The 2.0 version of rSNPBase

Variant report

Variant rs1198575
Chromosome Location chr1:98562260-98562261
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:98549400-98569400 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
2 chr1:98553200-98569600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:98553600-98567800 Weak transcription HSMM muscle
4 chr1:98553600-98567800 Weak transcription NH-A brain
5 chr1:98556000-98566400 Weak transcription HUVEC blood vessel
6 chr1:98556800-98564000 Weak transcription A549 lung
7 chr1:98557000-98564800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr1:98560400-98567600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
9 chr1:98560600-98563200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:98560600-98569400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr1:98561800-98562400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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Last update: Aug 31, 2015