Variant report

Variant rs4291478
Chromosome Location chr1:86917139-86917140
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:86897200-86922600 Strong transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:86897200-86922800 Strong transcription HMEC breast
3 chr1:86903400-86926800 Weak transcription Esophagus oesophagus
4 chr1:86914600-86930800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr1:86915200-86920000 Strong transcription NHEK skin
6 chr1:86915400-86917400 Enhancers HUVEC blood vessel
7 chr1:86915600-86919400 Weak transcription K562 blood
8 chr1:86916400-86917400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:86916400-86921600 Strong transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr1:86916800-86917200 Enhancers HUES6 Cell Line embryonic stem cell
11 chr1:86916800-86917400 Enhancers Primary hematopoietic stem cells short term culture blood
12 chr1:86917000-86930600 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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