Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 136853 |
| ensemblid | ENSG00000146700.9 |
| hgncid | 14461 |
| symbol | SSC4D |
| name | scavenger receptor cysteine rich family member with 4 domains |
| refseq_nuc | NM_080744.2 |
| refseq_prot | NP_542782.1 |
| ensembl_nuc | ENST00000275560.4 |
| ensembl_prot | ENSP00000275560.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 76389337 |
| end | 76409697 |
| strand | - |
| ver | v1.2 |
| region | chr7:76389337-76409697 |
| region5000 | chr7:76384337-76414697 |
| regionname0 | SSC4D_chr7_76389337_76409697 |
| regionname5000 | SSC4D_chr7_76384337_76414697 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 575 | 223 | 48 | 44 | 83 | 14 | 32 | 61 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0002 | 0/0 | 575 | 67 | 3 | 14 | 39 | 1 | 10 | 31 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0003 | 0/0 | 575 | 49 | 15 | 7 | 25 | 1 | 1 | 23 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0004 | 0/0 | 575 | 27 | 25 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0005 | 0/0 | 575 | 6 | 0 | 0 | 6 | 0 | 0 | 4 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0006 | 0/0 | 575 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0007 | 0/0 | 575 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0008 | 0/0 | 575 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0009 | 0/0 | 575 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0010 | 0/0 | 575 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0011 | 0/0 | 575 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0012 | 0/0 | 575 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0013 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| a0014 | 0/0 | 575 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | MHKEA others(570): Show |
chr7 | 76384337 | 76414697 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1725 | 154 | 32 | 30 | 60 | 9 | 22 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0004 | 0/1 | 1725 | 29 | 10 | 6 | 1 | 4 | 7 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0005 | 0/0 | 1725 | 29 | 0 | 5 | 22 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0007 | 0/0 | 1725 | 8 | 5 | 3 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0016 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0017 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0001c0022 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0002c0002 | 0/0 | 1725 | 66 | 3 | 14 | 38 | 1 | 10 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0002c0014 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0003c0003 | 0/0 | 1725 | 48 | 14 | 7 | 25 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0003c0013 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0004c0006 | 0/0 | 1725 | 25 | 23 | 2 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0004c0011 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0005c0008 | 0/0 | 1725 | 6 | 0 | 0 | 6 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0006c0009 | 0/0 | 1725 | 5 | 0 | 0 | 5 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0007c0010 | 0/0 | 1725 | 3 | 3 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0008c0012 | 0/0 | 1725 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0009c0015 | 0/0 | 1725 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0010c0021 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0011c0023 | 0/0 | 1725 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0012c0020 | 0/0 | 1725 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0013c0019 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 | ||
| a0014c0018 | 0/0 | 1725 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | ATGCA others(1720): Show |
chr7 | 76384337 | 76414697 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2800 | 131 | 18 | 28 | 59 | 8 | 17 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0001t0004 | 0/0 | 2800 | 21 | 14 | 2 | 0 | 1 | 4 | SSC4D_chr7_76384337_76414697 | SSC4D | CGTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0001t0007 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0001t0008 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0004t0001 | 0/0 | 2800 | 5 | 5 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0004t0003 | 0/1 | 2800 | 23 | 4 | 6 | 1 | 4 | 7 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0004t0004 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CGTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0005t0001 | 0/0 | 2800 | 18 | 0 | 1 | 15 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0005t0002 | 0/0 | 2800 | 11 | 0 | 4 | 7 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0007t0001 | 0/0 | 2800 | 8 | 5 | 3 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0016t0004 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CGTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0017t0009 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0001c0022t0001 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0002c0002t0001 | 0/0 | 2800 | 4 | 3 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0002c0002t0002 | 0/0 | 2800 | 61 | 0 | 14 | 36 | 1 | 10 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0002c0002t0006 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0002c0014t0001 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0003c0003t0001 | 0/0 | 2800 | 48 | 14 | 7 | 25 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0003c0013t0001 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0004c0006t0001 | 0/0 | 2800 | 25 | 23 | 2 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0004c0011t0001 | 0/0 | 2800 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0005c0008t0001 | 0/0 | 2800 | 6 | 0 | 0 | 6 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0006c0009t0003 | 0/0 | 2800 | 5 | 0 | 0 | 5 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0007c0010t0003 | 0/0 | 2800 | 3 | 3 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0008c0012t0001 | 0/0 | 2800 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0009c0015t0001 | 0/0 | 2800 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0010c0021t0001 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0011c0023t0001 | 0/0 | 2800 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0012c0020t0005 | 0/0 | 2800 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0013c0019t0001 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| a0014c0018t0002 | 0/0 | 2800 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | CTTTT others(2795): Show |
chr7 | 76384337 | 76414697 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 11 | 0 | 1 | 6 | 2 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0003 | 0/0 | 10 | 2 | 2 | 4 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0005 | 1/0 | 8 | 0 | 2 | 5 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0006 | 0/0 | 5 | 0 | 1 | 2 | 0 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0032 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0004g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0001t0008g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0057 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0004t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0007t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0016t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0017t0009g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0001c0022t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0001 | 0/0 | 13 | 0 | 11 | 0 | 1 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0004 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0010 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0002t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0002c0014t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0011 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0003t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0003c0013t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0007 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0011t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0004c0011t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0005c0008t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0005c0008t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0005c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0005c0008t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0005c0008t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0006c0009t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0006c0009t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0006c0009t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0006c0009t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0006c0009t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0007c0010t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0007c0010t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0007c0010t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0008c0012t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0008c0012t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0009c0015t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0010c0021t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0011c0023t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0012c0020t0005g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0013c0019t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| a0014c0018t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0004 | t0003 | g0091 | EUR | GBR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | GBR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00140 | hp2 | a0001 | c0004 | t0003 | g0103 | EUR | GBR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00280 | hp2 | a0001 | c0005 | t0001 | g0278 | EUR | FIN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00323 | hp1 | a0003 | c0003 | t0001 | g0162 | EUR | FIN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00423 | hp2 | a0002 | c0002 | t0006 | g0066 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00544 | hp1 | a0001 | c0005 | t0001 | g0285 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00558 | hp2 | a0001 | c0005 | t0001 | g0282 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00597 | hp2 | a0003 | c0003 | t0001 | g0142 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00609 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0046 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00673 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00733 | hp2 | a0001 | c0007 | t0001 | g0081 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00735 | hp1 | a0001 | c0004 | t0003 | g0071 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0138 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0022 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01081 | hp2 | a0001 | c0004 | t0003 | g0072 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01099 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01109 | hp2 | a0004 | c0006 | t0001 | g0250 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0025 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0051 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01243 | hp1 | a0004 | c0006 | t0001 | g0249 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01243 | hp2 | a0001 | c0007 | t0001 | g0009 | AMR | PUR | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01256 | hp1 | a0002 | c0002 | t0002 | g0119 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01258 | hp2 | a0009 | c0015 | t0001 | g0241 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01261 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01261 | hp2 | a0001 | c0004 | t0003 | g0092 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0010 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01358 | hp2 | a0001 | c0004 | t0003 | g0090 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01433 | hp1 | a0001 | c0005 | t0002 | g0041 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01433 | hp2 | a0001 | c0007 | t0001 | g0078 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01496 | hp2 | a0001 | c0005 | t0002 | g0041 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0254 | EUR | IBS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01515 | hp2 | a0001 | c0004 | t0003 | g0070 | EUR | IBS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | IBS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0243 | EUR | IBS | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0007 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01884 | hp2 | a0003 | c0003 | t0001 | g0110 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01943 | hp2 | a0003 | c0003 | t0001 | g0153 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0164 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01975 | hp1 | a0003 | c0003 | t0001 | g0145 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01993 | hp2 | a0001 | c0004 | t0003 | g0093 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0118 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02015 | hp2 | a0005 | c0008 | t0001 | g0220 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02040 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0043 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02056 | hp2 | a0001 | c0005 | t0002 | g0276 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02071 | hp2 | a0001 | c0005 | t0002 | g0040 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02083 | hp1 | a0001 | c0005 | t0002 | g0040 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02129 | hp2 | a0001 | c0005 | t0001 | g0292 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02135 | hp2 | a0006 | c0009 | t0003 | g0096 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0027 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02145 | hp2 | a0004 | c0006 | t0001 | g0247 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | CDX | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CDX | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02257 | hp1 | a0004 | c0006 | t0001 | g0258 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02258 | hp1 | a0007 | c0010 | t0003 | g0102 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02258 | hp2 | a0004 | c0006 | t0001 | g0007 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02273 | hp1 | a0001 | c0005 | t0001 | g0288 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02273 | hp2 | a0003 | c0003 | t0001 | g0147 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02280 | hp1 | a0003 | c0003 | t0001 | g0027 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02280 | hp2 | a0004 | c0006 | t0001 | g0248 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02293 | hp1 | a0001 | c0005 | t0002 | g0284 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02300 | hp1 | a0001 | c0005 | t0002 | g0131 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02300 | hp2 | a0003 | c0003 | t0001 | g0151 | AMR | PEL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0054 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02523 | hp1 | a0001 | c0005 | t0001 | g0279 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02572 | hp1 | a0001 | c0001 | t0004 | g0047 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02572 | hp2 | a0001 | c0016 | t0004 | g0053 