Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2571 |
| ensemblid | ENSG00000128683.14 |
| hgncid | 4092 |
| symbol | GAD1 |
| name | glutamate decarboxylase 1 |
| refseq_nuc | NM_000817.3 |
| refseq_prot | NP_000808.2 |
| ensembl_nuc | ENST00000358196.8 |
| ensembl_prot | ENSP00000350928.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 170816887 |
| end | 170861151 |
| strand | + |
| ver | v1.2 |
| region | chr2:170816887-170861151 |
| region5000 | chr2:170811887-170866151 |
| regionname0 | GAD1_chr2_170816887_170861151 |
| regionname5000 | GAD1_chr2_170811887_170866151 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 594 | 379 | 69 | 67 | 184 | 15 | 42 | 144 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0002 | 0/0 | 594 | 23 | 23 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0003 | 0/0 | 594 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0004 | 0/0 | 594 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0005 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0006 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0007 | 0/0 | 594 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| a0008 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | MASST others(589): Show |
chr2 | 170811887 | 170866151 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1782 | 207 | 43 | 40 | 86 | 9 | 27 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0001c0002 | 0/0 | 1782 | 153 | 11 | 25 | 96 | 6 | 15 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0001c0004 | 0/0 | 1782 | 16 | 14 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0001c0007 | 0/0 | 1782 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0001c0013 | 0/0 | 1782 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0002c0003 | 0/0 | 1782 | 17 | 17 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0002c0005 | 0/0 | 1782 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0003c0006 | 0/0 | 1782 | 5 | 0 | 0 | 5 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0004c0012 | 0/0 | 1782 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0005c0008 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0006c0010 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0007c0011 | 0/0 | 1782 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 | ||
| a0008c0009 | 0/0 | 1782 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | ATGGC others(1777): Show |
chr2 | 170811887 | 170866151 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3279 | 50 | 24 | 11 | 8 | 3 | 4 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0002 | 1/0 | 3279 | 60 | 5 | 9 | 30 | 2 | 13 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0003 | 0/1 | 3279 | 73 | 0 | 12 | 48 | 3 | 9 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0004 | 0/0 | 3279 | 7 | 7 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0006 | 0/0 | 3279 | 5 | 5 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0007 | 0/0 | 3279 | 3 | 0 | 3 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0008 | 0/0 | 3279 | 4 | 0 | 3 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0010 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0011 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0012 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0015 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0001t0018 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0001 | 0/0 | 3279 | 126 | 10 | 24 | 71 | 6 | 15 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0002 | 0/0 | 3279 | 22 | 0 | 1 | 21 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0006 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0009 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0016 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0002t0017 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0004t0001 | 0/0 | 3279 | 16 | 14 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0007t0002 | 0/0 | 3279 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0001c0013t0001 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0002c0003t0001 | 0/0 | 3279 | 14 | 14 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0002c0003t0005 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0002c0003t0013 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0002c0003t0014 | 0/0 | 3279 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0002c0005t0005 | 0/0 | 3279 | 6 | 6 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0003c0006t0002 | 0/0 | 3279 | 5 | 0 | 0 | 5 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0004c0012t0001 | 0/0 | 3279 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0005c0008t0001 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0006c0010t0003 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0007c0011t0007 | 0/0 | 3279 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| a0008c0009t0003 | 0/0 | 3279 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | CTCTT others(3274): Show |
chr2 | 170811887 | 170866151 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0282 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0335 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0356 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0003g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0004g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0006g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0007g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0007g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0008g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0008g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0008g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0008g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0010g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0011g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0012g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0015g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0001t0018g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0001 | 0/0 | 9 | 0 | 3 | 4 | 1 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0007 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0009g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0002t0017g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0004t0001g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0007t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0007t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0001c0013t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0001g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0013g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0003t0014g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0005t0005g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0005t0005g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0005t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0005t0005g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0002c0005t0005g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0003c0006t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0003c0006t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0003c0006t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0003c0006t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0003c0006t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0004c0012t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0005c0008t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0006c0010t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0007c0011t0007g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| a0008c0009t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0011 | g0248 | EUR | GBR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | GBR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0206 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0090 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0227 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | FIN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00408 | hp1 | a0003 | c0006 | t0002 | g0089 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00423 | hp1 | a0001 | c0002 | t0016 | g0001 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0352 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00438 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0302 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00597 | hp2 | a0001 | c0002 | t0001 | g0193 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0265 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00733 | hp1 | a0001 | c0001 | t0008 | g0355 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00733 | hp2 | a0001 | c0004 | t0001 | g0274 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0331 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0162 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0082 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0166 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0118 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0060 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01109 | hp2 | a0001 | c0001 | t0008 | g0276 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01168 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0131 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0027 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0110 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0313 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0272 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01255 | hp1 | a0001 | c0001 | t0003 | g0370 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0024 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0172 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01261 | hp2 | a0001 | c0004 | t0001 | g0234 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01346 | hp1 | a0001 | c0001 | t0012 | g0311 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0307 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0120 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0152 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01516 | hp1 | a0004 | c0012 | t0001 | g0180 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0334 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0019 | EUR | IBS | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0362 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01891 | hp1 | a0001 | c0004 | t0001 | g0254 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01891 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01928 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0202 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01943 | hp1 | a0001 | c0001 | t0010 | g0368 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0316 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0367 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0201 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0315 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02040 | hp1 | a0003 | c0006 | t0002 | g0130 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02040 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0317 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02056 | hp2 | a0001 | c0002 | t0001 | g0196 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02074 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02074 | hp2 | a0005 | c0008 | t0001 | g0036 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02083 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02132 | hp1 | a0006 | c0010 | t0003 | g0309 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0291 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02135 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0029 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0016 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | CDX | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02258 | hp1 | a0002 | c0005 | t0005 | g0168 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0005 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0167 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0116 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02300 | hp2 | a0007 | c0011 | t0007 | g0369 | AMR | PEL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02451 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02451 | hp2 | a0002 | c0003 | t0001 | g0366 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0267 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | KHV | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0145 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0253 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02615 | hp2 | a0001 | c0004 | t0001 | g0255 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02622 | hp1 | a0002 | c0003 | t0005 | g0303 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0204 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0348 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02647 | hp1 | a0001 | c0004 | t0001 | g0122 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02723 | hp1 | a0002 | c0003 | t0013 | g0212 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02735 | hp2 | a0001 | c0002 | t0001 | g0197 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0165 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02809 | hp1 | a0001 | c0004 | t0001 | g0363 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02809 | hp2 | a0001 | c0013 | t0001 | g0124 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02818 | hp1 | a0001 | c0001 | t0018 | g0273 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02818 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02886 | hp1 | a0002 | c0003 | t0001 | g0337 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0164 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0361 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02896 | hp1 | a0001 | c0004 | t0001 | g0123 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02897 | hp2 | a0001 | c0004 | t0001 | g0177 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02922 | hp1 | a0001 | c0001 | t0015 | g0320 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02922 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0306 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02970 | hp2 | a0001 | c0004 | t0001 | g0176 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03041 | hp2 | a0001 | c0004 | t0001 | g0252 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0353 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03098 | hp2 | a0001 | c0001 | t0006 | g0343 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03130 | hp2 | a0002 | c0003 | t0001 | g0032 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03139 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0242 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03195 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03225 | hp1 | a0002 | c0003 | t0001 | g0251 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03225 | hp2 | a0002 | c0003 | t0014 | g0365 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03486 | hp2 | a0001 | c0004 | t0001 | g0211 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03516 | hp1 | a0002 | c0003 | t0001 | g0354 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03516 | hp2 | a0002 | c0003 | t0001 | g0349 | AFR | ESN | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0210 | AFR | GWD | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0278 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0323 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0328 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0158 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0330 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0240 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0198 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03704 | hp1 | a0001 | c0002 | t0001 | g0205 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0072 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0199 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0014 | SAS | PJL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0357 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0327 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0285 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03927 | hp2 | a0001 | c0001 | t0008 | g0301 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0086 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0305 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0296 | SAS | BEB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0326 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0215 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04204 | hp2 | a0001 | c0001 | t0003 | g0214 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG04228 | hp2 | a0001 | c0002 | t0001 | g0061 | SAS | STU | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18522 | hp1 | a0002 | c0003 | t0001 | g0360 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18522 | hp2 | a0002 | c0005 | t0005 | g0170 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | CHB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | CHB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0351 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18941 | hp1 | a0001 | c0007 | t0002 | g0015 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18942 | hp1 | a0003 | c0006 | t0002 | g0088 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18943 | hp2 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18944 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18945 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18947 | hp2 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18948 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18949 | hp2 | a0001 | c0002 | t0017 | g0121 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18951 | hp1 | a0001 | c0002 | t0001 | g0203 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0270 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18957 | hp1 | a0001 | c0002 | t0009 | g0147 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0338 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18964 | hp1 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0345 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18968 | hp2 | a0001 | c0002 | t0002 | g0262 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18969 | hp1 | a0001 | c0007 | t0002 | g0161 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0359 