Variant report

Variant rs35147271
Chromosome Location chr15:76053168-76053169
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:76051400-76053600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr15:76051400-76054000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
3 chr15:76051400-76055600 Weak transcription Pancreas Pancrea
4 chr15:76051400-76057000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr15:76051400-76059000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr15:76051400-76063200 Weak transcription Right Atrium heart
7 chr15:76051600-76054600 Enhancers Fetal Heart heart
8 chr15:76051800-76053200 Weak transcription HepG2 liver
9 chr15:76051800-76054800 Weak transcription Fetal Brain Female brain
10 chr15:76052000-76053600 Enhancers Right Ventricle heart
11 chr15:76052200-76053600 Enhancers K562 blood
12 chr15:76052200-76053800 Weak transcription Stomach Mucosa stomach
13 chr15:76052400-76055600 Weak transcription Liver Liver
14 chr15:76052600-76053800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin

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