Variant report

Variant rs13191872
Chromosome Location chr6:32375095-32375096
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 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 chr6:32374400-32378800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
3 chr6:32374600-32375400 Enhancers Fetal Intestine Large intestine
4 chr6:32374600-32375400 Enhancers Fetal Intestine Small intestine
5 chr6:32374600-32375600 Enhancers HUES64 Cell Line embryonic stem cell
6 chr6:32374600-32375800 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr6:32374800-32375200 Enhancers ES-I3 Cell Line embryonic stem cell
8 chr6:32374800-32375200 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr6:32374800-32375200 Enhancers H9 Cell Line embryonic stem cell
10 chr6:32374800-32375200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr6:32374800-32375200 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr6:32374800-32375200 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr6:32374800-32375200 Flanking Active TSS Duodenum Mucosa Duodenum
14 chr6:32375000-32375200 Bivalent Enhancer Sigmoid Colon Sigmoid Colon
15 chr6:32375000-32375400 Enhancers HUES48 Cell Line embryonic stem cell
16 chr6:32375000-32375400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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