Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10590 |
| ensemblid | ENSG00000079689.15 |
| hgncid | 16941 |
| symbol | SCGN |
| name | secretagogin, EF-hand calcium binding protein |
| refseq_nuc | NM_006998.4 |
| refseq_prot | NP_008929.2 |
| ensembl_nuc | ENST00000377961.3 |
| ensembl_prot | ENSP00000367197.2 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 25652215 |
| end | 25701783 |
| strand | + |
| ver | v1.2 |
| region | chr6:25652215-25701783 |
| region5000 | chr6:25647215-25706783 |
| regionname0 | SCGN_chr6_25652215_25701783 |
| regionname5000 | SCGN_chr6_25647215_25706783 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 276 | 350 | 77 | 65 | 149 | 17 | 40 | 116 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0002 | 0/0 | 276 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0003 | 0/0 | 276 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0004 | 0/0 | 276 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0005 | 0/0 | 276 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0006 | 0/0 | 276 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0007 | 0/0 | 276 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0008 | 0/0 | 276 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| a0009 | 0/0 | 276 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | MDSSR others(271): Show |
chr6 | 25647215 | 25706783 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 828 | 346 | 76 | 65 | 146 | 17 | 40 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0001c0004 | 0/0 | 828 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0001c0006 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0002c0002 | 0/0 | 828 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0003c0003 | 0/0 | 828 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0004c0005 | 0/0 | 828 | 2 | 1 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0005c0008 | 0/0 | 828 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0006c0007 | 0/0 | 828 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0007c0009 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0008c0011 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 | ||
| a0009c0010 | 0/0 | 828 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | ATGGA others(823): Show |
chr6 | 25647215 | 25706783 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1469 | 108 | 9 | 21 | 71 | 4 | 3 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0002 | 0/1 | 1469 | 81 | 24 | 10 | 22 | 6 | 18 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0003 | 0/0 | 1469 | 51 | 23 | 13 | 4 | 4 | 7 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0004 | 0/0 | 1468 | 39 | 0 | 12 | 22 | 1 | 4 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0005 | 0/0 | 1468 | 26 | 2 | 4 | 14 | 1 | 5 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0006 | 0/0 | 1468 | 18 | 3 | 1 | 10 | 1 | 3 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0007 | 0/0 | 1467 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1462): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0008 | 0/0 | 1469 | 6 | 3 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0009 | 0/0 | 1468 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0010 | 1/0 | 1468 | 2 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0012 | 0/0 | 1468 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0013 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0014 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0015 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0016 | 0/0 | 1468 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0017 | 0/0 | 1469 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0001t0018 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0004t0001 | 0/0 | 1469 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0001c0004t0004 | 0/0 | 1468 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0001c0006t0003 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0002c0002t0003 | 0/0 | 1469 | 6 | 6 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0003c0003t0003 | 0/0 | 1469 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0004c0005t0004 | 0/0 | 1468 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1463): Show |
chr6 | 25647215 | 25706783 |
| a0004c0005t0011 | 0/0 | 1467 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1462): Show |
chr6 | 25647215 | 25706783 |
| a0005c0008t0001 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0006c0007t0002 | 0/0 | 1469 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0007c0009t0001 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0008c0011t0003 | 0/0 | 1469 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| a0009c0010t0003 | 0/0 | 1469 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | GCTGA others(1464): Show |
chr6 | 25647215 | 25706783 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0005 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0008 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0004 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0004g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0005g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0006g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0007g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0007g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0007g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0008g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0008g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0008g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0008g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0009g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0010g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0010g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0012g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0014g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0015g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0016g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0017g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0001t0018g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0004t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0004t0004g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0001c0006t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0002c0002t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0002c0002t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0002c0002t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0002c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0002c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0003c0003t0003g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0003c0003t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0003c0003t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0004c0005t0004g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0004c0005t0011g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0005c0008t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0006c0007t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0007c0009t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0008c0011t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| a0009c0010t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0006 | g0257 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0159 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0022 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00323 | hp1 | a0005 | c0008 | t0001 | g0169 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | FIN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0305 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00438 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00544 | hp1 | a0001 | c0001 | t0004 | g0264 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00609 | hp1 | a0006 | c0007 | t0002 | g0203 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00609 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00642 | hp2 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0143 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00673 | hp2 | a0001 | c0001 | t0005 | g0025 | EAS | CHS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00738 | hp1 | a0001 | c0001 | t0005 | g0278 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01069 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0175 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01071 | hp2 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01081 | hp2 | a0001 | c0001 | t0008 | g0024 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01106 | hp1 | a0001 | c0001 | t0006 | g0254 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0303 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01167 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01168 | hp2 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0026 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01192 | hp1 | a0001 | c0001 | t0004 | g0279 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0079 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0148 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01346 | hp1 | a0001 | c0001 | t0004 | g0028 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01358 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01361 | hp1 | a0001 | c0001 | t0008 | g0189 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01433 | hp1 | a0001 | c0001 | t0005 | g0298 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01496 | hp2 | a0001 | c0001 | t0004 | g0294 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0165 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01516 | hp1 | a0001 | c0001 | t0005 | g0243 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0085 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0014 | EUR | IBS | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01884 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01891 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0291 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01943 | hp2 | a0001 | c0001 | t0004 | g0285 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01993 | hp1 | a0001 | c0001 | t0017 | g0073 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0297 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02055 | hp1 | a0001 | c0001 | t0008 | g0152 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0065 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0277 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0253 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0269 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0227 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0284 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | CDX | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02257 | hp1 | a0003 | c0003 | t0003 | g0010 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02257 | hp2 | a0001 | c0006 | t0003 | g0051 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0071 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02280 | hp2 | a0003 | c0003 | t0003 | g0312 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02300 | hp2 | a0004 | c0005 | t0004 | g0275 | AMR | PEL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0094 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0008 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02602 | hp2 | a0001 | c0001 | t0004 | g0287 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02615 | hp1 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0235 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02818 | hp2 | a0002 | c0002 | t0003 | g0092 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0174 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02895 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02895 | hp2 | a0001 | c0001 | t0008 | g0061 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02896 | hp2 | a0002 | c0002 | t0003 | g0091 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0233 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02922 | hp2 | a0004 | c0005 | t0011 | g0247 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02970 | hp1 | a0001 | c0001 | t0009 | g0245 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03017 | hp1 | a0007 | c0009 | t0001 | g0001 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03017 | hp2 | a0001 | c0001 | t0004 | g0296 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0237 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03130 | hp1 | a0001 | c0001 | t0006 | g0249 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0153 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0313 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03195 | hp1 | a0003 | c0003 | t0003 | g0311 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03209 | hp1 | a0008 | c0011 | t0003 | g0318 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0004 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0317 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03225 | hp2 | a0001 | c0001 | t0010 | g0211 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0280 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03453 | hp1 | a0001 | c0001 | t0005 | g0234 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03486 | hp2 | a0002 | c0002 | t0003 | g0093 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03490 | hp1 | a0001 | c0001 | t0005 | g0238 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03491 | hp2 | a0001 | c0001 | t0006 | g0251 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03516 | hp2 | a0001 | c0001 | t0013 | g0101 | AFR | ESN | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0086 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03654 | hp1 | a0001 | c0001 | t0005 | g0272 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0039 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03669 | hp1 | a0009 | c0010 | t0003 | g0038 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0190 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0239 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0242 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0149 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0128 | SAS | PJL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03831 | hp1 | a0001 | c0001 | t0006 | g0268 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0289 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0151 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0288 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0135 | SAS | BEB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04228 | hp1 | a0001 | c0001 | t0006 | g0290 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | STU | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | CHB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | CHB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18940 | hp1 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18943 | hp1 | a0001 | c0001 | t0005 | g0292 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0295 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18948 | hp1 | a0001 | c0001 | t0004 | g0035 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18948 | hp2 | a0001 | c0004 | t0004 | g0274 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18956 | hp2 | a0001 | c0001 | t0005 | g0240 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18957 | hp1 | a0001 | c0001 | t0006 | g0310 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18957 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0282 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18963 | hp2 | a0001 | c0001 | t0004 | g0267 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18965 | hp2 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18974 | hp1 | a0001 | c0001 | t0004 | g0309 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18974 | hp2 | a0001 | c0004 | t0001 | g0121 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18975 | hp2 | a0001 | c0001 | t0004 | g0244 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18977 | hp1 | a0001 | c0001 | t0018 | g0120 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18979 | hp2 | a0001 | c0001 | t0015 | g0129 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18982 | hp1 | a0001 | c0001 | t0006 | g0283 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18983 | hp1 | a0001 | c0004 | t0001 | g0111 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18984 | hp2 | a0001 | c0001 | t0004 | g0255 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18986 | hp1 | a0001 | c0001 | t0004 | g0263 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18986 | hp2 | a0001 | c0001 | t0005 | g0276 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18987 | hp1 | a0001 | c0001 | t0004 | g0302 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19003 | hp2 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0286 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0241 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0308 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0087 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0316 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0293 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19055 | hp1 | a0001 | c0001 | t0012 | g0299 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19056 | hp2 | a0001 | c0001 | t0006 | g0031 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19058 | hp1 | a0001 | c0001 | t0006 | g0300 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0261 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19064 | hp1 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19068 | hp2 | a0001 | c0001 | t0004 | g0270 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0131 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19070 | hp2 | a0001 | c0001 | t0004 | g0260 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0304 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19079 | hp2 | a0001 | c0001 | t0004 | g0265 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19081 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0307 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19089 | hp2 | a0001 | c0001 | t0006 | g0306 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19091 | hp1 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0002 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0236 | AFR | YRI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20129 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ASW | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0014 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0112 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20805 | hp1 | a0001 | c0001 | t0004 | g0248 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0219 | EUR | TSI | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | GIH | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0262 | SAS | GIH | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02109 | hp1 | a0001 | c0001 | t0007 | g0009 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0246 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | ACB | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03471 | hp1 | a0001 | c0001 | t0014 | g0195 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0009 | AFR | MSL | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18955 | hp1 | a0001 | c0001 | t0004 | g0252 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | USA | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | USA | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0259 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| NA21309 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | LWK | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0059 | REF | REF | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0163 | REF | REF | SCGN_chr6_25647215_25706783 | SCGN | chr6 | 25647215 | 25706783 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:25653400 | A | T | 1 | a0008 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.101A>T | p.Glu34Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/11 | 290/1468 | 101/831 | 34/276 | chr6 | 25653400 | |||
