Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1390 |
| ensemblid | ENSG00000095794.21 |
| hgncid | 2352 |
| symbol | CREM |
| name | cAMP responsive element modulator |
| refseq_nuc | NM_183011.2 |
| refseq_prot | NP_898829.1 |
| ensembl_nuc | ENST00000685392.1 |
| ensembl_prot | ENSP00000509489.1 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 35126846 |
| end | 35212953 |
| strand | + |
| ver | v1.2 |
| region | chr10:35126846-35212953 |
| region5000 | chr10:35121846-35217953 |
| regionname0 | CREM_chr10_35126846_35212953 |
| regionname5000 | CREM_chr10_35121846_35217953 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 299 | 292 | 79 | 54 | 102 | 14 | 41 | 78 | CREM_chr10_35121846_35217953 | CREM | MSKCA others(294): Show |
chr10 | 35121846 | 35217953 |
| a0002 | 0/0 | 299 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | MSKCA others(294): Show |
chr10 | 35121846 | 35217953 |
| a0003 | 0/0 | 299 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | MSKCA others(294): Show |
chr10 | 35121846 | 35217953 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 897 | 277 | 69 | 49 | 102 | 14 | 41 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 | ||
| a0001c0002 | 0/0 | 897 | 12 | 9 | 3 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 | ||
| a0001c0003 | 0/0 | 897 | 2 | 1 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 | ||
| a0001c0004 | 0/0 | 897 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 | ||
| a0002c0006 | 0/0 | 897 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 | ||
| a0003c0005 | 0/0 | 897 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATGAG others(892): Show |
chr10 | 35121846 | 35217953 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2857 | 153 | 52 | 23 | 48 | 8 | 21 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0002 | 0/0 | 2856 | 72 | 6 | 14 | 40 | 5 | 7 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2851): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0003 | 0/0 | 2857 | 31 | 2 | 9 | 8 | 1 | 11 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0005 | 0/0 | 2857 | 4 | 4 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0006 | 0/0 | 2857 | 3 | 0 | 2 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0007 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2851): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0008 | 0/0 | 2857 | 2 | 0 | 0 | 0 | 0 | 2 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0009 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0010 | 0/1 | 2857 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0011 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0012 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0014 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0015 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0016 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2851): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0017 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0018 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0001t0019 | 0/0 | 2857 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0002t0004 | 0/0 | 2858 | 11 | 9 | 2 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2853): Show |
chr10 | 35121846 | 35217953 |
| a0001c0002t0020 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0001c0003t0002 | 0/0 | 2856 | 2 | 1 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2851): Show |
chr10 | 35121846 | 35217953 |
| a0001c0004t0013 | 0/0 | 2857 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0002c0006t0003 | 0/0 | 2857 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| a0003c0005t0001 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | ATTGT others(2852): Show |
chr10 | 35121846 | 35217953 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0002g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0003g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0005g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0006g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0006g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0007g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0007g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0008g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0009g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0010g0244 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0011g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0012g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0014g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0015g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0017g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0018g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0001t0019g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0004g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0002t0020g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0003t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0001c0004t0013g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0002c0006t0003g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| a0003c0005t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | GBR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0164 | EUR | GBR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0200 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0066 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00735 | hp1 | a0001 | c0001 | t0012 | g0273 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00738 | hp2 | a0001 | c0002 | t0004 | g0110 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01071 | hp1 | a0001 | c0002 | t0020 | g0290 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0042 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0117 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0034 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01261 | hp1 | a0001 | c0001 | t0006 | g0242 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0024 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0252 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0100 | EUR | IBS | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01891 | hp1 | a0001 | c0001 | t0015 | g0262 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01928 | hp2 | a0001 | c0001 | t0006 | g0241 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02257 | hp2 | a0001 | c0002 | t0004 | g0111 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0040 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02572 | hp2 | a0001 | c0002 | t0004 | g0289 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02615 | hp2 | a0001 | c0002 | t0004 | g0113 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0283 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02647 | hp1 | a0001 | c0002 | t0004 | g0114 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02723 | hp1 | a0001 | c0002 | t0004 | g0116 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0282 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02809 | hp1 | a0001 | c0002 | t0004 | g0112 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02895 | hp1 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0109 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02896 | hp2 | a0001 | c0001 | t0005 | g0002 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0115 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0126 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0021 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0039 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0011 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03486 | hp1 | a0001 | c0001 | t0018 | g0287 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0030 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03579 | hp2 | a0001 | c0003 | t0002 | g0043 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0025 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0106 | SAS | PJL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03834 | hp2 | a0001 | c0001 | t0008 | g0247 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0029 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04115 | hp2 | a0002 | c0006 | t0003 | g0032 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0033 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG04204 | hp2 | a0001 | c0001 | t0008 | g0245 | SAS | STU | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | CHB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18941 | hp2 | a0001 | c0001 | t0006 | g0145 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18959 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18960 | hp1 | a0001 | c0001 | t0014 | g0193 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18960 | hp2 | a0001 | c0001 | t0019 | g0159 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18974 | hp1 | a0001 | c0001 | t0017 | g0214 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18980 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19043 | hp1 | a0003 | c0005 | t0001 | g0152 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19063 | hp2 | a0001 | c0001 | t0016 | g0196 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19089 | hp1 | a0001 | c0001 | t0011 | g0210 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19089 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA19240 | hp2 | a0001 | c0002 | t0004 | g0036 | AFR | YRI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ASW | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ASW | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0207 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0038 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | GIH | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | GIH | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01123 | hp1 | a0001 | c0004 | t0013 | g0270 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0288 | AFR | ACB | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG03471 | hp2 | a0001 | c0002 | t0004 | g0108 | AFR | MSL | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0091 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | USA | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | LWK | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0244 | REF | REF | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0153 | REF | REF | CREM_chr10_35121846_35217953 | CREM | chr10 | 35121846 | 35217953 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:35148447 | G | C | 1 | a0003 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.124G>C | p.Val42Leu | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/8 | 526/2857 | 124/900 | 42/299 | chr10 | 35148447 | |||
| chr10:35179265 | C | A | 1 | a0002 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.398C>A | p.Thr133Lys | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/8 | 800/2857 | 398/900 | 133/299 | chr10 | 35179265 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:35148446 | T | C | 1 | a0001c0004 | 1 | HG01123.hp1 | synonymous_variant | LOW | c.123T>C | p.His41His | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/8 | 525/2857 | 123/900 | 41/299 | chr10 | 35148446 | |||
| chr10:35179179 | G | A | 1 | a0001c0002 | 12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
synonymous_variant | LOW | c.312G>A | p.Lys104Lys | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/8 | 714/2857 | 312/900 | 104/299 | chr10 | 35179179 | |||
| chr10:35207028 | A | G | 1 | a0001c0003 | 2 | HG01099.hp2 HG03579.hp2 |
synonymous_variant | LOW | c.732A>G | p.Arg244Arg | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/8 | 1134/2857 | 732/900 | 244/299 | chr10 | 35207028 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:35126855 | T | C | 1 | a0001c0001t0009 | 1 | HG02559.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-393T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | chr10 | 35126855 | |||||||
| chr10:35126892 | C | T | 1 | a0001c0001t0008 | 2 | HG03834.hp2 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-356C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10944 | chr10 | 35126892 | ||||||
| chr10:35126922 | G | T | 2 | a0001c0002t0004 a0001c0002t0020 |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-326G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10914 | chr10 | 35126922 | ||||||
| chr10:35126939 | C | T | 2 | a0001c0002t0004 a0001c0002t0020 |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-309C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | chr10 | 35126939 | |||||||
| chr10:35127047 | G | A | 1 | a0001c0001t0005 | 4 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-201G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10789 | chr10 | 35127047 | ||||||
| chr10:35127114 | C | G | 1 | a0001c0001t0019 | 1 | NA18960.hp2 | 5_prime_UTR_variant | MODIFIER | c.-134C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/8 | 10722 | chr10 | 35127114 | ||||||
| chr10:35137827 | A | G | 9 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0007 others(6): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-9A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/8 | chr10 | 35137827 | |||||||
| chr10:35211766 | C | A | 1 | a0001c0001t0011 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*368C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 368 | chr10 | 35211766 | ||||||
| chr10:35211846 | T | C | 1 | a0001c0001t0012 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*448T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 448 | chr10 | 35211846 | ||||||
| chr10:35212007 | G | A | 1 | a0001c0001t0006 | 3 | HG01261.hp1 HG01928.hp2 NA18941.hp2 |
3_prime_UTR_variant | MODIFIER | c.*609G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 609 | chr10 | 35212007 | ||||||
| chr10:35212054 | C | T | 1 | a0001c0001t0017 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*656C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 656 | chr10 | 35212054 | ||||||
| chr10:35212068 | C | A | 1 | a0001c0001t0007 | 2 | HG02280.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*670C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 670 | chr10 | 35212068 | ||||||
| chr10:35212193 | T | A | 1 | a0001c0001t0018 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*795T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 795 | chr10 | 35212193 | ||||||
| chr10:35212303 | T | TA | 1 | a0001c0002t0004 | 11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*916dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 917 | INFO_REALIGN_3_PRIME | chr10 | 35212303 | |||||
| chr10:35212303 | TA | T | 4 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 others(1): Show |
77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*916delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 916 | INFO_REALIGN_3_PRIME | chr10 | 35212303 | |||||
| chr10:35212394 | G | A | 1 | a0001c0004t0013 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*996G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 996 | chr10 | 35212394 | ||||||
| chr10:35212510 | A | G | 5 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0016 others(2): Show |
88 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*1112A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1112 | chr10 | 35212510 | ||||||
| chr10:35212727 | G | A | 1 | a0001c0001t0014 | 1 | NA18960.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1329G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1329 | chr10 | 35212727 | ||||||
| chr10:35212734 | G | A | 1 | a0001c0001t0015 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1336G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 8/8 | 1336 | chr10 | 35212734 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:35127505 | C | T | 2 | a0001c0002t0004g0289 a0001c0002t0020g0290 |
2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-55+312C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127505 | |||||||
| chr10:35127527 | A | G | 2 | a0001c0001t0009g0288 a0001c0001t0018g0287 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-55+334A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127527 | |||||||
| chr10:35127585 | G | C | 116 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(113): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-55+392G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127585 | |||||||
| chr10:35127641 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-55+448G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127641 | |||||||
| chr10:35127744 | G | T | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.-55+551G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127744 | |||||||
| chr10:35127854 | C | CT | 114 | a0001c0001t0002g0001 a0001c0001t0002g0041 a0001c0001t0002g0044 others(111): Show |
115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.-55+672dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35127854 | ||||||
| chr10:35127857 | T | TG | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-55+664_-55+665ins others(1): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35127857 | |||||||
| chr10:35128098 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-55+905A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128098 | |||||||
| chr10:35128253 | A | G | 1 | a0001c0001t0001g0279 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-55+1060A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128253 | |||||||
| chr10:35128274 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-55+1081C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128274 | |||||||
| chr10:35128526 | C | CT | 24 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0271 others(21): Show |
24 | HG00735.hp1 HG00738.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-55+1350dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35128526 | ||||||
| chr10:35128526 | CT | C | 100 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0002g0001 others(97): Show |
101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.-55+1350delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35128526 | ||||||
| chr10:35128545 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-55+1352A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128545 | |||||||
| chr10:35128559 | T | G | 1 | a0001c0001t0002g0041 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-55+1366T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128559 | |||||||
| chr10:35128650 | T | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+1457T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128650 | |||||||
| chr10:35128794 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.-55+1601G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128794 | |||||||
| chr10:35128854 | G | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-55+1661G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128854 | |||||||
| chr10:35128938 | C | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-55+1745C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35128938 | |||||||
| chr10:35129024 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.-55+1831A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129024 | |||||||
| chr10:35129589 | T | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-55+2396T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129589 | |||||||
| chr10:35129598 | G | A | 116 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(113): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-55+2405G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129598 | |||||||
| chr10:35129641 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-55+2448G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129641 | |||||||
| chr10:35129688 | G | C | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.-55+2495G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129688 | |||||||
| chr10:35129776 | C | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+2583C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129776 | |||||||
| chr10:35129796 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-55+2603G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35129796 | |||||||
| chr10:35130052 | C | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+2859C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130052 | |||||||
| chr10:35130071 | C | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-55+2878C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130071 | |||||||
| chr10:35130112 | C | G | 2 | a0001c0001t0002g0103 a0001c0001t0002g0107 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.-55+2919C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130112 | |||||||
| chr10:35130190 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+2997C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130190 | |||||||
| chr10:35130196 | C | CA | 14 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(11): Show |
14 | HG00741.hp1 HG01358.hp1 HG02015.hp2 others(11): Show |
intron_variant | MODIFIER | c.-55+3026dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130196 | ||||||
| chr10:35130196 | CA | C | 88 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(85): Show |
89 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-55+3026delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130196 | ||||||
| chr10:35130219 | AT | A | 10 | a0001c0001t0003g0035 a0001c0001t0007g0040 a0001c0002t0004g0108 others(7): Show |
10 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-55+3034delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35130219 | ||||||
| chr10:35130220 | T | A | 14 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0191 others(11): Show |
14 | HG00438.hp1 HG00438.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.-55+3027T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130220 | |||||||
| chr10:35130265 | A | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-55+3072A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130265 | |||||||
| chr10:35130464 | A | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-55+3271A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130464 | |||||||
| chr10:35130720 | A | G | 1 | a0001c0001t0003g0033 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-55+3527A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130720 | |||||||
| chr10:35130722 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-55+3529A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130722 | |||||||
| chr10:35130781 | T | C | 1 | a0001c0004t0013g0270 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-55+3588T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35130781 | |||||||
| chr10:35131081 | G | A | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-55+3888G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131081 | |||||||
| chr10:35131392 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-55+4199A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131392 | |||||||
| chr10:35131631 | A | G | 1 | a0001c0001t0001g0269 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-55+4438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131631 | |||||||
| chr10:35131693 | T | G | 1 | a0001c0001t0001g0254 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-55+4500T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131693 | |||||||
| chr10:35131924 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-55+4731G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131924 | |||||||
| chr10:35131981 | C | G | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-55+4788C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35131981 | |||||||
| chr10:35132057 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-55+4864T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132057 | |||||||
| chr10:35132076 | G | C | 112 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0143 others(109): Show |
113 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.-55+4883G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132076 | |||||||
| chr10:35132081 | A | G | 1 | a0001c0001t0002g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-55+4888A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132081 | |||||||
| chr10:35132156 | G | A | 1 | a0001c0001t0006g0145 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-55+4963G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132156 | |||||||
| chr10:35132201 | CA | C | 7 | a0001c0001t0001g0249 a0001c0001t0002g0281 a0001c0001t0002g0282 others(4): Show |
7 | HG01169.hp2 HG01192.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-55+5024delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132201 | ||||||
| chr10:35132214 | A | G | 3 | a0001c0002t0004g0108 a0001c0002t0004g0116 a0001c0002t0004g0117 |
3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.-55+5021A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132214 | |||||||
| chr10:35132215 | AAAG | A | 60 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(57): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.-55+5025_-55+5027d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132215 | ||||||
| chr10:35132216 | AAG | A | 6 | a0001c0001t0002g0041 a0001c0001t0002g0054 a0001c0001t0002g0079 others(3): Show |
6 | HG02486.hp1 HG03225.hp2 NA18991.hp1 others(3): Show |
intron_variant | MODIFIER | c.-55+5025_-55+5026d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35132216 | ||||||
| chr10:35132217 | AG | A | 3 | a0001c0001t0003g0015 a0001c0001t0003g0025 a0002c0006t0003g0032 |
3 | HG03669.hp2 HG04115.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.-55+5025delG | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132217 | |||||||
| chr10:35132218 | G | A | 29 | a0001c0001t0002g0080 a0001c0001t0003g0005 a0001c0001t0003g0006 others(26): Show |
29 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.-55+5025G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132218 | |||||||
| chr10:35132254 | G | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-55+5061G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132254 | |||||||
| chr10:35132476 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-55+5283G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132476 | |||||||
| chr10:35132707 | T | C | 2 | a0001c0003t0002g0042 a0001c0003t0002g0043 |
2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-54-5075T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132707 | |||||||
| chr10:35132804 | C | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-4978C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132804 | |||||||
| chr10:35132907 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-4875T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35132907 | |||||||
| chr10:35133011 | C | G | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.-54-4771C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133011 | |||||||
| chr10:35133175 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-4607G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133175 | |||||||
| chr10:35133188 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-54-4594G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133188 | |||||||
| chr10:35133263 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-4519G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133263 | |||||||
| chr10:35133308 | A | AT | 8 | a0001c0001t0001g0141 a0001c0001t0001g0144 a0001c0001t0001g0243 others(5): Show |
8 | HG02145.hp2 HG02647.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-54-4457dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | ||||||
