The 2.0 version of rSNPBase

Variant report

Variant rs1812500
Chromosome Location chr2:173072323-173072324
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr2:173069400-173073200 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr2:173069800-173072400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
5 chr2:173070000-173072800 Weak transcription Primary hematopoietic stem cells short term culture blood
6 chr2:173070000-173073200 Weak transcription Fetal Adrenal Gland Adrenal Gland
7 chr2:173070000-173077800 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr2:173070200-173078600 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr2:173070400-173073000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
10 chr2:173070600-173076800 Enhancers Primary monocytes fromperipheralblood blood
11 chr2:173070600-173077600 Weak transcription iPS-18 Cell Line embryonic stem cell
12 chr2:173070800-173073200 Enhancers Monocytes-CD14+_RO01746 blood
13 chr2:173071800-173073400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
14 chr2:173071800-173074600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
15 chr2:173072000-173073000 Weak transcription HMEC breast
16 chr2:173072000-173073200 Weak transcription Osteobl bone
17 chr2:173072000-173073400 Enhancers NHLF lung
18 chr2:173072000-173074800 Enhancers Fetal Intestine Small intestine

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Last update: Aug 31, 2015