Variant report

Variant rs6938337
Chromosome Location chr6:32381041-32381042
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:32368400-32385600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr6:32378800-32381200 Enhancers Fetal Intestine Large intestine
3 chr6:32378800-32381200 Enhancers Fetal Intestine Small intestine
4 chr6:32379400-32383400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr6:32379800-32381600 Enhancers Duodenum Mucosa Duodenum
6 chr6:32381000-32381200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
7 chr6:32381000-32381400 Bivalent Enhancer ES-I3 Cell Line embryonic stem cell
8 chr6:32381000-32381400 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
9 chr6:32381000-32381400 Bivalent Enhancer Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr6:32381000-32381600 Enhancers Primary B cells from peripheral blood blood
11 chr6:32381000-32381600 Enhancers Colonic Mucosa Colon
12 chr6:32381000-32381600 Flanking Active TSS Hela-S3 cervix
13 chr6:32381000-32381800 Enhancers Breast Myoepithelial Primary Cells Breast

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