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02602 | hp1 | a0001 | c0022 | t0001 | g0252 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02615 | hp1 | a0003 | c0003 | t0001 | g0136 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02615 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02622 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02630 | hp2 | a0001 | c0007 | t0001 | g0080 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02647 | hp1 | a0010 | c0021 | t0001 | g0148 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02647 | hp2 | a0004 | c0006 | t0001 | g0260 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0050 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0001 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02717 | hp1 | a0001 | c0004 | t0001 | g0219 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0111 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0044 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02735 | hp1 | a0001 | c0017 | t0009 | g0294 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02809 | hp1 | a0001 | c0004 | t0003 | g0088 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02809 | hp2 | a0004 | c0011 | t0001 | g0263 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02818 | hp2 | a0008 | c0012 | t0001 | g0079 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02886 | hp2 | a0003 | c0013 | t0001 | g0137 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02895 | hp1 | a0001 | c0004 | t0003 | g0107 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02895 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02896 | hp1 | a0004 | c0006 | t0001 | g0265 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02897 | hp2 | a0003 | c0003 | t0001 | g0024 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02922 | hp1 | a0004 | c0006 | t0001 | g0262 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02922 | hp2 | a0001 | c0007 | t0001 | g0009 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02965 | hp2 | a0004 | c0006 | t0001 | g0251 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02970 | hp1 | a0004 | c0011 | t0001 | g0196 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02976 | hp2 | a0011 | c0023 | t0001 | g0210 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03017 | hp1 | a0012 | c0020 | t0005 | g0055 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0010 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0049 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03098 | hp2 | a0004 | c0006 | t0001 | g0261 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03130 | hp1 | a0004 | c0006 | t0001 | g0056 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03130 | hp2 | a0004 | c0006 | t0001 | g0060 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03139 | hp1 | a0004 | c0006 | t0001 | g0257 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03139 | hp2 | a0007 | c0010 | t0003 | g0097 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03195 | hp1 | a0001 | c0004 | t0001 | g0269 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0128 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03209 | hp1 | a0004 | c0006 | t0001 | g0181 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03209 | hp2 | a0004 | c0006 | t0001 | g0259 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03225 | hp1 | a0001 | c0004 | t0001 | g0274 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03225 | hp2 | a0004 | c0006 | t0001 | g0246 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0048 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03453 | hp2 | a0001 | c0007 | t0001 | g0083 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03490 | hp1 | a0001 | c0004 | t0003 | g0089 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03492 | hp2 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03516 | hp1 | a0004 | c0006 | t0001 | g0264 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0132 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03540 | hp2 | a0001 | c0007 | t0001 | g0009 | AFR | GWD | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03579 | hp1 | a0001 | c0004 | t0001 | g0268 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0115 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0074 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03704 | hp2 | a0001 | c0004 | t0003 | g0100 | SAS | PJL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03831 | hp1 | a0001 | c0001 | t0007 | g0207 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0120 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0022 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0059 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03927 | hp1 | a0001 | c0004 | t0003 | g0108 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03942 | hp1 | a0002 | c0002 | t0002 | g0124 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03942 | hp2 | a0001 | c0004 | t0003 | g0106 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0114 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0130 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04184 | hp2 | a0001 | c0004 | t0003 | g0094 | SAS | BEB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04199 | hp1 | a0001 | c0005 | t0001 | g0271 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04199 | hp2 | a0001 | c0004 | t0003 | g0098 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG04228 | hp2 | a0003 | c0003 | t0001 | g0011 | SAS | STU | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18522 | hp1 | a0004 | c0006 | t0001 | g0007 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0052 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | CHB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18747 | hp1 | a0006 | c0009 | t0003 | g0095 | EAS | CHB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18747 | hp2 | a0005 | c0008 | t0001 | g0224 | EAS | CHB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18906 | hp1 | a0001 | c0004 | t0003 | g0104 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0045 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18939 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18939 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18942 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18945 | hp1 | a0005 | c0008 | t0001 | g0034 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0188 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18950 | hp1 | a0002 | c0002 | t0002 | g0127 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18950 | hp2 | a0005 | c0008 | t0001 | g0212 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18951 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18952 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18956 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18956 | hp2 | a0006 | c0009 | t0003 | g0109 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18957 | hp2 | a0001 | c0005 | t0001 | g0286 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18963 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18964 | hp2 | a0001 | c0005 | t0001 | g0289 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0121 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18969 | hp1 | a0001 | c0005 | t0001 | g0287 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18972 | hp2 | a0001 | c0005 | t0002 | g0275 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18974 | hp1 | a0006 | c0009 | t0003 | g0141 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18975 | hp2 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0125 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18983 | hp1 | a0002 | c0014 | t0001 | g0129 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0160 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0122 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18988 | hp1 | a0003 | c0003 | t0001 | g0155 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18988 | hp2 | a0001 | c0005 | t0001 | g0281 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18990 | hp1 | a0013 | c0019 | t0001 | g0273 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18990 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18992 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18993 | hp1 | a0003 | c0003 | t0001 | g0166 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18994 | hp2 | a0005 | c0008 | t0001 | g0182 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18997 | hp1 | a0002 | c0002 | t0002 | g0113 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18997 | hp2 | a0003 | c0003 | t0001 | g0167 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19000 | hp2 | a0001 | c0005 | t0001 | g0293 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19002 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19002 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19003 | hp1 | a0001 | c0005 | t0002 | g0290 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19005 | hp2 | a0003 | c0003 | t0001 | g0029 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19009 | hp1 | a0001 | c0005 | t0002 | g0277 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19009 | hp2 | a0003 | c0003 | t0001 | g0154 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19012 | hp2 | a0003 | c0003 | t0001 | g0146 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19030 | hp1 | a0003 | c0003 | t0001 | g0134 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0084 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19043 | hp2 | a0003 | c0003 | t0001 | g0135 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19054 | hp1 | a0006 | c0009 | t0003 | g0099 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19056 | hp1 | a0014 | c0018 | t0002 | g0291 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19057 | hp1 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19057 | hp2 | a0001 | c0005 | t0001 | g0280 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19060 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19062 | hp2 | a0003 | c0003 | t0001 | g0159 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19065 | hp2 | a0003 | c0003 | t0001 | g0150 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19074 | hp1 | a0001 | c0005 | t0001 | g0008 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19080 | hp1 | a0003 | c0003 | t0001 | g0028 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19082 | hp1 | a0003 | c0003 | t0001 | g0157 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19085 | hp2 | a0001 | c0005 | t0001 | g0272 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19088 | hp1 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19089 | hp1 | a0001 | c0005 | t0002 | g0283 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19090 | hp1 | a0001 | c0004 | t0003 | g0086 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19240 | hp1 | a0004 | c0006 | t0001 | g0039 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0112 | AFR | YRI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20129 | hp2 | a0004 | c0006 | t0001 | g0007 | AFR | ASW | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0001 | EUR | TSI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20752 | hp2 | a0001 | c0004 | t0003 | g0073 | EUR | TSI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0173 | EUR | TSI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20805 | hp2 | a0001 | c0001 | t0004 | g0042 | EUR | TSI | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20905 | hp1 | a0001 | c0004 | t0003 | g0085 | SAS | GIH | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01123 | hp1 | a0001 | c0004 | t0003 | g0101 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02109 | hp1 | a0008 | c0012 | t0001 | g0082 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02109 | hp2 | a0003 | c0003 | t0001 | g0025 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02486 | hp1 | a0007 | c0010 | t0003 | g0105 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02559 | hp1 | a0004 | c0006 | t0001 | g0039 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG02559 | hp2 | a0001 | c0004 | t0001 | g0270 | AFR | ACB | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03471 | hp1 | a0004 | c0006 | t0001 | g0061 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG03471 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | MSL | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG06807 | hp1 | a0001 | c0004 | t0003 | g0087 | AFR | USA | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| HG06807 | hp2 | a0001 | c0001 | t0004 | g0019 | AFR | USA | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18955 | hp1 | a0005 | c0008 | t0001 | g0034 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA18955 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | USA | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA20300 | hp2 | a0004 | c0006 | t0001 | g0256 | AFR | USA | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | LWK | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0003 | g0057 | REF | REF | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | SSC4D_chr7_76384337_76414697 | SSC4D | chr7 | 76384337 | 76414697 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76390159 | C | T | 1 | a0005 | 6 | HG02015.hp2 NA18747.hp2 NA18945.hp1 others(3): Show |
missense_variant | MODERATE | c.1628G>A | p.Arg543His | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 1978/2800 | 1628/1728 | 543/575 | chr7 | 76390159 | |||
| chr7:76390273 | C | T | 3 | a0003 a0010 a0012 |
51 | HG00323.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
missense_variant | MODERATE | c.1514G>A | p.Arg505Gln | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 1864/2800 | 1514/1728 | 505/575 | chr7 | 76390273 | |||
| chr7:76390333 | C | T | 1 | a0013 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1454G>A | p.Arg485His | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 1804/2800 | 1454/1728 | 485/575 | chr7 | 76390333 | |||
| chr7:76392041 | C | G | 1 | a0014 | 1 | NA19056.hp1 | missense_variant&splice_region_variant | MODERATE | c.1334G>C | p.Gly445Ala | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/11 | 1684/2800 | 1334/1728 | 445/575 | chr7 | 76392041 | |||
| chr7:76393414 | G | A | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1324C>T | p.Leu442Phe | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/11 | 1674/2800 | 1324/1728 | 442/575 | chr7 | 76393414 | |||
| chr7:76395280 | C | A | 1 | a0008 | 2 | HG02109.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.919G>T | p.Asp307Tyr | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/11 | 1269/2800 | 919/1728 | 307/575 | chr7 | 76395280 | |||
| chr7:76395322 | G | A | 1 | a0010 | 1 | HG02647.hp1 | missense_variant | MODERATE | c.877C>T | p.Pro293Ser | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/11 | 1227/2800 | 877/1728 | 293/575 | chr7 | 76395322 | |||
| chr7:76397619 | A | C | 1 | a0009 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.767T>G | p.Val256Gly | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/11 | 1117/2800 | 767/1728 | 256/575 | chr7 | 76397619 | |||
| chr7:76398740 | G | A | 1 | a0004 | 27 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