| chr6:25661633 | C | T | 1 | a0009 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.235C>T | p.Arg79Trp | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/11 | 424/1468 | 235/831 | 79/276 | chr6 | 25661633 | |||
| chr6:25664994 | C | T | 1 | a0007 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.298C>T | p.Arg100Trp | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/11 | 487/1468 | 298/831 | 100/276 | chr6 | 25664994 | |||
| chr6:25669566 | G | A | 1 | a0004 | 2 | HG02300.hp2 HG02922.hp2 |
missense_variant&splice_region_variant | MODERATE | c.392G>A | p.Arg131His | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/11 | 581/1468 | 392/831 | 131/276 | chr6 | 25669566 | |||
| chr6:25670014 | C | G | 1 | a0005 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.409C>G | p.Leu137Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/11 | 598/1468 | 409/831 | 137/276 | chr6 | 25670014 | |||
| chr6:25670035 | G | C | 1 | a0006 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.430G>C | p.Ala144Pro | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/11 | 619/1468 | 430/831 | 144/276 | chr6 | 25670035 | |||
| chr6:25691069 | C | T | 1 | a0003 | 5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
missense_variant | MODERATE | c.647C>T | p.Ala216Val | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/11 | 836/1468 | 647/831 | 216/276 | chr6 | 25691069 | |||
| chr6:25701256 | G | A | 1 | a0002 | 6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
missense_variant | MODERATE | c.752G>A | p.Arg251His | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 941/1468 | 752/831 | 251/276 | chr6 | 25701256 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:25669555 | T | C | 1 | a0001c0006 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.381T>C | p.Ala127Ala | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/11 | 570/1468 | 381/831 | 127/276 | chr6 | 25669555 | |||
| chr6:25691124 | G | A | 1 | a0001c0004 | 3 | NA18948.hp2 NA18974.hp2 NA18983.hp1 |
splice_region_variant&synonymous_variant | LOW | c.702G>A | p.Gln234Gln | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/11 | 891/1468 | 702/831 | 234/276 | chr6 | 25691124 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:25652340 | AG | A | 9 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(6): Show |
95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
5_prime_UTR_variant | MODIFIER | c.-62delG | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/11 | 62 | INFO_REALIGN_3_PRIME | chr6 | 25652340 | |||||
| chr6:25701439 | T | C | 1 | a0001c0001t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*104T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 104 | chr6 | 25701439 | ||||||
| chr6:25701463 | C | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(24): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
3_prime_UTR_variant | MODIFIER | c.*128C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 128 | chr6 | 25701463 | ||||||
| chr6:25701470 | G | T | 2 | a0001c0001t0008 a0001c0001t0009 |
8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*135G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 135 | chr6 | 25701470 | ||||||
| chr6:25701490 | G | A | 8 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0014 others(5): Show |
154 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
3_prime_UTR_variant | MODIFIER | c.*155G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 155 | chr6 | 25701490 | ||||||
| chr6:25701630 | G | T | 2 | a0001c0001t0012 a0001c0001t0018 |
2 | NA18977.hp1 NA19055.hp1 |
3_prime_UTR_variant | MODIFIER | c.*295G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 295 | chr6 | 25701630 | ||||||
| chr6:25701675 | G | A | 10 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0015 others(7): Show |
86 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*340G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 340 | chr6 | 25701675 | ||||||
| chr6:25701676 | T | C | 1 | a0001c0001t0015 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*341T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 341 | chr6 | 25701676 | ||||||
| chr6:25701692 | T | A | 1 | a0001c0001t0014 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*357T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 357 | chr6 | 25701692 | ||||||
| chr6:25701739 | A | AT | 25 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(22): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*411dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 412 | INFO_REALIGN_3_PRIME | chr6 | 25701739 | |||||
| chr6:25701747 | G | T | 1 | a0001c0001t0017 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 11/11 | 412 | chr6 | 25701747 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:25652499 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0003g0032 |
3 | HG02572.hp1 HG03540.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.82+14G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652499 | |||||||
| chr6:25652644 | T | C | 1 | a0001c0001t0004g0035 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.82+159T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652644 | |||||||
| chr6:25652741 | A | G | 1 | a0001c0001t0001g0319 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.82+256A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652741 | |||||||
| chr6:25652852 | TCA | T | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82+369_82+370delAC | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr6 | 25652852 | ||||||
| chr6:25652862 | G | T | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.82+377G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25652862 | |||||||
| chr6:25653047 | C | T | 6 | a0001c0001t0002g0313 a0001c0001t0002g0315 a0001c0001t0003g0314 others(3): Show |
8 | HG01106.hp2 HG01884.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-335C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653047 | |||||||
| chr6:25653173 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0222 a0001c0001t0001g0223 others(9): Show |
15 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.83-209A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653173 | |||||||
| chr6:25653208 | T | G | 27 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(24): Show |
28 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.83-174T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653208 | |||||||
| chr6:25653220 | C | T | 1 | a0001c0001t0002g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.83-162C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653220 | |||||||
| chr6:25653236 | T | G | 6 | a0001c0001t0005g0234 a0001c0001t0007g0009 a0001c0001t0007g0235 others(3): Show |
8 | HG01884.hp1 HG02109.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.83-146T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653236 | |||||||
| chr6:25653317 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-65T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653317 | |||||||
| chr6:25653334 | G | A | 1 | a0001c0001t0005g0238 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.83-48G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653334 | |||||||
| chr6:25653338 | T | TA | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.83-44_83-43insA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653338 | |||||||
| chr6:25653380 | AG | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0220 a0001c0001t0003g0221 |
7 | HG02486.hp1 HG02615.hp2 HG02965.hp1 others(4): Show |
splice_acceptor_variant&intron_variant | HIGH | c.83-1delG | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 1/10 | chr6 | 25653380 | |||||||
| chr6:25653484 | G | A | 1 | a0001c0001t0008g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.153+32G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653484 | |||||||
| chr6:25653501 | G | A | 1 | a0001c0001t0004g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.153+49G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653501 | |||||||
| chr6:25653597 | T | C | 10 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(7): Show |
13 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+145T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653597 | |||||||
| chr6:25653607 | T | C | 1 | a0001c0001t0005g0240 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.153+155T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653607 | |||||||
| chr6:25653614 | T | G | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+162T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653614 | |||||||
| chr6:25653633 | T | A | 1 | a0001c0001t0003g0316 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.153+181T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653633 | |||||||
| chr6:25653861 | C | G | 32 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(29): Show |
33 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.153+409C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653861 | |||||||
| chr6:25653920 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.153+468G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25653920 | |||||||
| chr6:25654000 | T | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0003 others(19): Show |
30 | HG01243.hp1 HG01891.hp1 HG01993.hp1 others(27): Show |
intron_variant | MODIFIER | c.153+548T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654000 | |||||||
| chr6:25654037 | T | A | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(98): Show |
123 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.153+585T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654037 | |||||||
| chr6:25654120 | C | G | 1 | a0001c0001t0006g0310 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.153+668C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654120 | |||||||
| chr6:25654120 | C | T | 3 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0216 |
3 | HG01167.hp2 HG01169.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.153+668C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654120 | |||||||
| chr6:25654231 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.153+779C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654231 | |||||||
| chr6:25654326 | G | T | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.153+874G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654326 | |||||||
| chr6:25654358 | G | T | 1 | a0001c0001t0004g0309 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.153+906G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654358 | |||||||
| chr6:25654397 | C | G | 2 | a0001c0001t0005g0307 a0001c0001t0005g0308 |
2 | NA19011.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.153+945C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654397 | |||||||
| chr6:25654489 | T | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0085 |
3 | HG01516.hp2 HG01517.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.153+1037T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654489 | |||||||
| chr6:25654759 | C | T | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1307C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654759 | |||||||
| chr6:25654771 | T | C | 1 | a0001c0001t0004g0241 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.153+1319T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654771 | |||||||
| chr6:25654829 | G | T | 2 | a0001c0001t0002g0210 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153+1377G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654829 | |||||||
| chr6:25654831 | C | T | 10 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(7): Show |
13 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(10): Show |
intron_variant | MODIFIER | c.153+1379C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654831 | |||||||
| chr6:25654833 | G | T | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+1381G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654833 | |||||||
| chr6:25654876 | T | C | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1424T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654876 | |||||||
| chr6:25654933 | G | A | 2 | a0001c0001t0002g0210 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.153+1481G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654933 | |||||||
| chr6:25654950 | A | T | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+1498A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25654950 | |||||||
| chr6:25655013 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.153+1561C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655013 | |||||||
| chr6:25655061 | C | A | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.153+1609C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655061 | |||||||
| chr6:25655067 | A | G | 1 | a0001c0001t0002g0011 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.153+1615A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655067 | |||||||
| chr6:25655194 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.153+1742G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655194 | |||||||
| chr6:25655303 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.153+1851T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655303 | |||||||
| chr6:25655447 | G | A | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+1995G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655447 | |||||||
| chr6:25655611 | T | G | 93 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(90): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.153+2159T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655611 | |||||||
| chr6:25655665 | A | AT | 86 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(83): Show |
95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.153+2220dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25655665 | ||||||
| chr6:25655695 | C | G | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.153+2243C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655695 | |||||||
| chr6:25655699 | T | C | 1 | a0001c0001t0005g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.153+2247T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655699 | |||||||
| chr6:25655867 | T | G | 2 | a0001c0001t0008g0152 a0001c0001t0008g0153 |
2 | HG02055.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.153+2415T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655867 | |||||||
| chr6:25655984 | G | A | 1 | a0001c0001t0004g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.153+2532G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25655984 | |||||||
| chr6:25656293 | A | G | 2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.153+2841A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656293 | |||||||
| chr6:25656433 | C | G | 80 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(77): Show |
89 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.153+2981C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656433 | |||||||
| chr6:25656466 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.153+3014A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656466 | |||||||
| chr6:25656485 | T | C | 1 | a0001c0001t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.153+3033T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656485 | |||||||
| chr6:25656747 | G | A | 3 | a0001c0001t0002g0062 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02630.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.153+3295G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25656747 | |||||||
| chr6:25657058 | C | T | 3 | a0001c0001t0002g0056 a0001c0001t0002g0057 a0001c0001t0002g0058 |
3 | HG01346.hp2 HG01433.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.153+3606C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657058 | |||||||