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0294 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18972 | hp2 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18974 | hp1 | a0001 | c0002 | t0001 | g0106 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0149 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18975 | hp1 | a0001 | c0002 | t0001 | g0332 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18975 | hp2 | a0003 | c0006 | t0002 | g0085 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0299 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18979 | hp1 | a0001 | c0001 | t0003 | g0298 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18981 | hp2 | a0001 | c0002 | t0002 | g0010 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18983 | hp1 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0295 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18987 | hp2 | a0001 | c0002 | t0002 | g0015 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18989 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18994 | hp1 | a0001 | c0002 | t0002 | g0105 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0339 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18995 | hp1 | a0008 | c0009 | t0003 | g0250 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0288 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0358 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19002 | hp2 | a0001 | c0002 | t0001 | g0150 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19003 | hp1 | a0001 | c0001 | t0003 | g0356 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19003 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19005 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19009 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0340 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19043 | hp1 | a0001 | c0002 | t0006 | g0190 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19054 | hp2 | a0001 | c0002 | t0001 | g0271 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19055 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0344 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0269 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0292 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19064 | hp2 | a0001 | c0002 | t0001 | g0119 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19066 | hp2 | a0001 | c0002 | t0009 | g0004 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19068 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0059 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19072 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0079 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19075 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19079 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0341 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19082 | hp1 | a0001 | c0002 | t0002 | g0040 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19085 | hp1 | a0003 | c0006 | t0002 | g0178 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19085 | hp2 | a0001 | c0001 | t0003 | g0322 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0264 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19088 | hp1 | a0001 | c0001 | t0003 | g0293 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19240 | hp1 | a0002 | c0003 | t0001 | g0364 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA19240 | hp2 | a0002 | c0005 | t0005 | g0011 | AFR | YRI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20129 | hp1 | a0002 | c0003 | t0001 | g0336 | AFR | ASW | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20129 | hp2 | a0001 | c0004 | t0001 | g0236 | AFR | ASW | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0151 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0019 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20805 | hp1 | a0001 | c0002 | t0001 | g0192 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | TSI | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0191 | SAS | GIH | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0221 | SAS | GIH | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0113 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0052 | AMR | CLM | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02109 | hp2 | a0002 | c0005 | t0005 | g0187 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02559 | hp1 | a0002 | c0005 | t0005 | g0169 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0256 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | MSL | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG06807 | hp1 | a0002 | c0005 | t0005 | g0011 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0007 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA18955 | hp2 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0018 | AFR | USA | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | LWK | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0335 | REF | REF | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0282 | REF | REF | GAD1_chr2_170811887_170866151 | GAD1 | chr2 | 170811887 | 170866151 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170818671 | C | A | 1 | a0003 | 5 | HG00408.hp1 HG02040.hp1 NA18942.hp1 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.80C>A | p.Thr27Lys | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/17 | 305/3279 | 80/1785 | 27/594 | chr2 | 170818671 | |||
| chr2:170829576 | G | A | 1 | a0008 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.247G>A | p.Asp83Asn | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 472/3279 | 247/1785 | 83/594 | chr2 | 170829576 | |||
| chr2:170829597 | C | T | 1 | a0005 | 1 | HG02074.hp2 | missense_variant | MODERATE | c.268C>T | p.Arg90Cys | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 493/3279 | 268/1785 | 90/594 | chr2 | 170829597 | |||
| chr2:170844088 | A | C | 1 | a0004 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.682A>C | p.Ile228Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/17 | 907/3279 | 682/1785 | 228/594 | chr2 | 170844088 | |||
| chr2:170845769 | A | T | 1 | a0007 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.931A>T | p.Ile311Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 9/17 | 1156/3279 | 931/1785 | 311/594 | chr2 | 170845769 | |||
| chr2:170846058 | C | G | 1 | a0006 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.997C>G | p.Gln333Glu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/17 | 1222/3279 | 997/1785 | 333/594 | chr2 | 170846058 | |||
| chr2:170858877 | G | A | 1 | a0002 | 23 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(20): Show |
missense_variant | MODERATE | c.1595G>A | p.Arg532Gln | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/17 | 1820/3279 | 1595/1785 | 532/594 | chr2 | 170858877 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170822115 | T | C | 4 | a0001c0002 a0001c0007 a0002c0005 others(1): Show |
162 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(159): Show |
synonymous_variant | LOW | c.111T>C | p.His37His | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/17 | 336/3279 | 111/1785 | 37/594 | chr2 | 170822115 | |||
| chr2:170829578 | C | T | 1 | a0001c0013 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.249C>T | p.Asp83Asp | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/17 | 474/3279 | 249/1785 | 83/594 | chr2 | 170829578 | |||
| chr2:170852729 | C | T | 1 | a0001c0007 | 2 | NA18941.hp1 NA18969.hp1 |
synonymous_variant | LOW | c.1200C>T | p.Thr400Thr | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/17 | 1425/3279 | 1200/1785 | 400/594 | chr2 | 170852729 | |||
| chr2:170857054 | C | T | 2 | a0001c0004 a0001c0013 |
17 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(14): Show |
synonymous_variant | LOW | c.1450C>T | p.Leu484Leu | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/17 | 1675/3279 | 1450/1785 | 484/594 | chr2 | 170857054 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170816954 | G | A | 3 | a0001c0001t0007 a0001c0001t0010 a0007c0011t0007 |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-158G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/17 | 1638 | chr2 | 170816954 | ||||||
| chr2:170816965 | G | A | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0011 others(3): Show |
80 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
5_prime_UTR_variant | MODIFIER | c.-147G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/17 | 1627 | chr2 | 170816965 | ||||||
| chr2:170818553 | A | C | 1 | a0001c0001t0018 | 1 | HG02818.hp1 | 5_prime_UTR_variant | MODIFIER | c.-39A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/17 | 39 | chr2 | 170818553 | ||||||
| chr2:170859949 | A | G | 3 | a0001c0001t0007 a0001c0001t0012 a0007c0011t0007 |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 67 | chr2 | 170859949 | ||||||
| chr2:170860124 | A | C | 1 | a0001c0002t0009 | 2 | NA18957.hp1 NA19066.hp2 |
3_prime_UTR_variant | MODIFIER | c.*242A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 242 | chr2 | 170860124 | ||||||
| chr2:170860124 | A | G | 1 | a0001c0002t0017 | 1 | NA18949.hp2 | 3_prime_UTR_variant | MODIFIER | c.*242A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 242 | chr2 | 170860124 | ||||||
| chr2:170860293 | G | A | 26 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(23): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*411G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 411 | chr2 | 170860293 | ||||||
| chr2:170860307 | T | C | 1 | a0002c0003t0013 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*425T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 425 | chr2 | 170860307 | ||||||
| chr2:170860395 | C | T | 2 | a0001c0001t0006 a0001c0002t0006 |
6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 513 | chr2 | 170860395 | ||||||
| chr2:170860582 | C | T | 2 | a0002c0003t0005 a0002c0005t0005 |
7 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*700C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 700 | chr2 | 170860582 | ||||||
| chr2:170860666 | G | A | 1 | a0002c0003t0014 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 784 | chr2 | 170860666 | ||||||
| chr2:170860685 | T | C | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*803T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 803 | chr2 | 170860685 | ||||||
| chr2:170860872 | G | A | 1 | a0001c0002t0016 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*990G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 990 | chr2 | 170860872 | ||||||
| chr2:170860890 | C | T | 1 | a0001c0001t0004 | 7 | HG01884.hp2 HG02630.hp2 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 1008 | chr2 | 170860890 | ||||||
| chr2:170861087 | G | A | 1 | a0001c0001t0011 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1205G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 17/17 | 1205 | chr2 | 170861087 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:170817122 | G | A | 1 | a0001c0001t0003g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-64+74G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817122 | |||||||
| chr2:170817202 | C | G | 1 | a0001c0001t0003g0370 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-64+154C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817202 | |||||||
| chr2:170817225 | A | AC | 38 | a0001c0001t0001g0225 a0001c0001t0001g0226 a0001c0001t0001g0233 others(35): Show |
39 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(36): Show |
intron_variant | MODIFIER | c.-64+190dupC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACC | 45 | a0001c0001t0001g0185 a0001c0001t0001g0208 a0001c0001t0001g0216 others(42): Show |
48 | HG00280.hp1 HG00544.hp2 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.-64+189_-64+190dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCC | 51 | a0001c0001t0001g0012 a0001c0001t0001g0173 a0001c0001t0001g0179 others(48): Show |
64 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-64+188_-64+190dup others(3): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCCC | 39 | a0001c0001t0001g0002 a0001c0001t0001g0126 a0001c0001t0001g0128 others(36): Show |
44 | HG00423.hp2 HG00639.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.-64+187_-64+190dup others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCCCC | 36 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0096 others(33): Show |
38 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.-64+186_-64+190dup others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCCCCC | 21 | a0001c0001t0001g0070 a0001c0001t0002g0064 a0001c0001t0002g0065 others(18): Show |
22 | HG00609.hp2 HG01109.hp1 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.-64+185_-64+190dup others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCCCCCC | 17 | a0001c0001t0001g0047 a0001c0001t0002g0048 a0001c0001t0002g0049 others(14): Show |
17 | HG01081.hp2 HG01361.hp1 HG02074.hp2 others(14): Show |
intron_variant | MODIFIER | c.-64+184_-64+190dup others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | ACCCCCCC others(3): Show |
1 | a0001c0001t0002g0033 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-64+181_-64+190dup others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817225 | A | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+177A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817225 | |||||||
| chr2:170817225 | AC | A | 41 | a0001c0001t0001g0031 a0001c0001t0001g0333 a0001c0001t0001g0342 others(38): Show |
48 | HG00438.hp1 HG00733.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.-64+190delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr2 | 170817225 | ||||||
| chr2:170817234 | C | A | 2 | a0001c0001t0001g0031 a0002c0003t0001g0032 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-64+186C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817234 | |||||||
| chr2:170817251 | A | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+203A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817251 | |||||||
| chr2:170817342 | G | A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-64+294G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817342 | |||||||
| chr2:170817441 | C | T | 1 | a0001c0002t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-64+393C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817441 | |||||||
| chr2:170817494 | G | T | 1 | a0001c0002t0001g0332 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-64+446G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817494 | |||||||
| chr2:170817588 | C | G | 77 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(74): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.-64+540C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817588 | |||||||
| chr2:170817602 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-64+554G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817602 | |||||||
| chr2:170817822 | T | C | 4 | a0001c0001t0001g0185 a0001c0001t0001g0225 a0001c0001t0001g0226 others(1): Show |
4 | HG01069.hp2 HG01975.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.-63-707T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817822 | |||||||
| chr2:170817937 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-63-592C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170817937 | |||||||
| chr2:170818031 | C | T | 1 | a0001c0001t0001g0325 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-63-498C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818031 | |||||||
| chr2:170818068 | T | G | 1 | a0001c0002t0001g0143 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-63-461T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818068 | |||||||
| chr2:170818090 | C | G | 4 | a0001c0001t0001g0218 a0001c0001t0002g0223 a0001c0001t0002g0224 others(1): Show |
4 | HG03486.hp1 NA18950.hp1 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.-63-439C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818090 | |||||||
| chr2:170818159 | A | C | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-63-370A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818159 | |||||||
| chr2:170818186 | T | C | 238 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(235): Show |
265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.-63-343T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818186 | |||||||
| chr2:170818198 | C | A | 1 | a0001c0001t0002g0326 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-63-331C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818198 | |||||||
| chr2:170818392 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0260 |
3 | NA18950.hp1 NA19054.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.-63-137G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818392 | |||||||
| chr2:170818433 | T | A | 1 | a0001c0002t0001g0332 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-63-96T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 1/16 | chr2 | 170818433 | |||||||
| chr2:170818805 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.82+132C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170818805 | |||||||
| chr2:170818871 | A | G | 235 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(232): Show |
262 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.82+198A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170818871 | |||||||
| chr2:170819228 | C | G | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82+555C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819228 | |||||||
| chr2:170819289 | GAGAA | G | 3 | a0001c0002t0001g0046 a0001c0002t0001g0063 a0001c0002t0017g0121 |
3 | NA18949.hp2 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.82+618_82+621delGA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819289 | ||||||
| chr2:170819291 | G | GAAAT | 75 | a0001c0001t0001g0031 a0001c0001t0001g0318 a0001c0001t0001g0319 others(72): Show |
79 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.82+640_82+643dupAA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819291 | G | GAAATAAA others(1): Show |
7 | a0001c0001t0001g0235 a0001c0001t0003g0284 a0001c0001t0003g0287 others(4): Show |
7 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.82+636_82+643dupAA others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819291 | G | GAAATAAA others(5): Show |
2 | a0001c0001t0001g0280 a0001c0001t0015g0320 |
2 | HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.82+632_82+643dupAA others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819291 | GAAAT | G | 225 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(222): Show |
