Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285051 |
| ensemblid | ENSG00000239605.11 |
| hgncid | 26850 |
| symbol | STPG4 |
| name | sperm-tail PG-rich repeat containing 4 |
| refseq_nuc | NM_001163561.2 |
| refseq_prot | NP_001157033.1 |
| ensembl_nuc | ENST00000445927.7 |
| ensembl_prot | ENSP00000408527.2 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 47086991 |
| end | 47155308 |
| strand | - |
| ver | v1.2 |
| region | chr2:47086991-47155308 |
| region5000 | chr2:47081991-47160308 |
| regionname0 | STPG4_chr2_47086991_47155308 |
| regionname5000 | STPG4_chr2_47081991_47160308 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 248 | 235 | 54 | 35 | 109 | 10 | 25 | 85 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0002 | 0/0 | 248 | 51 | 20 | 13 | 7 | 2 | 9 | 4 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0003 | 0/0 | 248 | 46 | 11 | 6 | 23 | 1 | 5 | 18 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0004 | 0/0 | 36 | 11 | 1 | 5 | 5 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(31): Show |
chr2 | 47081991 | 47160308 |
| a0005 | 0/0 | 248 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0006 | 0/0 | 248 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0007 | 0/0 | 248 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0008 | 0/0 | 248 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0009 | 0/0 | 248 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| a0010 | 0/0 | 248 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | MDQPA others(243): Show |
chr2 | 47081991 | 47160308 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 744 | 233 | 53 | 35 | 109 | 10 | 24 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0001c0012 | 0/0 | 744 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0001c0015 | 0/0 | 744 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0002c0002 | 0/0 | 744 | 51 | 20 | 13 | 7 | 2 | 9 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0003c0003 | 0/0 | 744 | 45 | 10 | 6 | 23 | 1 | 5 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0003c0011 | 0/0 | 744 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0004c0004 | 0/0 | 745 | 8 | 0 | 4 | 4 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(740): Show |
chr2 | 47081991 | 47160308 | ||
| a0004c0005 | 0/0 | 745 | 2 | 0 | 1 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(740): Show |
chr2 | 47081991 | 47160308 | ||
| a0004c0009 | 0/0 | 745 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(740): Show |
chr2 | 47081991 | 47160308 | ||
| a0005c0008 | 0/0 | 744 | 2 | 1 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0006c0006 | 0/0 | 744 | 2 | 0 | 2 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0007c0007 | 0/0 | 744 | 2 | 2 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0008c0013 | 0/0 | 744 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0009c0014 | 0/0 | 744 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 | ||
| a0010c0010 | 0/0 | 744 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | ATGGA others(739): Show |
chr2 | 47081991 | 47160308 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 821 | 230 | 50 | 35 | 109 | 10 | 24 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0001c0001t0002 | 0/0 | 821 | 3 | 3 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0001c0012t0001 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0001c0015t0001 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0002c0002t0001 | 0/0 | 821 | 51 | 20 | 13 | 7 | 2 | 9 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0003c0003t0001 | 0/0 | 821 | 45 | 10 | 6 | 23 | 1 | 5 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0003c0011t0001 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0004c0004t0001 | 0/0 | 822 | 8 | 0 | 4 | 4 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(817): Show |
chr2 | 47081991 | 47160308 |
| a0004c0005t0001 | 0/0 | 822 | 2 | 0 | 1 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(817): Show |
chr2 | 47081991 | 47160308 |
| a0004c0009t0001 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(817): Show |
chr2 | 47081991 | 47160308 |
| a0005c0008t0001 | 0/0 | 821 | 2 | 1 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0006c0006t0001 | 0/0 | 821 | 2 | 0 | 2 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0007c0007t0001 | 0/0 | 821 | 2 | 2 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0008c0013t0001 | 0/0 | 821 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0009c0014t0001 | 0/0 | 821 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| a0010c0010t0001 | 0/0 | 821 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | ACACC others(816): Show |
chr2 | 47081991 | 47160308 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0343 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0012t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0001c0015t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0002c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0003c0011t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0004t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0005t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0005t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0004c0009t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0005c0008t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0005c0008t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0006c0006t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0006c0006t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0007c0007t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0007c0007t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0008c0013t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0009c0014t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| a0010c0010t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | GBR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0242 | EUR | GBR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0283 | EUR | GBR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0036 | EUR | FIN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0055 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00438 | hp1 | a0003 | c0003 | t0001 | g0061 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0049 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0300 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0285 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0050 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00673 | hp2 | a0004 | c0004 | t0001 | g0012 | EAS | CHS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00735 | hp1 | a0004 | c0004 | t0001 | g0010 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00738 | hp2 | a0005 | c0008 | t0001 | g0345 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0038 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0334 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0289 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01099 | hp1 | a0002 | c0002 | t0001 | g0281 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0272 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01109 | hp2 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01175 | hp1 | a0004 | c0004 | t0001 | g0008 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0280 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01255 | hp2 | a0004 | c0004 | t0001 | g0016 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01256 | hp2 | a0003 | c0003 | t0001 | g0030 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01257 | hp2 | a0006 | c0006 | t0001 | g0130 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01258 | hp1 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01258 | hp2 | a0006 | c0006 | t0001 | g0129 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0060 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01261 | hp2 | a0003 | c0003 | t0001 | g0062 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0279 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0344 | EUR | IBS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01515 | hp2 | a0008 | c0013 | t0001 | g0174 | EUR | IBS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | IBS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0194 | EUR | IBS | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0019 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0333 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01891 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01943 | hp2 | a0004 | c0005 | t0001 | g0013 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0305 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0282 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0306 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02027 | hp2 | a0004 | c0004 | t0001 | g0011 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02080 | hp1 | a0004 | c0004 | t0001 | g0009 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02080 | hp2 | a0004 | c0005 | t0001 | g0014 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0302 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02145 | hp1 | a0005 | c0008 | t0001 | g0346 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | CDX | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CDX | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0336 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0311 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0037 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0312 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02300 | hp1 | a0003 | c0003 | t0001 | g0059 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0331 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0335 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02630 | hp1 | a0009 | c0014 | t0001 | g0107 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0325 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0292 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0330 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02738 | hp2 | a0010 | c0010 | t0001 | g0028 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0284 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02896 | hp1 | a0002 | c0002 | t0001 | g0278 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02896 | hp2 | a0003 | c0003 | t0001 | g0027 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0277 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02965 | hp1 | a0003 | c0003 | t0001 | g0039 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02970 | hp1 | a0007 | c0007 | t0001 | g0338 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0310 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0291 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0301 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03017 | hp2 | a0003 | c0003 | t0001 | g0032 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0332 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0337 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03139 | hp2 | a0004 | c0009 | t0001 | g0006 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0329 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03490 | hp1 | a0003 | c0003 | t0001 | g0031 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0307 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0299 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | ESN | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0316 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0293 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03669 | hp2 | a0003 | c0003 | t0001 | g0033 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0308 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0309 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0034 | SAS | BEB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0287 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04204 | hp1 | a0003 | c0003 | t0001 | g0035 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18522 | hp1 | a0007 | c0007 | t0001 | g0339 | AFR | YRI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18522 | hp2 | a0003 | c0011 | t0001 | g0018 | AFR | YRI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18612 | hp1 | a0003 | c0003 | t0001 | g0052 | EAS | CHB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | CHB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18940 | hp2 | a0003 | c0003 | t0001 | g0045 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18942 | hp2 | a0003 | c0003 | t0001 | g0040 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18944 | hp1 | a0003 | c0003 | t0001 | g0047 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18948 | hp2 | a0003 | c0003 | t0001 | g0053 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18954 | hp2 | a0003 | c0003 | t0001 | g0043 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18957 | hp2 | a0003 | c0003 | t0001 | g0058 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18962 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0297 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18987 | hp2 | a0003 | c0003 | t0001 | g0057 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0044 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18997 | hp2 | a0003 | c0003 | t0001 | g0054 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18998 | hp2 | a0002 | c0002 | t0001 | g0295 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19005 | hp1 | a0003 | c0003 | t0001 | g0051 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0025 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0056 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0296 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19056 | hp1 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19066 | hp1 | a0003 | c0003 | t0001 | g0048 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19083 | hp1 | a0004 | c0004 | t0001 | g0015 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19084 | hp2 | a0003 | c0003 | t0001 | g0063 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19085 | hp1 | a0003 | c0003 | t0001 | g0046 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | YRI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20129 | hp1 | a0003 | c0003 | t0001 | g0020 | AFR | ASW | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0313 | AFR | ASW | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0286 | EUR | TSI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0243 | EUR | TSI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0256 | EUR | TSI | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20905 | hp1 | a0001 | c0015 | t0001 | g0164 | SAS | GIH | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0288 | SAS | GIH | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0290 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02559 | hp1 | a0002 | c0002 | t0001 | g0273 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03471 | hp1 | a0001 | c0012 | t0001 | g0122 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG06807 | hp1 | a0003 | c0003 | t0001 | g0017 | AFR | USA | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0021 | AFR | USA | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | USA | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | USA | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| NA21309 | hp2 | a0003 | c0003 | t0001 | g0022 | AFR | LWK | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0343 | REF | REF | STPG4_chr2_47081991_47160308 | STPG4 | chr2 | 47081991 | 47160308 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47087059 | C | A | 1 | a0008 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.696G>T | p.Met232Ile | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 7/7 | 753/821 | 696/747 | 232/248 | chr2 | 47087059 | |||
| chr2:47090313 | G | C | 1 | a0009 | 1 | HG02630.hp1 | missense_variant | MODERATE | c.581C>G | p.Ser194Cys | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/7 | 638/821 | 581/747 | 194/248 | chr2 | 47090313 | |||
| chr2:47151306 | G | C | 1 | a0007 | 2 | HG02970.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.351C>G | p.Phe117Leu | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/7 | 408/821 | 351/747 | 117/248 | chr2 | 47151306 | |||
| chr2:47151425 | C | T | 1 | a0010 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.232G>A | p.Glu78Lys | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/7 | 289/821 | 232/747 | 78/248 | chr2 | 47151425 | |||
| chr2:47151472 | T | C | 1 | a0006 | 2 | HG01257.hp2 HG01258.hp2 |
missense_variant | MODERATE | c.185A>G | p.Glu62Gly | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/7 | 242/821 | 185/747 | 62/248 | chr2 | 47151472 | |||
| chr2:47153006 | T | C | 3 | a0002 a0004 a0007 |
55 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
missense_variant | MODERATE | c.92A>G | p.Gln31Arg | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/7 | 149/821 | 92/747 | 31/248 | chr2 | 47153006 | |||
| chr2:47155203 | G | T | 3 | a0003 a0004 a0010 |
48 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(45): Show |
missense_variant | MODERATE | c.49C>A | p.Leu17Met | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/7 | 106/821 | 49/747 | 17/248 | chr2 | 47155203 | |||
| chr2:47155204 | G | C | 1 | a0005 | 2 | HG00738.hp2 HG02145.hp1 |
missense_variant | MODERATE | c.48C>G | p.Asp16Glu | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/7 | 105/821 | 48/747 | 16/248 | chr2 | 47155204 | |||
| chr2:47155227 | C | CG | 1 | a0004 | 11 | HG00673.hp2 HG00735.hp1 HG01109.hp2 others(8): Show |
frameshift_variant | HIGH | c.24dupC | p.Ala9fs | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/7 | 81/821 | 24/747 | 8/248 | chr2 | 47155227 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47090273 | A | G | 2 | a0001c0012 a0003c0011 |
2 | HG03471.hp1 NA18522.hp2 |
synonymous_variant | LOW | c.621T>C | p.Cys207Cys | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/7 | 678/821 | 621/747 | 207/248 | chr2 | 47090273 | |||
| chr2:47130210 | G | A | 1 | a0001c0015 | 1 | NA20905.hp1 | synonymous_variant | LOW | c.450C>T | p.Pro150Pro | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 4/7 | 507/821 | 450/747 | 150/248 | chr2 | 47130210 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47155275 | T | C | 1 | a0001c0001t0002 | 3 | HG02109.hp1 HG02922.hp1 NA19240.hp1 |
5_prime_UTR_variant | MODIFIER | c.-24A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/7 | 24 | chr2 | 47155275 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:47087161 | G | C | 1 | a0001c0001t0001g0120 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.625-31C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087161 | |||||||
| chr2:47087237 | T | A | 2 | a0001c0001t0001g0320 a0002c0002t0001g0313 |
2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.625-107A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087237 | |||||||
| chr2:47087283 | C | T | 1 | a0002c0002t0001g0284 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.625-153G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087283 | |||||||
| chr2:47087312 | C | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0067 others(130): Show |
135 | HG00140.hp1 HG00323.hp1 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.625-182G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087312 | |||||||
| chr2:47087317 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.625-187G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087317 | |||||||
| chr2:47087321 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.625-191A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087321 | |||||||
| chr2:47087353 | A | G | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.625-223T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087353 | |||||||
| chr2:47087401 | G | A | 1 | a0001c0001t0001g0001 | 2 | NA18941.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.625-271C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087401 | |||||||
| chr2:47087472 | C | T | 57 | a0001c0001t0001g0003 a0001c0001t0001g0075 a0001c0001t0001g0081 others(54): Show |
58 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.625-342G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087472 | |||||||
| chr2:47087499 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0067 others(128): Show |
133 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(130): Show |
intron_variant | MODIFIER | c.625-369C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087499 | |||||||
| chr2:47087574 | C | T | 19 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0090 others(16): Show |
19 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.625-444G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087574 | |||||||
| chr2:47087587 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.625-457G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087587 | |||||||
| chr2:47087709 | T | C | 2 | a0001c0001t0001g0321 a0001c0001t0001g0322 |
2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.625-579A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087709 | |||||||
| chr2:47087841 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0067 others(127): Show |
132 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.625-711G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087841 | |||||||
| chr2:47087892 | G | A | 138 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(135): Show |
139 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.625-762C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087892 | |||||||
| chr2:47087918 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0067 others(132): Show |
137 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(134): Show |
intron_variant | MODIFIER | c.625-788T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087918 | |||||||
| chr2:47087985 | T | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(317): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.625-855A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087985 | |||||||
| chr2:47087989 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.625-859C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47087989 | |||||||
| chr2:47088005 | C | T | 1 | a0003c0003t0001g0046 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.625-875G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088005 | |||||||
| chr2:47088080 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.625-950A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088080 | |||||||
| chr2:47088081 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.625-951C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088081 | |||||||
| chr2:47088088 | G | GT | 9 | a0001c0001t0001g0088 a0001c0001t0001g0219 a0001c0001t0001g0245 others(6): Show |
9 | HG00741.hp2 HG01169.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.625-959dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088088 | |||||||
| chr2:47088182 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.625-1052G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088182 | |||||||
| chr2:47088402 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.625-1272G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088402 | |||||||
| chr2:47088700 | G | T | 2 | a0001c0001t0001g0324 a0004c0004t0001g0016 |
2 | HG01255.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.624+1570C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088700 | |||||||
| chr2:47088742 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0320 a0002c0002t0001g0313 |
3 | HG03453.hp1 HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.624+1528G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088742 | |||||||
| chr2:47088817 | A | G | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(309): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.624+1453T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088817 | |||||||
| chr2:47088836 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.624+1434G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088836 | |||||||
| chr2:47088859 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0320 a0001c0001t0001g0324 others(3): Show |
6 | HG01255.hp2 HG02572.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+1411T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088859 | |||||||
| chr2:47088936 | A | C | 3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0341 |
3 | HG02886.hp2 HG02895.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.624+1334T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47088936 | |||||||
| chr2:47089013 | T | A | 65 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0076 others(62): Show |
66 | HG00609.hp1 HG00741.hp2 HG01074.hp2 others(63): Show |
intron_variant | MODIFIER | c.624+1257A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089013 | |||||||
| chr2:47089030 | C | A | 60 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0076 others(57): Show |
61 | HG00140.hp1 HG00609.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.624+1240G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089030 | |||||||
| chr2:47089036 | G | A | 188 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0066 others(185): Show |
190 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.624+1234C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089036 | |||||||
| chr2:47089058 | A | G | 57 | a0001c0001t0001g0065 a0001c0001t0001g0074 a0001c0001t0001g0076 others(54): Show |
58 | HG00140.hp1 HG00609.hp1 HG00741.hp2 others(55): Show |
intron_variant | MODIFIER | c.624+1212T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089058 | |||||||
| chr2:47089066 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.624+1204A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089066 | |||||||
| chr2:47089482 | T | C | 10 | a0001c0001t0001g0099 a0001c0001t0001g0119 a0001c0001t0001g0203 others(7): Show |
10 | HG00639.hp2 HG00735.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.624+788A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089482 | |||||||
| chr2:47089498 | C | T | 8 | a0001c0001t0001g0117 a0001c0001t0001g0316 a0001c0001t0001g0340 others(5): Show |
8 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.624+772G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089498 | |||||||
| chr2:47089601 | T | C | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(88): Show |
94 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.624+669A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089601 | |||||||
| chr2:47089602 | A | G | 108 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(105): Show |
111 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.624+668T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089602 | |||||||
| chr2:47089654 | T | TA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0067 others(34): Show |
39 | HG00639.hp2 HG00735.hp1 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.624+615dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089654 | |||||||
| chr2:47089654 | T | TAA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0070 others(40): Show |
44 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.624+614_624+615dup others(2): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089654 | |||||||
| chr2:47089737 | T | G | 29 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0090 others(26): Show |
30 | HG00323.hp1 HG00741.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.624+533A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089737 | |||||||
| chr2:47089757 | T | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(178): Show |
184 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.624+513A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089757 | |||||||
| chr2:47089759 | T | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.624+511A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089759 | |||||||
| chr2:47089933 | T | C | 1 | a0001c0012t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.624+337A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089933 | |||||||
| chr2:47089935 | G | A | 1 | a0003c0003t0001g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.624+335C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089935 | |||||||
| chr2:47089981 | T | C | 1 | a0003c0003t0001g0063 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.624+289A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089981 | |||||||
| chr2:47089986 | T | A | 4 | a0001c0001t0001g0087 a0001c0001t0001g0244 a0001c0001t0001g0245 others(1): Show |
4 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.624+284A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47089986 | |||||||
| chr2:47090111 | T | C | 2 | a0002c0002t0001g0279 a0003c0003t0001g0059 |
2 | HG01358.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.624+159A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47090111 | |||||||
| chr2:47090219 | C | T | 2 | a0001c0001t0001g0324 a0004c0004t0001g0016 |
2 | HG01255.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.624+51G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47090219 | |||||||
| chr2:47090228 | A | T | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.624+42T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47090228 | |||||||
| chr2:47090240 | G | A | 9 | a0001c0001t0001g0117 a0001c0001t0001g0316 a0001c0001t0001g0340 others(6): Show |
9 | HG01081.hp2 HG01884.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.624+30C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 6/6 | chr2 | 47090240 | |||||||
| chr2:47090450 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0012t0001g0122 others(1): Show |
4 | HG03225.hp2 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-76T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090450 | |||||||
| chr2:47090492 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0066 a0001c0001t0001g0073 others(36): Show |
40 | HG00140.hp2 HG00621.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.520-118T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090492 | |||||||
| chr2:47090600 | C | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0118 a0001c0012t0001g0122 others(1): Show |
4 | HG03041.hp1 HG03453.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-226G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090600 | |||||||
| chr2:47090802 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0323 a0001c0001t0002g0347 |
3 | HG02109.hp1 HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.520-428T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090802 | |||||||
| chr2:47090813 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(61): Show |
67 | HG00639.hp2 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.520-439G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090813 | |||||||
| chr2:47090899 | GAC | G | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(65): Show |
71 | HG00621.hp1 HG00639.hp2 HG00735.hp1 others(68): Show |
intron_variant | MODIFIER | c.520-527_520-526del others(2): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090899 | |||||||
