The 2.0 version of rSNPBase

Variant report

Variant rs1947118
Chromosome Location chr2:72770662-72770663
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:72761400-72783000 Weak transcription Aorta Aorta
2 chr2:72766400-72775600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr2:72766400-72782800 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr2:72766600-72773600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr2:72766600-72774600 Weak transcription Fetal Lung lung
6 chr2:72766600-72786400 Weak transcription ES-WA7 Cell Line embryonic stem cell
7 chr2:72766800-72774000 Weak transcription A549 lung
8 chr2:72766800-72781400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr2:72766800-72788000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr2:72766800-72788600 Weak transcription NH-A brain
11 chr2:72766800-72789200 Weak transcription NHEK skin
12 chr2:72768800-72786800 Weak transcription Primary T helper naive cells from peripheral blood blood
13 chr2:72769600-72780200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr2:72769800-72772200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr2:72770000-72771400 Enhancers HUVEC blood vessel
16 chr2:72770200-72771000 Enhancers Small Intestine intestine
17 chr2:72770200-72771200 Enhancers Fetal Heart heart
18 chr2:72770400-72771200 Flanking Active TSS K562 blood
19 chr2:72770600-72771000 Enhancers Fetal Adrenal Gland Adrenal Gland
20 chr2:72770600-72771200 Enhancers Fetal Intestine Large intestine
21 chr2:72770600-72771400 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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Last update: Aug 31, 2015