| chr10:35133308 | AT | A | 19 | a0001c0001t0001g0120 a0001c0001t0001g0146 a0001c0001t0001g0147 others(16): Show |
19 | HG01071.hp1 HG01109.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.-54-4457delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | ||||||
| chr10:35133308 | ATT | A | 98 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(95): Show |
99 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.-54-4458_-54-4457d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35133308 | ||||||
| chr10:35133414 | T | A | 1 | a0001c0001t0002g0046 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-54-4368T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133414 | |||||||
| chr10:35133499 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-54-4283A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133499 | |||||||
| chr10:35133571 | T | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-54-4211T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133571 | |||||||
| chr10:35133578 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-54-4204C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133578 | |||||||
| chr10:35133591 | G | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-54-4191G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133591 | |||||||
| chr10:35133614 | T | A | 1 | a0001c0001t0003g0035 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-54-4168T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133614 | |||||||
| chr10:35133784 | G | T | 3 | a0001c0001t0006g0145 a0001c0001t0006g0241 a0001c0001t0006g0242 |
3 | HG01261.hp1 HG01928.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.-54-3998G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133784 | |||||||
| chr10:35133812 | C | T | 68 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-54-3970C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133812 | |||||||
| chr10:35133939 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-54-3843G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35133939 | |||||||
| chr10:35134029 | T | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.-54-3753T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134029 | |||||||
| chr10:35134048 | G | GT | 3 | a0001c0001t0007g0039 a0001c0001t0007g0040 a0001c0001t0009g0288 |
3 | HG02280.hp1 HG02559.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-54-3728dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35134048 | ||||||
| chr10:35134055 | G | GT | 37 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0220 others(34): Show |
37 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.-54-3712dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35134055 | ||||||
| chr10:35134055 | G | T | 9 | a0001c0001t0002g0001 a0001c0001t0002g0082 a0001c0001t0002g0083 others(6): Show |
9 | HG00423.hp2 HG01261.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.-54-3727G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134055 | |||||||
| chr10:35134455 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-54-3327G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134455 | |||||||
| chr10:35134546 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-54-3236A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134546 | |||||||
| chr10:35134591 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54-3191G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134591 | |||||||
| chr10:35134632 | T | C | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-54-3150T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134632 | |||||||
| chr10:35134641 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-3141A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134641 | |||||||
| chr10:35134726 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-54-3056T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134726 | |||||||
| chr10:35134931 | A | G | 277 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(274): Show |
280 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(277): Show |
intron_variant | MODIFIER | c.-54-2851A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134931 | |||||||
| chr10:35134968 | G | A | 1 | a0001c0002t0004g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-54-2814G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35134968 | |||||||
| chr10:35135016 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.-54-2766C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135016 | |||||||
| chr10:35135033 | G | A | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-2749G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135033 | |||||||
| chr10:35135119 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-54-2663G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135119 | |||||||
| chr10:35135210 | A | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54-2572A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135210 | |||||||
| chr10:35135245 | A | C | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-54-2537A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135245 | |||||||
| chr10:35135522 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-54-2260G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135522 | |||||||
| chr10:35135721 | GA | G | 138 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.-54-2039delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135721 | ||||||
| chr10:35135721 | GAA | G | 22 | a0001c0001t0001g0120 a0001c0001t0001g0132 a0001c0001t0001g0144 others(19): Show |
22 | HG00544.hp2 HG00621.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.-54-2040_-54-2039d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135721 | ||||||
| chr10:35135737 | AAAAAAAG others(2): Show |
A | 6 | a0001c0001t0003g0020 a0001c0001t0003g0021 a0001c0001t0003g0022 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.-54-2043_-54-2035d others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135737 | ||||||
| chr10:35135738 | AAAAAAGA others(1): Show |
A | 25 | a0001c0001t0002g0061 a0001c0001t0003g0005 a0001c0001t0003g0006 others(22): Show |
25 | HG00639.hp1 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.-54-2042_-54-2035d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135738 | ||||||
| chr10:35135739 | AAAAAGAG | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(66): Show |
70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-54-2041_-54-2035d others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135739 | ||||||
| chr10:35135830 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-54-1952G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135830 | |||||||
| chr10:35135872 | G | GTA | 7 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0229 others(4): Show |
7 | HG02080.hp2 NA18612.hp1 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.-54-1909_-54-1908d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35135872 | ||||||
| chr10:35135885 | G | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-1897G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35135885 | |||||||
| chr10:35136208 | C | CAAAAT | 109 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.-54-1573_-54-1572i others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136208 | ||||||
| chr10:35136362 | G | A | 4 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | NA18612.hp2 NA18953.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.-54-1420G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136362 | |||||||
| chr10:35136426 | C | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-1356C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136426 | |||||||
| chr10:35136443 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-54-1339G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136443 | |||||||
| chr10:35136484 | T | C | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-54-1298T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136484 | |||||||
| chr10:35136490 | T | G | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-54-1292T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136490 | |||||||
| chr10:35136585 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-54-1197T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136585 | |||||||
| chr10:35136618 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-54-1164A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136618 | |||||||
| chr10:35136622 | C | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.-54-1160C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136622 | |||||||
| chr10:35136790 | GT | G | 115 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(112): Show |
117 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.-54-972delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | ||||||
| chr10:35136790 | GTT | G | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(144): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-54-973_-54-972del others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | ||||||
| chr10:35136790 | GTTT | G | 11 | a0001c0001t0001g0232 a0001c0002t0004g0036 a0001c0002t0004g0108 others(8): Show |
11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-54-974_-54-972del others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35136790 | ||||||
| chr10:35136810 | T | G | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-972T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136810 | |||||||
| chr10:35136890 | G | A | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-54-892G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136890 | |||||||
| chr10:35136891 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-54-891G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136891 | |||||||
| chr10:35136914 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-54-868G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35136914 | |||||||
| chr10:35137004 | A | G | 2 | a0001c0002t0004g0289 a0001c0002t0020g0290 |
2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.-54-778A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137004 | |||||||
| chr10:35137030 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-54-752T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137030 | |||||||
| chr10:35137040 | C | G | 1 | a0001c0002t0004g0108 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-54-742C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137040 | |||||||
| chr10:35137083 | G | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-699G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137083 | |||||||
| chr10:35137161 | T | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-54-621T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137161 | |||||||
| chr10:35137197 | TAAAG | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.-54-583_-54-580del others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr10 | 35137197 | ||||||
| chr10:35137282 | T | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.-54-500T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137282 | |||||||
| chr10:35137308 | A | G | 1 | a0003c0005t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-54-474A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137308 | |||||||
| chr10:35137396 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.-54-386G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137396 | |||||||
| chr10:35137686 | T | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-54-96T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 1/7 | chr10 | 35137686 | |||||||
| chr10:35137907 | T | G | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+28T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35137907 | |||||||
| chr10:35138326 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.44+447C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138326 | |||||||
| chr10:35138467 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+588G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138467 | |||||||
| chr10:35138526 | A | AT | 28 | a0001c0001t0001g0125 a0001c0001t0001g0140 a0001c0001t0001g0218 others(25): Show |
28 | HG00423.hp1 HG00738.hp2 HG01071.hp1 others(25): Show |
intron_variant | MODIFIER | c.44+666dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35138526 | ||||||
| chr10:35138682 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+803C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138682 | |||||||
| chr10:35138697 | T | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.44+818T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138697 | |||||||
| chr10:35138733 | T | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 |
3 | HG02258.hp2 HG02970.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.44+854T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138733 | |||||||
| chr10:35138745 | C | T | 3 | a0001c0001t0001g0217 a0001c0001t0001g0222 a0001c0001t0001g0232 |
3 | HG00438.hp2 NA18974.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.44+866C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138745 | |||||||
| chr10:35138746 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.44+867G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138746 | |||||||
| chr10:35138786 | G | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.44+907G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138786 | |||||||
| chr10:35138872 | T | C | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44+993T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138872 | |||||||
| chr10:35138876 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44+997A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35138876 | |||||||
| chr10:35139122 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0243 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.44+1243T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139122 | |||||||
| chr10:35139127 | A | AT | 18 | a0001c0001t0001g0213 a0001c0001t0001g0215 a0001c0001t0001g0216 others(15): Show |
18 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.44+1262dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35139127 | ||||||
| chr10:35139127 | AT | A | 107 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(104): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.44+1262delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35139127 | ||||||
| chr10:35139135 | T | C | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.44+1256T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139135 | |||||||
| chr10:35139152 | G | C | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.44+1273G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139152 | |||||||
| chr10:35139272 | G | A | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+1393G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139272 | |||||||
| chr10:35139304 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+1425G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139304 | |||||||
| chr10:35139309 | G | A | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.44+1430G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139309 | |||||||
| chr10:35139327 | C | G | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.44+1448C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139327 | |||||||
| chr10:35139336 | C | T | 109 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.44+1457C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139336 | |||||||
| chr10:35139368 | C | G | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44+1489C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139368 | |||||||
| chr10:35139666 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.44+1787G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139666 | |||||||
| chr10:35139812 | C | G | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.44+1933C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35139812 | |||||||
| chr10:35140072 | A | G | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+2193A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140072 | |||||||
| chr10:35140182 | G | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.44+2303G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140182 | |||||||
| chr10:35140198 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.44+2319C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140198 | |||||||
| chr10:35140220 | T | C | 1 | a0001c0001t0019g0159 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.44+2341T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140220 | |||||||
| chr10:35140528 | G | C | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.44+2649G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140528 | |||||||
| chr10:35140577 | A | G | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.44+2698A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140577 | |||||||
| chr10:35140897 | C | T | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+3018C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35140897 | |||||||
| chr10:35141187 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.44+3308T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141187 | |||||||
| chr10:35141227 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.44+3348T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141227 | |||||||
| chr10:35141357 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(131): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.44+3478A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141357 | |||||||
| chr10:35141519 | C | T | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.44+3640C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141519 | |||||||
| chr10:35141571 | T | C | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+3692T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141571 | |||||||
| chr10:35141634 | G | A | 1 | a0001c0001t0003g0015 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.44+3755G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141634 | |||||||
| chr10:35141636 | T | C | 1 | a0001c0001t0003g0015 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.44+3757T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141636 | |||||||
| chr10:35141934 | ATGT | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.44+4059_44+4061del others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35141934 | ||||||
| chr10:35141982 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.44+4103A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35141982 | |||||||
| chr10:35142171 | G | A | 1 | a0001c0004t0013g0270 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.44+4292G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142171 | |||||||
| chr10:35142508 | C | T | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.44+4629C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142508 | |||||||
| chr10:35142708 | T | C | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.44+4829T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142708 | |||||||
| chr10:35142756 | T | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.44+4877T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142756 | |||||||
| chr10:35142782 | T | C | 1 | a0001c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.44+4903T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142782 | |||||||
| chr10:35142887 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+5008C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142887 | |||||||
| chr10:35142970 | A | G | 1 | a0001c0001t0008g0245 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.44+5091A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35142970 | |||||||
| chr10:35143035 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.44+5156A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143035 | |||||||
| chr10:35143189 | T | TTTA | 3 | a0001c0001t0001g0121 a0001c0001t0001g0209 a0001c0001t0011g0210 |
3 | NA18944.hp2 NA18975.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.45-5178_45-5176dup others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35143189 | ||||||
| chr10:35143422 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-4946G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143422 | |||||||
| chr10:35143477 | T | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-4891T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143477 | |||||||
| chr10:35143484 | A | G | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.45-4884A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143484 | |||||||
| chr10:35143488 | G | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45-4880G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143488 | |||||||
| chr10:35143636 | T | C | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-4732T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143636 | |||||||
| chr10:35143793 | G | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-4575G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143793 | |||||||
| chr10:35143817 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4551C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143817 | |||||||
| chr10:35143835 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4533G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143835 | |||||||
| chr10:35143836 | T | G | 1 | a0001c0001t0001g0120 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4532T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143836 | |||||||
| chr10:35143837 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4531G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143837 | |||||||
| chr10:35143914 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4454T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143914 | |||||||
| chr10:35143933 | A | T | 1 | a0001c0001t0001g0120 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.45-4435A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35143933 | |||||||
| chr10:35144090 | T | A | 1 | a0001c0001t0001g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.45-4278T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144090 | |||||||
| chr10:35144149 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-4219C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144149 | |||||||
| chr10:35144209 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-4159G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144209 | |||||||
| chr10:35144271 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-4097G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144271 | |||||||
| chr10:35144551 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-3817A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144551 | |||||||
| chr10:35144566 | C | A | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0217 others(2): Show |
5 | HG00438.hp2 NA18972.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-3802C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144566 | |||||||
| chr10:35144738 | C | CT | 105 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(102): Show |
106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.45-3617dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35144738 | ||||||
| chr10:35144800 | G | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-3568G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144800 | |||||||
| chr10:35144818 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.45-3550G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35144818 | |||||||
| chr10:35145018 | G | A | 1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-3350G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145018 | |||||||
| chr10:35145066 | C | T | 68 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.45-3302C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145066 | |||||||
| chr10:35145144 | G | GAGCA | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-3221_45-3218dup others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145144 | ||||||
| chr10:35145160 | C | CA | 18 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0001c0001t0001g0129 others(15): Show |
18 | HG01071.hp1 HG01175.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.45-3188dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | ||||||
| chr10:35145160 | C | CAA | 65 | a0001c0001t0002g0001 a0001c0001t0002g0044 a0001c0001t0002g0045 others(62): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.45-3189_45-3188dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | ||||||
| chr10:35145160 | C | CAAA | 13 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0041 others(10): Show |
13 | HG00733.hp2 HG01258.hp2 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.45-3190_45-3188dup others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | ||||||
| chr10:35145160 | CA | C | 8 | a0001c0001t0001g0226 a0001c0001t0001g0238 a0001c0001t0002g0281 others(5): Show |
8 | HG01099.hp1 HG01192.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.45-3188delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | ||||||
| chr10:35145160 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0205 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.45-3197_45-3188del others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145160 | ||||||
| chr10:35145168 | A | AAG | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-3199_45-3198ins others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145168 | ||||||
| chr10:35145407 | T | C | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.45-2961T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145407 | |||||||
| chr10:35145445 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-2923T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145445 | |||||||
| chr10:35145513 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.45-2855C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145513 | |||||||
| chr10:35145605 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0275 others(1): Show |
4 | HG01123.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-2763A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145605 | |||||||
| chr10:35145609 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45-2759C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145609 | |||||||
| chr10:35145676 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45-2692G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145676 | |||||||
| chr10:35145680 | A | G | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.45-2688A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145680 | |||||||
| chr10:35145692 | C | T | 2 | a0001c0003t0002g0042 a0001c0003t0002g0043 |
2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.45-2676C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145692 | |||||||
| chr10:35145776 | C | CA | 205 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0119 others(202): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.45-2569dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | ||||||
| chr10:35145776 | C | CAA | 28 | a0001c0001t0001g0003 a0001c0001t0001g0121 a0001c0001t0001g0134 others(25): Show |
29 | HG00323.hp2 HG01175.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.45-2570_45-2569dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | ||||||
| chr10:35145776 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0012 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.45-2579_45-2569del others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35145776 | ||||||
