Variant report

Variant rs186945635
Chromosome Location chr5:107459534-107459535
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:107388400-107510800 Weak transcription Primary B cells from cord blood blood
2 chr5:107437800-107463800 Weak transcription Esophagus oesophagus
3 chr5:107449000-107467200 Weak transcription Aorta Aorta
4 chr5:107457000-107459600 Weak transcription Fetal Intestine Small intestine
5 chr5:107457800-107460000 Enhancers HUES6 Cell Line embryonic stem cell
6 chr5:107458400-107459800 Enhancers ES-I3 Cell Line embryonic stem cell
7 chr5:107458400-107459800 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr5:107458400-107460200 Enhancers HUES64 Cell Line embryonic stem cell
9 chr5:107458400-107460600 Enhancers iPS-20b Cell Line embryonic stem cell
10 chr5:107458600-107460600 Enhancers iPS-18 Cell Line embryonic stem cell
11 chr5:107459000-107459800 Weak transcription Pancreatic Islets Pancreatic Islet
12 chr5:107459200-107459800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
13 chr5:107459200-107460600 Enhancers HUES48 Cell Line embryonic stem cell

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