252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.82+640_82+643delAA others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819291 | GAAATAAA others(1): Show |
G | 3 | a0001c0001t0003g0246 a0001c0001t0003g0307 a0001c0001t0012g0311 |
3 | HG01106.hp1 HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.82+636_82+643delAA others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819291 | GAAATAAA others(5): Show |
G | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82+632_82+643delAA others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819291 | ||||||
| chr2:170819355 | A | C | 2 | a0001c0001t0001g0031 a0002c0003t0001g0032 |
2 | HG03130.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.82+682A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819355 | |||||||
| chr2:170819479 | A | G | 2 | a0001c0002t0001g0062 a0001c0002t0001g0079 |
2 | NA19010.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.82+806A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819479 | |||||||
| chr2:170819485 | G | A | 50 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0034 others(47): Show |
53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+812G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819485 | |||||||
| chr2:170819499 | C | T | 1 | a0001c0001t0018g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+826C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819499 | |||||||
| chr2:170819629 | T | A | 2 | a0001c0001t0002g0065 a0001c0001t0002g0082 |
2 | HG01070.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.82+956T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819629 | |||||||
| chr2:170819712 | G | A | 1 | a0001c0001t0002g0127 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.82+1039G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819712 | |||||||
| chr2:170819955 | T | TC | 90 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(87): Show |
108 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.82+1285dupC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr2 | 170819955 | ||||||
| chr2:170819959 | G | T | 1 | a0001c0001t0002g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.82+1286G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170819959 | |||||||
| chr2:170820008 | G | C | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82+1335G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820008 | |||||||
| chr2:170820074 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82+1401G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820074 | |||||||
| chr2:170820191 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.82+1518G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820191 | |||||||
| chr2:170820255 | C | T | 8 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(5): Show |
8 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.82+1582C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820255 | |||||||
| chr2:170820258 | C | T | 50 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0034 others(47): Show |
53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.82+1585C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820258 | |||||||
| chr2:170820262 | G | A | 4 | a0001c0001t0001g0235 a0001c0004t0001g0234 a0001c0004t0001g0236 others(1): Show |
4 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.82+1589G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820262 | |||||||
| chr2:170820289 | A | C | 54 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(51): Show |
58 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.82+1616A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820289 | |||||||
| chr2:170820322 | C | A | 1 | a0001c0001t0001g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.82+1649C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820322 | |||||||
| chr2:170820441 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(5): Show |
8 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-1646G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820441 | |||||||
| chr2:170820688 | G | T | 1 | a0001c0002t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.83-1399G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820688 | |||||||
| chr2:170820713 | C | A | 140 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0004 others(137): Show |
161 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.83-1374C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170820713 | |||||||
| chr2:170821213 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.83-874T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821213 | |||||||
| chr2:170821225 | T | A | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.83-862T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821225 | |||||||
| chr2:170821235 | G | C | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.83-852G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821235 | |||||||
| chr2:170821242 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0010g0368 a0001c0002t0001g0142 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-845C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821242 | |||||||
| chr2:170821578 | C | T | 1 | a0002c0003t0001g0366 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.83-509C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821578 | |||||||
| chr2:170821582 | C | G | 1 | a0001c0002t0001g0207 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.83-505C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821582 | |||||||
| chr2:170821759 | G | A | 3 | a0001c0001t0007g0029 a0001c0001t0010g0368 a0007c0011t0007g0369 |
4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-328G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821759 | |||||||
| chr2:170821869 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(228): Show |
258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.83-218C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170821869 | |||||||
| chr2:170822059 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.83-28G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 2/16 | chr2 | 170822059 | |||||||
| chr2:170822155 | T | C | 2 | a0001c0002t0001g0046 a0001c0002t0001g0063 |
2 | NA18982.hp1 NA18987.hp1 |
splice_region_variant&intron_variant | LOW | c.145+6T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822155 | |||||||
| chr2:170822373 | A | G | 9 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(6): Show |
9 | HG01069.hp2 HG01975.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.145+224A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822373 | |||||||
| chr2:170822446 | C | T | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145+297C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822446 | |||||||
| chr2:170822641 | C | T | 1 | a0002c0003t0014g0365 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.145+492C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822641 | |||||||
| chr2:170822810 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.145+661G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822810 | |||||||
| chr2:170822819 | G | C | 50 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0034 others(47): Show |
53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.145+670G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170822819 | |||||||
| chr2:170823005 | G | A | 76 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(73): Show |
81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.145+856G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823005 | |||||||
| chr2:170823144 | A | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+995A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823144 | |||||||
| chr2:170823145 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(75): Show |
83 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.145+996G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823145 | |||||||
| chr2:170823168 | C | T | 2 | a0001c0002t0001g0120 a0001c0002t0001g0206 |
2 | HG00280.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.145+1019C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823168 | |||||||
| chr2:170823174 | A | G | 2 | a0001c0002t0001g0076 a0001c0002t0001g0109 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.145+1025A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823174 | |||||||
| chr2:170823202 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.145+1053G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823202 | |||||||
| chr2:170823324 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+1175C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823324 | |||||||
| chr2:170823532 | A | G | 145 | a0001c0001t0001g0218 a0001c0001t0007g0029 a0001c0001t0007g0367 others(142): Show |
167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.145+1383A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823532 | |||||||
| chr2:170823566 | G | A | 7 | a0001c0002t0001g0034 a0001c0002t0001g0051 a0001c0002t0002g0035 others(4): Show |
7 | HG02074.hp2 NA18945.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+1417G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823566 | |||||||
| chr2:170823570 | A | G | 145 | a0001c0001t0001g0218 a0001c0001t0007g0029 a0001c0001t0007g0367 others(142): Show |
167 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.145+1421A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823570 | |||||||
| chr2:170823698 | T | C | 1 | a0001c0001t0018g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.145+1549T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823698 | |||||||
| chr2:170823807 | G | GA | 4 | a0001c0001t0003g0019 a0001c0001t0003g0024 a0001c0001t0003g0334 others(1): Show |
6 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+1658_145+1659i others(3): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823807 | |||||||
| chr2:170823808 | G | A | 4 | a0001c0001t0003g0019 a0001c0001t0003g0024 a0001c0001t0003g0334 others(1): Show |
6 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+1659G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823808 | |||||||
| chr2:170823809 | G | C | 1 | a0003c0006t0002g0085 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.145+1660G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170823809 | |||||||
| chr2:170824008 | C | T | 1 | a0007c0011t0007g0369 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.145+1859C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824008 | |||||||
| chr2:170824051 | G | C | 91 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0002t0001g0001 others(88): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1902G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824051 | |||||||
| chr2:170824052 | G | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0002t0001g0001 others(88): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1903G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824052 | |||||||
| chr2:170824077 | C | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0002t0001g0001 others(88): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.145+1928C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824077 | |||||||
| chr2:170824205 | C | T | 50 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0034 others(47): Show |
53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.145+2056C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824205 | |||||||
| chr2:170824378 | T | TAC | 49 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0104 others(46): Show |
50 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.145+2270_145+2271d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | T | TACAC | 21 | a0001c0001t0001g0047 a0001c0001t0001g0219 a0001c0001t0001g0280 others(18): Show |
21 | HG00280.hp2 HG00408.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.145+2268_145+2271d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | T | TACACACA others(1): Show |
4 | a0001c0001t0001g0237 a0001c0001t0002g0086 a0001c0001t0004g0175 others(1): Show |
4 | HG03195.hp1 HG03579.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+2264_145+2271d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | T | TACACACA others(3): Show |
1 | a0001c0001t0002g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.145+2262_145+2271d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | T | TACACACA others(5): Show |
1 | a0001c0004t0001g0211 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.145+2260_145+2271d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | T | TACACACA others(9): Show |
1 | a0001c0001t0004g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.145+2256_145+2271d others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TAC | T | 41 | a0001c0001t0001g0031 a0001c0001t0001g0216 a0001c0001t0001g0304 others(38): Show |
43 | HG00544.hp1 HG00597.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.145+2270_145+2271d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACAC | T | 45 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0001g0321 others(42): Show |
55 | HG00140.hp1 HG00733.hp1 HG01106.hp1 others(52): Show |
intron_variant | MODIFIER | c.145+2268_145+2271d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACAC | T | 7 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(4): Show |
7 | HG02647.hp1 HG02809.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.145+2266_145+2271d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACACA others(1): Show |
T | 12 | a0001c0001t0001g0235 a0001c0004t0001g0217 a0001c0004t0001g0234 others(9): Show |
12 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+2264_145+2271d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0185 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.145+2262_145+2271d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACACA others(7): Show |
T | 12 | a0001c0001t0001g0070 a0001c0001t0001g0173 a0001c0001t0001g0208 others(9): Show |
12 | HG00741.hp1 HG01069.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.145+2258_145+2271d others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACACA others(9): Show |
T | 8 | a0001c0001t0001g0080 a0001c0001t0007g0029 a0001c0001t0007g0367 others(5): Show |
9 | HG01243.hp2 HG01928.hp1 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.145+2256_145+2271d others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824378 | TACACACA others(11): Show |
T | 140 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0126 others(137): Show |
165 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.145+2254_145+2271d others(20): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824378 | ||||||
| chr2:170824417 | ACAC | A | 5 | a0001c0001t0001g0353 a0001c0001t0003g0245 a0001c0001t0003g0307 others(2): Show |
5 | HG00438.hp1 HG01346.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.145+2270_145+2272d others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824417 | ||||||
| chr2:170824419 | A | C | 1 | a0001c0002t0002g0006 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.145+2270A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824419 | |||||||
| chr2:170824419 | AC | A | 4 | a0001c0001t0001g0342 a0001c0001t0003g0240 a0001c0001t0003g0285 others(1): Show |
4 | HG02723.hp1 HG02723.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+2274delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824419 | ||||||
| chr2:170824660 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0010g0368 others(1): Show |
5 | HG01928.hp1 HG01943.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.145+2511C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824660 | |||||||
| chr2:170824671 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.145+2522C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824671 | |||||||
| chr2:170824782 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.145+2633T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170824782 | |||||||
| chr2:170824929 | C | CGT | 10 | a0001c0001t0003g0239 a0001c0002t0001g0037 a0001c0002t0001g0145 others(7): Show |
11 | HG00408.hp2 HG02109.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.145+2801_145+2802d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170824929 | C | CGTGT | 115 | a0001c0001t0001g0080 a0001c0001t0003g0019 a0001c0001t0003g0020 others(112): Show |
128 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.145+2799_145+2802d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170824929 | C | CGTGTGT | 65 | a0001c0001t0001g0031 a0001c0001t0001g0235 a0001c0001t0001g0237 others(62): Show |
67 | HG00733.hp2 HG01109.hp2 HG01884.hp2 others(64): Show |
intron_variant | MODIFIER | c.145+2797_145+2802d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170824929 | C | CGTGTGTG others(1): Show |
72 | a0001c0001t0001g0047 a0001c0001t0001g0070 a0001c0001t0001g0096 others(69): Show |
74 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.145+2795_145+2802d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170824929 | C | CGTGTGTG others(3): Show |
13 | a0001c0001t0001g0104 a0001c0001t0001g0218 a0001c0001t0002g0064 others(10): Show |
13 | HG00323.hp2 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.145+2793_145+2802d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170824929 | CGTGT | C | 10 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(7): Show |
10 | HG01069.hp2 HG01975.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.145+2799_145+2802d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170824929 | ||||||
| chr2:170825191 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.145+3042G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825191 | |||||||
| chr2:170825473 | A | G | 151 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0091 others(148): Show |
176 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.145+3324A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825473 | |||||||
| chr2:170825568 | A | C | 4 | a0001c0001t0001g0325 a0001c0001t0001g0361 a0001c0001t0004g0324 others(1): Show |
4 | HG01884.hp2 HG02615.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.145+3419A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825568 | |||||||
| chr2:170825606 | C | T | 3 | a0001c0002t0002g0006 a0001c0002t0002g0045 a0001c0002t0002g0059 |
4 | HG00609.hp2 HG02083.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.145+3457C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825606 | |||||||
| chr2:170825624 | C | T | 73 | a0001c0001t0001g0047 a0001c0001t0001g0070 a0001c0001t0001g0096 others(70): Show |