| chr10:35145876 | G | A | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.45-2492G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35145876 | |||||||
| chr10:35146009 | A | G | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.45-2359A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146009 | |||||||
| chr10:35146080 | T | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-2288T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146080 | |||||||
| chr10:35146158 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2210C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146158 | |||||||
| chr10:35146190 | G | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0246 |
2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.45-2178G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146190 | |||||||
| chr10:35146304 | GGTTT | G | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-2058_45-2055del others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35146304 | ||||||
| chr10:35146313 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-2055G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146313 | |||||||
| chr10:35146348 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.45-2020G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146348 | |||||||
| chr10:35146387 | T | C | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-1981T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146387 | |||||||
| chr10:35146544 | C | T | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.45-1824C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146544 | |||||||
| chr10:35146690 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.45-1678C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146690 | |||||||
| chr10:35146780 | T | G | 2 | a0001c0001t0001g0259 a0001c0001t0001g0260 |
2 | HG00621.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.45-1588T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146780 | |||||||
| chr10:35146948 | T | C | 1 | a0001c0001t0002g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.45-1420T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146948 | |||||||
| chr10:35146999 | A | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-1369A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35146999 | |||||||
| chr10:35147041 | G | GT | 75 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0130 others(72): Show |
75 | HG00099.hp2 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.45-1300dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | ||||||
| chr10:35147041 | G | GTT | 17 | a0001c0001t0001g0140 a0001c0001t0001g0150 a0001c0001t0001g0158 others(14): Show |
17 | HG00280.hp1 HG00621.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-1301_45-1300dup others(2): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | ||||||
| chr10:35147041 | GTTTTTTT others(3): Show |
G | 3 | a0001c0001t0002g0091 a0001c0001t0003g0012 a0001c0001t0003g0018 |
3 | HG00639.hp1 HG06807.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.45-1309_45-1300del others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | ||||||
| chr10:35147041 | GTTTTTTT others(4): Show |
G | 100 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(97): Show |
101 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.45-1310_45-1300del others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35147041 | ||||||
| chr10:35147055 | T | G | 9 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(6): Show |
10 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-1313T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147055 | |||||||
| chr10:35147067 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.45-1301T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147067 | |||||||
| chr10:35147146 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.45-1222G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147146 | |||||||
| chr10:35147152 | G | T | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.45-1216G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147152 | |||||||
| chr10:35147210 | C | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-1158C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147210 | |||||||
| chr10:35147211 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.45-1157G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147211 | |||||||
| chr10:35147215 | G | A | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.45-1153G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147215 | |||||||
| chr10:35147275 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-1093G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147275 | |||||||
| chr10:35147348 | C | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.45-1020C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147348 | |||||||
| chr10:35147931 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.45-437G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147931 | |||||||
| chr10:35147942 | A | G | 1 | a0001c0002t0004g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.45-426A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147942 | |||||||
| chr10:35147946 | T | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.45-422T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147946 | |||||||
| chr10:35147981 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.45-387G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35147981 | |||||||
| chr10:35148061 | A | T | 1 | a0001c0001t0001g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.45-307A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148061 | |||||||
| chr10:35148165 | A | G | 5 | a0001c0001t0002g0087 a0001c0001t0002g0088 a0001c0001t0002g0089 others(2): Show |
5 | HG02040.hp1 HG02135.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.45-203A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148165 | |||||||
| chr10:35148295 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.45-73G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | chr10 | 35148295 | |||||||
| chr10:35148311 | A | AT | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.45-54dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr10 | 35148311 | ||||||
| chr10:35148592 | C | G | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+101C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148592 | |||||||
| chr10:35148644 | G | GTAAT | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+156_168+159dup others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35148644 | ||||||
| chr10:35148689 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168+198C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148689 | |||||||
| chr10:35148929 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.168+438C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148929 | |||||||
| chr10:35148964 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.168+473T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148964 | |||||||
| chr10:35148974 | A | G | 11 | a0001c0001t0001g0134 a0001c0001t0001g0160 a0001c0001t0001g0161 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+483A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35148974 | |||||||
| chr10:35149018 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.168+527T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149018 | |||||||
| chr10:35149031 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.168+540T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149031 | |||||||
| chr10:35149409 | T | C | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+918T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149409 | |||||||
| chr10:35149486 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+995T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149486 | |||||||
| chr10:35149582 | G | A | 1 | a0001c0001t0019g0159 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.168+1091G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149582 | |||||||
| chr10:35149888 | AAACACAC others(10): Show |
A | 2 | a0001c0001t0002g0041 a0001c0001t0002g0093 |
2 | NA19000.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.168+1399_168+1415d others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149888 | ||||||
| chr10:35149889 | A | AAC | 16 | a0001c0001t0001g0175 a0001c0001t0001g0186 a0001c0001t0001g0235 others(13): Show |
16 | HG00621.hp2 HG00639.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.168+1447_168+1448d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACAC | 16 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0198 others(13): Show |
16 | HG00544.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.168+1445_168+1448d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACAC | 21 | a0001c0001t0001g0138 a0001c0001t0001g0150 a0001c0001t0001g0158 others(18): Show |
21 | HG00741.hp2 HG01168.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.168+1443_168+1448d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(1): Show |
15 | a0001c0001t0001g0133 a0001c0001t0001g0143 a0001c0001t0001g0181 others(12): Show |
15 | HG00558.hp1 HG01109.hp2 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.168+1441_168+1448d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(3): Show |
16 | a0001c0001t0001g0125 a0001c0001t0001g0137 a0001c0001t0001g0139 others(13): Show |
16 | HG00099.hp2 HG01261.hp2 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.168+1439_168+1448d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(5): Show |
29 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0001t0001g0122 others(26): Show |
29 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.168+1437_168+1448d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(7): Show |
15 | a0001c0001t0001g0123 a0001c0001t0001g0141 a0001c0001t0001g0163 others(12): Show |
15 | HG00438.hp1 HG02135.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+1435_168+1448d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(9): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0131 others(11): Show |
15 | HG00438.hp2 HG00621.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.168+1433_168+1448d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(11): Show |
7 | a0001c0001t0001g0132 a0001c0001t0001g0172 a0001c0001t0001g0185 others(4): Show |
7 | HG00741.hp1 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1431_168+1448d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(13): Show |
5 | a0001c0001t0001g0142 a0001c0001t0001g0171 a0001c0001t0001g0190 others(2): Show |
5 | HG00099.hp1 HG00738.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.168+1429_168+1448d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(15): Show |
1 | a0001c0001t0001g0215 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.168+1427_168+1448d others(24): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | AACACACA others(17): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0199 |
2 | HG03453.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.168+1425_168+1448d others(26): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | A | ACACACAC others(6): Show |
1 | a0001c0001t0011g0210 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.168+1398_168+1399i others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149889 | |||||||
| chr10:35149889 | AAC | A | 12 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(9): Show |
12 | HG01109.hp1 HG02258.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+1447_168+1448d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACAC | A | 11 | a0001c0001t0001g0140 a0001c0001t0001g0167 a0001c0001t0001g0254 others(8): Show |
11 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+1445_168+1448d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACAC | A | 7 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0002t0004g0110 others(4): Show |
7 | HG00738.hp2 HG01071.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+1443_168+1448d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACACA others(3): Show |
A | 1 | a0001c0001t0001g0161 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.168+1439_168+1448d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACACA others(5): Show |
A | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.168+1437_168+1448d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACACA others(7): Show |
A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+1435_168+1448d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACACA others(9): Show |
A | 31 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(28): Show |
31 | HG00323.hp1 HG00544.hp1 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+1433_168+1448d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149889 | AACACACA others(11): Show |
A | 34 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(31): Show |
35 | HG00280.hp2 HG00423.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.168+1431_168+1448d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149889 | ||||||
| chr10:35149924 | ACACACAC others(8): Show |
A | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.168+1435_168+1449d others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149924 | ||||||
| chr10:35149938 | A | ACACACAC others(7): Show |
1 | a0001c0001t0001g0148 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | ||||||
| chr10:35149938 | A | ACACACAC others(5): Show |
1 | a0001c0001t0001g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | ||||||
| chr10:35149938 | A | ACACACAC others(3): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0147 a0001c0001t0001g0149 |
3 | NA19057.hp1 NA19076.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.168+1448_168+1449i others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | ||||||
| chr10:35149938 | A | ACACC | 2 | a0001c0001t0001g0176 a0001c0001t0005g0002 |
3 | HG00558.hp2 HG02895.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.168+1448_168+1449i others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35149938 | ||||||
| chr10:35149939 | C | CACACACA others(8): Show |
1 | a0001c0001t0001g0177 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149939 | |||||||
| chr10:35149939 | C | CACACACA others(10): Show |
1 | a0001c0001t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.168+1448_168+1449i others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35149939 | |||||||
| chr10:35150224 | T | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+1733T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150224 | |||||||
| chr10:35150232 | T | C | 1 | a0001c0001t0002g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.168+1741T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150232 | |||||||
| chr10:35150261 | T | C | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+1770T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150261 | |||||||
| chr10:35150333 | A | G | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+1842A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150333 | |||||||
| chr10:35150696 | C | CTGT | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+2206_168+2208d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35150696 | ||||||
| chr10:35150828 | AAAAGTGT others(58): Show |
A | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.168+2403_168+2467d others(67): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35150828 | ||||||
| chr10:35150953 | G | A | 1 | a0001c0001t0001g0253 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.168+2462G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35150953 | |||||||
| chr10:35151072 | A | G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+2581A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151072 | |||||||
| chr10:35151100 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.168+2609C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151100 | |||||||
| chr10:35151194 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.168+2703A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151194 | |||||||
| chr10:35151213 | G | A | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.168+2722G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151213 | |||||||
| chr10:35151257 | A | G | 1 | a0003c0005t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.168+2766A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151257 | |||||||
| chr10:35151285 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.168+2794T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151285 | |||||||
| chr10:35151365 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+2874G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151365 | |||||||
| chr10:35151399 | A | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+2908A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151399 | |||||||
| chr10:35151404 | A | G | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.168+2913A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151404 | |||||||
| chr10:35151444 | C | G | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+2953C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151444 | |||||||
| chr10:35151501 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+3010G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151501 | |||||||
| chr10:35151509 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+3018G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151509 | |||||||
| chr10:35151530 | C | A | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+3039C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151530 | |||||||
| chr10:35151532 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+3041C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151532 | |||||||
| chr10:35151653 | T | C | 121 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.168+3162T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151653 | |||||||
| chr10:35151758 | C | A | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.168+3267C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151758 | |||||||
| chr10:35151808 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.168+3317A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151808 | |||||||
| chr10:35151941 | A | G | 4 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0275 others(1): Show |
4 | HG01123.hp1 HG02622.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+3450A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35151941 | |||||||
| chr10:35152072 | T | A | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+3581T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152072 | |||||||
| chr10:35152113 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+3622G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152113 | |||||||
| chr10:35152241 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+3750A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152241 | |||||||
| chr10:35152284 | T | G | 1 | a0001c0004t0013g0270 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.168+3793T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152284 | |||||||
| chr10:35152297 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.168+3806A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152297 | |||||||
| chr10:35152314 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+3823A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152314 | |||||||
| chr10:35152540 | C | T | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.168+4049C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152540 | |||||||
| chr10:35152584 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+4093C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152584 | |||||||
| chr10:35152671 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+4180G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152671 | |||||||
| chr10:35152783 | GTACAA | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+4298_168+4302d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35152783 | ||||||
| chr10:35152825 | C | T | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168+4334C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35152825 | |||||||
| chr10:35153067 | TAAA | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+4580_168+4582d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35153067 | ||||||
| chr10:35153089 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+4598A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153089 | |||||||
| chr10:35153153 | TGGATTGC others(9): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.168+4666_168+4681d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35153153 | ||||||
| chr10:35153535 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0016g0196 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.168+5044G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153535 | |||||||
| chr10:35153681 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5190C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153681 | |||||||
| chr10:35153891 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.168+5400A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153891 | |||||||
| chr10:35153920 | G | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.168+5429G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35153920 | |||||||
| chr10:35154112 | G | A | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.168+5621G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154112 | |||||||
| chr10:35154292 | A | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+5801A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154292 | |||||||
| chr10:35154389 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5898C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154389 | |||||||
| chr10:35154403 | G | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+5912G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154403 | |||||||
| chr10:35154422 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.168+5931T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154422 | |||||||
| chr10:35154543 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.168+6052A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154543 | |||||||
| chr10:35154715 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+6224A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154715 | |||||||
| chr10:35154985 | C | T | 3 | a0001c0001t0001g0178 a0001c0001t0001g0203 a0001c0001t0001g0225 |
3 | HG02145.hp1 HG02257.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.168+6494C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35154985 | |||||||
| chr10:35155054 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.168+6563T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155054 | |||||||
| chr10:35155055 | G | A | 1 | a0001c0004t0013g0270 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.168+6564G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155055 | |||||||
| chr10:35155214 | G | A | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+6723G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155214 | |||||||
| chr10:35155529 | CA | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+7046delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155529 | ||||||
| chr10:35155630 | TC | T | 7 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(4): Show |
7 | HG01071.hp1 HG01123.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.168+7140delC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155630 | |||||||
| chr10:35155631 | C | T | 26 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(23): Show |
26 | HG00621.hp1 HG00738.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.168+7140C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155631 | |||||||
| chr10:35155631 | CT | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(246): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.168+7151delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155631 | ||||||
| chr10:35155632 | T | A | 1 | a0001c0001t0003g0008 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.168+7141T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155632 | |||||||
| chr10:35155733 | A | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0274 a0001c0001t0017g0214 |
3 | HG00438.hp1 HG02080.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.168+7242A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155733 | |||||||
| chr10:35155859 | G | A | 1 | a0001c0001t0002g0101 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.168+7368G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155859 | |||||||
| chr10:35155945 | CT | C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(99): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.168+7466delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35155945 | ||||||
| chr10:35155963 | A | G | 109 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+7472A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35155963 | |||||||
| chr10:35156253 | C | CT | 105 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0002g0001 others(102): Show |
106 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.168+7773dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35156253 | ||||||
| chr10:35156291 | C | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+7800C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156291 | |||||||
| chr10:35156467 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0224 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.168+7976C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156467 | |||||||
| chr10:35156660 | A | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+8169A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156660 | |||||||
| chr10:35156665 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.168+8174A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156665 | |||||||
| chr10:35156727 | G | C | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+8236G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156727 | |||||||
| chr10:35156924 | A | G | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.168+8433A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156924 | |||||||
| chr10:35156958 | T | G | 1 | a0001c0001t0001g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.168+8467T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35156958 | |||||||
| chr10:35157276 | C | CAACT | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+8789_168+8792d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157276 | ||||||
| chr10:35157447 | C | A | 2 | a0001c0001t0001g0143 a0001c0001t0001g0246 |
2 | HG01109.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.168+8956C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157447 | |||||||
| chr10:35157635 | C | CA | 12 | a0001c0001t0001g0130 a0001c0001t0001g0227 a0001c0001t0001g0259 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+9165dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | ||||||
| chr10:35157635 | CA | C | 109 | a0001c0001t0001g0195 a0001c0001t0001g0249 a0001c0001t0002g0001 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.168+9165delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | ||||||
| chr10:35157635 | CAA | C | 6 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(3): Show |
6 | HG00639.hp1 HG01071.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.168+9164_168+9165d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157635 | ||||||
