Variant report

Variant rs11624178
Chromosome Location chr14:32261618-32261619
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:32222600-32270200 Weak transcription Aorta Aorta
2 chr14:32244400-32270200 Weak transcription Ovary ovary
3 chr14:32250600-32322400 Weak transcription Primary T helper cells fromperipheralblood blood
4 chr14:32250800-32270200 Weak transcription Primary T helper cells PMA-I stimulated --
5 chr14:32251200-32272600 Weak transcription Primary T cells from cord blood blood
6 chr14:32252600-32268000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr14:32257600-32272200 Weak transcription Pancreas Pancrea
8 chr14:32257600-32281200 Weak transcription HepG2 liver
9 chr14:32258000-32270600 Weak transcription Gastric stomach
10 chr14:32258200-32267200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr14:32261200-32268400 Weak transcription Primary hematopoietic stem cells blood
12 chr14:32261400-32263000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr14:32261600-32262800 Enhancers NHEK skin

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