | 19 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(16): Show |
22 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.99-414A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914191 | |||||||
| chr9:111914217 | G | T | 1 | a0001c0001t0001g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.99-388G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914217 | |||||||
| chr9:111914249 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99-356A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914249 | |||||||
| chr9:111914274 | G | A | 1 | a0001c0001t0003g0147 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99-331G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914274 | |||||||
| chr9:111914393 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.99-212G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914393 | |||||||
| chr9:111914425 | C | T | 9 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(6): Show |
9 | NA18943.hp2 NA18944.hp2 NA18946.hp2 others(6): Show |
intron_variant | MODIFIER | c.99-180C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 1/8 | chr9 | 111914425 | |||||||
| chr9:111914766 | TTTTTG | T | 208 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(205): Show |
235 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(232): Show |
intron_variant | MODIFIER | c.240+43_240+47delTT others(3): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111914766 | ||||||
| chr9:111914883 | C | T | 2 | a0001c0003t0008g0136 a0001c0003t0008g0141 |
2 | HG00558.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.240+137C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111914883 | |||||||
| chr9:111914899 | C | T | 22 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(19): Show |
22 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.240+153C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111914899 | |||||||
| chr9:111915144 | G | T | 1 | a0001c0002t0002g0083 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.240+398G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915144 | |||||||
| chr9:111915152 | C | G | 1 | a0001c0002t0006g0354 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.240+406C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915152 | |||||||
| chr9:111915225 | A | C | 2 | a0001c0002t0002g0010 a0001c0002t0002g0082 |
3 | HG02965.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.240+479A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915225 | |||||||
| chr9:111915330 | T | C | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.240+584T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915330 | |||||||
| chr9:111915353 | T | C | 1 | a0001c0001t0003g0148 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.240+607T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915353 | |||||||
| chr9:111915449 | T | C | 2 | a0001c0001t0028g0143 a0001c0001t0028g0172 |
2 | NA18952.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.240+703T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915449 | |||||||
| chr9:111915482 | A | G | 1 | a0001c0001t0004g0273 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.240+736A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915482 | |||||||
| chr9:111915486 | T | C | 1 | a0001c0004t0020g0321 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.240+740T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915486 | |||||||
| chr9:111915523 | T | C | 1 | a0001c0001t0003g0177 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.240+777T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111915523 | |||||||
| chr9:111916209 | A | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(72): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.240+1463A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916209 | |||||||
| chr9:111916221 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.240+1475C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916221 | |||||||
| chr9:111916222 | G | A | 1 | a0001c0001t0001g0247 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.240+1476G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916222 | |||||||
| chr9:111916227 | A | G | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+1481A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916227 | |||||||
| chr9:111916423 | C | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+1677C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916423 | |||||||
| chr9:111916476 | G | A | 1 | a0001c0001t0005g0281 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.240+1730G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916476 | |||||||
| chr9:111916567 | T | G | 343 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(340): Show |
382 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.240+1821T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916567 | |||||||
| chr9:111916641 | T | C | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+1895T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916641 | |||||||
| chr9:111916834 | A | G | 1 | a0001c0002t0002g0127 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.240+2088A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916834 | |||||||
| chr9:111916854 | G | A | 2 | a0001c0002t0009g0089 a0001c0002t0009g0094 |
2 | NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.240+2108G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916854 | |||||||
| chr9:111916870 | C | T | 33 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
35 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.240+2124C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111916870 | |||||||
| chr9:111917095 | A | G | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.240+2349A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917095 | |||||||
| chr9:111917133 | A | G | 3 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0003g0179 |
3 | HG00738.hp1 HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.240+2387A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917133 | |||||||
| chr9:111917212 | C | T | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+2466C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917212 | |||||||
| chr9:111917213 | T | G | 339 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(336): Show |
378 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(375): Show |
intron_variant | MODIFIER | c.240+2467T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917213 | |||||||
| chr9:111917377 | C | T | 1 | a0001c0002t0002g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.240+2631C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917377 | |||||||
| chr9:111917449 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.240+2703C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917449 | |||||||
| chr9:111917532 | A | G | 3 | a0001c0002t0002g0125 a0001c0002t0002g0126 a0001c0002t0002g0127 |
3 | HG00639.hp1 HG01361.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.240+2786A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917532 | |||||||
| chr9:111917891 | T | G | 190 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(187): Show |
217 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(214): Show |