| chr10:35157800 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.168+9309A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157800 | |||||||
| chr10:35157822 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.168+9331G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157822 | |||||||
| chr10:35157875 | A | AT | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+9385dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35157875 | ||||||
| chr10:35157910 | C | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+9419C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157910 | |||||||
| chr10:35157917 | T | C | 1 | a0001c0001t0003g0011 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.168+9426T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157917 | |||||||
| chr10:35157937 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+9446A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157937 | |||||||
| chr10:35157950 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.168+9459G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35157950 | |||||||
| chr10:35158347 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.168+9856C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158347 | |||||||
| chr10:35158615 | G | C | 2 | a0001c0001t0001g0238 a0001c0001t0001g0240 |
2 | HG01261.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.168+10124G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158615 | |||||||
| chr10:35158794 | T | C | 32 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(29): Show |
32 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.168+10303T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158794 | |||||||
| chr10:35158798 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0002g0091 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.168+10318_168+1034 others(28): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158798 | ||||||
| chr10:35158799 | T | TG | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10308_168+1030 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158799 | |||||||
| chr10:35158800 | T | G | 2 | a0001c0001t0009g0288 a0001c0001t0018g0287 |
2 | HG02559.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.168+10309T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158800 | |||||||
| chr10:35158805 | TTTTGTTG others(5): Show |
T | 24 | a0001c0001t0002g0051 a0001c0001t0002g0052 a0001c0001t0002g0053 others(21): Show |
24 | HG00639.hp1 HG00639.hp2 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.168+10321_168+1033 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158805 | ||||||
| chr10:35158806 | TTTGTTGT others(4): Show |
T | 36 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0045 others(33): Show |
36 | HG00323.hp1 HG00423.hp2 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.168+10318_168+1032 others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158806 | ||||||
| chr10:35158807 | T | G | 13 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(10): Show |
13 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.168+10316T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158807 | |||||||
| chr10:35158807 | TTGTTGTT others(3): Show |
T | 23 | a0001c0001t0002g0001 a0001c0001t0002g0038 a0001c0001t0002g0041 others(20): Show |
23 | HG00280.hp2 HG00544.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.168+10318_168+1032 others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35158807 | ||||||
| chr10:35158808 | TGTTGTTT others(6): Show |
T | 20 | a0001c0001t0002g0086 a0001c0001t0003g0005 a0001c0001t0003g0006 others(17): Show |
20 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.168+10318_168+1033 others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158808 | |||||||
| chr10:35158809 | G | T | 35 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
35 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.168+10318G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158809 | |||||||
| chr10:35158812 | G | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10321G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158812 | |||||||
| chr10:35158817 | G | T | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+10326G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158817 | |||||||
| chr10:35158818 | T | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10327T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158818 | |||||||
| chr10:35158821 | G | T | 102 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(99): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.168+10330G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158821 | |||||||
| chr10:35158942 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10451G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35158942 | |||||||
| chr10:35159121 | G | A | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+10630G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159121 | |||||||
| chr10:35159260 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+10769C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159260 | |||||||
| chr10:35159262 | C | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+10771C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159262 | |||||||
| chr10:35159440 | C | T | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.168+10949C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159440 | |||||||
| chr10:35159476 | G | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.168+10985G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159476 | |||||||
| chr10:35159527 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+11036C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159527 | |||||||
| chr10:35159792 | G | A | 68 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.168+11301G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159792 | |||||||
| chr10:35159907 | C | G | 1 | a0001c0001t0001g0236 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.168+11416C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159907 | |||||||
| chr10:35159910 | G | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+11419G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159910 | |||||||
| chr10:35159979 | T | G | 1 | a0001c0001t0001g0175 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.168+11488T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35159979 | |||||||
| chr10:35160261 | C | T | 1 | a0001c0001t0002g0053 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.168+11770C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160261 | |||||||
| chr10:35160281 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.168+11790G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160281 | |||||||
| chr10:35160300 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+11809A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160300 | |||||||
| chr10:35160349 | C | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0213 |
2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.168+11858C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160349 | |||||||
| chr10:35160350 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.168+11859G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160350 | |||||||
| chr10:35160387 | A | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+11896A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160387 | |||||||
| chr10:35160409 | C | CT | 40 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(37): Show |
40 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.168+11927dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160409 | ||||||
| chr10:35160433 | C | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+11942C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160433 | |||||||
| chr10:35160511 | G | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12020G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160511 | |||||||
| chr10:35160660 | C | T | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.168+12169C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160660 | |||||||
| chr10:35160694 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.168+12203A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160694 | |||||||
| chr10:35160695 | TAAC | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+12206_168+1220 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160695 | ||||||
| chr10:35160752 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12261A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160752 | |||||||
| chr10:35160899 | TCATATCC others(5): Show |
T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+12412_168+1242 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35160899 | ||||||
| chr10:35160985 | C | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.168+12494C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160985 | |||||||
| chr10:35160989 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(4): Show |
8 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.168+12498G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35160989 | |||||||
| chr10:35161187 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+12696T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161187 | |||||||
| chr10:35161205 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.168+12714C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161205 | |||||||
| chr10:35161206 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.168+12715G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161206 | |||||||
| chr10:35161211 | A | G | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12720A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161211 | |||||||
| chr10:35161218 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+12727C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161218 | |||||||
| chr10:35161219 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+12728C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161219 | |||||||
| chr10:35161222 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+12731C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161222 | |||||||
| chr10:35161244 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12753C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161244 | |||||||
| chr10:35161262 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0212 |
2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.168+12771G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161262 | |||||||
| chr10:35161350 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.168+12859G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161350 | |||||||
| chr10:35161368 | G | A | 1 | a0001c0001t0016g0196 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.168+12877G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161368 | |||||||
| chr10:35161398 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+12907G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161398 | |||||||
| chr10:35161495 | A | T | 1 | a0001c0002t0004g0117 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.168+13004A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161495 | |||||||
| chr10:35161663 | CA | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+13183delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35161663 | ||||||
| chr10:35161679 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+13188G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161679 | |||||||
| chr10:35161680 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13189A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161680 | |||||||
| chr10:35161827 | G | C | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.168+13336G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161827 | |||||||
| chr10:35161929 | A | G | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+13438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161929 | |||||||
| chr10:35161937 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13446G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161937 | |||||||
| chr10:35161940 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13449A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35161940 | |||||||
| chr10:35162012 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+13521C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162012 | |||||||
| chr10:35162024 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.168+13533C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162024 | |||||||
| chr10:35162208 | A | C | 1 | a0001c0001t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.168+13717A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162208 | |||||||
| chr10:35162378 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+13887A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162378 | |||||||
| chr10:35162405 | T | C | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.168+13914T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162405 | |||||||
| chr10:35162415 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0140 others(7): Show |
11 | HG00741.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.168+13924A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162415 | |||||||
| chr10:35162424 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.168+13933T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162424 | |||||||
| chr10:35162670 | G | A | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.168+14179G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162670 | |||||||
| chr10:35162673 | G | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.168+14182G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162673 | |||||||
| chr10:35162728 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.168+14237G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162728 | |||||||
| chr10:35162770 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+14279C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162770 | |||||||
| chr10:35162865 | T | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.168+14374T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162865 | |||||||
| chr10:35162896 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.168+14405A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35162896 | |||||||
| chr10:35163018 | C | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+14527C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163018 | |||||||
| chr10:35163045 | C | CA | 70 | a0001c0001t0001g0131 a0001c0001t0002g0001 a0001c0001t0002g0037 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+14565dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163045 | ||||||
| chr10:35163159 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.168+14668G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163159 | |||||||
| chr10:35163177 | T | G | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.168+14686T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163177 | |||||||
| chr10:35163213 | G | A | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.168+14722G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163213 | |||||||
| chr10:35163261 | G | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+14770G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163261 | |||||||
| chr10:35163333 | CTT | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.168+14845_168+1484 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163333 | ||||||
| chr10:35163396 | A | T | 1 | a0001c0001t0002g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.168+14905A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163396 | |||||||
| chr10:35163420 | A | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.168+14929A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163420 | |||||||
| chr10:35163428 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.168+14937A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163428 | |||||||
| chr10:35163435 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.168+14944A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163435 | |||||||
| chr10:35163441 | T | C | 1 | a0001c0001t0001g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.168+14950T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163441 | |||||||
| chr10:35163449 | C | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.168+14958C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163449 | |||||||
| chr10:35163450 | G | A | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.168+14959G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163450 | |||||||
| chr10:35163478 | GTTCGAGA others(5): Show |
G | 1 | a0001c0001t0002g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.168+14988_168+1499 others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163478 | |||||||
| chr10:35163482 | G | C | 5 | a0001c0002t0004g0110 a0001c0002t0004g0111 a0001c0002t0004g0112 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+14991G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163482 | |||||||
| chr10:35163558 | G | A | 6 | a0001c0001t0001g0121 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG03098.hp2 HG03579.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.168+15067G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163558 | |||||||
| chr10:35163580 | A | G | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.168+15089A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163580 | |||||||
| chr10:35163752 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.169-15137C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163752 | |||||||
| chr10:35163917 | G | A | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-14972G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35163917 | |||||||
| chr10:35163974 | C | CA | 9 | a0001c0001t0001g0134 a0001c0001t0001g0207 a0001c0001t0001g0227 others(6): Show |
10 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-14902dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35163974 | ||||||
| chr10:35164053 | AAGT | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0160 a0001c0001t0001g0205 |
3 | HG01258.hp1 HG02273.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.169-14832_169-1483 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35164053 | ||||||
| chr10:35164282 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.169-14607G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164282 | |||||||
| chr10:35164473 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-14416G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164473 | |||||||
| chr10:35164526 | T | C | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-14363T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164526 | |||||||
| chr10:35164577 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.169-14312A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164577 | |||||||
| chr10:35164614 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-14275C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164614 | |||||||
| chr10:35164773 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.169-14116G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35164773 | |||||||
| chr10:35165056 | C | CAA | 9 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(6): Show |
9 | HG01884.hp2 HG02559.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-13812_169-1381 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | C | CAAA | 7 | a0001c0001t0002g0055 a0001c0001t0002g0059 a0001c0001t0002g0061 others(4): Show |
7 | HG01516.hp2 HG01975.hp1 HG03540.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13813_169-1381 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | C | CAAAA | 63 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(60): Show |
64 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.169-13814_169-1381 others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | C | CAAAAA | 6 | a0001c0001t0002g0052 a0001c0001t0002g0065 a0001c0001t0002g0081 others(3): Show |
6 | HG00544.hp1 HG01069.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.169-13815_169-1381 others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | C | CAAAAAAA | 21 | a0001c0001t0003g0007 a0001c0001t0003g0008 a0001c0001t0003g0009 others(18): Show |
21 | HG00639.hp1 HG00735.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.169-13817_169-1381 others(11): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0003g0005 a0001c0001t0003g0015 a0001c0001t0003g0016 others(4): Show |
7 | HG00741.hp2 NA18959.hp1 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13818_169-1381 others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165056 | CAA | C | 8 | a0001c0002t0004g0108 a0001c0002t0004g0111 a0001c0002t0004g0112 others(5): Show |
8 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-13812_169-1381 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35165056 | ||||||
| chr10:35165057 | A | C | 1 | a0001c0002t0004g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.169-13832A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165057 | |||||||
| chr10:35165058 | A | T | 1 | a0001c0002t0004g0110 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.169-13831A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165058 | |||||||
| chr10:35165066 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.169-13823A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165066 | |||||||
| chr10:35165069 | A | T | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-13820A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165069 | |||||||
| chr10:35165070 | A | AT | 7 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0189 others(4): Show |
7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-13819_169-1381 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165070 | |||||||
| chr10:35165070 | A | T | 7 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0138 others(4): Show |
7 | HG00735.hp1 HG02015.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-13819A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165070 | |||||||
| chr10:35165074 | A | AT | 9 | a0001c0001t0001g0120 a0001c0001t0001g0140 a0001c0001t0001g0182 others(6): Show |
9 | HG01261.hp2 HG02572.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.169-13815_169-1381 others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | |||||||
| chr10:35165074 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.169-13815A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | |||||||
| chr10:35165074 | A | T | 123 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(120): Show |
125 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.169-13815A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165074 | |||||||
| chr10:35165078 | A | AAAG | 10 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0263 others(7): Show |
10 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-13811_169-1381 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165078 | |||||||
| chr10:35165079 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.169-13810G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165079 | |||||||
| chr10:35165178 | T | C | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-13711T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165178 | |||||||
| chr10:35165271 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-13618A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165271 | |||||||
| chr10:35165369 | C | T | 1 | a0001c0001t0002g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.169-13520C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165369 | |||||||
| chr10:35165422 | A | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-13467A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165422 | |||||||
| chr10:35165477 | A | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-13412A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165477 | |||||||
| chr10:35165590 | A | T | 3 | a0001c0002t0004g0108 a0001c0002t0004g0116 a0001c0002t0004g0117 |
3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-13299A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165590 | |||||||
| chr10:35165712 | T | C | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-13177T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35165712 | |||||||
| chr10:35166048 | C | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.169-12841C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166048 | |||||||
| chr10:35166050 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.169-12839A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166050 | |||||||
| chr10:35166166 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-12723C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166166 | |||||||
| chr10:35166266 | C | CA | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-12615dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166266 | ||||||
| chr10:35166359 | C | T | 6 | a0001c0001t0001g0189 a0001c0001t0002g0281 a0001c0001t0002g0282 others(3): Show |
6 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-12530C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166359 | |||||||
| chr10:35166378 | T | C | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.169-12511T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166378 | |||||||
| chr10:35166408 | A | G | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-12481A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166408 | |||||||
| chr10:35166564 | C | CA | 14 | a0001c0001t0001g0143 a0001c0001t0001g0268 a0001c0001t0002g0059 others(11): Show |
14 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.169-12310dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | ||||||
| chr10:35166564 | C | CAA | 73 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(70): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.169-12311_169-1231 others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | ||||||
| chr10:35166564 | C | CAAA | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.169-12312_169-1231 others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35166564 | ||||||
| chr10:35166600 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-12289G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166600 | |||||||
| chr10:35166701 | C | T | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-12188C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166701 | |||||||
| chr10:35166831 | A | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.169-12058A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166831 | |||||||
| chr10:35166863 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-12026C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35166863 | |||||||
| chr10:35167001 | C | T | 2 | a0001c0001t0003g0109 a0001c0001t0009g0288 |
2 | HG02559.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.169-11888C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167001 | |||||||
| chr10:35167150 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0014g0193 |
2 | NA18960.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.169-11739A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167150 | |||||||
| chr10:35167230 | C | T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
6 | HG00438.hp2 NA18972.hp1 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.169-11659C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167230 | |||||||
| chr10:35167287 | G | A | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-11602G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167287 | |||||||