missense_variant | MODERATE | c.533C>T | p.Thr178Met | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/11 | 883/2800 | 533/1728 | 178/575 | chr7 | 76398740 | |||
| chr7:76400378 | C | T | 1 | a0002 | 67 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(64): Show |
missense_variant | MODERATE | c.383G>A | p.Arg128His | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 733/2800 | 383/1728 | 128/575 | chr7 | 76400378 | |||
| chr7:76400481 | C | T | 1 | a0007 | 3 | HG02258.hp1 HG02486.hp1 HG03139.hp2 |
missense_variant | MODERATE | c.280G>A | p.Val94Ile | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 630/2800 | 280/1728 | 94/575 | chr7 | 76400481 | |||
| chr7:76400559 | G | A | 1 | a0011 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.202C>T | p.Arg68Trp | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 552/2800 | 202/1728 | 68/575 | chr7 | 76400559 | |||
| chr7:76401038 | C | T | 1 | a0006 | 5 | HG02135.hp2 NA18747.hp1 NA18956.hp2 others(2): Show |
missense_variant | MODERATE | c.139G>A | p.Ala47Thr | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/11 | 489/2800 | 139/1728 | 47/575 | chr7 | 76401038 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76393523 | G | T | 1 | a0001c0016 | 1 | HG02572.hp2 | synonymous_variant | LOW | c.1215C>A | p.Pro405Pro | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/11 | 1565/2800 | 1215/1728 | 405/575 | chr7 | 76393523 | |||
| chr7:76393712 | T | C | 16 | a0001c0004 a0001c0005 a0001c0007 others(13): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
synonymous_variant | LOW | c.1026A>G | p.Gly342Gly | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/11 | 1376/2800 | 1026/1728 | 342/575 | chr7 | 76393712 | |||
| chr7:76393900 | T | G | 1 | a0001c0017 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.951A>C | p.Thr317Thr | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 8/11 | 1301/2800 | 951/1728 | 317/575 | chr7 | 76393900 | |||
| chr7:76395308 | T | C | 1 | a0004c0011 | 2 | HG02809.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.891A>G | p.Thr297Thr | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/11 | 1241/2800 | 891/1728 | 297/575 | chr7 | 76395308 | |||
| chr7:76400356 | G | A | 3 | a0001c0005 a0013c0019 a0014c0018 |
31 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(28): Show |
synonymous_variant | LOW | c.405C>T | p.Ser135Ser | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 755/2800 | 405/1728 | 135/575 | chr7 | 76400356 | |||
| chr7:76400443 | G | A | 4 | a0003c0003 a0003c0013 a0010c0021 others(1): Show |
51 | HG00323.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
synonymous_variant | LOW | c.318C>T | p.Pro106Pro | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 668/2800 | 318/1728 | 106/575 | chr7 | 76400443 | |||
| chr7:76400536 | G | A | 1 | a0001c0022 | 1 | HG02602.hp1 | synonymous_variant | LOW | c.225C>T | p.His75His | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 575/2800 | 225/1728 | 75/575 | chr7 | 76400536 | |||
| chr7:76400572 | G | T | 1 | a0003c0013 | 1 | HG02886.hp2 | synonymous_variant | LOW | c.189C>A | p.Gly63Gly | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/11 | 539/2800 | 189/1728 | 63/575 | chr7 | 76400572 | |||
| chr7:76401039 | G | A | 2 | a0001c0007 a0008c0012 |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
synonymous_variant | LOW | c.138C>T | p.Ser46Ser | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/11 | 488/2800 | 138/1728 | 46/575 | chr7 | 76401039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76389477 | A | T | 1 | a0002c0002t0006 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*582T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 582 | chr7 | 76389477 | ||||||
| chr7:76389698 | C | T | 4 | a0001c0005t0002 a0002c0002t0002 a0002c0002t0006 others(1): Show |
74 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*361G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 361 | chr7 | 76389698 | ||||||
| chr7:76389896 | G | A | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 11/11 | 163 | chr7 | 76389896 | ||||||
| chr7:76404453 | G | C | 1 | a0001c0001t0008 | 1 | NA18945.hp2 | 5_prime_UTR_variant | MODIFIER | c.-14C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/11 | 14 | chr7 | 76404453 | ||||||
| chr7:76404488 | A | T | 3 | a0001c0004t0003 a0006c0009t0003 a0007c0010t0003 |
30 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(27): Show |
5_prime_UTR_variant | MODIFIER | c.-49T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/11 | 49 | chr7 | 76404488 | ||||||
| chr7:76409518 | A | G | 1 | a0012c0020t0005 | 1 | HG03017.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-171T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/11 | chr7 | 76409518 | |||||||
| chr7:76409531 | A | G | 3 | a0001c0001t0004 a0001c0004t0004 a0001c0016t0004 |
23 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-184T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/11 | 5092 | chr7 | 76409531 | ||||||
| chr7:76409606 | G | A | 1 | a0001c0017t0009 | 1 | HG02735.hp1 | 5_prime_UTR_variant | MODIFIER | c.-259C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/11 | 5167 | chr7 | 76409606 | ||||||
| chr7:76409696 | A | C | 3 | a0001c0001t0004 a0001c0004t0004 a0001c0016t0004 |
23 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(20): Show |
5_prime_UTR_variant | MODIFIER | c.-349T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/11 | 5257 | chr7 | 76409696 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:76390429 | C | G | 38 | a0001c0004t0001g0219 a0001c0004t0001g0268 a0001c0004t0001g0269 others(35): Show |
38 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1412-54G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76390429 | |||||||
| chr7:76390537 | G | A | 43 | a0003c0003t0001g0011 a0003c0003t0001g0024 a0003c0003t0001g0025 others(40): Show |
51 | HG00323.hp1 HG00597.hp2 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.1412-162C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76390537 | |||||||
| chr7:76390654 | A | G | 1 | a0004c0011t0001g0196 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1412-279T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76390654 | |||||||
| chr7:76390816 | C | T | 1 | a0001c0004t0003g0093 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1412-441G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76390816 | |||||||
| chr7:76390859 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1412-484A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76390859 | |||||||
| chr7:76391050 | T | C | 2 | a0004c0006t0001g0060 a0004c0006t0001g0061 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1412-675A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391050 | |||||||
| chr7:76391075 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1412-700C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391075 | |||||||
| chr7:76391083 | C | T | 1 | a0004c0006t0001g0181 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1412-708G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391083 | |||||||
| chr7:76391084 | G | A | 61 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(58): Show |
90 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.1412-709C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391084 | |||||||
| chr7:76391233 | T | A | 177 | a0001c0004t0001g0219 a0001c0004t0001g0268 a0001c0004t0001g0269 others(174): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1411+731A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391233 | |||||||
| chr7:76391327 | C | G | 23 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0056 others(20): Show |
27 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.1411+637G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391327 | |||||||
| chr7:76391348 | C | T | 49 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(46): Show |
75 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1411+616G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391348 | |||||||
| chr7:76391507 | C | T | 2 | a0004c0006t0001g0060 a0004c0006t0001g0061 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1411+457G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391507 | |||||||
| chr7:76391826 | A | C | 1 | a0006c0009t0003g0096 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1411+138T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391826 | |||||||
| chr7:76391935 | C | T | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1411+29G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 10/10 | chr7 | 76391935 | |||||||
| chr7:76392364 | A | C | 1 | a0004c0011t0001g0263 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1334-323T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392364 | |||||||
| chr7:76392379 | G | A | 1 | a0004c0006t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1334-338C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392379 | |||||||
| chr7:76392420 | T | C | 1 | a0002c0002t0002g0122 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1334-379A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392420 | |||||||
| chr7:76392432 | C | T | 1 | a0004c0006t0001g0060 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1334-391G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392432 | |||||||
| chr7:76392443 | A | G | 129 | a0001c0004t0001g0219 a0001c0004t0003g0070 a0001c0004t0003g0071 others(126): Show |
165 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.1334-402T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392443 | |||||||
| chr7:76392538 | C | CA | 16 | a0001c0001t0007g0207 a0001c0004t0001g0274 a0001c0005t0001g0008 others(13): Show |
19 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(16): Show |
intron_variant | MODIFIER | c.1334-498dupT | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392538 | |||||||
| chr7:76392572 | C | T | 6 | a0003c0003t0001g0026 a0003c0003t0001g0028 a0003c0003t0001g0149 others(3): Show |
8 | HG00323.hp1 NA18939.hp2 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1334-531G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392572 | |||||||
| chr7:76392700 | G | C | 33 | a0003c0003t0001g0011 a0003c0003t0001g0025 a0003c0003t0001g0026 others(30): Show |
40 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.1334-659C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392700 | |||||||
| chr7:76392744 | G | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0240 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1333+661C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392744 | |||||||
| chr7:76392809 | G | A | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1333+596C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392809 | |||||||
| chr7:76392810 | A | G | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1333+595T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392810 | |||||||
| chr7:76392810 | A | T | 1 | a0001c0001t0001g0206 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1333+595T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76392810 | |||||||
| chr7:76393101 | T | A | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1333+304A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393101 | |||||||
| chr7:76393180 | A | C | 134 | a0001c0004t0001g0219 a0001c0004t0001g0268 a0001c0004t0001g0269 others(131): Show |
170 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.1333+225T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393180 | |||||||
| chr7:76393204 | T | G | 1 | a0012c0020t0005g0055 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1333+201A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393204 | |||||||
| chr7:76393228 | TCGCCCCG others(35): Show |
T | 3 | a0002c0002t0002g0123 a0002c0002t0002g0126 a0002c0002t0002g0133 |
3 | NA18944.hp1 NA19002.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.1333+135_1333+176d others(44): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393228 | |||||||
| chr7:76393339 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1333+66C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393339 | |||||||
| chr7:76393371 | C | CCGCTGTC others(11): Show |
1 | a0001c0001t0001g0195 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1333+16_1333+33dup others(18): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393371 | |||||||
| chr7:76393387 | C | T | 2 | a0002c0002t0002g0121 a0002c0002t0002g0122 |
2 | NA18965.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1333+18G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393387 | |||||||
| chr7:76393396 | C | T | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1333+9G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 9/10 | chr7 | 76393396 | |||||||
| chr7:76393724 | G | A | 33 | a0003c0003t0001g0011 a0003c0003t0001g0025 a0003c0003t0001g0026 others(30): Show |
40 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(37): Show |
splice_region_variant&intron_variant | LOW | c.1022-8C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 8/10 | chr7 | 76393724 | |||||||
| chr7:76393744 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1022-28T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 8/10 | chr7 | 76393744 | |||||||
| chr7:76393767 | C | T | 49 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(46): Show |
75 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.1022-51G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 8/10 | chr7 | 76393767 | |||||||
| chr7:76394107 | G | T | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.947-203C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394107 | |||||||
| chr7:76394120 | T | A | 2 | a0004c0006t0001g0060 a0004c0006t0001g0061 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.947-216A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394120 | |||||||
| chr7:76394135 | A | G | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.947-231T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394135 | |||||||
| chr7:76394167 | C | T | 2 | a0001c0001t0004g0018 a0001c0001t0004g0051 |
3 | HG01192.hp2 HG03041.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.947-263G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394167 | |||||||
| chr7:76394335 | C | T | 51 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(48): Show |
78 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.947-431G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394335 | |||||||
| chr7:76394398 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.947-494A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394398 | |||||||
| chr7:76394408 | A | AT | 15 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0170 others(12): Show |
18 | HG00140.hp1 HG00597.hp1 HG01192.hp2 others(15): Show |
intron_variant | MODIFIER | c.947-505dupA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394408 | |||||||
| chr7:76394408 | AT | A | 115 | a0001c0001t0001g0036 a0001c0001t0001g0058 a0001c0001t0001g0216 others(112): Show |
158 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(155): Show |
intron_variant | MODIFIER | c.947-505delA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394408 | |||||||
| chr7:76394445 | G | C | 16 | a0001c0005t0001g0008 a0001c0005t0001g0271 a0001c0005t0001g0272 others(13): Show |