| chr6:25657063 | A | G | 7 | a0001c0001t0003g0014 a0001c0001t0003g0021 a0001c0001t0003g0085 others(4): Show |
9 | HG01255.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.153+3611A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657063 | |||||||
| chr6:25657175 | A | T | 29 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(26): Show |
30 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.153+3723A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657175 | |||||||
| chr6:25657235 | A | C | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(276): Show |
320 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.153+3783A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657235 | |||||||
| chr6:25657312 | A | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(276): Show |
320 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.153+3860A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657312 | |||||||
| chr6:25657334 | A | G | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.153+3882A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657334 | |||||||
| chr6:25657362 | A | G | 45 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(42): Show |
51 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.153+3910A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657362 | |||||||
| chr6:25657482 | G | A | 1 | a0001c0001t0002g0154 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153+4030G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657482 | |||||||
| chr6:25657534 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.154-4018G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657534 | |||||||
| chr6:25657617 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
13 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3935G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657617 | |||||||
| chr6:25657657 | A | ATATATAT others(17): Show |
1 | a0001c0001t0002g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.154-3893_154-3870d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25657657 | ||||||
| chr6:25657681 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0005g0246 a0001c0001t0009g0245 |
3 | HG02486.hp2 HG02970.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.154-3871G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657681 | |||||||
| chr6:25657685 | A | G | 7 | a0001c0001t0002g0008 a0001c0001t0002g0154 a0001c0001t0002g0184 others(4): Show |
9 | HG01243.hp2 HG02055.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-3867A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657685 | |||||||
| chr6:25657808 | C | T | 1 | a0001c0001t0004g0271 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.154-3744C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657808 | |||||||
| chr6:25657822 | G | A | 6 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0008g0024 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-3730G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657822 | |||||||
| chr6:25657883 | C | T | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0213 others(1): Show |
4 | HG01358.hp1 HG01496.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3669C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657883 | |||||||
| chr6:25657995 | A | G | 1 | a0001c0001t0005g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.154-3557A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25657995 | |||||||
| chr6:25658002 | CCTTTTTT others(4): Show |
C | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.154-3549_154-3539d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(8): Show |
C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-3549_154-3535d others(17): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(16): Show |
C | 1 | a0001c0001t0006g0306 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.154-3549_154-3527d others(25): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(17): Show |
C | 11 | a0001c0001t0004g0302 a0001c0001t0004g0303 a0001c0001t0005g0240 others(8): Show |
13 | HG00408.hp1 HG01109.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3549_154-3526d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(18): Show |
C | 33 | a0001c0001t0002g0313 a0001c0001t0002g0315 a0001c0001t0003g0314 others(30): Show |
37 | HG00738.hp1 HG01069.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.154-3549_154-3525d others(27): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(19): Show |
C | 11 | a0001c0001t0004g0241 a0001c0001t0004g0266 a0001c0001t0004g0267 others(8): Show |
11 | HG02074.hp1 HG02300.hp2 HG03130.hp1 others(8): Show |
intron_variant | MODIFIER | c.154-3549_154-3524d others(28): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(20): Show |
C | 29 | a0001c0001t0004g0035 a0001c0001t0004g0239 a0001c0001t0004g0248 others(26): Show |
32 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.154-3549_154-3523d others(29): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(21): Show |
C | 5 | a0001c0001t0002g0054 a0001c0001t0002g0055 a0001c0001t0004g0244 others(2): Show |
5 | HG00741.hp2 HG02922.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.154-3549_154-3522d others(30): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(22): Show |
C | 4 | a0001c0001t0001g0050 a0001c0001t0002g0052 a0001c0001t0002g0053 others(1): Show |
4 | HG01074.hp1 HG02080.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.154-3549_154-3521d others(31): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(23): Show |
C | 17 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
18 | HG00323.hp2 HG00733.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.154-3549_154-3520d others(32): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658002 | CCTTTTTT others(28): Show |
C | 1 | a0001c0001t0005g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.154-3549_154-3515d others(37): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658002 | |||||||
| chr6:25658003 | CTTT | C | 13 | a0001c0001t0001g0162 a0001c0001t0001g0178 a0001c0001t0001g0194 others(10): Show |
13 | HG00280.hp1 HG01192.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.154-3497_154-3495d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTT | C | 16 | a0001c0001t0001g0023 a0001c0001t0001g0157 a0001c0001t0001g0180 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.154-3498_154-3495d others(6): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTT | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0166 others(8): Show |
11 | HG01943.hp1 HG01993.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.154-3499_154-3495d others(7): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(1): Show |
C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0125 a0001c0001t0001g0222 others(3): Show |
7 | HG02630.hp1 HG02717.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-3502_154-3495d others(10): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(2): Show |
C | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(5): Show |
9 | HG01081.hp1 HG02155.hp1 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.154-3503_154-3495d others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(3): Show |
C | 7 | a0001c0001t0001g0001 a0001c0001t0001g0118 a0001c0001t0002g0141 others(4): Show |
7 | HG01517.hp2 HG03195.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-3504_154-3495d others(12): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(4): Show |
C | 14 | a0001c0001t0001g0013 a0001c0001t0001g0102 a0001c0001t0001g0108 others(11): Show |
17 | HG00621.hp1 HG01255.hp1 HG01516.hp2 others(14): Show |
intron_variant | MODIFIER | c.154-3505_154-3495d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(5): Show |
C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(45): Show |
52 | HG00438.hp2 HG00544.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.154-3506_154-3495d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(6): Show |
C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(32): Show |
39 | HG00280.hp2 HG00408.hp2 HG01123.hp2 others(36): Show |
intron_variant | MODIFIER | c.154-3507_154-3495d others(15): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(7): Show |
C | 9 | a0001c0001t0001g0033 a0001c0001t0001g0064 a0001c0001t0002g0006 others(6): Show |
12 | HG01515.hp1 HG01517.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.154-3508_154-3495d others(16): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(8): Show |
C | 4 | a0001c0001t0001g0034 a0001c0001t0003g0218 a0003c0003t0003g0010 others(1): Show |
4 | HG01884.hp2 HG03195.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.154-3509_154-3495d others(17): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(9): Show |
C | 1 | a0001c0001t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.154-3510_154-3495d others(18): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(14): Show |
C | 2 | a0001c0001t0002g0176 a0001c0001t0002g0317 |
2 | HG03225.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.154-3515_154-3495d others(23): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(15): Show |
C | 2 | a0001c0001t0002g0177 a0008c0011t0003g0318 |
2 | HG02723.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.154-3516_154-3495d others(24): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0003g0316 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.154-3517_154-3495d others(25): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(17): Show |
C | 3 | a0001c0001t0001g0155 a0001c0001t0001g0156 a0001c0001t0001g0171 |
3 | HG01070.hp1 HG01071.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.154-3518_154-3495d others(26): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(18): Show |
C | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-3519_154-3495d others(27): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(20): Show |
C | 1 | a0006c0007t0002g0203 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.154-3521_154-3495d others(29): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(22): Show |
C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0002g0206 others(3): Show |
6 | HG01167.hp2 HG01496.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.154-3523_154-3495d others(31): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(23): Show |
C | 2 | a0001c0001t0001g0170 a0001c0001t0003g0215 |
2 | HG01069.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.154-3524_154-3495d others(32): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(26): Show |
C | 1 | a0001c0001t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.154-3527_154-3495d others(35): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(29): Show |
C | 7 | a0001c0001t0002g0219 a0001c0001t0003g0190 a0001c0001t0003g0191 others(4): Show |
8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.154-3530_154-3495d others(38): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658003 | CTTTTTTT others(31): Show |
C | 1 | a0001c0001t0002g0008 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.154-3532_154-3495d others(40): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658003 | ||||||
| chr6:25658149 | C | T | 1 | a0001c0001t0005g0298 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.154-3403C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658149 | |||||||
| chr6:25658186 | C | T | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.154-3366C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658186 | |||||||
| chr6:25658197 | G | A | 6 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(3): Show |
6 | HG01106.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.154-3355G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658197 | |||||||
| chr6:25658267 | C | A | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-3285C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658267 | |||||||
| chr6:25658352 | T | C | 45 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.154-3200T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658352 | |||||||
| chr6:25658405 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-3147T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658405 | |||||||
| chr6:25658490 | G | A | 3 | a0001c0001t0002g0313 a0001c0001t0002g0315 a0001c0001t0003g0314 |
3 | HG01106.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.154-3062G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658490 | |||||||
| chr6:25658547 | A | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0006c0007t0002g0203 |
3 | HG00609.hp1 HG02135.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.154-3005A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658547 | |||||||
| chr6:25658679 | T | C | 86 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(83): Show |
95 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.154-2873T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658679 | |||||||
| chr6:25658793 | CA | C | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-2753delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25658793 | ||||||
| chr6:25658812 | A | G | 6 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0008g0024 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.154-2740A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658812 | |||||||
| chr6:25658901 | A | G | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-2651A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658901 | |||||||
| chr6:25658923 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.154-2629T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658923 | |||||||
| chr6:25658944 | G | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.154-2608G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658944 | |||||||
| chr6:25658991 | G | A | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-2561G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25658991 | |||||||
| chr6:25659031 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-2521G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659031 | |||||||
| chr6:25659042 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.154-2510T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659042 | |||||||
| chr6:25659077 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0192 a0001c0001t0001g0194 others(26): Show |
32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.154-2475C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659077 | |||||||
| chr6:25659094 | C | G | 1 | a0001c0001t0005g0297 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.154-2458C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659094 | |||||||
| chr6:25659203 | G | T | 2 | a0001c0001t0002g0210 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.154-2349G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659203 | |||||||
| chr6:25659525 | G | T | 1 | a0001c0001t0003g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.154-2027G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659525 | |||||||
| chr6:25659609 | T | C | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-1943T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659609 | |||||||
| chr6:25659725 | C | A | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.154-1827C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659725 | |||||||
| chr6:25659763 | T | C | 6 | a0001c0001t0002g0090 a0002c0002t0003g0015 a0002c0002t0003g0091 others(3): Show |
7 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.154-1789T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659763 | |||||||
| chr6:25659787 | CCAGGCTA others(1661): Show |
C | 1 | a0001c0001t0004g0244 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.154-1762_154-95del | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr6 | 25659787 | ||||||
| chr6:25659825 | G | C | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.154-1727G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659825 | |||||||
| chr6:25659930 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0048 |
2 | HG00323.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.154-1622C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659930 | |||||||
| chr6:25659969 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.154-1583G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25659969 | |||||||
| chr6:25660079 | A | G | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.154-1473A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660079 | |||||||
| chr6:25660119 | G | A | 3 | a0003c0003t0003g0010 a0003c0003t0003g0311 a0003c0003t0003g0312 |
5 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.154-1433G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660119 | |||||||
| chr6:25660123 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.154-1429G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660123 | |||||||
| chr6:25660263 | C | A | 2 | a0001c0001t0005g0246 a0001c0001t0009g0245 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.154-1289C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660263 | |||||||
| chr6:25660282 | G | A | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.154-1270G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660282 | |||||||
| chr6:25660414 | G | T | 1 | a0004c0005t0004g0275 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.154-1138G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660414 | |||||||
| chr6:25660422 | T | G | 1 | a0001c0001t0001g0033 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.154-1130T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660422 | |||||||
| chr6:25660545 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.154-1007G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660545 | |||||||
| chr6:25660580 | C | T | 38 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(35): Show |
42 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(39): Show |
intron_variant | MODIFIER | c.154-972C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660580 | |||||||
| chr6:25660659 | C | T | 1 | a0001c0001t0004g0255 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.154-893C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660659 | |||||||