| chr2:47090952 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.520-578G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47090952 | |||||||
| chr2:47091012 | C | A | 48 | a0001c0001t0001g0001 a0001c0001t0001g0078 a0001c0001t0001g0081 others(45): Show |
49 | HG00621.hp1 HG00735.hp2 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.520-638G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091012 | |||||||
| chr2:47091046 | C | CCACGGGG others(6): Show |
1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.520-685_520-673dup others(13): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091046 | |||||||
| chr2:47091111 | G | A | 2 | a0003c0003t0001g0031 a0003c0003t0001g0032 |
2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.520-737C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091111 | |||||||
| chr2:47091164 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.520-790C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091164 | |||||||
| chr2:47091250 | A | G | 26 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0173 others(23): Show |
26 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.520-876T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091250 | |||||||
| chr2:47091726 | T | C | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.520-1352A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091726 | |||||||
| chr2:47091786 | G | A | 1 | a0004c0004t0001g0011 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.520-1412C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091786 | |||||||
| chr2:47091823 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.520-1449A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091823 | |||||||
| chr2:47091850 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18980.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.520-1476G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091850 | |||||||
| chr2:47091851 | A | G | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.520-1477T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091851 | |||||||
| chr2:47091973 | T | C | 284 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.520-1599A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47091973 | |||||||
| chr2:47092024 | C | A | 1 | a0002c0002t0001g0312 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.520-1650G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092024 | |||||||
| chr2:47092065 | A | G | 15 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0099 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-1691T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092065 | |||||||
| chr2:47092115 | C | G | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(279): Show |
286 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.520-1741G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092115 | |||||||
| chr2:47092126 | T | A | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.520-1752A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092126 | |||||||
| chr2:47092141 | T | TGCATTTT others(330): Show |
1 | a0002c0002t0001g0332 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(339): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(331): Show |
1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(340): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(306): Show |
1 | a0001c0001t0001g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.520-1768_520-1767i others(315): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(308): Show |
1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(317): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(310): Show |
2 | a0001c0001t0001g0169 a0004c0004t0001g0012 |
2 | HG00673.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(319): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(316): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0322 |
2 | HG02622.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(325): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(317): Show |
1 | a0001c0001t0001g0321 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.520-1768_520-1767i others(326): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(318): Show |
3 | a0001c0001t0001g0139 a0001c0001t0001g0159 a0001c0001t0001g0196 |
3 | HG03688.hp1 NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(327): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(320): Show |
3 | a0001c0001t0001g0069 a0001c0001t0001g0118 a0001c0001t0001g0167 |
3 | HG01361.hp2 HG02738.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(329): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(321): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0099 others(9): Show |
13 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(330): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(323): Show |
1 | a0001c0001t0001g0077 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(332): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(322): Show |
2 | a0001c0001t0001g0079 a0001c0001t0001g0252 |
2 | HG03927.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(331): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(323): Show |
2 | a0001c0001t0001g0264 a0002c0002t0001g0278 |
2 | HG02896.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(332): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(323): Show |
1 | a0001c0001t0001g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(332): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(324): Show |
4 | a0001c0001t0001g0121 a0002c0002t0001g0277 a0004c0004t0001g0011 others(1): Show |
4 | HG02027.hp2 HG02897.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(333): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(329): Show |
4 | a0001c0001t0001g0178 a0004c0004t0001g0016 a0006c0006t0001g0129 others(1): Show |
4 | HG01255.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(338): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(330): Show |
10 | a0001c0001t0001g0074 a0001c0001t0001g0127 a0001c0001t0001g0148 others(7): Show |
10 | HG01070.hp2 HG01515.hp2 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(339): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(331): Show |
32 | a0001c0001t0001g0065 a0001c0001t0001g0095 a0001c0001t0001g0115 others(29): Show |
32 | HG00609.hp1 HG00738.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(340): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(332): Show |
38 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0096 others(35): Show |
38 | HG00408.hp1 HG00621.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(341): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(333): Show |
1 | a0001c0001t0001g0140 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(342): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(333): Show |
1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(342): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(333): Show |
45 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0081 others(42): Show |
45 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(342): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(334): Show |
30 | a0001c0001t0001g0070 a0001c0001t0001g0093 a0001c0001t0001g0137 others(27): Show |
30 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(343): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(335): Show |
17 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0075 others(14): Show |
17 | HG00140.hp1 HG01167.hp1 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(344): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(336): Show |
29 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0080 others(26): Show |
31 | HG00642.hp1 HG00741.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(345): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(337): Show |
18 | a0001c0001t0001g0138 a0001c0001t0001g0142 a0001c0001t0001g0143 others(15): Show |
18 | HG01175.hp1 HG01175.hp2 HG02083.hp1 others(15): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(346): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(338): Show |
8 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0223 others(5): Show |
8 | HG00597.hp1 HG00741.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(347): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(339): Show |
1 | a0002c0002t0001g0306 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(348): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(340): Show |
1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(349): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(341): Show |
1 | a0001c0001t0002g0005 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(350): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(342): Show |
1 | a0003c0003t0001g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.520-1768_520-1767i others(351): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(343): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0152 a0003c0003t0001g0041 |
3 | NA18955.hp2 NA19064.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.520-1768_520-1767i others(352): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(344): Show |
4 | a0001c0001t0001g0153 a0001c0001t0001g0268 a0003c0003t0001g0025 others(1): Show |
4 | NA18954.hp1 NA18962.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-1768_520-1767i others(353): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092141 | T | TGCATTTT others(345): Show |
1 | a0003c0003t0001g0040 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.520-1768_520-1767i others(354): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092141 | |||||||
| chr2:47092181 | A | G | 282 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0066 others(279): Show |
285 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(282): Show |
intron_variant | MODIFIER | c.520-1807T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092181 | |||||||
| chr2:47092363 | C | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.520-1989G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092363 | |||||||
| chr2:47092407 | G | A | 5 | a0001c0001t0001g0092 a0001c0001t0001g0170 a0001c0001t0001g0218 others(2): Show |
5 | HG02080.hp1 NA18941.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-2033C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092407 | |||||||
| chr2:47092508 | A | C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0221 |
2 | HG02071.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.520-2134T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092508 | |||||||
| chr2:47092521 | C | CAAGAAAA others(5): Show |
288 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(285): Show |
292 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.520-2159_520-2148d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092521 | |||||||
| chr2:47092521 | C | CAAGAAAA others(5): Show |
1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.520-2148_520-2147i others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092521 | |||||||
| chr2:47092530 | A | AAAAAAAG others(5): Show |
1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.520-2157_520-2156i others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092530 | |||||||
| chr2:47092531 | A | AAAAAGAA others(39): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0241 |
2 | HG01993.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.520-2158_520-2157i others(48): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092531 | |||||||
| chr2:47092534 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.520-2160C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092534 | |||||||
| chr2:47092539 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2165C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092539 | |||||||
| chr2:47092540 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2166C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092540 | |||||||
| chr2:47092542 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2168C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092542 | |||||||
| chr2:47092544 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2170C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092544 | |||||||
| chr2:47092545 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2171C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092545 | |||||||
| chr2:47092548 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2174C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092548 | |||||||
| chr2:47092549 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.520-2175T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092549 | |||||||
| chr2:47092551 | A | AGGGAGGG others(10): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02572.hp1 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-2194_520-2178d others(19): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092551 | |||||||
| chr2:47092551 | A | AGGGAGGG others(27): Show |
2 | a0001c0001t0001g0274 a0002c0002t0001g0272 |
2 | HG01109.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.520-2211_520-2178d others(36): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092551 | |||||||
| chr2:47092551 | A | AGGGAGGG others(44): Show |
3 | a0001c0001t0001g0114 a0002c0002t0001g0273 a0002c0002t0001g0313 |
3 | HG02559.hp1 NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.520-2228_520-2178d others(53): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092551 | |||||||
| chr2:47092551 | A | G | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2177T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092551 | |||||||
| chr2:47092551 | AGGGAGGG others(10): Show |
A | 2 | a0003c0003t0001g0031 a0003c0003t0001g0032 |
2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.520-2194_520-2178d others(19): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092551 | |||||||
| chr2:47092559 | G | C | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.520-2185C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092559 | |||||||
| chr2:47092568 | G | A | 2 | a0001c0001t0001g0116 a0002c0002t0001g0290 |
2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.520-2194C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092568 | |||||||
| chr2:47092586 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.520-2212C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092586 | |||||||
| chr2:47092640 | G | C | 23 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(20): Show |
24 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.520-2266C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092640 | |||||||
| chr2:47092799 | GT | G | 157 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0065 others(154): Show |
159 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.520-2426delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092799 | |||||||
| chr2:47092799 | GTT | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(128): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.520-2427_520-2426d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092799 | |||||||
| chr2:47092940 | G | A | 1 | a0003c0003t0001g0059 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.520-2566C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47092940 | |||||||
| chr2:47093012 | C | T | 129 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(126): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.520-2638G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093012 | |||||||
| chr2:47093033 | T | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | HG01099.hp2 HG01993.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.520-2659A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093033 | |||||||
| chr2:47093076 | A | C | 148 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0001g0068 others(145): Show |
149 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(146): Show |
intron_variant | MODIFIER | c.520-2702T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093076 | |||||||
| chr2:47093153 | T | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(292): Show |
299 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.520-2779A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093153 | |||||||
| chr2:47093182 | T | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.520-2808A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093182 | |||||||
| chr2:47093344 | G | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0065 a0001c0001t0001g0099 others(12): Show |
16 | HG00639.hp2 HG00735.hp1 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.520-2970C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093344 | |||||||
| chr2:47093439 | G | A | 12 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(9): Show |
12 | HG00738.hp2 HG01884.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-3065C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093439 | |||||||
| chr2:47093551 | T | A | 22 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(19): Show |
23 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(20): Show |
intron_variant | MODIFIER | c.520-3177A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093551 | |||||||
| chr2:47093667 | T | C | 6 | a0001c0001t0001g0117 a0002c0002t0001g0332 a0003c0003t0001g0019 others(3): Show |
6 | HG00738.hp2 HG01884.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-3293A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093667 | |||||||
| chr2:47093675 | G | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.520-3301C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093675 | |||||||
| chr2:47093705 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0186 |
2 | NA18946.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.520-3331C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093705 | |||||||
| chr2:47093707 | C | T | 84 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0081 others(81): Show |
84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-3333G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093707 | |||||||
| chr2:47093724 | C | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(289): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.520-3350G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093724 | |||||||
| chr2:47093760 | A | C | 23 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(20): Show |
24 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.520-3386T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093760 | |||||||
| chr2:47093761 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-3387G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093761 | |||||||
| chr2:47093789 | T | C | 3 | a0001c0001t0001g0076 a0001c0001t0001g0083 a0001c0001t0001g0180 |
3 | HG02132.hp1 NA18967.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.520-3415A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093789 | |||||||
| chr2:47093806 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.520-3432T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093806 | |||||||
| chr2:47093807 | G | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.520-3433C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093807 | |||||||
| chr2:47093852 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.520-3478C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093852 | |||||||
| chr2:47093856 | C | T | 4 | a0001c0001t0001g0114 a0002c0002t0001g0272 a0002c0002t0001g0273 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-3482G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093856 | |||||||
| chr2:47093909 | G | A | 1 | a0007c0007t0001g0338 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.520-3535C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093909 | |||||||
| chr2:47093949 | G | A | 2 | a0001c0001t0001g0170 a0002c0002t0001g0297 |
2 | NA18941.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.520-3575C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093949 | |||||||
| chr2:47093977 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-3603C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093977 | |||||||
| chr2:47093992 | T | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.520-3618A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47093992 | |||||||
| chr2:47094073 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.520-3699A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094073 | |||||||
| chr2:47094194 | A | T | 133 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(130): Show |
135 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.520-3820T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094194 | |||||||
| chr2:47094269 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(289): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.520-3895C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094269 | |||||||
| chr2:47094313 | C | T | 23 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(20): Show |
24 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.520-3939G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094313 | |||||||
| chr2:47094340 | G | T | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.520-3966C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094340 | |||||||
| chr2:47094579 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.520-4205A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094579 | |||||||
| chr2:47094677 | A | T | 1 | a0008c0013t0001g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.520-4303T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094677 | |||||||
| chr2:47094729 | G | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0340 a0003c0003t0001g0019 others(2): Show |
5 | HG00738.hp2 HG01884.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-4355C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094729 | |||||||
| chr2:47094761 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.520-4387A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094761 | |||||||
| chr2:47094826 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(129): Show |
134 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.520-4452C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094826 | |||||||
| chr2:47094884 | G | A | 1 | a0001c0012t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.520-4510C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094884 | |||||||
| chr2:47094896 | C | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(133): Show |
138 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.520-4522G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094896 | |||||||
| chr2:47094978 | T | C | 294 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(291): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.520-4604A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094978 | |||||||
| chr2:47094990 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.520-4616C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47094990 | |||||||
| chr2:47095031 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.520-4657A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095031 | |||||||
| chr2:47095046 | G | A | 3 | a0001c0001t0001g0067 a0001c0001t0001g0116 a0002c0002t0001g0290 |
3 | HG02486.hp1 HG02622.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.520-4672C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095046 | |||||||
| chr2:47095083 | C | T | 128 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(125): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.520-4709G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095083 | |||||||
| chr2:47095084 | A | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(293): Show |
300 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(297): Show |
intron_variant | MODIFIER | c.520-4710T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095084 | |||||||
| chr2:47095191 | G | A | 292 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(289): Show |
296 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(293): Show |
intron_variant | MODIFIER | c.520-4817C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095191 | |||||||
| chr2:47095218 | A | C | 4 | a0001c0001t0001g0114 a0002c0002t0001g0272 a0002c0002t0001g0273 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-4844T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095218 | |||||||
| chr2:47095242 | T | C | 4 | a0001c0001t0001g0114 a0002c0002t0001g0272 a0002c0002t0001g0273 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.520-4868A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095242 | |||||||
| chr2:47095279 | C | T | 3 | a0001c0001t0001g0169 a0001c0001t0001g0217 a0004c0004t0001g0012 |
3 | HG00673.hp2 HG02040.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.520-4905G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095279 | |||||||
| chr2:47095290 | G | C | 84 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0081 others(81): Show |
84 | HG00408.hp1 HG00597.hp1 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.520-4916C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095290 | |||||||
| chr2:47095437 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.520-5063G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095437 | |||||||
| chr2:47095499 | C | T | 1 | a0009c0014t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.520-5125G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095499 | |||||||
| chr2:47095531 | C | G | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(290): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.520-5157G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095531 | |||||||
| chr2:47095617 | C | T | 15 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0078 others(12): Show |
15 | HG00438.hp2 HG00597.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.520-5243G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095617 | |||||||
| chr2:47095649 | A | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.520-5275T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095649 | |||||||
| chr2:47095652 | G | A | 23 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(20): Show |
24 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.520-5278C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095652 | |||||||
| chr2:47095754 | C | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(132): Show |
137 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.520-5380G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095754 | |||||||
| chr2:47095995 | T | A | 2 | a0002c0002t0001g0291 a0003c0003t0001g0021 |
2 | HG02976.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.520-5621A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47095995 | |||||||
| chr2:47096013 | A | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(276): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.520-5639T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096013 | |||||||
| chr2:47096014 | A | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(276): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.520-5640T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096014 | |||||||
| chr2:47096046 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.520-5672T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096046 | |||||||
| chr2:47096155 | C | T | 11 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0340 others(8): Show |
11 | HG00738.hp2 HG01884.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-5781G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096155 | |||||||
| chr2:47096160 | C | G | 23 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(20): Show |
24 | HG00741.hp1 HG01175.hp1 HG02451.hp2 others(21): Show |
intron_variant | MODIFIER | c.520-5786G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096160 | |||||||
| chr2:47096208 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.520-5834T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096208 | |||||||
| chr2:47096210 | C | A | 4 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0116 others(1): Show |
4 | HG02486.hp1 HG02622.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-5836G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096210 | |||||||
| chr2:47096226 | G | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0341 |
2 | HG01891.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.520-5852C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096226 | |||||||
| chr2:47096228 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.520-5854C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096228 | |||||||
| chr2:47096293 | T | C | 137 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(134): Show |
139 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.520-5919A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096293 | |||||||
| chr2:47096305 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.520-5931C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096305 | |||||||
| chr2:47096472 | T | C | 141 | a0001c0001t0001g0003 a0001c0001t0001g0066 a0001c0001t0001g0069 others(138): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.520-6098A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096472 | |||||||
| chr2:47096502 | A | C | 1 | a0003c0011t0001g0018 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.520-6128T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096502 | |||||||
| chr2:47096585 | C | G | 1 | a0002c0002t0001g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.520-6211G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096585 | |||||||
| chr2:47096792 | A | G | 1 | a0007c0007t0001g0338 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.520-6418T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096792 | |||||||
| chr2:47096893 | A | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0078 others(29): Show |
32 | HG00438.hp2 HG00597.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.520-6519T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096893 | |||||||
| chr2:47096942 | G | A | 138 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0065 others(135): Show |
139 | HG00438.hp2 HG00597.hp2 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.520-6568C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47096942 | |||||||
| chr2:47097000 | G | A | 63 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0071 others(60): Show |
63 | HG00609.hp1 HG00621.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.520-6626C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097000 | |||||||
| chr2:47097175 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-6801A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097175 | |||||||
| chr2:47097253 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0199 |
2 | HG01255.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.520-6879T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097253 | |||||||
| chr2:47097310 | C | T | 51 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0086 others(48): Show |
54 | HG00642.hp1 HG00738.hp2 HG00741.hp1 others(51): Show |
intron_variant | MODIFIER | c.520-6936G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097310 | |||||||
