The 2.0 version of rSNPBase

Variant report

Variant rs17117613
Chromosome Location chr1:98576274-98576275
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:98573800-98576400 Weak transcription HSMMtube muscle
2 chr1:98574200-98576400 Weak transcription HMEC breast
3 chr1:98574200-98576400 Weak transcription NHDF-Ad bronchial
4 chr1:98575800-98576600 Enhancers A549 lung
5 chr1:98576000-98576800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
6 chr1:98576000-98576800 Enhancers HUVEC blood vessel
7 chr1:98576000-98577000 Enhancers Muscle Satellite Cultured Cells --
8 chr1:98576000-98577000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
9 chr1:98576200-98576600 Enhancers NHLF lung
10 chr1:98576200-98576800 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
11 chr1:98576200-98576800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr1:98576200-98576800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr1:98576200-98576800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
14 chr1:98576200-98576800 Enhancers HSMM muscle
15 chr1:98576200-98576800 Enhancers Osteobl bone
16 chr1:98576200-98577000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
17 chr1:98576200-98577000 Enhancers Hela-S3 cervix

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Last update: Aug 31, 2015