| chr6:25660744 | A | G | 91 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(88): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-808A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660744 | |||||||
| chr6:25660836 | G | A | 91 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(88): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-716G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660836 | |||||||
| chr6:25660899 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0003g0212 |
2 | HG01358.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.154-653C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25660899 | |||||||
| chr6:25661140 | A | C | 91 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(88): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.154-412A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661140 | |||||||
| chr6:25661321 | T | C | 27 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(24): Show |
28 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.154-231T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661321 | |||||||
| chr6:25661470 | T | G | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.154-82T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 2/10 | chr6 | 25661470 | |||||||
| chr6:25661659 | A | T | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+15A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661659 | |||||||
| chr6:25661735 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+91A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661735 | |||||||
| chr6:25661756 | T | G | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+112T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661756 | |||||||
| chr6:25661914 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.246+270A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661914 | |||||||
| chr6:25661932 | C | G | 1 | a0001c0001t0004g0296 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.246+288C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661932 | |||||||
| chr6:25661946 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+302A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661946 | |||||||
| chr6:25661948 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+304C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661948 | |||||||
| chr6:25661951 | C | A | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+307C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661951 | |||||||
| chr6:25661952 | T | A | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+308T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661952 | |||||||
| chr6:25661953 | A | G | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+309A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661953 | |||||||
| chr6:25661954 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+310T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661954 | |||||||
| chr6:25661955 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.246+311T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25661955 | |||||||
| chr6:25662034 | T | A | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+390T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662034 | |||||||
| chr6:25662104 | G | C | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+460G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662104 | |||||||
| chr6:25662357 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.246+713A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662357 | |||||||
| chr6:25662458 | G | A | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.246+814G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662458 | |||||||
| chr6:25662525 | G | A | 3 | a0001c0001t0005g0246 a0001c0001t0009g0245 a0004c0005t0011g0247 |
3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.246+881G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662525 | |||||||
| chr6:25662560 | T | C | 6 | a0001c0001t0001g0005 a0001c0001t0001g0222 a0001c0001t0001g0223 others(3): Show |
9 | HG01928.hp1 HG01943.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.246+916T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662560 | |||||||
| chr6:25662562 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.246+918T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662562 | |||||||
| chr6:25662575 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.246+931T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662575 | |||||||
| chr6:25662645 | A | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
13 | HG00140.hp2 HG00280.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.246+1001A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662645 | |||||||
| chr6:25662685 | A | G | 4 | a0001c0001t0002g0206 a0001c0001t0002g0207 a0001c0001t0002g0213 others(1): Show |
4 | HG01358.hp1 HG01496.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1041A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662685 | |||||||
| chr6:25662763 | A | C | 1 | a0001c0001t0003g0049 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.246+1119A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662763 | |||||||
| chr6:25662895 | A | G | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.246+1251A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662895 | |||||||
| chr6:25662997 | C | T | 1 | a0001c0001t0004g0271 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.246+1353C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25662997 | |||||||
| chr6:25663034 | C | A | 3 | a0001c0001t0002g0070 a0001c0001t0002g0071 a0001c0001t0002g0072 |
3 | HG02258.hp1 HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.246+1390C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663034 | |||||||
| chr6:25663072 | G | T | 1 | a0001c0001t0002g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.246+1428G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663072 | |||||||
| chr6:25663094 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.246+1450A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663094 | |||||||
| chr6:25663123 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0002g0317 a0001c0001t0003g0316 others(1): Show |
4 | HG00621.hp2 HG03209.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.246+1479G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663123 | |||||||
| chr6:25663132 | C | T | 27 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(24): Show |
28 | HG00323.hp2 HG00733.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.246+1488C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663132 | |||||||
| chr6:25663280 | A | G | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.246+1636A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663280 | |||||||
| chr6:25663291 | T | C | 1 | a0001c0001t0004g0252 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.246+1647T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663291 | |||||||
| chr6:25663296 | A | G | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.247-1647A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663296 | |||||||
| chr6:25663305 | C | A | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.247-1638C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663305 | |||||||
| chr6:25663343 | C | A | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.247-1600C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663343 | |||||||
| chr6:25663382 | T | G | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.247-1561T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663382 | |||||||
| chr6:25663675 | A | G | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.247-1268A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663675 | |||||||
| chr6:25663920 | T | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.247-1023T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663920 | |||||||
| chr6:25663957 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(44): Show |
53 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.247-986T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25663957 | |||||||
| chr6:25664028 | A | T | 2 | a0001c0001t0002g0210 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.247-915A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664028 | |||||||
| chr6:25664451 | C | T | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.247-492C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664451 | |||||||
| chr6:25664753 | T | A | 278 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(275): Show |
319 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.247-190T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664753 | |||||||
| chr6:25664813 | C | T | 128 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(125): Show |
141 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.247-130C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664813 | |||||||
| chr6:25664863 | C | T | 3 | a0001c0001t0005g0246 a0001c0001t0009g0245 a0004c0005t0011g0247 |
3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.247-80C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 3/10 | chr6 | 25664863 | |||||||
| chr6:25665098 | G | C | 2 | a0001c0001t0001g0096 a0001c0001t0001g0097 |
2 | HG02129.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.336+66G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665098 | |||||||
| chr6:25665298 | C | T | 1 | a0001c0001t0002g0011 | 2 | HG02080.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.336+266C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665298 | |||||||
| chr6:25665334 | A | G | 3 | a0001c0001t0005g0246 a0001c0001t0009g0245 a0004c0005t0011g0247 |
3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.336+302A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665334 | |||||||
| chr6:25665415 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.336+383C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665415 | |||||||
| chr6:25665651 | A | G | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.336+619A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665651 | |||||||
| chr6:25665682 | C | A | 1 | a0001c0001t0005g0238 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.336+650C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665682 | |||||||
| chr6:25665836 | AT | A | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+813delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25665836 | ||||||
| chr6:25665936 | G | A | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+904G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665936 | |||||||
| chr6:25665944 | T | A | 5 | a0001c0001t0003g0190 a0001c0001t0008g0024 a0001c0001t0008g0152 others(2): Show |
6 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+912T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665944 | |||||||
| chr6:25665947 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.336+915T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25665947 | |||||||
| chr6:25666033 | T | A | 2 | a0001c0001t0001g0194 a0001c0001t0002g0193 |
2 | NA18980.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.336+1001T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666033 | |||||||
| chr6:25666177 | TA | T | 91 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0037 others(88): Show |
100 | HG00323.hp2 HG00408.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.336+1166delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25666177 | ||||||
| chr6:25666177 | TAA | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(182): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.336+1165_336+1166d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25666177 | ||||||
| chr6:25666246 | C | T | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.336+1214C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666246 | |||||||
| chr6:25666285 | G | A | 1 | a0009c0010t0003g0038 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.336+1253G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666285 | |||||||
| chr6:25666304 | T | C | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.336+1272T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666304 | |||||||
| chr6:25666456 | T | G | 95 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0002g0231 others(92): Show |
104 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.336+1424T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666456 | |||||||
| chr6:25666586 | C | T | 45 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(42): Show |
51 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.336+1554C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666586 | |||||||
| chr6:25666782 | A | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(96): Show |
121 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.336+1750A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666782 | |||||||
| chr6:25666788 | A | G | 1 | a0001c0001t0004g0248 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.336+1756A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666788 | |||||||
| chr6:25666839 | T | C | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.336+1807T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666839 | |||||||
| chr6:25666916 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.336+1884C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25666916 | |||||||
| chr6:25667000 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02155.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.336+1968C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667000 | |||||||
| chr6:25667278 | A | G | 1 | a0001c0001t0003g0143 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.337-2233A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667278 | |||||||
| chr6:25667470 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-2041A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667470 | |||||||
| chr6:25667557 | C | T | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA19006.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.337-1954C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667557 | |||||||
| chr6:25667639 | G | A | 4 | a0001c0001t0003g0218 a0003c0003t0003g0010 a0003c0003t0003g0311 others(1): Show |
6 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1872G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667639 | |||||||
| chr6:25667709 | C | T | 6 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0008g0024 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1802C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667709 | |||||||
| chr6:25667711 | G | A | 178 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(175): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.337-1800G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667711 | |||||||
| chr6:25667783 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.337-1728T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667783 | |||||||
| chr6:25667802 | C | T | 1 | a0004c0005t0004g0275 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.337-1709C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667802 | |||||||
| chr6:25667803 | A | G | 16 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(13): Show |
19 | HG01175.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.337-1708A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667803 | |||||||
| chr6:25667836 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.337-1675T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667836 | |||||||
| chr6:25667847 | C | A | 90 | a0001c0001t0002g0242 a0001c0001t0002g0313 a0001c0001t0002g0315 others(87): Show |
99 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.337-1664C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667847 | |||||||
| chr6:25667898 | A | G | 3 | a0001c0001t0004g0248 a0001c0001t0006g0249 a0001c0001t0006g0250 |
3 | HG02145.hp1 HG03130.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.337-1613A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667898 | |||||||
| chr6:25667904 | T | A | 1 | a0001c0001t0002g0315 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.337-1607T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667904 | |||||||
| chr6:25667909 | A | T | 3 | a0001c0001t0002g0313 a0001c0001t0002g0315 a0001c0001t0003g0314 |
3 | HG01106.hp2 HG02723.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.337-1602A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667909 | |||||||
| chr6:25667931 | G | A | 6 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0008g0024 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1580G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667931 | |||||||
| chr6:25667990 | C | G | 6 | a0001c0001t0003g0190 a0001c0001t0003g0191 a0001c0001t0008g0024 others(3): Show |
7 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.337-1521C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25667990 | |||||||
| chr6:25668183 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.337-1328C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668183 | |||||||
| chr6:25668217 | GA | G | 174 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(171): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.337-1280delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25668217 | ||||||
| chr6:25668378 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.337-1133C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668378 | |||||||
| chr6:25668396 | C | T | 2 | a0001c0001t0005g0246 a0001c0001t0009g0245 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.337-1115C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668396 | |||||||
| chr6:25668452 | A | T | 1 | a0001c0001t0002g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.337-1059A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668452 | |||||||
| chr6:25668472 | T | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0192 a0001c0001t0001g0194 others(26): Show |
