Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57606 |
| ensemblid | ENSG00000109171.15 |
| hgncid | 29282 |
| symbol | SLAIN2 |
| name | SLAIN motif family member 2 |
| refseq_nuc | NM_020846.2 |
| refseq_prot | NP_065897.1 |
| ensembl_nuc | ENST00000264313.11 |
| ensembl_prot | ENSP00000264313.5 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48341529 |
| end | 48426201 |
| strand | + |
| ver | v1.2 |
| region | chr4:48341529-48426201 |
| region5000 | chr4:48336529-48431201 |
| regionname0 | SLAIN2_chr4_48341529_48426201 |
| regionname5000 | SLAIN2_chr4_48336529_48431201 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 581 | 342 | 83 | 60 | 139 | 18 | 40 | 114 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(576): Show |
chr4 | 48336529 | 48431201 |
| a0002 | 0/0 | 581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(576): Show |
chr4 | 48336529 | 48431201 |
| a0003 | 0/0 | 350 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(345): Show |
chr4 | 48336529 | 48431201 |
| a0004 | 0/0 | 581 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(576): Show |
chr4 | 48336529 | 48431201 |
| a0005 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(576): Show |
chr4 | 48336529 | 48431201 |
| a0006 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(570): Show |
chr4 | 48336529 | 48431201 |
| a0007 | 0/0 | 581 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | MEDVN others(576): Show |
chr4 | 48336529 | 48431201 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1743 | 312 | 64 | 56 | 138 | 16 | 36 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0001c0002 | 0/0 | 1743 | 15 | 4 | 4 | 1 | 2 | 4 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0001c0003 | 0/0 | 1743 | 11 | 11 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0001c0004 | 0/0 | 1743 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0001c0006 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0002c0010 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0003c0007 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0004c0009 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0005c0011 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 | ||
| a0006c0005 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1720): Show |
chr4 | 48336529 | 48431201 | ||
| a0007c0008 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | ATGGA others(1738): Show |
chr4 | 48336529 | 48431201 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 6081 | 142 | 35 | 22 | 64 | 9 | 10 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0002 | 0/0 | 6080 | 72 | 16 | 16 | 24 | 3 | 13 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0003 | 0/0 | 6081 | 41 | 2 | 11 | 16 | 4 | 8 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCT others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0004 | 0/0 | 6080 | 26 | 3 | 1 | 19 | 0 | 3 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0007 | 0/0 | 6081 | 4 | 0 | 0 | 4 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0008 | 0/0 | 6081 | 4 | 0 | 4 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0010 | 0/0 | 6081 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0011 | 0/0 | 6081 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0013 | 0/0 | 6080 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0015 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0016 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0017 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0018 | 0/0 | 6080 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0019 | 0/0 | 6080 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0021 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0022 | 0/0 | 6082 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6077): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0023 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0024 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0025 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0026 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0027 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0028 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0029 | 0/0 | 6079 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6074): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0032 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0033 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0001t0034 | 0/0 | 6081 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCT others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0001c0002t0005 | 0/0 | 6080 | 9 | 3 | 2 | 0 | 2 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0002t0009 | 0/0 | 6079 | 4 | 0 | 2 | 0 | 0 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6074): Show |
chr4 | 48336529 | 48431201 |
| a0001c0002t0030 | 0/0 | 6079 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6074): Show |
chr4 | 48336529 | 48431201 |
| a0001c0002t0031 | 0/0 | 6079 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6074): Show |
chr4 | 48336529 | 48431201 |
| a0001c0003t0006 | 0/0 | 6076 | 8 | 8 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6071): Show |
chr4 | 48336529 | 48431201 |
| a0001c0003t0012 | 0/0 | 6076 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6071): Show |
chr4 | 48336529 | 48431201 |
| a0001c0003t0014 | 0/0 | 6076 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6071): Show |
chr4 | 48336529 | 48431201 |
| a0001c0004t0002 | 0/0 | 6080 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0001c0006t0001 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0002c0010t0001 | 0/0 | 6081 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| a0003c0007t0002 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0004c0009t0002 | 0/0 | 6080 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0005c0011t0020 | 0/0 | 6080 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6075): Show |
chr4 | 48336529 | 48431201 |
| a0006c0005t0001 | 0/0 | 6063 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6058): Show |
chr4 | 48336529 | 48431201 |
| a0007c0008t0001 | 0/0 | 6081 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | AATCC others(6076): Show |
chr4 | 48336529 | 48431201 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0005 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0149 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0003 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0004g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0007g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0011g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0013g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0015g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0016g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0017g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0018g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0019g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0021g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0022g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0023g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0024g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0025g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0026g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0027g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0028g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0029g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0032g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0033g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0001t0034g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0009g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0030g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0002t0031g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0012g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0003t0014g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0001c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0002c0010t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0003c0007t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0004c0009t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0005c0011t0020g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0006c0005t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| a0007c0008t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0204 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0290 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0065 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0003 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0116 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0166 | EUR | FIN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00408 | hp1 | a0001 | c0001 | t0033 | g0284 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0248 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0165 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0208 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00738 | hp1 | a0002 | c0010 | t0001 | g0136 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0186 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0200 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01069 | hp2 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01074 | hp1 | a0001 | c0002 | t0009 | g0174 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01099 | hp1 | a0001 | c0001 | t0028 | g0264 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0301 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01109 | hp1 | a0003 | c0007 | t0002 | g0300 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01109 | hp2 | a0001 | c0002 | t0005 | g0008 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0187 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0203 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01256 | hp2 | a0001 | c0001 | t0008 | g0145 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0185 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0003 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0207 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0307 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0142 | AMR | CLM | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01516 | hp1 | a0001 | c0001 | t0003 | g0180 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | IBS | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01891 | hp2 | a0001 | c0003 | t0014 | g0153 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01943 | hp1 | a0001 | c0001 | t0008 | g0144 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0315 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0305 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01978 | hp2 | a0004 | c0009 | t0002 | g0324 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG01981 | hp2 | a0001 | c0001 | t0008 | g0146 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02004 | hp1 | a0001 | c0001 | t0021 | g0294 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02015 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02040 | hp1 | a0005 | c0011 | t0020 | g0254 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02055 | hp1 | a0001 | c0002 | t0005 | g0172 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0310 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02056 | hp2 | a0001 | c0001 | t0013 | g0283 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0320 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02145 | hp2 | a0001 | c0003 | t0006 | g0213 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02148 | hp2 | a0006 | c0005 | t0001 | g0106 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CDX | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0235 | EAS | CDX | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0332 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02258 | hp1 | a0001 | c0001 | t0029 | g0163 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02258 | hp2 | a0001 | c0003 | t0006 | g0033 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0329 | AMR | PEL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02451 | hp1 | a0001 | c0004 | t0002 | g0230 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02451 | hp2 | a0001 | c0003 | t0006 | g0211 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02523 | hp1 | a0001 | c0002 | t0031 | g0175 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0256 | EAS | KHV | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0268 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0288 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02615 | hp1 | a0001 | c0001 | t0016 | g0333 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02615 | hp2 | a0001 | c0003 | t0012 | g0214 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0242 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02630 | hp2 | a0001 | c0001 | t0023 | g0035 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0194 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0295 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0243 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0289 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0281 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0327 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02809 | hp2 | a0001 | c0001 | t0011 | g0031 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02895 | hp1 | a0007 | c0008 | t0001 | g0123 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02922 | hp2 | a0001 | c0003 | t0006 | g0032 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0097 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03017 | hp1 | a0001 | c0001 | t0017 | g0234 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03041 | hp1 | a0001 | c0002 | t0005 | g0169 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03098 | hp1 | a0001 | c0003 | t0006 | g0212 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0229 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03139 | hp2 | a0001 | c0001 | t0027 | g0179 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03195 | hp2 | a0001 | c0004 | t0002 | g0231 | AFR | ESN | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0269 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03225 | hp2 | a0001 | c0001 | t0015 | g0293 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03453 | hp1 | a0001 | c0003 | t0006 | g0216 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03453 | hp2 | a0001 | c0001 | t0018 | g0280 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0298 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03490 | hp2 | a0001 | c0002 | t0005 | g0199 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03492 | hp2 | a0001 | c0002 | t0005 | g0173 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03540 | hp1 | a0001 | c0003 | t0012 | g0215 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0021 | AFR | GWD | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0220 | AFR | MSL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03654 | hp2 | a0001 | c0001 | t0004 | g0312 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0009 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0192 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03831 | hp2 | a0001 | c0001 | t0019 | g0303 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0253 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03927 | hp2 | a0001 | c0002 | t0009 | g0177 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0304 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04184 | hp1 | a0001 | c0002 | t0009 | g0176 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04184 | hp2 | a0001 | c0001 | t0004 | g0238 | SAS | BEB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0191 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0311 | SAS | STU | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18612 | hp2 | a0001 | c0001 | t0004 | g0250 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0197 | EAS | CHB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0326 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18939 | hp1 | a0001 | c0001 | t0025 | g0047 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0249 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18942 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18943 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18944 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18946 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0317 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18964 | hp1 | a0001 | c0001 | t0024 | g0014 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18965 | hp2 | a0001 | c0001 | t0004 | g0313 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18969 | hp2 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18975 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0323 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0319 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0318 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18999 | hp2 | a0001 | c0001 | t0004 | g0316 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19000 | hp1 | a0001 | c0001 | t0007 | g0314 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19005 | hp2 | a0001 | c0001 | t0026 | g0070 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0331 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0224 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19030 | hp1 | a0001 | c0002 | t0030 | g0201 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19043 | hp1 | a0001 | c0003 | t0006 | g0036 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0202 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19055 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19056 | hp2 | a0001 | c0001 | t0022 | g0089 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19064 | hp1 | a0001 | c0001 | t0034 | g0183 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19078 | hp2 | a0001 | c0001 | t0007 | g0330 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19079 | hp2 | a0001 | c0001 | t0032 | g0055 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19080 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19086 | hp2 | a0001 | c0001 | t0010 | g0090 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19090 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0328 | AFR | YRI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20129 | hp1 | a0001 | c0002 | t0005 | g0178 | AFR | ASW | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ASW | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20752 | hp1 | a0001 | c0002 | t0005 | g0171 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20805 | hp2 | a0001 | c0002 | t0005 | g0170 | EUR | TSI | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | GIH | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0287 | SAS | GIH | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0244 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG02559 | hp2 | a0001 | c0003 | t0006 | g0034 | AFR | ACB | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0149 | REF | REF | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0029 | REF | REF | SLAIN2_chr4_48336529_48431201 | SLAIN2 | chr4 | 48336529 | 48431201 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341909 | C | T | 1 | a0005 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.170C>T | p.Pro57Leu | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 381/6081 | 170/1746 | 57/581 | chr4 | 48341909 | |||
| chr4:48341960 | AGTCGGGC others(11): Show |
A | 1 | a0006 | 1 | HG02148.hp2 | conservative_inframe_deletion | MODERATE | c.229_246delGGCGGGCC others(10): Show |
p.Gly77_Gly82del | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 440/6081 | 229/1746 | 77/581 | INFO_REALIGN_3_PRIME | chr4 | 48341960 | ||
| chr4:48342076 | C | G | 1 | a0002 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.337C>G | p.Arg113Gly | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 548/6081 | 337/1746 | 113/581 | chr4 | 48342076 | |||
| chr4:48379710 | A | G | 1 | a0004 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.724A>G | p.Arg242Gly | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/8 | 935/6081 | 724/1746 | 242/581 | chr4 | 48379710 | |||
| chr4:48379782 | A | G | 1 | a0007 | 1 | HG02895.hp1 | missense_variant | MODERATE | c.796A>G | p.Ile266Val | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/8 | 1007/6081 | 796/1746 | 266/581 | chr4 | 48379782 | |||
| chr4:48382756 | C | T | 1 | a0003 | 1 | HG01109.hp1 | stop_gained | HIGH | c.1051C>T | p.Arg351* | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/8 | 1262/6081 | 1051/1746 | 351/581 | chr4 | 48382756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341751 | T | C | 1 | a0001c0004 | 3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
synonymous_variant | LOW | c.12T>C | p.Val4Val | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 223/6081 | 12/1746 | 4/581 | chr4 | 48341751 | |||
| chr4:48342072 | G | C | 1 | a0001c0006 | 1 | HG02965.hp2 | synonymous_variant | LOW | c.333G>C | p.Pro111Pro | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 544/6081 | 333/1746 | 111/581 | chr4 | 48342072 | |||
| chr4:48382602 | G | A | 1 | a0001c0003 | 11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
synonymous_variant | LOW | c.897G>A | p.Arg299Arg | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/8 | 1108/6081 | 897/1746 | 299/581 | chr4 | 48382602 | |||
| chr4:48422041 | C | T | 1 | a0001c0002 | 15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
synonymous_variant | LOW | c.1710C>T | p.Ser570Ser | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1921/6081 | 1710/1746 | 570/581 | chr4 | 48422041 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48341533 | C | T | 2 | a0001c0001t0003 a0001c0001t0034 |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
5_prime_UTR_variant | MODIFIER | c.-207C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 207 | chr4 | 48341533 | ||||||
| chr4:48341633 | G | C | 1 | a0001c0003t0014 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-107G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 107 | chr4 | 48341633 | ||||||
| chr4:48341671 | C | T | 2 | a0001c0001t0013 a0001c0001t0033 |
3 | HG00408.hp1 HG02056.hp2 HG02155.hp2 |
5_prime_UTR_variant | MODIFIER | c.-69C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 69 | chr4 | 48341671 | ||||||
| chr4:48341676 | G | A | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(12): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
5_prime_UTR_variant | MODIFIER | c.-64G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 64 | chr4 | 48341676 | ||||||
| chr4:48341685 | C | T | 1 | a0001c0001t0032 | 1 | NA19079.hp2 | 5_prime_UTR_variant | MODIFIER | c.-55C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/8 | 55 | chr4 | 48341685 | ||||||
| chr4:48422418 | A | G | 1 | a0001c0001t0034 | 1 | NA19064.hp1 | 3_prime_UTR_variant | MODIFIER | c.*341A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 341 | chr4 | 48422418 | ||||||
| chr4:48422634 | T | A | 1 | a0001c0001t0033 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*557T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 557 | chr4 | 48422634 | ||||||
| chr4:48423113 | C | G | 1 | a0001c0002t0031 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1036C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1036 | chr4 | 48423113 | ||||||
| chr4:48423179 | G | C | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1102G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1102 | chr4 | 48423179 | ||||||
| chr4:48423191 | A | T | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1114A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1114 | chr4 | 48423191 | ||||||
| chr4:48423275 | TA | T | 14 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(11): Show |
113 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1208delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1208 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | |||||
| chr4:48423275 | TAA | T | 5 | a0001c0001t0029 a0001c0002t0005 a0001c0002t0009 others(2): Show |
16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1207_*1208delAA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1207 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | |||||
| chr4:48423275 | TAAAAA | T | 3 | a0001c0003t0006 a0001c0003t0012 a0001c0003t0014 |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1204_*1208delAAAA others(1): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1204 | INFO_REALIGN_3_PRIME | chr4 | 48423275 | |||||
| chr4:48423338 | T | G | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1261T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1261 | chr4 | 48423338 | ||||||
| chr4:48423431 | G | T | 1 | a0001c0001t0021 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1354G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1354 | chr4 | 48423431 | ||||||
| chr4:48423461 | A | C | 1 | a0005c0011t0020 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1384A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1384 | chr4 | 48423461 | ||||||
| chr4:48423670 | C | G | 1 | a0001c0001t0019 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1593C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1593 | chr4 | 48423670 | ||||||
| chr4:48424049 | A | T | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(12): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*1972A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 1972 | chr4 | 48424049 | ||||||
| chr4:48424470 | A | G | 1 | a0001c0001t0027 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2393A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2393 | chr4 | 48424470 | ||||||
| chr4:48424565 | A | G | 1 | a0001c0001t0018 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2488A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2488 | chr4 | 48424565 | ||||||
| chr4:48424585 | T | G | 2 | a0001c0001t0008 a0001c0001t0022 |
5 | HG01256.hp2 HG01496.hp2 HG01943.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2508T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2508 | chr4 | 48424585 | ||||||
| chr4:48424748 | C | T | 1 | a0001c0001t0026 | 1 | NA19005.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2671C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2671 | chr4 | 48424748 | ||||||
| chr4:48424766 | T | TA | 2 | a0001c0001t0022 a0001c0002t0005 |
10 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2700dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2701 | INFO_REALIGN_3_PRIME | chr4 | 48424766 | |||||
| chr4:48424929 | G | A | 3 | a0001c0003t0006 a0001c0003t0012 a0001c0003t0014 |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2852G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2852 | chr4 | 48424929 | ||||||
| chr4:48424998 | A | G | 1 | a0001c0001t0025 | 1 | NA18939.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2921A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 2921 | chr4 | 48424998 | ||||||
| chr4:48425243 | C | T | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(23): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*3166C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3166 | chr4 | 48425243 | ||||||
| chr4:48425273 | A | G | 1 | a0001c0001t0004 | 26 | HG00609.hp1 HG01099.hp2 HG02074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*3196A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3196 | chr4 | 48425273 | ||||||
| chr4:48425442 | C | T | 1 | a0001c0001t0024 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3365C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3365 | chr4 | 48425442 | ||||||
| chr4:48425452 | T | C | 1 | a0001c0001t0015 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3375T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3375 | chr4 | 48425452 | ||||||
| chr4:48425605 | A | T | 1 | a0001c0001t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3528A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3528 | chr4 | 48425605 | ||||||
| chr4:48425612 | A | G | 3 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0031 |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3535A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3535 | chr4 | 48425612 | ||||||
| chr4:48425702 | C | T | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(12): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3625C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3625 | chr4 | 48425702 | ||||||
| chr4:48425756 | G | A | 15 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0007 others(12): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
3_prime_UTR_variant | MODIFIER | c.*3679G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3679 | chr4 | 48425756 | ||||||
| chr4:48425860 | G | A | 1 | a0001c0001t0010 | 2 | HG02015.hp1 NA19086.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3783G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3783 | chr4 | 48425860 | ||||||
| chr4:48425974 | A | G | 1 | a0001c0001t0011 | 2 | HG02809.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3897A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3897 | chr4 | 48425974 | ||||||
| chr4:48426009 | C | G | 1 | a0001c0001t0017 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3932C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3932 | chr4 | 48426009 | ||||||
| chr4:48426075 | C | T | 1 | a0001c0003t0012 | 2 | HG02615.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3998C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 3998 | chr4 | 48426075 | ||||||