74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.145+3475C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825624 | |||||||
| chr2:170825676 | A | G | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.145+3527A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825676 | |||||||
| chr2:170825707 | G | A | 10 | a0001c0002t0001g0004 a0001c0002t0001g0111 a0001c0002t0001g0112 others(7): Show |
11 | HG00673.hp2 HG02135.hp2 NA18948.hp2 others(8): Show |
intron_variant | MODIFIER | c.145+3558G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825707 | |||||||
| chr2:170825709 | G | A | 41 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(38): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.145+3560G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825709 | |||||||
| chr2:170825734 | G | A | 1 | a0001c0002t0001g0038 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.145+3585G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825734 | |||||||
| chr2:170825829 | C | T | 48 | a0001c0002t0001g0007 a0001c0002t0001g0018 a0001c0002t0001g0034 others(45): Show |
51 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.146-3646C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825829 | |||||||
| chr2:170825836 | C | T | 3 | a0001c0001t0007g0029 a0001c0001t0010g0368 a0007c0011t0007g0369 |
4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-3639C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825836 | |||||||
| chr2:170825894 | G | T | 3 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0257 |
3 | HG02683.hp2 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.146-3581G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825894 | |||||||
| chr2:170825897 | T | A | 1 | a0001c0002t0001g0144 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.146-3578T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825897 | |||||||
| chr2:170825965 | A | G | 1 | a0001c0001t0002g0102 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.146-3510A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170825965 | |||||||
| chr2:170826230 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0091 others(96): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.146-3245C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826230 | |||||||
| chr2:170826276 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.146-3199G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826276 | |||||||
| chr2:170826289 | G | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0091 others(91): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.146-3186G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826289 | |||||||
| chr2:170826314 | C | A | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-3161C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826314 | |||||||
| chr2:170826332 | C | T | 3 | a0001c0002t0001g0046 a0001c0002t0001g0063 a0001c0002t0017g0121 |
3 | NA18949.hp2 NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.146-3143C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826332 | |||||||
| chr2:170826517 | G | A | 41 | a0001c0001t0001g0173 a0001c0001t0001g0185 a0001c0001t0001g0208 others(38): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.146-2958G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826517 | |||||||
| chr2:170826567 | C | CA | 149 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0070 others(146): Show |
175 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(172): Show |
intron_variant | MODIFIER | c.146-2891dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | ||||||
| chr2:170826567 | C | CAA | 70 | a0001c0001t0001g0047 a0001c0001t0001g0096 a0001c0001t0001g0104 others(67): Show |
71 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.146-2892_146-2891d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | ||||||
| chr2:170826567 | CA | C | 8 | a0001c0001t0001g0350 a0001c0001t0002g0351 a0001c0001t0003g0316 others(5): Show |
8 | HG01943.hp2 HG01975.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-2891delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170826567 | ||||||
| chr2:170826597 | C | T | 253 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(250): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.146-2878C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826597 | |||||||
| chr2:170826601 | C | T | 3 | a0001c0001t0007g0029 a0001c0001t0010g0368 a0007c0011t0007g0369 |
4 | HG01928.hp1 HG01943.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2874C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826601 | |||||||
| chr2:170826657 | G | A | 1 | a0001c0002t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.146-2818G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826657 | |||||||
| chr2:170826682 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0002g0008 |
4 | NA18980.hp2 NA18986.hp2 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2793A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826682 | |||||||
| chr2:170826824 | A | T | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-2651A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826824 | |||||||
| chr2:170826916 | C | T | 1 | a0001c0001t0003g0024 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.146-2559C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826916 | |||||||
| chr2:170826965 | A | G | 1 | a0001c0002t0001g0119 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.146-2510A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170826965 | |||||||
| chr2:170827158 | G | A | 45 | a0001c0001t0003g0021 a0001c0002t0001g0007 a0001c0002t0001g0018 others(42): Show |
49 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.146-2317G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827158 | |||||||
| chr2:170827193 | C | G | 2 | a0001c0001t0003g0299 a0001c0001t0003g0300 |
2 | HG00597.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.146-2282C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827193 | |||||||
| chr2:170827230 | G | A | 1 | a0001c0001t0003g0310 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.146-2245G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827230 | |||||||
| chr2:170827248 | C | A | 49 | a0001c0001t0003g0021 a0001c0002t0001g0007 a0001c0002t0001g0018 others(46): Show |
53 | HG00438.hp2 HG00609.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.146-2227C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827248 | |||||||
| chr2:170827257 | C | T | 1 | a0002c0003t0001g0032 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.146-2218C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827257 | |||||||
| chr2:170827272 | C | T | 8 | a0001c0001t0003g0214 a0001c0001t0003g0215 a0001c0001t0003g0240 others(5): Show |
8 | HG02602.hp1 HG02738.hp2 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.146-2203C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827272 | |||||||
| chr2:170827455 | C | T | 4 | a0001c0002t0001g0043 a0001c0002t0001g0044 a0001c0002t0001g0269 others(1): Show |
4 | NA18952.hp2 NA18962.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-2020C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827455 | |||||||
| chr2:170827456 | G | A | 4 | a0001c0001t0001g0173 a0001c0001t0001g0208 a0001c0001t0001g0233 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-2019G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827456 | |||||||
| chr2:170827522 | T | C | 2 | a0001c0001t0002g0141 a0001c0001t0018g0273 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.146-1953T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827522 | |||||||
| chr2:170827530 | C | T | 1 | a0002c0003t0001g0323 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.146-1945C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827530 | |||||||
| chr2:170827554 | C | T | 1 | a0001c0002t0001g0146 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.146-1921C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827554 | |||||||
| chr2:170827565 | G | T | 12 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0217 others(9): Show |
12 | HG00733.hp2 HG01261.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.146-1910G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827565 | |||||||
| chr2:170827687 | T | C | 2 | a0001c0002t0001g0051 a0005c0008t0001g0036 |
2 | HG02074.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.146-1788T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827687 | |||||||
| chr2:170827777 | C | T | 1 | a0001c0002t0002g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.146-1698C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827777 | |||||||
| chr2:170827780 | A | G | 1 | a0001c0001t0003g0283 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.146-1695A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827780 | |||||||
| chr2:170827834 | T | C | 4 | a0001c0001t0018g0273 a0001c0002t0001g0145 a0002c0003t0001g0317 others(1): Show |
4 | HG02055.hp2 HG02572.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1641T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827834 | |||||||
| chr2:170827873 | T | G | 302 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(299): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.146-1602T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827873 | |||||||
| chr2:170827905 | G | C | 1 | a0001c0001t0002g0351 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.146-1570G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827905 | |||||||
| chr2:170827990 | G | A | 8 | a0001c0001t0001g0346 a0001c0001t0001g0350 a0001c0004t0001g0217 others(5): Show |
8 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.146-1485G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170827990 | |||||||
| chr2:170828043 | ATCCTCAC others(31): Show |
A | 140 | a0001c0001t0001g0031 a0001c0001t0001g0070 a0001c0001t0001g0080 others(137): Show |
153 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.146-1384_146-1347d others(40): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828043 | ||||||
| chr2:170828057 | T | C | 50 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0185 others(47): Show |
54 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.146-1418T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828057 | |||||||
| chr2:170828067 | GTCCTCCC others(54): Show |
G | 1 | a0001c0001t0001g0318 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-1384_146-1324d others(63): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828067 | ||||||
| chr2:170828085 | TCACCCCT others(311): Show |
T | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1384_146-1067d others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828085 | ||||||
| chr2:170828087 | AC | A | 218 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(215): Show |
244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.146-1384delC | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828087 | ||||||
| chr2:170828090 | CCTCCTCC others(8): Show |
C | 6 | a0001c0001t0003g0291 a0001c0001t0006g0242 a0001c0001t0006g0243 others(3): Show |
6 | HG01884.hp1 HG02132.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.146-1384_146-1370d others(17): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828090 | |||||||
| chr2:170828098 | T | C | 218 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(215): Show |
244 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(241): Show |
intron_variant | MODIFIER | c.146-1377T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828098 | |||||||
| chr2:170828105 | G | GTCCTCAC others(2): Show |
167 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(164): Show |
188 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(185): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(11): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | ||||||
| chr2:170828105 | G | GTCCTCAC others(25): Show |
44 | a0001c0001t0001g0185 a0001c0001t0003g0021 a0001c0001t0003g0298 others(41): Show |
48 | HG00438.hp2 HG00609.hp2 HG01123.hp2 others(45): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(34): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | ||||||
| chr2:170828105 | G | GTCCTCAC others(140): Show |
4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1365_146-1364i others(149): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | ||||||
| chr2:170828105 | G | GTCCTCAC others(853): Show |
1 | a0001c0001t0004g0348 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146-1365_146-1364i others(862): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828105 | ||||||
| chr2:170828108 | C | CTCACCCT others(306): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.146-1365_146-1364i others(315): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828108 | ||||||
| chr2:170828138 | T | A | 1 | a0001c0001t0004g0348 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.146-1337T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828138 | |||||||
| chr2:170828140 | C | A | 1 | a0001c0001t0002g0277 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.146-1335C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828140 | |||||||
| chr2:170828147 | C | CACCCTCC others(39): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18986.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.146-1305_146-1304i others(48): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828147 | ||||||
| chr2:170828147 | C | CACCCTCC others(16): Show |
4 | a0001c0001t0001g0219 a0001c0001t0001g0222 a0001c0001t0001g0258 others(1): Show |
4 | HG00544.hp2 HG00621.hp1 NA18961.hp2 others(1): Show |
intron_variant | MODIFIER | c.146-1306_146-1305i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828147 | ||||||
| chr2:170828147 | C | T | 48 | a0001c0001t0001g0185 a0001c0001t0001g0235 a0001c0001t0003g0021 others(45): Show |
52 | HG00438.hp2 HG00609.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.146-1328C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828147 | |||||||
| chr2:170828154 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0128 |
2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.146-1321C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828154 | |||||||
| chr2:170828171 | G | A | 25 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0001g0318 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.146-1304G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828171 | |||||||
| chr2:170828176 | CCT | C | 60 | a0001c0001t0001g0179 a0001c0001t0002g0008 a0001c0001t0002g0033 others(57): Show |
63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.146-1292_146-1291d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828176 | ||||||
| chr2:170828180 | T | C | 25 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0001g0318 others(22): Show |
25 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.146-1295T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828180 | |||||||
| chr2:170828194 | A | G | 4 | a0001c0001t0001g0237 a0001c0001t0003g0291 a0001c0001t0008g0276 others(1): Show |
4 | HG01109.hp2 HG02132.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1281A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828194 | |||||||
| chr2:170828196 | CT | C | 24 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0049 others(21): Show |
24 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.146-1278delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828196 | |||||||
| chr2:170828197 | TCTCCTCT others(17): Show |
T | 40 | a0001c0001t0001g0096 a0001c0001t0001g0225 a0001c0001t0001g0261 others(37): Show |
44 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.146-1270_146-1247d others(26): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828197 | ||||||
| chr2:170828202 | T | TCCCTCTG others(14): Show |
19 | a0001c0001t0001g0133 a0001c0001t0002g0049 a0001c0001t0002g0064 others(16): Show |
19 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.146-1272_146-1271i others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828202 | ||||||
| chr2:170828204 | T | C | 1 | a0001c0001t0008g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1271T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828204 | |||||||
| chr2:170828212 | A | ATCCTCAC others(3): Show |
1 | a0001c0001t0002g0008 | 2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.146-1257_146-1248d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828212 | ||||||
| chr2:170828212 | A | G | 23 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0049 others(20): Show |
23 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.146-1263A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828212 | |||||||
| chr2:170828221 | C | T | 22 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0049 others(19): Show |
22 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.146-1254C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828221 | |||||||
| chr2:170828222 | CTCCTCTT others(7): Show |
C | 61 | a0001c0001t0001g0179 a0001c0001t0002g0033 a0001c0001t0002g0048 others(58): Show |
63 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.146-1247_146-1234d others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828222 | ||||||
| chr2:170828228 | T | C | 1 | a0001c0001t0008g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1247T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828228 | |||||||
| chr2:170828229 | T | C | 27 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0008 others(24): Show |
28 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.146-1246T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828229 | |||||||
| chr2:170828235 | T | TATCCTCA others(3): Show |
21 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0049 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-1240_146-1239i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828235 | |||||||
| chr2:170828236 | G | A | 1 | a0002c0003t0001g0366 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.146-1239G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828236 | |||||||
| chr2:170828236 | G | C | 21 | a0001c0001t0001g0133 a0001c0001t0001g0237 a0001c0001t0002g0049 others(18): Show |
21 | HG00140.hp2 HG00280.hp2 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.146-1239G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828236 | |||||||
| chr2:170828236 | G | GTCCTCAC others(71): Show |
1 | a0001c0001t0008g0301 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.146-1230_146-1229i others(80): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828236 | ||||||