32 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.337-1039T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668472 | |||||||
| chr6:25668693 | G | A | 7 | a0001c0001t0002g0090 a0001c0001t0013g0101 a0002c0002t0003g0015 others(4): Show |
8 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.337-818G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668693 | |||||||
| chr6:25668700 | A | AGATATAC others(12): Show |
3 | a0001c0001t0005g0246 a0001c0001t0009g0245 a0004c0005t0011g0247 |
3 | HG02486.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.337-809_337-808ins others(19): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25668700 | ||||||
| chr6:25668763 | A | G | 3 | a0001c0001t0002g0062 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | HG02630.hp1 HG02717.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.337-748A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668763 | |||||||
| chr6:25668929 | G | A | 98 | a0001c0001t0002g0090 a0001c0001t0002g0231 a0001c0001t0002g0242 others(95): Show |
108 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.337-582G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668929 | |||||||
| chr6:25668955 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(40): Show |
49 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.337-556C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668955 | |||||||
| chr6:25668966 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.337-545C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25668966 | |||||||
| chr6:25669050 | G | T | 46 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(43): Show |
52 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.337-461G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669050 | |||||||
| chr6:25669077 | G | C | 92 | a0001c0001t0002g0231 a0001c0001t0002g0242 a0001c0001t0002g0313 others(89): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.337-434G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669077 | |||||||
| chr6:25669110 | C | CA | 144 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(141): Show |
172 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.337-385dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | ||||||
| chr6:25669110 | C | CAA | 105 | a0001c0001t0001g0102 a0001c0001t0001g0192 a0001c0001t0001g0194 others(102): Show |
114 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.337-386_337-385dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | ||||||
| chr6:25669110 | C | CAAA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0197 a0001c0001t0001g0222 others(21): Show |
28 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.337-387_337-385dup others(3): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr6 | 25669110 | ||||||
| chr6:25669268 | A | G | 101 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0090 others(98): Show |
112 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.337-243A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669268 | |||||||
| chr6:25669297 | G | A | 37 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(34): Show |
43 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.337-214G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669297 | |||||||
| chr6:25669408 | A | T | 101 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0090 others(98): Show |
112 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.337-103A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669408 | |||||||
| chr6:25669441 | G | A | 38 | a0001c0001t0001g0005 a0001c0001t0001g0064 a0001c0001t0001g0067 others(35): Show |
44 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.337-70G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 4/10 | chr6 | 25669441 | |||||||
| chr6:25669605 | T | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0090 others(53): Show |
61 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.393+38T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/10 | chr6 | 25669605 | |||||||
| chr6:25669797 | T | A | 1 | a0001c0001t0001g0192 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.394-202T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 5/10 | chr6 | 25669797 | |||||||
| chr6:25670123 | C | A | 16 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(13): Show |
19 | HG01175.hp2 HG01358.hp1 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.471+47C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670123 | |||||||
| chr6:25670257 | A | C | 1 | a0001c0001t0002g0040 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.471+181A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670257 | |||||||
| chr6:25670303 | G | A | 1 | a0001c0001t0006g0310 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.471+227G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670303 | |||||||
| chr6:25670564 | T | C | 91 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0231 others(88): Show |
101 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.471+488T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670564 | |||||||
| chr6:25670597 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(88): Show |
108 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.471+521C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670597 | |||||||
| chr6:25670718 | A | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0004g0035 others(33): Show |
40 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
intron_variant | MODIFIER | c.471+642A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670718 | |||||||
| chr6:25670805 | C | G | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+729C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670805 | |||||||
| chr6:25670995 | C | G | 2 | a0001c0001t0002g0206 a0001c0001t0002g0207 |
2 | HG01496.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.471+919C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25670995 | |||||||
| chr6:25671037 | AAG | A | 45 | a0001c0001t0004g0027 a0001c0001t0004g0028 a0001c0001t0004g0029 others(42): Show |
51 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.471+964_471+965del others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25671037 | ||||||
| chr6:25671171 | T | A | 1 | a0001c0001t0003g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+1095T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671171 | |||||||
| chr6:25671252 | A | G | 1 | a0001c0001t0003g0151 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.471+1176A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671252 | |||||||
| chr6:25671398 | CT | C | 90 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0231 others(87): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.471+1323delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671398 | |||||||
| chr6:25671571 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+1495G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671571 | |||||||
| chr6:25671618 | A | T | 87 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0003g0214 others(84): Show |
97 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.471+1542A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671618 | |||||||
| chr6:25671645 | C | T | 90 | a0001c0001t0001g0013 a0001c0001t0001g0082 a0001c0001t0002g0231 others(87): Show |
100 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.471+1569C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671645 | |||||||
| chr6:25671661 | C | A | 2 | a0001c0001t0003g0215 a0001c0001t0003g0216 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.471+1585C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671661 | |||||||
| chr6:25671715 | C | T | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471+1639C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671715 | |||||||
| chr6:25671716 | C | T | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.471+1640C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25671716 | |||||||
| chr6:25672048 | C | A | 2 | a0001c0001t0002g0210 a0001c0001t0010g0211 |
2 | HG02109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.471+1972C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672048 | |||||||
| chr6:25672051 | C | A | 1 | a0001c0001t0003g0316 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.471+1975C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672051 | |||||||
| chr6:25672086 | C | T | 7 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(4): Show |
10 | HG01175.hp2 HG01515.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+2010C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672086 | |||||||
| chr6:25672151 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0066 |
3 | HG01515.hp1 HG01517.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.471+2075C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672151 | |||||||
| chr6:25672333 | A | G | 1 | a0001c0001t0004g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.471+2257A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672333 | |||||||
| chr6:25672583 | G | A | 7 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+2507G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672583 | |||||||
| chr6:25672669 | A | G | 50 | a0001c0001t0001g0139 a0001c0001t0002g0231 a0001c0001t0002g0242 others(47): Show |
54 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.471+2593A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672669 | |||||||
| chr6:25672813 | A | G | 1 | a0001c0001t0005g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.471+2737A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25672813 | |||||||
| chr6:25673039 | A | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(278): Show |
322 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.471+2963A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673039 | |||||||
| chr6:25673045 | A | G | 21 | a0001c0001t0001g0005 a0001c0001t0001g0194 a0001c0001t0001g0204 others(18): Show |
24 | HG00140.hp2 HG00280.hp1 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.471+2969A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673045 | |||||||
| chr6:25673052 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+2976T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673052 | |||||||
| chr6:25673078 | G | A | 1 | a0001c0001t0002g0063 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.471+3002G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673078 | |||||||
| chr6:25673136 | T | C | 1 | a0001c0001t0002g0006 | 3 | HG03239.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.471+3060T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673136 | |||||||
| chr6:25673335 | A | G | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.471+3259A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673335 | |||||||
| chr6:25673398 | C | T | 1 | a0001c0001t0002g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.471+3322C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673398 | |||||||
| chr6:25673532 | C | G | 1 | a0001c0001t0009g0245 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.471+3456C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673532 | |||||||
| chr6:25673533 | G | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(17): Show |
24 | HG00642.hp2 HG01081.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.471+3457G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673533 | |||||||
| chr6:25673579 | T | C | 1 | a0001c0001t0004g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.471+3503T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673579 | |||||||
| chr6:25673736 | G | A | 1 | a0001c0001t0009g0233 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.471+3660G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673736 | |||||||
| chr6:25673860 | G | T | 1 | a0001c0001t0003g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.471+3784G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25673860 | |||||||
| chr6:25674017 | A | C | 1 | a0001c0001t0003g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.471+3941A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674017 | |||||||
| chr6:25674281 | A | G | 104 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(101): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.471+4205A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674281 | |||||||
| chr6:25674315 | C | A | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.471+4239C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674315 | |||||||
| chr6:25674485 | C | A | 1 | a0001c0001t0003g0220 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.471+4409C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674485 | |||||||
| chr6:25674497 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(77): Show |
93 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.471+4421T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674497 | |||||||
| chr6:25674507 | G | A | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(99): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.471+4431G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674507 | |||||||
| chr6:25674668 | C | T | 47 | a0001c0001t0001g0179 a0001c0001t0002g0219 a0001c0001t0004g0027 others(44): Show |
53 | HG00408.hp1 HG00738.hp1 HG01069.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+4592C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674668 | |||||||
| chr6:25674691 | A | G | 144 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0033 others(141): Show |
160 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.471+4615A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674691 | |||||||
| chr6:25674780 | T | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0217 others(9): Show |
13 | HG00280.hp2 HG00673.hp1 NA18943.hp2 others(10): Show |
intron_variant | MODIFIER | c.471+4704T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674780 | |||||||
| chr6:25674806 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.471+4730T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25674806 | |||||||
| chr6:25675013 | G | A | 1 | a0001c0001t0003g0079 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+4937G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675013 | |||||||
| chr6:25675049 | G | T | 1 | a0001c0001t0001g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.471+4973G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675049 | |||||||
| chr6:25675140 | C | T | 142 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0033 others(139): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.471+5064C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675140 | |||||||
| chr6:25675144 | C | T | 2 | a0001c0001t0005g0292 a0001c0001t0005g0293 |
2 | NA18943.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.471+5068C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675144 | |||||||
| chr6:25675234 | C | T | 2 | a0001c0001t0004g0261 a0001c0001t0006g0268 |
2 | HG03831.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.471+5158C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675234 | |||||||
| chr6:25675426 | G | A | 2 | a0001c0001t0003g0086 a0001c0001t0016g0087 |
2 | HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.471+5350G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675426 | |||||||
| chr6:25675452 | C | T | 3 | a0001c0001t0002g0231 a0001c0001t0003g0232 a0001c0001t0014g0195 |
3 | HG02559.hp2 HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.471+5376C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675452 | |||||||
| chr6:25675472 | A | C | 1 | a0001c0001t0001g0138 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.471+5396A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675472 | |||||||
| chr6:25675536 | T | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.471+5460T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675536 | |||||||
| chr6:25675607 | G | A | 1 | a0001c0001t0002g0012 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.471+5531G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675607 | |||||||
| chr6:25675626 | C | T | 102 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(99): Show |
122 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.471+5550C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675626 | |||||||
| chr6:25675775 | C | G | 1 | a0008c0011t0003g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.471+5699C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675775 | |||||||
| chr6:25675886 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.471+5810T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25675886 | |||||||
| chr6:25676045 | C | G | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.472-5906C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676045 | |||||||
| chr6:25676169 | G | A | 245 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(242): Show |
281 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.472-5782G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676169 | |||||||
| chr6:25676301 | C | T | 1 | a0001c0001t0004g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.472-5650C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676301 | |||||||
| chr6:25676307 | C | T | 1 | a0001c0001t0014g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-5644C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676307 | |||||||
| chr6:25676512 | T | C | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.472-5439T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676512 | |||||||
| chr6:25676542 | A | C | 7 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-5409A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676542 | |||||||
| chr6:25676587 | G | A | 142 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0033 others(139): Show |
158 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.472-5364G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676587 | |||||||
