Variant report

Variant rs2857633
Chromosome Location chr22:30114333-30114334
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr22:30098800-30115600 Weak transcription Right Atrium heart
2 chr22:30110600-30114800 Enhancers Fetal Brain Male brain
3 chr22:30111000-30114600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr22:30112800-30116600 Weak transcription Pancreas Pancrea
5 chr22:30113000-30115000 Weak transcription Spleen Spleen
6 chr22:30113200-30114400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr22:30113600-30114600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr22:30113600-30114600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr22:30113600-30114600 Weak transcription Fetal Brain Female brain
10 chr22:30113800-30114400 Enhancers HMEC breast
11 chr22:30114000-30114400 Bivalent Enhancer NHEK skin
12 chr22:30114000-30114600 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast

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