intron_variant | MODIFIER | c.240+3145T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917891 | |||||||
| chr9:111917925 | T | C | 1 | a0001c0001t0013g0028 | 2 | HG00323.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.240+3179T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917925 | |||||||
| chr9:111917972 | A | G | 1 | a0001c0001t0003g0180 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.240+3226A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111917972 | |||||||
| chr9:111918011 | A | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.240+3265A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918011 | |||||||
| chr9:111918041 | T | G | 1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.240+3295T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918041 | |||||||
| chr9:111918112 | G | A | 1 | a0001c0001t0004g0257 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.240+3366G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918112 | |||||||
| chr9:111918134 | C | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.240+3388C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918134 | |||||||
| chr9:111918167 | G | A | 121 | a0001c0001t0015g0092 a0001c0001t0026g0355 a0001c0001t0026g0356 others(118): Show |
136 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.240+3421G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918167 | |||||||
| chr9:111918700 | G | A | 111 | a0001c0001t0027g0001 a0001c0001t0027g0080 a0001c0001t0039g0030 others(108): Show |
124 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.240+3954G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918700 | |||||||
| chr9:111918705 | G | A | 182 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(179): Show |
206 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.240+3959G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918705 | |||||||
| chr9:111918748 | C | T | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.240+4002C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918748 | |||||||
| chr9:111918799 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.241-4050C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918799 | |||||||
| chr9:111918872 | C | T | 1 | a0001c0002t0002g0069 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.241-3977C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918872 | |||||||
| chr9:111918878 | T | A | 1 | a0001c0001t0031g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.241-3971T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918878 | |||||||
| chr9:111918903 | C | T | 58 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(55): Show |
67 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-3946C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918903 | |||||||
| chr9:111918912 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0210 |
2 | NA18971.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.241-3937G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918912 | |||||||
| chr9:111918924 | C | CA | 122 | a0001c0001t0001g0223 a0001c0001t0004g0278 a0001c0001t0026g0355 others(119): Show |
137 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(134): Show |
intron_variant | MODIFIER | c.241-3913dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111918924 | ||||||
| chr9:111918950 | A | C | 1 | a0001c0001t0005g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-3899A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918950 | |||||||
| chr9:111918952 | C | A | 1 | a0001c0001t0005g0284 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.241-3897C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918952 | |||||||
| chr9:111918952 | C | CA | 119 | a0001c0001t0007g0302 a0001c0001t0026g0355 a0001c0001t0026g0356 others(116): Show |
134 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.241-3888dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111918952 | ||||||
| chr9:111918952 | C | CAA | 62 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(59): Show |
71 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.241-3889_241-3888d others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111918952 | ||||||
| chr9:111918962 | C | A | 287 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(284): Show |
321 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.241-3887C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111918962 | |||||||
| chr9:111919022 | A | G | 75 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(72): Show |
82 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.241-3827A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919022 | |||||||
| chr9:111919122 | GT | G | 3 | a0001c0001t0003g0167 a0001c0001t0003g0168 a0001c0001t0003g0179 |
3 | HG00738.hp1 HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.241-3721delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111919122 | ||||||
| chr9:111919303 | C | A | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.241-3546C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919303 | |||||||
| chr9:111919347 | G | A | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.241-3502G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919347 | |||||||
| chr9:111919373 | C | T | 1 | a0001c0002t0002g0074 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.241-3476C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919373 | |||||||
| chr9:111919619 | G | A | 2 | a0001c0002t0002g0117 a0001c0002t0002g0118 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.241-3230G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919619 | |||||||
| chr9:111919687 | C | T | 1 | a0001c0001t0003g0178 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.241-3162C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919687 | |||||||
| chr9:111919711 | C | T | 58 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(55): Show |
67 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-3138C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919711 | |||||||
| chr9:111919714 | GA | G | 58 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(55): Show |
67 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.241-3133delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111919714 | ||||||
| chr9:111919751 | C | T | 1 | a0001c0002t0006g0008 | 3 | HG02145.hp2 HG02257.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.241-3098C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919751 | |||||||
| chr9:111919772 | G | T | 33 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(30): Show |
35 | HG00323.hp1 HG00323.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.241-3077G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919772 | |||||||
| chr9:111919794 | C | CA | 23 | a0001c0001t0001g0191 a0001c0001t0003g0180 a0001c0001t0024g0364 others(20): Show |
23 | HG00558.hp1 HG00642.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.241-3037dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111919794 | ||||||
| chr9:111919794 | C | CAA | 59 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(56): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.241-3038_241-3037d others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111919794 | ||||||