| chr10:35167306 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-11583A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167306 | |||||||
| chr10:35167314 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.169-11575C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167314 | |||||||
| chr10:35167367 | C | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-11522C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167367 | |||||||
| chr10:35167461 | G | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-11428G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167461 | |||||||
| chr10:35167476 | C | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-11413C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167476 | |||||||
| chr10:35167785 | A | T | 1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.169-11104A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167785 | |||||||
| chr10:35167890 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10999A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167890 | |||||||
| chr10:35167980 | A | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-10909A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35167980 | |||||||
| chr10:35167983 | CT | C | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-10899delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35167983 | ||||||
| chr10:35168158 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0034 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.169-10731C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168158 | |||||||
| chr10:35168247 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.169-10642C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168247 | |||||||
| chr10:35168269 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03098.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.169-10620C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168269 | |||||||
| chr10:35168286 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.169-10603G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168286 | |||||||
| chr10:35168335 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.169-10554T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168335 | |||||||
| chr10:35168385 | T | C | 2 | a0001c0001t0002g0037 a0001c0001t0002g0038 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.169-10504T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168385 | |||||||
| chr10:35168528 | T | C | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-10361T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168528 | |||||||
| chr10:35168545 | G | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10344G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168545 | |||||||
| chr10:35168591 | T | G | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.169-10298T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168591 | |||||||
| chr10:35168677 | C | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-10212C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168677 | |||||||
| chr10:35168754 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-10135C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168754 | |||||||
| chr10:35168850 | A | G | 1 | a0001c0001t0002g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.169-10039A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168850 | |||||||
| chr10:35168971 | A | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-9918A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35168971 | |||||||
| chr10:35169114 | G | GT | 5 | a0001c0001t0001g0148 a0001c0001t0002g0081 a0001c0001t0002g0092 others(2): Show |
5 | HG01169.hp1 HG01993.hp1 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-9769dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169114 | ||||||
| chr10:35169232 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-9657A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169232 | |||||||
| chr10:35169263 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0187 |
2 | HG02015.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.169-9626T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169263 | |||||||
| chr10:35169332 | T | A | 1 | a0001c0001t0001g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.169-9557T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169332 | |||||||
| chr10:35169376 | C | T | 1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.169-9513C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169376 | |||||||
| chr10:35169390 | C | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-9499C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169390 | |||||||
| chr10:35169597 | G | C | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-9292G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169597 | |||||||
| chr10:35169845 | G | A | 43 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(40): Show |
43 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.169-9044G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169845 | |||||||
| chr10:35169852 | A | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.169-9037A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169852 | |||||||
| chr10:35169893 | G | T | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.169-8996G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169893 | |||||||
| chr10:35169965 | C | CT | 84 | a0001c0001t0001g0138 a0001c0001t0001g0259 a0001c0001t0001g0260 others(81): Show |
85 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.169-8909dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | ||||||
| chr10:35169965 | C | CTT | 10 | a0001c0001t0001g0258 a0001c0001t0003g0025 a0001c0001t0003g0026 others(7): Show |
10 | HG02145.hp2 HG03491.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-8910_169-8909d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | ||||||
| chr10:35169965 | C | CTTT | 22 | a0001c0001t0001g0184 a0001c0001t0003g0005 a0001c0001t0003g0006 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-8911_169-8909d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35169965 | ||||||
| chr10:35169994 | G | A | 2 | a0001c0001t0003g0025 a0002c0006t0003g0032 |
2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.169-8895G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35169994 | |||||||
| chr10:35170014 | G | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-8875G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170014 | |||||||
| chr10:35170064 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-8825G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170064 | |||||||
| chr10:35170111 | C | T | 1 | a0003c0005t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.169-8778C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170111 | |||||||
| chr10:35170189 | T | G | 1 | a0001c0001t0007g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.169-8700T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170189 | |||||||
| chr10:35170201 | G | A | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.169-8688G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170201 | |||||||
| chr10:35170209 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.169-8680C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170209 | |||||||
| chr10:35170335 | C | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-8554C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170335 | |||||||
| chr10:35170359 | C | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-8530C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170359 | |||||||
| chr10:35170524 | T | C | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.169-8365T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170524 | |||||||
| chr10:35170569 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.169-8320A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170569 | |||||||
| chr10:35170747 | T | A | 3 | a0001c0002t0004g0108 a0001c0002t0004g0116 a0001c0002t0004g0117 |
3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.169-8142T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170747 | |||||||
| chr10:35170768 | G | C | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.169-8121G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35170768 | |||||||
| chr10:35171048 | G | A | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.169-7841G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171048 | |||||||
| chr10:35171147 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-7742A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171147 | |||||||
| chr10:35171161 | C | CT | 55 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(52): Show |
56 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.169-7703dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | C | CTT | 35 | a0001c0001t0001g0138 a0001c0001t0001g0190 a0001c0001t0001g0191 others(32): Show |
35 | HG00438.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.169-7704_169-7703d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | C | CTTT | 60 | a0001c0001t0002g0001 a0001c0001t0002g0038 a0001c0001t0002g0044 others(57): Show |
61 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.169-7705_169-7703d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | C | CTTTT | 12 | a0001c0001t0002g0037 a0001c0001t0002g0041 a0001c0001t0002g0059 others(9): Show |
12 | HG00733.hp2 HG01168.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-7706_169-7703d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | CT | C | 10 | a0001c0001t0001g0131 a0001c0001t0001g0254 a0001c0001t0001g0255 others(7): Show |
10 | HG01884.hp2 HG02559.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-7703delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | CTT | C | 7 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(4): Show |
7 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.169-7704_169-7703d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171161 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0157 others(1): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-7713_169-7703d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35171161 | ||||||
| chr10:35171295 | A | C | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7594A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171295 | |||||||
| chr10:35171296 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7593T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171296 | |||||||
| chr10:35171299 | G | T | 68 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(65): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.169-7590G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171299 | |||||||
| chr10:35171309 | T | C | 1 | a0001c0001t0001g0246 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.169-7580T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171309 | |||||||
| chr10:35171392 | G | C | 2 | a0001c0002t0004g0289 a0001c0002t0020g0290 |
2 | HG01071.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.169-7497G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171392 | |||||||
| chr10:35171419 | G | C | 1 | a0001c0001t0002g0079 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.169-7470G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171419 | |||||||
| chr10:35171424 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.169-7465G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171424 | |||||||
| chr10:35171491 | T | C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-7398T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171491 | |||||||
| chr10:35171578 | A | G | 2 | a0001c0001t0003g0011 a0001c0001t0003g0012 |
2 | HG00639.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.169-7311A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171578 | |||||||
| chr10:35171849 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169-7040A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171849 | |||||||
| chr10:35171850 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.169-7039T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35171850 | |||||||
| chr10:35172011 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.169-6878T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172011 | |||||||
| chr10:35172046 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.169-6843G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172046 | |||||||
| chr10:35172082 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-6807G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172082 | |||||||
| chr10:35172110 | T | C | 125 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(122): Show |
126 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.169-6779T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172110 | |||||||
| chr10:35172129 | CTTTGTTT others(3): Show |
C | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-6751_169-6742d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172129 | ||||||
| chr10:35172203 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.169-6686C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172203 | |||||||
| chr10:35172332 | A | G | 10 | a0001c0001t0003g0005 a0001c0001t0003g0007 a0001c0001t0003g0008 others(7): Show |
10 | HG01123.hp2 HG01981.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.169-6557A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172332 | |||||||
| chr10:35172385 | G | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0189 others(4): Show |
7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-6504G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172385 | |||||||
| chr10:35172414 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.169-6475C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172414 | |||||||
| chr10:35172419 | A | G | 2 | a0001c0001t0003g0025 a0002c0006t0003g0032 |
2 | HG03669.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.169-6470A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172419 | |||||||
| chr10:35172470 | CAG | C | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-6418_169-6417d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172470 | |||||||
| chr10:35172572 | GT | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(277): Show |
284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.169-6304delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172572 | ||||||
| chr10:35172574 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.169-6315T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172574 | |||||||
| chr10:35172690 | T | A | 2 | a0001c0001t0008g0245 a0001c0001t0008g0247 |
2 | HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.169-6199T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172690 | |||||||
| chr10:35172709 | A | AC | 81 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(78): Show |
82 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.169-6173dupC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35172709 | ||||||
| chr10:35172820 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-6069C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172820 | |||||||
| chr10:35172875 | A | T | 1 | a0001c0001t0001g0233 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.169-6014A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35172875 | |||||||
| chr10:35173022 | G | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.169-5867G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173022 | |||||||
| chr10:35173030 | T | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-5859T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173030 | |||||||
| chr10:35173351 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.169-5538A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173351 | |||||||
| chr10:35173432 | A | G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-5457A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173432 | |||||||
| chr10:35173474 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-5415G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173474 | |||||||
| chr10:35173711 | A | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-5178A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173711 | |||||||
| chr10:35173983 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-4906C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35173983 | |||||||
| chr10:35174134 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.169-4755A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174134 | |||||||
| chr10:35174243 | G | C | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.169-4646G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174243 | |||||||
| chr10:35174798 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.169-4091G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174798 | |||||||
| chr10:35174821 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.169-4068C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174821 | |||||||
| chr10:35174880 | G | A | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.169-4009G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35174880 | |||||||
| chr10:35175031 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.169-3858G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175031 | |||||||
| chr10:35175173 | T | C | 1 | a0001c0001t0002g0082 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.169-3716T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175173 | |||||||
| chr10:35175240 | G | A | 128 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(125): Show |
129 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.169-3649G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175240 | |||||||
| chr10:35175244 | G | A | 130 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(127): Show |
131 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.169-3645G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175244 | |||||||
| chr10:35175260 | A | AC | 39 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(36): Show |
39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3629_169-3628i others(3): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175260 | |||||||
| chr10:35175261 | T | A | 39 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(36): Show |
39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3628T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175261 | |||||||
| chr10:35175262 | G | T | 39 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(36): Show |
39 | HG00621.hp1 HG00738.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.169-3627G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175262 | |||||||
| chr10:35175274 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.169-3615G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175274 | |||||||
| chr10:35175307 | G | A | 7 | a0001c0001t0002g0051 a0001c0001t0002g0053 a0001c0001t0002g0056 others(4): Show |
7 | HG01258.hp2 HG01358.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.169-3582G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175307 | |||||||
| chr10:35175445 | C | CA | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-3434dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35175445 | ||||||
| chr10:35175503 | G | T | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-3386G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175503 | |||||||
| chr10:35175547 | G | A | 2 | a0001c0001t0007g0040 a0001c0001t0018g0287 |
2 | HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.169-3342G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175547 | |||||||
| chr10:35175610 | C | T | 1 | a0001c0001t0001g0168 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.169-3279C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175610 | |||||||
| chr10:35175744 | G | A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.169-3145G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175744 | |||||||
| chr10:35175850 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.169-3039C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175850 | |||||||
| chr10:35175905 | T | C | 1 | a0001c0001t0002g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.169-2984T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35175905 | |||||||
| chr10:35176060 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.169-2829C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176060 | |||||||
| chr10:35176173 | G | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.169-2716G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176173 | |||||||
| chr10:35176243 | C | T | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.169-2646C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176243 | |||||||
| chr10:35176251 | G | A | 5 | a0001c0001t0002g0044 a0001c0001t0002g0047 a0001c0001t0002g0048 others(2): Show |
5 | HG02129.hp1 NA18612.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.169-2638G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176251 | |||||||
| chr10:35176262 | T | A | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2627T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176262 | |||||||
| chr10:35176351 | G | C | 101 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(98): Show |
102 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.169-2538G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176351 | |||||||
| chr10:35176409 | CT | C | 11 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0194 others(8): Show |
11 | HG00558.hp1 HG01884.hp2 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.169-2464delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35176409 | ||||||
| chr10:35176424 | T | G | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2465T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176424 | |||||||
| chr10:35176469 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2420A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176469 | |||||||
| chr10:35176508 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.169-2381C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176508 | |||||||
| chr10:35176533 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.169-2356G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176533 | |||||||
| chr10:35176535 | G | A | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.169-2354G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176535 | |||||||
| chr10:35176630 | T | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-2259T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176630 | |||||||
| chr10:35176671 | A | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0076 |
2 | NA18946.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.169-2218A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176671 | |||||||
| chr10:35176688 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.169-2201C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176688 | |||||||
| chr10:35176818 | G | A | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.169-2071G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176818 | |||||||
| chr10:35176848 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-2041C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176848 | |||||||
| chr10:35176952 | T | C | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-1937T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35176952 | |||||||
| chr10:35177077 | CA | C | 59 | a0001c0001t0001g0137 a0001c0001t0001g0170 a0001c0001t0001g0172 others(56): Show |
59 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.169-1801delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr10 | 35177077 | ||||||
| chr10:35177132 | T | C | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.169-1757T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177132 | |||||||
| chr10:35177222 | A | G | 1 | a0001c0001t0001g0284 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.169-1667A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177222 | |||||||
| chr10:35177257 | T | G | 120 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.169-1632T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177257 | |||||||
| chr10:35177259 | C | T | 1 | a0001c0001t0001g0230 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.169-1630C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177259 | |||||||
| chr10:35177305 | T | C | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.169-1584T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177305 | |||||||
| chr10:35177451 | A | G | 33 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(30): Show |
33 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.169-1438A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177451 | |||||||
| chr10:35177554 | C | T | 1 | a0001c0001t0001g0131 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.169-1335C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177554 | |||||||
| chr10:35177568 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.169-1321G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177568 | |||||||
| chr10:35177843 | G | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.169-1046G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177843 | |||||||
| chr10:35177999 | G | A | 4 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0001c0001t0001g0263 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.169-890G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35177999 | |||||||
| chr10:35178139 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.169-750T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178139 | |||||||
| chr10:35178434 | T | C | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0275 |
3 | HG02622.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.169-455T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178434 | |||||||
| chr10:35178743 | C | T | 124 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(121): Show |
125 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.169-146C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 3/7 | chr10 | 35178743 | |||||||
| chr10:35179342 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.409+66A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35179342 | |||||||
| chr10:35180112 | A | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.409+836A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180112 | |||||||
| chr10:35180157 | G | C | 2 | a0001c0001t0001g0227 a0001c0001t0001g0231 |
2 | NA18984.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.409+881G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180157 | |||||||
| chr10:35180250 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.409+974G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180250 | |||||||
| chr10:35180734 | G | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.409+1458G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180734 | |||||||
| chr10:35180769 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0167 |
4 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1493G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180769 | |||||||
| chr10:35180845 | G | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+1569G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35180845 | |||||||
| chr10:35181047 | T | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.409+1771T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181047 | |||||||
| chr10:35181214 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.409+1938C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181214 | |||||||
