The 2.0 version of rSNPBase

Variant report

Variant rs71416564
Chromosome Location chr2:114597064-114597065
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:114574200-114603600 Weak transcription Primary B cells from cord blood blood
2 chr2:114586400-114601000 Weak transcription Primary T cells from cord blood blood
3 chr2:114589200-114600200 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr2:114589200-114600200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr2:114589200-114600200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:114591600-114597800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr2:114592400-114597600 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr2:114592600-114597400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:114592800-114599400 Weak transcription Placenta Placenta
10 chr2:114595600-114598600 Enhancers HepG2 liver
11 chr2:114596200-114597400 Enhancers Fetal Adrenal Gland Adrenal Gland
12 chr2:114596400-114621000 Weak transcription Aorta Aorta
13 chr2:114596600-114603400 Weak transcription Primary T helper naive cells fromperipheralblood blood
14 chr2:114596600-114611600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
15 chr2:114596800-114632800 Weak transcription Primary T helper cells fromperipheralblood blood

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Last update: Aug 31, 2015