| chr4:48426084 | C | T | 3 | a0001c0002t0005 a0001c0002t0009 a0001c0002t0031 |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4007C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 4007 | chr4 | 48426084 | ||||||
| chr4:48426136 | G | A | 1 | a0001c0002t0030 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4059G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 8/8 | 4059 | chr4 | 48426136 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48342137 | G | T | 116 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(113): Show |
118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.389+9G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342137 | |||||||
| chr4:48342182 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.389+54A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342182 | |||||||
| chr4:48342313 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.389+185C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342313 | |||||||
| chr4:48342340 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.389+212C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342340 | |||||||
| chr4:48342592 | G | T | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+464G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342592 | |||||||
| chr4:48342593 | C | T | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+465C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342593 | |||||||
| chr4:48342711 | C | CT | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(104): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(108): Show |
intron_variant | MODIFIER | c.389+607dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTT | 27 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(24): Show |
27 | HG00735.hp2 HG01167.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.389+606_389+607dup others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTT | 89 | a0001c0001t0001g0162 a0001c0001t0001g0217 a0001c0001t0002g0010 others(86): Show |
91 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.389+605_389+607dup others(3): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTT | 43 | a0001c0001t0002g0308 a0001c0001t0002g0309 a0001c0001t0002g0310 others(40): Show |
46 | HG00323.hp2 HG00733.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.389+604_389+607dup others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTTT | 26 | a0001c0001t0002g0332 a0001c0001t0003g0009 a0001c0001t0003g0181 others(23): Show |
27 | HG00738.hp2 HG00741.hp2 HG01175.hp1 others(24): Show |
intron_variant | MODIFIER | c.389+603_389+607dup others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTTTT | 9 | a0001c0001t0003g0003 a0001c0001t0003g0203 a0001c0001t0003g0204 others(6): Show |
11 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+602_389+607dup others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTTTTT others(5): Show |
1 | a0001c0003t0006g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.389+596_389+607dup others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTTTTT others(6): Show |
4 | a0001c0003t0006g0212 a0001c0003t0006g0213 a0001c0003t0012g0214 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+595_389+607dup others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342711 | C | CTTTTTTT others(7): Show |
1 | a0001c0003t0006g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.389+594_389+607dup others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48342711 | ||||||
| chr4:48342766 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+638C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342766 | |||||||
| chr4:48342772 | C | G | 1 | a0001c0001t0007g0330 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.389+644C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342772 | |||||||
| chr4:48342774 | G | A | 33 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
38 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.389+646G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342774 | |||||||
| chr4:48342913 | A | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+785A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342913 | |||||||
| chr4:48342999 | C | T | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.389+871C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48342999 | |||||||
| chr4:48343118 | T | C | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+990T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343118 | |||||||
| chr4:48343213 | A | G | 1 | a0001c0001t0001g0161 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.389+1085A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343213 | |||||||
| chr4:48343434 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+1306A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343434 | |||||||
| chr4:48343734 | T | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(10): Show |
14 | HG02074.hp2 NA18939.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.389+1606T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343734 | |||||||
| chr4:48343887 | T | A | 2 | a0001c0001t0003g0198 a0001c0001t0003g0210 |
2 | NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.389+1759T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343887 | |||||||
| chr4:48343989 | C | T | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+1861C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48343989 | |||||||
| chr4:48344085 | G | GT | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+1960dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48344085 | ||||||
| chr4:48344266 | T | A | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+2138T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344266 | |||||||
| chr4:48344511 | A | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+2383A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344511 | |||||||
| chr4:48344564 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+2436G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344564 | |||||||
| chr4:48344686 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.389+2558T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344686 | |||||||
| chr4:48344721 | T | C | 3 | a0001c0001t0004g0224 a0001c0001t0004g0225 a0001c0001t0004g0226 |
3 | NA18946.hp2 NA19012.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.389+2593T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344721 | |||||||
| chr4:48344802 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+2674C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344802 | |||||||
| chr4:48344807 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.389+2679A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344807 | |||||||
| chr4:48344868 | G | T | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+2740G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344868 | |||||||
| chr4:48344929 | A | G | 1 | a0002c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.389+2801A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344929 | |||||||
| chr4:48344976 | T | A | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+2848T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48344976 | |||||||
| chr4:48345284 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.389+3156C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345284 | |||||||
| chr4:48345300 | C | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389+3172C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345300 | |||||||
| chr4:48345369 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.389+3241G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345369 | |||||||
| chr4:48345407 | T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+3279T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345407 | |||||||
| chr4:48345414 | C | T | 13 | a0001c0001t0029g0163 a0001c0002t0030g0201 a0001c0003t0006g0032 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+3286C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345414 | |||||||
| chr4:48345580 | C | A | 2 | a0001c0001t0002g0232 a0001c0001t0002g0233 |
2 | HG00597.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.389+3452C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345580 | |||||||
| chr4:48345596 | A | G | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+3468A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345596 | |||||||
| chr4:48345729 | TGTTA | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(5): Show |
9 | HG01070.hp1 HG01433.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+3605_389+3608d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48345729 | ||||||
| chr4:48345746 | A | G | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+3618A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345746 | |||||||
| chr4:48345921 | A | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+3793A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345921 | |||||||
| chr4:48345959 | C | A | 1 | a0001c0001t0003g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.389+3831C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48345959 | |||||||
| chr4:48345990 | T | TGAAA | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.389+3864_389+3865i others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48345990 | ||||||
| chr4:48346009 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+3881G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346009 | |||||||
| chr4:48346731 | G | A | 1 | a0001c0001t0017g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.389+4603G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346731 | |||||||
| chr4:48346797 | GAATCAGA others(456): Show |
G | 3 | a0001c0004t0002g0229 a0001c0004t0002g0230 a0001c0004t0002g0231 |
3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.389+4673_389+5135d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346797 | ||||||
| chr4:48346835 | C | CT | 17 | a0001c0001t0001g0108 a0001c0001t0001g0119 a0001c0001t0001g0157 others(14): Show |
17 | HG01167.hp1 HG01243.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.389+4727dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | ||||||
| chr4:48346835 | CT | C | 116 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0064 others(113): Show |
118 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.389+4727delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | ||||||
| chr4:48346835 | CTT | C | 15 | a0001c0001t0002g0221 a0001c0001t0002g0305 a0001c0001t0002g0306 others(12): Show |
15 | HG01891.hp2 HG01975.hp2 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+4726_389+4727d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48346835 | ||||||
| chr4:48346855 | T | A | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+4727T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346855 | |||||||
| chr4:48346942 | A | G | 13 | a0001c0001t0029g0163 a0001c0002t0030g0201 a0001c0003t0006g0032 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.389+4814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48346942 | |||||||
| chr4:48347252 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5124G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347252 | |||||||
| chr4:48347315 | G | A | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.389+5187G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347315 | |||||||
| chr4:48347344 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5216C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347344 | |||||||
| chr4:48347390 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+5262C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347390 | |||||||
| chr4:48347397 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5269C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347397 | |||||||
| chr4:48347427 | T | G | 3 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0034g0183 |
3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.389+5299T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347427 | |||||||
| chr4:48347449 | A | G | 1 | a0001c0001t0002g0307 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.389+5321A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347449 | |||||||
| chr4:48347468 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+5340C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347468 | |||||||
| chr4:48347635 | A | G | 1 | a0001c0001t0002g0306 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.389+5507A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347635 | |||||||
| chr4:48347673 | A | G | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+5545A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347673 | |||||||
| chr4:48347694 | A | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+5566A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347694 | |||||||
| chr4:48347761 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5633G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347761 | |||||||
| chr4:48347781 | G | A | 1 | a0001c0001t0013g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.389+5653G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347781 | |||||||
| chr4:48347782 | C | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+5654C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347782 | |||||||
| chr4:48347897 | A | T | 5 | a0001c0002t0009g0174 a0001c0002t0009g0176 a0001c0002t0009g0177 others(2): Show |
5 | HG00741.hp2 HG01074.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.389+5769A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347897 | |||||||
| chr4:48347925 | T | G | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+5797T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347925 | |||||||
| chr4:48347962 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.389+5834A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48347962 | |||||||
| chr4:48348022 | A | C | 1 | a0001c0001t0011g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.389+5894A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348022 | |||||||
| chr4:48348025 | A | C | 1 | a0001c0001t0001g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.389+5897A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348025 | |||||||
| chr4:48348029 | A | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+5901A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348029 | |||||||
| chr4:48348044 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.389+5916C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348044 | |||||||
| chr4:48348117 | CT | C | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+5990delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348117 | |||||||
| chr4:48348137 | T | C | 1 | a0001c0001t0013g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.389+6009T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348137 | |||||||
| chr4:48348155 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.389+6027G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348155 | |||||||
| chr4:48348183 | A | C | 1 | a0001c0001t0002g0329 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.389+6055A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348183 | |||||||
| chr4:48348237 | T | A | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+6109T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348237 | |||||||
| chr4:48348247 | T | TAAAAA | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6120_389+6121i others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348247 | ||||||
| chr4:48348252 | TA | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6131delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348252 | ||||||
| chr4:48348560 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.389+6432G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348560 | |||||||
| chr4:48348648 | C | G | 1 | a0001c0001t0003g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.389+6520C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348648 | |||||||
| chr4:48348689 | C | CA | 45 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(42): Show |
46 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.389+6578dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | ||||||
| chr4:48348689 | C | CAA | 73 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(70): Show |
74 | HG00597.hp2 HG00609.hp1 HG01099.hp1 others(71): Show |
intron_variant | MODIFIER | c.389+6577_389+6578d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | ||||||
| chr4:48348689 | C | CAAA | 11 | a0001c0001t0002g0220 a0001c0001t0002g0227 a0001c0001t0002g0236 others(8): Show |
11 | HG01891.hp1 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.389+6576_389+6578d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348689 | ||||||
| chr4:48348704 | AAAG | A | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+6581_389+6583d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48348704 | ||||||
| chr4:48348740 | G | A | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.389+6612G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348740 | |||||||
| chr4:48348770 | C | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6642C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348770 | |||||||
| chr4:48348771 | A | G | 15 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(12): Show |
16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.389+6643A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348771 | |||||||
| chr4:48348827 | C | T | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.389+6699C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348827 | |||||||
| chr4:48348828 | C | T | 1 | a0001c0001t0003g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.389+6700C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348828 | |||||||
| chr4:48348883 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+6755A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348883 | |||||||
| chr4:48348973 | C | A | 5 | a0001c0001t0002g0282 a0001c0001t0007g0323 a0001c0001t0013g0235 others(2): Show |
5 | HG00408.hp1 HG02056.hp2 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.389+6845C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348973 | |||||||
| chr4:48348996 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.389+6868A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48348996 | |||||||
| chr4:48349047 | T | C | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.389+6919T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349047 | |||||||
| chr4:48349079 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+6951T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349079 | |||||||
| chr4:48349551 | C | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.389+7423C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349551 | |||||||
| chr4:48349561 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.389+7433A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349561 | |||||||
| chr4:48349623 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+7495C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48349623 | |||||||
| chr4:48349964 | C | CA | 14 | a0001c0001t0001g0139 a0001c0002t0005g0008 a0001c0002t0005g0169 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.389+7844dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48349964 | ||||||
| chr4:48350213 | G | C | 1 | a0004c0009t0002g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.389+8085G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350213 | |||||||
| chr4:48350219 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.389+8091G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350219 | |||||||
| chr4:48350315 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00558.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.389+8187A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350315 | |||||||
| chr4:48350511 | G | A | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.389+8383G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350511 | |||||||
| chr4:48350906 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.389+8778A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48350906 | |||||||
| chr4:48351016 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0281 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.389+8888A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351016 | |||||||
| chr4:48351268 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9140A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351268 | |||||||
| chr4:48351303 | A | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+9175A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351303 | |||||||
| chr4:48351325 | G | A | 71 | a0001c0001t0002g0010 a0001c0001t0002g0221 a0001c0001t0002g0232 others(68): Show |
72 | HG00597.hp2 HG00609.hp1 HG01099.hp1 others(69): Show |
intron_variant | MODIFIER | c.389+9197G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351325 | |||||||
| chr4:48351462 | T | C | 1 | a0001c0001t0004g0241 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.389+9334T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351462 | |||||||
| chr4:48351464 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9336A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351464 | |||||||
| chr4:48351669 | A | T | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+9541A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351669 | |||||||
| chr4:48351697 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9569C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351697 | |||||||
| chr4:48351701 | C | T | 1 | a0001c0001t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.389+9573C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351701 | |||||||
| chr4:48351740 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+9612G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351740 | |||||||
| chr4:48351754 | G | A | 1 | a0001c0001t0003g0181 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.389+9626G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351754 | |||||||
| chr4:48351816 | T | C | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+9688T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351816 | |||||||
| chr4:48351861 | T | C | 1 | a0001c0001t0004g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.389+9733T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351861 | |||||||
| chr4:48351880 | C | T | 6 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(3): Show |
7 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9752C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351880 | |||||||
| chr4:48351955 | G | A | 7 | a0001c0001t0002g0220 a0001c0001t0002g0227 a0001c0001t0002g0228 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9827G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48351955 | |||||||
| chr4:48352040 | C | T | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+9912C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352040 | |||||||
| chr4:48352049 | T | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+9921T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352049 | |||||||
| chr4:48352112 | A | AT | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9985dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48352112 | ||||||
| chr4:48352114 | G | T | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9986G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352114 | |||||||
| chr4:48352115 | C | T | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.389+9987C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352115 | |||||||
| chr4:48352116 | T | G | 7 | a0001c0001t0002g0220 a0001c0001t0002g0227 a0001c0001t0002g0228 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+9988T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352116 | |||||||
| chr4:48352269 | A | G | 1 | a0001c0001t0002g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.389+10141A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352269 | |||||||
| chr4:48352328 | T | C | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.389+10200T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352328 | |||||||
| chr4:48352405 | A | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.389+10277A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352405 | |||||||
| chr4:48352498 | G | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+10370G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352498 | |||||||
| chr4:48352542 | T | A | 2 | a0001c0001t0003g0184 a0001c0001t0003g0206 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.389+10414T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352542 | |||||||
| chr4:48352604 | T | C | 178 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.389+10476T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352604 | |||||||
| chr4:48352648 | A | T | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.389+10520A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352648 | |||||||
| chr4:48352664 | A | C | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.389+10536A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352664 | |||||||
| chr4:48352680 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.389+10552G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48352680 | |||||||
| chr4:48353102 | A | T | 1 | a0001c0001t0002g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.389+10974A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353102 | |||||||
| chr4:48353172 | G | A | 4 | a0001c0001t0002g0243 a0001c0001t0002g0244 a0001c0001t0002g0309 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.389+11044G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353172 | |||||||
| chr4:48353387 | T | C | 2 | a0001c0001t0002g0282 a0001c0001t0007g0323 |
2 | NA18977.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.389+11259T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353387 | |||||||
| chr4:48353427 | T | TCATGGTC others(242): Show |
1 | a0001c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389+11312_389+1131 others(253): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48353427 | ||||||
| chr4:48353527 | G | A | 189 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.389+11399G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353527 | |||||||
| chr4:48353587 | CAG | C | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.389+11461_389+1146 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48353587 | ||||||
| chr4:48353734 | A | G | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+11606A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353734 | |||||||
| chr4:48353816 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+11688G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353816 | |||||||
| chr4:48353931 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.389+11803A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353931 | |||||||
| chr4:48353942 | C | T | 189 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.389+11814C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48353942 | |||||||
| chr4:48354013 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+11885C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354013 | |||||||
| chr4:48354046 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.389+11918C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354046 | |||||||
| chr4:48354079 | T | G | 3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.389+11951T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354079 | |||||||
| chr4:48354130 | T | G | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+12002T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354130 | |||||||
| chr4:48354136 | TAA | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12017_389+1201 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354136 | ||||||
| chr4:48354206 | T | C | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12078T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354206 | |||||||
| chr4:48354298 | A | G | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.389+12170A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354298 | |||||||
| chr4:48354316 | G | A | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+12188G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354316 | |||||||
| chr4:48354461 | C | T | 173 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(170): Show |
180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.389+12333C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354461 | |||||||
| chr4:48354466 | AT | A | 166 | a0001c0001t0001g0056 a0001c0001t0001g0154 a0001c0001t0001g0155 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.389+12349delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354466 | ||||||
| chr4:48354472 | T | C | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12344T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354472 | |||||||
| chr4:48354476 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12348T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354476 | |||||||
| chr4:48354477 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.389+12349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354477 | |||||||
| chr4:48354552 | T | C | 1 | a0001c0001t0003g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.389+12424T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354552 | |||||||
| chr4:48354612 | A | G | 1 | a0001c0001t0019g0303 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.389+12484A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354612 | |||||||
