Variant report

Variant rs3817766
Chromosome Location chr6:167720757-167720758
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167711600-167721600 Weak transcription Fetal Intestine Large intestine
2 chr6:167716200-167721200 Weak transcription Liver Liver
3 chr6:167717200-167721800 Strong transcription Fetal Intestine Small intestine
4 chr6:167717800-167724000 Weak transcription Fetal Brain Female brain
5 chr6:167720200-167720800 Weak transcription HepG2 liver
6 chr6:167720200-167722200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
7 chr6:167720200-167723200 Weak transcription Rectal Smooth Muscle rectum
8 chr6:167720200-167723200 Weak transcription Stomach Mucosa stomach
9 chr6:167720400-167726400 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr6:167720400-167727600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
11 chr6:167720600-167722800 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell

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