Variant report

Variant rs72995399
Chromosome Location chr1:147190825-147190826
allele C/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 chr1:147188400-147191000 Enhancers Primary T helper 17 cells PMA-I stimulated --
3 chr1:147188600-147191800 Enhancers HMEC breast
4 chr1:147188800-147191800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:147189000-147191000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:147189000-147192400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:147189400-147191800 Enhancers Left Ventricle heart
8 chr1:147189400-147191800 Enhancers Pancreas Pancrea
9 chr1:147189400-147193000 Enhancers Esophagus oesophagus
10 chr1:147189600-147191200 Enhancers Fetal Muscle Leg muscle
11 chr1:147189600-147192000 Weak transcription A549 lung
12 chr1:147189600-147192000 Enhancers HSMMtube muscle
13 chr1:147190000-147191000 Weak transcription Placenta Placenta
14 chr1:147190000-147192000 Enhancers Stomach Mucosa stomach
15 chr1:147190200-147191000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
16 chr1:147190200-147194200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
17 chr1:147190200-147198800 Weak transcription Right Atrium heart
18 chr1:147190400-147191200 Weak transcription Right Ventricle heart
19 chr1:147190400-147191400 Weak transcription NHEK skin
20 chr1:147190600-147193600 Weak transcription Primary neutrophils fromperipheralblood blood
21 chr1:147190800-147191200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast

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