| chr4:48354651 | G | C | 2 | a0001c0001t0003g0184 a0001c0001t0003g0206 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.389+12523G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354651 | |||||||
| chr4:48354690 | C | T | 1 | a0001c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.389+12562C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354690 | |||||||
| chr4:48354725 | G | A | 188 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.389+12597G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354725 | |||||||
| chr4:48354734 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.389+12606G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354734 | |||||||
| chr4:48354760 | A | G | 2 | a0001c0002t0005g0173 a0001c0002t0005g0199 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.389+12632A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354760 | |||||||
| chr4:48354884 | ATTTTC | A | 142 | a0001c0001t0002g0010 a0001c0001t0002g0220 a0001c0001t0002g0221 others(139): Show |
148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.389+12771_389+1277 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354884 | ||||||
| chr4:48354895 | TTTTC | T | 11 | a0001c0001t0002g0011 a0001c0001t0002g0296 a0001c0001t0002g0297 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12771_389+1277 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48354895 | ||||||
| chr4:48354906 | T | C | 11 | a0001c0001t0002g0011 a0001c0001t0002g0296 a0001c0001t0002g0297 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12778T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354906 | |||||||
| chr4:48354907 | C | T | 11 | a0001c0001t0002g0011 a0001c0001t0002g0296 a0001c0001t0002g0297 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.389+12779C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354907 | |||||||
| chr4:48354990 | C | T | 1 | a0001c0001t0003g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.389+12862C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48354990 | |||||||
| chr4:48355016 | G | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.389+12888G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355016 | |||||||
| chr4:48355022 | C | T | 1 | a0001c0003t0006g0211 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.389+12894C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355022 | |||||||
| chr4:48355027 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.389+12899G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355027 | |||||||
| chr4:48355066 | G | A | 10 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(7): Show |
11 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.389+12938G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355066 | |||||||
| chr4:48355079 | G | C | 11 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(8): Show |
12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.389+12951G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355079 | |||||||
| chr4:48355088 | G | C | 1 | a0001c0001t0004g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.389+12960G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355088 | |||||||
| chr4:48355160 | G | A | 2 | a0001c0003t0006g0036 a0001c0003t0014g0153 |
2 | HG01891.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.389+13032G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355160 | |||||||
| chr4:48355219 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.389+13091G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355219 | |||||||
| chr4:48355272 | C | T | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.389+13144C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355272 | |||||||
| chr4:48355510 | A | G | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.389+13382A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355510 | |||||||
| chr4:48355607 | G | C | 1 | a0001c0001t0002g0332 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.389+13479G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355607 | |||||||
| chr4:48355666 | C | T | 2 | a0001c0001t0002g0275 a0001c0001t0002g0276 |
2 | HG01928.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.389+13538C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355666 | |||||||
| chr4:48355717 | T | A | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+13589T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355717 | |||||||
| chr4:48355718 | C | A | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.389+13590C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355718 | |||||||
| chr4:48355736 | C | T | 2 | a0001c0001t0001g0111 a0001c0001t0002g0328 |
2 | NA19086.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.389+13608C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48355736 | |||||||
| chr4:48356005 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-13844C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356005 | |||||||
| chr4:48356345 | G | T | 1 | a0001c0003t0006g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.390-13504G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356345 | |||||||
| chr4:48356425 | T | C | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-13424T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356425 | |||||||
| chr4:48356434 | CTGTACTA others(15): Show |
C | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-13393_390-1337 others(26): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48356434 | ||||||
| chr4:48356438 | A | G | 1 | a0001c0001t0003g0191 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.390-13411A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356438 | |||||||
| chr4:48356456 | A | C | 2 | a0001c0001t0001g0159 a0001c0001t0029g0163 |
2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.390-13393A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356456 | |||||||
| chr4:48356504 | G | A | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-13345G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356504 | |||||||
| chr4:48356703 | T | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-13146T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356703 | |||||||
| chr4:48356710 | T | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(1): Show |
6 | HG02486.hp2 HG02572.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.390-13139T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356710 | |||||||
| chr4:48356743 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.390-13106C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356743 | |||||||
| chr4:48356793 | C | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18946.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.390-13056C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356793 | |||||||
| chr4:48356979 | C | T | 2 | a0001c0001t0001g0107 a0006c0005t0001g0106 |
2 | HG02148.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.390-12870C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356979 | |||||||
| chr4:48356997 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-12852C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48356997 | |||||||
| chr4:48357158 | T | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-12691T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357158 | |||||||
| chr4:48357170 | C | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-12679C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357170 | |||||||
| chr4:48357201 | A | G | 1 | a0001c0001t0002g0295 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.390-12648A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357201 | |||||||
| chr4:48357273 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.390-12576G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357273 | |||||||
| chr4:48357306 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.390-12543A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357306 | |||||||
| chr4:48357375 | CT | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-12463delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48357375 | ||||||
| chr4:48357709 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-12140C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357709 | |||||||
| chr4:48357735 | G | A | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.390-12114G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357735 | |||||||
| chr4:48357744 | A | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-12105A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357744 | |||||||
| chr4:48357755 | A | G | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.390-12094A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357755 | |||||||
| chr4:48357888 | A | G | 1 | a0001c0001t0003g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-11961A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357888 | |||||||
| chr4:48357998 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.390-11851C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48357998 | |||||||
| chr4:48358267 | A | G | 4 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0321 others(1): Show |
4 | HG01358.hp1 HG01928.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-11582A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358267 | |||||||
| chr4:48358323 | C | CT | 113 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(110): Show |
115 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(112): Show |
intron_variant | MODIFIER | c.390-11513dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48358323 | ||||||
| chr4:48358341 | C | T | 2 | a0001c0001t0001g0048 a0001c0002t0030g0201 |
2 | NA18998.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.390-11508C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358341 | |||||||
| chr4:48358353 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390-11496C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358353 | |||||||
| chr4:48358380 | C | T | 1 | a0001c0001t0004g0311 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.390-11469C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358380 | |||||||
| chr4:48358464 | C | T | 1 | a0001c0001t0002g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.390-11385C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358464 | |||||||
| chr4:48358465 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.390-11384G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358465 | |||||||
| chr4:48358535 | C | T | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-11314C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358535 | |||||||
| chr4:48358559 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.390-11290G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358559 | |||||||
| chr4:48358608 | G | A | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-11241G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358608 | |||||||
| chr4:48358686 | G | C | 1 | a0001c0001t0001g0057 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.390-11163G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358686 | |||||||
| chr4:48358728 | A | AT | 109 | a0001c0001t0001g0104 a0001c0001t0002g0010 a0001c0001t0002g0011 others(106): Show |
111 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(108): Show |
intron_variant | MODIFIER | c.390-11112dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48358728 | ||||||
| chr4:48358814 | G | A | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.390-11035G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358814 | |||||||
| chr4:48358815 | G | C | 1 | a0001c0001t0001g0058 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.390-11034G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358815 | |||||||
| chr4:48358920 | A | C | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-10929A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358920 | |||||||
| chr4:48358922 | T | C | 1 | a0001c0001t0003g0195 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.390-10927T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358922 | |||||||
| chr4:48358960 | A | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-10889A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48358960 | |||||||
| chr4:48359118 | T | C | 1 | a0001c0001t0002g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.390-10731T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359118 | |||||||
| chr4:48359304 | G | C | 1 | a0001c0001t0003g0166 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.390-10545G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359304 | |||||||
| chr4:48359490 | C | G | 116 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(113): Show |
118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.390-10359C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359490 | |||||||
| chr4:48359709 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.390-10140T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359709 | |||||||
| chr4:48359883 | C | T | 1 | a0001c0001t0002g0278 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.390-9966C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359883 | |||||||
| chr4:48359970 | G | A | 166 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(163): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.390-9879G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359970 | |||||||
| chr4:48359971 | T | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-9878T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48359971 | |||||||
| chr4:48360151 | C | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-9698C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360151 | |||||||
| chr4:48360153 | C | CA | 46 | a0001c0001t0001g0059 a0001c0001t0002g0289 a0001c0001t0003g0003 others(43): Show |
51 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.390-9681dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48360153 | ||||||
| chr4:48360153 | CA | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0124 a0001c0001t0002g0270 others(4): Show |
7 | HG01255.hp1 HG02451.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-9681delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48360153 | ||||||
| chr4:48360402 | C | G | 3 | a0001c0001t0004g0242 a0001c0001t0004g0268 a0001c0001t0004g0269 |
3 | HG02572.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.390-9447C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360402 | |||||||
| chr4:48360481 | A | G | 3 | a0001c0001t0002g0265 a0001c0001t0002g0266 a0001c0001t0002g0267 |
3 | NA18957.hp1 NA18970.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.390-9368A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360481 | |||||||
| chr4:48360504 | A | G | 1 | a0001c0001t0002g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.390-9345A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360504 | |||||||
| chr4:48360524 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(304): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.390-9325A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360524 | |||||||
| chr4:48360534 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.390-9315G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360534 | |||||||
| chr4:48360560 | C | T | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.390-9289C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360560 | |||||||
| chr4:48360688 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-9161C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360688 | |||||||
| chr4:48360839 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-9010A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360839 | |||||||
| chr4:48360867 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-8982G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360867 | |||||||
| chr4:48360892 | T | C | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-8957T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48360892 | |||||||
| chr4:48361045 | G | A | 1 | a0001c0001t0003g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.390-8804G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361045 | |||||||
| chr4:48361199 | A | T | 3 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0034g0183 |
3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.390-8650A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361199 | |||||||
| chr4:48361226 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.390-8623G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361226 | |||||||
| chr4:48361228 | A | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-8621A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361228 | |||||||
| chr4:48361352 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.390-8497C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361352 | |||||||
| chr4:48361467 | G | C | 2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG02015.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.390-8382G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361467 | |||||||
| chr4:48361500 | T | C | 4 | a0001c0001t0003g0180 a0001c0001t0003g0198 a0001c0001t0003g0202 others(1): Show |
4 | HG01516.hp1 NA18943.hp2 NA18955.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-8349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361500 | |||||||
| chr4:48361624 | A | AT | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-8215dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48361624 | ||||||
| chr4:48361651 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(10): Show |
14 | HG02074.hp2 NA18939.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-8198C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361651 | |||||||
| chr4:48361657 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.390-8192T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361657 | |||||||
| chr4:48361824 | GTCT | G | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-8020_390-8018d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48361824 | ||||||
| chr4:48361966 | A | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-7883A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48361966 | |||||||
| chr4:48362019 | G | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-7830G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362019 | |||||||
| chr4:48362232 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-7617C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362232 | |||||||
| chr4:48362358 | T | C | 1 | a0001c0001t0007g0330 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-7491T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362358 | |||||||
| chr4:48362359 | G | T | 1 | a0001c0001t0007g0330 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-7490G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362359 | |||||||
| chr4:48362423 | C | CT | 30 | a0001c0001t0002g0272 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
33 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.390-7412dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362423 | ||||||
| chr4:48362423 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.390-7426C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362423 | |||||||
| chr4:48362423 | CT | C | 12 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0060 others(9): Show |
12 | HG00558.hp1 HG01167.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.390-7412delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362423 | ||||||
| chr4:48362458 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-7391G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362458 | |||||||
| chr4:48362489 | G | A | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-7360G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362489 | |||||||
| chr4:48362499 | ACCTCTGA others(2): Show |
A | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-7346_390-7338d others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362499 | ||||||
| chr4:48362566 | G | A | 1 | a0001c0001t0001g0067 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.390-7283G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362566 | |||||||
| chr4:48362576 | G | A | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.390-7273G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362576 | |||||||
| chr4:48362586 | ATTTTTTT others(30): Show |
A | 25 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-7260_390-7224d others(39): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362586 | ||||||
| chr4:48362662 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.390-7187G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362662 | |||||||
| chr4:48362732 | C | CT | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(245): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.390-7103dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | ||||||
| chr4:48362732 | C | CTT | 40 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0126 others(37): Show |
46 | HG00099.hp1 HG00280.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.390-7104_390-7103d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | ||||||
| chr4:48362732 | CTTTTTTT others(12): Show |
C | 8 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(5): Show |
8 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.390-7102_390-7084d others(21): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | ||||||
| chr4:48362732 | CTTTTTTT others(13): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.390-7101_390-7082d others(22): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362732 | ||||||
| chr4:48362750 | C | CT | 9 | a0001c0001t0016g0333 a0001c0001t0029g0163 a0001c0002t0005g0008 others(6): Show |
10 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-7083dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362750 | ||||||
| chr4:48362750 | CT | C | 119 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0072 others(116): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.390-7083delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48362750 | ||||||
| chr4:48362766 | T | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0245 others(1): Show |
4 | HG00642.hp1 HG03486.hp2 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-7083T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362766 | |||||||
| chr4:48362767 | A | T | 21 | a0001c0001t0001g0103 a0001c0001t0002g0220 a0001c0001t0002g0227 others(18): Show |
22 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.390-7082A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362767 | |||||||
| chr4:48362880 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-6969C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362880 | |||||||
| chr4:48362933 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6916A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362933 | |||||||
| chr4:48362934 | T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6915T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362934 | |||||||
| chr4:48362951 | T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6898T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48362951 | |||||||
| chr4:48363006 | A | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6843A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363006 | |||||||
| chr4:48363044 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-6805C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363044 | |||||||
| chr4:48363061 | A | G | 1 | a0001c0001t0025g0047 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.390-6788A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363061 | |||||||
| chr4:48363095 | C | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.390-6754C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363095 | |||||||
| chr4:48363133 | T | C | 180 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.390-6716T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363133 | |||||||
| chr4:48363277 | C | T | 2 | a0001c0001t0002g0011 a0001c0001t0004g0301 |
3 | HG01074.hp2 HG01099.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.390-6572C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363277 | |||||||
| chr4:48363303 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-6546G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363303 | |||||||
| chr4:48363339 | C | T | 1 | a0001c0001t0002g0332 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.390-6510C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363339 | |||||||
| chr4:48363372 | C | T | 1 | a0001c0001t0002g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.390-6477C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363372 | |||||||
| chr4:48363409 | CCCTCCCG others(42): Show |
C | 1 | a0001c0001t0001g0105 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.390-6414_390-6366d others(51): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363409 | ||||||
| chr4:48363419 | C | T | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-6430C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363419 | |||||||
| chr4:48363433 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-6416G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363433 | |||||||
| chr4:48363437 | GGGGGGCT others(523): Show |
G | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-6401_390-5872d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363437 | ||||||
| chr4:48363458 | A | C | 178 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.390-6391A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363458 | |||||||
| chr4:48363460 | C | T | 1 | a0001c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.390-6389C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363460 | |||||||
| chr4:48363484 | A | G | 178 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(175): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.390-6365A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363484 | |||||||
| chr4:48363551 | C | T | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.390-6298C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363551 | |||||||
| chr4:48363563 | C | T | 1 | a0001c0001t0002g0308 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.390-6286C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363563 | |||||||
| chr4:48363574 | ACCCCCCA others(42): Show |
A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6253_390-6205d others(51): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363574 | ||||||
| chr4:48363674 | CACTTCCC others(18): Show |
C | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-6174_390-6150d others(27): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363674 | |||||||
| chr4:48363674 | CACTTCCC others(171): Show |
C | 1 | a0001c0001t0017g0234 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.390-6130_390-5953d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363674 | ||||||
| chr4:48363685 | AGGGGCGG others(467): Show |
A | 1 | a0001c0001t0003g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.390-6146_390-5673d others(2): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363685 | ||||||
| chr4:48363691 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-6158G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363691 | |||||||
| chr4:48363749 | AC | A | 149 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.390-6092delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363749 | ||||||
| chr4:48363773 | G | T | 14 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(11): Show |
14 | HG00140.hp1 HG00323.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.390-6076G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363773 | |||||||
| chr4:48363777 | C | T | 3 | a0001c0001t0003g0180 a0001c0001t0003g0198 a0001c0001t0003g0210 |
3 | HG01516.hp1 NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.390-6072C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363777 | |||||||
| chr4:48363806 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.390-6043G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363806 | |||||||
| chr4:48363869 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0001g0063 |
2 | HG01169.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.390-5980G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363869 | |||||||
| chr4:48363896 | C | T | 1 | a0001c0002t0031g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.390-5953C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363896 | |||||||
| chr4:48363917 | C | CG | 37 | a0001c0001t0002g0327 a0001c0001t0003g0003 a0001c0001t0003g0006 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5926dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363917 | ||||||
| chr4:48363935 | ACCTC | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5907_390-5904d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48363935 | ||||||
| chr4:48363946 | G | A | 152 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(149): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.390-5903G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363946 | |||||||
| chr4:48363955 | G | T | 36 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(33): Show |
41 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(38): Show |
intron_variant | MODIFIER | c.390-5894G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363955 | |||||||
| chr4:48363967 | A | G | 188 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.390-5882A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363967 | |||||||
| chr4:48363969 | G | T | 1 | a0001c0001t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.390-5880G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48363969 | |||||||