| chr2:170828252 | T | C | 1 | a0001c0001t0002g0008 | 2 | NA18980.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.146-1223T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828252 | |||||||
| chr2:170828276 | T | TTCCCTCT others(16): Show |
5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | ||||||
| chr2:170828276 | T | TTCCCTCT others(16): Show |
48 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0185 others(45): Show |
52 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | ||||||
| chr2:170828276 | T | TTCCCTCT others(17): Show |
12 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(9): Show |
13 | HG01346.hp1 HG01891.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.146-1190_146-1189i others(26): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828276 | ||||||
| chr2:170828286 | T | C | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1189T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828286 | |||||||
| chr2:170828296 | C | CTCCTCCC others(59): Show |
4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1154_146-1153i others(68): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828296 | ||||||
| chr2:170828299 | C | CTCCCTCT others(16): Show |
4 | a0001c0002t0001g0001 a0001c0002t0001g0003 a0001c0002t0001g0114 others(1): Show |
6 | NA18945.hp2 NA18980.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1162_146-1140d others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828299 | ||||||
| chr2:170828322 | T | TTCCCTCT others(13): Show |
1 | a0001c0001t0003g0310 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.146-1139_146-1120d others(22): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828322 | ||||||
| chr2:170828349 | T | C | 1 | a0001c0002t0001g0016 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.146-1126T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828349 | |||||||
| chr2:170828365 | T | TTCCCTCT others(39): Show |
1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.146-1089_146-1044d others(48): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828365 | ||||||
| chr2:170828380 | TCACCCTC others(16): Show |
T | 5 | a0001c0001t0003g0023 a0001c0001t0003g0028 a0001c0001t0003g0315 others(2): Show |
6 | HG01167.hp1 HG01192.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.146-1072_146-1050d others(25): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828380 | ||||||
| chr2:170828383 | C | T | 61 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0185 others(58): Show |
65 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.146-1092C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828383 | |||||||
| chr2:170828431 | C | G | 1 | a0001c0002t0001g0171 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.146-1044C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828431 | |||||||
| chr2:170828446 | G | A | 5 | a0001c0001t0001g0333 a0001c0001t0001g0353 a0001c0002t0001g0145 others(2): Show |
5 | HG02055.hp2 HG02572.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.146-1029G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828446 | |||||||
| chr2:170828447 | C | T | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-1028C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828447 | |||||||
| chr2:170828448 | G | A | 7 | a0001c0001t0002g0209 a0001c0004t0001g0122 a0001c0004t0001g0123 others(4): Show |
7 | HG02559.hp2 HG02647.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.146-1027G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828448 | |||||||
| chr2:170828455 | G | A | 1 | a0001c0004t0001g0253 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.146-1020G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828455 | |||||||
| chr2:170828458 | G | GTCCTCCC others(16): Show |
1 | a0001c0001t0001g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.146-973_146-951dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828458 | ||||||
| chr2:170828458 | GTCCTCCC others(16): Show |
G | 154 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0136 others(151): Show |
162 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.146-973_146-951del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828458 | ||||||
| chr2:170828481 | C | CTCCTCCC others(823): Show |
4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.146-823_146-822ins others(830): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828481 | ||||||
| chr2:170828555 | A | ACCTCTGC others(15): Show |
1 | a0001c0001t0001g0318 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.146-902_146-881dup others(22): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828555 | ||||||
| chr2:170828619 | G | GCCCTCCT others(16): Show |
1 | a0001c0002t0001g0202 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.146-822_146-800dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828619 | ||||||
| chr2:170828619 | GCCCTCCT others(16): Show |
G | 82 | a0001c0001t0001g0104 a0001c0001t0001g0133 a0001c0001t0001g0179 others(79): Show |
85 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.146-822_146-800del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828619 | ||||||
| chr2:170828670 | C | T | 1 | a0001c0002t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146-805C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828670 | |||||||
| chr2:170828740 | CCCTCTGC others(16): Show |
C | 1 | a0002c0003t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146-720_146-698del others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828740 | ||||||
| chr2:170828831 | T | C | 1 | a0002c0003t0001g0336 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.146-644T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828831 | |||||||
| chr2:170828952 | C | CTCCTCCC others(16): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0216 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146-513_146-491dup others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr2 | 170828952 | ||||||
| chr2:170828987 | C | G | 76 | a0001c0001t0001g0133 a0001c0001t0002g0008 a0001c0001t0002g0033 others(73): Show |
79 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.146-488C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170828987 | |||||||
| chr2:170829006 | T | C | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-469T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829006 | |||||||
| chr2:170829007 | C | T | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.146-468C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829007 | |||||||
| chr2:170829188 | A | C | 2 | a0001c0001t0001g0031 a0001c0001t0001g0216 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.146-287A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 3/16 | chr2 | 170829188 | |||||||
| chr2:170829681 | T | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.304+48T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170829681 | |||||||
| chr2:170829818 | T | G | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+185T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170829818 | |||||||
| chr2:170830049 | C | T | 206 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0031 others(203): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.304+416C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830049 | |||||||
| chr2:170830486 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305-464C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830486 | |||||||
| chr2:170830812 | T | C | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.305-138T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830812 | |||||||
| chr2:170830839 | C | A | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.305-111C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830839 | |||||||
| chr2:170830913 | G | C | 1 | a0001c0002t0001g0204 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.305-37G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 4/16 | chr2 | 170830913 | |||||||
| chr2:170831201 | G | A | 1 | a0001c0004t0001g0252 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.547+9G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831201 | |||||||
| chr2:170831275 | T | G | 1 | a0001c0001t0001g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.547+83T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831275 | |||||||
| chr2:170831384 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.547+192G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831384 | |||||||
| chr2:170831453 | G | A | 1 | a0001c0001t0001g0318 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.547+261G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831453 | |||||||
| chr2:170831591 | C | T | 1 | a0001c0002t0001g0112 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.547+399C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831591 | |||||||
| chr2:170831594 | A | ATG | 43 | a0001c0001t0001g0047 a0001c0001t0001g0070 a0001c0001t0001g0096 others(40): Show |
44 | HG01081.hp1 HG01258.hp2 HG01361.hp1 others(41): Show |
intron_variant | MODIFIER | c.547+442_547+443dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTG | 67 | a0001c0001t0001g0133 a0001c0001t0001g0136 a0001c0001t0001g0137 others(64): Show |
70 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.547+440_547+443dup others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTGTG | 47 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0002g0008 others(44): Show |
50 | HG00673.hp1 HG01081.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.547+438_547+443dup others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTGTGT others(1): Show |
15 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0068 others(12): Show |
15 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(12): Show |
intron_variant | MODIFIER | c.547+436_547+443dup others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTGTGT others(3): Show |
6 | a0001c0001t0002g0082 a0001c0001t0002g0209 a0001c0001t0002g0328 others(3): Show |
6 | HG01070.hp1 HG02559.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+434_547+443dup others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0002g0220 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.547+432_547+443dup others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | A | ATGTGTGT others(9): Show |
2 | a0001c0001t0002g0087 a0002c0003t0001g0032 |
2 | HG03130.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.547+428_547+443dup others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | ATG | A | 55 | a0001c0001t0001g0031 a0001c0001t0001g0361 a0001c0001t0003g0025 others(52): Show |
61 | HG00597.hp1 HG01168.hp1 HG01169.hp2 others(58): Show |
intron_variant | MODIFIER | c.547+442_547+443del others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | ATGTG | A | 4 | a0001c0001t0001g0225 a0001c0001t0001g0261 a0001c0001t0003g0239 others(1): Show |
4 | HG00408.hp2 HG01069.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+440_547+443del others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831594 | ATGTGTGT others(5): Show |
A | 4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+432_547+443del others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831594 | ||||||
| chr2:170831628 | GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0002g0097 a0001c0001t0002g0099 a0001c0001t0002g0134 others(1): Show |
4 | HG02027.hp2 HG02155.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+438_547+445del others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831628 | ||||||
| chr2:170831634 | G | A | 6 | a0001c0004t0001g0217 a0001c0004t0001g0253 a0001c0004t0001g0254 others(3): Show |
6 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+442G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831634 | |||||||
| chr2:170831634 | G | GTA | 4 | a0001c0002t0001g0013 a0001c0002t0001g0017 a0001c0002t0001g0152 others(1): Show |
5 | HG00323.hp1 HG00621.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+447_547+448dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTA | 2 | a0001c0001t0001g0002 a0001c0001t0001g0012 |
5 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTGT others(3): Show |
1 | a0001c0001t0001g0002 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTGT others(5): Show |
4 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0176 others(1): Show |
4 | HG02647.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTGT others(7): Show |
1 | a0001c0004t0001g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTGT others(9): Show |
5 | a0001c0001t0001g0235 a0001c0004t0001g0125 a0001c0004t0001g0211 others(2): Show |
5 | HG00733.hp2 HG02809.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+443_547+444ins others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831634 | G | GTGTGTGT others(11): Show |
1 | a0001c0004t0001g0234 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.547+443_547+444ins others(18): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831634 | ||||||
| chr2:170831636 | A | G | 78 | a0001c0001t0001g0318 a0001c0001t0002g0008 a0001c0001t0002g0033 others(75): Show |
81 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.547+444A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831636 | |||||||
| chr2:170831682 | TAATA | T | 6 | a0001c0001t0001g0091 a0001c0001t0001g0280 a0001c0001t0007g0029 others(3): Show |
7 | HG01099.hp1 HG01346.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.547+500_547+503del others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831682 | ||||||
| chr2:170831725 | T | TAA | 23 | a0001c0001t0001g0235 a0001c0001t0006g0242 a0001c0001t0006g0243 others(20): Show |
23 | HG00733.hp2 HG01261.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.547+535_547+536dup others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831725 | ||||||
| chr2:170831759 | AAATATTT others(6): Show |
A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+579_547+591del others(13): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170831759 | ||||||
| chr2:170831862 | T | C | 2 | a0001c0001t0003g0291 a0001c0001t0003g0345 |
2 | HG02132.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.547+670T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170831862 | |||||||
| chr2:170832083 | C | G | 66 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0237 others(63): Show |
75 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.547+891C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832083 | |||||||
| chr2:170832083 | C | T | 2 | a0001c0002t0002g0040 a0001c0002t0002g0266 |
2 | HG02056.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.547+891C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832083 | |||||||
| chr2:170832093 | C | T | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+901C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832093 | |||||||
| chr2:170832250 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.547+1058C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832250 | |||||||
| chr2:170832257 | T | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0077 |
2 | HG01255.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.547+1065T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832257 | |||||||
| chr2:170832311 | G | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1119G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832311 | |||||||
| chr2:170832313 | T | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1121T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832313 | |||||||
| chr2:170832315 | T | G | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1123T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832315 | |||||||
| chr2:170832316 | T | G | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1124T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832316 | |||||||
| chr2:170832317 | G | T | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1125G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832317 | |||||||
| chr2:170832341 | G | C | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1149G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832341 | |||||||
| chr2:170832342 | C | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1150C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832342 | |||||||
| chr2:170832344 | T | C | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1152T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832344 | |||||||
| chr2:170832345 | G | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1153G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832345 | |||||||
| chr2:170832346 | T | G | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1154T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832346 | |||||||
| chr2:170832350 | T | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1158T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832350 | |||||||
| chr2:170832355 | C | T | 17 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1163C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832355 | |||||||
| chr2:170832381 | A | C | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1189A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832381 | |||||||
| chr2:170832383 | G | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1191G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832383 | |||||||
| chr2:170832391 | T | G | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1199T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832391 | |||||||
| chr2:170832404 | T | A | 1 | a0001c0002t0002g0074 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.547+1212T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832404 | |||||||
| chr2:170832651 | TGC | T | 9 | a0001c0001t0001g0031 a0001c0001t0002g0069 a0001c0001t0002g0174 others(6): Show |
9 | HG00323.hp1 HG01074.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.547+1472_547+1473d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832651 | ||||||
| chr2:170832653 | C | T | 1 | a0001c0002t0001g0004 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.547+1461C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832653 | |||||||
| chr2:170832656 | GCGCGCGC others(5): Show |
G | 17 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1466_547+1477d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832656 | ||||||
| chr2:170832658 | G | A | 1 | a0001c0002t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.547+1466G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832658 | |||||||
| chr2:170832660 | G | GCACA | 3 | a0001c0001t0001g0222 a0001c0001t0003g0021 a0001c0002t0001g0034 |