| chr6:25676669 | T | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.472-5282T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676669 | |||||||
| chr6:25676741 | A | C | 29 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(26): Show |
34 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-5210A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676741 | |||||||
| chr6:25676768 | TTTCCATC others(5): Show |
T | 104 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(101): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.472-5168_472-5157d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25676768 | ||||||
| chr6:25676819 | G | A | 1 | a0001c0001t0005g0272 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.472-5132G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676819 | |||||||
| chr6:25676980 | C | G | 1 | a0001c0001t0008g0061 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.472-4971C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25676980 | |||||||
| chr6:25677087 | G | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.472-4864G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677087 | |||||||
| chr6:25677108 | C | G | 32 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(29): Show |
37 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.472-4843C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677108 | |||||||
| chr6:25677320 | T | C | 1 | a0001c0001t0014g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-4631T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677320 | |||||||
| chr6:25677339 | G | T | 1 | a0001c0001t0008g0024 | 2 | HG00642.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.472-4612G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677339 | |||||||
| chr6:25677378 | G | A | 1 | a0001c0001t0014g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-4573G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677378 | |||||||
| chr6:25677559 | A | T | 1 | a0001c0001t0003g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472-4392A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677559 | |||||||
| chr6:25677660 | A | G | 1 | a0001c0001t0004g0260 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.472-4291A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677660 | |||||||
| chr6:25677705 | A | G | 103 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(100): Show |
123 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-4246A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677705 | |||||||
| chr6:25677726 | A | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0033 others(140): Show |
159 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.472-4225A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677726 | |||||||
| chr6:25677826 | A | G | 1 | a0001c0001t0004g0291 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.472-4125A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677826 | |||||||
| chr6:25677945 | A | C | 1 | a0001c0001t0002g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-4006A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25677945 | |||||||
| chr6:25678011 | T | C | 7 | a0001c0001t0001g0194 a0001c0001t0001g0204 a0001c0001t0001g0205 others(4): Show |
7 | HG00609.hp1 HG02135.hp1 NA18940.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-3940T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678011 | |||||||
| chr6:25678450 | C | T | 101 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(98): Show |
121 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.472-3501C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678450 | |||||||
| chr6:25678657 | C | T | 1 | a0001c0001t0010g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.472-3294C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678657 | |||||||
| chr6:25678680 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18973.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.472-3271G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678680 | |||||||
| chr6:25678683 | A | T | 15 | a0001c0001t0002g0003 a0001c0001t0002g0070 a0001c0001t0002g0071 others(12): Show |
18 | HG01243.hp1 HG01891.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.472-3268A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678683 | |||||||
| chr6:25678799 | C | T | 1 | a0001c0001t0003g0191 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.472-3152C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678799 | |||||||
| chr6:25678804 | G | T | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.472-3147G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678804 | |||||||
| chr6:25678815 | C | T | 1 | a0001c0001t0005g0269 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.472-3136C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678815 | |||||||
| chr6:25678816 | A | G | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.472-3135A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678816 | |||||||
| chr6:25678868 | C | T | 2 | a0001c0001t0005g0246 a0001c0001t0009g0245 |
2 | HG02486.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.472-3083C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678868 | |||||||
| chr6:25678951 | A | C | 1 | a0001c0001t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.472-3000A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25678951 | |||||||
| chr6:25679142 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.472-2809G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679142 | |||||||
| chr6:25679171 | G | A | 1 | a0001c0001t0014g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.472-2780G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679171 | |||||||
| chr6:25679430 | A | G | 29 | a0001c0001t0001g0064 a0001c0001t0001g0067 a0001c0001t0002g0006 others(26): Show |
34 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-2521A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679430 | |||||||
| chr6:25679483 | GGT | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(102): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.472-2456_472-2455d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25679483 | ||||||
| chr6:25679560 | TC | T | 3 | a0001c0001t0002g0158 a0001c0001t0002g0181 a0001c0001t0003g0159 |
3 | HG00099.hp2 HG03704.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.472-2390delC | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679560 | |||||||
| chr6:25679732 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(108): Show |
132 | HG00280.hp2 HG00408.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.472-2219A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679732 | |||||||
| chr6:25679899 | AAAT | A | 99 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(96): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.472-2051_472-2049d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679899 | |||||||
| chr6:25679927 | T | C | 1 | a0001c0001t0002g0193 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.472-2024T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679927 | |||||||
| chr6:25679955 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.472-1996G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679955 | |||||||
| chr6:25679974 | A | G | 2 | a0001c0001t0002g0176 a0001c0001t0002g0177 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.472-1977A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25679974 | |||||||
| chr6:25680045 | CAA | C | 105 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(102): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.472-1904_472-1903d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25680045 | ||||||
| chr6:25680103 | A | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(291): Show |
340 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.472-1848A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680103 | |||||||
| chr6:25680182 | A | C | 4 | a0001c0001t0003g0218 a0003c0003t0003g0010 a0003c0003t0003g0311 others(1): Show |
6 | HG01884.hp2 HG01891.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-1769A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680182 | |||||||
| chr6:25680221 | CATAATGT others(4): Show |
C | 1 | a0001c0001t0006g0259 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.472-1727_472-1717d others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr6 | 25680221 | ||||||
| chr6:25680295 | T | C | 1 | a0001c0001t0002g0317 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.472-1656T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680295 | |||||||
| chr6:25680301 | T | C | 1 | a0008c0011t0003g0318 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.472-1650T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680301 | |||||||
| chr6:25680538 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18978.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.472-1413T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680538 | |||||||
| chr6:25680556 | C | A | 1 | a0001c0001t0003g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.472-1395C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680556 | |||||||
| chr6:25680573 | C | T | 1 | a0004c0005t0011g0247 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.472-1378C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680573 | |||||||
| chr6:25680913 | C | T | 104 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(101): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.472-1038C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680913 | |||||||
| chr6:25680939 | A | G | 1 | a0001c0001t0003g0065 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.472-1012A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25680939 | |||||||
| chr6:25681027 | G | A | 3 | a0001c0001t0005g0026 a0001c0001t0005g0278 a0001c0001t0005g0298 |
4 | HG00738.hp1 HG01168.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-924G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681027 | |||||||
| chr6:25681255 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.472-696T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681255 | |||||||
| chr6:25681263 | C | A | 1 | a0001c0001t0002g0141 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.472-688C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681263 | |||||||
| chr6:25681462 | G | A | 1 | a0001c0001t0005g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.472-489G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681462 | |||||||
| chr6:25681525 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(101): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.472-426G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681525 | |||||||
| chr6:25681816 | T | G | 1 | a0001c0001t0004g0255 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.472-135T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681816 | |||||||
| chr6:25681835 | C | T | 1 | a0001c0001t0004g0029 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.472-116C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 6/10 | chr6 | 25681835 | |||||||
| chr6:25682034 | A | C | 101 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(98): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.527+28A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682034 | |||||||
| chr6:25682213 | G | A | 5 | a0001c0001t0003g0214 a0001c0001t0004g0248 a0001c0001t0006g0249 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+207G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682213 | |||||||
| chr6:25682350 | G | A | 3 | a0001c0001t0002g0317 a0001c0001t0003g0316 a0008c0011t0003g0318 |
3 | HG03209.hp1 HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.527+344G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682350 | |||||||
| chr6:25682386 | C | CA | 280 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(277): Show |
321 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.527+380_527+381ins others(1): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682386 | |||||||
| chr6:25682397 | G | GCACTTCA others(4): Show |
5 | a0001c0001t0003g0214 a0001c0001t0004g0248 a0001c0001t0006g0249 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+395_527+396ins others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25682397 | ||||||
| chr6:25682415 | G | C | 1 | a0003c0003t0003g0311 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.527+409G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682415 | |||||||
| chr6:25682482 | G | A | 1 | a0004c0005t0004g0275 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.527+476G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682482 | |||||||
| chr6:25682506 | A | C | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+500A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682506 | |||||||
| chr6:25682507 | A | T | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+501A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682507 | |||||||
| chr6:25682537 | C | T | 2 | a0001c0001t0002g0231 a0001c0001t0003g0232 |
2 | HG02559.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+531C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682537 | |||||||
| chr6:25682701 | C | G | 107 | a0001c0001t0001g0005 a0001c0001t0001g0033 a0001c0001t0001g0034 others(104): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.527+695C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25682701 | |||||||
| chr6:25683052 | A | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(273): Show |
317 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.527+1046A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683052 | |||||||
| chr6:25683097 | C | A | 1 | a0001c0001t0001g0037 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.527+1091C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683097 | |||||||
| chr6:25683142 | G | T | 4 | a0001c0001t0002g0210 a0001c0001t0005g0246 a0001c0001t0009g0245 others(1): Show |
4 | HG02109.hp2 HG02486.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+1136G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683142 | |||||||
| chr6:25683164 | A | C | 1 | a0001c0001t0004g0241 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.527+1158A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683164 | |||||||
| chr6:25683185 | C | T | 1 | a0001c0001t0001g0023 | 2 | NA18970.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.527+1179C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683185 | |||||||
| chr6:25683186 | G | A | 5 | a0001c0001t0003g0214 a0001c0001t0004g0248 a0001c0001t0006g0249 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+1180G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683186 | |||||||
| chr6:25683200 | C | T | 5 | a0001c0001t0003g0214 a0001c0001t0004g0248 a0001c0001t0006g0249 others(2): Show |
5 | HG02145.hp1 HG02922.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+1194C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683200 | |||||||
| chr6:25683300 | G | A | 1 | a0001c0001t0003g0172 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.527+1294G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683300 | |||||||
| chr6:25683338 | G | A | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.527+1332G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683338 | |||||||
| chr6:25683412 | C | A | 3 | a0001c0001t0003g0089 a0001c0001t0003g0099 a0001c0001t0003g0106 |
3 | HG01934.hp2 HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.527+1406C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683412 | |||||||
| chr6:25683446 | G | C | 2 | a0001c0001t0004g0271 a0001c0001t0005g0025 |
3 | HG00609.hp2 HG00673.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.527+1440G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683446 | |||||||
| chr6:25683539 | T | C | 2 | a0001c0001t0001g0200 a0001c0001t0002g0199 |
2 | NA18975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.527+1533T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683539 | |||||||
| chr6:25683630 | G | GT | 38 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0064 others(35): Show |
41 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(38): Show |
intron_variant | MODIFIER | c.527+1625dupT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25683630 | ||||||
| chr6:25683716 | G | C | 1 | a0001c0001t0003g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.527+1710G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683716 | |||||||
| chr6:25683726 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(77): Show |
96 | HG00621.hp1 HG01074.hp2 HG01081.hp1 others(93): Show |
intron_variant | MODIFIER | c.527+1720C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683726 | |||||||
| chr6:25683727 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.527+1721G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683727 | |||||||
| chr6:25683922 | G | T | 15 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0002g0060 others(12): Show |
16 | HG01106.hp2 HG01358.hp1 HG01993.hp1 others(13): Show |
intron_variant | MODIFIER | c.527+1916G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25683922 | |||||||
| chr6:25684051 | A | G | 179 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0033 others(176): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.527+2045A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684051 | |||||||
| chr6:25684054 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18978.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.527+2048C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684054 | |||||||
| chr6:25684081 | C | T | 1 | a0001c0001t0002g0069 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.527+2075C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684081 | |||||||
| chr6:25684140 | C | A | 1 | a0001c0001t0001g0225 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.527+2134C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684140 | |||||||
| chr6:25684177 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0018 others(167): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.527+2171T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684177 | |||||||