| chr10:35181215 | A | C | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.409+1939A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181215 | |||||||
| chr10:35181221 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.409+1945C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181221 | |||||||
| chr10:35181373 | A | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0034 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.409+2097A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181373 | |||||||
| chr10:35181518 | G | T | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02559.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+2242G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181518 | |||||||
| chr10:35181525 | G | T | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0267 others(1): Show |
4 | HG02258.hp1 HG02258.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+2249G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181525 | |||||||
| chr10:35181656 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | NA20129.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.409+2380T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181656 | |||||||
| chr10:35181830 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.409+2554A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181830 | |||||||
| chr10:35181913 | A | T | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.409+2637A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181913 | |||||||
| chr10:35181997 | A | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.409+2721A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35181997 | |||||||
| chr10:35182023 | C | T | 3 | a0001c0002t0004g0108 a0001c0002t0004g0116 a0001c0002t0004g0117 |
3 | HG01109.hp1 HG02723.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.409+2747C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182023 | |||||||
| chr10:35182154 | A | G | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.409+2878A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182154 | |||||||
| chr10:35182175 | G | A | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.409+2899G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182175 | |||||||
| chr10:35182355 | A | G | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.409+3079A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182355 | |||||||
| chr10:35182369 | C | T | 5 | a0001c0002t0004g0110 a0001c0002t0004g0111 a0001c0002t0004g0112 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.409+3093C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182369 | |||||||
| chr10:35182382 | A | AT | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.409+3114dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35182382 | ||||||
| chr10:35182443 | C | T | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.409+3167C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182443 | |||||||
| chr10:35182482 | T | G | 3 | a0001c0001t0001g0259 a0001c0001t0001g0260 a0001c0001t0001g0264 |
3 | HG00621.hp1 HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.409+3206T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182482 | |||||||
| chr10:35182668 | GACTT | G | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.409+3396_409+3399d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35182668 | ||||||
| chr10:35182672 | T | G | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.409+3396T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182672 | |||||||
| chr10:35182793 | A | G | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+3517A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182793 | |||||||
| chr10:35182813 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.409+3537A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182813 | |||||||
| chr10:35182945 | G | A | 140 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
141 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.409+3669G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35182945 | |||||||
| chr10:35183222 | T | C | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.409+3946T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183222 | |||||||
| chr10:35183271 | A | G | 121 | a0001c0001t0001g0136 a0001c0001t0002g0001 a0001c0001t0002g0037 others(118): Show |
122 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.409+3995A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183271 | |||||||
| chr10:35183504 | T | C | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.409+4228T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183504 | |||||||
| chr10:35183546 | A | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.409+4270A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183546 | |||||||
| chr10:35183627 | C | A | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.409+4351C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183627 | |||||||
| chr10:35183813 | G | A | 1 | a0001c0001t0002g0061 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.410-4387G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183813 | |||||||
| chr10:35183817 | G | A | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.410-4383G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183817 | |||||||
| chr10:35183827 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.410-4373C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183827 | |||||||
| chr10:35183891 | A | G | 1 | a0001c0001t0002g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.410-4309A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183891 | |||||||
| chr10:35183905 | T | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-4295T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35183905 | |||||||
| chr10:35184107 | G | A | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-4093G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184107 | |||||||
| chr10:35184116 | C | T | 2 | a0001c0001t0005g0002 a0001c0001t0005g0127 |
3 | HG02895.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.410-4084C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184116 | |||||||
| chr10:35184128 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410-4072T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184128 | |||||||
| chr10:35184185 | C | A | 4 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(1): Show |
4 | HG01192.hp1 HG02622.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-4015C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184185 | |||||||
| chr10:35184557 | G | A | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-3643G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184557 | |||||||
| chr10:35184624 | T | C | 3 | a0001c0002t0004g0036 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.410-3576T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184624 | |||||||
| chr10:35184707 | G | T | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-3493G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184707 | |||||||
| chr10:35184786 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-3414C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184786 | |||||||
| chr10:35184797 | AAAAG | A | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-3397_410-3394d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35184797 | ||||||
| chr10:35184814 | G | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.410-3386G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184814 | |||||||
| chr10:35184880 | A | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-3320A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184880 | |||||||
| chr10:35184950 | T | G | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.410-3250T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184950 | |||||||
| chr10:35184985 | A | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-3215A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184985 | |||||||
| chr10:35184999 | T | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.410-3201T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35184999 | |||||||
| chr10:35185033 | C | CCATT | 147 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(144): Show |
150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.410-3137_410-3134d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | ||||||
| chr10:35185033 | C | CCATTCAT others(1): Show |
12 | a0001c0001t0001g0119 a0001c0001t0001g0138 a0001c0001t0001g0140 others(9): Show |
12 | HG00423.hp1 HG00621.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-3141_410-3134d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | ||||||
| chr10:35185033 | CCATT | C | 3 | a0001c0001t0003g0009 a0001c0001t0003g0109 a0001c0001t0018g0287 |
3 | HG01081.hp1 HG02895.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.410-3137_410-3134d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | ||||||
| chr10:35185033 | CCATTCAT others(1): Show |
C | 102 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(99): Show |
103 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.410-3141_410-3134d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185033 | ||||||
| chr10:35185067 | T | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-3133T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185067 | |||||||
| chr10:35185085 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.410-3115T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185085 | |||||||
| chr10:35185101 | T | C | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-3099T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185101 | |||||||
| chr10:35185106 | CT | C | 114 | a0001c0001t0001g0174 a0001c0001t0001g0286 a0001c0001t0002g0001 others(111): Show |
115 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.410-3078delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35185106 | ||||||
| chr10:35185189 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410-3011G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185189 | |||||||
| chr10:35185205 | C | T | 1 | a0001c0001t0014g0193 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.410-2995C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185205 | |||||||
| chr10:35185292 | C | T | 5 | a0001c0001t0001g0138 a0001c0001t0001g0201 a0001c0001t0003g0025 others(2): Show |
5 | HG03669.hp2 HG04115.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-2908C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185292 | |||||||
| chr10:35185350 | A | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-2850A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185350 | |||||||
| chr10:35185462 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.410-2738C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185462 | |||||||
| chr10:35185493 | A | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(134): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.410-2707A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185493 | |||||||
| chr10:35185628 | A | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-2572A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185628 | |||||||
| chr10:35185631 | A | G | 1 | a0001c0001t0003g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410-2569A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185631 | |||||||
| chr10:35185708 | A | G | 1 | a0001c0001t0001g0207 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.410-2492A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185708 | |||||||
| chr10:35185771 | T | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-2429T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185771 | |||||||
| chr10:35185835 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-2365C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185835 | |||||||
| chr10:35185889 | T | C | 1 | a0003c0005t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.410-2311T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185889 | |||||||
| chr10:35185978 | C | T | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.410-2222C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35185978 | |||||||
| chr10:35186111 | C | A | 1 | a0001c0001t0001g0235 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.410-2089C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186111 | |||||||
| chr10:35186112 | T | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-2088T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186112 | |||||||
| chr10:35186190 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.410-2010T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186190 | |||||||
| chr10:35186222 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.410-1978G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186222 | |||||||
| chr10:35186234 | T | C | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.410-1966T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186234 | |||||||
| chr10:35186380 | T | G | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1820T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186380 | |||||||
| chr10:35186382 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1818A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186382 | |||||||
| chr10:35186383 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1817G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186383 | |||||||
| chr10:35186387 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1813T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186387 | |||||||
| chr10:35186390 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1810A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186390 | |||||||
| chr10:35186393 | G | A | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1807G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186393 | |||||||
| chr10:35186394 | A | G | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1806A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186394 | |||||||
| chr10:35186395 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.410-1805A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186395 | |||||||
| chr10:35186650 | A | G | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-1550A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186650 | |||||||
| chr10:35186656 | C | T | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.410-1544C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186656 | |||||||
| chr10:35186671 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0121 others(59): Show |
63 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.410-1529A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186671 | |||||||
| chr10:35186707 | A | T | 1 | a0001c0001t0002g0083 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.410-1493A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186707 | |||||||
| chr10:35186713 | CAT | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-1481_410-1480d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186713 | ||||||
| chr10:35186723 | T | TATATATA others(46): Show |
1 | a0001c0001t0001g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.410-1475_410-1423d others(55): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186723 | ||||||
| chr10:35186828 | A | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0243 |
3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410-1372A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186828 | |||||||
| chr10:35186843 | T | C | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.410-1357T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186843 | |||||||
| chr10:35186845 | C | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-1355C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186845 | |||||||
| chr10:35186846 | G | C | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.410-1354G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186846 | |||||||
| chr10:35186902 | TATA | T | 103 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(100): Show |
104 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.410-1292_410-1290d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186902 | ||||||
| chr10:35186909 | A | G | 27 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0055 others(24): Show |
27 | HG00544.hp1 HG02015.hp1 HG02040.hp1 others(24): Show |
intron_variant | MODIFIER | c.410-1291A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186909 | |||||||
| chr10:35186947 | T | TTA | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-1244_410-1243d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186947 | ||||||
| chr10:35186981 | G | A | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186981 | |||||||
| chr10:35186984 | ATATATAT others(51): Show |
A | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.410-1208_410-1151d others(60): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186984 | ||||||
| chr10:35186999 | T | C | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-1201T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35186999 | |||||||
| chr10:35186999 | TATATATA others(5): Show |
T | 1 | a0001c0001t0001g0238 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.410-1188_410-1177d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35186999 | ||||||
| chr10:35187001 | TATATA | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0243 |
3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.410-1188_410-1184d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187001 | ||||||
| chr10:35187004 | A | T | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1196A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187004 | |||||||
| chr10:35187005 | T | A | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1195T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187005 | |||||||
| chr10:35187006 | A | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-1194A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187006 | |||||||
| chr10:35187006 | A | T | 7 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(4): Show |
7 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.410-1194A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187006 | |||||||
| chr10:35187029 | C | T | 87 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(84): Show |
88 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.410-1171C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187029 | |||||||
| chr10:35187049 | T | A | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.410-1151T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187049 | |||||||
| chr10:35187060 | T | TA | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.410-1139dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187060 | ||||||
| chr10:35187075 | AAT | A | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1117_410-1116d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187075 | ||||||
| chr10:35187077 | TATATATA others(7): Show |
T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-1115_410-1102d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187077 | ||||||
| chr10:35187082 | ATAATATA others(4): Show |
A | 22 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(19): Show |
22 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.410-1117_410-1107d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187082 | |||||||
| chr10:35187084 | A | C | 1 | a0001c0001t0001g0271 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.410-1116A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187084 | |||||||
| chr10:35187092 | A | ATAATT | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-1106_410-1105i others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187092 | ||||||
| chr10:35187099 | TGA | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.410-1100_410-1099d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187099 | |||||||
| chr10:35187100 | G | A | 32 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(29): Show |
32 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.410-1100G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187100 | |||||||
| chr10:35187100 | G | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-1100G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187100 | |||||||
| chr10:35187101 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.410-1099A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187101 | |||||||
| chr10:35187108 | T | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.410-1092T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187108 | |||||||
| chr10:35187119 | T | C | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-1081T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187119 | |||||||
| chr10:35187122 | A | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410-1078A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187122 | |||||||
| chr10:35187130 | T | A | 6 | a0001c0001t0001g0131 a0001c0002t0004g0110 a0001c0002t0004g0111 others(3): Show |
6 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.410-1070T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187130 | |||||||
| chr10:35187130 | TAATATAT others(18): Show |
T | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1068_410-1044d others(27): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187130 | ||||||
| chr10:35187131 | A | T | 107 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(104): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.410-1069A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187131 | |||||||
| chr10:35187131 | AAT | A | 4 | a0001c0002t0004g0036 a0001c0002t0004g0115 a0001c0002t0004g0289 others(1): Show |
4 | HG01071.hp1 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-1064_410-1063d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187131 | ||||||
| chr10:35187136 | AT | A | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1062delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187136 | ||||||
| chr10:35187142 | A | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.410-1058A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187142 | |||||||
| chr10:35187147 | A | T | 9 | a0001c0001t0001g0166 a0001c0002t0004g0108 a0001c0002t0004g0110 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1053A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187147 | |||||||
| chr10:35187148 | TATATATA others(39): Show |
T | 1 | a0001c0001t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.410-1028_410-983de others(47): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187148 | ||||||
| chr10:35187152 | TATAATAT others(49): Show |
T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.410-1047_410-992de others(57): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187152 | |||||||
| chr10:35187155 | A | T | 60 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(57): Show |
60 | HG00621.hp1 HG00639.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.410-1045A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187155 | |||||||
| chr10:35187156 | A | T | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1044A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187156 | |||||||
| chr10:35187162 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1038A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187162 | |||||||
| chr10:35187163 | T | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1037T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187163 | |||||||
| chr10:35187163 | TTATATAT others(9): Show |
T | 35 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(32): Show |
35 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.410-1030_410-1015d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187163 | ||||||
| chr10:35187165 | AT | A | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1034delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187165 | |||||||
| chr10:35187170 | T | A | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1030T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187170 | |||||||
| chr10:35187171 | T | A | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1029T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187171 | |||||||
| chr10:35187172 | A | T | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1028A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187172 | |||||||
| chr10:35187176 | T | TATAATAT others(8): Show |
1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.410-1024_410-1023i others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187176 | |||||||
| chr10:35187176 | T | TATTTATA others(26): Show |
8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410-1024_410-1023i others(35): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187176 | |||||||
| chr10:35187177 | T | A | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1023T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187177 | |||||||
| chr10:35187179 | A | ATATATTT others(32): Show |
1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.410-1016_410-1015i others(41): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187179 | ||||||
| chr10:35187179 | A | ATATATTT others(32): Show |
3 | a0001c0002t0004g0115 a0001c0002t0004g0289 a0001c0002t0020g0290 |
3 | HG01071.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.410-1016_410-1015i others(41): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187179 | ||||||
| chr10:35187179 | A | T | 9 | a0001c0001t0003g0109 a0001c0002t0004g0108 a0001c0002t0004g0110 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.410-1021A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187179 | |||||||
| chr10:35187185 | A | T | 8 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(5): Show |
9 | HG02895.hp1 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.410-1015A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187185 | |||||||
| chr10:35187186 | A | T | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1014A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187186 | |||||||
| chr10:35187190 | TA | T | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG01192.hp1 HG01884.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.410-1009delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187190 | |||||||
| chr10:35187193 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.410-1007T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187193 | |||||||
| chr10:35187197 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.410-1003A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187197 | |||||||
| chr10:35187209 | T | A | 1 | a0001c0001t0001g0158 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.410-991T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187209 | |||||||
| chr10:35187210 | T | A | 2 | a0001c0001t0001g0150 a0001c0001t0016g0196 |
2 | NA18947.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.410-990T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187210 | |||||||
| chr10:35187218 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.410-982T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187218 | |||||||
| chr10:35187235 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.410-965T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187235 | |||||||
| chr10:35187271 | GT | G | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.410-918delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr10 | 35187271 | ||||||
| chr10:35187273 | T | G | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.410-927T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187273 | |||||||
