The 2.0 version of rSNPBase

Variant report

Variant rs35893878
Chromosome Location chr2:114597946-114597947
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 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 chr2:114592800-114599400 Weak transcription Placenta Placenta
7 chr2:114595600-114598600 Enhancers HepG2 liver
8 chr2:114596400-114621000 Weak transcription Aorta Aorta
9 chr2:114596600-114603400 Weak transcription Primary T helper naive cells fromperipheralblood blood
10 chr2:114596600-114611600 Weak transcription Primary mononuclear cells fromperipheralblood Blood
11 chr2:114596800-114632800 Weak transcription Primary T helper cells fromperipheralblood blood
12 chr2:114597400-114599200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr2:114597400-114600200 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr2:114597600-114598600 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr2:114597600-114631400 Weak transcription Primary T helper cells PMA-I stimulated --
16 chr2:114597800-114598000 Enhancers HUES6 Cell Line embryonic stem cell
17 chr2:114597800-114598200 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr2:114597800-114598400 Enhancers H9 Cell Line embryonic stem cell

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Last update: Aug 31, 2015