| chr4:48364011 | T | C | 189 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.390-5838T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364011 | |||||||
| chr4:48364063 | C | G | 5 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0045 others(2): Show |
5 | HG02074.hp2 NA18965.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.390-5786C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364063 | |||||||
| chr4:48364113 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.390-5736C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364113 | |||||||
| chr4:48364145 | C | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-5704C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364145 | |||||||
| chr4:48364159 | C | T | 2 | a0001c0001t0001g0119 a0001c0001t0029g0163 |
2 | HG02258.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.390-5690C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364159 | |||||||
| chr4:48364259 | C | T | 1 | a0002c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.390-5590C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364259 | |||||||
| chr4:48364280 | C | T | 3 | a0001c0001t0004g0242 a0001c0001t0004g0268 a0001c0001t0004g0269 |
3 | HG02572.hp1 HG02630.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.390-5569C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364280 | |||||||
| chr4:48364284 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0077 a0001c0001t0001g0103 |
3 | HG00280.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.390-5565G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364284 | |||||||
| chr4:48364360 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.390-5489C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364360 | |||||||
| chr4:48364429 | C | T | 154 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.390-5420C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364429 | |||||||
| chr4:48364430 | G | A | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-5419G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364430 | |||||||
| chr4:48364437 | G | A | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.390-5412G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364437 | |||||||
| chr4:48364468 | C | CG | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0078 others(3): Show |
6 | HG01978.hp2 HG02056.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.390-5377dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364468 | ||||||
| chr4:48364468 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-5381C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364468 | |||||||
| chr4:48364500 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-5349G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364500 | |||||||
| chr4:48364547 | C | T | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-5302C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364547 | |||||||
| chr4:48364552 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.390-5297C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364552 | |||||||
| chr4:48364639 | C | T | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.390-5210C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364639 | |||||||
| chr4:48364653 | C | T | 1 | a0001c0001t0004g0246 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.390-5196C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364653 | |||||||
| chr4:48364677 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-5172C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364677 | |||||||
| chr4:48364682 | C | G | 2 | a0001c0002t0005g0173 a0001c0002t0005g0199 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.390-5167C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364682 | |||||||
| chr4:48364682 | C | T | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.390-5167C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364682 | |||||||
| chr4:48364690 | A | G | 154 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.390-5159A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364690 | |||||||
| chr4:48364702 | T | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.390-5147T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364702 | |||||||
| chr4:48364742 | G | A | 7 | a0001c0001t0002g0220 a0001c0001t0002g0227 a0001c0001t0002g0228 others(4): Show |
7 | HG01243.hp2 HG01891.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.390-5107G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364742 | |||||||
| chr4:48364747 | C | T | 25 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-5102C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364747 | |||||||
| chr4:48364758 | C | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.390-5091C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364758 | |||||||
| chr4:48364851 | C | T | 2 | a0001c0001t0002g0237 a0001c0001t0029g0163 |
2 | HG02258.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.390-4998C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364851 | |||||||
| chr4:48364868 | G | A | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-4981G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364868 | |||||||
| chr4:48364873 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0003g0180 |
2 | HG01516.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.390-4976A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48364873 | |||||||
| chr4:48364873 | AGGGAGG | A | 19 | a0001c0001t0001g0119 a0001c0001t0001g0155 a0001c0001t0007g0330 others(16): Show |
20 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.390-4956_390-4951d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364873 | ||||||
| chr4:48364883 | A | AG | 7 | a0001c0001t0001g0132 a0001c0001t0003g0194 a0001c0001t0004g0269 others(4): Show |
7 | HG01099.hp1 HG02004.hp1 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.390-4961dupG | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48364883 | ||||||
| chr4:48365044 | C | T | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.390-4805C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365044 | |||||||
| chr4:48365054 | G | A | 1 | a0001c0001t0003g0168 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.390-4795G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365054 | |||||||
| chr4:48365075 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-4774A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365075 | |||||||
| chr4:48365096 | C | G | 4 | a0001c0001t0001g0068 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
4 | HG01069.hp1 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-4753C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365096 | |||||||
| chr4:48365108 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.390-4741T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365108 | |||||||
| chr4:48365142 | G | A | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(325): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.390-4707G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365142 | |||||||
| chr4:48365217 | C | T | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-4632C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365217 | |||||||
| chr4:48365285 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.390-4564A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365285 | |||||||
| chr4:48365300 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-4549C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365300 | |||||||
| chr4:48365331 | G | A | 11 | a0001c0002t0005g0178 a0001c0003t0006g0032 a0001c0003t0006g0033 others(8): Show |
11 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.390-4518G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365331 | |||||||
| chr4:48365362 | C | T | 1 | a0001c0001t0024g0014 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.390-4487C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365362 | |||||||
| chr4:48365444 | C | CA | 105 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0039 others(102): Show |
107 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.390-4384dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | ||||||
| chr4:48365444 | C | CAA | 26 | a0001c0001t0001g0104 a0001c0001t0002g0232 a0001c0001t0002g0237 others(23): Show |
26 | HG00609.hp1 HG01255.hp2 HG01346.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-4385_390-4384d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | ||||||
| chr4:48365444 | C | CAAA | 16 | a0001c0001t0023g0035 a0001c0002t0005g0008 a0001c0002t0005g0169 others(13): Show |
17 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.390-4386_390-4384d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | ||||||
| chr4:48365444 | CAA | C | 10 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(7): Show |
10 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-4385_390-4384d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365444 | ||||||
| chr4:48365468 | A | G | 1 | a0001c0001t0028g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.390-4381A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365468 | |||||||
| chr4:48365549 | GTTTA | G | 3 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 |
3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.390-4284_390-4281d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365549 | ||||||
| chr4:48365611 | A | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-4238A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365611 | |||||||
| chr4:48365909 | T | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.390-3940T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365909 | |||||||
| chr4:48365939 | TGTAA | T | 25 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.390-3907_390-3904d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48365939 | ||||||
| chr4:48365951 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.390-3898A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365951 | |||||||
| chr4:48365958 | A | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-3891A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48365958 | |||||||
| chr4:48366072 | T | C | 1 | a0001c0001t0003g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.390-3777T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366072 | |||||||
| chr4:48366082 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.390-3767G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366082 | |||||||
| chr4:48366159 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.390-3690C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366159 | |||||||
| chr4:48366402 | C | T | 2 | a0001c0003t0006g0032 a0001c0003t0006g0033 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.390-3447C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366402 | |||||||
| chr4:48366605 | A | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.390-3244A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366605 | |||||||
| chr4:48366690 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.390-3159A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366690 | |||||||
| chr4:48366748 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.390-3101C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366748 | |||||||
| chr4:48366821 | G | GT | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-3021dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48366821 | ||||||
| chr4:48366942 | T | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(113): Show |
119 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.390-2907T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48366942 | |||||||
| chr4:48367198 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-2651C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367198 | |||||||
| chr4:48367378 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.390-2471A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367378 | |||||||
| chr4:48367693 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.390-2156A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367693 | |||||||
| chr4:48367789 | A | T | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-2060A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367789 | |||||||
| chr4:48367801 | A | G | 1 | a0001c0001t0002g0262 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.390-2048A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367801 | |||||||
| chr4:48367806 | C | T | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-2043C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367806 | |||||||
| chr4:48367917 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.390-1932A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367917 | |||||||
| chr4:48367952 | C | A | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-1897C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48367952 | |||||||
| chr4:48368051 | C | CTTTTTTT others(3): Show |
96 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(93): Show |
98 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.390-1794_390-1785d others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0002g0278 a0001c0001t0002g0279 a0001c0001t0002g0288 others(8): Show |
11 | HG02074.hp1 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.390-1795_390-1785d others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(5): Show |
5 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(2): Show |
5 | HG00642.hp1 HG03225.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.390-1796_390-1785d others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0002g0227 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.390-1797_390-1785d others(15): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(7): Show |
12 | a0001c0001t0001g0081 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
12 | HG01243.hp2 HG02145.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(8): Show |
17 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(14): Show |
19 | HG01070.hp1 HG01167.hp1 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(9): Show |
96 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(93): Show |
100 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(10): Show |
42 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0023 others(39): Show |
42 | HG00323.hp1 HG00597.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368051 | C | CTTTTTTT others(11): Show |
10 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0069 others(7): Show |
10 | HG01257.hp1 HG01361.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.390-1785_390-1784i others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368051 | ||||||
| chr4:48368099 | G | C | 4 | a0001c0001t0008g0142 a0001c0001t0008g0144 a0001c0001t0008g0145 others(1): Show |
4 | HG01256.hp2 HG01496.hp2 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.390-1750G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368099 | |||||||
| chr4:48368419 | A | AGTACATG others(8): Show |
1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.390-1427_390-1413d others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr4 | 48368419 | ||||||
| chr4:48368424 | A | C | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-1425A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368424 | |||||||
| chr4:48368480 | ATT | A | 10 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(7): Show |
10 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.390-1368_390-1367d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368480 | |||||||
| chr4:48368495 | A | G | 1 | a0001c0001t0004g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.390-1354A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368495 | |||||||
| chr4:48368525 | A | T | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.390-1324A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368525 | |||||||
| chr4:48368595 | AC | A | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.390-1253delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368595 | |||||||
| chr4:48368608 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.390-1241T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368608 | |||||||
| chr4:48368799 | G | C | 1 | a0001c0001t0007g0330 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.390-1050G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48368799 | |||||||
| chr4:48369381 | C | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.390-468C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369381 | |||||||
| chr4:48369501 | T | C | 116 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(113): Show |
118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.390-348T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369501 | |||||||
| chr4:48369741 | A | G | 1 | a0001c0001t0002g0297 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.390-108A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369741 | |||||||
| chr4:48369751 | C | T | 1 | a0001c0001t0001g0092 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.390-98C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 1/7 | chr4 | 48369751 | |||||||
| chr4:48370001 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | splice_region_variant&intron_variant | LOW | c.538+4T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370001 | |||||||
| chr4:48370046 | C | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0083 |
2 | HG00558.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.538+49C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370046 | |||||||
| chr4:48370068 | T | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.538+71T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370068 | |||||||
| chr4:48370202 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.538+205A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370202 | |||||||
| chr4:48370389 | G | C | 15 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(12): Show |
16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+392G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370389 | |||||||
| chr4:48370537 | A | G | 1 | a0001c0001t0003g0185 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.538+540A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370537 | |||||||
| chr4:48370718 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.538+721C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48370718 | |||||||
| chr4:48371102 | T | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.538+1105T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371102 | |||||||
| chr4:48371109 | G | GT | 21 | a0001c0001t0001g0043 a0001c0001t0001g0058 a0001c0001t0001g0069 others(18): Show |
21 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.538+1126dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371109 | ||||||
| chr4:48371109 | GT | G | 25 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.538+1126delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371109 | ||||||
| chr4:48371114 | T | G | 2 | a0001c0001t0001g0084 a0001c0001t0001g0111 |
2 | NA19010.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.538+1117T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371114 | |||||||
| chr4:48371253 | T | G | 1 | a0001c0001t0001g0118 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538+1256T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371253 | |||||||
| chr4:48371270 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.538+1273A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371270 | |||||||
| chr4:48371510 | A | T | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538+1513A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371510 | |||||||
| chr4:48371663 | A | C | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1666A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371663 | |||||||
| chr4:48371665 | T | A | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1668T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371665 | |||||||
| chr4:48371666 | C | T | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1669C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371666 | |||||||
| chr4:48371667 | C | A | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1670C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371667 | |||||||
| chr4:48371668 | T | C | 4 | a0001c0001t0002g0236 a0001c0001t0003g0180 a0001c0001t0003g0198 others(1): Show |
4 | HG01516.hp1 NA18940.hp2 NA18943.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1671T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371668 | |||||||
| chr4:48371670 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1673G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371670 | |||||||
| chr4:48371673 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1676G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371673 | |||||||
| chr4:48371675 | C | A | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1678C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371675 | |||||||
| chr4:48371677 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1680A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371677 | |||||||
| chr4:48371678 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1681G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371678 | |||||||
| chr4:48371679 | G | T | 1 | a0001c0001t0002g0236 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.538+1682G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371679 | |||||||
| chr4:48371771 | A | G | 15 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(12): Show |
16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.538+1774A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371771 | |||||||
| chr4:48371926 | G | A | 1 | a0001c0001t0002g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.538+1929G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371926 | |||||||
| chr4:48371940 | CCAAAA | C | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.538+1958_538+1962d others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371940 | ||||||
| chr4:48371971 | T | TAC | 3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.538+1991_538+1992d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | ||||||
| chr4:48371971 | TAC | T | 234 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(231): Show |
240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.538+1991_538+1992d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | ||||||
| chr4:48371971 | TACAC | T | 24 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(21): Show |
26 | HG01255.hp1 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.538+1989_538+1992d others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | ||||||
| chr4:48371971 | TACACAC | T | 17 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(14): Show |
18 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.538+1987_538+1992d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371971 | ||||||
| chr4:48371972 | ACACACAC others(15): Show |
A | 4 | a0001c0001t0002g0299 a0001c0001t0002g0302 a0001c0001t0002g0305 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.538+1993_538+2014d others(24): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48371972 | ||||||
| chr4:48371986 | A | G | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.538+1989A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371986 | |||||||
| chr4:48371988 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(156): Show |
165 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.538+1991A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371988 | |||||||
| chr4:48371994 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0002g0243 a0001c0001t0002g0309 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.538+1997G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371994 | |||||||
| chr4:48371996 | A | G | 29 | a0001c0001t0001g0043 a0001c0001t0001g0124 a0001c0001t0002g0279 others(26): Show |
30 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.538+1999A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371996 | |||||||
| chr4:48371998 | A | G | 3 | a0001c0002t0030g0201 a0001c0003t0006g0032 a0001c0003t0006g0033 |
3 | HG02258.hp2 HG02922.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.538+2001A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48371998 | |||||||
| chr4:48372029 | TATATATA others(7): Show |
T | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2046_538+2059d others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372029 | ||||||
| chr4:48372031 | TATATAC | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2046_538+2051d others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372031 | ||||||
| chr4:48372037 | CATATACA others(9): Show |
C | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG02145.hp2 HG02258.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+2046_538+2061d others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372037 | ||||||
| chr4:48372039 | T | C | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.538+2042T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372039 | |||||||
| chr4:48372051 | CAT | C | 128 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(125): Show |
131 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(128): Show |
intron_variant | MODIFIER | c.538+2066_538+2067d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48372051 | ||||||
| chr4:48372063 | T | C | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2066T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372063 | |||||||
| chr4:48372125 | T | A | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.538+2128T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372125 | |||||||
| chr4:48372187 | T | C | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.538+2190T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372187 | |||||||
| chr4:48372201 | A | C | 1 | a0001c0001t0001g0015 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.538+2204A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372201 | |||||||
| chr4:48372315 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+2318T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372315 | |||||||
| chr4:48372351 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0219 |
3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.538+2354T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372351 | |||||||
| chr4:48372388 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.538+2391A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372388 | |||||||
| chr4:48372400 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.538+2403T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372400 | |||||||
| chr4:48372500 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.538+2503A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372500 | |||||||
| chr4:48372505 | A | G | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.538+2508A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372505 | |||||||
| chr4:48372532 | G | A | 11 | a0001c0001t0029g0163 a0001c0003t0006g0032 a0001c0003t0006g0033 others(8): Show |
11 | HG02145.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+2535G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372532 | |||||||
| chr4:48372572 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.538+2575A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372572 | |||||||
| chr4:48372635 | C | T | 125 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(122): Show |
127 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.538+2638C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372635 | |||||||
| chr4:48372888 | T | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.538+2891T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372888 | |||||||
| chr4:48372986 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.538+2989C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372986 | |||||||
| chr4:48372997 | A | G | 1 | a0001c0001t0013g0283 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.538+3000A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48372997 | |||||||
| chr4:48373257 | C | T | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.538+3260C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373257 | |||||||
| chr4:48373568 | G | A | 2 | a0001c0001t0003g0009 a0001c0001t0003g0208 |
3 | HG00735.hp1 HG03704.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.538+3571G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373568 | |||||||
| chr4:48373573 | G | C | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.538+3576G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373573 | |||||||
| chr4:48373762 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.538+3765C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373762 | |||||||
| chr4:48373773 | GCTTACAC others(14): Show |
G | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.538+3780_538+3800d others(23): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48373773 | ||||||
| chr4:48373838 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.538+3841C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373838 | |||||||
| chr4:48373843 | C | A | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.538+3846C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373843 | |||||||
| chr4:48373920 | C | T | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG02258.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.538+3923C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373920 | |||||||
