The 2.0 version of rSNPBase

Variant report

Variant rs7115142
Chromosome Location chr11:10241871-10241872
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:10219000-10242200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:10227800-10242600 Weak transcription Esophagus oesophagus
3 chr11:10230600-10246800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
4 chr11:10231000-10254400 Weak transcription NHDF-Ad bronchial
5 chr11:10231000-10254400 Weak transcription NHLF lung
6 chr11:10235400-10263400 Weak transcription Breast Myoepithelial Primary Cells Breast
7 chr11:10237800-10243400 Weak transcription HepG2 liver
8 chr11:10240000-10242400 ZNF genes & repeats Ganglion Eminence derived primary cultured neurospheres brain
9 chr11:10240400-10242800 Weak transcription Right Atrium heart
10 chr11:10240600-10259800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
11 chr11:10241000-10242200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr11:10241000-10253600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr11:10241200-10242000 Weak transcription Fetal Adrenal Gland Adrenal Gland
14 chr11:10241200-10252800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr11:10241200-10255200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
16 chr11:10241800-10242200 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
17 chr11:10241800-10254800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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Last update: Aug 31, 2015