3 | HG00621.hp1 NA19084.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.547+1469_547+1470i others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832660 | G | GCACACA | 22 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0258 others(19): Show |
23 | HG00438.hp2 HG02074.hp2 HG03704.hp2 others(20): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832660 | G | GCACACAC others(1): Show |
9 | a0001c0001t0001g0179 a0001c0001t0001g0219 a0001c0001t0003g0021 others(6): Show |
9 | HG00544.hp2 HG00609.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832660 | G | GCACACAC others(3): Show |
4 | a0001c0001t0001g0259 a0001c0002t0002g0006 a0001c0002t0002g0059 others(1): Show |
4 | HG02083.hp1 NA18984.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.547+1469_547+1470i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832660 | GCGCGCAC others(3): Show |
G | 9 | a0001c0001t0001g0235 a0001c0001t0002g0081 a0001c0001t0002g0086 others(6): Show |
9 | HG00673.hp1 HG00733.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.547+1470_547+1479d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832660 | GCGCGCAC others(5): Show |
G | 67 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(64): Show |
71 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.547+1470_547+1481d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832660 | ||||||
| chr2:170832661 | C | T | 2 | a0001c0002t0001g0160 a0001c0002t0001g0192 |
2 | HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.547+1469C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832661 | |||||||
| chr2:170832662 | G | A | 36 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(33): Show |
39 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.547+1470G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832662 | |||||||
| chr2:170832662 | G | GCA | 17 | a0001c0001t0001g0319 a0001c0001t0003g0028 a0001c0001t0003g0288 others(14): Show |
17 | HG00140.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | G | GCACA | 20 | a0001c0001t0001g0080 a0001c0001t0001g0321 a0001c0001t0001g0342 others(17): Show |
24 | HG00544.hp1 HG00609.hp1 HG01167.hp1 others(21): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | G | GCACACA | 14 | a0001c0001t0001g0070 a0001c0001t0001g0185 a0001c0001t0001g0290 others(11): Show |
15 | HG01192.hp2 HG01256.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | G | GCACACAC others(1): Show |
6 | a0001c0001t0003g0314 a0001c0001t0003g0316 a0001c0002t0001g0037 others(3): Show |
6 | HG01943.hp2 HG02074.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.547+1471_547+1472i others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | G | GCACACAC others(3): Show |
2 | a0001c0002t0001g0052 a0001c0002t0001g0186 |
2 | HG01123.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.547+1471_547+1472i others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | GCGCA | G | 34 | a0001c0001t0001g0173 a0001c0001t0001g0218 a0001c0001t0002g0087 others(31): Show |
39 | HG00140.hp2 HG00423.hp1 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.547+1472_547+1475d others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | GCGCACA | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(110): Show |
129 | HG00280.hp1 HG00408.hp2 HG00597.hp1 others(126): Show |
intron_variant | MODIFIER | c.547+1472_547+1477d others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | GCGCACAC others(1): Show |
G | 5 | a0001c0001t0001g0304 a0001c0001t0001g0347 a0001c0001t0003g0249 others(2): Show |
5 | HG00438.hp1 HG02132.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+1472_547+1479d others(10): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832662 | GCGCACAC others(3): Show |
G | 2 | a0001c0001t0004g0348 a0001c0002t0001g0167 |
2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.547+1472_547+1481d others(12): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832662 | ||||||
| chr2:170832664 | G | A | 112 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0136 others(109): Show |
124 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.547+1472G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832664 | |||||||
| chr2:170832664 | G | GCA | 3 | a0001c0001t0002g0213 a0002c0003t0001g0349 a0002c0003t0001g0354 |
3 | HG03516.hp1 HG03516.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.547+1503_547+1504d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832664 | ||||||
| chr2:170832664 | G | GCACACAC others(5): Show |
1 | a0001c0001t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.547+1493_547+1504d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170832664 | ||||||
| chr2:170832672 | A | G | 17 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(14): Show |
17 | HG01884.hp1 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.547+1480A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832672 | |||||||
| chr2:170832691 | C | G | 5 | a0001c0001t0002g0033 a0001c0001t0002g0050 a0001c0001t0002g0066 others(2): Show |
5 | NA18941.hp2 NA18959.hp2 NA19080.hp1 others(2): Show |
intron_variant | MODIFIER | c.547+1499C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832691 | |||||||
| chr2:170832853 | G | A | 89 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(86): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+1661G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832853 | |||||||
| chr2:170832911 | C | G | 141 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(138): Show |
163 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.547+1719C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170832911 | |||||||
| chr2:170833013 | G | C | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.547+1821G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833013 | |||||||
| chr2:170833126 | C | G | 32 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0003g0019 others(29): Show |
38 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.547+1934C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833126 | |||||||
| chr2:170833210 | G | T | 89 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(86): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+2018G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833210 | |||||||
| chr2:170833340 | A | C | 94 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(91): Show |
98 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.547+2148A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833340 | |||||||
| chr2:170833460 | A | G | 89 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(86): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.547+2268A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833460 | |||||||
| chr2:170833603 | C | T | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2411C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833603 | |||||||
| chr2:170833611 | T | C | 64 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0290 others(61): Show |
73 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.547+2419T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833611 | |||||||
| chr2:170833765 | G | A | 67 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.547+2573G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833765 | |||||||
| chr2:170833781 | G | A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.547+2589G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833781 | |||||||
| chr2:170833816 | TG | T | 214 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0031 others(211): Show |
245 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.547+2627delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170833816 | ||||||
| chr2:170833861 | G | A | 1 | a0001c0001t0003g0285 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.547+2669G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833861 | |||||||
| chr2:170833931 | C | T | 1 | a0003c0006t0002g0130 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.547+2739C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833931 | |||||||
| chr2:170833932 | G | A | 3 | a0001c0002t0001g0046 a0001c0002t0001g0076 a0001c0002t0001g0109 |
3 | HG02647.hp2 HG03540.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.547+2740G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833932 | |||||||
| chr2:170833954 | T | C | 152 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(149): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.547+2762T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170833954 | |||||||
| chr2:170834000 | C | CA | 52 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(49): Show |
56 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.548-2780dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834000 | ||||||
| chr2:170834000 | C | CAA | 6 | a0001c0001t0001g0235 a0001c0002t0001g0269 a0001c0004t0001g0211 others(3): Show |
6 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.548-2781_548-2780d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834000 | ||||||
| chr2:170834013 | AG | A | 4 | a0001c0001t0002g0087 a0001c0002t0002g0015 a0001c0002t0002g0074 others(1): Show |
4 | NA18959.hp1 NA18987.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.548-2779delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834013 | |||||||
| chr2:170834014 | G | A | 93 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(90): Show |
96 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.548-2779G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834014 | |||||||
| chr2:170834221 | C | T | 1 | a0001c0001t0003g0297 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.548-2572C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834221 | |||||||
| chr2:170834314 | G | A | 67 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(64): Show |
70 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.548-2479G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834314 | |||||||
| chr2:170834451 | TAAAAG | T | 89 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(86): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.548-2340_548-2336d others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834451 | ||||||
| chr2:170834571 | C | T | 1 | a0001c0001t0003g0315 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.548-2222C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834571 | |||||||
| chr2:170834592 | T | A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-2201T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834592 | |||||||
| chr2:170834765 | C | CT | 11 | a0001c0001t0001g0133 a0001c0001t0001g0173 a0001c0001t0001g0208 others(8): Show |
13 | HG01928.hp1 HG01975.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.548-2011dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | ||||||
| chr2:170834765 | CT | C | 73 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(70): Show |
77 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.548-2011delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | ||||||
| chr2:170834765 | CTT | C | 65 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(62): Show |
68 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.548-2012_548-2011d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170834765 | ||||||
| chr2:170834824 | G | A | 1 | a0001c0001t0008g0355 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.548-1969G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834824 | |||||||
| chr2:170834825 | C | A | 1 | a0001c0001t0008g0355 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.548-1968C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834825 | |||||||
| chr2:170834987 | G | C | 1 | a0001c0001t0002g0141 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.548-1806G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170834987 | |||||||
| chr2:170835181 | T | A | 13 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(10): Show |
13 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.548-1612T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835181 | |||||||
| chr2:170835203 | T | A | 1 | a0001c0001t0002g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.548-1590T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835203 | |||||||
| chr2:170835204 | A | T | 1 | a0001c0001t0002g0101 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.548-1589A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835204 | |||||||
| chr2:170835213 | T | A | 93 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.548-1580T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835213 | |||||||
| chr2:170835219 | A | G | 89 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(86): Show |
92 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.548-1574A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835219 | |||||||
| chr2:170835279 | T | C | 1 | a0001c0013t0001g0124 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.548-1514T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835279 | |||||||
| chr2:170835292 | A | T | 1 | a0001c0002t0001g0108 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.548-1501A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835292 | |||||||
| chr2:170835314 | T | C | 1 | a0001c0002t0001g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.548-1479T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835314 | |||||||
| chr2:170835347 | G | A | 93 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.548-1446G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835347 | |||||||
| chr2:170835417 | A | G | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-1376A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835417 | |||||||
| chr2:170835469 | T | C | 7 | a0001c0001t0004g0175 a0001c0001t0004g0210 a0001c0001t0004g0278 others(4): Show |
7 | HG01884.hp2 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.548-1324T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835469 | |||||||
| chr2:170835490 | C | T | 1 | a0001c0002t0002g0110 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.548-1303C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835490 | |||||||
| chr2:170835577 | T | A | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.548-1216T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835577 | |||||||
| chr2:170835779 | A | G | 1 | a0001c0001t0002g0087 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.548-1014A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835779 | |||||||
| chr2:170835941 | A | T | 1 | a0001c0002t0002g0040 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.548-852A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835941 | |||||||
| chr2:170835978 | G | A | 1 | a0001c0002t0001g0171 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.548-815G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170835978 | |||||||
| chr2:170836111 | C | CT | 6 | a0001c0001t0002g0095 a0001c0001t0003g0214 a0001c0001t0006g0242 others(3): Show |
6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.548-669dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr2 | 170836111 | ||||||
| chr2:170836259 | A | T | 4 | a0001c0002t0001g0062 a0001c0002t0001g0072 a0001c0002t0001g0073 others(1): Show |
4 | HG02155.hp2 HG03704.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.548-534A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836259 | |||||||
| chr2:170836302 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.548-491A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836302 | |||||||
| chr2:170836314 | T | C | 1 | a0001c0002t0001g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.548-479T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836314 | |||||||
| chr2:170836485 | T | C | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.548-308T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836485 | |||||||
| chr2:170836508 | A | G | 1 | a0001c0001t0004g0281 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.548-285A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836508 | |||||||
| chr2:170836574 | T | G | 1 | a0001c0002t0001g0206 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.548-219T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 5/16 | chr2 | 170836574 | |||||||
| chr2:170836945 | A | C | 75 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(72): Show |
78 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.638+62A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170836945 | |||||||
| chr2:170836987 | T | C | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.638+104T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170836987 | |||||||
| chr2:170837054 | A | G | 1 | a0001c0004t0001g0363 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.638+171A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837054 | |||||||
| chr2:170837129 | C | G | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+246C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837129 | |||||||
| chr2:170837198 | G | C | 79 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(76): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.638+315G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837198 | |||||||
| chr2:170837264 | T | C | 1 | a0001c0001t0001g0318 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.638+381T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837264 | |||||||
| chr2:170837554 | A | G | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+671A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837554 | |||||||
| chr2:170837596 | AG | A | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+717delG | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170837596 | ||||||
| chr2:170837655 | T | G | 3 | a0001c0001t0002g0049 a0001c0001t0002g0069 a0001c0001t0008g0276 |
3 | HG01081.hp2 HG01109.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.638+772T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837655 | |||||||
| chr2:170837719 | T | C | 1 | a0001c0001t0002g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.638+836T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170837719 | |||||||
| chr2:170838182 | C | T | 1 | a0001c0001t0018g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+1299C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838182 | |||||||
| chr2:170838560 | A | G | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+1677A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838560 | |||||||
| chr2:170838805 | C | T | 6 | a0001c0002t0001g0038 a0001c0002t0001g0054 a0001c0002t0001g0057 others(3): Show |
6 | NA18975.hp1 NA18983.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+1922C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838805 | |||||||