| chr4:48373993 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-3903G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48373993 | |||||||
| chr4:48374081 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-3815G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374081 | |||||||
| chr4:48374093 | G | C | 1 | a0001c0001t0002g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.539-3803G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374093 | |||||||
| chr4:48374179 | A | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-3717A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374179 | |||||||
| chr4:48374260 | G | A | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.539-3636G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374260 | |||||||
| chr4:48374339 | C | T | 1 | a0001c0001t0003g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.539-3557C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374339 | |||||||
| chr4:48374396 | C | G | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.539-3500C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374396 | |||||||
| chr4:48374586 | G | A | 2 | a0001c0001t0002g0227 a0001c0001t0002g0308 |
2 | HG01891.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.539-3310G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374586 | |||||||
| chr4:48374762 | A | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-3134A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374762 | |||||||
| chr4:48374782 | G | T | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.539-3114G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374782 | |||||||
| chr4:48374785 | A | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.539-3111A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374785 | |||||||
| chr4:48374789 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(114): Show |
121 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(118): Show |
intron_variant | MODIFIER | c.539-3107A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374789 | |||||||
| chr4:48374802 | A | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.539-3094A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374802 | |||||||
| chr4:48374834 | T | A | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-3062T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48374834 | |||||||
| chr4:48375036 | T | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.539-2860T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375036 | |||||||
| chr4:48375109 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-2787G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375109 | |||||||
| chr4:48375119 | G | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-2777G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375119 | |||||||
| chr4:48375120 | A | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.539-2776A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375120 | |||||||
| chr4:48375223 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.539-2673G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375223 | |||||||
| chr4:48375271 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-2625C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375271 | |||||||
| chr4:48375302 | T | A | 2 | a0001c0003t0006g0032 a0001c0003t0006g0033 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.539-2594T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375302 | |||||||
| chr4:48375390 | C | T | 1 | a0001c0001t0004g0285 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.539-2506C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375390 | |||||||
| chr4:48375495 | C | CT | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(2): Show |
5 | HG02109.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.539-2393dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48375495 | ||||||
| chr4:48375616 | A | G | 3 | a0001c0004t0002g0229 a0001c0004t0002g0230 a0001c0004t0002g0231 |
3 | HG02451.hp1 HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.539-2280A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375616 | |||||||
| chr4:48375670 | G | A | 1 | a0002c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.539-2226G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375670 | |||||||
| chr4:48375845 | A | G | 15 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(12): Show |
16 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.539-2051A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375845 | |||||||
| chr4:48375911 | C | T | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.539-1985C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48375911 | |||||||
| chr4:48376144 | G | T | 1 | a0001c0002t0005g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.539-1752G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376144 | |||||||
| chr4:48376228 | C | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.539-1668C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376228 | |||||||
| chr4:48376246 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.539-1650G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376246 | |||||||
| chr4:48376251 | C | T | 1 | a0001c0001t0002g0261 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.539-1645C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376251 | |||||||
| chr4:48376369 | C | A | 25 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.539-1527C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376369 | |||||||
| chr4:48376411 | C | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1485C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376411 | |||||||
| chr4:48376456 | GAA | G | 125 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(122): Show |
127 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.539-1423_539-1422d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376456 | ||||||
| chr4:48376456 | GAAA | G | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.539-1424_539-1422d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376456 | ||||||
| chr4:48376475 | G | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.539-1421G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376475 | |||||||
| chr4:48376562 | A | C | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.539-1334A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376562 | |||||||
| chr4:48376619 | C | CT | 19 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0037 others(16): Show |
19 | HG00738.hp1 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.539-1257dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | ||||||
| chr4:48376619 | CT | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0030 others(17): Show |
20 | HG00741.hp2 HG01255.hp1 HG01943.hp1 others(17): Show |
intron_variant | MODIFIER | c.539-1257delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | ||||||
| chr4:48376619 | CTT | C | 139 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(136): Show |
142 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.539-1258_539-1257d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376619 | ||||||
| chr4:48376639 | T | G | 2 | a0001c0001t0011g0021 a0001c0001t0011g0031 |
2 | HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.539-1257T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376639 | |||||||
| chr4:48376744 | C | T | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.539-1152C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376744 | |||||||
| chr4:48376771 | C | G | 1 | a0001c0001t0004g0260 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.539-1125C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376771 | |||||||
| chr4:48376824 | C | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.539-1072C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376824 | |||||||
| chr4:48376833 | G | A | 1 | a0001c0003t0006g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.539-1063G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376833 | |||||||
| chr4:48376853 | C | T | 1 | a0001c0001t0004g0259 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.539-1043C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376853 | |||||||
| chr4:48376902 | C | T | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.539-994C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376902 | |||||||
| chr4:48376913 | C | CT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0039 others(29): Show |
34 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.539-962dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376913 | ||||||
| chr4:48376913 | CT | C | 176 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0023 others(173): Show |
179 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.539-962delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376913 | ||||||
| chr4:48376965 | G | C | 1 | a0001c0001t0002g0309 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.539-931G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376965 | |||||||
| chr4:48376989 | TA | T | 25 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.539-897delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48376989 | ||||||
| chr4:48376999 | A | T | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.539-897A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48376999 | |||||||
| chr4:48377102 | A | T | 1 | a0001c0001t0003g0182 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.539-794A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377102 | |||||||
| chr4:48377185 | T | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
174 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(171): Show |
intron_variant | MODIFIER | c.539-711T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377185 | |||||||
| chr4:48377194 | A | T | 1 | a0001c0001t0010g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.539-702A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377194 | |||||||
| chr4:48377207 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.539-689G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377207 | |||||||
| chr4:48377316 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.539-580T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377316 | |||||||
| chr4:48377336 | A | AT | 259 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(256): Show |
268 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.539-539dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48377336 | ||||||
| chr4:48377336 | AT | A | 6 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0157 others(3): Show |
6 | HG01167.hp1 HG01256.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.539-539delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr4 | 48377336 | ||||||
| chr4:48377398 | C | T | 1 | a0002c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.539-498C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377398 | |||||||
| chr4:48377447 | G | A | 14 | a0001c0001t0027g0179 a0001c0002t0005g0008 a0001c0002t0005g0169 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.539-449G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377447 | |||||||
| chr4:48377849 | C | G | 3 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 |
3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.539-47C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 2/7 | chr4 | 48377849 | |||||||
| chr4:48378078 | T | C | 1 | a0001c0003t0006g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.703+18T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378078 | |||||||
| chr4:48378191 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.703+131G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378191 | |||||||
| chr4:48378229 | C | T | 3 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0034g0183 |
3 | NA18963.hp2 NA18992.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.703+169C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378229 | |||||||
| chr4:48378342 | T | G | 13 | a0001c0001t0029g0163 a0001c0002t0030g0201 a0001c0003t0006g0032 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.703+282T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378342 | |||||||
| chr4:48378463 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(154): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.703+403A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378463 | |||||||
| chr4:48378531 | A | G | 3 | a0001c0001t0003g0203 a0001c0001t0003g0204 a0001c0001t0003g0205 |
3 | HG00099.hp1 HG00642.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.703+471A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378531 | |||||||
| chr4:48378580 | C | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.703+520C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378580 | |||||||
| chr4:48378582 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.703+522A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378582 | |||||||
| chr4:48378775 | G | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.703+715G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378775 | |||||||
| chr4:48378847 | T | C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.703+787T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48378847 | |||||||
| chr4:48379048 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.704-642C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379048 | |||||||
| chr4:48379265 | T | C | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.704-425T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379265 | |||||||
| chr4:48379305 | C | T | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.704-385C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379305 | |||||||
| chr4:48379558 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.704-132A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | chr4 | 48379558 | |||||||
| chr4:48379673 | CT | C | 9 | a0001c0001t0001g0038 a0001c0001t0001g0042 a0001c0001t0001g0156 others(6): Show |
9 | HG01256.hp2 HG02615.hp1 HG02809.hp2 others(6): Show |
splice_region_variant&intron_variant | LOW | c.704-4delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr4 | 48379673 | ||||||
| chr4:48379893 | T | C | 13 | a0001c0001t0029g0163 a0001c0002t0030g0201 a0001c0003t0006g0032 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.862+45T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48379893 | |||||||
| chr4:48379942 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+94T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48379942 | |||||||
| chr4:48380000 | A | G | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.862+152A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380000 | |||||||
| chr4:48380066 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+218A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380066 | |||||||
| chr4:48380096 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+248A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380096 | |||||||
| chr4:48380526 | C | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(291): Show |
303 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(300): Show |
intron_variant | MODIFIER | c.862+678C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380526 | |||||||
| chr4:48380775 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.862+927C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48380775 | |||||||
| chr4:48381075 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.862+1227G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381075 | |||||||
| chr4:48381475 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.863-1093A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381475 | |||||||
| chr4:48381548 | C | T | 1 | a0001c0001t0002g0271 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.863-1020C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381548 | |||||||
| chr4:48381655 | C | A | 1 | a0001c0001t0003g0210 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.863-913C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381655 | |||||||
| chr4:48381753 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.863-815G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48381753 | |||||||
| chr4:48382482 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.863-86T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 4/7 | chr4 | 48382482 | |||||||
| chr4:48382974 | G | A | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1222+47G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48382974 | |||||||
| chr4:48383038 | C | T | 1 | a0001c0001t0002g0228 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1222+111C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383038 | |||||||
| chr4:48383080 | A | C | 1 | a0001c0001t0002g0297 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1222+153A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383080 | |||||||
| chr4:48383102 | A | C | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1222+175A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383102 | |||||||
| chr4:48383167 | TC | T | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1222+241delC | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383167 | |||||||
| chr4:48383168 | C | CA | 7 | a0001c0001t0002g0326 a0001c0001t0004g0250 a0001c0001t0004g0285 others(4): Show |
7 | HG03139.hp2 HG03225.hp2 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.1222+262dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | ||||||
| chr4:48383168 | CA | C | 17 | a0001c0001t0001g0069 a0001c0001t0001g0071 a0001c0001t0001g0080 others(14): Show |
17 | HG01070.hp2 HG01257.hp1 HG01515.hp1 others(14): Show |
intron_variant | MODIFIER | c.1222+262delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | ||||||
| chr4:48383168 | CAA | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(143): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.1222+261_1222+262d others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | ||||||
| chr4:48383168 | CAAA | C | 17 | a0001c0001t0001g0023 a0001c0001t0001g0038 a0001c0001t0001g0040 others(14): Show |
17 | HG00733.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1222+260_1222+262d others(5): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr4 | 48383168 | ||||||
| chr4:48383185 | A | G | 3 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0096 |
3 | NA18943.hp1 NA19012.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1222+258A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383185 | |||||||
| chr4:48383194 | C | A | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1222+267C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383194 | |||||||
| chr4:48383240 | A | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1222+313A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383240 | |||||||
| chr4:48383487 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1223-160C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383487 | |||||||
| chr4:48383604 | T | C | 1 | a0001c0001t0003g0188 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1223-43T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 5/7 | chr4 | 48383604 | |||||||
| chr4:48383958 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1360+174A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48383958 | |||||||
| chr4:48384056 | A | G | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1360+272A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384056 | |||||||
| chr4:48384076 | TTTTGCTT others(17): Show |
T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+293_1360+316d others(26): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384076 | |||||||
| chr4:48384145 | C | T | 1 | a0001c0001t0007g0323 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+361C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384145 | |||||||
| chr4:48384158 | T | C | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1360+374T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384158 | |||||||
| chr4:48384206 | T | G | 1 | a0001c0001t0002g0287 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1360+422T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384206 | |||||||
| chr4:48384251 | A | G | 1 | a0001c0001t0003g0181 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1360+467A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384251 | |||||||
| chr4:48384312 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+528C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384312 | |||||||
| chr4:48384335 | A | G | 1 | a0001c0001t0004g0226 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1360+551A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384335 | |||||||
| chr4:48384581 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360+797A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384581 | |||||||
| chr4:48384800 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1360+1016C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384800 | |||||||
| chr4:48384874 | C | T | 2 | a0001c0001t0002g0279 a0001c0001t0007g0330 |
2 | HG02602.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1360+1090C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384874 | |||||||
| chr4:48384905 | T | G | 1 | a0001c0001t0004g0249 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1360+1121T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384905 | |||||||
| chr4:48384914 | A | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+1130A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48384914 | |||||||
| chr4:48385056 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1360+1272T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385056 | |||||||
| chr4:48385505 | T | C | 1 | a0001c0001t0002g0306 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1360+1721T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385505 | |||||||
| chr4:48385638 | C | CT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1360+1864dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48385638 | ||||||
| chr4:48385748 | G | A | 1 | a0001c0001t0034g0183 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1360+1964G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385748 | |||||||
| chr4:48385811 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1360+2027T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385811 | |||||||
| chr4:48385834 | T | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(34): Show |
40 | HG00140.hp2 HG00438.hp2 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.1360+2050T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385834 | |||||||
| chr4:48385942 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1360+2158G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48385942 | |||||||
| chr4:48385942 | G | GT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0083 others(3): Show |
7 | HG00558.hp1 HG02155.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+2171dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48385942 | ||||||
| chr4:48386090 | GA | G | 11 | a0001c0001t0001g0071 a0001c0001t0001g0073 a0001c0001t0001g0074 others(8): Show |
11 | HG00408.hp1 HG02056.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+2325delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48386090 | ||||||
| chr4:48386090 | GAA | G | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+2324_1360+232 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48386090 | ||||||
| chr4:48386100 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1360+2316A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386100 | |||||||
| chr4:48386107 | A | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(175): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(182): Show |
intron_variant | MODIFIER | c.1360+2323A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386107 | |||||||
| chr4:48386275 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1360+2491C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386275 | |||||||
| chr4:48386286 | A | G | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+2502A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386286 | |||||||
| chr4:48386357 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1360+2573G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386357 | |||||||
| chr4:48386489 | A | G | 1 | a0001c0001t0002g0258 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1360+2705A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386489 | |||||||
| chr4:48386594 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | NA18946.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1360+2810A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386594 | |||||||
| chr4:48386640 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1360+2856C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386640 | |||||||
| chr4:48386752 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | HG00558.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.1360+2968G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386752 | |||||||
| chr4:48386758 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1360+2974T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386758 | |||||||
| chr4:48386806 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+3022C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386806 | |||||||
| chr4:48386844 | G | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+3060G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386844 | |||||||
| chr4:48386865 | A | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+3081A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386865 | |||||||
| chr4:48386962 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360+3178C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48386962 | |||||||
| chr4:48387094 | C | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3310C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387094 | |||||||
| chr4:48387124 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3340C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387124 | |||||||
| chr4:48387133 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1360+3349T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387133 | |||||||
| chr4:48387208 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+3424A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387208 | |||||||
| chr4:48387220 | T | A | 2 | a0001c0001t0002g0292 a0001c0001t0002g0304 |
2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+3436T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387220 | |||||||
| chr4:48387244 | A | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0219 |
3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+3460A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387244 | |||||||
| chr4:48387416 | A | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+3632A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387416 | |||||||
| chr4:48387486 | A | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+3702A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387486 | |||||||
| chr4:48387577 | G | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+3793G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387577 | |||||||
| chr4:48387643 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+3859C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387643 | |||||||
| chr4:48387692 | A | G | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+3908A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387692 | |||||||
| chr4:48387764 | A | G | 1 | a0001c0001t0002g0305 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1360+3980A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48387764 | |||||||
| chr4:48387801 | AATAT | A | 4 | a0001c0001t0002g0295 a0001c0001t0002g0326 a0001c0001t0015g0293 others(1): Show |
4 | HG02717.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1360+4022_1360+402 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48387801 | ||||||
| chr4:48388560 | T | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+4776T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388560 | |||||||
| chr4:48388608 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1360+4824A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388608 | |||||||
| chr4:48388812 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1360+5028C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48388812 | |||||||
| chr4:48389109 | TAA | T | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+5326_1360+532 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389109 | |||||||
| chr4:48389200 | A | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+5416A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389200 | |||||||
| chr4:48389362 | C | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(139): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.1360+5578C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389362 | |||||||
| chr4:48389392 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1360+5608A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389392 | |||||||
| chr4:48389471 | A | G | 1 | a0001c0001t0002g0223 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1360+5687A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389471 | |||||||
| chr4:48389483 | T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+5699T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389483 | |||||||
| chr4:48389511 | C | T | 1 | a0001c0001t0004g0260 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1360+5727C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389511 | |||||||
