Variant report

Variant rs4709163
Chromosome Location chr6:167723641-167723642
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
2 chr6:167720400-167726400 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:167721600-167724400 Enhancers Fetal Intestine Large intestine
5 chr6:167721800-167728000 Enhancers Fetal Brain Male brain
6 chr6:167722000-167723800 Flanking Active TSS HepG2 liver
7 chr6:167722000-167724200 Enhancers Fetal Intestine Small intestine
8 chr6:167722800-167725000 Enhancers Liver Liver
9 chr6:167722800-167727400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr6:167723200-167723800 Enhancers Rectal Smooth Muscle rectum
11 chr6:167723200-167724800 Enhancers Stomach Mucosa stomach
12 chr6:167723400-167724600 Weak transcription Brain Inferior Temporal Lobe brain
13 chr6:167723400-167724800 Enhancers Fetal Stomach stomach
14 chr6:167723600-167724400 Weak transcription Duodenum Smooth Muscle Duodenum
15 chr6:167723600-167724600 Weak transcription Brain Germinal Matrix brain
16 chr6:167723600-167725600 Enhancers Stomach Smooth Muscle stomach

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