| chr2:47097442 | G | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.520-7068C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097442 | |||||||
| chr2:47097462 | T | G | 19 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(16): Show |
20 | HG00741.hp1 HG01175.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.520-7088A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097462 | |||||||
| chr2:47097500 | G | A | 2 | a0001c0001t0001g0319 a0002c0002t0001g0289 |
2 | HG01081.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.520-7126C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097500 | |||||||
| chr2:47097617 | T | C | 5 | a0001c0001t0001g0117 a0001c0001t0001g0315 a0001c0001t0001g0317 others(2): Show |
5 | HG01891.hp1 HG02257.hp2 NA19240.hp2 others(2): Show |
intron_variant | MODIFIER | c.520-7243A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097617 | |||||||
| chr2:47097619 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.520-7245C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097619 | |||||||
| chr2:47097721 | T | G | 62 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0074 others(59): Show |
62 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.520-7347A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097721 | |||||||
| chr2:47097752 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.520-7378G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097752 | |||||||
| chr2:47097795 | A | G | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0315 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-7421T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097795 | |||||||
| chr2:47097910 | G | C | 6 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0315 others(3): Show |
6 | HG01891.hp1 HG02257.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-7536C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097910 | |||||||
| chr2:47097953 | T | TA | 31 | a0001c0001t0001g0079 a0001c0001t0001g0083 a0001c0001t0001g0092 others(28): Show |
31 | HG00408.hp1 HG01169.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.520-7580dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097953 | |||||||
| chr2:47097953 | TA | T | 22 | a0001c0001t0001g0001 a0001c0001t0001g0108 a0001c0001t0001g0124 others(19): Show |
23 | HG00323.hp1 HG00597.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.520-7580delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097953 | |||||||
| chr2:47097953 | TAAA | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0247 others(22): Show |
27 | HG00642.hp1 HG00738.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.520-7582_520-7580d others(5): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47097953 | |||||||
| chr2:47098029 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0217 |
2 | HG02040.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.520-7655C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098029 | |||||||
| chr2:47098133 | G | C | 56 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0074 others(53): Show |
56 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.520-7759C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098133 | |||||||
| chr2:47098160 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG01891.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-7786G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098160 | |||||||
| chr2:47098200 | C | T | 2 | a0002c0002t0001g0289 a0009c0014t0001g0107 |
2 | HG01081.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.520-7826G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098200 | |||||||
| chr2:47098222 | C | T | 2 | a0001c0001t0001g0315 a0001c0001t0001g0317 |
2 | HG02257.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.520-7848G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098222 | |||||||
| chr2:47098252 | C | A | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG02486.hp1 HG02622.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-7878G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098252 | |||||||
| chr2:47098258 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.520-7884C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098258 | |||||||
| chr2:47098296 | A | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02257.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-7922T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098296 | |||||||
| chr2:47098401 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.520-8027G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098401 | |||||||
| chr2:47098402 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.520-8028C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098402 | |||||||
| chr2:47098425 | C | T | 5 | a0002c0002t0001g0004 a0002c0002t0001g0304 a0002c0002t0001g0305 others(2): Show |
6 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.520-8051G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098425 | |||||||
| chr2:47098596 | T | C | 1 | a0002c0002t0001g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.520-8222A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098596 | |||||||
| chr2:47098607 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.520-8233C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098607 | |||||||
| chr2:47098608 | A | T | 1 | a0001c0001t0001g0077 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.520-8234T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098608 | |||||||
| chr2:47098694 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0119 a0001c0001t0001g0260 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-8320G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098694 | |||||||
| chr2:47098733 | T | C | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520-8359A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098733 | |||||||
| chr2:47098740 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0260 a0009c0014t0001g0107 |
3 | HG01891.hp2 HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.520-8366G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098740 | |||||||
| chr2:47098757 | G | GA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0070 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.520-8384dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098757 | |||||||
| chr2:47098757 | G | GAA | 51 | a0001c0001t0001g0067 a0001c0001t0001g0069 a0001c0001t0001g0095 others(48): Show |
51 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.520-8385_520-8384d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098757 | |||||||
| chr2:47098757 | GA | G | 8 | a0001c0001t0001g0066 a0001c0001t0001g0119 a0001c0001t0001g0123 others(5): Show |
8 | HG01891.hp2 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-8384delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098757 | |||||||
| chr2:47098834 | C | T | 175 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0070 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.520-8460G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098834 | |||||||
| chr2:47098882 | G | A | 7 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(4): Show |
7 | HG00738.hp2 HG02145.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-8508C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098882 | |||||||
| chr2:47098890 | T | G | 8 | a0001c0001t0001g0086 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
9 | HG02109.hp1 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.520-8516A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098890 | |||||||
| chr2:47098927 | C | G | 272 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(269): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.520-8553G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47098927 | |||||||
| chr2:47099053 | C | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-8679G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099053 | |||||||
| chr2:47099072 | G | A | 3 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 |
3 | HG02622.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.520-8698C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099072 | |||||||
| chr2:47099078 | G | C | 20 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(17): Show |
21 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.520-8704C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099078 | |||||||
| chr2:47099117 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.520-8743T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099117 | |||||||
| chr2:47099227 | TTTTC | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0073 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.520-8857_520-8854d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099227 | |||||||
| chr2:47099237 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(29): Show |
33 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.520-8863T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099237 | |||||||
| chr2:47099241 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-8867G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099241 | |||||||
| chr2:47099258 | A | G | 10 | a0001c0001t0001g0068 a0001c0001t0001g0117 a0001c0001t0001g0315 others(7): Show |
10 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.520-8884T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099258 | |||||||
| chr2:47099408 | G | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-9034C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099408 | |||||||
| chr2:47099462 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-9088A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099462 | |||||||
| chr2:47099588 | G | A | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-9214C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099588 | |||||||
| chr2:47099598 | G | A | 1 | a0001c0001t0001g0265 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.520-9224C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099598 | |||||||
| chr2:47099630 | G | A | 2 | a0003c0003t0001g0029 a0003c0003t0001g0030 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.520-9256C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099630 | |||||||
| chr2:47099693 | G | T | 1 | a0009c0014t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.520-9319C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099693 | |||||||
| chr2:47099720 | A | G | 1 | a0001c0001t0001g0175 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.520-9346T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099720 | |||||||
| chr2:47099762 | C | T | 1 | a0002c0002t0001g0286 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.520-9388G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099762 | |||||||
| chr2:47099768 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.520-9394C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099768 | |||||||
| chr2:47099823 | AGAGCAGC others(7541): Show |
A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-16997_520-9450 others(3): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099823 | |||||||
| chr2:47099833 | G | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-9459C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099833 | |||||||
| chr2:47099868 | G | C | 1 | a0001c0001t0001g0240 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.520-9494C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099868 | |||||||
| chr2:47099946 | G | A | 1 | a0002c0002t0001g0300 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.520-9572C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099946 | |||||||
| chr2:47099982 | G | A | 1 | a0003c0003t0001g0017 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.520-9608C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099982 | |||||||
| chr2:47099996 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.520-9622T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47099996 | |||||||
| chr2:47100062 | G | A | 1 | a0004c0004t0001g0007 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.520-9688C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100062 | |||||||
| chr2:47100098 | C | A | 1 | a0005c0008t0001g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.520-9724G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100098 | |||||||
| chr2:47100116 | G | A | 2 | a0003c0003t0001g0019 a0003c0003t0001g0021 |
2 | HG01884.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.520-9742C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100116 | |||||||
| chr2:47100125 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-9751C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100125 | |||||||
| chr2:47100157 | C | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0072 others(158): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.520-9783G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100157 | |||||||
| chr2:47100163 | G | C | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-9789C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100163 | |||||||
| chr2:47100164 | TGGGATCC others(7540): Show |
T | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.520-17337_520-9791 others(3): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100164 | |||||||
| chr2:47100172 | A | C | 1 | a0004c0004t0001g0012 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.520-9798T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100172 | |||||||
| chr2:47100177 | G | A | 18 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(15): Show |
18 | HG00738.hp2 HG02257.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.520-9803C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100177 | |||||||
| chr2:47100258 | A | G | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-9884T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100258 | |||||||
| chr2:47100266 | G | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-9892C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100266 | |||||||
| chr2:47100289 | C | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0068 others(206): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.520-9915G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100289 | |||||||
| chr2:47100298 | CAGCACCC others(7538): Show |
C | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-17469_520-9925 others(3): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100298 | |||||||
| chr2:47100342 | C | T | 3 | a0002c0002t0001g0293 a0003c0003t0001g0031 a0003c0003t0001g0032 |
3 | HG03017.hp2 HG03490.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.520-9968G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100342 | |||||||
| chr2:47100378 | A | AACCTTTG others(7): Show |
1 | a0003c0003t0001g0054 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.520-10018_520-1000 others(18): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100378 | |||||||
| chr2:47100417 | G | A | 1 | a0003c0003t0001g0050 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.520-10043C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100417 | |||||||
| chr2:47100449 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.520-10075C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100449 | |||||||
| chr2:47100458 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.520-10084G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100458 | |||||||
| chr2:47100493 | G | A | 19 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0001g0089 others(16): Show |
20 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.520-10119C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100493 | |||||||
| chr2:47100511 | G | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0092 others(153): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.520-10137C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100511 | |||||||
| chr2:47100516 | G | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0072 others(169): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(171): Show |
intron_variant | MODIFIER | c.520-10142C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100516 | |||||||
| chr2:47100553 | G | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-10179C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100553 | |||||||
| chr2:47100574 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10200A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100574 | |||||||
| chr2:47100659 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0068 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.520-10285C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100659 | |||||||
| chr2:47100686 | G | A | 201 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0068 others(198): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.520-10312C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100686 | |||||||
| chr2:47100710 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10336C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100710 | |||||||
| chr2:47100787 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10413G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100787 | |||||||
| chr2:47100807 | C | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10433G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100807 | |||||||
| chr2:47100820 | T | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10446A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100820 | |||||||
| chr2:47100826 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10452C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100826 | |||||||
| chr2:47100834 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10460T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100834 | |||||||
| chr2:47100847 | CTCCGAAC others(3): Show |
C | 1 | a0003c0003t0001g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.520-10483_520-1047 others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100847 | |||||||
| chr2:47100851 | G | A | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520-10477C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100851 | |||||||
| chr2:47100866 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(73): Show |
78 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.520-10492A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100866 | |||||||
| chr2:47100869 | G | C | 1 | a0004c0004t0001g0012 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.520-10495C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100869 | |||||||
| chr2:47100889 | C | T | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-10515G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100889 | |||||||
| chr2:47100890 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.520-10516C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100890 | |||||||
| chr2:47100926 | C | T | 18 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(15): Show |
18 | HG00738.hp2 HG02257.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.520-10552G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100926 | |||||||
| chr2:47100928 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.520-10554G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100928 | |||||||
| chr2:47100986 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.520-10612G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47100986 | |||||||
| chr2:47101004 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10630A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101004 | |||||||
| chr2:47101038 | G | A | 16 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0001g0131 others(13): Show |
16 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.520-10664C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101038 | |||||||
| chr2:47101057 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10683T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101057 | |||||||
| chr2:47101093 | A | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10719T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101093 | |||||||
| chr2:47101167 | G | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10793C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101167 | |||||||
| chr2:47101189 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0092 a0001c0001t0001g0106 others(106): Show |
110 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(107): Show |
intron_variant | MODIFIER | c.520-10815C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101189 | |||||||
| chr2:47101201 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.520-10827T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101201 | |||||||
| chr2:47101209 | G | C | 1 | a0001c0001t0001g0249 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.520-10835C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101209 | |||||||
| chr2:47101230 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10856C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101230 | |||||||
| chr2:47101283 | G | A | 15 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
15 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-10909C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101283 | |||||||
| chr2:47101287 | C | G | 15 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
15 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.520-10913G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101287 | |||||||
| chr2:47101305 | T | C | 7 | a0001c0001t0001g0177 a0001c0001t0001g0190 a0001c0001t0001g0195 others(4): Show |
7 | HG00099.hp1 HG00735.hp2 HG02300.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-10931A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101305 | |||||||
| chr2:47101321 | C | T | 1 | a0003c0003t0001g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.520-10947G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101321 | |||||||
| chr2:47101322 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-10948C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101322 | |||||||
| chr2:47101422 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11048G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101422 | |||||||
| chr2:47101528 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.520-11154G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101528 | |||||||
| chr2:47101538 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-11164G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101538 | |||||||
| chr2:47101596 | C | G | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-11222G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101596 | |||||||
| chr2:47101626 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(70): Show |
75 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.520-11252C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101626 | |||||||
| chr2:47101787 | G | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11413C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101787 | |||||||
| chr2:47101788 | C | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11414G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101788 | |||||||
| chr2:47101809 | C | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-11435G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101809 | |||||||
| chr2:47101897 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11523G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101897 | |||||||
| chr2:47101908 | G | C | 1 | a0003c0003t0001g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.520-11534C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101908 | |||||||
| chr2:47101935 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.520-11561C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101935 | |||||||
| chr2:47101936 | A | C | 1 | a0007c0007t0001g0338 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.520-11562T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101936 | |||||||
| chr2:47101943 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-11569C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101943 | |||||||
| chr2:47101974 | C | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11600G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47101974 | |||||||
| chr2:47102030 | G | T | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-11656C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102030 | |||||||
| chr2:47102054 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11680T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102054 | |||||||
| chr2:47102061 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11687A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102061 | |||||||
| chr2:47102063 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11689A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102063 | |||||||
| chr2:47102105 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11731C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102105 | |||||||
| chr2:47102110 | G | A | 2 | a0001c0001t0001g0118 a0004c0009t0001g0006 |
2 | HG03139.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.520-11736C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102110 | |||||||
| chr2:47102130 | C | G | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520-11756G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102130 | |||||||
| chr2:47102145 | G | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(120): Show |
126 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(123): Show |
intron_variant | MODIFIER | c.520-11771C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102145 | |||||||
| chr2:47102151 | C | T | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG00741.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.520-11777G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102151 | |||||||
| chr2:47102152 | G | A | 17 | a0001c0001t0001g0109 a0001c0001t0001g0126 a0001c0001t0001g0131 others(14): Show |
17 | HG00741.hp2 HG01175.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-11778C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102152 | |||||||
| chr2:47102154 | TGCAGGTT others(85): Show |
T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11872_520-1178 others(96): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102154 | |||||||
| chr2:47102200 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-11826C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102200 | |||||||
| chr2:47102209 | C | A | 69 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(66): Show |
71 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.520-11835G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102209 | |||||||
| chr2:47102212 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.520-11838T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102212 | |||||||
| chr2:47102233 | T | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(68): Show |
73 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.520-11859A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102233 | |||||||
| chr2:47102245 | G | C | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02257.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.520-11871C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102245 | |||||||
| chr2:47102288 | T | C | 5 | a0001c0001t0001g0119 a0001c0001t0001g0260 a0003c0003t0001g0017 others(2): Show |
5 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-11914A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102288 | |||||||
| chr2:47102370 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-11996A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102370 | |||||||
| chr2:47102410 | C | T | 2 | a0001c0001t0001g0229 a0002c0002t0001g0325 |
2 | HG02523.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.520-12036G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102410 | |||||||
| chr2:47102432 | C | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG01070.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-12058G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102432 | |||||||
| chr2:47102511 | C | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-12137G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102511 | |||||||
| chr2:47102628 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.520-12254A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102628 | |||||||
| chr2:47102727 | T | TA | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-12354dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102727 | |||||||
| chr2:47102770 | G | C | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-12396C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102770 | |||||||
| chr2:47102819 | T | G | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-12445A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102819 | |||||||
| chr2:47102888 | G | A | 4 | a0001c0001t0001g0119 a0001c0001t0001g0260 a0003c0003t0001g0017 others(1): Show |
4 | HG01891.hp2 HG02630.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.520-12514C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102888 | |||||||
| chr2:47102932 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-12558T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102932 | |||||||
| chr2:47102962 | C | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-12588G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47102962 | |||||||
| chr2:47103008 | G | A | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-12634C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103008 | |||||||
| chr2:47103064 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-12690C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103064 | |||||||
| chr2:47103142 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.520-12768C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103142 | |||||||
| chr2:47103151 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-12777G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103151 | |||||||
| chr2:47103191 | G | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-12817C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103191 | |||||||
| chr2:47103194 | C | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.520-12820G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103194 | |||||||
| chr2:47103205 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.520-12831G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103205 | |||||||
| chr2:47103231 | C | T | 17 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(14): Show |
17 | HG00738.hp2 HG02257.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.520-12857G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103231 | |||||||
| chr2:47103280 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-12906G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103280 | |||||||
| chr2:47103281 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-12907C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103281 | |||||||
| chr2:47103370 | G | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(70): Show |
75 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(72): Show |