| chr9:111919794 | CA | C | 12 | a0001c0001t0005g0306 a0001c0001t0007g0315 a0001c0002t0002g0067 others(9): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.241-3037delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111919794 | ||||||
| chr9:111919799 | A | C | 6 | a0001c0001t0010g0029 a0001c0001t0010g0351 a0001c0001t0010g0352 others(3): Show |
7 | HG00323.hp1 HG00733.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.241-3050A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111919799 | |||||||
| chr9:111920057 | G | A | 182 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(179): Show |
206 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.241-2792G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920057 | |||||||
| chr9:111920254 | G | A | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.241-2595G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920254 | |||||||
| chr9:111920313 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.241-2536C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920313 | |||||||
| chr9:111920384 | G | A | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241-2465G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920384 | |||||||
| chr9:111920465 | A | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-2384A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920465 | |||||||
| chr9:111920603 | G | A | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.241-2246G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920603 | |||||||
| chr9:111920619 | C | T | 1 | a0001c0001t0026g0357 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.241-2230C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920619 | |||||||
| chr9:111920651 | A | C | 1 | a0001c0002t0002g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.241-2198A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920651 | |||||||
| chr9:111920696 | A | G | 3 | a0001c0001t0024g0364 a0001c0001t0024g0365 a0001c0001t0024g0366 |
3 | HG00642.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.241-2153A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920696 | |||||||
| chr9:111920810 | G | A | 1 | a0001c0001t0005g0294 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.241-2039G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920810 | |||||||
| chr9:111920813 | C | A | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.241-2036C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920813 | |||||||
| chr9:111920914 | T | TG | 64 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(61): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.241-1935_241-1934i others(3): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920914 | |||||||
| chr9:111920948 | G | T | 2 | a0001c0002t0002g0010 a0001c0002t0002g0082 |
3 | HG02965.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.241-1901G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111920948 | |||||||
| chr9:111921048 | G | A | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.241-1801G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921048 | |||||||
| chr9:111921347 | A | G | 1 | a0001c0001t0010g0359 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.241-1502A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921347 | |||||||
| chr9:111921369 | T | C | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1480T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921369 | |||||||
| chr9:111921429 | A | T | 1 | a0001c0001t0004g0258 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.241-1420A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921429 | |||||||
| chr9:111921458 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.241-1391C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921458 | |||||||
| chr9:111921490 | C | G | 64 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(61): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.241-1359C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921490 | |||||||
| chr9:111921622 | A | G | 184 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(181): Show |
208 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.241-1227A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921622 | |||||||
| chr9:111921648 | C | CA | 119 | a0001c0001t0019g0112 a0001c0001t0026g0355 a0001c0001t0026g0356 others(116): Show |
134 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.241-1186dupA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921648 | ||||||
| chr9:111921648 | C | CAA | 7 | a0001c0002t0002g0040 a0001c0002t0002g0075 a0001c0002t0002g0085 others(4): Show |
7 | HG01106.hp1 HG01261.hp2 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-1187_241-1186d others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921648 | ||||||
| chr9:111921664 | G | A | 209 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(206): Show |
236 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(233): Show |
intron_variant | MODIFIER | c.241-1185G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921664 | |||||||
| chr9:111921740 | A | AT | 21 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(18): Show |
24 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.241-1107dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921740 | ||||||
| chr9:111921802 | A | AT | 9 | a0001c0001t0003g0014 a0001c0001t0003g0163 a0001c0001t0003g0164 others(6): Show |
10 | HG01192.hp2 HG01255.hp1 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.241-1021dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATT | 27 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0346 others(24): Show |
31 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.241-1022_241-1021d others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTT | 59 | a0001c0001t0001g0239 a0001c0001t0001g0332 a0001c0001t0001g0333 others(56): Show |
71 | HG00099.hp2 HG00408.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.241-1023_241-1021d others(5): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTT | 29 | a0001c0001t0001g0328 a0001c0001t0001g0335 a0001c0001t0001g0339 others(26): Show |
29 | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(26): Show |
intron_variant | MODIFIER | c.241-1024_241-1021d others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTT | 6 | a0001c0001t0001g0336 a0001c0001t0018g0128 a0001c0001t0029g0111 others(3): Show |
6 | HG00738.hp2 HG01074.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-1025_241-1021d others(7): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT | 7 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0325 others(4): Show |
9 | HG00558.hp1 HG01261.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.241-1027_241-1021d others(9): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(1): Show |
16 | a0001c0002t0006g0323 a0001c0002t0006g0324 a0001c0002t0006g0326 others(13): Show |
16 | HG02486.hp2 HG02630.hp2 HG03209.hp2 others(13): Show |
intron_variant | MODIFIER | c.241-1028_241-1021d others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(2): Show |
14 | a0001c0001t0001g0015 a0001c0001t0001g0192 a0001c0001t0001g0203 others(11): Show |
15 | HG01361.hp1 HG02040.hp2 HG02071.hp1 others(12): Show |