| chr6:25684328 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.527+2322A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684328 | |||||||
| chr6:25684356 | C | T | 1 | a0001c0001t0004g0267 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.527+2350C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684356 | |||||||
| chr6:25684378 | C | T | 5 | a0001c0001t0003g0004 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.527+2372C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684378 | |||||||
| chr6:25684425 | G | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(151): Show |
174 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.527+2419G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684425 | |||||||
| chr6:25684507 | G | A | 12 | a0001c0001t0002g0003 a0001c0001t0002g0062 a0001c0001t0002g0068 others(9): Show |
15 | HG02630.hp1 HG02717.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.527+2501G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684507 | |||||||
| chr6:25684527 | G | T | 6 | a0001c0001t0001g0205 a0001c0001t0002g0193 a0001c0001t0002g0196 others(3): Show |
6 | HG02135.hp1 NA18940.hp2 NA19003.hp1 others(3): Show |
intron_variant | MODIFIER | c.527+2521G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684527 | |||||||
| chr6:25684542 | C | T | 3 | a0001c0001t0002g0040 a0001c0001t0005g0026 a0001c0001t0005g0262 |
4 | HG01168.hp2 HG01169.hp1 HG04184.hp1 others(1): Show |
intron_variant | MODIFIER | c.527+2536C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684542 | |||||||
| chr6:25684574 | C | A | 7 | a0001c0001t0001g0050 a0001c0001t0001g0155 a0001c0001t0001g0156 others(4): Show |
7 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.527+2568C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684574 | |||||||
| chr6:25684708 | G | A | 15 | a0001c0001t0002g0003 a0001c0001t0002g0060 a0001c0001t0002g0074 others(12): Show |
18 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.527+2702G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684708 | |||||||
| chr6:25684725 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(155): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.527+2719G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684725 | |||||||
| chr6:25684844 | A | G | 1 | a0001c0001t0002g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.527+2838A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684844 | |||||||
| chr6:25684922 | CAATAGAC others(5): Show |
C | 3 | a0001c0001t0008g0061 a0001c0001t0009g0233 a0001c0001t0009g0245 |
3 | HG02895.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.527+2923_527+2934d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25684922 | ||||||
| chr6:25684925 | T | C | 2 | a0001c0001t0003g0036 a0001c0001t0003g0232 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.527+2919T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25684925 | |||||||
| chr6:25685019 | A | G | 76 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(73): Show |
87 | HG00408.hp2 HG00438.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.527+3013A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685019 | |||||||
| chr6:25685083 | T | C | 5 | a0001c0001t0003g0079 a0001c0001t0003g0081 a0001c0001t0003g0214 others(2): Show |
5 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+3077T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685083 | |||||||
| chr6:25685132 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527+3126G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685132 | |||||||
| chr6:25685134 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.527+3128G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685134 | |||||||
| chr6:25685172 | A | G | 7 | a0001c0001t0008g0024 a0001c0001t0008g0061 a0001c0001t0008g0152 others(4): Show |
8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.527+3166A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685172 | |||||||
| chr6:25685236 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.527+3230G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685236 | |||||||
| chr6:25685261 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(4): Show |
10 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.527+3255G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685261 | |||||||
| chr6:25685264 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(157): Show |
179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.527+3258G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685264 | |||||||
| chr6:25685488 | A | G | 11 | a0001c0001t0002g0008 a0001c0001t0002g0052 a0001c0001t0002g0053 others(8): Show |
13 | HG02055.hp2 HG02080.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.527+3482A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685488 | |||||||
| chr6:25685529 | G | A | 16 | a0001c0001t0002g0008 a0001c0001t0002g0052 a0001c0001t0002g0053 others(13): Show |
18 | HG02055.hp2 HG02080.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.527+3523G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685529 | |||||||
| chr6:25685635 | C | G | 1 | a0001c0001t0016g0087 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.528-3537C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685635 | |||||||
| chr6:25685650 | G | GTATAAT | 5 | a0001c0001t0003g0004 a0001c0001t0003g0173 a0001c0001t0003g0174 others(2): Show |
8 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.528-3505_528-3500d others(8): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25685650 | ||||||
| chr6:25685650 | GTATAATT others(5): Show |
G | 1 | a0001c0001t0002g0207 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.528-3511_528-3500d others(14): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25685650 | ||||||
| chr6:25685661 | A | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(135): Show |
154 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(151): Show |
intron_variant | MODIFIER | c.528-3511A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685661 | |||||||
| chr6:25685805 | G | T | 79 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.528-3367G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25685805 | |||||||
| chr6:25686153 | T | G | 1 | a0001c0001t0004g0287 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.528-3019T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686153 | |||||||
| chr6:25686177 | C | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(141): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.528-2995C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686177 | |||||||
| chr6:25686586 | T | G | 1 | a0001c0001t0005g0276 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.528-2586T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686586 | |||||||
| chr6:25686602 | TTATCAGA others(9): Show |
T | 1 | a0001c0001t0005g0258 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.528-2569_528-2554d others(18): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686602 | |||||||
| chr6:25686614 | T | C | 1 | a0001c0001t0004g0252 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.528-2558T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686614 | |||||||
| chr6:25686752 | A | G | 3 | a0001c0001t0001g0224 a0001c0001t0004g0263 a0001c0001t0004g0265 |
3 | NA18964.hp1 NA18986.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.528-2420A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686752 | |||||||
| chr6:25686865 | T | C | 3 | a0001c0001t0008g0061 a0001c0001t0009g0233 a0001c0001t0009g0245 |
3 | HG02895.hp2 HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.528-2307T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686865 | |||||||
| chr6:25686959 | C | T | 2 | a0001c0001t0001g0208 a0001c0001t0001g0209 |
2 | HG01261.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.528-2213C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25686959 | |||||||
| chr6:25687351 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(136): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.528-1821T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687351 | |||||||
| chr6:25687397 | C | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0032 a0001c0001t0003g0220 |
7 | HG02486.hp1 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.528-1775C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687397 | |||||||
| chr6:25687525 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.528-1647A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687525 | |||||||
| chr6:25687579 | T | C | 1 | a0001c0004t0001g0121 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.528-1593T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687579 | |||||||
| chr6:25687667 | T | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(136): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.528-1505T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687667 | |||||||
| chr6:25687759 | T | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0074 a0001c0001t0002g0075 others(2): Show |
8 | NA18945.hp2 NA18955.hp2 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.528-1413T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687759 | |||||||
| chr6:25687818 | T | C | 5 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(2): Show |
5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-1354T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25687818 | |||||||
| chr6:25687850 | AT | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(18): Show |
25 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(22): Show |
intron_variant | MODIFIER | c.528-1314delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25687850 | ||||||
| chr6:25688456 | A | C | 1 | a0002c0002t0003g0094 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.528-716A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688456 | |||||||
| chr6:25688577 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.528-595G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688577 | |||||||
| chr6:25688687 | A | C | 1 | a0001c0001t0003g0173 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.528-485A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688687 | |||||||
| chr6:25688801 | C | CAA | 8 | a0001c0001t0004g0303 a0001c0001t0008g0024 a0001c0001t0008g0061 others(5): Show |
9 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.528-358_528-357dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | ||||||
| chr6:25688801 | C | CAAAAAAA others(3): Show |
10 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0054 others(7): Show |
11 | HG00741.hp2 HG01515.hp1 HG01517.hp1 others(8): Show |
intron_variant | MODIFIER | c.528-366_528-357dup others(10): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | ||||||
| chr6:25688801 | C | CAAAAAAA others(4): Show |
14 | a0001c0001t0001g0048 a0001c0001t0001g0096 a0001c0001t0001g0170 others(11): Show |
16 | HG00323.hp2 HG01069.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.528-367_528-357dup others(11): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | ||||||
| chr6:25688801 | C | CAAAAAAA others(5): Show |
104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(101): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.528-368_528-357dup others(12): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | ||||||
| chr6:25688801 | C | CAAAAAAA others(6): Show |
18 | a0001c0001t0001g0018 a0001c0001t0001g0043 a0001c0001t0001g0113 others(15): Show |
19 | HG00438.hp1 HG00544.hp2 HG01109.hp2 others(16): Show |
intron_variant | MODIFIER | c.528-369_528-357dup others(13): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25688801 | ||||||
| chr6:25688942 | T | G | 1 | a0006c0007t0002g0203 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.528-230T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688942 | |||||||
| chr6:25688996 | C | T | 5 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(2): Show |
5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.528-176C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25688996 | |||||||
| chr6:25689145 | C | T | 6 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0080 others(3): Show |
6 | HG01496.hp1 HG02258.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.528-27C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | chr6 | 25689145 | |||||||
| chr6:25689150 | AT | A | 259 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.528-9delT | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr6 | 25689150 | ||||||
| chr6:25689228 | A | T | 10 | a0001c0001t0002g0060 a0001c0001t0002g0090 a0001c0001t0002g0210 others(7): Show |
10 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.573+11A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689228 | |||||||
| chr6:25689259 | G | C | 160 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(157): Show |
179 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.573+42G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689259 | |||||||
| chr6:25689361 | G | T | 5 | a0001c0001t0002g0098 a0001c0001t0002g0141 a0001c0001t0002g0142 others(2): Show |
5 | NA18956.hp1 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-112G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 8/10 | chr6 | 25689361 | |||||||
| chr6:25689563 | A | G | 1 | a0001c0001t0003g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.633+31A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689563 | |||||||
| chr6:25689630 | A | G | 2 | a0001c0001t0003g0036 a0001c0001t0003g0232 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.633+98A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689630 | |||||||
| chr6:25689933 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.633+401A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25689933 | |||||||
| chr6:25690062 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(76): Show |
96 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.633+530G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690062 | |||||||
| chr6:25690118 | T | C | 1 | a0001c0001t0001g0124 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.633+586T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690118 | |||||||
| chr6:25690172 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.633+640C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690172 | |||||||
| chr6:25690175 | G | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0170 |
3 | HG01069.hp1 HG01515.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.633+643G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690175 | |||||||
| chr6:25690223 | A | G | 7 | a0001c0001t0008g0024 a0001c0001t0008g0061 a0001c0001t0008g0152 others(4): Show |
8 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.633+691A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690223 | |||||||
| chr6:25690708 | C | A | 47 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0014 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.634-348C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690708 | |||||||
| chr6:25690912 | T | C | 1 | a0001c0001t0004g0256 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.634-144T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690912 | |||||||
| chr6:25690949 | A | G | 5 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(2): Show |
5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.634-107A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 9/10 | chr6 | 25690949 | |||||||
| chr6:25691134 | C | T | 16 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0054 others(13): Show |
17 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.702+10C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691134 | |||||||
| chr6:25691596 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.702+472G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691596 | |||||||
| chr6:25691637 | T | G | 1 | a0001c0001t0001g0125 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.702+513T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691637 | |||||||
| chr6:25691669 | C | T | 2 | a0001c0001t0003g0036 a0001c0001t0003g0232 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+545C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691669 | |||||||
| chr6:25691670 | G | A | 47 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0014 others(44): Show |
60 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.702+546G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691670 | |||||||
| chr6:25691688 | A | T | 2 | a0001c0001t0003g0036 a0001c0001t0003g0232 |
2 | HG01255.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.702+564A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691688 | |||||||
| chr6:25691728 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.702+604A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691728 | |||||||
| chr6:25691793 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(17): Show |
24 | HG00438.hp2 HG01496.hp2 HG01928.hp1 others(21): Show |
intron_variant | MODIFIER | c.702+669T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691793 | |||||||
| chr6:25691923 | C | A | 16 | a0001c0001t0002g0003 a0001c0001t0002g0060 a0001c0001t0002g0074 others(13): Show |
19 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.702+799C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25691923 | |||||||
| chr6:25692012 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.702+888T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692012 | |||||||
| chr6:25692685 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.702+1561G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692685 | |||||||
| chr6:25692909 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.702+1785G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692909 | |||||||
| chr6:25692966 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0197 |
4 | NA18965.hp1 NA18987.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1842G>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25692966 | |||||||
