Variant report

Variant rs188182161
Chromosome Location chrX:76705538-76705539
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chrX:76703800-76706200 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --
2 chrX:76704200-76705600 Flanking Active TSS Primary hematopoietic stem cells G-CSF-mobilized Female --
3 chrX:76704200-76705800 Active TSS Fetal Muscle Trunk muscle
4 chrX:76704600-76706000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
5 chrX:76704800-76705600 Enhancers iPS-15b Cell Line embryonic stem cell
6 chrX:76704800-76705600 Weak transcription Skeletal Muscle Male skeletal muscle
7 chrX:76704800-76705800 Weak transcription Left Ventricle heart
8 chrX:76704800-76709000 Weak transcription Right Atrium heart
9 chrX:76705000-76705600 Enhancers Primary hematopoietic stem cells short term culture blood
10 chrX:76705000-76710600 Weak transcription H1 Cell Line embryonic stem cell
11 chrX:76705000-76713800 Weak transcription Primary hematopoietic stem cells blood
12 chrX:76705200-76705800 Enhancers ES-I3 Cell Line embryonic stem cell
13 chrX:76705400-76705600 Enhancers NH-A brain
14 chrX:76705400-76705800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
15 chrX:76705400-76706000 Flanking Active TSS Fetal Muscle Leg muscle
16 chrX:76705400-76707200 Enhancers HUVEC blood vessel
17 chrX:76705400-76707400 Enhancers Hela-S3 cervix

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