| chr4:48389667 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0219 |
3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1360+5883G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389667 | |||||||
| chr4:48389764 | A | T | 1 | a0001c0004t0002g0230 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1360+5980A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389764 | |||||||
| chr4:48389811 | A | G | 1 | a0001c0001t0003g0196 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1360+6027A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389811 | |||||||
| chr4:48389927 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1360+6143T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389927 | |||||||
| chr4:48389945 | A | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(183): Show |
intron_variant | MODIFIER | c.1360+6161A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48389945 | |||||||
| chr4:48390078 | CTTTTTCT others(6): Show |
C | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1360+6300_1360+631 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48390078 | ||||||
| chr4:48390084 | C | CT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(137): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.1360+6314dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48390084 | ||||||
| chr4:48390191 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+6407C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390191 | |||||||
| chr4:48390226 | C | T | 1 | a0001c0001t0002g0257 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1360+6442C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390226 | |||||||
| chr4:48390245 | T | C | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+6461T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390245 | |||||||
| chr4:48390266 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1360+6482A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390266 | |||||||
| chr4:48390622 | A | G | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1360+6838A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390622 | |||||||
| chr4:48390641 | T | G | 1 | a0001c0003t0006g0216 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1360+6857T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390641 | |||||||
| chr4:48390741 | G | A | 1 | a0001c0001t0013g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1360+6957G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390741 | |||||||
| chr4:48390924 | A | C | 25 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(22): Show |
27 | HG00642.hp1 HG01255.hp1 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+7140A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48390924 | |||||||
| chr4:48391193 | G | A | 1 | a0001c0001t0002g0309 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1360+7409G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391193 | |||||||
| chr4:48391417 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1360+7633G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391417 | |||||||
| chr4:48391542 | T | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+7758T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391542 | |||||||
| chr4:48391663 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(150): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.1360+7879A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391663 | |||||||
| chr4:48391704 | A | G | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+7920A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391704 | |||||||
| chr4:48391977 | C | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+8193C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48391977 | |||||||
| chr4:48392062 | CAG | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+8281_1360+828 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48392062 | ||||||
| chr4:48392101 | G | A | 1 | a0001c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+8317G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392101 | |||||||
| chr4:48392307 | G | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0198 |
2 | HG01516.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1360+8523G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392307 | |||||||
| chr4:48392337 | T | A | 20 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0016 others(17): Show |
22 | HG01255.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.1360+8553T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392337 | |||||||
| chr4:48392397 | A | G | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+8613A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392397 | |||||||
| chr4:48392433 | T | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1360+8649T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392433 | |||||||
| chr4:48392557 | G | A | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+8773G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392557 | |||||||
| chr4:48392576 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.1360+8792T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392576 | |||||||
| chr4:48392576 | T | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+8792T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392576 | |||||||
| chr4:48392598 | A | G | 1 | a0001c0001t0002g0322 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1360+8814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392598 | |||||||
| chr4:48392796 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1360+9012C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392796 | |||||||
| chr4:48392798 | A | G | 116 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(113): Show |
118 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(115): Show |
intron_variant | MODIFIER | c.1360+9014A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392798 | |||||||
| chr4:48392858 | T | G | 2 | a0001c0001t0004g0317 a0001c0001t0004g0318 |
2 | NA18950.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1360+9074T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392858 | |||||||
| chr4:48392900 | A | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9116A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392900 | |||||||
| chr4:48392980 | G | A | 13 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0068 others(10): Show |
13 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1360+9196G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392980 | |||||||
| chr4:48392996 | A | G | 1 | a0001c0001t0026g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1360+9212A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392996 | |||||||
| chr4:48392999 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1360+9215A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48392999 | |||||||
| chr4:48393312 | C | T | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9528C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393312 | |||||||
| chr4:48393386 | T | TTG | 8 | a0001c0001t0001g0083 a0001c0001t0001g0217 a0001c0001t0003g0184 others(5): Show |
8 | HG02155.hp1 HG02886.hp1 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.1360+9638_1360+963 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTG | 9 | a0001c0001t0001g0057 a0001c0001t0001g0103 a0001c0001t0001g0105 others(6): Show |
9 | HG01515.hp2 HG02015.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9636_1360+963 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTG | 72 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(69): Show |
75 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.1360+9634_1360+963 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTGT others(1): Show |
160 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0013 others(157): Show |
166 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.1360+9632_1360+963 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTGT others(3): Show |
17 | a0001c0001t0001g0020 a0001c0001t0001g0068 a0001c0001t0001g0082 others(14): Show |
17 | HG00642.hp1 HG01069.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1360+9630_1360+963 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTGT others(5): Show |
7 | a0001c0001t0002g0256 a0001c0001t0002g0290 a0001c0001t0002g0292 others(4): Show |
7 | HG00099.hp2 HG02523.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+9628_1360+963 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTGT others(7): Show |
5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0002g0222 others(2): Show |
5 | HG00558.hp2 HG01255.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9626_1360+963 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTGTGTGT others(9): Show |
6 | a0001c0001t0002g0325 a0001c0002t0009g0174 a0001c0002t0009g0176 others(3): Show |
6 | HG00741.hp1 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+9624_1360+963 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTTGTGTG others(6): Show |
1 | a0001c0003t0012g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1360+9603_1360+960 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | T | TTTGTGTG others(12): Show |
1 | a0001c0003t0012g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1360+9603_1360+960 others(23): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393386 | TTG | T | 5 | a0001c0001t0001g0158 a0001c0001t0003g0180 a0001c0001t0003g0198 others(2): Show |
5 | HG00099.hp1 HG01433.hp1 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+9638_1360+963 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48393386 | ||||||
| chr4:48393387 | TGTGTGTG others(8): Show |
T | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1360+9604_1360+961 others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393387 | |||||||
| chr4:48393439 | G | C | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+9655G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393439 | |||||||
| chr4:48393735 | C | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+9951C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393735 | |||||||
| chr4:48393781 | A | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+9997A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393781 | |||||||
| chr4:48393801 | A | G | 1 | a0001c0002t0005g0178 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1360+10017A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393801 | |||||||
| chr4:48393972 | A | G | 3 | a0001c0001t0002g0299 a0001c0001t0002g0302 a0001c0001t0002g0305 |
3 | HG01070.hp2 HG01071.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1360+10188A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393972 | |||||||
| chr4:48393991 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1360+10207G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393991 | |||||||
| chr4:48393993 | A | G | 27 | a0001c0001t0016g0333 a0001c0001t0029g0163 a0001c0002t0005g0008 others(24): Show |
28 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.1360+10209A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48393993 | |||||||
| chr4:48394150 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+10366C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394150 | |||||||
| chr4:48394319 | A | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+10535A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394319 | |||||||
| chr4:48394479 | C | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(292): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.1360+10695C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394479 | |||||||
| chr4:48394736 | G | T | 3 | a0001c0001t0002g0243 a0001c0001t0002g0309 a0001c0001t0002g0310 |
3 | HG02055.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1360+10952G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394736 | |||||||
| chr4:48394767 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+10983A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394767 | |||||||
| chr4:48394924 | T | A | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+11140T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48394924 | |||||||
| chr4:48395014 | A | G | 1 | a0001c0001t0002g0267 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1360+11230A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395014 | |||||||
| chr4:48395031 | C | T | 1 | a0001c0002t0005g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1360+11247C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395031 | |||||||
| chr4:48395043 | G | T | 1 | a0001c0001t0007g0323 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+11259G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395043 | |||||||
| chr4:48395139 | A | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1360+11355A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395139 | |||||||
| chr4:48395260 | C | G | 11 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0068 others(8): Show |
11 | HG00408.hp2 HG00438.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+11476C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395260 | |||||||
| chr4:48395445 | G | T | 2 | a0001c0001t0002g0292 a0001c0001t0002g0304 |
2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+11661G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395445 | |||||||
| chr4:48395445 | GA | G | 107 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(104): Show |
109 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(106): Show |
intron_variant | MODIFIER | c.1360+11671delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395445 | ||||||
| chr4:48395446 | A | G | 2 | a0001c0001t0002g0292 a0001c0001t0002g0304 |
2 | HG03942.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1360+11662A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395446 | |||||||
| chr4:48395458 | A | G | 1 | a0001c0001t0002g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1360+11674A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395458 | |||||||
| chr4:48395477 | C | T | 38 | a0001c0001t0002g0221 a0001c0001t0002g0232 a0001c0001t0002g0233 others(35): Show |
38 | HG00597.hp2 HG01346.hp1 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.1360+11693C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395477 | |||||||
| chr4:48395607 | G | A | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+11823G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395607 | |||||||
| chr4:48395675 | A | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+11891A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395675 | |||||||
| chr4:48395729 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0088 |
2 | NA18941.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1360+11945T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395729 | |||||||
| chr4:48395780 | G | T | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+11996G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395780 | |||||||
| chr4:48395810 | C | CTTT | 6 | a0001c0003t0006g0036 a0001c0003t0006g0211 a0001c0003t0006g0212 others(3): Show |
6 | HG01891.hp2 HG02145.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1360+12042_1360+12 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTT | 9 | a0001c0001t0001g0012 a0001c0001t0001g0059 a0001c0001t0001g0064 others(6): Show |
9 | HG01070.hp1 HG01175.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12041_1360+12 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTT | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(128): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.1360+12040_1360+12 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTT | 102 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0143 others(99): Show |
104 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(101): Show |
intron_variant | MODIFIER | c.1360+12039_1360+12 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT | 15 | a0001c0001t0001g0098 a0001c0001t0002g0236 a0001c0001t0002g0237 others(12): Show |
15 | HG00741.hp1 HG02004.hp1 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+12038_1360+12 others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0003g0180 a0001c0001t0003g0198 a0001c0001t0003g0210 others(4): Show |
7 | HG01516.hp1 HG02630.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+12036_1360+12 others(15): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT others(3): Show |
11 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(8): Show |
11 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+12035_1360+12 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+12031_1360+12 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT others(14): Show |
1 | a0001c0003t0012g0215 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1360+12044_1360+12 others(27): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | C | CTTTTTTT others(15): Show |
1 | a0001c0003t0012g0214 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1360+12044_1360+12 others(28): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395810 | CTTTTT | C | 11 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(8): Show |
12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1360+12040_1360+12 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48395810 | ||||||
| chr4:48395901 | A | G | 1 | a0001c0006t0001g0097 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1360+12117A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395901 | |||||||
| chr4:48395909 | A | G | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1360+12125A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395909 | |||||||
| chr4:48395982 | G | T | 1 | a0001c0001t0002g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1360+12198G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48395982 | |||||||
| chr4:48396219 | A | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12435A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396219 | |||||||
| chr4:48396331 | A | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(309): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1360+12547A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396331 | |||||||
| chr4:48396334 | G | A | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1360+12550G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396334 | |||||||
| chr4:48396405 | A | C | 1 | a0001c0001t0026g0070 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1360+12621A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396405 | |||||||
| chr4:48396466 | A | G | 1 | a0001c0001t0025g0047 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1360+12682A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396466 | |||||||
| chr4:48396660 | C | A | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+12876C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396660 | |||||||
| chr4:48396718 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+12934C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396718 | |||||||
| chr4:48396760 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+12976G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396760 | |||||||
| chr4:48396798 | C | T | 1 | a0001c0001t0002g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1360+13014C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396798 | |||||||
| chr4:48396958 | G | A | 3 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 |
3 | HG02258.hp2 HG02559.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1360+13174G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48396958 | |||||||
| chr4:48397283 | T | C | 1 | a0001c0001t0002g0272 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1360+13499T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397283 | |||||||
| chr4:48397362 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+13578T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397362 | |||||||
| chr4:48397404 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+13620T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397404 | |||||||
| chr4:48397471 | T | C | 4 | a0001c0003t0006g0211 a0001c0003t0006g0212 a0001c0003t0006g0213 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+13687T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397471 | |||||||
| chr4:48397498 | T | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+13714T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397498 | |||||||
| chr4:48397627 | A | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+13843A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397627 | |||||||
| chr4:48397664 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1360+13880C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397664 | |||||||
| chr4:48397861 | C | T | 188 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1360+14077C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397861 | |||||||
| chr4:48397894 | C | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1360+14110C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397894 | |||||||
| chr4:48397895 | G | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1360+14111G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397895 | |||||||
| chr4:48397978 | A | G | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1360+14194A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48397978 | |||||||
| chr4:48398024 | C | T | 1 | a0001c0001t0013g0235 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1360+14240C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398024 | |||||||
| chr4:48398133 | A | G | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+14349A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398133 | |||||||
| chr4:48398146 | T | C | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+14362T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398146 | |||||||
| chr4:48398154 | G | C | 1 | a0004c0009t0002g0324 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1360+14370G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398154 | |||||||
| chr4:48398470 | C | T | 1 | a0001c0002t0005g0169 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1360+14686C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398470 | |||||||
| chr4:48398707 | G | A | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1360+14923G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398707 | |||||||
| chr4:48398708 | C | A | 1 | a0001c0001t0003g0198 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1360+14924C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398708 | |||||||
| chr4:48398781 | G | A | 1 | a0001c0001t0003g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1360+14997G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398781 | |||||||
| chr4:48398876 | T | C | 3 | a0001c0001t0003g0180 a0001c0001t0003g0198 a0001c0001t0003g0210 |
3 | HG01516.hp1 NA18943.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1360+15092T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398876 | |||||||
| chr4:48398894 | C | G | 188 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(185): Show |
196 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.1360+15110C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398894 | |||||||
| chr4:48398941 | G | A | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+15157G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398941 | |||||||
| chr4:48398967 | T | A | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1360+15183T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398967 | |||||||
| chr4:48398976 | G | C | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1360+15192G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398976 | |||||||
| chr4:48398998 | G | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+15214G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48398998 | |||||||
| chr4:48399126 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1360+15342C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399126 | |||||||
| chr4:48399132 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1360+15348A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399132 | |||||||
| chr4:48399152 | C | A | 4 | a0001c0002t0009g0174 a0001c0002t0009g0177 a0001c0002t0009g0200 others(1): Show |
4 | HG00741.hp2 HG01074.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+15368C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399152 | |||||||
| chr4:48399266 | T | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+15482T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399266 | |||||||
| chr4:48399400 | T | G | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1360+15616T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399400 | |||||||
| chr4:48399622 | A | G | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1360+15838A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399622 | |||||||
| chr4:48399894 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+16110G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399894 | |||||||
| chr4:48399897 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1360+16113C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48399897 | |||||||
| chr4:48400031 | A | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1360+16247A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400031 | |||||||
| chr4:48400377 | G | A | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1360+16593G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400377 | |||||||
| chr4:48400388 | CT | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(125): Show |
134 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.1360+16630delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | ||||||
| chr4:48400388 | CTTTTTTT | C | 8 | a0001c0001t0002g0228 a0001c0001t0002g0237 a0001c0001t0002g0247 others(5): Show |
8 | HG01243.hp2 HG01346.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+16624_1360+16 others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | ||||||
| chr4:48400388 | CTTTTTTT others(1): Show |
C | 143 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(140): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1360+16623_1360+16 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | ||||||
| chr4:48400388 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+16620_1360+16 others(17): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | ||||||
| chr4:48400388 | CTTTTTTT others(5): Show |
C | 25 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(22): Show |
26 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.1360+16619_1360+16 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400388 | ||||||
| chr4:48400608 | G | T | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1360+16824G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400608 | |||||||
| chr4:48400746 | A | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1360+16962A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400746 | |||||||
| chr4:48400766 | CGTTT | C | 14 | a0001c0001t0004g0312 a0001c0002t0005g0008 a0001c0002t0005g0169 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+16999_1360+17 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48400766 | ||||||
| chr4:48400898 | G | C | 1 | a0001c0001t0001g0122 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1360+17114G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400898 | |||||||
| chr4:48400923 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1360+17139C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48400923 | |||||||
| chr4:48401006 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1360+17222G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401006 | |||||||
| chr4:48401103 | G | C | 1 | a0001c0001t0007g0323 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1360+17319G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401103 | |||||||
| chr4:48401284 | A | G | 1 | a0001c0002t0009g0177 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1360+17500A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401284 | |||||||
| chr4:48401295 | T | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1360+17511T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401295 | |||||||
| chr4:48401388 | A | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1360+17604A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401388 | |||||||
| chr4:48401403 | G | T | 1 | a0001c0001t0001g0019 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1360+17619G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401403 | |||||||
| chr4:48401419 | G | C | 2 | a0001c0001t0002g0223 a0001c0001t0002g0281 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1360+17635G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401419 | |||||||
| chr4:48401442 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1360+17658A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401442 | |||||||
| chr4:48401523 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+17739G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401523 | |||||||
| chr4:48401906 | T | C | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1360+18122T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48401906 | |||||||
| chr4:48402046 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-18079T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402046 | |||||||
| chr4:48402050 | A | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0117 |
2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1361-18075A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402050 | |||||||
| chr4:48402057 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1361-18068G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402057 | |||||||