intron_variant | MODIFIER | c.241-1029_241-1021d others(11): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(3): Show |
28 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0191 others(25): Show |
31 | HG00408.hp1 HG00558.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.241-1030_241-1021d others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(4): Show |
22 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
24 | HG00280.hp1 HG00280.hp2 HG00423.hp2 others(21): Show |
intron_variant | MODIFIER | c.241-1031_241-1021d others(13): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(5): Show |
12 | a0001c0001t0001g0017 a0001c0001t0001g0199 a0001c0001t0001g0218 others(9): Show |
13 | HG03831.hp1 NA18950.hp2 NA18966.hp2 others(10): Show |
intron_variant | MODIFIER | c.241-1032_241-1021d others(14): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(6): Show |
4 | a0001c0001t0001g0232 a0001c0001t0026g0356 a0001c0001t0026g0357 others(1): Show |
4 | HG02135.hp1 HG03490.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1033_241-1021d others(15): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(9): Show |
1 | a0001c0002t0002g0114 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.241-1036_241-1021d others(18): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(10): Show |
14 | a0001c0002t0002g0048 a0001c0002t0002g0073 a0001c0002t0002g0074 others(11): Show |
16 | HG00544.hp2 HG00621.hp1 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.241-1037_241-1021d others(19): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(11): Show |
21 | a0001c0001t0027g0001 a0001c0001t0027g0080 a0001c0002t0002g0001 others(18): Show |
28 | HG00423.hp1 HG00597.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.241-1038_241-1021d others(20): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(12): Show |
13 | a0001c0002t0002g0009 a0001c0002t0002g0031 a0001c0002t0002g0034 others(10): Show |
14 | HG01175.hp1 HG01952.hp2 HG02004.hp2 others(11): Show |
intron_variant | MODIFIER | c.241-1039_241-1021d others(21): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(13): Show |
4 | a0001c0002t0002g0056 a0001c0002t0002g0086 a0001c0002t0021g0264 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1040_241-1021d others(22): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(14): Show |
4 | a0001c0002t0002g0010 a0001c0002t0002g0077 a0001c0002t0002g0119 others(1): Show |
5 | HG02155.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-1041_241-1021d others(23): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(15): Show |
5 | a0001c0002t0002g0038 a0001c0002t0002g0082 a0001c0002t0002g0117 others(2): Show |
5 | HG01517.hp1 HG02602.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.241-1042_241-1021d others(24): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(16): Show |
4 | a0001c0002t0002g0066 a0001c0002t0002g0118 a0001c0002t0002g0120 others(1): Show |
4 | HG01258.hp2 HG01516.hp2 HG02056.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1043_241-1021d others(25): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(17): Show |
4 | a0001c0002t0002g0059 a0001c0002t0002g0123 a0001c0002t0002g0126 others(1): Show |
4 | HG00140.hp2 HG01978.hp2 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.241-1044_241-1021d others(26): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(18): Show |
3 | a0001c0002t0002g0060 a0001c0002t0002g0061 a0001c0002t0021g0263 |
3 | HG01358.hp1 HG02083.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.241-1045_241-1021d others(27): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(19): Show |
3 | a0001c0002t0002g0040 a0001c0002t0002g0062 a0001c0002t0002g0063 |
3 | HG02132.hp2 NA18951.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.241-1046_241-1021d others(28): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(20): Show |
1 | a0001c0002t0002g0064 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.241-1021_241-1020i others(29): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(21): Show |
2 | a0001c0002t0012g0096 a0001c0002t0022g0100 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.241-1021_241-1020i others(30): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(22): Show |
1 | a0001c0002t0012g0101 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.241-1021_241-1020i others(31): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(23): Show |
1 | a0002c0005t0014g0065 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.241-1021_241-1020i others(32): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(24): Show |
1 | a0001c0002t0022g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.241-1021_241-1020i others(33): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(27): Show |
1 | a0001c0002t0012g0103 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.241-1021_241-1020i others(36): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(28): Show |
1 | a0001c0002t0009g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.241-1021_241-1020i others(37): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | A | ATTTTTTT others(29): Show |
1 | a0001c0002t0012g0104 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.241-1021_241-1020i others(38): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | ATTTT | A | 5 | a0001c0001t0013g0028 a0001c0001t0013g0341 a0001c0001t0013g0343 others(2): Show |
6 | HG00323.hp2 HG01167.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.241-1024_241-1021d others(6): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921802 | ATTTTTTT others(2): Show |
A | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG00642.hp2 HG01884.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.241-1029_241-1021d others(11): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr9 | 111921802 | ||||||
| chr9:111921848 | T | C | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.241-1001T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921848 | |||||||
| chr9:111921914 | C | A | 1 | a0001c0002t0002g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.241-935C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111921914 | |||||||
| chr9:111922010 | G | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(18): Show |
24 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.241-839G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922010 | |||||||
| chr9:111922280 | T | C | 64 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(61): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.241-569T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922280 | |||||||
| chr9:111922429 | A | G | 103 | a0001c0001t0027g0001 a0001c0001t0027g0080 a0001c0002t0002g0001 others(100): Show |
114 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.241-420A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922429 | |||||||
| chr9:111922444 | A | T | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241-405A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922444 | |||||||
| chr9:111922694 | A | G | 1 | a0001c0001t0005g0285 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.241-155A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922694 | |||||||
| chr9:111922725 | C | G | 60 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(57): Show |