| chr10:35187385 | G | A | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.410-815G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187385 | |||||||
| chr10:35187395 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.410-805G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187395 | |||||||
| chr10:35187506 | T | C | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.410-694T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187506 | |||||||
| chr10:35187540 | G | T | 1 | a0001c0001t0002g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.410-660G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187540 | |||||||
| chr10:35187822 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.410-378A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187822 | |||||||
| chr10:35187925 | T | G | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.410-275T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187925 | |||||||
| chr10:35187991 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0012g0273 |
2 | HG00735.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.410-209A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35187991 | |||||||
| chr10:35188004 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0121 others(61): Show |
65 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.410-196T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 5/7 | chr10 | 35188004 | |||||||
| chr10:35188424 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.598+36A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188424 | |||||||
| chr10:35188574 | C | T | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.598+186C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188574 | |||||||
| chr10:35188642 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.598+254G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188642 | |||||||
| chr10:35188659 | A | AT | 14 | a0001c0001t0001g0120 a0001c0001t0001g0130 a0001c0001t0001g0248 others(11): Show |
14 | HG00621.hp1 HG01891.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.598+289dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35188659 | ||||||
| chr10:35188659 | AT | A | 115 | a0001c0001t0001g0226 a0001c0001t0001g0232 a0001c0001t0001g0252 others(112): Show |
116 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.598+289delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35188659 | ||||||
| chr10:35188672 | T | G | 2 | a0001c0001t0001g0276 a0001c0001t0012g0273 |
2 | HG00735.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.598+284T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188672 | |||||||
| chr10:35188685 | A | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0034 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598+297A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188685 | |||||||
| chr10:35188691 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+303G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188691 | |||||||
| chr10:35188847 | G | A | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+459G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188847 | |||||||
| chr10:35188937 | G | A | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+549G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188937 | |||||||
| chr10:35188974 | A | G | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(213): Show |
220 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(217): Show |
intron_variant | MODIFIER | c.598+586A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35188974 | |||||||
| chr10:35189132 | T | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+744T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189132 | |||||||
| chr10:35189177 | G | GT | 70 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(67): Show |
71 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.598+798dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189177 | ||||||
| chr10:35189183 | T | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+795T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189183 | |||||||
| chr10:35189187 | G | T | 113 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(110): Show |
114 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.598+799G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189187 | |||||||
| chr10:35189195 | G | GT | 9 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(6): Show |
9 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+814dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189195 | ||||||
| chr10:35189199 | T | G | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.598+811T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189199 | |||||||
| chr10:35189333 | C | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+945C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189333 | |||||||
| chr10:35189463 | A | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+1075A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189463 | |||||||
| chr10:35189469 | A | G | 1 | a0001c0002t0004g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598+1081A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189469 | |||||||
| chr10:35189481 | TTTGC | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+1101_598+1104d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189481 | ||||||
| chr10:35189489 | CTTGT | C | 73 | a0001c0001t0001g0206 a0001c0001t0002g0001 a0001c0001t0002g0037 others(70): Show |
74 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.598+1116_598+1119d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35189489 | ||||||
| chr10:35189582 | C | T | 2 | a0001c0001t0003g0030 a0001c0001t0003g0031 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.598+1194C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189582 | |||||||
| chr10:35189601 | C | T | 107 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(104): Show |
108 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.598+1213C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189601 | |||||||
| chr10:35189725 | A | C | 1 | a0001c0001t0003g0035 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.598+1337A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189725 | |||||||
| chr10:35189726 | G | A | 1 | a0001c0001t0003g0035 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.598+1338G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189726 | |||||||
| chr10:35189852 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.598+1464A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35189852 | |||||||
| chr10:35190044 | C | G | 7 | a0001c0001t0002g0050 a0001c0001t0002g0054 a0001c0001t0002g0080 others(4): Show |
7 | HG00280.hp2 HG01081.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+1656C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190044 | |||||||
| chr10:35190184 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0034 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598+1796C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190184 | |||||||
| chr10:35190336 | G | T | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+1948G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190336 | |||||||
| chr10:35190562 | A | G | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.598+2174A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190562 | |||||||
| chr10:35190576 | G | T | 109 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(106): Show |
110 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.598+2188G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190576 | |||||||
| chr10:35190669 | A | AT | 6 | a0001c0001t0001g0206 a0001c0001t0002g0281 a0001c0001t0002g0282 others(3): Show |
6 | HG01192.hp1 HG02129.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.598+2291dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35190669 | ||||||
| chr10:35190780 | G | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+2392G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190780 | |||||||
| chr10:35190915 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.598+2527G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190915 | |||||||
| chr10:35190958 | A | G | 108 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(105): Show |
109 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(106): Show |
intron_variant | MODIFIER | c.598+2570A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35190958 | |||||||
| chr10:35191086 | T | TTTTATTT others(1): Show |
150 | a0001c0001t0001g0004 a0001c0001t0001g0118 a0001c0001t0001g0119 others(147): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.598+2713_598+2720d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(5): Show |
18 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0166 others(15): Show |
19 | HG00621.hp1 HG01071.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.598+2709_598+2720d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(9): Show |
30 | a0001c0001t0001g0167 a0001c0001t0003g0005 a0001c0001t0003g0007 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.598+2705_598+2720d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(13): Show |
16 | a0001c0001t0002g0037 a0001c0001t0002g0061 a0001c0001t0002g0080 others(13): Show |
16 | HG00733.hp2 HG01081.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+2701_598+2720d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(17): Show |
55 | a0001c0001t0002g0038 a0001c0001t0002g0044 a0001c0001t0002g0045 others(52): Show |
55 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.598+2720_598+2721i others(26): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(21): Show |
15 | a0001c0001t0002g0001 a0001c0001t0002g0041 a0001c0001t0002g0048 others(12): Show |
16 | HG00423.hp2 HG02040.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.598+2720_598+2721i others(30): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(25): Show |
1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+2720_598+2721i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTATTT others(25): Show |
1 | a0001c0001t0002g0283 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.598+2720_598+2721i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191086 | T | TTTTTTTT others(25): Show |
1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598+2701_598+2702i others(34): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191086 | ||||||
| chr10:35191147 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.598+2759C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191147 | |||||||
| chr10:35191150 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0213 |
2 | NA18954.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.598+2762G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191150 | |||||||
| chr10:35191383 | T | C | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+2995T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191383 | |||||||
| chr10:35191444 | T | A | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.598+3056T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191444 | |||||||
| chr10:35191652 | C | A | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.598+3264C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191652 | |||||||
| chr10:35191688 | C | T | 1 | a0001c0001t0002g0063 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.598+3300C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191688 | |||||||
| chr10:35191694 | T | G | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+3306T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191694 | |||||||
| chr10:35191821 | C | T | 1 | a0001c0001t0001g0208 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.598+3433C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191821 | |||||||
| chr10:35191822 | G | A | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+3434G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35191822 | |||||||
| chr10:35191938 | C | CCCACCTG others(3): Show |
119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.598+3551_598+3552i others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35191938 | ||||||
| chr10:35192054 | C | G | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+3666C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192054 | |||||||
| chr10:35192238 | G | C | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+3850G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192238 | |||||||
| chr10:35192241 | A | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+3853A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192241 | |||||||
| chr10:35192351 | C | T | 1 | a0001c0001t0003g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.598+3963C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192351 | |||||||
| chr10:35192484 | G | T | 1 | a0001c0001t0002g0089 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.598+4096G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192484 | |||||||
| chr10:35192613 | T | C | 1 | a0001c0001t0001g0202 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.598+4225T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192613 | |||||||
| chr10:35192791 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598+4403A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192791 | |||||||
| chr10:35192811 | C | T | 2 | a0001c0001t0003g0007 a0001c0001t0003g0008 |
2 | HG01123.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.598+4423C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192811 | |||||||
| chr10:35192844 | T | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+4456T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35192844 | |||||||
| chr10:35193037 | G | T | 120 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.598+4649G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193037 | |||||||
| chr10:35193039 | TC | T | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+4655delC | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35193039 | ||||||
| chr10:35193121 | T | G | 1 | a0001c0001t0006g0241 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.598+4733T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193121 | |||||||
| chr10:35193264 | G | T | 1 | a0001c0001t0001g0169 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.598+4876G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193264 | |||||||
| chr10:35193379 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.598+4991T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193379 | |||||||
| chr10:35193382 | T | C | 1 | a0001c0002t0004g0117 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.598+4994T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193382 | |||||||
| chr10:35193498 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+5110C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193498 | |||||||
| chr10:35193610 | C | A | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+5222C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193610 | |||||||
| chr10:35193624 | T | TA | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+5238dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35193624 | ||||||
| chr10:35193634 | G | T | 9 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(6): Show |
9 | HG03491.hp1 HG03492.hp1 HG03669.hp2 others(6): Show |
intron_variant | MODIFIER | c.598+5246G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193634 | |||||||
| chr10:35193636 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.598+5248C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193636 | |||||||
| chr10:35193683 | T | C | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.598+5295T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193683 | |||||||
| chr10:35193702 | G | C | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.598+5314G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35193702 | |||||||
| chr10:35194001 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+5613G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194001 | |||||||
| chr10:35194097 | C | CA | 45 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(42): Show |
45 | HG00438.hp1 HG00558.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.598+5736dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAA | 8 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+5732_598+5736d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0001 a0001c0001t0002g0041 a0001c0001t0002g0047 others(4): Show |
8 | HG00423.hp2 HG01515.hp1 HG02040.hp2 others(5): Show |
intron_variant | MODIFIER | c.598+5727_598+5736d others(12): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(4): Show |
17 | a0001c0001t0002g0037 a0001c0001t0002g0038 a0001c0001t0002g0051 others(14): Show |
17 | HG00733.hp2 HG01081.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.598+5726_598+5736d others(13): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(5): Show |
32 | a0001c0001t0002g0046 a0001c0001t0002g0052 a0001c0001t0002g0055 others(29): Show |
32 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.598+5725_598+5736d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(6): Show |
25 | a0001c0001t0002g0045 a0001c0001t0002g0062 a0001c0001t0002g0064 others(22): Show |
25 | HG01074.hp1 HG01081.hp1 HG01169.hp1 others(22): Show |
intron_variant | MODIFIER | c.598+5724_598+5736d others(15): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0027 others(1): Show |
4 | HG00639.hp1 HG03492.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+5723_598+5736d others(16): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0060 a0001c0001t0003g0026 a0001c0001t0003g0028 |
3 | HG03688.hp2 HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.598+5722_598+5736d others(17): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0003g0029 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.598+5721_598+5736d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0002g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.598+5720_598+5736d others(19): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0003g0025 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.598+5719_598+5736d others(20): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(12): Show |
2 | a0001c0001t0002g0050 a0001c0001t0003g0033 |
2 | HG00280.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.598+5718_598+5736d others(21): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | C | CAAAAAAA others(13): Show |
1 | a0002c0006t0003g0032 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.598+5717_598+5736d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194097 | CA | C | 7 | a0001c0001t0001g0149 a0001c0001t0001g0169 a0001c0001t0001g0174 others(4): Show |
7 | HG01167.hp2 HG01168.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.598+5736delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194097 | ||||||
| chr10:35194322 | TA | T | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.598+5942delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194322 | ||||||
| chr10:35194426 | A | G | 1 | a0001c0002t0004g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.598+6038A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194426 | |||||||
| chr10:35194450 | A | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+6062A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194450 | |||||||
| chr10:35194515 | C | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.598+6127C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194515 | |||||||
| chr10:35194611 | T | G | 1 | a0001c0001t0001g0216 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.598+6223T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194611 | |||||||
| chr10:35194741 | GT | G | 16 | a0001c0001t0001g0140 a0001c0001t0001g0157 a0001c0001t0001g0167 others(13): Show |
16 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.598+6367delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194741 | ||||||
| chr10:35194741 | GTT | G | 106 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(103): Show |
107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.598+6366_598+6367d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194741 | ||||||
| chr10:35194841 | A | G | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+6453A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194841 | |||||||
| chr10:35194899 | G | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.598+6511G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35194899 | |||||||
| chr10:35194901 | C | CATT | 31 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(28): Show |
32 | HG00621.hp1 HG01168.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.598+6538_598+6540d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | ||||||
| chr10:35194901 | C | CATTATT | 4 | a0001c0001t0001g0168 a0001c0001t0001g0199 a0001c0001t0003g0025 others(1): Show |
4 | HG03453.hp2 HG03669.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+6535_598+6540d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | ||||||
| chr10:35194901 | CATT | C | 91 | a0001c0001t0001g0258 a0001c0001t0002g0001 a0001c0001t0002g0037 others(88): Show |
92 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.598+6538_598+6540d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35194901 | ||||||
| chr10:35195053 | T | C | 1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.598+6665T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195053 | |||||||
| chr10:35195261 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.598+6873T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195261 | |||||||
| chr10:35195292 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598+6904G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195292 | |||||||
| chr10:35195491 | C | G | 4 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0001c0001t0001g0263 others(1): Show |
4 | HG01891.hp1 HG02145.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.598+7103C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195491 | |||||||
| chr10:35195549 | G | C | 1 | a0001c0001t0002g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.598+7161G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195549 | |||||||
| chr10:35195598 | A | G | 1 | a0001c0001t0007g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.598+7210A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195598 | |||||||
| chr10:35195622 | G | C | 1 | a0001c0001t0011g0210 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.598+7234G>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195622 | |||||||
| chr10:35195801 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.598+7413G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35195801 | |||||||
| chr10:35196021 | T | G | 126 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(123): Show |
127 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.598+7633T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196021 | |||||||
| chr10:35196135 | T | C | 1 | a0001c0001t0016g0196 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.598+7747T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196135 | |||||||
| chr10:35196469 | A | C | 1 | a0001c0001t0002g0102 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.598+8081A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196469 | |||||||
| chr10:35196585 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.598+8197A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196585 | |||||||
| chr10:35196607 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.598+8219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196607 | |||||||
| chr10:35196710 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.598+8322C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196710 | |||||||
| chr10:35196736 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.598+8348A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196736 | |||||||
| chr10:35196761 | A | T | 122 | a0001c0001t0001g0261 a0001c0001t0002g0001 a0001c0001t0002g0037 others(119): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.598+8373A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196761 | |||||||
| chr10:35196808 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.598+8420G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196808 | |||||||
| chr10:35196822 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.598+8434C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196822 | |||||||
| chr10:35196865 | C | CT | 18 | a0001c0001t0001g0122 a0001c0001t0001g0146 a0001c0001t0001g0167 others(15): Show |
18 | HG00280.hp1 HG00544.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.598+8499dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | ||||||
| chr10:35196865 | C | CTT | 10 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(7): Show |
10 | HG00621.hp1 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.598+8498_598+8499d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | ||||||
| chr10:35196865 | C | CTTT | 12 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(9): Show |
12 | HG00738.hp2 HG01071.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.598+8497_598+8499d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | ||||||
| chr10:35196865 | C | CTTTTTT | 67 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(64): Show |
68 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.598+8494_598+8499d others(8): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | ||||||
| chr10:35196865 | C | CTTTTTTT | 31 | a0001c0001t0001g0261 a0001c0001t0002g0041 a0001c0001t0002g0044 others(28): Show |
31 | HG00280.hp2 HG00741.hp2 HG01081.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+8493_598+8499d others(9): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35196865 | ||||||
| chr10:35196895 | G | A | 122 | a0001c0001t0001g0261 a0001c0001t0002g0001 a0001c0001t0002g0037 others(119): Show |
123 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.598+8507G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196895 | |||||||
| chr10:35196930 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0157 others(1): Show |
5 | HG02572.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+8542C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196930 | |||||||
| chr10:35196932 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.598+8544C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35196932 | |||||||
| chr10:35197218 | A | G | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+8830A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197218 | |||||||
| chr10:35197346 | T | A | 5 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 others(2): Show |
5 | HG01192.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+8958T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197346 | |||||||
| chr10:35197416 | C | CTTTA | 30 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0136 others(27): Show |
32 | HG00099.hp1 HG00733.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.598+9076_598+9079d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197416 | CTTTA | C | 141 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0128 others(138): Show |
142 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.598+9076_598+9079d others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197416 | CTTTATTT others(1): Show |
C | 10 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0275 others(7): Show |
