Variant report

Variant rs73073546
Chromosome Location chr2:211423086-211423087
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:211416800-211425800 Weak transcription Duodenum Mucosa Duodenum
2 chr2:211418200-211424400 Genic enhancers Fetal Intestine Large intestine
3 chr2:211418600-211443200 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:211419600-211423800 Enhancers Fetal Intestine Small intestine
5 chr2:211421000-211423600 Enhancers H1 Cell Line embryonic stem cell
6 chr2:211421000-211423600 Enhancers iPS-20b Cell Line embryonic stem cell
7 chr2:211421200-211423600 Enhancers HUES48 Cell Line embryonic stem cell
8 chr2:211421200-211424600 Active TSS Hela-S3 cervix
9 chr2:211421200-211425400 Active TSS Liver Liver
10 chr2:211421400-211423400 Enhancers HUES64 Cell Line embryonic stem cell
11 chr2:211421600-211423200 Enhancers iPS-15b Cell Line embryonic stem cell
12 chr2:211421600-211423400 Weak transcription H9 Cell Line embryonic stem cell
13 chr2:211421600-211423800 Enhancers iPS-18 Cell Line embryonic stem cell
14 chr2:211421800-211423600 Weak transcription Fetal Adrenal Gland Adrenal Gland
15 chr2:211422000-211424600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
16 chr2:211422400-211423800 Enhancers Breast Myoepithelial Primary Cells Breast
17 chr2:211422600-211427800 Weak transcription Fetal Kidney kidney
18 chr2:211423000-211426000 Weak transcription ES-I3 Cell Line embryonic stem cell

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