The 2.0 version of rSNPBase

Variant report

Variant rs10930528
Chromosome Location chr2:173069855-173069856
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173065400-173072600 Weak transcription Primary hematopoietic stem cells blood
2 chr2:173065400-173073600 Weak transcription NHEK skin
3 chr2:173068800-173070000 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr2:173069000-173070000 Enhancers Primary hematopoietic stem cells short term culture blood
5 chr2:173069000-173070200 Enhancers Primary monocytes fromperipheralblood blood
6 chr2:173069000-173070400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr2:173069000-173070400 Enhancers Monocytes-CD14+_RO01746 blood
8 chr2:173069400-173070200 Enhancers iPS-20b Cell Line embryonic stem cell
9 chr2:173069400-173070400 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
10 chr2:173069400-173070400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr2:173069400-173070600 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr2:173069400-173073200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr2:173069600-173071800 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:173069600-173072000 Weak transcription NHLF lung
15 chr2:173069800-173070000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
16 chr2:173069800-173072400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --

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Last update: Aug 31, 2015