The 2.0 version of rSNPBase

Variant report

Variant rs7517145
Chromosome Location chr1:223675204-223675205
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:223672600-223675800 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr1:223674200-223675600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
3 chr1:223674400-223676400 Weak transcription Stomach Mucosa stomach
4 chr1:223674400-223677800 Weak transcription HUVEC blood vessel
5 chr1:223674400-223678000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:223674400-223678400 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr1:223674600-223677600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
8 chr1:223674600-223677800 Weak transcription NHDF-Ad bronchial
9 chr1:223674600-223678400 Weak transcription Esophagus oesophagus
10 chr1:223674800-223677600 Weak transcription Osteobl bone
11 chr1:223674800-223678000 Weak transcription Muscle Satellite Cultured Cells --
12 chr1:223675000-223676800 Weak transcription NHEK skin
13 chr1:223675000-223677400 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr1:223675000-223677600 Weak transcription NH-A brain
15 chr1:223675000-223677800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
16 chr1:223675200-223675600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
17 chr1:223675200-223675600 Weak transcription HMEC breast

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Last update: Aug 31, 2015