The 2.0 version of rSNPBase

Variant report

Variant esv2132834
Chromosome Location chr15:75478891-75478892
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:75473000-75487600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr15:75473200-75483200 Weak transcription Aorta Aorta
3 chr15:75473200-75483400 Weak transcription Left Ventricle heart
4 chr15:75475400-75487800 Weak transcription Right Atrium heart
5 chr15:75475600-75480600 Weak transcription HepG2 liver
6 chr15:75475600-75481600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr15:75475600-75487600 Weak transcription Pancreas Pancrea
8 chr15:75476400-75479000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr15:75476600-75479200 Enhancers Primary monocytes fromperipheralblood blood
10 chr15:75476800-75479000 Enhancers Primary hematopoietic stem cells blood
11 chr15:75476800-75479800 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr15:75477200-75492600 Weak transcription Spleen Spleen
13 chr15:75477800-75479200 Enhancers iPS-15b Cell Line embryonic stem cell
14 chr15:75478600-75486200 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr15:75478800-75480800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr15:75478800-75483400 Weak transcription Fetal Heart heart

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Last update: Aug 31, 2015