| chr2:170838877 | T | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+1994T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170838877 | |||||||
| chr2:170839006 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0233 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.638+2123A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839006 | |||||||
| chr2:170839142 | T | C | 1 | a0001c0001t0004g0348 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.638+2259T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839142 | |||||||
| chr2:170839149 | G | A | 1 | a0001c0001t0002g0141 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.638+2266G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839149 | |||||||
| chr2:170839340 | T | C | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2457T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839340 | |||||||
| chr2:170839352 | C | T | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+2469C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839352 | |||||||
| chr2:170839613 | C | CA | 16 | a0001c0001t0001g0126 a0001c0001t0001g0179 a0001c0001t0003g0247 others(13): Show |
16 | HG00597.hp2 HG02027.hp1 HG02148.hp2 others(13): Show |
intron_variant | MODIFIER | c.638+2747dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839613 | ||||||
| chr2:170839613 | CA | C | 6 | a0001c0001t0001g0342 a0001c0001t0002g0049 a0001c0001t0002g0182 others(3): Show |
6 | HG01081.hp2 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.638+2747delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839613 | ||||||
| chr2:170839633 | T | A | 1 | a0001c0001t0018g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.638+2750T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839633 | |||||||
| chr2:170839655 | T | C | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2772T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839655 | |||||||
| chr2:170839677 | AT | A | 5 | a0001c0001t0001g0235 a0001c0004t0001g0211 a0001c0004t0001g0234 others(2): Show |
5 | HG00733.hp2 HG01261.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.638+2795delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839677 | |||||||
| chr2:170839679 | ATTC | A | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2804_638+2806d others(5): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170839679 | ||||||
| chr2:170839696 | C | T | 1 | a0001c0001t0003g0344 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.638+2813C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839696 | |||||||
| chr2:170839721 | G | C | 54 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(51): Show |
59 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.638+2838G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839721 | |||||||
| chr2:170839962 | T | C | 152 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(149): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.638+3079T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170839962 | |||||||
| chr2:170840081 | G | A | 6 | a0001c0002t0001g0038 a0001c0002t0001g0054 a0001c0002t0001g0057 others(3): Show |
6 | NA18975.hp1 NA18983.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.638+3198G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840081 | |||||||
| chr2:170840173 | C | T | 43 | a0001c0001t0001g0096 a0001c0001t0001g0225 a0001c0001t0001g0261 others(40): Show |
47 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.638+3290C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840173 | |||||||
| chr2:170840189 | G | A | 2 | a0001c0001t0003g0022 a0001c0002t0001g0231 |
3 | NA18942.hp2 NA18978.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.638+3306G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840189 | |||||||
| chr2:170840270 | A | G | 148 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(145): Show |
155 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.638+3387A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840270 | |||||||
| chr2:170840508 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.639-3537C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840508 | |||||||
| chr2:170840597 | A | G | 2 | a0001c0001t0001g0031 a0001c0001t0001g0216 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.639-3448A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840597 | |||||||
| chr2:170840643 | A | G | 105 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(102): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.639-3402A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840643 | |||||||
| chr2:170840658 | A | AAGGGAGG others(5): Show |
1 | a0001c0001t0002g0331 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.639-3373_639-3362d others(14): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | ||||||
| chr2:170840658 | A | AAGGGAGG others(14): Show |
4 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(1): Show |
4 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.639-3380_639-3379i others(23): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | ||||||
| chr2:170840658 | A | AAGGGAGG others(18): Show |
77 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(74): Show |
80 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.639-3380_639-3379i others(27): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | ||||||
| chr2:170840658 | A | AAGGGAGG others(22): Show |
1 | a0001c0002t0002g0265 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.639-3380_639-3379i others(31): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170840658 | ||||||
| chr2:170840735 | C | A | 2 | a0001c0001t0002g0277 a0001c0001t0018g0273 |
2 | HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.639-3310C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170840735 | |||||||
| chr2:170841015 | G | A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-3030G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841015 | |||||||
| chr2:170841054 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-2991C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841054 | |||||||
| chr2:170841195 | A | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(79): Show |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-2850A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841195 | |||||||
| chr2:170841285 | T | C | 16 | a0001c0001t0001g0235 a0001c0001t0007g0029 a0001c0001t0007g0367 others(13): Show |
17 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.639-2760T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841285 | |||||||
| chr2:170841531 | T | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.639-2514T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841531 | |||||||
| chr2:170841539 | CAAAAT | C | 82 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(79): Show |
100 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.639-2492_639-2488d others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170841539 | ||||||
| chr2:170841741 | G | C | 16 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0082 others(13): Show |
16 | HG00280.hp2 HG00323.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.639-2304G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841741 | |||||||
| chr2:170841836 | A | G | 1 | a0001c0001t0018g0273 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.639-2209A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170841836 | |||||||
| chr2:170842124 | T | G | 3 | a0001c0001t0001g0346 a0001c0001t0001g0350 a0001c0001t0004g0348 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.639-1921T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842124 | |||||||
| chr2:170842162 | T | C | 90 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(87): Show |
93 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.639-1883T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842162 | |||||||
| chr2:170842255 | C | G | 1 | a0001c0001t0004g0348 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.639-1790C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842255 | |||||||
| chr2:170842309 | C | T | 6 | a0001c0001t0004g0175 a0001c0001t0004g0210 a0001c0001t0004g0278 others(3): Show |
6 | HG01884.hp2 HG03139.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.639-1736C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842309 | |||||||
| chr2:170842664 | C | T | 1 | a0001c0002t0017g0121 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.639-1381C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842664 | |||||||
| chr2:170842808 | T | G | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.639-1237T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842808 | |||||||
| chr2:170842889 | T | A | 83 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(80): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.639-1156T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842889 | |||||||
| chr2:170842896 | T | C | 1 | a0001c0001t0003g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.639-1149T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170842896 | |||||||
| chr2:170843047 | G | A | 2 | a0001c0001t0002g0181 a0001c0001t0002g0182 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.639-998G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843047 | |||||||
| chr2:170843182 | C | T | 1 | a0001c0001t0003g0297 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.639-863C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843182 | |||||||
| chr2:170843612 | C | A | 6 | a0001c0002t0001g0017 a0001c0002t0001g0171 a0001c0002t0001g0194 others(3): Show |
7 | HG00621.hp2 HG02056.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.639-433C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843612 | |||||||
| chr2:170843619 | C | CT | 8 | a0001c0001t0001g0222 a0001c0001t0001g0290 a0001c0001t0001g0353 others(5): Show |
9 | HG00621.hp1 HG02280.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.639-408dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | ||||||
| chr2:170843619 | CT | C | 111 | a0001c0001t0001g0031 a0001c0001t0001g0183 a0001c0001t0001g0216 others(108): Show |
114 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.639-408delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | ||||||
| chr2:170843619 | CTT | C | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0257 others(4): Show |
8 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.639-409_639-408del others(2): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chr2 | 170843619 | ||||||
| chr2:170843849 | C | T | 79 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(76): Show |
82 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.639-196C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170843849 | |||||||
| chr2:170844036 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.639-9C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 6/16 | chr2 | 170844036 | |||||||
| chr2:170844159 | T | G | 1 | a0001c0001t0004g0210 | 1 | HG03540.hp2 | splice_donor_variant&intron_variant | HIGH | c.751+2T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844159 | |||||||
| chr2:170844219 | G | A | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.751+62G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844219 | |||||||
| chr2:170844248 | A | AT | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.751+99dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844248 | ||||||
| chr2:170844291 | G | C | 1 | a0001c0002t0001g0106 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.751+134G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844291 | |||||||
| chr2:170844298 | A | G | 1 | a0001c0001t0004g0210 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.751+141A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844298 | |||||||
| chr2:170844394 | T | C | 2 | a0001c0001t0001g0070 a0001c0001t0001g0080 |
2 | HG01243.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.751+237T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844394 | |||||||
| chr2:170844407 | C | CT | 14 | a0001c0001t0003g0284 a0001c0001t0003g0296 a0001c0001t0003g0297 others(11): Show |
15 | HG00280.hp1 HG00621.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.751+269dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844407 | ||||||
| chr2:170844407 | CT | C | 87 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(84): Show |
91 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.751+269delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr2 | 170844407 | ||||||
| chr2:170844425 | T | C | 1 | a0001c0001t0002g0209 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.751+268T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844425 | |||||||
| chr2:170844426 | T | G | 1 | a0004c0012t0001g0180 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.751+269T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844426 | |||||||
| chr2:170844506 | T | C | 1 | a0001c0001t0003g0292 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.751+349T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170844506 | |||||||
| chr2:170845220 | C | T | 2 | a0001c0002t0001g0046 a0001c0002t0001g0063 |
2 | NA18982.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.752-286C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845220 | |||||||
| chr2:170845253 | G | C | 1 | a0001c0001t0003g0308 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.752-253G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845253 | |||||||
| chr2:170845254 | C | G | 152 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(149): Show |
160 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.752-252C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845254 | |||||||
| chr2:170845276 | C | T | 1 | a0001c0001t0003g0341 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.752-230C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 7/16 | chr2 | 170845276 | |||||||
| chr2:170845665 | G | A | 2 | a0001c0001t0001g0290 a0001c0001t0001g0342 |
2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.868-41G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 8/16 | chr2 | 170845665 | |||||||
| chr2:170845970 | C | T | 105 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(102): Show |
109 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.948-39C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 9/16 | chr2 | 170845970 | |||||||
| chr2:170846075 | G | A | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1002+12G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846075 | |||||||
| chr2:170846362 | G | A | 1 | a0001c0002t0006g0190 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1002+299G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846362 | |||||||
| chr2:170846368 | T | C | 1 | a0002c0003t0001g0366 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1002+305T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846368 | |||||||
| chr2:170846450 | G | A | 71 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(68): Show |
74 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(71): Show |
intron_variant | MODIFIER | c.1002+387G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846450 | |||||||
| chr2:170846831 | C | A | 10 | a0001c0001t0001g0226 a0001c0001t0003g0214 a0001c0001t0003g0245 others(7): Show |
12 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.1002+768C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170846831 | |||||||
| chr2:170847010 | A | T | 1 | a0001c0001t0002g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1003-666A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847010 | |||||||
| chr2:170847110 | C | A | 1 | a0001c0002t0001g0156 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1003-566C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847110 | |||||||
| chr2:170847167 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1003-509C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847167 | |||||||
| chr2:170847174 | A | G | 1 | a0001c0002t0001g0042 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1003-502A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | chr2 | 170847174 | |||||||
| chr2:170847406 | A | ACAGAATT others(321): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0216 |
2 | HG02486.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1003-259_1003-258i others(330): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr2 | 170847406 | ||||||
| chr2:170847875 | G | A | 1 | a0001c0001t0003g0027 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1119+83G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170847875 | |||||||
| chr2:170847886 | C | G | 1 | a0004c0012t0001g0180 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1119+94C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170847886 | |||||||
| chr2:170848009 | C | T | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1119+217C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848009 | |||||||
| chr2:170848259 | C | T | 1 | a0001c0002t0001g0056 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1119+467C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848259 | |||||||
| chr2:170848436 | G | A | 1 | a0001c0002t0001g0113 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1119+644G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848436 | |||||||
| chr2:170848454 | G | A | 1 | a0001c0001t0002g0351 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1119+662G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848454 | |||||||
| chr2:170848456 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1119+664C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848456 | |||||||
| chr2:170848496 | C | CA | 59 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0179 others(56): Show |
64 | HG00438.hp2 HG00544.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.1119+720dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 170848496 | ||||||
| chr2:170848496 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1119+704C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848496 | |||||||
| chr2:170848507 | A | G | 1 | a0002c0003t0001g0337 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1119+715A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848507 | |||||||
| chr2:170848647 | AT | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(81): Show |
102 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1120-628delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr2 | 170848647 | ||||||
| chr2:170848936 | C | T | 3 | a0002c0003t0001g0005 a0002c0003t0001g0349 a0002c0003t0001g0354 |