intron_variant | MODIFIER | c.520-12996C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103370 | |||||||
| chr2:47103419 | T | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-13045A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103419 | |||||||
| chr2:47103466 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.520-13092C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103466 | |||||||
| chr2:47103578 | C | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-13204G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103578 | |||||||
| chr2:47103596 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-13222C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103596 | |||||||
| chr2:47103657 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-13283T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103657 | |||||||
| chr2:47103691 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.520-13317T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103691 | |||||||
| chr2:47103754 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.520-13380A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103754 | |||||||
| chr2:47103910 | G | A | 1 | a0001c0001t0001g0191 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.520-13536C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103910 | |||||||
| chr2:47103946 | T | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0134 |
3 | NA18952.hp1 NA18980.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.520-13572A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103946 | |||||||
| chr2:47103969 | T | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-13595A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47103969 | |||||||
| chr2:47104121 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-13747A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104121 | |||||||
| chr2:47104139 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-13765T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104139 | |||||||
| chr2:47104202 | C | A | 2 | a0001c0001t0001g0235 a0001c0001t0001g0314 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.520-13828G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104202 | |||||||
| chr2:47104260 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(27): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.520-13886G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104260 | |||||||
| chr2:47104275 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0072 a0001c0001t0001g0092 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.520-13901G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104275 | |||||||
| chr2:47104332 | T | C | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-13958A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104332 | |||||||
| chr2:47104368 | A | C | 30 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(27): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.520-13994T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104368 | |||||||
| chr2:47104393 | T | C | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-14019A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104393 | |||||||
| chr2:47104451 | C | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-14077G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104451 | |||||||
| chr2:47104496 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.520-14122C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104496 | |||||||
| chr2:47104502 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-14128C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104502 | |||||||
| chr2:47104581 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(273): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.520-14207C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104581 | |||||||
| chr2:47104591 | T | C | 129 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(126): Show |
132 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(129): Show |
intron_variant | MODIFIER | c.520-14217A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104591 | |||||||
| chr2:47104742 | G | C | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.520-14368C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104742 | |||||||
| chr2:47104789 | C | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0067 others(121): Show |
127 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(124): Show |
intron_variant | MODIFIER | c.520-14415G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104789 | |||||||
| chr2:47104791 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.520-14417T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104791 | |||||||
| chr2:47104817 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-14443C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104817 | |||||||
| chr2:47104822 | C | T | 2 | a0002c0002t0001g0277 a0002c0002t0001g0278 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.520-14448G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104822 | |||||||
| chr2:47104838 | G | A | 94 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0068 others(91): Show |
96 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.520-14464C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104838 | |||||||
| chr2:47104857 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-14483G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47104857 | |||||||
| chr2:47105046 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.520-14672C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105046 | |||||||
| chr2:47105127 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.520-14753C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105127 | |||||||
| chr2:47105193 | G | A | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.520-14819C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105193 | |||||||
| chr2:47105231 | G | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(286): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.520-14857C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105231 | |||||||
| chr2:47105281 | G | A | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-14907C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105281 | |||||||
| chr2:47105310 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-14936C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105310 | |||||||
| chr2:47105443 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-15069G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105443 | |||||||
| chr2:47105484 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.520-15110C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105484 | |||||||
| chr2:47105531 | C | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-15157G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105531 | |||||||
| chr2:47105567 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-15193G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105567 | |||||||
| chr2:47105745 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.520-15371G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105745 | |||||||
| chr2:47105836 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-15462A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105836 | |||||||
| chr2:47105844 | G | A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-15470C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105844 | |||||||
| chr2:47105928 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-15554T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105928 | |||||||
| chr2:47105960 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.520-15586G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47105960 | |||||||
| chr2:47106146 | A | T | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.520-15772T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106146 | |||||||
| chr2:47106188 | A | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-15814T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106188 | |||||||
| chr2:47106248 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-15874G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106248 | |||||||
| chr2:47106334 | C | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.520-15960G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106334 | |||||||
| chr2:47106363 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0073 others(48): Show |
52 | HG00408.hp2 HG00438.hp2 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.520-15989G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106363 | |||||||
| chr2:47106417 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.520-16043C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106417 | |||||||
| chr2:47106432 | G | T | 33 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(30): Show |
34 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.520-16058C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106432 | |||||||
| chr2:47106545 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-16171G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106545 | |||||||
| chr2:47106587 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-16213G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106587 | |||||||
| chr2:47106678 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0258 |
2 | HG00738.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.520-16304C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106678 | |||||||
| chr2:47106682 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-16308C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106682 | |||||||
| chr2:47106684 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.520-16310G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106684 | |||||||
| chr2:47106698 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.520-16324G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106698 | |||||||
| chr2:47106701 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-16327A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106701 | |||||||
| chr2:47106958 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-16584G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106958 | |||||||
| chr2:47106973 | C | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0196 a0003c0003t0001g0060 |
3 | HG01069.hp2 HG01261.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.520-16599G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47106973 | |||||||
| chr2:47107140 | G | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-16766C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107140 | |||||||
| chr2:47107205 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.520-16831C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107205 | |||||||
| chr2:47107286 | G | A | 1 | a0001c0001t0001g0076 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.520-16912C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107286 | |||||||
| chr2:47107288 | G | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-16914C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107288 | |||||||
| chr2:47107311 | G | A | 72 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(69): Show |
74 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.520-16937C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107311 | |||||||
| chr2:47107312 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-16938A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107312 | |||||||
| chr2:47107365 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-16991C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107365 | |||||||
| chr2:47107393 | G | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0196 a0003c0003t0001g0060 |
3 | HG01069.hp2 HG01261.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.520-17019C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107393 | |||||||
| chr2:47107396 | C | T | 2 | a0003c0003t0001g0038 a0003c0003t0001g0039 |
2 | HG00741.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.520-17022G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107396 | |||||||
| chr2:47107399 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17025C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107399 | |||||||
| chr2:47107405 | C | T | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.520-17031G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107405 | |||||||
| chr2:47107422 | G | A | 18 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.520-17048C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107422 | |||||||
| chr2:47107430 | G | A | 1 | a0004c0009t0001g0006 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.520-17056C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107430 | |||||||
| chr2:47107436 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17062T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107436 | |||||||
| chr2:47107480 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.520-17106C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107480 | |||||||
| chr2:47107496 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.520-17122G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107496 | |||||||
| chr2:47107538 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17164G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107538 | |||||||
| chr2:47107543 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.520-17169G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107543 | |||||||
| chr2:47107544 | G | A | 1 | a0003c0003t0001g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.520-17170C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107544 | |||||||
| chr2:47107675 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(75): Show |
80 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-17301G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107675 | |||||||
| chr2:47107676 | G | A | 3 | a0001c0001t0001g0136 a0003c0003t0001g0046 a0003c0003t0001g0047 |
3 | NA18944.hp1 NA18961.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.520-17302C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107676 | |||||||
| chr2:47107808 | A | ACT | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17436_520-1743 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107808 | |||||||
| chr2:47107843 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.520-17469A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107843 | |||||||
| chr2:47107963 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(75): Show |
80 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.520-17589C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107963 | |||||||
| chr2:47107970 | T | C | 3 | a0001c0001t0001g0092 a0001c0001t0001g0142 a0001c0001t0001g0143 |
3 | NA18949.hp2 NA18980.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.520-17596A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47107970 | |||||||
| chr2:47108042 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17668T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108042 | |||||||
| chr2:47108080 | G | A | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.520-17706C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108080 | |||||||
| chr2:47108082 | G | T | 1 | a0001c0001t0001g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.520-17708C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108082 | |||||||
| chr2:47108168 | C | G | 1 | a0003c0003t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.520-17794G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108168 | |||||||
| chr2:47108176 | G | A | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.520-17802C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108176 | |||||||
| chr2:47108197 | C | T | 6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(3): Show |
6 | HG01175.hp1 HG02572.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-17823G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108197 | |||||||
| chr2:47108221 | G | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.520-17847C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108221 | |||||||
| chr2:47108240 | A | T | 1 | a0001c0001t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.520-17866T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108240 | |||||||
| chr2:47108251 | G | A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 |
3 | NA18987.hp1 NA18997.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.520-17877C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108251 | |||||||
| chr2:47108277 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-17903T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108277 | |||||||
| chr2:47108336 | G | C | 1 | a0001c0001t0001g0216 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.520-17962C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108336 | |||||||
| chr2:47108360 | T | C | 12 | a0001c0001t0001g0068 a0001c0001t0001g0126 a0001c0001t0001g0131 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.520-17986A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108360 | |||||||
| chr2:47108420 | C | G | 3 | a0001c0001t0001g0260 a0004c0009t0001g0006 a0009c0014t0001g0107 |
3 | HG02630.hp1 HG02735.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.520-18046G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108420 | |||||||
| chr2:47108428 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.520-18054G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108428 | |||||||
| chr2:47108520 | G | A | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.520-18146C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108520 | |||||||
| chr2:47108582 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.520-18208T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108582 | |||||||
| chr2:47108616 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.520-18242A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108616 | |||||||
| chr2:47108782 | G | A | 59 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(56): Show |
60 | HG00323.hp1 HG01074.hp1 HG01099.hp2 others(57): Show |
intron_variant | MODIFIER | c.520-18408C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108782 | |||||||
| chr2:47108909 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-18535G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108909 | |||||||
| chr2:47108981 | G | A | 3 | a0001c0001t0001g0069 a0002c0002t0001g0279 a0003c0003t0001g0059 |
3 | HG01358.hp2 HG01361.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.520-18607C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47108981 | |||||||
| chr2:47109112 | C | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0319 a0003c0003t0001g0017 |
3 | HG01891.hp2 HG03540.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.520-18738G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109112 | |||||||
| chr2:47109129 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.520-18755A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109129 | |||||||
| chr2:47109268 | A | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-18894T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109268 | |||||||
| chr2:47109269 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-18895C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109269 | |||||||
| chr2:47109354 | C | T | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-18980G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109354 | |||||||
| chr2:47109355 | A | G | 14 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(11): Show |
14 | HG00741.hp2 HG01243.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.520-18981T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109355 | |||||||
| chr2:47109443 | G | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0154 a0001c0001t0001g0155 others(8): Show |
12 | NA18941.hp2 NA18942.hp1 NA18943.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-19069C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109443 | |||||||
| chr2:47109556 | G | GA | 10 | a0001c0001t0001g0068 a0001c0001t0001g0072 a0001c0001t0001g0092 others(7): Show |
10 | HG00741.hp2 HG01256.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-19183dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109556 | |||||||
| chr2:47109556 | GA | G | 89 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(86): Show |
91 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.520-19183delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109556 | |||||||
| chr2:47109609 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.520-19235A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109609 | |||||||
| chr2:47109744 | G | A | 24 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(21): Show |
24 | HG00738.hp2 HG01891.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.520-19370C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109744 | |||||||
| chr2:47109861 | T | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-19487A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109861 | |||||||
| chr2:47109926 | GATC | G | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-19555_520-1955 others(7): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109926 | |||||||
| chr2:47109931 | T | C | 1 | a0003c0003t0001g0035 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.520-19557A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109931 | |||||||
| chr2:47109941 | A | G | 8 | a0001c0001t0001g0108 a0002c0002t0001g0296 a0002c0002t0001g0330 others(5): Show |
8 | HG01074.hp1 HG01884.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.520-19567T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109941 | |||||||
| chr2:47109965 | T | C | 1 | a0009c0014t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.520-19591A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47109965 | |||||||
| chr2:47110007 | T | TAAGAAAT others(141): Show |
11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-19634_520-1963 others(152): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110007 | |||||||
| chr2:47110049 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.520-19675G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110049 | |||||||
| chr2:47110060 | G | A | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.520-19686C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110060 | |||||||
| chr2:47110081 | G | A | 1 | a0009c0014t0001g0107 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.520-19707C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110081 | |||||||
| chr2:47110176 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+19765G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110176 | |||||||
| chr2:47110328 | T | A | 6 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(3): Show |
6 | HG00738.hp2 HG02451.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+19613A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110328 | |||||||
| chr2:47110362 | G | A | 3 | a0001c0001t0001g0260 a0004c0009t0001g0006 a0009c0014t0001g0107 |
3 | HG02630.hp1 HG02735.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.519+19579C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110362 | |||||||
| chr2:47110377 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+19564G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110377 | |||||||
| chr2:47110405 | C | A | 1 | a0001c0001t0001g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.519+19536G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110405 | |||||||
| chr2:47110457 | G | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0067 a0001c0001t0001g0069 others(73): Show |
78 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.519+19484C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110457 | |||||||
| chr2:47110683 | T | C | 2 | a0001c0001t0001g0099 a0004c0004t0001g0010 |
2 | HG00639.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.519+19258A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110683 | |||||||
| chr2:47110695 | G | C | 10 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0119 others(7): Show |
10 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.519+19246C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110695 | |||||||
| chr2:47110699 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+19242A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110699 | |||||||
| chr2:47110856 | A | G | 6 | a0003c0003t0001g0045 a0003c0003t0001g0048 a0003c0003t0001g0049 others(3): Show |
6 | HG00621.hp1 NA18940.hp2 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+19085T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110856 | |||||||
| chr2:47110877 | T | A | 75 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0093 others(72): Show |
77 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(74): Show |
intron_variant | MODIFIER | c.519+19064A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110877 | |||||||
| chr2:47110881 | A | G | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+19060T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110881 | |||||||
| chr2:47110899 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+19042G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110899 | |||||||
| chr2:47110964 | T | A | 1 | a0008c0013t0001g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.519+18977A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110964 | |||||||
| chr2:47110987 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18954T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47110987 | |||||||
| chr2:47111078 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18863T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111078 | |||||||
| chr2:47111166 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.519+18775C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111166 | |||||||
| chr2:47111184 | T | A | 22 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(19): Show |
22 | HG00738.hp2 HG01891.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.519+18757A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111184 | |||||||
| chr2:47111212 | T | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18729A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111212 | |||||||
| chr2:47111225 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+18716C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111225 | |||||||
| chr2:47111238 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18703A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111238 | |||||||
| chr2:47111272 | C | G | 1 | a0002c0002t0001g0310 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.519+18669G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111272 | |||||||
| chr2:47111375 | A | C | 2 | a0003c0003t0001g0029 a0003c0003t0001g0030 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.519+18566T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111375 | |||||||
| chr2:47111384 | T | A | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+18557A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111384 | |||||||
| chr2:47111484 | C | T | 68 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0093 others(65): Show |
70 | HG00140.hp2 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.519+18457G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111484 | |||||||
| chr2:47111488 | T | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18453A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111488 | |||||||
| chr2:47111543 | C | T | 2 | a0001c0001t0001g0324 a0004c0004t0001g0016 |
2 | HG01255.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.519+18398G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111543 | |||||||
| chr2:47111590 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18351A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111590 | |||||||
| chr2:47111606 | C | G | 1 | a0002c0002t0001g0296 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.519+18335G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111606 | |||||||
| chr2:47111611 | C | G | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02083.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.519+18330G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111611 | |||||||
| chr2:47111671 | TA | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18269delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111671 | |||||||
| chr2:47111719 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.519+18222C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111719 | |||||||
| chr2:47111727 | C | A | 24 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0001g0247 others(21): Show |
26 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.519+18214G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111727 | |||||||
| chr2:47111802 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18139G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111802 | |||||||
| chr2:47111823 | G | T | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.519+18118C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111823 | |||||||
| chr2:47111842 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+18099T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111842 | |||||||
| chr2:47111931 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+18010T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47111931 | |||||||
| chr2:47112009 | A | G | 1 | a0001c0001t0001g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.519+17932T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112009 | |||||||
| chr2:47112020 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.519+17921G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112020 | |||||||
| chr2:47112081 | TA | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17859delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112081 | |||||||
| chr2:47112088 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.519+17853G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112088 | |||||||
| chr2:47112189 | C | A | 95 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0114 others(92): Show |
97 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.519+17752G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112189 | |||||||
| chr2:47112222 | A | G | 9 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+17719T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112222 | |||||||
| chr2:47112227 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17714G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112227 | |||||||
| chr2:47112305 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17636A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112305 | |||||||
| chr2:47112339 | G | GT | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+17601dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112339 | |||||||
| chr2:47112339 | GT | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17601delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112339 | |||||||