69 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.241-124C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 2/8 | chr9 | 111922725 | |||||||
| chr9:111922960 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.343+9C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111922960 | |||||||
| chr9:111923080 | T | C | 1 | a0001c0002t0002g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.343+129T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923080 | |||||||
| chr9:111923145 | A | G | 1 | a0001c0001t0041g0160 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.343+194A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923145 | |||||||
| chr9:111923361 | G | A | 64 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(61): Show |
73 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.343+410G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923361 | |||||||
| chr9:111923363 | GT | G | 115 | a0001c0001t0003g0150 a0001c0001t0027g0001 a0001c0001t0027g0080 others(112): Show |
130 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.343+425delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 111923363 | ||||||
| chr9:111923363 | GTT | G | 67 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(64): Show |
76 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.343+424_343+425del others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 111923363 | ||||||
| chr9:111923409 | C | A | 374 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(371): Show |
421 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(418): Show |
intron_variant | MODIFIER | c.343+458C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923409 | |||||||
| chr9:111923413 | A | G | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.343+462A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923413 | |||||||
| chr9:111923556 | G | A | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.343+605G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923556 | |||||||
| chr9:111923562 | G | T | 1 | a0001c0001t0001g0328 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.343+611G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923562 | |||||||
| chr9:111923625 | G | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0002t0012g0097 others(1): Show |
4 | HG02109.hp2 HG02572.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.343+674G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923625 | |||||||
| chr9:111923946 | C | T | 1 | a0001c0001t0026g0357 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.344-831C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111923946 | |||||||
| chr9:111924068 | G | C | 1 | a0001c0001t0050g0240 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.344-709G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924068 | |||||||
| chr9:111924130 | T | C | 340 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
379 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.344-647T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924130 | |||||||
| chr9:111924148 | A | G | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.344-629A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924148 | |||||||
| chr9:111924177 | C | T | 2 | a0001c0001t0029g0110 a0001c0001t0029g0111 |
2 | HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.344-600C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924177 | |||||||
| chr9:111924237 | T | A | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.344-540T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924237 | |||||||
| chr9:111924325 | A | G | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.344-452A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924325 | |||||||
| chr9:111924480 | G | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.344-297G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924480 | |||||||
| chr9:111924483 | A | G | 1 | a0001c0002t0009g0091 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.344-294A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924483 | |||||||
| chr9:111924649 | TTAAA | T | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.344-124_344-121del others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr9 | 111924649 | ||||||
| chr9:111924666 | A | G | 6 | a0001c0002t0009g0089 a0001c0002t0009g0090 a0001c0002t0009g0091 others(3): Show |
6 | HG00544.hp2 HG00621.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.344-111A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924666 | |||||||
| chr9:111924719 | C | T | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.344-58C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 3/8 | chr9 | 111924719 | |||||||
| chr9:111924884 | G | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
splice_region_variant&intron_variant | LOW | c.445+6G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111924884 | |||||||
| chr9:111925053 | C | A | 1 | a0001c0001t0003g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.445+175C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925053 | |||||||
| chr9:111925178 | C | G | 1 | a0001c0001t0019g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.445+300C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925178 | |||||||
| chr9:111925189 | G | T | 2 | a0001c0001t0016g0189 a0001c0001t0054g0190 |
2 | HG00673.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.445+311G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925189 | |||||||
| chr9:111925415 | T | C | 3 | a0001c0002t0002g0031 a0001c0002t0002g0049 a0001c0002t0002g0067 |
3 | NA18945.hp2 NA18991.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.445+537T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925415 | |||||||
| chr9:111925559 | T | C | 1 | a0001c0001t0019g0174 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.445+681T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925559 | |||||||
| chr9:111925661 | C | T | 10 | a0001c0002t0012g0095 a0001c0002t0012g0096 a0001c0002t0012g0097 others(7): Show |
10 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.446-723C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925661 | |||||||
| chr9:111925823 | A | G | 340 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
379 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.446-561A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925823 | |||||||
| chr9:111925923 | C | T | 1 | a0001c0001t0019g0112 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.446-461C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111925923 | |||||||
| chr9:111926152 | T | C | 3 | a0001c0002t0002g0052 a0001c0002t0021g0264 a0001c0002t0021g0265 |
3 | HG01167.hp1 HG01169.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.446-232T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926152 | |||||||
| chr9:111926208 | T | C | 1 | a0001c0001t0003g0152 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.446-176T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926208 | |||||||
| chr9:111926267 | T | C | 11 | a0001c0001t0005g0005 a0001c0001t0005g0023 a0001c0001t0005g0289 others(8): Show |
13 | HG01081.hp1 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.446-117T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926267 | |||||||
