Variant report

Variant rs17202466
Chromosome Location chr3:110430026-110430027
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:110427200-110433400 Enhancers Fetal Intestine Small intestine
2 chr3:110427600-110430200 Weak transcription HUES6 Cell Line embryonic stem cell
3 chr3:110427800-110432600 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr3:110428200-110432600 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr3:110428200-110433000 Enhancers HUES64 Cell Line embryonic stem cell
6 chr3:110428200-110434200 Enhancers Fetal Intestine Large intestine
7 chr3:110428400-110431200 Enhancers Liver Liver
8 chr3:110428400-110431600 Enhancers HUES48 Cell Line embryonic stem cell
9 chr3:110428400-110432600 Enhancers H1 Cell Line embryonic stem cell
10 chr3:110429400-110430800 Weak transcription H9 Cell Line embryonic stem cell
11 chr3:110429400-110431200 Enhancers HepG2 liver
12 chr3:110429600-110431800 Enhancers iPS-18 Cell Line embryonic stem cell
13 chr3:110429800-110431400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
14 chr3:110430000-110431000 Enhancers Duodenum Mucosa Duodenum
15 chr3:110430000-110431200 Enhancers Pancreatic Islets Pancreatic Islet
16 chr3:110430000-110431600 Enhancers Stomach Mucosa stomach
17 chr3:110430000-110431800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
18 chr3:110430000-110431800 Enhancers iPS-20b Cell Line embryonic stem cell

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