| chr2:47112401 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+17540G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112401 | |||||||
| chr2:47112423 | G | A | 6 | a0001c0001t0001g0188 a0001c0001t0001g0204 a0001c0001t0001g0260 others(3): Show |
6 | HG00597.hp1 HG01257.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+17518C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112423 | |||||||
| chr2:47112438 | T | TG | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17502dupC | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112438 | |||||||
| chr2:47112503 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.519+17438C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112503 | |||||||
| chr2:47112512 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17429G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112512 | |||||||
| chr2:47112521 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.519+17420A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112521 | |||||||
| chr2:47112590 | A | G | 3 | a0002c0002t0001g0310 a0002c0002t0001g0311 a0002c0002t0001g0312 |
3 | HG02258.hp2 HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.519+17351T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112590 | |||||||
| chr2:47112603 | G | C | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.519+17338C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112603 | |||||||
| chr2:47112621 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.519+17320T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112621 | |||||||
| chr2:47112673 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.519+17268A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112673 | |||||||
| chr2:47112690 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.519+17251T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112690 | |||||||
| chr2:47112710 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0072 others(137): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.519+17231A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112710 | |||||||
| chr2:47112760 | T | C | 92 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0114 others(89): Show |
94 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.519+17181A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112760 | |||||||
| chr2:47112828 | T | C | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.519+17113A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112828 | |||||||
| chr2:47112889 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+17052T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112889 | |||||||
| chr2:47112965 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+16976G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112965 | |||||||
| chr2:47112989 | CA | C | 52 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(49): Show |
53 | HG00597.hp2 HG00738.hp1 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.519+16951delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112989 | |||||||
| chr2:47112989 | CAA | C | 22 | a0001c0001t0001g0002 a0001c0001t0001g0067 a0001c0001t0001g0068 others(19): Show |
23 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.519+16950_519+1695 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112989 | |||||||
| chr2:47112989 | CAAA | C | 39 | a0001c0001t0001g0072 a0001c0001t0001g0093 a0001c0001t0001g0094 others(36): Show |
39 | HG00642.hp2 HG00738.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.519+16949_519+1695 others(7): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112989 | |||||||
| chr2:47112989 | CAAAA | C | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(206): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.519+16948_519+1695 others(8): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112989 | |||||||
| chr2:47112989 | CAAAAAA | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+16946_519+1695 others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47112989 | |||||||
| chr2:47113232 | C | A | 27 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(24): Show |
28 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.519+16709G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113232 | |||||||
| chr2:47113286 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.519+16655C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113286 | |||||||
| chr2:47113540 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+16401C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113540 | |||||||
| chr2:47113696 | C | T | 35 | a0001c0001t0001g0068 a0001c0001t0001g0113 a0001c0001t0001g0116 others(32): Show |
35 | HG00738.hp2 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.519+16245G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113696 | |||||||
| chr2:47113751 | T | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0070 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.519+16190A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113751 | |||||||
| chr2:47113801 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+16140C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113801 | |||||||
| chr2:47113816 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0001g0172 |
2 | NA19081.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.519+16125G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113816 | |||||||
| chr2:47113861 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+16080G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113861 | |||||||
| chr2:47113896 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+16045A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113896 | |||||||
| chr2:47113965 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+15976G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113965 | |||||||
| chr2:47113978 | G | A | 1 | a0002c0002t0001g0282 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.519+15963C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113978 | |||||||
| chr2:47113983 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+15958C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47113983 | |||||||
| chr2:47114007 | C | A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+15934G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114007 | |||||||
| chr2:47114022 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+15919A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114022 | |||||||
| chr2:47114033 | AAAAAAC | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+15902_519+1590 others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114033 | |||||||
| chr2:47114040 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+15901T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114040 | |||||||
| chr2:47114085 | A | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+15856T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114085 | |||||||
| chr2:47114149 | T | C | 1 | a0002c0002t0001g0306 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.519+15792A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114149 | |||||||
| chr2:47114284 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+15657G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114284 | |||||||
| chr2:47114305 | G | A | 1 | a0002c0002t0001g0288 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.519+15636C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114305 | |||||||
| chr2:47114379 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+15562G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114379 | |||||||
| chr2:47114477 | C | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+15464G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114477 | |||||||
| chr2:47114478 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+15463C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114478 | |||||||
| chr2:47114547 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0082 a0001c0001t0001g0104 |
3 | NA18986.hp1 NA19064.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.519+15394G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114547 | |||||||
| chr2:47114631 | A | G | 1 | a0010c0010t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.519+15310T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114631 | |||||||
| chr2:47114777 | AT | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+15163delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114777 | |||||||
| chr2:47114861 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+15080C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114861 | |||||||
| chr2:47114960 | G | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+14981C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47114960 | |||||||
| chr2:47115061 | C | A | 1 | a0001c0001t0001g0205 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.519+14880G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115061 | |||||||
| chr2:47115171 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+14770T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115171 | |||||||
| chr2:47115182 | T | A | 4 | a0001c0001t0001g0238 a0002c0002t0001g0280 a0002c0002t0001g0281 others(1): Show |
4 | HG01099.hp1 HG01192.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+14759A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115182 | |||||||
| chr2:47115204 | T | C | 41 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0147 others(38): Show |
41 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+14737A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115204 | |||||||
| chr2:47115385 | T | C | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.519+14556A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115385 | |||||||
| chr2:47115399 | G | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0136 a0001c0001t0001g0137 others(84): Show |
88 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.519+14542C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115399 | |||||||
| chr2:47115501 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.519+14440G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115501 | |||||||
| chr2:47115543 | T | C | 1 | a0002c0002t0001g0303 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.519+14398A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115543 | |||||||
| chr2:47115551 | G | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+14390C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115551 | |||||||
| chr2:47115651 | G | GTT | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+14289_519+1429 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115651 | |||||||
| chr2:47115652 | C | CT | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0066 others(219): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.519+14288dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115652 | |||||||
| chr2:47115652 | C | CTT | 26 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0072 others(23): Show |
26 | HG00438.hp2 HG00597.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.519+14287_519+1428 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115652 | |||||||
| chr2:47115652 | C | CTTT | 23 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(20): Show |
24 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.519+14286_519+1428 others(7): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115652 | |||||||
| chr2:47115652 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+14289G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115652 | |||||||
| chr2:47115675 | C | T | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+14266G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115675 | |||||||
| chr2:47115677 | G | C | 2 | a0001c0001t0001g0216 a0009c0014t0001g0107 |
2 | HG02109.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.519+14264C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115677 | |||||||
| chr2:47115684 | G | A | 1 | a0010c0010t0001g0028 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.519+14257C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115684 | |||||||
| chr2:47115844 | G | A | 8 | a0001c0001t0001g0119 a0001c0001t0001g0321 a0001c0001t0001g0322 others(5): Show |
8 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.519+14097C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115844 | |||||||
| chr2:47115924 | G | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+14017C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115924 | |||||||
| chr2:47115933 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0002c0002t0001g0299 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+14008G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47115933 | |||||||
| chr2:47116001 | G | A | 19 | a0001c0001t0001g0247 a0002c0002t0001g0004 a0002c0002t0001g0292 others(16): Show |
20 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.519+13940C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116001 | |||||||
| chr2:47116178 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0131 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.519+13763A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116178 | |||||||
| chr2:47116180 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.519+13761G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116180 | |||||||
| chr2:47116186 | C | G | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.519+13755G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116186 | |||||||
| chr2:47116204 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.519+13737C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116204 | |||||||
| chr2:47116212 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.519+13729C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116212 | |||||||
| chr2:47116277 | G | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 |
3 | HG02647.hp1 HG03130.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.519+13664C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116277 | |||||||
| chr2:47116311 | G | T | 9 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.519+13630C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116311 | |||||||
| chr2:47116782 | A | G | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.519+13159T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116782 | |||||||
| chr2:47116811 | A | G | 1 | a0002c0002t0001g0302 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.519+13130T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116811 | |||||||
| chr2:47116871 | T | TCAAAATC | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+13069_519+1307 others(11): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116871 | |||||||
| chr2:47116957 | A | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12984T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116957 | |||||||
| chr2:47116972 | G | T | 6 | a0001c0001t0001g0095 a0001c0001t0001g0132 a0001c0001t0001g0133 others(3): Show |
6 | HG02004.hp2 NA18961.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+12969C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47116972 | |||||||
| chr2:47117126 | G | A | 1 | a0001c0012t0001g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.519+12815C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117126 | |||||||
| chr2:47117189 | C | G | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12752G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117189 | |||||||
| chr2:47117200 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.519+12741G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117200 | |||||||
| chr2:47117329 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.519+12612G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117329 | |||||||
| chr2:47117335 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12606C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117335 | |||||||
| chr2:47117350 | G | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(40): Show |
44 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.519+12591C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117350 | |||||||
| chr2:47117413 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12528A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117413 | |||||||
| chr2:47117455 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12486A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117455 | |||||||
| chr2:47117485 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0324 others(1): Show |
4 | HG01255.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+12456T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117485 | |||||||
| chr2:47117486 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.519+12455C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117486 | |||||||
| chr2:47117749 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12192G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117749 | |||||||
| chr2:47117801 | T | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+12140A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117801 | |||||||
| chr2:47117877 | G | C | 1 | a0003c0003t0001g0053 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.519+12064C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117877 | |||||||
| chr2:47117915 | CAT | C | 17 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0123 others(14): Show |
17 | HG00738.hp2 HG01167.hp2 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.519+12024_519+1202 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117915 | |||||||
| chr2:47117927 | TA | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0073 others(85): Show |
89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.519+12013delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117927 | |||||||
| chr2:47117929 | TA | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 others(73): Show |
78 | HG00323.hp2 HG00609.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.519+12011delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117929 | |||||||
| chr2:47117930 | A | ATATATAT others(4): Show |
7 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(4): Show |
7 | HG01884.hp1 HG02723.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+12010_519+1201 others(15): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117930 | |||||||
| chr2:47117930 | A | ATATATAT others(4): Show |
2 | a0003c0003t0001g0022 a0003c0003t0001g0023 |
2 | HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.519+12010_519+1201 others(15): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117930 | |||||||
| chr2:47117930 | A | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0070 a0001c0001t0001g0073 others(98): Show |
102 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(99): Show |
intron_variant | MODIFIER | c.519+12011T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117930 | |||||||
| chr2:47117930 | AT | A | 7 | a0001c0001t0001g0116 a0001c0001t0001g0121 a0001c0001t0001g0140 others(4): Show |
7 | HG01884.hp2 HG02622.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+12010delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117930 | |||||||
| chr2:47117930 | ATT | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0075 a0001c0001t0001g0098 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+12009_519+1201 others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117930 | |||||||
| chr2:47117931 | T | TA | 4 | a0002c0002t0001g0285 a0002c0002t0001g0310 a0002c0002t0001g0311 others(1): Show |
4 | HG00642.hp2 HG02258.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+12009_519+1201 others(5): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117931 | |||||||
| chr2:47117932 | T | A | 13 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0079 others(10): Show |
13 | HG00738.hp1 HG01099.hp2 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.519+12009A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117932 | |||||||
| chr2:47117934 | T | A | 1 | a0001c0001t0001g0081 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.519+12007A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117934 | |||||||
| chr2:47117978 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+11963G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117978 | |||||||
| chr2:47117999 | G | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11942C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47117999 | |||||||
| chr2:47118111 | C | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+11830G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118111 | |||||||
| chr2:47118247 | C | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+11694G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118247 | |||||||
| chr2:47118291 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11650G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118291 | |||||||
| chr2:47118292 | G | A | 3 | a0002c0002t0001g0305 a0002c0002t0001g0306 a0004c0005t0001g0013 |
3 | HG01943.hp2 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.519+11649C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118292 | |||||||
| chr2:47118369 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11572G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118369 | |||||||
| chr2:47118418 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11523C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118418 | |||||||
| chr2:47118422 | C | G | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.519+11519G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118422 | |||||||
| chr2:47118440 | T | C | 43 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(40): Show |
44 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.519+11501A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118440 | |||||||
| chr2:47118441 | A | G | 3 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02145.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.519+11500T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118441 | |||||||
| chr2:47118537 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11404G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118537 | |||||||
| chr2:47118567 | G | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+11374C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118567 | |||||||
| chr2:47118604 | G | A | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.519+11337C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118604 | |||||||
| chr2:47118618 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+11323A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118618 | |||||||
| chr2:47118685 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.519+11256A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118685 | |||||||
| chr2:47118788 | T | C | 2 | a0003c0003t0001g0029 a0003c0003t0001g0030 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.519+11153A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118788 | |||||||
| chr2:47118789 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.519+11152C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118789 | |||||||
| chr2:47118827 | T | C | 24 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+11114A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118827 | |||||||
| chr2:47118831 | C | T | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+11110G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118831 | |||||||
| chr2:47118935 | G | T | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.519+11006C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118935 | |||||||
| chr2:47118965 | T | A | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+10976A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118965 | |||||||
| chr2:47118986 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.519+10955A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47118986 | |||||||
| chr2:47119046 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10895G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119046 | |||||||
| chr2:47119047 | G | A | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.519+10894C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119047 | |||||||
| chr2:47119127 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.519+10814C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119127 | |||||||
| chr2:47119190 | T | G | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(278): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.519+10751A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119190 | |||||||
| chr2:47119429 | C | G | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.519+10512G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119429 | |||||||
| chr2:47119655 | C | G | 5 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+10286G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119655 | |||||||
| chr2:47119664 | TA | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10276delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119664 | |||||||
| chr2:47119674 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.519+10267G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119674 | |||||||
| chr2:47119675 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(37): Show |
41 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.519+10266C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119675 | |||||||
| chr2:47119752 | A | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10189T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119752 | |||||||
| chr2:47119797 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.519+10144T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119797 | |||||||
| chr2:47119798 | G | C | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10143C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119798 | |||||||
| chr2:47119818 | T | C | 1 | a0001c0001t0001g0079 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.519+10123A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119818 | |||||||
| chr2:47119830 | TG | T | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0324 others(1): Show |
4 | HG01255.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+10110delC | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119830 | |||||||
| chr2:47119871 | G | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10070C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119871 | |||||||
| chr2:47119889 | G | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(36): Show |
40 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.519+10052C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119889 | |||||||
| chr2:47119950 | C | G | 290 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(287): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.519+9991G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119950 | |||||||
| chr2:47119961 | C | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.519+9980G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47119961 | |||||||
| chr2:47120250 | G | C | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0324 others(1): Show |
4 | HG01255.hp2 HG02572.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+9691C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120250 | |||||||
| chr2:47120354 | A | G | 1 | a0002c0002t0001g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.519+9587T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120354 | |||||||
| chr2:47120446 | G | A | 2 | a0006c0006t0001g0129 a0006c0006t0001g0130 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.519+9495C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120446 | |||||||
| chr2:47120532 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.519+9409T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120532 | |||||||
| chr2:47120566 | CA | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.519+9374delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120566 | |||||||
| chr2:47120627 | G | A | 2 | a0002c0002t0001g0277 a0002c0002t0001g0278 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.519+9314C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120627 | |||||||
| chr2:47120656 | G | T | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+9285C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120656 | |||||||
| chr2:47120750 | T | G | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(248): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.519+9191A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120750 | |||||||
| chr2:47120779 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519+9162C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47120779 | |||||||
| chr2:47121016 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+8925C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121016 | |||||||
| chr2:47121017 | C | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(21): Show |
25 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.519+8924G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121017 | |||||||
| chr2:47121018 | A | T | 5 | a0001c0001t0001g0118 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
5 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+8923T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121018 | |||||||
| chr2:47121038 | G | T | 2 | a0001c0001t0001g0152 a0001c0001t0001g0153 |
2 | NA18955.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.519+8903C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121038 | |||||||
| chr2:47121089 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+8852T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121089 | |||||||
| chr2:47121144 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+8797C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121144 | |||||||
| chr2:47121179 | A | T | 1 | a0002c0002t0001g0302 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.519+8762T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121179 | |||||||
| chr2:47121186 | C | T | 4 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0084 others(1): Show |
4 | HG00597.hp2 HG02027.hp1 HG02071.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+8755G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121186 | |||||||
| chr2:47121208 | C | T | 238 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.519+8733G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121208 | |||||||
| chr2:47121233 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.519+8708G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121233 | |||||||
| chr2:47121268 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+8673C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121268 | |||||||
| chr2:47121422 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.519+8519G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121422 | |||||||
| chr2:47121516 | A | G | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+8425T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121516 | |||||||
| chr2:47121616 | A | G | 12 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.519+8325T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121616 | |||||||