| chr9:111926285 | A | C | 3 | a0001c0002t0006g0008 a0001c0002t0006g0362 a0001c0002t0006g0363 |
5 | HG02145.hp2 HG02257.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.446-99A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926285 | |||||||
| chr9:111926315 | T | C | 19 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(16): Show |
22 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.446-69T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926315 | |||||||
| chr9:111926381 | T | C | 2 | a0001c0001t0004g0258 a0001c0001t0004g0275 |
2 | NA18970.hp1 NA19060.hp1 |
splice_region_variant&intron_variant | LOW | c.446-3T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 4/8 | chr9 | 111926381 | |||||||
| chr9:111926527 | A | G | 26 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(23): Show |
28 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.558+31A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111926527 | |||||||
| chr9:111926633 | GC | G | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+140delC | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926633 | ||||||
| chr9:111926713 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0015g0092 |
2 | HG02155.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.558+217C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111926713 | |||||||
| chr9:111926861 | C | CT | 32 | a0001c0001t0001g0194 a0001c0001t0003g0146 a0001c0001t0003g0152 others(29): Show |
34 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.558+394dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | C | CTT | 8 | a0001c0001t0001g0191 a0001c0001t0007g0024 a0001c0001t0007g0311 others(5): Show |
9 | HG01109.hp2 HG03490.hp2 HG03492.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+393_558+394dup others(2): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | C | CTTT | 13 | a0001c0001t0001g0021 a0001c0001t0007g0025 a0001c0001t0007g0301 others(10): Show |
15 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.558+392_558+394dup others(3): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | C | CTTTT | 9 | a0001c0001t0001g0236 a0001c0001t0001g0239 a0001c0001t0007g0302 others(6): Show |
9 | HG00438.hp1 HG02300.hp1 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+391_558+394dup others(4): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0026g0356 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.558+385_558+394dup others(10): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | CT | C | 152 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(149): Show |
173 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(170): Show |
intron_variant | MODIFIER | c.558+394delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | CTTTTTTT others(5): Show |
C | 4 | a0001c0001t0004g0257 a0001c0001t0004g0269 a0001c0001t0005g0290 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 NA18940.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+383_558+394del others(12): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | CTTTTTTT others(6): Show |
C | 54 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0258 others(51): Show |
63 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.558+382_558+394del others(13): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0004g0273 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.558+381_558+394del others(14): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926861 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0317 a0001c0001t0001g0318 |
2 | NA18950.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.558+380_558+394del others(15): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111926861 | ||||||
| chr9:111926916 | A | G | 1 | a0001c0003t0008g0142 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.558+420A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111926916 | |||||||
| chr9:111927127 | T | A | 1 | a0001c0001t0011g0116 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.558+631T>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927127 | |||||||
| chr9:111927147 | G | A | 1 | a0001c0001t0003g0177 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.558+651G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927147 | |||||||
| chr9:111927163 | G | A | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+667G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927163 | |||||||
| chr9:111927194 | C | T | 184 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(181): Show |
208 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.558+698C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927194 | |||||||
| chr9:111927438 | G | T | 1 | a0001c0001t0031g0084 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.558+942G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927438 | |||||||
| chr9:111927491 | G | C | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+995G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927491 | |||||||
| chr9:111927494 | C | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+998C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927494 | |||||||
| chr9:111927515 | G | A | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1019G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927515 | |||||||
| chr9:111927537 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1041C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927537 | |||||||
| chr9:111927544 | C | T | 7 | a0001c0001t0024g0364 a0001c0001t0024g0365 a0001c0001t0024g0366 others(4): Show |
7 | HG00642.hp2 HG01106.hp2 HG01168.hp1 others(4): Show |
intron_variant | MODIFIER | c.558+1048C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927544 | |||||||
| chr9:111927601 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.558+1105G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927601 | |||||||
| chr9:111927672 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.558+1176C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927672 | |||||||
| chr9:111927702 | C | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(6): Show |
10 | HG00323.hp2 HG00642.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.558+1206C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927702 | |||||||
| chr9:111927703 | T | G | 340 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
379 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.558+1207T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927703 | |||||||
| chr9:111927730 | C | T | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.558+1234C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927730 | |||||||
| chr9:111927747 | G | T | 1 | a0001c0006t0005g0287 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.558+1251G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927747 | |||||||
| chr9:111927973 | G | A | 74 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(71): Show |
81 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.558+1477G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111927973 | |||||||
| chr9:111928034 | AATGTT | A | 24 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(21): Show |
26 | HG00323.hp1 HG00323.hp2 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.559-1463_559-1459d others(7): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111928034 | ||||||
