Variant report

Variant rs2235198
Chromosome Location chr6:167722644-167722645
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
2 chr6:167720200-167723200 Weak transcription Rectal Smooth Muscle rectum
3 chr6:167720200-167723200 Weak transcription Stomach Mucosa stomach
4 chr6:167720400-167726400 Weak transcription HUES6 Cell Line embryonic stem cell
5 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:167720600-167722800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:167721600-167724400 Enhancers Fetal Intestine Large intestine
8 chr6:167721800-167728000 Enhancers Fetal Brain Male brain
9 chr6:167722000-167723800 Flanking Active TSS HepG2 liver
10 chr6:167722000-167724200 Enhancers Fetal Intestine Small intestine
11 chr6:167722400-167722800 Flanking Active TSS Liver Liver

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