19 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.947-541C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394445 | |||||||
| chr7:76394449 | C | T | 1 | a0002c0002t0002g0022 | 2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.947-545G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394449 | |||||||
| chr7:76394450 | G | A | 8 | a0001c0007t0001g0009 a0001c0007t0001g0078 a0001c0007t0001g0080 others(5): Show |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.947-546C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394450 | |||||||
| chr7:76394472 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0175 a0001c0001t0001g0176 |
4 | HG01070.hp1 HG01192.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.947-568C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394472 | |||||||
| chr7:76394588 | T | C | 7 | a0003c0003t0001g0143 a0003c0003t0001g0144 a0003c0003t0001g0146 others(4): Show |
7 | NA18959.hp1 NA18971.hp2 NA18972.hp1 others(4): Show |
intron_variant | MODIFIER | c.946+665A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394588 | |||||||
| chr7:76394740 | G | A | 1 | a0001c0007t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.946+513C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394740 | |||||||
| chr7:76394748 | A | AAT | 5 | a0001c0001t0001g0183 a0001c0001t0001g0204 a0001c0001t0001g0228 others(2): Show |
5 | HG00544.hp2 HG01928.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.946+503_946+504dup others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394748 | A | AATATATA others(5): Show |
1 | a0001c0004t0001g0270 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.946+493_946+504dup others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394748 | A | AATATATA others(7): Show |
2 | a0001c0004t0001g0268 a0001c0004t0001g0269 |
2 | HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.946+491_946+504dup others(14): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394748 | AAT | A | 84 | a0001c0001t0001g0178 a0001c0001t0001g0193 a0001c0001t0001g0194 others(81): Show |
99 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.946+503_946+504del others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394748 | AATAT | A | 89 | a0001c0005t0001g0008 a0001c0005t0001g0271 a0001c0005t0001g0272 others(86): Show |
118 | HG00280.hp2 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.946+501_946+504del others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394748 | AATATAT | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0016t0004g0053 |
3 | HG01070.hp1 HG01192.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.946+499_946+504del others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394748 | |||||||
| chr7:76394760 | T | A | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+493A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394760 | |||||||
| chr7:76394768 | T | A | 42 | a0001c0001t0001g0217 a0001c0004t0003g0103 a0003c0003t0001g0011 others(39): Show |
50 | HG00140.hp2 HG00323.hp1 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.946+485A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394768 | |||||||
| chr7:76394768 | T | TATATATA others(17): Show |
1 | a0001c0004t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.946+484_946+485ins others(24): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394768 | |||||||
| chr7:76394771 | A | T | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+482T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394771 | |||||||
| chr7:76394774 | A | G | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+479T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394774 | |||||||
| chr7:76394798 | A | T | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+455T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394798 | |||||||
| chr7:76394799 | A | ATATATAA others(28): Show |
1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+453_946+454ins others(35): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394799 | |||||||
| chr7:76394808 | A | G | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+445T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394808 | |||||||
| chr7:76394815 | G | A | 1 | a0001c0004t0003g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.946+438C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394815 | |||||||
| chr7:76394815 | G | GTATAATA others(29): Show |
62 | a0001c0001t0001g0194 a0001c0001t0001g0255 a0001c0004t0001g0219 others(59): Show |
69 | HG00099.hp1 HG00323.hp1 HG00597.hp2 others(66): Show |
intron_variant | MODIFIER | c.946+402_946+437dup others(36): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394815 | |||||||
| chr7:76394815 | G | GTATAATA others(65): Show |
4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0004t0003g0071 others(1): Show |
4 | HG00735.hp1 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+437_946+438ins others(72): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394815 | |||||||
| chr7:76394815 | G | GTATAATA others(65): Show |
1 | a0003c0003t0001g0147 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.946+437_946+438ins others(72): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394815 | |||||||
| chr7:76394818 | TAA | T | 4 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+433_946+434del others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394818 | |||||||
| chr7:76394836 | T | TTATATAT others(13): Show |
8 | a0001c0007t0001g0009 a0001c0007t0001g0078 a0001c0007t0001g0080 others(5): Show |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.946+397_946+416dup others(20): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394836 | |||||||
| chr7:76394861 | TATAAG | T | 23 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0056 others(20): Show |
27 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.946+387_946+391del others(5): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76394861 | |||||||
| chr7:76395010 | T | C | 1 | a0003c0003t0001g0150 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.946+243A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76395010 | |||||||
| chr7:76395167 | G | C | 16 | a0001c0005t0001g0008 a0001c0005t0001g0271 a0001c0005t0001g0272 others(13): Show |
19 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(16): Show |
intron_variant | MODIFIER | c.946+86C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76395167 | |||||||
| chr7:76395203 | C | T | 42 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0072 others(39): Show |
46 | HG00099.hp1 HG00735.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.946+50G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76395203 | |||||||
| chr7:76395246 | T | G | 1 | a0001c0001t0001g0237 | 1 | HG02071.hp1 | splice_region_variant&intron_variant | LOW | c.946+7A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 7/10 | chr7 | 76395246 | |||||||
| chr7:76395465 | C | T | 1 | a0001c0005t0001g0288 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.869-135G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395465 | |||||||
| chr7:76395482 | G | A | 1 | a0004c0006t0001g0248 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.869-152C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395482 | |||||||
| chr7:76395649 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.869-319G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395649 | |||||||
| chr7:76395657 | G | A | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.869-327C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395657 | |||||||
| chr7:76395658 | A | G | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.869-328T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395658 | |||||||
| chr7:76395659 | G | A | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.869-329C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395659 | |||||||
| chr7:76395690 | CTCCTCTT others(8): Show |
C | 1 | a0001c0004t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.869-375_869-361del others(15): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395690 | |||||||
| chr7:76395795 | G | A | 49 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(46): Show |
75 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.869-465C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395795 | |||||||
| chr7:76395887 | G | A | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.869-557C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395887 | |||||||
| chr7:76395923 | G | A | 2 | a0003c0003t0001g0110 a0003c0003t0001g0112 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.869-593C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395923 | |||||||
| chr7:76395947 | G | A | 2 | a0001c0001t0004g0048 a0001c0001t0004g0050 |
2 | HG02683.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.869-617C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76395947 | |||||||
| chr7:76396279 | C | G | 4 | a0003c0003t0001g0024 a0003c0003t0001g0136 a0003c0003t0001g0138 others(1): Show |
5 | HG01074.hp1 HG02615.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.869-949G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396279 | |||||||
| chr7:76396297 | A | T | 1 | a0003c0003t0001g0152 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.869-967T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396297 | |||||||
| chr7:76396443 | G | A | 2 | a0001c0001t0001g0218 a0001c0001t0001g0235 |
2 | NA18946.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.868+1075C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396443 | |||||||
| chr7:76396587 | A | G | 1 | a0002c0002t0002g0116 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.868+931T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396587 | |||||||
| chr7:76396751 | T | C | 13 | a0001c0005t0001g0008 a0001c0005t0001g0278 a0001c0005t0001g0279 others(10): Show |
16 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.868+767A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396751 | |||||||
| chr7:76396772 | C | T | 13 | a0001c0005t0001g0008 a0001c0005t0001g0278 a0001c0005t0001g0279 others(10): Show |
16 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.868+746G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76396772 | |||||||
| chr7:76397045 | A | G | 6 | a0001c0001t0001g0036 a0001c0001t0001g0195 a0001c0001t0001g0199 others(3): Show |
7 | HG01891.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.868+473T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397045 | |||||||
| chr7:76397141 | G | T | 92 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(89): Show |
126 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.868+377C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397141 | |||||||
| chr7:76397245 | G | C | 3 | a0003c0003t0001g0132 a0003c0003t0001g0134 a0003c0003t0001g0135 |
3 | HG03540.hp1 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.868+273C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397245 | |||||||
| chr7:76397305 | T | C | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.868+213A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397305 | |||||||
| chr7:76397318 | G | A | 5 | a0004c0006t0001g0256 a0004c0006t0001g0258 a0004c0006t0001g0260 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.868+200C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397318 | |||||||
| chr7:76397402 | C | T | 2 | a0001c0007t0001g0078 a0001c0007t0001g0080 |
2 | HG01433.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.868+116G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 6/10 | chr7 | 76397402 | |||||||
| chr7:76397918 | T | C | 182 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(179): Show |
226 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.554-86A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76397918 | |||||||
| chr7:76397985 | T | C | 3 | a0003c0003t0001g0110 a0003c0003t0001g0111 a0003c0003t0001g0112 |
3 | HG01884.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.554-153A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76397985 | |||||||
| chr7:76398155 | G | A | 1 | a0001c0007t0001g0084 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.554-323C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398155 | |||||||
| chr7:76398259 | C | T | 94 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(91): Show |
129 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.554-427G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398259 | |||||||
| chr7:76398283 | C | T | 1 | a0001c0004t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.553+437G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398283 | |||||||
| chr7:76398294 | G | A | 23 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0056 others(20): Show |
27 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.553+426C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398294 | |||||||
| chr7:76398309 | A | AT | 47 | a0001c0001t0001g0168 a0001c0001t0001g0183 a0001c0001t0001g0199 others(44): Show |
57 | HG00597.hp2 HG00735.hp2 HG01175.hp1 others(54): Show |
intron_variant | MODIFIER | c.553+410dupA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398309 | |||||||
| chr7:76398309 | A | T | 1 | a0001c0001t0004g0015 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.553+411T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398309 | |||||||
| chr7:76398309 | AT | A | 7 | a0001c0001t0001g0222 a0001c0001t0001g0236 a0001c0001t0004g0046 others(4): Show |
7 | HG00639.hp2 HG01074.hp1 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.553+410delA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398309 | |||||||
| chr7:76398309 | ATTT | A | 50 | a0001c0001t0004g0043 a0001c0004t0001g0219 a0001c0004t0003g0071 others(47): Show |
55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.553+408_553+410del others(3): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398309 | |||||||
| chr7:76398461 | C | T | 4 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.553+259G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398461 | |||||||
| chr7:76398584 | T | C | 80 | a0001c0001t0004g0043 a0001c0004t0001g0219 a0001c0004t0003g0070 others(77): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.553+136A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398584 | |||||||
| chr7:76398595 | A | G | 80 | a0001c0001t0004g0043 a0001c0004t0001g0219 a0001c0004t0003g0070 others(77): Show |
89 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.553+125T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398595 | |||||||
| chr7:76398600 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.553+120G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 5/10 | chr7 | 76398600 | |||||||
| chr7:76398846 | C | T | 32 | a0001c0001t0004g0043 a0001c0004t0001g0219 a0001c0004t0003g0070 others(29): Show |
32 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.476-49G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76398846 | |||||||
| chr7:76398850 | C | G | 2 | a0004c0006t0001g0060 a0004c0006t0001g0061 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.476-53G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76398850 | |||||||
| chr7:76398874 | G | A | 1 | a0001c0004t0003g0098 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.476-77C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76398874 | |||||||