| chr9:111928079 | A | C | 2 | a0001c0001t0004g0022 a0001c0001t0004g0276 |
3 | HG02040.hp1 HG02074.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.559-1421A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928079 | |||||||
| chr9:111928133 | T | C | 103 | a0001c0001t0027g0001 a0001c0001t0027g0080 a0001c0002t0002g0001 others(100): Show |
114 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.559-1367T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928133 | |||||||
| chr9:111928221 | G | C | 340 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(337): Show |
379 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.559-1279G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928221 | |||||||
| chr9:111928355 | T | C | 1 | a0001c0001t0003g0153 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.559-1145T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928355 | |||||||
| chr9:111928419 | C | T | 1 | a0001c0001t0005g0283 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.559-1081C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928419 | |||||||
| chr9:111928443 | AGTGTAG | A | 7 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0062 others(4): Show |
7 | HG02132.hp2 HG02273.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.559-1054_559-1049d others(8): Show |
UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111928443 | ||||||
| chr9:111928463 | A | G | 1 | a0001c0001t0004g0277 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.559-1037A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928463 | |||||||
| chr9:111928485 | A | G | 120 | a0001c0001t0026g0355 a0001c0001t0026g0356 a0001c0001t0026g0357 others(117): Show |
135 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.559-1015A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928485 | |||||||
| chr9:111928622 | T | C | 1 | a0001c0001t0005g0292 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.559-878T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928622 | |||||||
| chr9:111928625 | G | A | 1 | a0001c0001t0026g0355 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.559-875G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928625 | |||||||
| chr9:111928699 | C | G | 11 | a0001c0002t0002g0083 a0001c0002t0012g0095 a0001c0002t0012g0096 others(8): Show |
11 | HG02258.hp2 HG02451.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.559-801C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928699 | |||||||
| chr9:111928752 | A | G | 3 | a0001c0002t0002g0042 a0001c0002t0002g0044 a0001c0002t0021g0263 |
3 | NA18981.hp2 NA19063.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.559-748A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928752 | |||||||
| chr9:111928850 | C | T | 15 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(12): Show |
15 | HG00558.hp1 HG04115.hp2 NA18943.hp2 others(12): Show |
intron_variant | MODIFIER | c.559-650C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928850 | |||||||
| chr9:111928897 | C | G | 344 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(341): Show |
383 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(380): Show |
intron_variant | MODIFIER | c.559-603C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928897 | |||||||
| chr9:111928918 | C | T | 1 | a0001c0001t0003g0153 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.559-582C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928918 | |||||||
| chr9:111928996 | C | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.559-504C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111928996 | |||||||
| chr9:111929049 | A | AC | 91 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0020 others(88): Show |
99 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.559-445dupC | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr9 | 111929049 | ||||||
| chr9:111929056 | A | C | 2 | a0001c0002t0002g0123 a0001c0002t0006g0323 |
2 | HG01978.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.559-444A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111929056 | |||||||
| chr9:111929200 | T | C | 1 | a0001c0002t0035g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.559-300T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111929200 | |||||||
| chr9:111929219 | A | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-281A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111929219 | |||||||
| chr9:111929390 | A | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.559-110A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111929390 | |||||||
| chr9:111929391 | G | T | 2 | a0001c0001t0003g0182 a0001c0001t0003g0183 |
2 | HG00735.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.559-109G>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 5/8 | chr9 | 111929391 | |||||||
| chr9:111929872 | G | A | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+194G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111929872 | |||||||
| chr9:111929883 | A | T | 1 | a0001c0001t0015g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.737+205A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111929883 | |||||||
| chr9:111929909 | C | T | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.737+231C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111929909 | |||||||
| chr9:111929949 | C | T | 2 | a0001c0001t0001g0227 a0001c0001t0001g0229 |
2 | HG00280.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.737+271C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111929949 | |||||||
| chr9:111929980 | A | G | 3 | a0001c0001t0011g0013 a0001c0001t0028g0143 a0001c0001t0028g0172 |
4 | NA18952.hp1 NA19083.hp1 NA19090.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+302A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111929980 | |||||||
| chr9:111930001 | A | G | 1 | a0001c0003t0046g0344 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.737+323A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930001 | |||||||
| chr9:111930016 | T | C | 1 | a0001c0001t0005g0023 | 2 | HG01081.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.737+338T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930016 | |||||||
| chr9:111930097 | T | C | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.737+419T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930097 | |||||||
| chr9:111930129 | T | C | 1 | a0001c0001t0005g0283 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.737+451T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930129 | |||||||
| chr9:111930132 | T | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+454T>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930132 | |||||||
| chr9:111930220 | A | T | 4 | a0001c0001t0007g0302 a0001c0001t0007g0303 a0001c0001t0007g0304 others(1): Show |
4 | NA19000.hp1 NA19003.hp2 NA19063.hp2 others(1): Show |
intron_variant | MODIFIER | c.737+542A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930220 | |||||||
| chr9:111930321 | G | A | 2 | a0001c0001t0025g0367 a0001c0001t0025g0368 |
2 | HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.737+643G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930321 | |||||||
