The 2.0 version of rSNPBase

Variant report

Variant rs72707274
Chromosome Location chr1:178974858-178974859
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:178972200-178975200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:178972400-178976600 Weak transcription A549 lung
3 chr1:178972400-178976600 Weak transcription Osteobl bone
4 chr1:178972400-178977800 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
5 chr1:178972400-178986000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
6 chr1:178972600-178976400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr1:178972600-178977800 Weak transcription Stomach Smooth Muscle stomach
8 chr1:178972600-178978000 Weak transcription Adipose Nuclei Adipose
9 chr1:178972600-178981200 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr1:178972800-178978000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr1:178973000-178976600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
12 chr1:178973200-178977800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
13 chr1:178973200-178979600 Weak transcription Sigmoid Colon Sigmoid Colon
14 chr1:178973400-178980200 Weak transcription Fetal Intestine Small intestine
15 chr1:178973400-178980200 Weak transcription Rectal Mucosa Donor 29 rectum
16 chr1:178973600-178976600 Weak transcription Stomach Mucosa stomach
17 chr1:178973600-178983200 Weak transcription K562 blood
18 chr1:178973800-178976600 Weak transcription HepG2 liver
19 chr1:178974600-178975000 Active TSS Fetal Brain Male brain

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Last update: Aug 31, 2015