| chr7:76398967 | C | T | 1 | a0002c0002t0001g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.476-170G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76398967 | |||||||
| chr7:76399061 | G | A | 1 | a0001c0004t0003g0108 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.476-264C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399061 | |||||||
| chr7:76399085 | T | C | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.476-288A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399085 | |||||||
| chr7:76399097 | C | T | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.476-300G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399097 | |||||||
| chr7:76399113 | G | C | 1 | a0001c0005t0001g0287 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.476-316C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399113 | |||||||
| chr7:76399268 | T | C | 50 | a0001c0001t0004g0043 a0001c0004t0001g0219 a0001c0004t0001g0274 others(47): Show |
53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.476-471A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399268 | |||||||
| chr7:76399310 | G | C | 1 | a0002c0002t0002g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-513C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399310 | |||||||
| chr7:76399311 | C | G | 1 | a0002c0002t0002g0063 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.476-514G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399311 | |||||||
| chr7:76399426 | T | C | 1 | a0002c0002t0001g0128 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.476-629A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399426 | |||||||
| chr7:76399483 | G | A | 3 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0001c0001t0004g0051 |
4 | HG01192.hp2 HG03041.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.476-686C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399483 | |||||||
| chr7:76399510 | A | G | 51 | a0001c0005t0002g0040 a0001c0005t0002g0041 a0001c0005t0002g0131 others(48): Show |
78 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.476-713T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399510 | |||||||
| chr7:76399552 | C | T | 178 | a0001c0004t0001g0219 a0001c0004t0001g0268 a0001c0004t0001g0269 others(175): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.475+734G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399552 | |||||||
| chr7:76399862 | G | A | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.475+424C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399862 | |||||||
| chr7:76399863 | G | A | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.475+423C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399863 | |||||||
| chr7:76399918 | G | C | 33 | a0003c0003t0001g0011 a0003c0003t0001g0025 a0003c0003t0001g0026 others(30): Show |
40 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(37): Show |
intron_variant | MODIFIER | c.475+368C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399918 | |||||||
| chr7:76399974 | C | G | 48 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(45): Show |
51 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.475+312G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76399974 | |||||||
| chr7:76400008 | T | A | 4 | a0001c0001t0001g0209 a0001c0004t0001g0274 a0001c0016t0004g0053 others(1): Show |
4 | HG02572.hp2 HG03017.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.475+278A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400008 | |||||||
| chr7:76400027 | G | A | 47 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(44): Show |
50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.475+259C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400027 | |||||||
| chr7:76400062 | C | T | 1 | a0004c0006t0001g0265 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.475+224G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400062 | |||||||
| chr7:76400104 | A | G | 13 | a0001c0005t0001g0008 a0001c0005t0001g0278 a0001c0005t0001g0279 others(10): Show |
16 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(13): Show |
intron_variant | MODIFIER | c.475+182T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400104 | |||||||
| chr7:76400202 | G | A | 1 | a0002c0002t0002g0140 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.475+84C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400202 | |||||||
| chr7:76400276 | C | G | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.475+10G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 4/10 | chr7 | 76400276 | |||||||
| chr7:76400621 | G | T | 21 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0056 others(18): Show |
25 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.170-30C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/10 | chr7 | 76400621 | |||||||
| chr7:76400788 | G | A | 57 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(54): Show |
62 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(59): Show |
intron_variant | MODIFIER | c.170-197C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/10 | chr7 | 76400788 | |||||||
| chr7:76400817 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.169+191C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/10 | chr7 | 76400817 | |||||||
| chr7:76400919 | G | A | 1 | a0002c0002t0002g0118 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.169+89C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/10 | chr7 | 76400919 | |||||||
| chr7:76400991 | C | T | 2 | a0001c0001t0001g0192 a0003c0003t0001g0163 |
2 | NA18957.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.169+17G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 3/10 | chr7 | 76400991 | |||||||
| chr7:76401411 | TTTTTC | T | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-373_134-369del others(5): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401411 | |||||||
| chr7:76401520 | G | A | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.134-477C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401520 | |||||||
| chr7:76401541 | C | T | 5 | a0004c0006t0001g0256 a0004c0006t0001g0258 a0004c0006t0001g0260 others(2): Show |
5 | HG02257.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-498G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401541 | |||||||
| chr7:76401550 | G | A | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-507C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401550 | |||||||
| chr7:76401583 | A | G | 23 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0056 others(20): Show |
27 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.134-540T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401583 | |||||||
| chr7:76401613 | C | T | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.134-570G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401613 | |||||||
| chr7:76401747 | C | T | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.134-704G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401747 | |||||||
| chr7:76401749 | C | A | 1 | a0007c0010t0003g0105 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.134-706G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401749 | |||||||
| chr7:76401828 | A | G | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-785T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401828 | |||||||
| chr7:76401962 | A | T | 3 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 |
3 | HG02559.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.134-919T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76401962 | |||||||
| chr7:76402032 | C | T | 178 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(175): Show |
222 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.134-989G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402032 | |||||||
| chr7:76402182 | A | AT | 48 | a0001c0001t0001g0035 a0001c0001t0001g0171 a0001c0001t0001g0175 others(45): Show |
58 | HG00323.hp1 HG00597.hp2 HG00741.hp1 others(55): Show |
intron_variant | MODIFIER | c.134-1140dupA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402182 | |||||||
| chr7:76402182 | A | ATTTT | 39 | a0001c0004t0003g0072 a0001c0004t0003g0085 a0001c0004t0003g0086 others(36): Show |
44 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(41): Show |
intron_variant | MODIFIER | c.134-1143_134-1140d others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402182 | |||||||
| chr7:76402182 | A | ATTTTT | 14 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0073 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.134-1144_134-1140d others(7): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402182 | |||||||
| chr7:76402182 | AT | A | 29 | a0001c0001t0001g0195 a0001c0001t0001g0245 a0001c0001t0008g0188 others(26): Show |
33 | HG01109.hp2 HG01243.hp1 HG01256.hp1 others(30): Show |
intron_variant | MODIFIER | c.134-1140delA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402182 | |||||||
| chr7:76402184 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.134-1141A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402184 | |||||||
| chr7:76402278 | C | T | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.134-1235G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402278 | |||||||
| chr7:76402289 | C | T | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.134-1246G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402289 | |||||||
| chr7:76402360 | T | G | 2 | a0001c0001t0001g0253 a0001c0001t0001g0254 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.134-1317A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402360 | |||||||
| chr7:76402425 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0058 a0001c0001t0001g0189 others(1): Show |
6 | HG00738.hp2 HG00741.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.134-1382C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402425 | |||||||
| chr7:76402490 | T | A | 3 | a0003c0003t0001g0110 a0003c0003t0001g0111 a0003c0003t0001g0112 |
3 | HG01884.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.134-1447A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402490 | |||||||
| chr7:76402499 | G | A | 25 | a0001c0005t0001g0008 a0001c0005t0001g0271 a0001c0005t0001g0272 others(22): Show |
30 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.134-1456C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402499 | |||||||
| chr7:76402640 | A | G | 8 | a0001c0007t0001g0009 a0001c0007t0001g0078 a0001c0007t0001g0080 others(5): Show |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.134-1597T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402640 | |||||||
| chr7:76402718 | A | G | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.133+1589T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402718 | |||||||
| chr7:76402772 | T | C | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.133+1535A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402772 | |||||||
| chr7:76402895 | G | A | 1 | a0002c0002t0002g0022 | 2 | HG01081.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.133+1412C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402895 | |||||||
| chr7:76402912 | C | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1395G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402912 | |||||||
| chr7:76402913 | C | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1394G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402913 | |||||||
| chr7:76402914 | G | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1393C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402914 | |||||||
| chr7:76402917 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1390A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402917 | |||||||
| chr7:76402918 | C | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1389G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402918 | |||||||
| chr7:76402919 | A | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1388T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402919 | |||||||
| chr7:76402921 | C | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1386G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402921 | |||||||
| chr7:76402922 | C | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1385G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402922 | |||||||
| chr7:76402923 | T | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1384A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402923 | |||||||
| chr7:76402924 | C | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1383G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402924 | |||||||
| chr7:76402925 | C | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1382G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402925 | |||||||
| chr7:76402926 | C | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1381G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402926 | |||||||
| chr7:76402929 | A | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1378T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402929 | |||||||
| chr7:76402930 | G | T | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1377C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402930 | |||||||
| chr7:76402934 | T | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1373A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402934 | |||||||
| chr7:76402936 | G | T | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1371C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402936 | |||||||
| chr7:76402939 | T | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1368A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402939 | |||||||
| chr7:76402940 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1367A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402940 | |||||||
| chr7:76402942 | C | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1365G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402942 | |||||||
| chr7:76402945 | G | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1362C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402945 | |||||||
| chr7:76402946 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1361G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402946 | |||||||
| chr7:76402947 | G | A | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.133+1360C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402947 | |||||||
| chr7:76402950 | A | C | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1357T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402950 | |||||||
| chr7:76402951 | G | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1356C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402951 | |||||||
| chr7:76402955 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1352G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402955 | |||||||
| chr7:76402962 | C | T | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1345G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402962 | |||||||
| chr7:76402963 | G | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1344C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402963 | |||||||
| chr7:76402972 | T | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1335A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402972 | |||||||