| chr9:111930351 | C | G | 21 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(18): Show |
24 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.737+673C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930351 | |||||||
| chr9:111930423 | A | G | 1 | a0001c0002t0049g0358 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.737+745A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930423 | |||||||
| chr9:111930470 | G | GT | 13 | a0001c0001t0001g0334 a0001c0001t0001g0339 a0001c0001t0003g0150 others(10): Show |
13 | HG01069.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.738-784dupT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 111930470 | ||||||
| chr9:111930470 | GT | G | 213 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0016 others(210): Show |
238 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.738-784delT | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr9 | 111930470 | ||||||
| chr9:111930532 | A | G | 18 | a0001c0003t0008g0129 a0001c0003t0008g0130 a0001c0003t0008g0131 others(15): Show |
18 | HG00558.hp1 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.738-739A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930532 | |||||||
| chr9:111930711 | G | A | 59 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(56): Show |
68 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.738-560G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930711 | |||||||
| chr9:111930715 | G | A | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.738-556G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930715 | |||||||
| chr9:111930760 | A | G | 1 | a0001c0001t0003g0150 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.738-511A>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930760 | |||||||
| chr9:111930788 | G | A | 1 | a0001c0001t0003g0163 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.738-483G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111930788 | |||||||
| chr9:111931083 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.738-188C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111931083 | |||||||
| chr9:111931170 | C | A | 4 | a0001c0001t0003g0154 a0001c0001t0003g0157 a0001c0001t0003g0163 others(1): Show |
4 | HG01123.hp1 HG02738.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.738-101C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111931170 | |||||||
| chr9:111931211 | C | G | 1 | a0001c0001t0013g0343 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.738-60C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111931211 | |||||||
| chr9:111931218 | C | T | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.738-53C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 6/8 | chr9 | 111931218 | |||||||
| chr9:111931387 | G | A | 2 | a0001c0001t0018g0035 a0001c0001t0018g0036 |
2 | NA18985.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.824+30G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111931387 | |||||||
| chr9:111931405 | A | AG | 11 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0003g0177 others(8): Show |
11 | HG01109.hp1 HG01175.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.824+54dupG | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 111931405 | ||||||
| chr9:111931798 | G | A | 1 | a0001c0002t0021g0262 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.825-372G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111931798 | |||||||
| chr9:111931883 | C | T | 7 | a0001c0001t0011g0011 a0001c0001t0011g0012 a0001c0001t0011g0013 others(4): Show |
10 | HG00609.hp2 HG00673.hp2 HG03239.hp2 others(7): Show |
intron_variant | MODIFIER | c.825-287C>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111931883 | |||||||
| chr9:111931903 | C | A | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.825-267C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111931903 | |||||||
| chr9:111931934 | T | C | 8 | a0001c0002t0006g0026 a0001c0002t0006g0027 a0001c0002t0006g0323 others(5): Show |
10 | HG01261.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.825-236T>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111931934 | |||||||
| chr9:111932023 | TA | T | 181 | a0001c0001t0001g0191 a0001c0001t0004g0003 a0001c0001t0004g0022 others(178): Show |
205 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(202): Show |
intron_variant | MODIFIER | c.825-134delA | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr9 | 111932023 | ||||||
| chr9:111932032 | A | C | 182 | a0001c0001t0001g0191 a0001c0001t0003g0177 a0001c0001t0004g0003 others(179): Show |
206 | HG00099.hp2 HG00140.hp2 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.825-138A>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111932032 | |||||||
| chr9:111932037 | C | A | 21 | a0001c0001t0001g0328 a0001c0001t0001g0332 a0001c0001t0001g0333 others(18): Show |
22 | HG00323.hp2 HG01167.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.825-133C>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 7/8 | chr9 | 111932037 | |||||||
| chr9:111932562 | G | A | 16 | a0001c0001t0053g0211 a0001c0003t0008g0129 a0001c0003t0008g0130 others(13): Show |
16 | HG00558.hp1 HG04115.hp2 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.1014+203G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932562 | |||||||
| chr9:111932577 | C | G | 1 | a0001c0002t0006g0238 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1014+218C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932577 | |||||||
| chr9:111932578 | C | G | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1014+219C>G | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932578 | |||||||
| chr9:111932612 | G | C | 4 | a0001c0004t0020g0319 a0001c0004t0020g0320 a0001c0004t0020g0321 others(1): Show |
4 | HG01106.hp2 HG01168.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.1015-215G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932612 | |||||||
| chr9:111932631 | G | C | 16 | a0001c0001t0053g0211 a0001c0003t0008g0129 a0001c0003t0008g0130 others(13): Show |
16 | HG00558.hp1 HG04115.hp2 NA18941.hp1 others(13): Show |
intron_variant | MODIFIER | c.1015-196G>C | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932631 | |||||||
| chr9:111932711 | G | A | 31 | a0001c0001t0004g0003 a0001c0001t0004g0022 a0001c0001t0004g0257 others(28): Show |
38 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(35): Show |
intron_variant | MODIFIER | c.1015-116G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932711 | |||||||
| chr9:111932727 | A | T | 21 | a0001c0001t0001g0021 a0001c0001t0001g0236 a0001c0001t0001g0239 others(18): Show |
24 | HG00438.hp1 HG02080.hp2 HG02135.hp2 others(21): Show |
intron_variant | MODIFIER | c.1015-100A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932727 | |||||||
| chr9:111932746 | G | A | 2 | a0001c0001t0043g0149 a0001c0001t0060g0286 |
2 | HG01192.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1015-81G>A | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932746 | |||||||
| chr9:111932807 | A | T | 5 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(2): Show |
5 | HG01884.hp2 HG02109.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1015-20A>T | UGCG | ENSG00000148154.10 | transcript | ENST00000374279.4 | protein_coding | 8/8 | chr9 | 111932807 |