| chr2:47121777 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(27): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.519+8164G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121777 | |||||||
| chr2:47121847 | C | CGT | 11 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(8): Show |
11 | HG01099.hp2 HG01891.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+8092_519+8093d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGT | 16 | a0001c0001t0001g0067 a0001c0001t0001g0079 a0001c0001t0001g0083 others(13): Show |
16 | HG01074.hp1 HG01884.hp2 HG02132.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+8090_519+8093d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGTGT | 8 | a0001c0001t0001g0068 a0001c0001t0001g0108 a0001c0001t0001g0109 others(5): Show |
9 | HG02109.hp1 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.519+8088_519+8093d others(8): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGTGTG others(1): Show |
15 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0086 others(12): Show |
15 | HG01243.hp2 HG01255.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.519+8086_519+8093d others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGTGTG others(3): Show |
18 | a0001c0001t0001g0099 a0001c0001t0001g0117 a0001c0001t0001g0121 others(15): Show |
18 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.519+8084_519+8093d others(12): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGTGTG others(5): Show |
5 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0100 others(2): Show |
6 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+8082_519+8093d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | C | CGTGTGTG others(7): Show |
1 | a0002c0002t0001g0331 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.519+8080_519+8093d others(16): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | CGTGTGTG others(1): Show |
C | 11 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0136 others(8): Show |
11 | HG00099.hp2 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.519+8086_519+8093d others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | CGTGTGTG others(3): Show |
C | 225 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(222): Show |
228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.519+8084_519+8093d others(12): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | CGTGTGTG others(5): Show |
C | 15 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(12): Show |
15 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.519+8082_519+8093d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121847 | CGTGTGTG others(7): Show |
C | 2 | a0001c0001t0001g0148 a0001c0001t0001g0188 |
2 | HG00597.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.519+8080_519+8093d others(16): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121847 | |||||||
| chr2:47121972 | G | A | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(282): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.519+7969C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47121972 | |||||||
| chr2:47122054 | A | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0070 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.519+7887T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122054 | |||||||
| chr2:47122290 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(47): Show |
51 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.519+7651C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122290 | |||||||
| chr2:47122427 | T | G | 1 | a0003c0003t0001g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.519+7514A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122427 | |||||||
| chr2:47122672 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+7269C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122672 | |||||||
| chr2:47122686 | AT | A | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(240): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.519+7254delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122686 | |||||||
| chr2:47122697 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.519+7244A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122697 | |||||||
| chr2:47122801 | T | TTTTG | 91 | a0001c0001t0001g0069 a0001c0001t0001g0136 a0001c0001t0001g0147 others(88): Show |
92 | HG00140.hp2 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.519+7136_519+7139d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122801 | |||||||
| chr2:47122815 | C | T | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.519+7126G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122815 | |||||||
| chr2:47122951 | G | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.519+6990C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122951 | |||||||
| chr2:47122957 | C | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.519+6984G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122957 | |||||||
| chr2:47122971 | G | A | 1 | a0004c0004t0001g0016 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.519+6970C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122971 | |||||||
| chr2:47122982 | C | T | 1 | a0005c0008t0001g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.519+6959G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122982 | |||||||
| chr2:47122988 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.519+6953C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47122988 | |||||||
| chr2:47123076 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.519+6865A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123076 | |||||||
| chr2:47123237 | T | G | 1 | a0001c0001t0001g0159 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.519+6704A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123237 | |||||||
| chr2:47123333 | T | A | 1 | a0001c0001t0001g0342 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.519+6608A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123333 | |||||||
| chr2:47123546 | G | A | 11 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(8): Show |
11 | HG01109.hp1 HG01243.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+6395C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123546 | |||||||
| chr2:47123669 | A | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(318): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.519+6272T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123669 | |||||||
| chr2:47123707 | TAAATC | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(14): Show |
18 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.519+6229_519+6233d others(7): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123707 | |||||||
| chr2:47123723 | G | A | 14 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(11): Show |
14 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.519+6218C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123723 | |||||||
| chr2:47123973 | T | TTTTA | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+5964_519+5967d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123973 | |||||||
| chr2:47123988 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.519+5953A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123988 | |||||||
| chr2:47123993 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+5948T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47123993 | |||||||
| chr2:47124127 | C | T | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.519+5814G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124127 | |||||||
| chr2:47124136 | C | G | 2 | a0003c0003t0001g0029 a0003c0003t0001g0030 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.519+5805G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124136 | |||||||
| chr2:47124373 | C | A | 1 | a0002c0002t0001g0289 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.519+5568G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124373 | |||||||
| chr2:47124458 | T | C | 1 | a0001c0001t0001g0083 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.519+5483A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124458 | |||||||
| chr2:47124574 | T | C | 4 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | NA18942.hp1 NA18944.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+5367A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124574 | |||||||
| chr2:47124592 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.519+5349T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124592 | |||||||
| chr2:47124597 | G | C | 11 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.519+5344C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124597 | |||||||
| chr2:47124614 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0099 others(33): Show |
37 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.519+5327G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124614 | |||||||
| chr2:47124628 | G | A | 12 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+5313C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124628 | |||||||
| chr2:47124679 | T | C | 12 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+5262A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124679 | |||||||
| chr2:47124771 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+5170A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124771 | |||||||
| chr2:47124795 | AT | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0220 a0001c0001t0001g0221 |
3 | HG00438.hp2 NA18973.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.519+5145delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124795 | |||||||
| chr2:47124856 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.519+5085C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124856 | |||||||
| chr2:47124931 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.519+5010G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124931 | |||||||
| chr2:47124943 | T | C | 5 | a0001c0001t0001g0175 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG00438.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.519+4998A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124943 | |||||||
| chr2:47124967 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.519+4974G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47124967 | |||||||
| chr2:47125140 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.519+4801C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125140 | |||||||
| chr2:47125420 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.519+4521G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125420 | |||||||
| chr2:47125514 | C | A | 3 | a0003c0003t0001g0041 a0003c0003t0001g0042 a0003c0003t0001g0043 |
3 | NA18954.hp2 NA18962.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.519+4427G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125514 | |||||||
| chr2:47125523 | T | C | 3 | a0002c0002t0001g0302 a0002c0002t0001g0303 a0004c0005t0001g0014 |
3 | HG02080.hp2 HG02129.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.519+4418A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125523 | |||||||
| chr2:47125599 | C | T | 49 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0099 others(46): Show |
50 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.519+4342G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125599 | |||||||
| chr2:47125629 | G | C | 1 | a0001c0015t0001g0164 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.519+4312C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125629 | |||||||
| chr2:47125724 | A | AT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.519+4216dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125724 | |||||||
| chr2:47125724 | A | ATT | 52 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(49): Show |
53 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.519+4215_519+4216d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125724 | |||||||
| chr2:47125787 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+4154C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125787 | |||||||
| chr2:47125789 | G | T | 1 | a0002c0002t0001g0293 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.519+4152C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125789 | |||||||
| chr2:47125822 | G | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+4119C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125822 | |||||||
| chr2:47125961 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.519+3980G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47125961 | |||||||
| chr2:47126019 | A | G | 1 | a0003c0003t0001g0044 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.519+3922T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126019 | |||||||
| chr2:47126025 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02145.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.519+3916A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126025 | |||||||
| chr2:47126120 | A | T | 12 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(9): Show |
12 | HG00738.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+3821T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126120 | |||||||
| chr2:47126240 | T | G | 6 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0078 others(3): Show |
6 | HG00597.hp2 HG02027.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.519+3701A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126240 | |||||||
| chr2:47126271 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.519+3670A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126271 | |||||||
| chr2:47126282 | C | T | 12 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.519+3659G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126282 | |||||||
| chr2:47126292 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.519+3649A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126292 | |||||||
| chr2:47126348 | C | A | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.519+3593G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126348 | |||||||
| chr2:47126350 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.519+3591C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126350 | |||||||
| chr2:47126418 | T | C | 3 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02145.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.519+3523A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126418 | |||||||
| chr2:47126425 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0068 others(245): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.519+3516C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126425 | |||||||
| chr2:47126457 | A | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.519+3484T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126457 | |||||||
| chr2:47126534 | C | G | 4 | a0001c0001t0001g0154 a0001c0001t0001g0157 a0001c0001t0001g0158 others(1): Show |
4 | NA18942.hp1 NA18944.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+3407G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126534 | |||||||
| chr2:47126592 | G | A | 231 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.519+3349C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126592 | |||||||
| chr2:47126691 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(265): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.519+3250C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126691 | |||||||
| chr2:47126747 | GTATT | G | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+3190_519+3193d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126747 | |||||||
| chr2:47126801 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.519+3140T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126801 | |||||||
| chr2:47126802 | GT | G | 15 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0075 others(12): Show |
15 | HG01099.hp2 HG01978.hp1 HG01993.hp1 others(12): Show |
intron_variant | MODIFIER | c.519+3138delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126802 | |||||||
| chr2:47126816 | G | A | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.519+3125C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126816 | |||||||
| chr2:47126914 | T | C | 5 | a0002c0002t0001g0004 a0002c0002t0001g0304 a0002c0002t0001g0305 others(2): Show |
6 | HG00642.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+3027A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126914 | |||||||
| chr2:47126978 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2963C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47126978 | |||||||
| chr2:47127065 | G | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2876C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127065 | |||||||
| chr2:47127068 | C | T | 1 | a0001c0001t0001g0324 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.519+2873G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127068 | |||||||
| chr2:47127132 | G | T | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+2809C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127132 | |||||||
| chr2:47127165 | A | AT | 3 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02145.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.519+2775dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127165 | |||||||
| chr2:47127203 | T | C | 1 | a0008c0013t0001g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.519+2738A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127203 | |||||||
| chr2:47127245 | G | GCTCA | 29 | a0001c0001t0001g0068 a0001c0001t0001g0118 a0001c0001t0001g0119 others(26): Show |
29 | HG00738.hp2 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.519+2695_519+2696i others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127245 | |||||||
| chr2:47127248 | A | C | 19 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(16): Show |
20 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.519+2693T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127248 | |||||||
| chr2:47127249 | ATTCTTTT others(1): Show |
A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2684_519+2691d others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127249 | |||||||
| chr2:47127249 | ATTCTTTT others(5): Show |
A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+2680_519+2691d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127249 | |||||||
| chr2:47127249 | ATTCTTTT others(6): Show |
A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+2679_519+2691d others(15): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127249 | |||||||
| chr2:47127252 | C | CT | 19 | a0001c0001t0001g0120 a0001c0001t0001g0136 a0001c0012t0001g0122 others(16): Show |
19 | HG00323.hp1 HG00408.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.519+2688dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTT | 13 | a0001c0001t0001g0121 a0001c0001t0001g0147 a0001c0001t0001g0321 others(10): Show |
13 | HG00738.hp2 HG02280.hp1 HG02738.hp2 others(10): Show |
intron_variant | MODIFIER | c.519+2687_519+2688d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTT | 7 | a0001c0001t0001g0340 a0001c0001t0001g0341 a0003c0003t0001g0038 others(4): Show |
7 | HG00621.hp1 HG00741.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.519+2686_519+2688d others(5): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTT | 8 | a0001c0001t0001g0322 a0002c0002t0001g0311 a0002c0002t0001g0312 others(5): Show |
8 | HG02258.hp2 HG02280.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+2685_519+2688d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT | 10 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(7): Show |
10 | HG01884.hp1 HG01891.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.519+2682_519+2688d others(9): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT others(1): Show |
16 | a0001c0001t0001g0069 a0001c0001t0001g0263 a0001c0001t0001g0274 others(13): Show |
16 | HG01081.hp2 HG01099.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2681_519+2688d others(10): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT others(2): Show |
20 | a0001c0001t0001g0148 a0001c0001t0001g0275 a0002c0002t0001g0004 others(17): Show |
21 | HG00140.hp2 HG00609.hp1 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.519+2680_519+2688d others(11): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT others(3): Show |
3 | a0002c0002t0001g0277 a0002c0002t0001g0287 a0002c0002t0001g0305 |
3 | HG01952.hp1 HG02897.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.519+2679_519+2688d others(12): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0115 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.519+2678_519+2688d others(13): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0114 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.519+2677_519+2688d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CT | C | 38 | a0001c0001t0001g0066 a0001c0001t0001g0072 a0001c0001t0001g0075 others(35): Show |
39 | HG01074.hp1 HG01099.hp2 HG01255.hp2 others(36): Show |
intron_variant | MODIFIER | c.519+2688delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTT | C | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0068 others(4): Show |
7 | HG01891.hp2 HG01993.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.519+2687_519+2688d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0217 others(5): Show |
8 | HG01358.hp1 HG02027.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.519+2680_519+2688d others(11): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTTTTTTT others(3): Show |
C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0092 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.519+2679_519+2688d others(12): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTTTTTTT others(4): Show |
C | 1 | a0008c0013t0001g0174 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.519+2678_519+2688d others(13): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTTTTTTT others(5): Show |
C | 1 | a0004c0005t0001g0014 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.519+2677_519+2688d others(14): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127252 | CTTTTTTT others(6): Show |
C | 6 | a0002c0002t0001g0294 a0002c0002t0001g0295 a0002c0002t0001g0297 others(3): Show |
6 | HG00621.hp2 HG02129.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.519+2676_519+2688d others(15): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127252 | |||||||
| chr2:47127258 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2683A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127258 | |||||||
| chr2:47127260 | T | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2681A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127260 | |||||||
| chr2:47127261 | T | A | 15 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2680A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127261 | |||||||
| chr2:47127262 | T | C | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+2679A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127262 | |||||||
| chr2:47127263 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+2678A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127263 | |||||||
| chr2:47127264 | T | A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+2677A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127264 | |||||||
| chr2:47127264 | T | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(12): Show |
16 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.519+2677A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127264 | |||||||
| chr2:47127265 | T | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2676A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127265 | |||||||
| chr2:47127266 | T | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+2675A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127266 | |||||||
| chr2:47127268 | T | C | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+2673A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127268 | |||||||
| chr2:47127269 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.519+2672A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127269 | |||||||
| chr2:47127322 | G | A | 4 | a0001c0001t0001g0179 a0001c0001t0001g0184 a0001c0001t0001g0248 others(1): Show |
4 | HG00323.hp2 HG01074.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.519+2619C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127322 | |||||||
| chr2:47127333 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+2608T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127333 | |||||||
| chr2:47127450 | G | A | 12 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(9): Show |
12 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.519+2491C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127450 | |||||||
| chr2:47127451 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG00741.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.519+2490A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127451 | |||||||
| chr2:47127524 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.519+2417G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127524 | |||||||
| chr2:47127667 | T | A | 3 | a0001c0001t0001g0189 a0001c0001t0001g0222 a0001c0001t0001g0234 |
3 | HG02145.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.519+2274A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127667 | |||||||
| chr2:47127850 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.519+2091A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127850 | |||||||
| chr2:47127902 | G | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+2039C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127902 | |||||||
| chr2:47127960 | T | C | 2 | a0001c0001t0002g0005 a0001c0001t0002g0347 |
3 | HG02109.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.519+1981A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47127960 | |||||||
| chr2:47128004 | G | A | 147 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0070 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.519+1937C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128004 | |||||||
| chr2:47128009 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.519+1932T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128009 | |||||||
| chr2:47128137 | C | A | 52 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0099 others(49): Show |
53 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.519+1804G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128137 | |||||||
| chr2:47128177 | C | A | 1 | a0002c0002t0001g0334 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.519+1764G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128177 | |||||||
| chr2:47128239 | C | G | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(280): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.519+1702G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128239 | |||||||
| chr2:47128615 | T | C | 1 | a0001c0001t0001g0065 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.519+1326A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128615 | |||||||
| chr2:47128710 | G | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519+1231C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128710 | |||||||
| chr2:47128910 | A | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+1031T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128910 | |||||||
| chr2:47128988 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.519+953T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47128988 | |||||||
| chr2:47129052 | A | G | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.519+889T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129052 | |||||||
| chr2:47129106 | G | A | 2 | a0003c0003t0001g0031 a0003c0003t0001g0032 |
2 | HG03017.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.519+835C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129106 | |||||||
| chr2:47129236 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.519+705G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129236 | |||||||
| chr2:47129364 | C | T | 243 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0068 others(240): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.519+577G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129364 | |||||||
| chr2:47129425 | C | G | 1 | a0003c0003t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.519+516G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129425 | |||||||
| chr2:47129532 | C | A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+409G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129532 | |||||||
| chr2:47129632 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.519+309T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129632 | |||||||
| chr2:47129646 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.519+295G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129646 | |||||||
| chr2:47129726 | G | C | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.519+215C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129726 | |||||||
| chr2:47129856 | T | C | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.519+85A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 5/6 | chr2 | 47129856 | |||||||
| chr2:47130047 | G | A | 1 | a0002c0002t0001g0279 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.465-52C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 4/6 | chr2 | 47130047 | |||||||
| chr2:47130054 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.465-59C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 4/6 | chr2 | 47130054 | |||||||
| chr2:47130149 | T | A | 4 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0223 others(1): Show |
4 | HG02083.hp2 NA18955.hp2 NA18982.hp2 others(1): Show |
intron_variant | MODIFIER | c.464+47A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 4/6 | chr2 | 47130149 | |||||||
| chr2:47130287 | T | C | 3 | a0003c0003t0001g0027 a0003c0003t0001g0038 a0003c0003t0001g0039 |
3 | HG00741.hp1 HG02896.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.400-27A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130287 | |||||||
| chr2:47130319 | A | G | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.400-59T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130319 | |||||||
| chr2:47130330 | G | A | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.400-70C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130330 | |||||||
| chr2:47130425 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(183): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.400-165T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130425 | |||||||
| chr2:47130554 | C | T | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.400-294G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130554 | |||||||
| chr2:47130568 | T | A | 13 | a0001c0001t0001g0118 a0001c0001t0001g0126 a0001c0001t0001g0131 others(10): Show |
13 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.400-308A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130568 | |||||||