| chr7:76402974 | G | C | 177 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(174): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.133+1333C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402974 | |||||||
| chr7:76402975 | T | C | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1332A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402975 | |||||||
| chr7:76402976 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1331A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402976 | |||||||
| chr7:76402977 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1330A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402977 | |||||||
| chr7:76402979 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1328A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402979 | |||||||
| chr7:76402980 | T | A | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1327A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402980 | |||||||
| chr7:76402981 | T | G | 1 | a0003c0003t0001g0153 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.133+1326A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76402981 | |||||||
| chr7:76403177 | G | A | 8 | a0001c0007t0001g0009 a0001c0007t0001g0078 a0001c0007t0001g0080 others(5): Show |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+1130C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403177 | |||||||
| chr7:76403227 | C | T | 4 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(1): Show |
4 | HG02451.hp1 HG02559.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1080G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403227 | |||||||
| chr7:76403302 | T | C | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.133+1005A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403302 | |||||||
| chr7:76403313 | G | T | 1 | a0001c0001t0001g0230 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.133+994C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403313 | |||||||
| chr7:76403347 | C | CTTTTTTT others(4): Show |
3 | a0001c0005t0001g0281 a0001c0005t0002g0283 a0006c0009t0003g0099 |
3 | NA18988.hp2 NA19054.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.133+959_133+960ins others(11): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403347 | |||||||
| chr7:76403347 | C | CTTTTTTT others(5): Show |
49 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(46): Show |
54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.133+959_133+960ins others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403347 | |||||||
| chr7:76403347 | C | CTTTTTTT others(6): Show |
4 | a0001c0004t0003g0086 a0001c0005t0001g0279 a0001c0005t0001g0287 others(1): Show |
4 | HG02523.hp1 NA18969.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+959_133+960ins others(13): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403347 | |||||||
| chr7:76403349 | T | C | 94 | a0001c0005t0002g0131 a0001c0007t0001g0009 a0001c0007t0001g0078 others(91): Show |
129 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.133+958A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403349 | |||||||
| chr7:76403369 | G | A | 94 | a0001c0005t0002g0131 a0001c0007t0001g0009 a0001c0007t0001g0078 others(91): Show |
129 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.133+938C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403369 | |||||||
| chr7:76403393 | A | G | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.133+914T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403393 | |||||||
| chr7:76403547 | G | A | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.133+760C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403547 | |||||||
| chr7:76403625 | C | T | 3 | a0002c0002t0002g0115 a0002c0002t0002g0120 a0002c0002t0002g0124 |
3 | HG03688.hp1 HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.133+682G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403625 | |||||||
| chr7:76403692 | C | T | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.133+615G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403692 | |||||||
| chr7:76403819 | G | C | 56 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(53): Show |
61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.133+488C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76403819 | |||||||
| chr7:76404104 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.133+203C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76404104 | |||||||
| chr7:76404227 | T | C | 30 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0072 others(27): Show |
30 | HG00099.hp1 HG00140.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.133+80A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 2/10 | chr7 | 76404227 | |||||||
| chr7:76404580 | C | T | 2 | a0003c0003t0001g0110 a0003c0003t0001g0112 |
2 | HG01884.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-66-75G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404580 | |||||||
| chr7:76404589 | T | C | 140 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(137): Show |
177 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.-66-84A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404589 | |||||||
| chr7:76404639 | T | C | 147 | a0001c0004t0001g0274 a0001c0004t0003g0070 a0001c0004t0003g0071 others(144): Show |
186 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.-66-134A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404639 | |||||||
| chr7:76404797 | C | T | 22 | a0001c0005t0001g0008 a0001c0005t0001g0278 a0001c0005t0001g0279 others(19): Show |
27 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(24): Show |
intron_variant | MODIFIER | c.-66-292G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404797 | |||||||
| chr7:76404833 | C | G | 142 | a0001c0001t0001g0191 a0001c0004t0001g0268 a0001c0004t0001g0269 others(139): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-66-328G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404833 | |||||||
| chr7:76404899 | A | G | 142 | a0001c0001t0001g0191 a0001c0004t0001g0268 a0001c0004t0001g0269 others(139): Show |
179 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.-66-394T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76404899 | |||||||
| chr7:76405034 | C | T | 3 | a0003c0003t0001g0110 a0003c0003t0001g0111 a0003c0003t0001g0112 |
3 | HG01884.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-66-529G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405034 | |||||||
| chr7:76405136 | A | G | 192 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(189): Show |
241 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.-66-631T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405136 | |||||||
| chr7:76405270 | A | ATT | 3 | a0001c0004t0003g0092 a0001c0005t0002g0284 a0006c0009t0003g0109 |
3 | HG01261.hp2 HG02293.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.-66-767_-66-766dup others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405270 | |||||||
| chr7:76405271 | T | TATATATA others(6): Show |
1 | a0001c0001t0001g0235 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-66-767_-66-766ins others(13): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTA | 24 | a0001c0001t0001g0006 a0001c0001t0001g0179 a0001c0001t0001g0197 others(21): Show |
31 | HG01358.hp1 HG01496.hp1 HG01943.hp2 others(28): Show |
intron_variant | MODIFIER | c.-66-768_-66-767dup others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0058 others(24): Show |
40 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.-66-770_-66-767dup others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATA | 27 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0168 others(24): Show |
37 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.-66-772_-66-767dup others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(1): Show |
16 | a0001c0001t0001g0013 a0001c0001t0001g0030 a0001c0001t0001g0171 others(13): Show |
19 | HG00423.hp2 HG00741.hp1 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-66-774_-66-767dup others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(3): Show |
6 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0172 others(3): Show |
8 | HG01071.hp1 HG01071.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-776_-66-767dup others(10): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(5): Show |
7 | a0001c0001t0001g0014 a0001c0001t0001g0178 a0001c0001t0001g0226 others(4): Show |
10 | HG00323.hp1 HG00609.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.-66-778_-66-767dup others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(7): Show |
5 | a0001c0001t0001g0038 a0001c0001t0001g0228 a0001c0001t0001g0229 others(2): Show |
6 | HG00738.hp2 HG01928.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-780_-66-767dup others(14): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(9): Show |
6 | a0001c0001t0001g0173 a0001c0001t0001g0174 a0001c0001t0001g0230 others(3): Show |
6 | HG01255.hp2 HG01346.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-782_-66-767dup others(16): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTATATAT others(11): Show |
2 | a0001c0001t0001g0233 a0001c0001t0001g0234 |
2 | HG01109.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-66-784_-66-767dup others(18): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTA | 10 | a0001c0004t0003g0093 a0001c0004t0003g0094 a0001c0004t0003g0098 others(7): Show |
11 | HG00544.hp1 HG01433.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.-66-767_-66-766ins others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATA | 8 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0100 others(5): Show |
8 | HG00140.hp2 HG00735.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-767_-66-766ins others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(1): Show |
8 | a0001c0004t0003g0090 a0001c0004t0003g0106 a0001c0004t0003g0107 others(5): Show |
8 | HG01358.hp2 HG02273.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-767_-66-766ins others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(3): Show |
3 | a0001c0004t0003g0072 a0001c0005t0001g0008 a0001c0005t0002g0276 |
6 | HG00609.hp1 HG01081.hp2 HG02056.hp2 others(3): Show |
intron_variant | MODIFIER | c.-66-767_-66-766ins others(10): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(5): Show |
4 | a0001c0001t0001g0223 a0001c0004t0003g0073 a0001c0004t0003g0091 others(1): Show |
4 | HG00099.hp1 HG02602.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-767_-66-766ins others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(7): Show |
1 | a0001c0004t0003g0108 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-66-767_-66-766ins others(14): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(9): Show |
1 | a0001c0004t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-66-767_-66-766ins others(16): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(13): Show |
1 | a0001c0004t0003g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-66-767_-66-766ins others(20): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | T | TTTTATAT others(21): Show |
1 | a0001c0004t0003g0089 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-66-767_-66-766ins others(28): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTA | T | 14 | a0001c0001t0001g0191 a0001c0005t0002g0275 a0001c0007t0001g0009 others(11): Show |
19 | HG00597.hp2 HG01081.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-66-768_-66-767del others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATA | T | 13 | a0001c0001t0001g0190 a0001c0001t0004g0016 a0001c0004t0004g0054 others(10): Show |
18 | HG00733.hp2 HG01109.hp2 HG01433.hp2 others(15): Show |
intron_variant | MODIFIER | c.-66-770_-66-767del others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATA | T | 3 | a0001c0001t0001g0189 a0001c0001t0001g0244 a0004c0006t0001g0246 |
3 | HG00741.hp2 HG03225.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.-66-772_-66-767del others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(1): Show |
T | 3 | a0001c0001t0001g0187 a0001c0001t0008g0188 a0006c0009t0003g0141 |
3 | NA18945.hp2 NA18974.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.-66-774_-66-767del others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0186 a0002c0002t0001g0023 a0008c0012t0001g0079 |
4 | HG02622.hp1 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-776_-66-767del others(10): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(5): Show |
T | 4 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0003c0003t0001g0132 others(1): Show |
4 | HG00639.hp2 HG03540.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-778_-66-767del others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(11): Show |
T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0177 a0001c0001t0001g0185 others(2): Show |
6 | HG02165.hp2 HG02970.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.-66-784_-66-767del others(18): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(13): Show |
T | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-66-786_-66-767del others(20): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(19): Show |
T | 3 | a0001c0001t0001g0184 a0004c0006t0001g0060 a0004c0006t0001g0061 |
3 | HG03130.hp2 HG03471.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.-66-792_-66-767del others(26): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(21): Show |
T | 1 | a0001c0001t0001g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-66-794_-66-767del others(28): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405271 | TTATATAT others(23): Show |
T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0175 a0001c0001t0001g0176 |
4 | HG01070.hp1 HG01192.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-796_-66-767del others(30): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405271 | |||||||
| chr7:76405273 | A | T | 10 | a0001c0005t0001g0278 a0001c0005t0001g0279 a0001c0005t0001g0280 others(7): Show |
11 | HG00280.hp2 HG00558.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.-66-768T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405273 | |||||||
| chr7:76405275 | A | T | 1 | a0001c0005t0002g0275 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-66-770T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405275 | |||||||
| chr7:76405281 | A | T | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-66-776T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405281 | |||||||
| chr7:76405291 | A | T | 1 | a0001c0004t0003g0086 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-66-786T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405291 | |||||||
| chr7:76405297 | A | G | 14 | a0001c0001t0004g0015 a0001c0001t0004g0017 a0001c0001t0004g0018 others(11): Show |
18 | HG02055.hp1 HG02572.hp1 HG02723.hp1 others(15): Show |
intron_variant | MODIFIER | c.-66-792T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405297 | |||||||
| chr7:76405299 | A | ATTTT | 2 | a0001c0001t0004g0019 a0001c0001t0004g0044 |
3 | HG02723.hp1 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-66-795_-66-794ins others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405299 | |||||||
| chr7:76405299 | A | G | 1 | a0001c0001t0004g0051 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-66-794T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405299 | |||||||
