Variant report

Variant rs12568149
Chromosome Location chr1:147191616-147191617
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:147187800-147192000 Enhancers HepG2 liver
2 chr1:147188600-147191800 Enhancers HMEC breast
3 chr1:147188800-147191800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr1:147189000-147192400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr1:147189400-147191800 Enhancers Left Ventricle heart
6 chr1:147189400-147191800 Enhancers Pancreas Pancrea
7 chr1:147189400-147193000 Enhancers Esophagus oesophagus
8 chr1:147189600-147192000 Weak transcription A549 lung
9 chr1:147189600-147192000 Enhancers HSMMtube muscle
10 chr1:147190000-147192000 Enhancers Stomach Mucosa stomach
11 chr1:147190200-147194200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr1:147190200-147198800 Weak transcription Right Atrium heart
13 chr1:147190600-147193600 Weak transcription Primary neutrophils fromperipheralblood blood
14 chr1:147191000-147191800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
15 chr1:147191000-147194800 Enhancers Placenta Placenta
16 chr1:147191200-147191800 Enhancers Right Ventricle heart
17 chr1:147191200-147192000 ZNF genes & repeats HUES6 Cell Line embryonic stem cell
18 chr1:147191200-147192200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr1:147191200-147192400 Weak transcription Fetal Muscle Leg muscle
20 chr1:147191400-147192000 Enhancers NHEK skin
21 chr1:147191600-147194200 Weak transcription H1 Cell Line embryonic stem cell

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