Variant report

Variant rs13023992
Chromosome Location chr2:187171716-187171717
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:187168000-187172400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr2:187168000-187173000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr2:187168400-187172400 Weak transcription NHEK skin
4 chr2:187169600-187172400 Weak transcription HepG2 liver
5 chr2:187170600-187173800 Enhancers ES-I3 Cell Line embryonic stem cell
6 chr2:187170800-187173600 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr2:187170800-187174000 Enhancers HUES48 Cell Line embryonic stem cell
8 chr2:187171000-187174000 Enhancers HUES6 Cell Line embryonic stem cell
9 chr2:187171200-187171800 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr2:187171200-187171800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr2:187171200-187173400 Enhancers H9 Cell Line embryonic stem cell
12 chr2:187171200-187173400 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr2:187171200-187173800 Enhancers Fetal Intestine Large intestine
14 chr2:187171400-187179400 Weak transcription Brain Substantia Nigra brain
15 chr2:187171600-187171800 Flanking Active TSS iPS-18 Cell Line embryonic stem cell
16 chr2:187171600-187171800 Enhancers iPS-20b Cell Line embryonic stem cell
17 chr2:187171600-187172000 Weak transcription HUES64 Cell Line embryonic stem cell

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