Variant report

Variant rs4667079
Chromosome Location chr2:187174811-187174812
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187171400-187179400 Weak transcription Brain Substantia Nigra brain
2 chr2:187171800-187175200 Enhancers Fetal Adrenal Gland Adrenal Gland
3 chr2:187173200-187175400 Weak transcription Sigmoid Colon Sigmoid Colon
4 chr2:187173200-187176600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
5 chr2:187173200-187192200 Weak transcription Placenta Amnion Placenta Amnion
6 chr2:187173400-187175400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr2:187173400-187177200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
8 chr2:187173400-187177600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
9 chr2:187173600-187190000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:187173800-187176400 Weak transcription Fetal Intestine Large intestine
11 chr2:187174600-187175200 Strong transcription Fetal Intestine Small intestine
12 chr2:187174600-187175200 Enhancers Right Atrium heart
13 chr2:187174800-187175000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr2:187174800-187175200 Enhancers Pancreas Pancrea

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