| chr7:76405299 | ATATATAT others(17): Show |
A | 2 | a0003c0003t0001g0134 a0003c0003t0001g0135 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-66-818_-66-795del others(24): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405299 | |||||||
| chr7:76405301 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0004g0051 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-66-797_-66-796ins others(10): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405301 | |||||||
| chr7:76405301 | A | G | 3 | a0001c0001t0004g0016 a0001c0004t0004g0054 a0001c0005t0002g0277 |
4 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-796T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405301 | |||||||
| chr7:76405301 | A | T | 13 | a0001c0001t0001g0267 a0001c0001t0004g0015 a0001c0001t0004g0017 others(10): Show |
17 | HG02055.hp1 HG02572.hp1 HG02683.hp2 others(14): Show |
intron_variant | MODIFIER | c.-66-796T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405301 | |||||||
| chr7:76405303 | A | C | 3 | a0001c0001t0004g0019 a0001c0001t0004g0044 a0001c0001t0004g0051 |
4 | HG01192.hp2 HG02723.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-798T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405303 | |||||||
| chr7:76405303 | A | T | 10 | a0001c0001t0004g0015 a0001c0001t0004g0017 a0001c0001t0004g0018 others(7): Show |
13 | HG02055.hp1 HG02572.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.-66-798T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405303 | |||||||
| chr7:76405305 | A | G | 2 | a0001c0004t0001g0269 a0001c0004t0001g0270 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-66-800T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405305 | |||||||
| chr7:76405305 | A | T | 16 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(13): Show |
21 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-800T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405305 | |||||||
| chr7:76405307 | A | C | 13 | a0001c0001t0004g0015 a0001c0001t0004g0017 a0001c0001t0004g0018 others(10): Show |
17 | HG01192.hp2 HG02055.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.-66-802T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405307 | |||||||
| chr7:76405307 | A | G | 1 | a0001c0004t0001g0268 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-66-802T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405307 | |||||||
| chr7:76405307 | A | T | 3 | a0001c0001t0004g0016 a0001c0004t0004g0054 a0001c0005t0002g0277 |
4 | HG02451.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-802T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405307 | |||||||
| chr7:76405309 | A | G | 24 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0004t0003g0086 others(21): Show |
31 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-66-804T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405309 | |||||||
| chr7:76405309 | A | T | 16 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(13): Show |
21 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-804T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405309 | |||||||
| chr7:76405311 | A | C | 16 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(13): Show |
21 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-806T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405311 | |||||||
| chr7:76405313 | A | G | 22 | a0001c0004t0003g0089 a0001c0005t0001g0008 a0001c0005t0001g0285 others(19): Show |
27 | HG00544.hp1 HG00609.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-66-808T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405313 | |||||||
| chr7:76405313 | A | T | 42 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(39): Show |
54 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(51): Show |
intron_variant | MODIFIER | c.-66-808T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405313 | |||||||
| chr7:76405315 | A | C | 16 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(13): Show |
21 | HG01192.hp2 HG02055.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.-66-810T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405315 | |||||||
| chr7:76405315 | A | G | 1 | a0004c0006t0001g0256 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-66-810T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405315 | |||||||
| chr7:76405315 | A | T | 29 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0004t0001g0268 others(26): Show |
36 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-66-810T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405315 | |||||||
| chr7:76405317 | G | A | 11 | a0001c0005t0001g0278 a0001c0005t0001g0279 a0001c0005t0001g0280 others(8): Show |
12 | HG00280.hp2 HG00558.hp2 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.-66-812C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405317 | |||||||
| chr7:76405317 | G | T | 53 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(50): Show |
66 | HG00639.hp2 HG00733.hp2 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.-66-812C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405317 | |||||||
| chr7:76405319 | A | ATATATAT others(39): Show |
1 | a0001c0005t0001g0292 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-66-815_-66-814ins others(46): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | ATATATAT others(31): Show |
1 | a0001c0005t0001g0282 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-66-815_-66-814ins others(38): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | ATATATAT others(27): Show |
4 | a0001c0005t0001g0279 a0001c0005t0001g0280 a0001c0005t0001g0281 others(1): Show |
4 | HG02523.hp1 NA18988.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.-66-815_-66-814ins others(34): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | ATATATGT others(25): Show |
2 | a0001c0005t0001g0278 a0001c0005t0002g0040 |
3 | HG00280.hp2 HG02071.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.-66-815_-66-814ins others(32): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | ATGTATTT others(5): Show |
2 | a0001c0004t0003g0090 a0001c0004t0003g0091 |
2 | HG00099.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.-66-815_-66-814ins others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | C | 46 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(43): Show |
58 | HG00639.hp2 HG00733.hp2 HG01109.hp2 others(55): Show |
intron_variant | MODIFIER | c.-66-814T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405319 | A | T | 8 | a0002c0002t0002g0076 a0003c0003t0001g0029 a0003c0003t0001g0138 others(5): Show |
9 | HG01074.hp1 HG01952.hp2 HG03516.hp1 others(6): Show |
intron_variant | MODIFIER | c.-66-814T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405319 | |||||||
| chr7:76405321 | T | G | 1 | a0009c0015t0001g0241 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-66-816A>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405321 | |||||||
| chr7:76405323 | T | A | 1 | a0009c0015t0001g0241 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-66-818A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405323 | |||||||
| chr7:76405323 | T | C | 63 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(60): Show |
77 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(74): Show |
intron_variant | MODIFIER | c.-66-818A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405323 | |||||||
| chr7:76405323 | T | TTTTCTTT others(1): Show |
24 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0072 others(21): Show |
24 | HG00140.hp2 HG00735.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.-66-826_-66-819dup others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405323 | |||||||
| chr7:76405327 | C | T | 3 | a0003c0003t0001g0134 a0003c0003t0001g0135 a0009c0015t0001g0241 |
3 | HG01258.hp2 NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-66-822G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405327 | |||||||
| chr7:76405339 | C | CT | 8 | a0001c0001t0001g0168 a0001c0001t0001g0183 a0001c0001t0001g0244 others(5): Show |
8 | HG02559.hp2 HG03195.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.-66-835dupA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | C | CTT | 6 | a0001c0005t0001g0278 a0001c0005t0001g0279 a0001c0005t0001g0280 others(3): Show |
7 | HG00280.hp2 HG00558.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.-66-836_-66-835dup others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | C | CTTTCTTT others(4): Show |
1 | a0001c0005t0002g0277 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-66-835_-66-834ins others(11): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | C | CTTTCTTT others(7): Show |
3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0013c0019t0001g0273 |
3 | HG04199.hp1 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-66-835_-66-834ins others(14): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | C | CTTTCTTT others(15): Show |
10 | a0001c0005t0001g0008 a0001c0005t0001g0285 a0001c0005t0001g0286 others(7): Show |
14 | HG00544.hp1 HG00609.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.-66-835_-66-834ins others(22): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | C | CTTTCTTT others(16): Show |
2 | a0001c0005t0002g0275 a0001c0005t0002g0276 |
2 | HG02056.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-66-835_-66-834ins others(23): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405339 | CT | C | 29 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0236 others(26): Show |
35 | HG00733.hp2 HG01070.hp1 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.-66-835delA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405339 | |||||||
| chr7:76405340 | T | TTTC | 9 | a0002c0002t0002g0076 a0002c0014t0001g0129 a0003c0003t0001g0029 others(6): Show |
10 | HG01074.hp1 HG01952.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-66-836_-66-835ins others(3): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405340 | |||||||
| chr7:76405340 | T | TTTCTTTC | 77 | a0001c0004t0003g0087 a0001c0004t0003g0089 a0002c0002t0001g0128 others(74): Show |
108 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.-66-836_-66-835ins others(7): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405340 | |||||||
| chr7:76405340 | T | TTTCTTTC others(4): Show |
5 | a0001c0001t0004g0018 a0001c0001t0004g0049 a0003c0003t0001g0110 others(2): Show |
5 | HG01884.hp2 HG02717.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-66-836_-66-835ins others(11): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405340 | |||||||
| chr7:76405340 | T | TTTCTTTC others(16): Show |
1 | a0014c0018t0002g0291 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-66-836_-66-835ins others(23): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405340 | |||||||
| chr7:76405343 | T | C | 3 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0009c0015t0001g0241 |
3 | HG01258.hp2 HG01517.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.-66-838A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405343 | |||||||
| chr7:76405346 | T | C | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-66-841A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405346 | |||||||
| chr7:76405350 | T | C | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-66-845A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405350 | |||||||
| chr7:76405420 | G | A | 2 | a0004c0006t0001g0039 a0004c0006t0001g0250 |
3 | HG01109.hp2 HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-66-915C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405420 | |||||||
| chr7:76405425 | G | A | 1 | a0002c0002t0002g0133 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-66-920C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405425 | |||||||
| chr7:76405477 | A | G | 149 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(146): Show |
188 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-66-972T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405477 | |||||||
| chr7:76405629 | C | T | 3 | a0003c0003t0001g0110 a0003c0003t0001g0111 a0003c0003t0001g0112 |
3 | HG01884.hp2 HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-66-1124G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405629 | |||||||
| chr7:76405873 | G | T | 1 | a0001c0001t0004g0044 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-66-1368C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405873 | |||||||
| chr7:76405907 | C | G | 4 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(1): Show |
4 | HG02559.hp2 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-66-1402G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405907 | |||||||
| chr7:76405965 | C | CTTCCTTT others(2): Show |
17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-66-1461_-66-1460i others(11): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405965 | |||||||
| chr7:76405979 | C | T | 17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-66-1474G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405979 | |||||||
| chr7:76405983 | CTTTT | C | 32 | a0003c0003t0001g0011 a0003c0003t0001g0025 a0003c0003t0001g0026 others(29): Show |
39 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.-66-1482_-66-1479d others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76405983 | |||||||
| chr7:76406016 | C | T | 2 | a0004c0006t0001g0246 a0004c0006t0001g0247 |
2 | HG02145.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-66-1511G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406016 | |||||||
| chr7:76406029 | A | C | 1 | a0001c0004t0004g0054 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-66-1524T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406029 | |||||||
| chr7:76406055 | C | A | 148 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(145): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-66-1550G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406055 | |||||||
| chr7:76406203 | C | A | 114 | a0001c0005t0002g0131 a0001c0007t0001g0009 a0001c0007t0001g0078 others(111): Show |
153 | HG00323.hp1 HG00423.hp2 HG00558.hp1 others(150): Show |
intron_variant | MODIFIER | c.-66-1698G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406203 | |||||||
| chr7:76406268 | G | A | 2 | a0003c0003t0001g0134 a0003c0003t0001g0135 |
2 | NA19030.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.-66-1763C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406268 | |||||||
| chr7:76406463 | T | A | 1 | a0001c0001t0001g0244 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-66-1958A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406463 | |||||||
| chr7:76406530 | C | T | 148 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(145): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-66-2025G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406530 | |||||||
| chr7:76406630 | T | C | 148 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(145): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-66-2125A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406630 | |||||||
| chr7:76406643 | C | G | 7 | a0004c0006t0001g0007 a0004c0006t0001g0039 a0004c0006t0001g0246 others(4): Show |
11 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-66-2138G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406643 | |||||||
