Variant report

Variant rs4919560
Chromosome Location chr10:95597809-95597810
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:95594800-95599800 Enhancers Fetal Intestine Large intestine
2 chr10:95595200-95599800 Enhancers Fetal Intestine Small intestine
3 chr10:95597000-95598000 Weak transcription Small Intestine intestine
4 chr10:95597200-95598000 Enhancers Colonic Mucosa Colon
5 chr10:95597200-95598600 Enhancers Pancreas Pancrea
6 chr10:95597400-95599600 Enhancers Duodenum Mucosa Duodenum
7 chr10:95597600-95598000 Enhancers Cortex derived primary cultured neurospheres brain
8 chr10:95597600-95598000 Enhancers Brain Germinal Matrix brain
9 chr10:95597800-95598000 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
10 chr10:95597800-95598200 Enhancers Fetal Brain Female brain

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