| chr4:48402077 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-18048G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402077 | |||||||
| chr4:48402199 | A | AT | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-17926_1361-17 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402199 | |||||||
| chr4:48402200 | A | AT | 148 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(145): Show |
155 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1361-17911dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48402200 | ||||||
| chr4:48402200 | A | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-17925A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402200 | |||||||
| chr4:48402224 | C | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-17901C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402224 | |||||||
| chr4:48402225 | G | A | 1 | a0001c0001t0004g0248 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1361-17900G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402225 | |||||||
| chr4:48402246 | T | C | 2 | a0001c0001t0002g0278 a0001c0001t0002g0282 |
2 | NA18977.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.1361-17879T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402246 | |||||||
| chr4:48402248 | T | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-17877T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402248 | |||||||
| chr4:48402323 | T | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-17802T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402323 | |||||||
| chr4:48402549 | C | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-17576C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402549 | |||||||
| chr4:48402765 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-17360C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402765 | |||||||
| chr4:48402845 | T | A | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-17280T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402845 | |||||||
| chr4:48402908 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-17217G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48402908 | |||||||
| chr4:48403361 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1361-16764G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403361 | |||||||
| chr4:48403374 | A | C | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-16751A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403374 | |||||||
| chr4:48403417 | C | T | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-16708C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403417 | |||||||
| chr4:48403465 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-16660A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403465 | |||||||
| chr4:48403612 | C | T | 1 | a0001c0006t0001g0097 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361-16513C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403612 | |||||||
| chr4:48403626 | C | T | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-16499C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403626 | |||||||
| chr4:48403639 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1361-16486G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403639 | |||||||
| chr4:48403720 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1361-16405T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403720 | |||||||
| chr4:48403720 | T | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-16405T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403720 | |||||||
| chr4:48403846 | G | A | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-16279G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403846 | |||||||
| chr4:48403892 | G | A | 1 | a0001c0002t0005g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1361-16233G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48403892 | |||||||
| chr4:48404074 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-16051T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404074 | |||||||
| chr4:48404147 | A | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-15978A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404147 | |||||||
| chr4:48404247 | A | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-15878A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404247 | |||||||
| chr4:48404413 | T | G | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00323.hp1 HG01358.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-15712T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404413 | |||||||
| chr4:48404419 | C | CT | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-15704dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48404419 | ||||||
| chr4:48404555 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1361-15570A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404555 | |||||||
| chr4:48404674 | G | T | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-15451G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404674 | |||||||
| chr4:48404819 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1361-15306A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404819 | |||||||
| chr4:48404827 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1361-15298C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404827 | |||||||
| chr4:48404956 | C | T | 1 | a0001c0001t0002g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1361-15169C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48404956 | |||||||
| chr4:48405172 | C | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-14953C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405172 | |||||||
| chr4:48405272 | C | T | 1 | a0001c0001t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1361-14853C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405272 | |||||||
| chr4:48405335 | A | G | 1 | a0001c0001t0002g0326 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1361-14790A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405335 | |||||||
| chr4:48405359 | CCTTTTTG others(6): Show |
C | 1 | a0001c0001t0002g0307 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1361-14759_1361-14 others(19): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48405359 | ||||||
| chr4:48405527 | T | C | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-14598T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405527 | |||||||
| chr4:48405595 | A | G | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-14530A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405595 | |||||||
| chr4:48405656 | A | C | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-14469A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405656 | |||||||
| chr4:48405758 | G | A | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-14367G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405758 | |||||||
| chr4:48405969 | G | A | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1361-14156G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48405969 | |||||||
| chr4:48406024 | C | T | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-14101C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406024 | |||||||
| chr4:48406179 | A | G | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-13946A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406179 | |||||||
| chr4:48406296 | T | C | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-13829T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406296 | |||||||
| chr4:48406461 | T | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0069 a0001c0001t0001g0077 others(8): Show |
12 | HG00280.hp2 HG01070.hp1 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-13664T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406461 | |||||||
| chr4:48406472 | A | G | 1 | a0001c0001t0002g0290 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1361-13653A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406472 | |||||||
| chr4:48406516 | T | G | 1 | a0001c0001t0028g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1361-13609T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406516 | |||||||
| chr4:48406518 | T | G | 7 | a0001c0001t0001g0005 a0001c0001t0001g0126 a0001c0001t0001g0127 others(4): Show |
8 | HG01070.hp1 HG01433.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-13607T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406518 | |||||||
| chr4:48406525 | CT | C | 19 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0060 others(16): Show |
19 | HG00558.hp1 HG01169.hp1 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1361-13580delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | ||||||
| chr4:48406525 | CTT | C | 23 | a0001c0001t0001g0160 a0001c0001t0003g0190 a0001c0002t0005g0169 others(20): Show |
23 | HG00741.hp2 HG01074.hp1 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.1361-13581_1361-13 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | ||||||
| chr4:48406525 | CTTT | C | 143 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(140): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.1361-13582_1361-13 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | ||||||
| chr4:48406525 | CTTTT | C | 11 | a0001c0001t0002g0239 a0001c0001t0002g0261 a0001c0001t0002g0267 others(8): Show |
11 | HG01070.hp2 HG01256.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-13583_1361-13 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48406525 | ||||||
| chr4:48406527 | T | C | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-13598T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406527 | |||||||
| chr4:48406528 | T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-13597T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406528 | |||||||
| chr4:48406529 | T | C | 4 | a0001c0003t0006g0211 a0001c0003t0006g0212 a0001c0003t0006g0213 others(1): Show |
4 | HG02145.hp2 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-13596T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406529 | |||||||
| chr4:48406582 | C | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-13543C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406582 | |||||||
| chr4:48406609 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-13516A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406609 | |||||||
| chr4:48406725 | G | A | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-13400G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406725 | |||||||
| chr4:48406804 | A | G | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-13321A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406804 | |||||||
| chr4:48406894 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1361-13231T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48406894 | |||||||
| chr4:48407024 | A | G | 1 | a0006c0005t0001g0106 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1361-13101A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407024 | |||||||
| chr4:48407146 | T | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-12979T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407146 | |||||||
| chr4:48407176 | C | T | 331 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(328): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.1361-12949C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407176 | |||||||
| chr4:48407194 | C | T | 1 | a0002c0010t0001g0136 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1361-12931C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407194 | |||||||
| chr4:48407255 | T | C | 3 | a0001c0001t0002g0240 a0001c0001t0002g0252 a0001c0001t0002g0258 |
3 | NA18974.hp2 NA19065.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1361-12870T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407255 | |||||||
| chr4:48407270 | T | G | 154 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(151): Show |
161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1361-12855T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407270 | |||||||
| chr4:48407298 | C | T | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-12827C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407298 | |||||||
| chr4:48407324 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-12801C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407324 | |||||||
| chr4:48407330 | T | C | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-12795T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407330 | |||||||
| chr4:48407346 | C | T | 189 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(186): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.1361-12779C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407346 | |||||||
| chr4:48407538 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0048 others(59): Show |
63 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(60): Show |
intron_variant | MODIFIER | c.1361-12587A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407538 | |||||||
| chr4:48407748 | T | C | 1 | a0001c0001t0003g0192 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1361-12377T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407748 | |||||||
| chr4:48407954 | A | G | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-12171A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48407954 | |||||||
| chr4:48408098 | C | T | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-12027C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408098 | |||||||
| chr4:48408184 | G | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0198 |
2 | HG01516.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.1361-11941G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408184 | |||||||
| chr4:48408200 | C | T | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-11925C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408200 | |||||||
| chr4:48408229 | G | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11896G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408229 | |||||||
| chr4:48408333 | A | C | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-11792A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408333 | |||||||
| chr4:48408361 | C | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-11764C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408361 | |||||||
| chr4:48408437 | A | G | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11688A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408437 | |||||||
| chr4:48408446 | G | A | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-11679G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408446 | |||||||
| chr4:48408530 | C | CA | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(113): Show |
120 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.1361-11575dupA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | ||||||
| chr4:48408530 | C | CAA | 104 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0141 others(101): Show |
106 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1361-11576_1361-11 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | ||||||
| chr4:48408530 | C | CAAA | 53 | a0001c0001t0001g0218 a0001c0001t0002g0247 a0001c0001t0002g0262 others(50): Show |
58 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1361-11577_1361-11 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | ||||||
| chr4:48408530 | C | CAAAA | 14 | a0001c0001t0003g0165 a0001c0001t0003g0198 a0001c0002t0005g0008 others(11): Show |
15 | HG00733.hp1 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-11578_1361-11 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | ||||||
| chr4:48408530 | CA | C | 7 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0024 others(4): Show |
7 | HG01255.hp1 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-11575delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48408530 | ||||||
| chr4:48408672 | A | G | 1 | a0001c0001t0001g0158 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1361-11453A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408672 | |||||||
| chr4:48408687 | T | A | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-11438T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408687 | |||||||
| chr4:48408725 | C | G | 6 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(3): Show |
7 | HG01069.hp2 HG01109.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-11400C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408725 | |||||||
| chr4:48408904 | G | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-11221G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408904 | |||||||
| chr4:48408932 | C | T | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-11193C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48408932 | |||||||
| chr4:48409043 | T | C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-11082T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409043 | |||||||
| chr4:48409068 | A | G | 1 | a0001c0001t0010g0090 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1361-11057A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409068 | |||||||
| chr4:48409196 | A | G | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-10929A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409196 | |||||||
| chr4:48409287 | A | AT | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-10829dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48409287 | ||||||
| chr4:48409317 | A | T | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-10808A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409317 | |||||||
| chr4:48409470 | A | C | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10655A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409470 | |||||||
| chr4:48409514 | C | T | 1 | a0001c0001t0002g0281 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1361-10611C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409514 | |||||||
| chr4:48409774 | C | T | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10351C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409774 | |||||||
| chr4:48409837 | T | C | 2 | a0001c0001t0002g0279 a0001c0001t0007g0330 |
2 | HG02602.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.1361-10288T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409837 | |||||||
| chr4:48409901 | A | AATG | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-10223_1361-10 others(9): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48409901 | ||||||
| chr4:48409958 | T | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-10167T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409958 | |||||||
| chr4:48409992 | G | A | 4 | a0001c0001t0002g0275 a0001c0001t0002g0276 a0001c0001t0002g0321 others(1): Show |
4 | HG01358.hp1 HG01928.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-10133G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48409992 | |||||||
| chr4:48410141 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-9984G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410141 | |||||||
| chr4:48410279 | GT | G | 23 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(20): Show |
23 | HG01167.hp1 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.1361-9832delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48410279 | ||||||
| chr4:48410436 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-9689G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410436 | |||||||
| chr4:48410522 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1361-9603C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410522 | |||||||
| chr4:48410580 | C | T | 1 | a0001c0001t0002g0274 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1361-9545C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410580 | |||||||
| chr4:48410726 | T | G | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0219 |
3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1361-9399T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410726 | |||||||
| chr4:48410775 | G | A | 1 | a0001c0001t0002g0239 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1361-9350G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410775 | |||||||
| chr4:48410826 | C | A | 12 | a0001c0001t0029g0163 a0001c0003t0006g0032 a0001c0003t0006g0033 others(9): Show |
12 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-9299C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410826 | |||||||
| chr4:48410974 | C | T | 1 | a0005c0011t0020g0254 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1361-9151C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410974 | |||||||
| chr4:48410980 | C | T | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-9145C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48410980 | |||||||
| chr4:48411033 | G | T | 5 | a0001c0001t0004g0313 a0001c0001t0004g0316 a0001c0001t0004g0317 others(2): Show |
5 | HG02074.hp1 NA18950.hp1 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1361-9092G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411033 | |||||||
| chr4:48411186 | T | A | 1 | a0001c0002t0005g0170 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1361-8939T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411186 | |||||||
| chr4:48411231 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-8894A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411231 | |||||||
| chr4:48411281 | C | T | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-8844C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411281 | |||||||
| chr4:48411494 | A | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-8631A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411494 | |||||||
| chr4:48411581 | C | T | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-8544C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411581 | |||||||
| chr4:48411603 | G | GT | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-8510dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411603 | ||||||
| chr4:48411603 | GT | G | 152 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(149): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1361-8510delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411603 | ||||||
| chr4:48411624 | T | A | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-8501T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411624 | |||||||
| chr4:48411769 | A | AT | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-8349dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48411769 | ||||||
| chr4:48411783 | G | A | 1 | a0001c0001t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1361-8342G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411783 | |||||||
| chr4:48411902 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-8223T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48411902 | |||||||
| chr4:48412017 | A | AT | 115 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(112): Show |
117 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(114): Show |
intron_variant | MODIFIER | c.1361-8106dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412017 | ||||||
| chr4:48412038 | C | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-8087C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412038 | |||||||
| chr4:48412157 | A | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-7968A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412157 | |||||||
| chr4:48412193 | A | G | 1 | a0007c0008t0001g0123 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1361-7932A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412193 | |||||||
| chr4:48412212 | A | G | 1 | a0001c0001t0004g0320 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1361-7913A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412212 | |||||||
| chr4:48412311 | GGGTGGAG others(214): Show |
G | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-7810_1361-759 others(4): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412311 | ||||||
| chr4:48412325 | A | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-7800A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412325 | |||||||
| chr4:48412364 | G | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-7761G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412364 | |||||||
| chr4:48412365 | T | TAC | 19 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0053 others(16): Show |
19 | HG00323.hp1 HG00733.hp2 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1361-7710_1361-770 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | T | TACAC | 7 | a0001c0001t0001g0001 a0001c0001t0001g0022 a0001c0001t0001g0082 others(4): Show |
7 | HG01358.hp2 HG01361.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-7712_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | T | TACACAC | 3 | a0001c0001t0001g0025 a0001c0001t0001g0080 a0001c0001t0024g0014 |
3 | HG02809.hp1 NA18964.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1361-7714_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | T | TACACACA others(3): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | NA18995.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1361-7718_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TAC | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
41 | HG00280.hp2 HG00609.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1361-7710_1361-770 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACAC | T | 21 | a0001c0001t0001g0015 a0001c0001t0001g0049 a0001c0001t0001g0050 others(18): Show |
21 | HG00140.hp2 HG00642.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.1361-7712_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACAC | T | 6 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0126 others(3): Show |
6 | HG01433.hp2 HG02004.hp2 HG02273.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-7714_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(1): Show |
T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(11): Show |
15 | HG01167.hp1 HG02040.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-7716_1361-770 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0155 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1361-7718_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(5): Show |
T | 3 | a0001c0001t0001g0039 a0001c0001t0023g0035 a0001c0001t0027g0179 |
3 | HG02630.hp2 HG03139.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1361-7720_1361-770 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(9): Show |
13 | HG02074.hp2 HG02735.hp2 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.1361-7722_1361-770 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(9): Show |
T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0025g0047 |
3 | HG03098.hp2 HG03834.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1361-7724_1361-770 others(20): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412365 | TACACACA others(11): Show |
T | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG01070.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1361-7726_1361-770 others(22): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412365 | ||||||
| chr4:48412387 | CACACACA others(23): Show |
C | 5 | a0001c0001t0002g0296 a0001c0001t0002g0297 a0001c0001t0002g0298 others(2): Show |
5 | HG01109.hp1 HG01255.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.1361-7737_1361-770 others(34): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412387 | |||||||
| chr4:48412389 | CACACACA others(21): Show |
C | 3 | a0001c0001t0002g0287 a0001c0001t0002g0288 a0001c0001t0021g0294 |
3 | HG02004.hp1 HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1361-7735_1361-770 others(32): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412389 | |||||||
| chr4:48412390 | ACACACAC others(25): Show |
A | 11 | a0001c0001t0004g0241 a0001c0001t0004g0249 a0001c0001t0004g0251 others(8): Show |
11 | HG02074.hp1 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-7733_1361-770 others(36): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412390 | ||||||
| chr4:48412391 | CACACACA others(19): Show |
C | 96 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(93): Show |
98 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(95): Show |
intron_variant | MODIFIER | c.1361-7733_1361-770 others(30): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412391 | |||||||
| chr4:48412403 | CACACACA others(7): Show |
C | 1 | a0001c0001t0003g0206 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1361-7721_1361-770 others(18): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412403 | |||||||
| chr4:48412405 | CACACACA others(5): Show |
C | 2 | a0001c0001t0003g0167 a0001c0001t0016g0333 |
2 | HG02615.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1361-7719_1361-770 others(16): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412405 | |||||||
| chr4:48412407 | C | A | 4 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1361-7718C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412407 | |||||||
| chr4:48412407 | C | CAA | 4 | a0001c0003t0006g0036 a0001c0003t0006g0216 a0001c0003t0012g0214 others(1): Show |
4 | HG02615.hp2 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-7717_1361-771 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412407 | ||||||
| chr4:48412407 | C | CACAA | 3 | a0001c0003t0006g0211 a0001c0003t0006g0212 a0001c0003t0006g0213 |
3 | HG02145.hp2 HG02451.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1361-7715_1361-771 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412407 | ||||||
| chr4:48412407 | CACACACA others(3): Show |
C | 7 | a0001c0001t0003g0165 a0001c0001t0003g0184 a0001c0001t0003g0185 others(4): Show |
