Variant report

Variant rs4900619
Chromosome Location chr14:104782751-104782752
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:104781600-104785200 Weak transcription Right Atrium heart
2 chr14:104782000-104784600 Enhancers Spleen Spleen
3 chr14:104782000-104785000 Weak transcription Brain Germinal Matrix brain
4 chr14:104782200-104783000 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
5 chr14:104782200-104783600 Enhancers Colonic Mucosa Colon
6 chr14:104782200-104785600 Weak transcription Fetal Brain Female brain
7 chr14:104782400-104782800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
8 chr14:104782400-104783200 Enhancers Duodenum Mucosa Duodenum
9 chr14:104782400-104784000 Weak transcription Fetal Brain Male brain
10 chr14:104782600-104783000 Flanking Active TSS Rectal Mucosa Donor 31 rectum
11 chr14:104782600-104783000 Enhancers Right Ventricle heart
12 chr14:104782600-104783400 Enhancers Rectal Mucosa Donor 29 rectum

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