Variant report

Variant rs3806232
Chromosome Location chr1:153364130-153364131
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:153353400-153366400 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr1:153356800-153368200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
3 chr1:153361600-153366400 Active TSS Primary hematopoietic stem cells blood
4 chr1:153361800-153368600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:153362000-153364400 Enhancers NHEK skin
6 chr1:153362000-153364600 Enhancers HMEC breast
7 chr1:153362200-153364200 Active TSS Esophagus oesophagus
8 chr1:153362400-153364200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:153363000-153364200 Enhancers Hela-S3 cervix
10 chr1:153363000-153364400 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
11 chr1:153363200-153367400 Weak transcription Right Ventricle heart
12 chr1:153363400-153364400 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr1:153363600-153364400 Flanking Active TSS Primary monocytes fromperipheralblood blood
14 chr1:153363600-153365600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
15 chr1:153363800-153364200 Flanking Active TSS Primary B cells from cord blood blood
16 chr1:153364000-153364200 Enhancers Right Atrium heart
17 chr1:153364000-153364400 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
18 chr1:153364000-153366200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr1:153364000-153366200 Weak transcription Placenta Placenta

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