| chr2:47130568 | T | G | 1 | a0001c0001t0001g0185 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.400-308A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130568 | |||||||
| chr2:47130590 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-330C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130590 | |||||||
| chr2:47130655 | G | C | 278 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(275): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.400-395C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130655 | |||||||
| chr2:47130740 | C | A | 10 | a0001c0001t0001g0126 a0001c0001t0001g0131 a0001c0001t0001g0178 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-480G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130740 | |||||||
| chr2:47130785 | G | C | 1 | a0005c0008t0001g0346 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.400-525C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130785 | |||||||
| chr2:47130934 | C | T | 36 | a0001c0001t0001g0136 a0001c0001t0001g0147 a0003c0003t0001g0026 others(33): Show |
36 | HG00323.hp1 HG00408.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.400-674G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130934 | |||||||
| chr2:47130962 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0124 others(3): Show |
6 | HG01891.hp2 HG02615.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.400-702C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47130962 | |||||||
| chr2:47131211 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.400-951G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131211 | |||||||
| chr2:47131339 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0092 others(142): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.400-1079G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131339 | |||||||
| chr2:47131471 | C | T | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.400-1211G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131471 | |||||||
| chr2:47131499 | C | T | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0092 others(143): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.400-1239G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131499 | |||||||
| chr2:47131577 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.400-1317T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131577 | |||||||
| chr2:47131848 | C | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.400-1588G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131848 | |||||||
| chr2:47131857 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.400-1597A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131857 | |||||||
| chr2:47131922 | C | T | 155 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0068 others(152): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.400-1662G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131922 | |||||||
| chr2:47131989 | A | G | 1 | a0002c0002t0001g0283 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.400-1729T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47131989 | |||||||
| chr2:47132007 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.400-1747T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132007 | |||||||
| chr2:47132096 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.400-1836G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132096 | |||||||
| chr2:47132164 | GA | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0099 others(119): Show |
124 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.400-1905delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132164 | |||||||
| chr2:47132165 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0068 others(154): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.400-1905T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132165 | |||||||
| chr2:47132166 | A | G | 86 | a0001c0001t0001g0069 a0001c0001t0001g0114 a0001c0001t0001g0115 others(83): Show |
87 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.400-1906T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132166 | |||||||
| chr2:47132167 | A | G | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.400-1907T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132167 | |||||||
| chr2:47132226 | G | A | 1 | a0001c0001t0001g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.400-1966C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132226 | |||||||
| chr2:47132527 | A | T | 37 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(34): Show |
38 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.400-2267T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132527 | |||||||
| chr2:47132628 | G | C | 1 | a0001c0001t0001g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.400-2368C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132628 | |||||||
| chr2:47132650 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.400-2390G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132650 | |||||||
| chr2:47132671 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.400-2411G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132671 | |||||||
| chr2:47132715 | C | T | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-2455G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132715 | |||||||
| chr2:47132907 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.400-2647A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47132907 | |||||||
| chr2:47133087 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.400-2827C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133087 | |||||||
| chr2:47133173 | CT | C | 18 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0118 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.400-2914delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133173 | |||||||
| chr2:47133228 | C | T | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-2968G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133228 | |||||||
| chr2:47133474 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18980.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.400-3214G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133474 | |||||||
| chr2:47133570 | C | CT | 18 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0110 others(15): Show |
19 | HG01255.hp2 HG01884.hp1 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.400-3311dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTT | 11 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0067 others(8): Show |
11 | HG01891.hp1 HG02145.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.400-3312_400-3311d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTT | 10 | a0001c0001t0001g0136 a0001c0001t0001g0157 a0001c0001t0001g0186 others(7): Show |
10 | HG02523.hp2 HG02896.hp1 HG03491.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-3314_400-3311d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTT | 202 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(199): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.400-3315_400-3311d others(7): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTTT | 28 | a0001c0001t0001g0068 a0001c0001t0001g0132 a0001c0001t0001g0148 others(25): Show |
28 | HG00597.hp1 HG01175.hp1 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.400-3316_400-3311d others(8): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTTTT others(2): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0146 others(7): Show |
11 | HG00639.hp1 HG00639.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.400-3319_400-3311d others(11): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0264 a0004c0004t0001g0010 |
3 | HG00735.hp1 HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.400-3320_400-3311d others(12): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01167.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.400-3321_400-3311d others(13): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133570 | C | CTTTTTTT others(6): Show |
1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-3323_400-3311d others(15): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133570 | |||||||
| chr2:47133639 | G | A | 64 | a0001c0001t0001g0069 a0001c0001t0001g0136 a0001c0001t0001g0147 others(61): Show |
64 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.400-3379C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133639 | |||||||
| chr2:47133698 | C | T | 2 | a0001c0001t0001g0178 a0001c0001t0001g0250 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.400-3438G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133698 | |||||||
| chr2:47133923 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.400-3663C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133923 | |||||||
| chr2:47133932 | T | C | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-3672A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47133932 | |||||||
| chr2:47134037 | C | CATACAT | 28 | a0001c0001t0001g0093 a0001c0001t0001g0113 a0001c0001t0001g0119 others(25): Show |
28 | HG00323.hp2 HG00738.hp2 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.400-3783_400-3778d others(8): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134037 | |||||||
| chr2:47134037 | C | CATACATA others(17): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0146 others(11): Show |
15 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(12): Show |
intron_variant | MODIFIER | c.400-3801_400-3778d others(26): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134037 | |||||||
| chr2:47134037 | C | CATACATA others(23): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0258 |
2 | HG00738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.400-3778_400-3777i others(32): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134037 | |||||||
| chr2:47134148 | C | A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.400-3888G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134148 | |||||||
| chr2:47134153 | C | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(131): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.400-3893G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134153 | |||||||
| chr2:47134281 | T | G | 5 | a0001c0001t0001g0175 a0001c0001t0001g0227 a0001c0001t0001g0228 others(2): Show |
5 | HG00438.hp1 HG02165.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-4021A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134281 | |||||||
| chr2:47134287 | A | G | 9 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-4027T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134287 | |||||||
| chr2:47134330 | G | A | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.400-4070C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134330 | |||||||
| chr2:47134496 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.400-4236C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134496 | |||||||
| chr2:47134840 | T | C | 5 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(2): Show |
5 | HG00738.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-4580A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134840 | |||||||
| chr2:47134859 | C | T | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-4599G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47134859 | |||||||
| chr2:47135090 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(160): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.400-4830T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135090 | |||||||
| chr2:47135100 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.400-4840A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135100 | |||||||
| chr2:47135118 | C | T | 88 | a0001c0001t0001g0069 a0001c0001t0001g0114 a0001c0001t0001g0115 others(85): Show |
89 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
intron_variant | MODIFIER | c.400-4858G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135118 | |||||||
| chr2:47135235 | T | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(276): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.400-4975A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135235 | |||||||
| chr2:47135561 | A | G | 2 | a0001c0001t0001g0235 a0001c0001t0001g0314 |
2 | HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.400-5301T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135561 | |||||||
| chr2:47135588 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.400-5328A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135588 | |||||||
| chr2:47135665 | G | A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.400-5405C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135665 | |||||||
| chr2:47135732 | T | G | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.400-5472A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135732 | |||||||
| chr2:47135743 | A | G | 1 | a0005c0008t0001g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.400-5483T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135743 | |||||||
| chr2:47135790 | G | A | 4 | a0003c0003t0001g0029 a0003c0003t0001g0030 a0003c0003t0001g0034 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.400-5530C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135790 | |||||||
| chr2:47135828 | C | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.400-5568G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135828 | |||||||
| chr2:47135893 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.400-5633T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47135893 | |||||||
| chr2:47136207 | G | A | 3 | a0001c0001t0001g0258 a0002c0002t0001g0277 a0002c0002t0001g0278 |
3 | HG00738.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.400-5947C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136207 | |||||||
| chr2:47136290 | C | T | 8 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-6030G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136290 | |||||||
| chr2:47136292 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.400-6032G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136292 | |||||||
| chr2:47136302 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(274): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.400-6042A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136302 | |||||||
| chr2:47136389 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-6129C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136389 | |||||||
| chr2:47136390 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0064 a0001c0001t0001g0065 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.400-6130G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136390 | |||||||
| chr2:47136438 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(272): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.400-6178T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136438 | |||||||
| chr2:47136543 | G | A | 1 | a0002c0002t0001g0282 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.400-6283C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136543 | |||||||
| chr2:47136628 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0136 others(95): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.400-6368T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136628 | |||||||
| chr2:47136723 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-6463C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136723 | |||||||
| chr2:47136799 | T | C | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.400-6539A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136799 | |||||||
| chr2:47136815 | A | T | 5 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0340 others(2): Show |
5 | HG00738.hp2 HG02886.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-6555T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136815 | |||||||
| chr2:47136822 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.400-6562C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136822 | |||||||
| chr2:47136908 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-6648A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47136908 | |||||||
| chr2:47137073 | A | G | 2 | a0001c0001t0001g0274 a0001c0001t0001g0275 |
2 | HG00609.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.400-6813T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137073 | |||||||
| chr2:47137090 | T | C | 2 | a0001c0001t0001g0121 a0001c0012t0001g0122 |
2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.400-6830A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137090 | |||||||
| chr2:47137197 | A | G | 166 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0064 others(163): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.400-6937T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137197 | |||||||
| chr2:47137260 | T | C | 4 | a0003c0003t0001g0035 a0003c0003t0001g0036 a0003c0003t0001g0037 others(1): Show |
4 | HG00323.hp1 HG01261.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-7000A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137260 | |||||||
| chr2:47137321 | GATAA | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0145 |
3 | NA18987.hp1 NA18997.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.400-7065_400-7062d others(6): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137321 | |||||||
| chr2:47137340 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-7080G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137340 | |||||||
| chr2:47137365 | T | C | 1 | a0004c0004t0001g0010 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.400-7105A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137365 | |||||||
| chr2:47137379 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.400-7119G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137379 | |||||||
| chr2:47137440 | G | A | 10 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.400-7180C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137440 | |||||||
| chr2:47137483 | C | A | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.400-7223G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137483 | |||||||
| chr2:47137520 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.400-7260G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137520 | |||||||
| chr2:47137598 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.400-7338G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137598 | |||||||
| chr2:47137692 | T | G | 1 | a0003c0003t0001g0054 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.400-7432A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137692 | |||||||
| chr2:47137710 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-7450C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137710 | |||||||
| chr2:47137728 | T | C | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0260 others(1): Show |
4 | HG02622.hp1 HG02622.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-7468A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137728 | |||||||
| chr2:47137761 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.400-7501T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137761 | |||||||
| chr2:47137926 | C | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(247): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.400-7666G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47137926 | |||||||
| chr2:47138005 | T | G | 2 | a0001c0001t0001g0260 a0009c0014t0001g0107 |
2 | HG02630.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.400-7745A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138005 | |||||||
| chr2:47138351 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.400-8091C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138351 | |||||||
| chr2:47138393 | G | GT | 8 | a0001c0001t0001g0073 a0001c0001t0001g0084 a0001c0001t0001g0327 others(5): Show |
8 | HG02027.hp1 HG02523.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-8134dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138393 | |||||||
| chr2:47138393 | GT | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
8 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-8134delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138393 | |||||||
| chr2:47138460 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.400-8200G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138460 | |||||||
| chr2:47138570 | A | G | 4 | a0001c0001t0001g0146 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG01070.hp1 HG02735.hp2 HG03239.hp1 others(1): Show |
intron_variant | MODIFIER | c.400-8310T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138570 | |||||||
| chr2:47138675 | A | G | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(258): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.400-8415T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138675 | |||||||
| chr2:47138696 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.400-8436G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138696 | |||||||
| chr2:47138734 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.400-8474C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138734 | |||||||
| chr2:47138738 | C | G | 1 | a0002c0002t0001g0297 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.400-8478G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138738 | |||||||
| chr2:47138738 | C | T | 1 | a0003c0003t0001g0057 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.400-8478G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138738 | |||||||
| chr2:47138747 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.400-8487T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138747 | |||||||
| chr2:47138766 | T | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.400-8506A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138766 | |||||||
| chr2:47138873 | C | T | 3 | a0001c0001t0001g0099 a0001c0001t0001g0235 a0001c0001t0001g0314 |
3 | HG00639.hp2 HG03041.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.400-8613G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138873 | |||||||
| chr2:47138967 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.400-8707C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47138967 | |||||||
| chr2:47139367 | T | A | 12 | a0001c0001t0001g0068 a0001c0001t0001g0260 a0001c0001t0001g0315 others(9): Show |
12 | HG01257.hp2 HG01258.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.400-9107A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139367 | |||||||
| chr2:47139407 | A | AT | 7 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0163 others(4): Show |
7 | HG02486.hp1 HG02630.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.400-9148dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139407 | |||||||
| chr2:47139407 | A | ATT | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0068 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.400-9149_400-9148d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139407 | |||||||
| chr2:47139407 | A | ATTT | 19 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(16): Show |
20 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.400-9150_400-9148d others(5): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139407 | |||||||
| chr2:47139578 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.400-9318G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139578 | |||||||
| chr2:47139778 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-9518A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139778 | |||||||
| chr2:47139841 | T | A | 1 | a0003c0003t0001g0055 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.400-9581A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139841 | |||||||
| chr2:47139939 | C | G | 1 | a0003c0003t0001g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.400-9679G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139939 | |||||||
| chr2:47139957 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.400-9697C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139957 | |||||||
| chr2:47139978 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.400-9718C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47139978 | |||||||
| chr2:47140062 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.400-9802G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47140062 | |||||||
| chr2:47140274 | G | C | 2 | a0001c0001t0002g0005 a0001c0001t0002g0347 |
3 | HG02109.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.400-10014C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47140274 | |||||||
| chr2:47140651 | T | G | 1 | a0003c0003t0001g0042 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.400-10391A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47140651 | |||||||
| chr2:47140818 | C | A | 1 | a0001c0001t0001g0086 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.399+10440G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47140818 | |||||||
| chr2:47140894 | C | CT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(145): Show |
151 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.399+10363dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47140894 | |||||||
| chr2:47141045 | G | A | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18945.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.399+10213C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141045 | |||||||
| chr2:47141136 | C | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+10122G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141136 | |||||||
| chr2:47141177 | G | A | 1 | a0002c0002t0001g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.399+10081C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141177 | |||||||
| chr2:47141226 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.399+10032G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141226 | |||||||
| chr2:47141325 | C | CA | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
7 | HG02257.hp2 HG02630.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+9932dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141325 | |||||||
| chr2:47141325 | CA | C | 13 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0157 others(10): Show |
13 | HG01070.hp2 HG01515.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.399+9932delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141325 | |||||||
| chr2:47141336 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.399+9922T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141336 | |||||||
| chr2:47141339 | A | G | 149 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(146): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.399+9919T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141339 | |||||||
| chr2:47141430 | G | C | 1 | a0001c0001t0001g0234 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.399+9828C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141430 | |||||||
| chr2:47141557 | C | CA | 7 | a0001c0001t0001g0118 a0001c0001t0001g0135 a0001c0001t0001g0145 others(4): Show |
7 | HG03041.hp2 HG03453.hp1 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+9700dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141557 | |||||||
| chr2:47141557 | CA | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0068 a0001c0001t0001g0098 others(26): Show |
30 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.399+9700delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141557 | |||||||
| chr2:47141557 | CAA | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0120 others(96): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.399+9699_399+9700d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141557 | |||||||
| chr2:47141615 | T | C | 249 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0069 others(246): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.399+9643A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141615 | |||||||
| chr2:47141769 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0067 |
3 | HG03041.hp1 HG03139.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.399+9489G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141769 | |||||||
| chr2:47141774 | G | A | 11 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0084 others(8): Show |
11 | HG00597.hp2 HG01243.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.399+9484C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141774 | |||||||
| chr2:47141778 | T | G | 8 | a0001c0001t0001g0118 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.399+9480A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141778 | |||||||
| chr2:47141865 | C | G | 2 | a0002c0002t0001g0280 a0002c0002t0001g0281 |
2 | HG01099.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.399+9393G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141865 | |||||||
| chr2:47141885 | C | T | 4 | a0001c0001t0001g0113 a0001c0001t0001g0116 a0001c0001t0001g0119 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+9373G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141885 | |||||||
| chr2:47141913 | G | A | 1 | a0002c0002t0001g0309 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.399+9345C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47141913 | |||||||
| chr2:47142052 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+9206A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142052 | |||||||
| chr2:47142055 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.399+9203A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142055 | |||||||
| chr2:47142251 | T | C | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.399+9007A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142251 | |||||||
| chr2:47142274 | CA | C | 284 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(281): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.399+8983delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142274 | |||||||
| chr2:47142464 | T | A | 5 | a0003c0003t0001g0019 a0003c0003t0001g0020 a0003c0003t0001g0021 others(2): Show |
5 | HG01884.hp1 HG01891.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+8794A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142464 | |||||||
| chr2:47142525 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.399+8733C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142525 | |||||||
| chr2:47142531 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.399+8727G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142531 | |||||||
| chr2:47142570 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.399+8688A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142570 | |||||||
| chr2:47142649 | C | G | 1 | a0002c0002t0001g0295 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.399+8609G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142649 | |||||||
| chr2:47142836 | C | CT | 26 | a0001c0001t0001g0068 a0001c0001t0001g0071 a0001c0001t0001g0072 others(23): Show |
26 | HG01069.hp2 HG01070.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.399+8421dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142836 | |||||||
| chr2:47142836 | C | CTT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(138): Show |
intron_variant | MODIFIER | c.399+8420_399+8421d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142836 | |||||||
| chr2:47142836 | C | CTTT | 17 | a0001c0001t0001g0092 a0001c0001t0001g0151 a0001c0001t0001g0155 others(14): Show |
