The 2.0 version of rSNPBase

Variant report

Variant rs12615093
Chromosome Location chr2:114595008-114595009
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 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 chr2:114584600-114595600 Weak transcription HepG2 liver
3 chr2:114586400-114601000 Weak transcription Primary T cells from cord blood blood
4 chr2:114589200-114596400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
5 chr2:114589200-114600200 Weak transcription Breast Myoepithelial Primary Cells Breast
6 chr2:114589200-114600200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr2:114589200-114600200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:114591600-114597800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
9 chr2:114592000-114596200 Weak transcription Fetal Intestine Large intestine
10 chr2:114592400-114597600 Weak transcription ES-I3 Cell Line embryonic stem cell
11 chr2:114592600-114597400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
12 chr2:114592800-114599400 Weak transcription Placenta Placenta

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Last update: Aug 31, 2015