Variant report

Variant rs36110805
Chromosome Location chr6:167704994-167704995
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167696800-167705800 Weak transcription ES-WA7 Cell Line embryonic stem cell
2 chr6:167697200-167705200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr6:167697600-167706200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr6:167702600-167705600 Weak transcription iPS-18 Cell Line embryonic stem cell
5 chr6:167702800-167705600 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr6:167702800-167706200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:167703000-167705800 Weak transcription HUES64 Cell Line embryonic stem cell
8 chr6:167703800-167705000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr6:167703800-167706000 Weak transcription Placenta Amnion Placenta Amnion
10 chr6:167704400-167707400 Flanking Active TSS HepG2 liver
11 chr6:167704600-167705400 Flanking Active TSS Liver Liver
12 chr6:167704600-167705400 Enhancers Duodenum Mucosa Duodenum
13 chr6:167704800-167706000 Flanking Active TSS Fetal Intestine Small intestine
14 chr6:167704800-167706800 Flanking Active TSS Fetal Intestine Large intestine

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