17 | HG00438.hp1 HG01175.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+8419_399+8421d others(5): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142836 | |||||||
| chr2:47142836 | CT | C | 15 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(12): Show |
15 | HG00741.hp1 HG01109.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.399+8421delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47142836 | |||||||
| chr2:47143024 | G | C | 12 | a0001c0001t0001g0068 a0001c0001t0001g0108 a0001c0001t0001g0110 others(9): Show |
12 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.399+8234C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143024 | |||||||
| chr2:47143122 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 |
3 | NA18952.hp1 NA18980.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.399+8136C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143122 | |||||||
| chr2:47143286 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.399+7972C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143286 | |||||||
| chr2:47143433 | CT | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+7824delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143433 | |||||||
| chr2:47143517 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.399+7741C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143517 | |||||||
| chr2:47143531 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.399+7727C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143531 | |||||||
| chr2:47143545 | A | G | 297 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(294): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.399+7713T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143545 | |||||||
| chr2:47143587 | G | A | 4 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(1): Show |
4 | HG02257.hp2 HG02809.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+7671C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143587 | |||||||
| chr2:47143634 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.399+7624G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143634 | |||||||
| chr2:47143647 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.399+7611C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47143647 | |||||||
| chr2:47144052 | C | G | 3 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 |
3 | HG02257.hp2 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.399+7206G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144052 | |||||||
| chr2:47144651 | T | C | 1 | a0003c0003t0001g0061 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.399+6607A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144651 | |||||||
| chr2:47144656 | G | A | 1 | a0005c0008t0001g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.399+6602C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144656 | |||||||
| chr2:47144660 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.399+6598C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144660 | |||||||
| chr2:47144707 | A | G | 8 | a0001c0001t0001g0068 a0001c0001t0001g0315 a0001c0001t0001g0316 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.399+6551T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144707 | |||||||
| chr2:47144761 | T | C | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.399+6497A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144761 | |||||||
| chr2:47144794 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(273): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.399+6464T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144794 | |||||||
| chr2:47144833 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+6425G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144833 | |||||||
| chr2:47144839 | T | C | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.399+6419A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144839 | |||||||
| chr2:47144855 | C | T | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+6403G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144855 | |||||||
| chr2:47144865 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.399+6393C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144865 | |||||||
| chr2:47144923 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(142): Show |
146 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(143): Show |
intron_variant | MODIFIER | c.399+6335C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144923 | |||||||
| chr2:47144931 | T | C | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.399+6327A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144931 | |||||||
| chr2:47144949 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.399+6309G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144949 | |||||||
| chr2:47144965 | C | T | 1 | a0001c0001t0001g0318 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.399+6293G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144965 | |||||||
| chr2:47144977 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.399+6281C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47144977 | |||||||
| chr2:47145207 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(141): Show |
145 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(142): Show |
intron_variant | MODIFIER | c.399+6051G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145207 | |||||||
| chr2:47145286 | G | A | 148 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.399+5972C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145286 | |||||||
| chr2:47145301 | G | A | 1 | a0003c0003t0001g0062 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.399+5957C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145301 | |||||||
| chr2:47145335 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0069 a0001c0001t0001g0136 others(105): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.399+5923G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145335 | |||||||
| chr2:47145398 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5860G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145398 | |||||||
| chr2:47145490 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5768C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145490 | |||||||
| chr2:47145491 | C | G | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5767G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145491 | |||||||
| chr2:47145494 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5764A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145494 | |||||||
| chr2:47145495 | T | G | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5763A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145495 | |||||||
| chr2:47145496 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5762A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145496 | |||||||
| chr2:47145504 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.399+5754T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145504 | |||||||
| chr2:47145627 | A | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0098 a0001c0001t0001g0099 others(13): Show |
17 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.399+5631T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145627 | |||||||
| chr2:47145829 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.399+5429G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47145829 | |||||||
| chr2:47146157 | C | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(1): Show |
4 | HG02615.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.399+5101G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146157 | |||||||
| chr2:47146167 | T | C | 2 | a0001c0001t0001g0119 a0003c0003t0001g0017 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.399+5091A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146167 | |||||||
| chr2:47146238 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.399+5020C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146238 | |||||||
| chr2:47146244 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.399+5014C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146244 | |||||||
| chr2:47146307 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0012t0001g0122 |
3 | HG01243.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.399+4951C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146307 | |||||||
| chr2:47146538 | C | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(158): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.399+4720G>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146538 | |||||||
| chr2:47146564 | G | GA | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(175): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.399+4693dupT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146564 | |||||||
| chr2:47146564 | GA | G | 101 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0120 others(98): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.399+4693delT | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146564 | |||||||
| chr2:47146896 | G | T | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.399+4362C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47146896 | |||||||
| chr2:47147046 | G | A | 2 | a0002c0002t0001g0311 a0002c0002t0001g0312 |
2 | HG02258.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.399+4212C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147046 | |||||||
| chr2:47147102 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.399+4156C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147102 | |||||||
| chr2:47147258 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0068 a0001c0001t0001g0069 others(115): Show |
120 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.399+4000T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147258 | |||||||
| chr2:47147428 | C | T | 292 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(289): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.399+3830G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147428 | |||||||
| chr2:47147491 | G | A | 1 | a0002c0002t0001g0313 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.399+3767C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147491 | |||||||
| chr2:47147612 | G | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0116 |
2 | HG02622.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.399+3646C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147612 | |||||||
| chr2:47147665 | A | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0092 others(156): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): Show |
intron_variant | MODIFIER | c.399+3593T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147665 | |||||||
| chr2:47147691 | A | G | 3 | a0002c0002t0001g0272 a0002c0002t0001g0273 a0002c0002t0001g0313 |
3 | HG01109.hp1 HG02559.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.399+3567T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147691 | |||||||
| chr2:47147745 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.399+3513C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147745 | |||||||
| chr2:47147906 | A | C | 26 | a0001c0001t0001g0136 a0001c0001t0001g0151 a0001c0001t0001g0152 others(23): Show |
26 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+3352T>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147906 | |||||||
| chr2:47147912 | A | G | 85 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0148 others(82): Show |
86 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.399+3346T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147912 | |||||||
| chr2:47147949 | C | T | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(298): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.399+3309G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147949 | |||||||
| chr2:47147956 | C | CT | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(250): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.399+3301dupA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147956 | |||||||
| chr2:47147956 | C | CTT | 12 | a0001c0001t0001g0068 a0001c0001t0001g0150 a0001c0001t0001g0315 others(9): Show |
12 | HG01192.hp1 HG02257.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.399+3300_399+3301d others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147956 | |||||||
| chr2:47147975 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0012t0001g0122 |
3 | HG01243.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.399+3283G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147975 | |||||||
| chr2:47147976 | G | A | 76 | a0001c0001t0001g0069 a0001c0001t0001g0148 a0001c0001t0001g0263 others(73): Show |
77 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.399+3282C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147976 | |||||||
| chr2:47147984 | C | G | 2 | a0001c0001t0001g0126 a0001c0001t0001g0131 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.399+3274G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47147984 | |||||||
| chr2:47148011 | G | A | 85 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0148 others(82): Show |
86 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.399+3247C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148011 | |||||||
| chr2:47148045 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.399+3213C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148045 | |||||||
| chr2:47148095 | G | A | 1 | a0002c0002t0001g0291 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.399+3163C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148095 | |||||||
| chr2:47148467 | T | C | 1 | a0001c0001t0001g0250 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.399+2791A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148467 | |||||||
| chr2:47148702 | T | C | 184 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0064 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.399+2556A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148702 | |||||||
| chr2:47148750 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.399+2508T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47148750 | |||||||
| chr2:47149029 | A | T | 3 | a0002c0002t0001g0289 a0002c0002t0001g0290 a0002c0002t0001g0291 |
3 | HG01081.hp2 HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.399+2229T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149029 | |||||||
| chr2:47149033 | T | G | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.399+2225A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149033 | |||||||
| chr2:47149134 | A | G | 75 | a0001c0001t0001g0069 a0001c0001t0001g0148 a0001c0001t0001g0263 others(72): Show |
76 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.399+2124T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149134 | |||||||
| chr2:47149204 | C | T | 18 | a0001c0001t0001g0148 a0001c0001t0001g0263 a0001c0001t0001g0274 others(15): Show |
18 | HG00140.hp2 HG00609.hp1 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.399+2054G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149204 | |||||||
| chr2:47149216 | G | A | 2 | a0002c0002t0001g0277 a0002c0002t0001g0278 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.399+2042C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149216 | |||||||
| chr2:47149328 | C | T | 1 | a0001c0001t0001g0147 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.399+1930G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149328 | |||||||
| chr2:47149533 | T | C | 29 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0098 others(26): Show |
31 | HG00639.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.399+1725A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149533 | |||||||
| chr2:47149600 | T | C | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.399+1658A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149600 | |||||||
| chr2:47149852 | C | T | 11 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(8): Show |
11 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+1406G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149852 | |||||||
| chr2:47149856 | C | T | 69 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(66): Show |
70 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.399+1402G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149856 | |||||||
| chr2:47149957 | A | G | 60 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0263 others(57): Show |
61 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(58): Show |
intron_variant | MODIFIER | c.399+1301T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47149957 | |||||||
| chr2:47150161 | G | A | 58 | a0001c0001t0001g0263 a0001c0001t0001g0274 a0001c0001t0001g0275 others(55): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.399+1097C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150161 | |||||||
| chr2:47150230 | G | A | 1 | a0003c0003t0001g0024 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.399+1028C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150230 | |||||||
| chr2:47150333 | C | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0064 others(260): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.399+925G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150333 | |||||||
| chr2:47150384 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.399+874C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150384 | |||||||
| chr2:47150575 | A | G | 58 | a0001c0001t0001g0263 a0001c0001t0001g0274 a0001c0001t0001g0275 others(55): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.399+683T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150575 | |||||||
| chr2:47150619 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.399+639C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150619 | |||||||
| chr2:47150649 | AT | A | 235 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(232): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.399+608delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150649 | |||||||
| chr2:47150656 | T | C | 58 | a0001c0001t0001g0263 a0001c0001t0001g0274 a0001c0001t0001g0275 others(55): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.399+602A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150656 | |||||||
| chr2:47150694 | G | A | 58 | a0001c0001t0001g0263 a0001c0001t0001g0274 a0001c0001t0001g0275 others(55): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.399+564C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150694 | |||||||
| chr2:47150851 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02451.hp1 HG02572.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.399+407C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150851 | |||||||
| chr2:47150927 | C | T | 13 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 others(10): Show |
13 | HG02083.hp1 HG02165.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.399+331G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47150927 | |||||||
| chr2:47151007 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.399+251G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47151007 | |||||||
| chr2:47151130 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 |
3 | NA18961.hp1 NA19004.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.399+128G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 3/6 | chr2 | 47151130 | |||||||
| chr2:47151619 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.142-104G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151619 | |||||||
| chr2:47151716 | A | T | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(290): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.142-201T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151716 | |||||||
| chr2:47151740 | T | C | 13 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(10): Show |
13 | HG01257.hp2 HG01258.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-225A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151740 | |||||||
| chr2:47151797 | G | C | 1 | a0004c0004t0001g0011 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.142-282C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151797 | |||||||
| chr2:47151804 | A | G | 59 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(56): Show |
60 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.142-289T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151804 | |||||||
| chr2:47151827 | G | A | 1 | a0001c0001t0001g0264 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.142-312C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151827 | |||||||
| chr2:47151834 | A | G | 4 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(1): Show |
4 | NA18968.hp2 NA18983.hp1 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-319T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151834 | |||||||
| chr2:47151901 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.142-386G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151901 | |||||||
| chr2:47151919 | GT | G | 20 | a0001c0001t0001g0068 a0001c0001t0001g0081 a0001c0001t0001g0086 others(17): Show |
20 | HG00738.hp2 HG01255.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-405delA | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151919 | |||||||
| chr2:47151919 | GTT | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0118 a0001c0001t0001g0120 others(3): Show |
6 | HG01243.hp2 HG03225.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.142-406_142-405del others(2): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151919 | |||||||
| chr2:47151919 | GTTT | G | 6 | a0002c0002t0001g0279 a0002c0002t0001g0280 a0002c0002t0001g0281 others(3): Show |
6 | HG00642.hp2 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-407_142-405del others(3): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151919 | |||||||
| chr2:47151919 | GTTTT | G | 45 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(42): Show |
46 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.142-408_142-405del others(4): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151919 | |||||||
| chr2:47151922 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.142-407A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151922 | |||||||
| chr2:47151923 | T | TG | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(205): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.142-409_142-408ins others(1): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151923 | |||||||
| chr2:47151924 | T | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG03041.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.142-409A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151924 | |||||||
| chr2:47151928 | T | G | 162 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(159): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.142-413A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47151928 | |||||||
| chr2:47152043 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.142-528C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152043 | |||||||
| chr2:47152123 | T | C | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.142-608A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152123 | |||||||
| chr2:47152200 | ATG | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.142-687_142-686del others(2): Show |
STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152200 | |||||||
| chr2:47152205 | G | C | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.142-690C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152205 | |||||||
| chr2:47152206 | G | T | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.142-691C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152206 | |||||||
| chr2:47152255 | C | G | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+702G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152255 | |||||||
| chr2:47152335 | T | C | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.141+622A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152335 | |||||||
| chr2:47152382 | C | T | 1 | a0001c0001t0001g0274 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.141+575G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152382 | |||||||
| chr2:47152390 | T | C | 54 | a0002c0002t0001g0004 a0002c0002t0001g0272 a0002c0002t0001g0273 others(51): Show |
55 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.141+567A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152390 | |||||||
| chr2:47152430 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.141+527A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152430 | |||||||
| chr2:47152451 | G | T | 1 | a0001c0001t0001g0066 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.141+506C>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152451 | |||||||
| chr2:47152531 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.141+426A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152531 | |||||||
| chr2:47152748 | C | G | 38 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0029 others(35): Show |
38 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.141+209G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152748 | |||||||
| chr2:47152786 | G | A | 7 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(4): Show |
7 | HG01243.hp2 HG02615.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+171C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152786 | |||||||
| chr2:47152808 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.141+149G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152808 | |||||||
| chr2:47152936 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.141+21T>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 2/6 | chr2 | 47152936 | |||||||
| chr2:47153064 | T | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(209): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.82-48A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153064 | |||||||
| chr2:47153166 | C | T | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.82-150G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153166 | |||||||
| chr2:47153459 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.82-443A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153459 | |||||||
| chr2:47153533 | T | A | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.82-517A>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153533 | |||||||
| chr2:47153698 | C | T | 7 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(4): Show |
7 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.82-682G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153698 | |||||||
| chr2:47153705 | A | G | 58 | a0001c0001t0001g0106 a0001c0001t0001g0274 a0001c0001t0001g0275 others(55): Show |
59 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(56): Show |
intron_variant | MODIFIER | c.82-689T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153705 | |||||||
| chr2:47153779 | G | A | 52 | a0002c0002t0001g0004 a0002c0002t0001g0277 a0002c0002t0001g0278 others(49): Show |
53 | HG00140.hp2 HG00621.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.82-763C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153779 | |||||||
| chr2:47153780 | A | G | 1 | a0003c0003t0001g0027 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.82-764T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153780 | |||||||
| chr2:47153915 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.82-899C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153915 | |||||||
| chr2:47153958 | A | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(244): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.82-942T>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153958 | |||||||
| chr2:47153995 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.82-979C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47153995 | |||||||
| chr2:47154026 | C | T | 1 | a0003c0003t0001g0026 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.82-1010G>A | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154026 | |||||||
| chr2:47154106 | G | A | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(279): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.81+1065C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154106 | |||||||
| chr2:47154269 | T | G | 11 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(8): Show |
11 | HG01255.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+902A>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154269 | |||||||
| chr2:47154377 | T | C | 1 | a0004c0004t0001g0015 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.81+794A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154377 | |||||||
| chr2:47154538 | T | C | 59 | a0001c0001t0001g0274 a0001c0001t0001g0275 a0001c0001t0001g0276 others(56): Show |
60 | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.81+633A>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154538 | |||||||
| chr2:47154594 | G | A | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.81+577C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154594 | |||||||
| chr2:47154608 | G | C | 2 | a0001c0001t0001g0324 a0004c0004t0001g0016 |
2 | HG01255.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.81+563C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154608 | |||||||
| chr2:47154834 | G | C | 11 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(8): Show |
11 | HG01255.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+337C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154834 | |||||||
| chr2:47154846 | G | A | 1 | a0002c0002t0001g0325 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.81+325C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154846 | |||||||
| chr2:47154890 | G | A | 3 | a0001c0001t0001g0326 a0001c0001t0001g0327 a0001c0001t0001g0328 |
3 | HG02083.hp1 HG02523.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.81+281C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47154890 | |||||||
| chr2:47155014 | G | A | 11 | a0002c0002t0001g0329 a0002c0002t0001g0330 a0002c0002t0001g0331 others(8): Show |
11 | HG01074.hp1 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+157C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47155014 | |||||||
| chr2:47155070 | G | C | 2 | a0001c0001t0001g0340 a0001c0001t0001g0341 |
2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.81+101C>G | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47155070 | |||||||
| chr2:47155075 | C | G | 344 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(341): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.81+96G>C | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47155075 | |||||||
| chr2:47155130 | G | A | 1 | a0001c0001t0001g0344 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.81+41C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47155130 | |||||||
| chr2:47155161 | G | A | 38 | a0003c0003t0001g0026 a0003c0003t0001g0027 a0003c0003t0001g0029 others(35): Show |
38 | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(35): Show |
intron_variant | MODIFIER | c.81+10C>T | STPG4 | ENSG00000239605.11 | transcript | ENST00000445927.7 | protein_coding | 1/6 | chr2 | 47155161 |