10 | HG01258.hp2 HG01261.hp1 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+9072_598+9079d others(10): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197416 | CTTTATTT others(5): Show |
C | 9 | a0001c0001t0001g0123 a0001c0001t0001g0199 a0001c0001t0002g0082 others(6): Show |
10 | HG00423.hp2 HG01175.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.598+9068_598+9079d others(14): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197416 | CTTTATTT others(9): Show |
C | 4 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0202 others(1): Show |
4 | HG03195.hp2 HG03225.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.598+9064_598+9079d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197416 | CTTTATTT others(13): Show |
C | 1 | a0001c0001t0002g0281 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.598+9060_598+9079d others(22): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35197416 | ||||||
| chr10:35197452 | ATTTATTT others(9): Show |
A | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.598+9065_598+9080d others(18): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197452 | |||||||
| chr10:35197468 | T | A | 3 | a0001c0001t0001g0254 a0001c0001t0001g0256 a0001c0001t0001g0257 |
3 | HG01884.hp2 HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.598+9080T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197468 | |||||||
| chr10:35197470 | T | A | 1 | a0001c0001t0001g0119 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598+9082T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197470 | |||||||
| chr10:35197492 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+9104G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197492 | |||||||
| chr10:35197543 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.598+9155C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197543 | |||||||
| chr10:35197549 | T | C | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.598+9161T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197549 | |||||||
| chr10:35197618 | A | T | 5 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00438.hp1 HG00738.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.598+9230A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197618 | |||||||
| chr10:35197631 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.598+9243T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35197631 | |||||||
| chr10:35198102 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.599-8793C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198102 | |||||||
| chr10:35198263 | G | T | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-8632G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198263 | |||||||
| chr10:35198295 | C | T | 1 | a0001c0001t0001g0003 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.599-8600C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198295 | |||||||
| chr10:35198368 | C | T | 13 | a0001c0001t0002g0001 a0001c0001t0002g0041 a0001c0001t0002g0044 others(10): Show |
14 | HG02040.hp2 HG02129.hp1 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.599-8527C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198368 | |||||||
| chr10:35198384 | G | A | 1 | a0001c0001t0001g0227 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.599-8511G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198384 | |||||||
| chr10:35198676 | G | A | 1 | a0001c0001t0002g0098 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.599-8219G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198676 | |||||||
| chr10:35198678 | C | G | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-8217C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198678 | |||||||
| chr10:35198795 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.599-8100T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198795 | |||||||
| chr10:35198887 | C | T | 1 | a0001c0001t0003g0010 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.599-8008C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35198887 | |||||||
| chr10:35199333 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.599-7562A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199333 | |||||||
| chr10:35199334 | T | C | 2 | a0001c0001t0001g0250 a0001c0001t0001g0251 |
2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.599-7561T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199334 | |||||||
| chr10:35199336 | C | T | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-7559C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199336 | |||||||
| chr10:35199341 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-7554C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199341 | |||||||
| chr10:35199515 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.599-7380G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199515 | |||||||
| chr10:35199551 | C | T | 6 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0021 others(3): Show |
6 | HG00735.hp2 HG00741.hp2 HG01074.hp1 others(3): Show |
intron_variant | MODIFIER | c.599-7344C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199551 | |||||||
| chr10:35199576 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-7319G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199576 | |||||||
| chr10:35199664 | A | T | 1 | a0001c0001t0002g0056 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.599-7231A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199664 | |||||||
| chr10:35199864 | ATTATT | A | 69 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(66): Show |
70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.599-7027_599-7023d others(7): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199864 | ||||||
| chr10:35199887 | C | CT | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(148): Show |
153 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.599-6989dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | ||||||
| chr10:35199887 | C | CTT | 51 | a0001c0001t0001g0162 a0001c0001t0001g0186 a0001c0001t0001g0198 others(48): Show |
51 | HG00639.hp1 HG00735.hp2 HG00738.hp2 others(48): Show |
intron_variant | MODIFIER | c.599-6990_599-6989d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | ||||||
| chr10:35199887 | C | CTTT | 65 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(62): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.599-6991_599-6989d others(5): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35199887 | ||||||
| chr10:35199973 | T | C | 1 | a0001c0002t0004g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.599-6922T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35199973 | |||||||
| chr10:35200326 | G | A | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-6569G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200326 | |||||||
| chr10:35200411 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-6484A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200411 | |||||||
| chr10:35200431 | G | T | 1 | a0003c0005t0001g0152 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.599-6464G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200431 | |||||||
| chr10:35200485 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.599-6410T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200485 | |||||||
| chr10:35200651 | A | C | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-6244A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200651 | |||||||
| chr10:35200714 | C | G | 1 | a0001c0002t0004g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.599-6181C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200714 | |||||||
| chr10:35200947 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0219 |
2 | NA19002.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.599-5948C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35200947 | |||||||
| chr10:35200996 | G | GT | 30 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(27): Show |
30 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.599-5890dupT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35200996 | ||||||
| chr10:35201084 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-5811A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201084 | |||||||
| chr10:35201136 | T | C | 1 | a0001c0003t0002g0042 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.599-5759T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201136 | |||||||
| chr10:35201243 | G | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-5652G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201243 | |||||||
| chr10:35201483 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.599-5412G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201483 | |||||||
| chr10:35201597 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.599-5298G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201597 | |||||||
| chr10:35201679 | G | T | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.599-5216G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201679 | |||||||
| chr10:35201921 | C | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-4974C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201921 | |||||||
| chr10:35201954 | C | T | 1 | a0001c0002t0004g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.599-4941C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35201954 | |||||||
| chr10:35202144 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.599-4751C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202144 | |||||||
| chr10:35202187 | C | G | 1 | a0001c0001t0001g0142 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.599-4708C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202187 | |||||||
| chr10:35202566 | A | G | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-4329A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202566 | |||||||
| chr10:35202598 | T | G | 1 | a0001c0002t0004g0112 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.599-4297T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202598 | |||||||
| chr10:35202692 | C | G | 11 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(8): Show |
11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.599-4203C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202692 | |||||||
| chr10:35202730 | G | A | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.599-4165G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202730 | |||||||
| chr10:35202794 | A | T | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.599-4101A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35202794 | |||||||
| chr10:35203096 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3799T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203096 | |||||||
| chr10:35203198 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3697A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203198 | |||||||
| chr10:35203363 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.599-3532C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203363 | |||||||
| chr10:35203415 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.599-3480C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203415 | |||||||
| chr10:35203672 | G | A | 1 | a0001c0001t0009g0288 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.599-3223G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203672 | |||||||
| chr10:35203686 | T | C | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-3209T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203686 | |||||||
| chr10:35203904 | A | G | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2991A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203904 | |||||||
| chr10:35203936 | A | G | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.599-2959A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203936 | |||||||
| chr10:35203963 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.599-2932G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35203963 | |||||||
| chr10:35204050 | C | G | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.599-2845C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204050 | |||||||
| chr10:35204240 | A | T | 1 | a0001c0001t0001g0162 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.599-2655A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204240 | |||||||
| chr10:35204328 | A | G | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2567A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204328 | |||||||
| chr10:35204487 | CTACTCGG others(37): Show |
C | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.599-2407_599-2364d others(46): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204487 | |||||||
| chr10:35204492 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.599-2403C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204492 | |||||||
| chr10:35204590 | A | C | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.599-2305A>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35204590 | |||||||
| chr10:35204596 | C | CA | 7 | a0001c0001t0001g0120 a0001c0001t0001g0122 a0001c0001t0001g0147 others(4): Show |
7 | HG02280.hp2 HG03942.hp2 NA19030.hp1 others(4): Show |
intron_variant | MODIFIER | c.599-2278dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | ||||||
| chr10:35204596 | CA | C | 42 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0197 others(39): Show |
42 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.599-2278delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | ||||||
| chr10:35204596 | CAA | C | 72 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(69): Show |
73 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.599-2279_599-2278d others(4): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr10 | 35204596 | ||||||
| chr10:35205204 | A | G | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 |
3 | HG03098.hp2 HG03579.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.599-1691A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205204 | |||||||
| chr10:35205380 | T | C | 2 | a0001c0001t0002g0098 a0001c0001t0016g0196 |
2 | NA19005.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.599-1515T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205380 | |||||||
| chr10:35205624 | G | T | 1 | a0001c0003t0002g0043 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.599-1271G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205624 | |||||||
| chr10:35205680 | C | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-1215C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205680 | |||||||
| chr10:35205684 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.599-1211C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205684 | |||||||
| chr10:35205710 | A | G | 2 | a0001c0003t0002g0042 a0001c0003t0002g0043 |
2 | HG01099.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.599-1185A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35205710 | |||||||
| chr10:35206031 | G | A | 1 | a0001c0001t0002g0066 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.599-864G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206031 | |||||||
| chr10:35206079 | T | C | 69 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(66): Show |
70 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.599-816T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206079 | |||||||
| chr10:35206087 | A | T | 1 | a0001c0001t0003g0109 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.599-808A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206087 | |||||||
| chr10:35206109 | G | A | 1 | a0001c0001t0003g0007 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.599-786G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206109 | |||||||
| chr10:35206234 | C | T | 12 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0260 others(9): Show |
12 | HG00621.hp1 HG01891.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.599-661C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206234 | |||||||
| chr10:35206260 | AT | A | 67 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(64): Show |
68 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.599-634delT | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206260 | |||||||
| chr10:35206261 | T | A | 2 | a0001c0001t0002g0097 a0001c0001t0002g0107 |
2 | HG02738.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.599-634T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206261 | |||||||
| chr10:35206280 | G | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.599-615G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206280 | |||||||
| chr10:35206367 | T | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.599-528T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206367 | |||||||
| chr10:35206417 | G | A | 5 | a0001c0002t0004g0110 a0001c0002t0004g0111 a0001c0002t0004g0112 others(2): Show |
5 | HG00738.hp2 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.599-478G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206417 | |||||||
| chr10:35206542 | A | T | 1 | a0001c0001t0018g0287 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.599-353A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206542 | |||||||
| chr10:35206685 | G | A | 1 | a0001c0001t0002g0050 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.599-210G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206685 | |||||||
| chr10:35206770 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0132 a0001c0001t0001g0140 others(7): Show |
11 | HG00741.hp1 HG02572.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.599-125A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 6/7 | chr10 | 35206770 | |||||||
| chr10:35207167 | C | G | 3 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 |
3 | HG00544.hp2 NA18965.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.755+116C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207167 | |||||||
| chr10:35207197 | C | G | 1 | a0001c0001t0002g0077 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.755+146C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207197 | |||||||
| chr10:35207326 | G | A | 71 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(68): Show |
72 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.755+275G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207326 | |||||||
| chr10:35207343 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.755+292A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207343 | |||||||
| chr10:35207381 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.755+330G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207381 | |||||||
| chr10:35207425 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.755+374T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207425 | |||||||
| chr10:35207458 | C | T | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.755+407C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207458 | |||||||
| chr10:35207461 | TAAATAA | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+427_755+432del others(6): Show |
CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35207461 | ||||||
| chr10:35207512 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.755+461C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207512 | |||||||
| chr10:35207513 | C | T | 29 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(26): Show |
29 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.755+462C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207513 | |||||||
| chr10:35207540 | T | C | 118 | a0001c0001t0001g0162 a0001c0001t0002g0001 a0001c0001t0002g0037 others(115): Show |
119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.755+489T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207540 | |||||||
| chr10:35207545 | G | A | 11 | a0001c0001t0003g0009 a0001c0001t0003g0010 a0001c0001t0003g0011 others(8): Show |
11 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.755+494G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207545 | |||||||
| chr10:35207546 | C | A | 7 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0189 others(4): Show |
7 | HG01167.hp2 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.755+495C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207546 | |||||||
| chr10:35207551 | A | G | 1 | a0001c0001t0001g0227 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.755+500A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207551 | |||||||
| chr10:35207564 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.755+513A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207564 | |||||||
| chr10:35207594 | C | T | 11 | a0001c0001t0001g0258 a0001c0001t0001g0261 a0001c0001t0001g0263 others(8): Show |
11 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.755+543C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207594 | |||||||
| chr10:35207667 | G | T | 1 | a0001c0001t0001g0276 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.755+616G>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207667 | |||||||
| chr10:35207698 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0118 others(145): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.755+647C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207698 | |||||||
| chr10:35207699 | G | A | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+648G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207699 | |||||||
| chr10:35207729 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | HG01884.hp2 HG02293.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.755+678G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207729 | |||||||
| chr10:35207766 | C | T | 2 | a0001c0001t0007g0039 a0001c0001t0007g0040 |
2 | HG02280.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.755+715C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207766 | |||||||
| chr10:35207771 | TA | T | 31 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0007 others(28): Show |
31 | HG00639.hp1 HG00735.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.755+732delA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35207771 | ||||||
| chr10:35207797 | A | T | 1 | a0001c0001t0003g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.755+746A>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207797 | |||||||
| chr10:35207802 | A | G | 120 | a0001c0001t0001g0199 a0001c0001t0002g0001 a0001c0001t0002g0037 others(117): Show |
121 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.755+751A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207802 | |||||||
| chr10:35207835 | A | G | 1 | a0001c0001t0001g0268 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.755+784A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207835 | |||||||
| chr10:35207927 | A | G | 1 | a0001c0001t0003g0019 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.755+876A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207927 | |||||||
| chr10:35207940 | G | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.755+889G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207940 | |||||||
| chr10:35207944 | T | C | 2 | a0001c0001t0002g0062 a0001c0001t0002g0063 |
2 | HG02015.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.755+893T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35207944 | |||||||
| chr10:35208018 | G | A | 51 | a0001c0001t0001g0004 a0001c0001t0001g0120 a0001c0001t0001g0121 others(48): Show |
52 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.755+967G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208018 | |||||||
| chr10:35208503 | C | T | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.755+1452C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208503 | |||||||
| chr10:35208528 | A | G | 9 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(6): Show |
9 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.755+1477A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208528 | |||||||
| chr10:35208605 | C | G | 3 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0243 |
3 | HG03195.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.755+1554C>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208605 | |||||||
| chr10:35208606 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.755+1555G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208606 | |||||||
| chr10:35208631 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.755+1580A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208631 | |||||||
| chr10:35208808 | C | A | 4 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.755+1757C>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35208808 | |||||||
| chr10:35209176 | G | A | 3 | a0001c0001t0002g0281 a0001c0001t0002g0282 a0001c0001t0002g0283 |
3 | HG01192.hp1 HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.756-2078G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209176 | |||||||
| chr10:35209221 | T | C | 11 | a0001c0002t0004g0036 a0001c0002t0004g0108 a0001c0002t0004g0110 others(8): Show |
11 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.756-2033T>C | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209221 | |||||||
| chr10:35209530 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG01884.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.756-1724A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209530 | |||||||
| chr10:35209609 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.756-1645C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209609 | |||||||
| chr10:35209610 | G | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.756-1644G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209610 | |||||||
| chr10:35209860 | T | A | 123 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(120): Show |
124 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.756-1394T>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209860 | |||||||
| chr10:35209919 | A | G | 3 | a0001c0001t0001g0132 a0001c0001t0001g0182 a0001c0001t0001g0239 |
3 | HG00741.hp1 HG02647.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.756-1335A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209919 | |||||||
| chr10:35209961 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.756-1293G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35209961 | |||||||
| chr10:35210065 | T | TA | 16 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0125 others(13): Show |
17 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.756-1173dupA | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr10 | 35210065 | ||||||
| chr10:35210115 | G | A | 119 | a0001c0001t0002g0001 a0001c0001t0002g0037 a0001c0001t0002g0038 others(116): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.756-1139G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210115 | |||||||
| chr10:35210139 | T | G | 1 | a0001c0001t0001g0157 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.756-1115T>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210139 | |||||||
| chr10:35210223 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.756-1031A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210223 | |||||||
| chr10:35210350 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.756-904G>A | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210350 | |||||||
| chr10:35210555 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.756-699A>G | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35210555 | |||||||
| chr10:35211075 | C | T | 8 | a0001c0002t0004g0108 a0001c0002t0004g0110 a0001c0002t0004g0111 others(5): Show |
8 | HG00738.hp2 HG01109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.756-179C>T | CREM | ENSG00000095794.21 | transcript | ENST00000685392.1 | protein_coding | 7/7 | chr10 | 35211075 |