| chr6:25693046 | C | T | 38 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0017 others(35): Show |
45 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.702+1922C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693046 | |||||||
| chr6:25693173 | C | T | 5 | a0002c0002t0003g0015 a0002c0002t0003g0091 a0002c0002t0003g0092 others(2): Show |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+2049C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693173 | |||||||
| chr6:25693177 | C | T | 2 | a0001c0001t0002g0158 a0001c0001t0005g0288 |
2 | HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.702+2053C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693177 | |||||||
| chr6:25693180 | G | T | 1 | a0001c0001t0005g0305 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.702+2056G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693180 | |||||||
| chr6:25693204 | C | T | 5 | a0001c0001t0002g0098 a0001c0001t0002g0141 a0001c0001t0002g0142 others(2): Show |
5 | NA18956.hp1 NA18983.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+2080C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693204 | |||||||
| chr6:25693265 | C | T | 6 | a0001c0001t0002g0003 a0001c0001t0002g0074 a0001c0001t0002g0075 others(3): Show |
9 | NA18945.hp2 NA18955.hp2 NA18973.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2141C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693265 | |||||||
| chr6:25693287 | T | A | 1 | a0001c0001t0001g0118 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.702+2163T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693287 | |||||||
| chr6:25693353 | T | G | 158 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(155): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.702+2229T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693353 | |||||||
| chr6:25693437 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.702+2313G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693437 | |||||||
| chr6:25693447 | G | A | 158 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(155): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.702+2323G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693447 | |||||||
| chr6:25693451 | C | CA | 83 | a0001c0001t0001g0037 a0001c0001t0001g0043 a0001c0001t0001g0045 others(80): Show |
92 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.702+2352dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | ||||||
| chr6:25693451 | C | CAA | 21 | a0001c0001t0001g0044 a0001c0001t0001g0126 a0001c0001t0002g0012 others(18): Show |
22 | HG01192.hp2 HG01433.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.702+2351_702+2352d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | ||||||
| chr6:25693451 | CA | C | 21 | a0001c0001t0001g0048 a0001c0001t0001g0114 a0001c0001t0002g0076 others(18): Show |
23 | HG00323.hp1 HG00323.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.702+2352delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693451 | ||||||
| chr6:25693593 | T | G | 1 | a0001c0001t0005g0297 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.702+2469T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693593 | |||||||
| chr6:25693656 | GATT | G | 139 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(136): Show |
155 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.702+2535_702+2537d others(5): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693656 | ||||||
| chr6:25693674 | TTAAC | T | 16 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0054 others(13): Show |
17 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.702+2555_702+2558d others(6): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25693674 | ||||||
| chr6:25693878 | C | T | 2 | a0001c0001t0002g0184 a0001c0001t0002g0231 |
2 | HG01243.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.702+2754C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693878 | |||||||
| chr6:25693898 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.702+2774A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25693898 | |||||||
| chr6:25694080 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.702+2956C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694080 | |||||||
| chr6:25694130 | C | T | 4 | a0001c0001t0008g0024 a0001c0001t0008g0152 a0001c0001t0008g0153 others(1): Show |
5 | HG00642.hp2 HG01081.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.702+3006C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694130 | |||||||
| chr6:25694200 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.702+3076C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694200 | |||||||
| chr6:25694263 | T | G | 47 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0017 others(44): Show |
54 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(51): Show |
intron_variant | MODIFIER | c.702+3139T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694263 | |||||||
| chr6:25694456 | T | C | 49 | a0001c0001t0001g0013 a0001c0001t0001g0023 a0001c0001t0001g0033 others(46): Show |
52 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.702+3332T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694456 | |||||||
| chr6:25694574 | A | G | 16 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0054 others(13): Show |
17 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.702+3450A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694574 | |||||||
| chr6:25694776 | C | T | 9 | a0001c0001t0003g0079 a0001c0001t0003g0081 a0001c0001t0003g0086 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+3652C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694776 | |||||||
| chr6:25694999 | G | A | 1 | a0001c0001t0003g0036 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.702+3875G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25694999 | |||||||
| chr6:25695065 | T | G | 1 | a0001c0001t0003g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+3941T>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695065 | |||||||
| chr6:25695130 | C | T | 8 | a0001c0001t0002g0090 a0001c0001t0002g0210 a0001c0001t0002g0213 others(5): Show |
8 | HG01358.hp1 HG01993.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.702+4006C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695130 | |||||||
| chr6:25695213 | G | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(129): Show |
147 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.702+4089G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695213 | |||||||
| chr6:25695238 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.702+4114T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695238 | |||||||
| chr6:25695317 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(310): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.702+4193T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695317 | |||||||
| chr6:25695592 | T | C | 160 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0119 others(157): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.702+4468T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695592 | |||||||
| chr6:25695963 | T | C | 16 | a0001c0001t0002g0012 a0001c0001t0002g0039 a0001c0001t0002g0054 others(13): Show |
17 | HG00741.hp2 HG01433.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.702+4839T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25695963 | |||||||
| chr6:25696151 | A | T | 1 | a0001c0001t0004g0241 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.702+5027A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696151 | |||||||
| chr6:25696383 | T | A | 159 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(156): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.703-4824T>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696383 | |||||||
| chr6:25696750 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18973.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.703-4457A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25696750 | |||||||
| chr6:25697136 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0171 others(1): Show |
4 | HG02083.hp1 HG02129.hp2 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-4071A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697136 | |||||||
| chr6:25697175 | C | T | 1 | a0001c0001t0005g0238 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.703-4032C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697175 | |||||||
| chr6:25697316 | G | T | 5 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(2): Show |
5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-3891G>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697316 | |||||||
| chr6:25697348 | C | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(310): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(356): Show |
intron_variant | MODIFIER | c.703-3859C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697348 | |||||||
| chr6:25697400 | A | G | 2 | a0001c0001t0003g0002 a0001c0001t0003g0220 |
6 | HG02486.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-3807A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697400 | |||||||
| chr6:25697933 | C | T | 1 | a0001c0001t0005g0246 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.703-3274C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25697933 | |||||||
| chr6:25698232 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0319 |
3 | HG02165.hp2 NA18943.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.703-2975A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698232 | |||||||
| chr6:25698253 | C | T | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(128): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.703-2954C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698253 | |||||||
| chr6:25698566 | A | T | 9 | a0001c0001t0003g0079 a0001c0001t0003g0081 a0001c0001t0003g0086 others(6): Show |
9 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-2641A>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698566 | |||||||
| chr6:25698585 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0127 |
2 | NA19068.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.703-2622C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698585 | |||||||
| chr6:25698765 | A | G | 1 | a0001c0006t0003g0051 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.703-2442A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698765 | |||||||
| chr6:25698878 | G | A | 5 | a0002c0002t0003g0015 a0002c0002t0003g0091 a0002c0002t0003g0092 others(2): Show |
6 | HG02572.hp2 HG02615.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-2329G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698878 | |||||||
| chr6:25698895 | C | T | 9 | a0001c0001t0002g0008 a0001c0001t0002g0060 a0001c0001t0002g0154 others(6): Show |
11 | HG02055.hp2 HG02258.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.703-2312C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698895 | |||||||
| chr6:25698991 | G | A | 2 | a0001c0001t0002g0176 a0001c0001t0002g0207 |
2 | HG02818.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.703-2216G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25698991 | |||||||
| chr6:25699055 | C | A | 46 | a0001c0001t0002g0006 a0001c0001t0002g0011 a0001c0001t0002g0017 others(43): Show |
53 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(50): Show |
intron_variant | MODIFIER | c.703-2152C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699055 | |||||||
| chr6:25699088 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-2119G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699088 | |||||||
| chr6:25699122 | G | A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0042 |
2 | HG01168.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.703-2085G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699122 | |||||||
| chr6:25699170 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703-2037G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699170 | |||||||
| chr6:25699245 | A | G | 5 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0080 others(2): Show |
5 | HG01496.hp1 HG02258.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-1962A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699245 | |||||||
| chr6:25699422 | C | G | 1 | a0001c0001t0002g0242 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.703-1785C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699422 | |||||||
| chr6:25699446 | C | T | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.703-1761C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699446 | |||||||
| chr6:25699589 | C | CA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0033 a0001c0001t0001g0034 others(12): Show |
16 | HG00438.hp2 HG00673.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-1597dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | ||||||
| chr6:25699589 | C | CAA | 13 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(10): Show |
13 | HG01106.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-1598_703-1597d others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | ||||||
| chr6:25699589 | CA | C | 19 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0127 others(16): Show |
22 | HG00099.hp1 HG00323.hp2 HG00642.hp1 others(19): Show |
intron_variant | MODIFIER | c.703-1597delA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25699589 | ||||||
| chr6:25699607 | A | G | 1 | a0001c0001t0005g0243 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.703-1600A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699607 | |||||||
| chr6:25699635 | A | G | 1 | a0001c0004t0001g0111 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.703-1572A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699635 | |||||||
| chr6:25699691 | A | C | 1 | a0001c0001t0001g0165 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.703-1516A>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699691 | |||||||
| chr6:25699754 | C | T | 2 | a0002c0002t0003g0015 a0002c0002t0003g0094 |
3 | HG02572.hp2 HG02615.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.703-1453C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699754 | |||||||
| chr6:25699771 | A | G | 131 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(128): Show |
146 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.703-1436A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699771 | |||||||
| chr6:25699782 | G | A | 1 | a0001c0001t0002g0176 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.703-1425G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25699782 | |||||||
| chr6:25700021 | G | A | 1 | a0002c0002t0003g0091 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.703-1186G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700021 | |||||||
| chr6:25700055 | G | A | 1 | a0001c0001t0003g0218 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.703-1152G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700055 | |||||||
| chr6:25700079 | C | G | 1 | a0001c0001t0007g0236 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703-1128C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700079 | |||||||
| chr6:25700090 | C | G | 5 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0198 others(2): Show |
5 | NA18940.hp2 NA19003.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-1117C>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700090 | |||||||
| chr6:25700114 | G | A | 11 | a0001c0001t0003g0002 a0001c0001t0003g0004 a0001c0001t0003g0032 others(8): Show |
18 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.703-1093G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700114 | |||||||
| chr6:25700122 | G | A | 81 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0016 others(78): Show |
93 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.703-1085G>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700122 | |||||||
| chr6:25700180 | A | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0119 a0001c0001t0001g0136 others(156): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.703-1027A>G | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700180 | |||||||
| chr6:25700224 | C | T | 2 | a0001c0001t0003g0215 a0001c0001t0003g0216 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.703-983C>T | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700224 | |||||||
| chr6:25700241 | C | A | 1 | a0001c0001t0013g0101 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.703-966C>A | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700241 | |||||||
| chr6:25700241 | C | CA | 7 | a0001c0001t0001g0019 a0001c0001t0001g0223 a0001c0001t0002g0042 others(4): Show |
8 | HG01081.hp1 HG01243.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.703-945dupA | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | ||||||
| chr6:25700241 | C | CAA | 179 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(176): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.703-946_703-945dup others(2): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | ||||||
| chr6:25700241 | C | CAAA | 109 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0044 others(106): Show |
129 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.703-947_703-945dup others(3): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | ||||||
| chr6:25700241 | C | CAAAA | 15 | a0001c0001t0001g0136 a0001c0001t0001g0194 a0001c0001t0001g0225 others(12): Show |
15 | HG00741.hp1 HG02145.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.703-948_703-945dup others(4): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | ||||||
| chr6:25700241 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0232 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.703-960_703-945dup others(16): Show |
SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr6 | 25700241 | ||||||
| chr6:25700611 | T | C | 1 | a0001c0001t0002g0187 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.703-596T>C | SCGN | ENSG00000079689.15 | transcript | ENST00000377961.3 | protein_coding | 10/10 | chr6 | 25700611 |