Variant report

Variant rs7579391
Chromosome Location chr2:187174468-187174469
allele C/T
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 chr2:187171800-187174800 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr2:187171800-187175200 Enhancers Fetal Adrenal Gland Adrenal Gland
4 chr2:187172400-187174800 Enhancers HepG2 liver
5 chr2:187173200-187175400 Weak transcription Sigmoid Colon Sigmoid Colon
6 chr2:187173200-187176600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
7 chr2:187173200-187192200 Weak transcription Placenta Amnion Placenta Amnion
8 chr2:187173400-187175400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr2:187173400-187177200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr2:187173400-187177600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr2:187173600-187174800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
12 chr2:187173600-187190000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr2:187173800-187174600 Weak transcription Fetal Intestine Small intestine
14 chr2:187173800-187176400 Weak transcription Fetal Intestine Large intestine

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