5 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1120-350C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 11/16 | chr2 | 170848936 | |||||||
| chr2:170849355 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01074.hp1 | splice_region_variant&intron_variant | LOW | c.1184+5C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849355 | |||||||
| chr2:170849669 | T | C | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1184+319T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849669 | |||||||
| chr2:170849677 | T | C | 1 | a0001c0001t0001g0353 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1184+327T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849677 | |||||||
| chr2:170849737 | A | T | 83 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(80): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+387A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170849737 | |||||||
| chr2:170850036 | G | A | 2 | a0001c0001t0003g0339 a0001c0002t0001g0037 |
2 | NA18990.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.1184+686G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850036 | |||||||
| chr2:170850269 | C | T | 1 | a0001c0004t0001g0274 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1184+919C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850269 | |||||||
| chr2:170850275 | A | G | 7 | a0001c0001t0001g0126 a0001c0001t0001g0128 a0001c0001t0003g0249 others(4): Show |
7 | HG00597.hp2 HG01981.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1184+925A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850275 | |||||||
| chr2:170850487 | G | C | 1 | a0001c0004t0001g0217 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1184+1137G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850487 | |||||||
| chr2:170850585 | G | T | 1 | a0002c0003t0005g0303 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1184+1235G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850585 | |||||||
| chr2:170850619 | A | G | 1 | a0001c0002t0001g0232 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1184+1269A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850619 | |||||||
| chr2:170850733 | A | C | 83 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(80): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.1184+1383A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850733 | |||||||
| chr2:170850839 | C | A | 1 | a0001c0001t0003g0344 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1184+1489C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170850839 | |||||||
| chr2:170851024 | G | GA | 11 | a0001c0001t0001g0235 a0001c0004t0001g0122 a0001c0004t0001g0123 others(8): Show |
11 | HG00733.hp2 HG01261.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1185-1680dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 170851024 | ||||||
| chr2:170851024 | GA | G | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1185-1680delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr2 | 170851024 | ||||||
| chr2:170851376 | C | A | 4 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0205 others(1): Show |
4 | HG01081.hp1 HG02735.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.1185-1338C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851376 | |||||||
| chr2:170851384 | T | C | 1 | a0001c0002t0001g0037 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1185-1330T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851384 | |||||||
| chr2:170851537 | A | G | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1185-1177A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851537 | |||||||
| chr2:170851590 | G | A | 39 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0290 others(36): Show |
45 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1185-1124G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170851590 | |||||||
| chr2:170852289 | A | G | 1 | a0001c0002t0001g0060 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1185-425A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852289 | |||||||
| chr2:170852331 | G | A | 1 | a0001c0002t0001g0159 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1185-383G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852331 | |||||||
| chr2:170852474 | T | C | 6 | a0002c0003t0001g0354 a0002c0005t0005g0011 a0002c0005t0005g0168 others(3): Show |
7 | HG02109.hp2 HG02258.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1185-240T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852474 | |||||||
| chr2:170852505 | G | T | 1 | a0001c0002t0001g0207 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1185-209G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852505 | |||||||
| chr2:170852550 | C | T | 3 | a0001c0002t0001g0076 a0001c0002t0001g0109 a0001c0002t0002g0045 |
3 | HG02647.hp2 HG03540.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.1185-164C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 12/16 | chr2 | 170852550 | |||||||
| chr2:170852861 | G | T | 1 | a0001c0001t0004g0348 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1263+69G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852861 | |||||||
| chr2:170852920 | A | G | 111 | a0001c0001t0001g0235 a0001c0001t0002g0008 a0001c0001t0002g0033 others(108): Show |
116 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.1263+128A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852920 | |||||||
| chr2:170852937 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1263+145C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852937 | |||||||
| chr2:170852997 | T | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1263+205T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170852997 | |||||||
| chr2:170853011 | G | A | 49 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(46): Show |
52 | HG00408.hp1 HG00423.hp2 HG00673.hp1 others(49): Show |
intron_variant | MODIFIER | c.1263+219G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853011 | |||||||
| chr2:170853174 | T | C | 4 | a0001c0001t0001g0173 a0001c0001t0001g0208 a0001c0001t0001g0233 others(1): Show |
4 | HG02109.hp1 HG02970.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1263+382T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853174 | |||||||
| chr2:170853443 | T | A | 1 | a0001c0001t0003g0284 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1264-430T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853443 | |||||||
| chr2:170853489 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1264-384C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853489 | |||||||
| chr2:170853490 | G | A | 1 | a0001c0001t0004g0278 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1264-383G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853490 | |||||||
| chr2:170853633 | G | C | 1 | a0001c0001t0003g0288 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1264-240G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 13/16 | chr2 | 170853633 | |||||||
| chr2:170854044 | A | G | 2 | a0002c0003t0001g0317 a0002c0003t0001g0323 |
2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1413+22A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854044 | |||||||
| chr2:170854298 | T | C | 2 | a0002c0003t0001g0317 a0002c0003t0001g0323 |
2 | HG02055.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1413+276T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854298 | |||||||
| chr2:170854330 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1413+308A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854330 | |||||||
| chr2:170854353 | A | T | 2 | a0001c0001t0001g0047 a0001c0002t0001g0272 |
2 | HG01243.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1413+331A>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854353 | |||||||
| chr2:170854393 | A | C | 1 | a0001c0001t0002g0141 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1413+371A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854393 | |||||||
| chr2:170854397 | C | CT | 28 | a0001c0001t0001g0047 a0001c0001t0001g0183 a0001c0001t0001g0185 others(25): Show |
28 | HG00597.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.1413+396dupT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170854397 | ||||||
| chr2:170854397 | CT | C | 30 | a0001c0001t0001g0235 a0001c0001t0001g0342 a0001c0001t0002g0094 others(27): Show |
31 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(28): Show |
intron_variant | MODIFIER | c.1413+396delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170854397 | ||||||
| chr2:170854652 | A | C | 1 | a0001c0001t0002g0330 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1413+630A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854652 | |||||||
| chr2:170854701 | G | A | 1 | a0002c0003t0001g0366 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1413+679G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170854701 | |||||||
| chr2:170855075 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1413+1053A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855075 | |||||||
| chr2:170855098 | TCTAA | T | 4 | a0001c0001t0001g0183 a0001c0001t0001g0321 a0001c0001t0003g0370 others(1): Show |
4 | HG01255.hp1 HG02055.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1413+1082_1413+108 others(8): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855098 | ||||||
| chr2:170855112 | AAAC | A | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1413+1096_1413+109 others(7): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855112 | ||||||
| chr2:170855209 | CT | C | 14 | a0001c0001t0001g0136 a0001c0001t0002g0048 a0001c0001t0002g0094 others(11): Show |
15 | HG01074.hp1 HG01346.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.1413+1205delT | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855209 | ||||||
| chr2:170855271 | C | T | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1413+1249C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855271 | |||||||
| chr2:170855346 | T | A | 1 | a0001c0001t0003g0310 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1413+1324T>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855346 | |||||||
| chr2:170855540 | T | C | 2 | a0001c0001t0001g0333 a0001c0001t0001g0353 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1414-1478T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855540 | |||||||
| chr2:170855585 | T | C | 7 | a0001c0004t0001g0217 a0001c0004t0001g0252 a0001c0004t0001g0253 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1414-1433T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855585 | |||||||
| chr2:170855649 | C | T | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1414-1369C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855649 | |||||||
| chr2:170855673 | G | A | 97 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0002g0008 others(94): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1414-1345G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855673 | |||||||
| chr2:170855872 | C | CA | 54 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0001g0179 others(51): Show |
60 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1414-1123dupA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | ||||||
| chr2:170855872 | CA | C | 64 | a0001c0001t0001g0259 a0001c0001t0002g0008 a0001c0001t0002g0033 others(61): Show |
66 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.1414-1123delA | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | ||||||
| chr2:170855872 | CAA | C | 22 | a0001c0001t0001g0237 a0001c0001t0002g0048 a0001c0001t0002g0094 others(19): Show |
23 | HG00733.hp2 HG01261.hp2 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.1414-1124_1414-112 others(6): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | ||||||
| chr2:170855872 | CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0003g0293 a0004c0012t0001g0180 |
2 | HG01516.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1414-1134_1414-112 others(16): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | ||||||
| chr2:170855872 | CAAAAAAA others(6): Show |
C | 148 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0047 others(145): Show |
171 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.1414-1135_1414-112 others(17): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr2 | 170855872 | ||||||
| chr2:170855925 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1414-1093C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855925 | |||||||
| chr2:170855926 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1414-1092G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170855926 | |||||||
| chr2:170856055 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1414-963A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856055 | |||||||
| chr2:170856069 | T | G | 1 | a0001c0001t0002g0213 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1414-949T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856069 | |||||||
| chr2:170856094 | G | T | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-924G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856094 | |||||||
| chr2:170856164 | T | C | 4 | a0001c0001t0007g0029 a0001c0001t0007g0367 a0001c0001t0012g0311 others(1): Show |
5 | HG01346.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1414-854T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856164 | |||||||
| chr2:170856178 | C | G | 93 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0002g0008 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1414-840C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856178 | |||||||
| chr2:170856211 | C | T | 1 | a0001c0002t0001g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1414-807C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856211 | |||||||
| chr2:170856386 | T | C | 1 | a0001c0002t0001g0039 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1414-632T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856386 | |||||||
| chr2:170856634 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1414-384T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856634 | |||||||
| chr2:170856641 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1414-377A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856641 | |||||||
| chr2:170856766 | C | T | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.1414-252C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856766 | |||||||
| chr2:170856798 | T | C | 2 | a0001c0002t0001g0076 a0001c0002t0001g0109 |
2 | HG02647.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1414-220T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 14/16 | chr2 | 170856798 | |||||||
| chr2:170857456 | G | T | 1 | a0001c0002t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1521+331G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857456 | |||||||
| chr2:170857532 | G | T | 3 | a0001c0001t0001g0346 a0001c0001t0001g0350 a0001c0001t0004g0348 |
3 | HG02630.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1521+407G>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857532 | |||||||
| chr2:170857569 | G | C | 37 | a0001c0001t0001g0096 a0001c0001t0001g0225 a0001c0001t0001g0261 others(34): Show |
41 | HG00408.hp2 HG00597.hp1 HG01069.hp2 others(38): Show |
intron_variant | MODIFIER | c.1521+444G>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857569 | |||||||
| chr2:170857589 | A | C | 1 | a0001c0001t0001g0136 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1521+464A>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857589 | |||||||
| chr2:170857625 | C | T | 1 | a0001c0001t0003g0358 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1521+500C>T | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857625 | |||||||
| chr2:170857936 | T | C | 1 | a0001c0002t0001g0167 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1521+811T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857936 | |||||||
| chr2:170857946 | T | C | 6 | a0001c0004t0001g0122 a0001c0004t0001g0123 a0001c0004t0001g0125 others(3): Show |
6 | HG02647.hp1 HG02809.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521+821T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170857946 | |||||||
| chr2:170858010 | C | A | 3 | a0001c0002t0001g0013 a0001c0002t0001g0152 a0001c0002t0001g0227 |
4 | HG00323.hp1 HG00738.hp2 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1522-794C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858010 | |||||||
| chr2:170858039 | CCA | C | 31 | a0001c0001t0001g0070 a0001c0001t0001g0080 a0001c0001t0003g0019 others(28): Show |
37 | HG00140.hp1 HG00544.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1522-764_1522-763d others(4): Show |
GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858039 | |||||||
| chr2:170858323 | T | G | 1 | a0001c0001t0002g0064 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1522-481T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858323 | |||||||
| chr2:170858340 | C | A | 6 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(3): Show |
6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1522-464C>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858340 | |||||||
| chr2:170858556 | T | G | 16 | a0001c0001t0002g0049 a0001c0001t0002g0069 a0001c0001t0002g0087 others(13): Show |
17 | HG00609.hp2 HG01081.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1522-248T>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858556 | |||||||
| chr2:170858572 | G | A | 1 | a0001c0001t0001g0280 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1522-232G>A | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858572 | |||||||
| chr2:170858623 | C | G | 96 | a0001c0001t0002g0008 a0001c0001t0002g0033 a0001c0001t0002g0048 others(93): Show |
101 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.1522-181C>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 15/16 | chr2 | 170858623 | |||||||
| chr2:170859252 | T | C | 6 | a0001c0001t0006g0242 a0001c0001t0006g0243 a0001c0001t0006g0244 others(3): Show |
6 | HG01884.hp1 HG02818.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1611+359T>C | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859252 | |||||||
| chr2:170859476 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1612-233A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859476 | |||||||
| chr2:170859610 | A | G | 22 | a0001c0001t0001g0346 a0001c0001t0001g0350 a0002c0003t0001g0005 others(19): Show |
25 | HG01891.hp2 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.1612-99A>G | GAD1 | ENSG00000128683.14 | transcript | ENST00000358196.8 | protein_coding | 16/16 | chr2 | 170859610 |