7 | HG00099.hp1 HG00733.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-7717_1361-770 others(14): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412407 | |||||||
| chr4:48412409 | C | A | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-7716C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412409 | |||||||
| chr4:48412409 | CACACACA others(1): Show |
C | 7 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0009 others(4): Show |
7 | HG00280.hp1 HG00738.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-7715_1361-770 others(12): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412409 | |||||||
| chr4:48412411 | CACACAT | C | 17 | a0001c0001t0003g0003 a0001c0001t0003g0007 a0001c0001t0003g0164 others(14): Show |
18 | HG00642.hp2 HG00735.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1361-7713_1361-770 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412411 | |||||||
| chr4:48412413 | CACAT | C | 8 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0009 others(5): Show |
8 | HG00323.hp2 HG01243.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-7711_1361-770 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412413 | |||||||
| chr4:48412420 | CCT | C | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-7688_1361-768 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48412420 | ||||||
| chr4:48412426 | T | C | 11 | a0001c0001t0004g0241 a0001c0001t0004g0249 a0001c0001t0004g0251 others(8): Show |
11 | HG02074.hp1 NA18939.hp2 NA18942.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-7699T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412426 | |||||||
| chr4:48412470 | A | G | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-7655A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412470 | |||||||
| chr4:48412686 | C | T | 1 | a0001c0001t0002g0221 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1361-7439C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412686 | |||||||
| chr4:48412687 | G | A | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-7438G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412687 | |||||||
| chr4:48412955 | C | T | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-7170C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48412955 | |||||||
| chr4:48413142 | C | T | 1 | a0001c0001t0028g0264 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1361-6983C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413142 | |||||||
| chr4:48413209 | T | C | 1 | a0001c0001t0001g0217 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1361-6916T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413209 | |||||||
| chr4:48413227 | CA | C | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG01167.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1361-6883delA | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | ||||||
| chr4:48413227 | CAA | C | 71 | a0001c0001t0002g0220 a0001c0001t0002g0223 a0001c0001t0002g0228 others(68): Show |
77 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.1361-6884_1361-688 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | ||||||
| chr4:48413227 | CAAA | C | 108 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(105): Show |
110 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.1361-6885_1361-688 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48413227 | ||||||
| chr4:48413242 | A | G | 2 | a0001c0001t0003g0184 a0001c0001t0003g0206 |
2 | HG03017.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1361-6883A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413242 | |||||||
| chr4:48413311 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-6814A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413311 | |||||||
| chr4:48413345 | C | T | 3 | a0001c0001t0002g0299 a0001c0001t0002g0302 a0001c0001t0002g0305 |
3 | HG01070.hp2 HG01071.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1361-6780C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413345 | |||||||
| chr4:48413353 | C | A | 1 | a0001c0001t0008g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1361-6772C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413353 | |||||||
| chr4:48413491 | C | T | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1361-6634C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413491 | |||||||
| chr4:48413558 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1361-6567A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413558 | |||||||
| chr4:48413623 | G | T | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-6502G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413623 | |||||||
| chr4:48413818 | A | G | 1 | a0001c0001t0002g0277 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1361-6307A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48413818 | |||||||
| chr4:48414235 | T | C | 1 | a0001c0001t0001g0119 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1361-5890T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414235 | |||||||
| chr4:48414411 | A | G | 2 | a0001c0003t0006g0032 a0001c0003t0006g0033 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1361-5714A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414411 | |||||||
| chr4:48414460 | G | A | 1 | a0001c0002t0031g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1361-5665G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414460 | |||||||
| chr4:48414550 | A | AT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0104 a0001c0001t0001g0139 others(3): Show |
6 | HG01496.hp2 HG01981.hp2 NA19000.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-5555dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | ||||||
| chr4:48414550 | AT | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0037 a0001c0001t0001g0038 others(16): Show |
20 | HG01069.hp1 HG02074.hp2 HG02630.hp2 others(17): Show |
intron_variant | MODIFIER | c.1361-5555delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | ||||||
| chr4:48414550 | ATT | A | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-5556_1361-555 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | ||||||
| chr4:48414550 | ATTT | A | 10 | a0001c0001t0029g0163 a0001c0003t0006g0032 a0001c0003t0006g0033 others(7): Show |
10 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1361-5557_1361-555 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | ||||||
| chr4:48414550 | ATTTTTTT | A | 152 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(149): Show |
159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.1361-5561_1361-555 others(11): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414550 | ||||||
| chr4:48414568 | TTTA | T | 10 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(7): Show |
11 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.1361-5552_1361-555 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48414568 | ||||||
| chr4:48414673 | G | A | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-5452G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414673 | |||||||
| chr4:48414700 | C | T | 11 | a0001c0002t0005g0008 a0001c0002t0005g0170 a0001c0002t0005g0171 others(8): Show |
12 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1361-5425C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414700 | |||||||
| chr4:48414714 | C | T | 33 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
38 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.1361-5411C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414714 | |||||||
| chr4:48414805 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1361-5320G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414805 | |||||||
| chr4:48414828 | G | A | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-5297G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414828 | |||||||
| chr4:48414855 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1361-5270A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414855 | |||||||
| chr4:48414858 | T | C | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-5267T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414858 | |||||||
| chr4:48414973 | G | C | 2 | a0001c0001t0002g0287 a0001c0001t0002g0288 |
2 | HG02602.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1361-5152G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48414973 | |||||||
| chr4:48415008 | G | A | 1 | a0001c0001t0011g0021 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1361-5117G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415008 | |||||||
| chr4:48415058 | C | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-5067C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415058 | |||||||
| chr4:48415244 | A | T | 180 | a0001c0001t0001g0107 a0001c0001t0002g0010 a0001c0001t0002g0011 others(177): Show |
188 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(185): Show |
intron_variant | MODIFIER | c.1361-4881A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415244 | |||||||
| chr4:48415325 | C | T | 1 | a0001c0001t0003g0167 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1361-4800C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415325 | |||||||
| chr4:48415335 | T | C | 1 | a0001c0001t0003g0167 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1361-4790T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415335 | |||||||
| chr4:48415379 | A | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-4746A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415379 | |||||||
| chr4:48415385 | C | T | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-4740C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415385 | |||||||
| chr4:48415386 | A | G | 191 | a0001c0001t0001g0139 a0001c0001t0001g0154 a0001c0001t0001g0155 others(188): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.1361-4739A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415386 | |||||||
| chr4:48415390 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-4735A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415390 | |||||||
| chr4:48415446 | A | G | 2 | a0001c0003t0006g0032 a0001c0003t0006g0033 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1361-4679A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415446 | |||||||
| chr4:48415483 | C | A | 1 | a0001c0001t0001g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1361-4642C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415483 | |||||||
| chr4:48415513 | T | C | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-4612T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415513 | |||||||
| chr4:48415517 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0001g0155 |
2 | HG06807.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1361-4608C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415517 | |||||||
| chr4:48415562 | C | A | 104 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(101): Show |
106 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.1361-4563C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415562 | |||||||
| chr4:48415587 | G | T | 2 | a0001c0001t0002g0223 a0001c0001t0002g0281 |
2 | HG02735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1361-4538G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415587 | |||||||
| chr4:48415622 | G | A | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-4503G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415622 | |||||||
| chr4:48415641 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4484G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415641 | |||||||
| chr4:48415763 | C | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-4362C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415763 | |||||||
| chr4:48415820 | C | A | 1 | a0001c0006t0001g0097 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1361-4305C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415820 | |||||||
| chr4:48415841 | C | G | 8 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(5): Show |
8 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-4284C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415841 | |||||||
| chr4:48415877 | C | T | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-4248C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415877 | |||||||
| chr4:48415878 | G | A | 6 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(3): Show |
6 | HG01167.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1361-4247G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415878 | |||||||
| chr4:48415940 | G | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4185G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415940 | |||||||
| chr4:48415942 | A | G | 8 | a0001c0001t0002g0227 a0001c0001t0002g0295 a0001c0001t0002g0308 others(5): Show |
8 | HG01891.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1361-4183A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48415942 | |||||||
| chr4:48416036 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4089G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416036 | |||||||
| chr4:48416043 | G | A | 1 | a0001c0001t0002g0255 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1361-4082G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416043 | |||||||
| chr4:48416072 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1361-4053G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416072 | |||||||
| chr4:48416076 | G | GT | 153 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(150): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.1361-4043dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48416076 | ||||||
| chr4:48416160 | A | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-3965A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416160 | |||||||
| chr4:48416166 | A | C | 1 | a0001c0001t0002g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-3959A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416166 | |||||||
| chr4:48416168 | G | A | 1 | a0001c0001t0002g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-3957G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416168 | |||||||
| chr4:48416252 | G | C | 2 | a0001c0003t0012g0214 a0001c0003t0012g0215 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1361-3873G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416252 | |||||||
| chr4:48416264 | G | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-3861G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416264 | |||||||
| chr4:48416369 | G | A | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0160 |
3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1361-3756G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416369 | |||||||
| chr4:48416468 | G | A | 1 | a0001c0001t0003g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-3657G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416468 | |||||||
| chr4:48416469 | A | G | 1 | a0001c0001t0003g0189 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1361-3656A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416469 | |||||||
| chr4:48416490 | A | G | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-3635A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416490 | |||||||
| chr4:48416514 | A | C | 1 | a0001c0001t0003g0208 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1361-3611A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416514 | |||||||
| chr4:48416595 | A | G | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-3530A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416595 | |||||||
| chr4:48416608 | G | A | 13 | a0001c0001t0029g0163 a0001c0002t0030g0201 a0001c0003t0006g0032 others(10): Show |
13 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-3517G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416608 | |||||||
| chr4:48416609 | C | T | 1 | a0001c0001t0002g0237 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1361-3516C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416609 | |||||||
| chr4:48416610 | G | A | 13 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(10): Show |
14 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.1361-3515G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416610 | |||||||
| chr4:48416735 | A | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0193 |
3 | NA18957.hp2 NA19055.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1361-3390A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416735 | |||||||
| chr4:48416762 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1361-3363A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416762 | |||||||
| chr4:48416766 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1361-3359C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416766 | |||||||
| chr4:48416852 | C | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-3273C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416852 | |||||||
| chr4:48416915 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1361-3210T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416915 | |||||||
| chr4:48416984 | G | A | 1 | a0001c0003t0006g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1361-3141G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48416984 | |||||||
| chr4:48417084 | C | A | 114 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(111): Show |
116 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(113): Show |
intron_variant | MODIFIER | c.1361-3041C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417084 | |||||||
| chr4:48417099 | A | G | 1 | a0001c0001t0002g0279 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1361-3026A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417099 | |||||||
| chr4:48417113 | T | G | 1 | a0001c0003t0006g0036 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1361-3012T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417113 | |||||||
| chr4:48417116 | T | TAAAG | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1361-3006_1361-300 others(8): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48417116 | ||||||
| chr4:48417239 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1361-2886A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417239 | |||||||
| chr4:48417284 | C | A | 28 | a0001c0001t0002g0011 a0001c0001t0002g0222 a0001c0001t0002g0278 others(25): Show |
29 | HG00099.hp2 HG00408.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1361-2841C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417284 | |||||||
| chr4:48417284 | C | G | 1 | a0001c0001t0002g0220 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1361-2841C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417284 | |||||||
| chr4:48417348 | G | A | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-2777G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417348 | |||||||
| chr4:48417493 | G | C | 175 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(172): Show |
182 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.1361-2632G>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417493 | |||||||
| chr4:48417529 | C | T | 1 | a0001c0001t0002g0292 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1361-2596C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417529 | |||||||
| chr4:48417606 | A | G | 1 | a0001c0001t0023g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1361-2519A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417606 | |||||||
| chr4:48417642 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1361-2483C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417642 | |||||||
| chr4:48417699 | C | T | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-2426C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417699 | |||||||
| chr4:48417735 | G | A | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-2390G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417735 | |||||||
| chr4:48417765 | A | G | 1 | a0001c0001t0002g0321 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1361-2360A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417765 | |||||||
| chr4:48417907 | G | A | 1 | a0001c0003t0014g0153 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1361-2218G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417907 | |||||||
| chr4:48417936 | T | C | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-2189T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417936 | |||||||
| chr4:48417958 | T | C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-2167T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48417958 | |||||||
| chr4:48418071 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-2054T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418071 | |||||||
| chr4:48418074 | TTTC | T | 110 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0221 others(107): Show |
112 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.1361-2035_1361-203 others(7): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418074 | ||||||
| chr4:48418074 | TTTCTTC | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0219 |
3 | HG00642.hp1 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1361-2038_1361-203 others(10): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418074 | ||||||
| chr4:48418138 | CCTTCTTT others(10): Show |
C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1361-1984_1361-196 others(21): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418138 | ||||||
| chr4:48418163 | T | C | 1 | a0001c0001t0018g0280 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1361-1962T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418163 | |||||||
| chr4:48418168 | CT | C | 12 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(9): Show |
13 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-1945delT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418168 | ||||||
| chr4:48418393 | T | C | 37 | a0001c0001t0003g0003 a0001c0001t0003g0006 a0001c0001t0003g0007 others(34): Show |
42 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.1361-1732T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418393 | |||||||
| chr4:48418541 | A | G | 1 | a0001c0001t0027g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1361-1584A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418541 | |||||||
| chr4:48418558 | T | A | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-1567T>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418558 | |||||||
| chr4:48418602 | C | T | 1 | a0001c0001t0021g0294 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1361-1523C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418602 | |||||||
| chr4:48418603 | G | A | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1361-1522G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418603 | |||||||
| chr4:48418614 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1361-1511T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48418614 | |||||||
| chr4:48418851 | AGT | A | 111 | a0001c0001t0001g0074 a0001c0001t0002g0010 a0001c0001t0002g0011 others(108): Show |
113 | HG00099.hp2 HG00408.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.1361-1261_1361-126 others(6): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48418851 | ||||||
| chr4:48419012 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1361-1113A>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419012 | |||||||
| chr4:48419029 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-1096C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419029 | |||||||
| chr4:48419109 | C | CT | 149 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(146): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1361-1005dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48419109 | ||||||
| chr4:48419142 | G | A | 1 | a0001c0001t0002g0328 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1361-983G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419142 | |||||||
| chr4:48419170 | C | G | 1 | a0001c0001t0003g0180 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1361-955C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419170 | |||||||
| chr4:48419223 | C | G | 1 | a0001c0001t0016g0333 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1361-902C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419223 | |||||||
| chr4:48419350 | C | T | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-775C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419350 | |||||||
| chr4:48419355 | C | T | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-770C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419355 | |||||||
| chr4:48419362 | C | G | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-763C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419362 | |||||||
| chr4:48419384 | G | A | 26 | a0001c0001t0029g0163 a0001c0002t0005g0008 a0001c0002t0005g0169 others(23): Show |
27 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.1361-741G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419384 | |||||||
| chr4:48419469 | C | T | 11 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(8): Show |
11 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1361-656C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419469 | |||||||
| chr4:48419499 | C | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1361-626C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419499 | |||||||
| chr4:48419576 | G | GT | 14 | a0001c0002t0005g0008 a0001c0002t0005g0169 a0001c0002t0005g0170 others(11): Show |
15 | HG00741.hp2 HG01069.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.1361-543dupT | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr4 | 48419576 | ||||||
| chr4:48419697 | A | G | 1 | a0001c0003t0006g0033 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1361-428A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419697 | |||||||
| chr4:48419772 | A | G | 1 | a0001c0001t0004g0285 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1361-353A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419772 | |||||||
| chr4:48419779 | C | G | 9 | a0001c0003t0006g0032 a0001c0003t0006g0033 a0001c0003t0006g0034 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1361-346C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419779 | |||||||
| chr4:48419892 | A | G | 1 | a0001c0002t0030g0201 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1361-233A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 6/7 | chr4 | 48419892 | |||||||
| chr4:48420503 | T | G | 1 | a0001c0001t0029g0163 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1679+60T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420503 | |||||||
| chr4:48420570 | G | T | 9 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(6): Show |
9 | HG01167.hp1 HG02622.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1679+127G>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420570 | |||||||
| chr4:48420745 | C | T | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+302C>T | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420745 | |||||||
| chr4:48420751 | T | G | 190 | a0001c0001t0001g0154 a0001c0001t0001g0155 a0001c0001t0001g0156 others(187): Show |
198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.1679+308T>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420751 | |||||||
| chr4:48420828 | T | C | 71 | a0001c0001t0002g0010 a0001c0001t0002g0221 a0001c0001t0002g0232 others(68): Show |
72 | HG00597.hp2 HG00609.hp1 HG01099.hp2 others(69): Show |
intron_variant | MODIFIER | c.1679+385T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420828 | |||||||
| chr4:48420860 | C | A | 1 | a0001c0001t0004g0242 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1679+417C>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420860 | |||||||
| chr4:48420935 | A | G | 1 | a0001c0001t0002g0289 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1679+492A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48420935 | |||||||
| chr4:48421007 | TTTTTGTT others(4): Show |
T | 1 | a0001c0001t0001g0139 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1679+581_1679+591d others(13): Show |
SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr4 | 48421007 | ||||||
| chr4:48421057 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1679+614C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421057 | |||||||
| chr4:48421071 | G | A | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+628G>A | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421071 | |||||||
| chr4:48421084 | T | C | 179 | a0001c0001t0002g0010 a0001c0001t0002g0011 a0001c0001t0002g0220 others(176): Show |
187 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1679+641T>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421084 | |||||||
| chr4:48421095 | A | C | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1679+652A>C | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421095 | |||||||
| chr4:48421174 | C | G | 1 | a0001c0003t0006g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1679+731C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421174 | |||||||
| chr4:48421219 | C | G | 2 | a0001c0003t0006g0032 a0001c0003t0006g0033 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1679+776C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421219 | |||||||
| chr4:48421713 | A | G | 7 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0024 others(4): Show |
7 | HG01255.hp1 HG02559.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1680-298A>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421713 | |||||||
| chr4:48421808 | C | G | 5 | a0001c0001t0002g0220 a0001c0001t0002g0228 a0001c0004t0002g0229 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1680-203C>G | SLAIN2 | ENSG00000109171.15 | transcript | ENST00000264313.11 | protein_coding | 7/7 | chr4 | 48421808 |