| chr7:76406784 | G | GA | 7 | a0001c0001t0001g0245 a0001c0005t0001g0293 a0002c0002t0002g0069 others(4): Show |
8 | HG01074.hp1 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.-66-2280dupT | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406784 | |||||||
| chr7:76406849 | G | C | 127 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(124): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-66-2344C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406849 | |||||||
| chr7:76406858 | A | T | 1 | a0001c0004t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-66-2353T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406858 | |||||||
| chr7:76406892 | A | T | 1 | a0002c0002t0001g0180 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-66-2387T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406892 | |||||||
| chr7:76406911 | T | A | 1 | a0002c0002t0002g0139 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-66-2406A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406911 | |||||||
| chr7:76406953 | A | ATTAT | 8 | a0001c0007t0001g0009 a0001c0007t0001g0078 a0001c0007t0001g0080 others(5): Show |
10 | HG00733.hp2 HG01243.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.-66-2452_-66-2449d others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76406953 | |||||||
| chr7:76407047 | A | G | 165 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(162): Show |
209 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(206): Show |
intron_variant | MODIFIER | c.-67+2367T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407047 | |||||||
| chr7:76407063 | G | C | 148 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(145): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.-67+2351C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407063 | |||||||
| chr7:76407085 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-67+2329G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407085 | |||||||
| chr7:76407176 | G | A | 127 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(124): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-67+2238C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407176 | |||||||
| chr7:76407231 | A | C | 1 | a0002c0002t0002g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-67+2183T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407231 | |||||||
| chr7:76407252 | G | A | 127 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(124): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-67+2162C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407252 | |||||||
| chr7:76407266 | T | A | 3 | a0001c0005t0001g0271 a0001c0005t0001g0272 a0013c0019t0001g0273 |
3 | HG04199.hp1 NA18990.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-67+2148A>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407266 | |||||||
| chr7:76407338 | C | CTT | 125 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(122): Show |
160 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.-67+2074_-67+2075d others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407338 | |||||||
| chr7:76407400 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-67+2014G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407400 | |||||||
| chr7:76407434 | C | T | 127 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(124): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-67+1980G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407434 | |||||||
| chr7:76407435 | G | A | 1 | a0001c0022t0001g0252 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-67+1979C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407435 | |||||||
| chr7:76407753 | G | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0177 |
3 | HG02165.hp2 NA18612.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-67+1661C>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407753 | |||||||
| chr7:76407762 | C | G | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | HG01070.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.-67+1652G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407762 | |||||||
| chr7:76407805 | T | C | 130 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(127): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.-67+1609A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407805 | |||||||
| chr7:76407873 | C | G | 127 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(124): Show |
162 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.-67+1541G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407873 | |||||||
| chr7:76407938 | C | A | 25 | a0001c0005t0001g0008 a0001c0005t0001g0271 a0001c0005t0001g0272 others(22): Show |
30 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(27): Show |
intron_variant | MODIFIER | c.-67+1476G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407938 | |||||||
| chr7:76407969 | A | T | 7 | a0001c0001t0001g0030 a0001c0001t0001g0169 a0001c0001t0001g0170 others(4): Show |
8 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.-67+1445T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76407969 | |||||||
| chr7:76408068 | C | G | 1 | a0001c0001t0001g0168 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-67+1346G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408068 | |||||||
| chr7:76408093 | C | T | 17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+1321G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408093 | |||||||
| chr7:76408097 | A | G | 17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+1317T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408097 | |||||||
| chr7:76408177 | A | G | 17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+1237T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408177 | |||||||
| chr7:76408266 | A | G | 17 | a0001c0001t0004g0015 a0001c0001t0004g0016 a0001c0001t0004g0017 others(14): Show |
22 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.-67+1148T>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408266 | |||||||
| chr7:76408425 | G | A | 10 | a0004c0006t0001g0256 a0004c0006t0001g0257 a0004c0006t0001g0258 others(7): Show |
10 | HG02257.hp1 HG02647.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.-67+989C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408425 | |||||||
| chr7:76408475 | C | A | 1 | a0001c0001t0001g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-67+939G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408475 | |||||||
| chr7:76408610 | C | T | 13 | a0002c0002t0002g0020 a0002c0002t0002g0021 a0002c0002t0002g0062 others(10): Show |
15 | HG00423.hp2 HG00558.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.-67+804G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408610 | |||||||
| chr7:76408709 | A | C | 1 | a0001c0001t0004g0043 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-67+705T>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408709 | |||||||
| chr7:76408719 | C | A | 1 | a0006c0009t0003g0141 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-67+695G>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408719 | |||||||
| chr7:76408729 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-67+685C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408729 | |||||||
| chr7:76408742 | G | A | 32 | a0003c0003t0001g0011 a0003c0003t0001g0025 a0003c0003t0001g0026 others(29): Show |
39 | HG00323.hp1 HG00597.hp2 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.-67+672C>T | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408742 | |||||||
| chr7:76408836 | A | T | 123 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0072 others(120): Show |
158 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.-67+578T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408836 | |||||||
| chr7:76408873 | C | T | 1 | a0001c0016t0004g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-67+541G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76408873 | |||||||
| chr7:76409297 | C | CCT | 13 | a0001c0004t0003g0070 a0001c0004t0003g0071 a0001c0004t0003g0072 others(10): Show |
14 | HG00423.hp2 HG00558.hp1 HG00735.hp1 others(11): Show |
intron_variant | MODIFIER | c.-67+115_-67+116dup others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409297 | |||||||
| chr7:76409297 | C | CCTCT | 26 | a0001c0004t0001g0274 a0001c0005t0001g0008 a0001c0005t0001g0278 others(23): Show |
31 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.-67+113_-67+116dup others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409297 | |||||||
| chr7:76409314 | C | G | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-67+100G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409314 | |||||||
| chr7:76409317 | TCTGTCTC others(3): Show |
T | 1 | a0001c0001t0001g0058 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-67+87_-67+96delTG others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409317 | |||||||
| chr7:76409318 | CTG | C | 5 | a0001c0001t0004g0045 a0001c0001t0004g0046 a0001c0004t0004g0054 others(2): Show |
5 | HG00639.hp2 HG02451.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-67+94_-67+95delCA | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409318 | |||||||
| chr7:76409320 | G | C | 23 | a0001c0001t0001g0033 a0001c0001t0001g0255 a0001c0001t0004g0015 others(20): Show |
28 | HG01192.hp2 HG01255.hp1 HG02015.hp2 others(25): Show |
intron_variant | MODIFIER | c.-67+94C>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409320 | |||||||
| chr7:76409322 | C | G | 3 | a0001c0001t0001g0033 a0005c0008t0001g0220 a0005c0008t0001g0224 |
3 | HG02015.hp2 NA18747.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-67+92G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409322 | |||||||
| chr7:76409323 | T | TCA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0234 |
3 | HG00280.hp1 HG00323.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.-67+89_-67+90dupTG | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCA | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
108 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.-67+89_-67+90delTG | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACA | T | 21 | a0001c0001t0001g0012 a0001c0001t0001g0189 a0001c0001t0001g0253 others(18): Show |
27 | HG00741.hp2 HG01099.hp1 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.-67+87_-67+90delTG others(2): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACACA | T | 32 | a0001c0001t0001g0203 a0001c0001t0001g0229 a0001c0001t0001g0233 others(29): Show |
44 | HG00735.hp2 HG00738.hp2 HG01109.hp1 others(41): Show |
intron_variant | MODIFIER | c.-67+85_-67+90delTG others(4): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACACAC others(1): Show |
T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0004t0001g0268 others(105): Show |
132 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.-67+83_-67+90delTG others(6): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACACAC others(3): Show |
T | 22 | a0001c0005t0001g0008 a0001c0005t0001g0278 a0001c0005t0001g0279 others(19): Show |
26 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(23): Show |
intron_variant | MODIFIER | c.-67+81_-67+90delTG others(8): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACACAC others(5): Show |
T | 7 | a0002c0002t0002g0001 a0004c0006t0001g0251 a0006c0009t0003g0095 others(4): Show |
7 | HG02135.hp2 HG02148.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-67+79_-67+90delTG others(10): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409323 | TCACACAC others(7): Show |
T | 1 | a0001c0004t0001g0274 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-67+77_-67+90delTG others(12): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409323 | |||||||
| chr7:76409324 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-67+90G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409324 | |||||||
| chr7:76409325 | A | T | 9 | a0001c0001t0001g0033 a0001c0001t0001g0255 a0001c0001t0004g0045 others(6): Show |
9 | HG00639.hp2 HG01255.hp1 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.-67+89T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409325 | |||||||
| chr7:76409326 | C | G | 2 | a0001c0004t0004g0054 a0001c0016t0004g0053 |
2 | HG02451.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-67+88G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409326 | |||||||
| chr7:76409327 | A | T | 6 | a0001c0001t0001g0255 a0001c0001t0004g0045 a0001c0001t0004g0046 others(3): Show |
6 | HG00639.hp2 HG01255.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+87T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409327 | |||||||
| chr7:76409328 | C | G | 14 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0018 others(11): Show |
18 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-67+86G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409328 | |||||||
| chr7:76409329 | A | T | 16 | a0001c0001t0004g0016 a0001c0001t0004g0017 a0001c0001t0004g0018 others(13): Show |
20 | HG00639.hp2 HG01192.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.-67+85T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409329 | |||||||
| chr7:76409330 | C | G | 5 | a0001c0001t0004g0015 a0001c0001t0004g0042 a0001c0005t0001g0271 others(2): Show |
6 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+84G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409330 | |||||||
| chr7:76409331 | A | T | 5 | a0001c0001t0004g0015 a0001c0001t0004g0042 a0001c0005t0001g0271 others(2): Show |
6 | HG03490.hp2 HG03492.hp2 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+83T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409331 | |||||||
| chr7:76409333 | A | T | 6 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(3): Show |
6 | HG02559.hp2 HG03195.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.-67+81T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409333 | |||||||
| chr7:76409334 | C | G | 3 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 |
3 | HG02559.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-67+80G>C | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409334 | |||||||
| chr7:76409335 | A | T | 3 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 |
3 | HG02559.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-67+79T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409335 | |||||||
| chr7:76409337 | A | T | 3 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 |
3 | HG02559.hp2 HG03195.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-67+77T>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409337 | |||||||
| chr7:76409400 | T | C | 29 | a0001c0004t0001g0268 a0001c0004t0001g0269 a0001c0004t0001g0270 others(26): Show |
34 | HG00280.hp2 HG00544.hp1 HG00558.hp2 others(31): Show |
intron_variant | MODIFIER | c.-67+14A>G | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409400 | |||||||
| chr7:76409404 | G | GATCATAG others(24): Show |
1 | a0004c0006t0001g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-67+9_-67+10insTCT others(28): Show |
SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409404 | |||||||
| chr7:76409413 | C | T | 1 | a0004c0006t0001g0056 | 1 | HG03130.hp1 | splice_donor_variant&intron_variant | HIGH | c.-67+1G>A | SSC4D | ENSG00000146700.9 | transcript | ENST00000275560.4 | protein_coding | 1/10 | chr7 | 76409413 |