Variant report

Variant rs547132409
Chromosome Location chr6:167663268-167663269
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167654800-167664800 Weak transcription Right Atrium heart
2 chr6:167660800-167663800 Enhancers H1 Cell Line embryonic stem cell
3 chr6:167661200-167663400 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr6:167661200-167663600 Enhancers HUES48 Cell Line embryonic stem cell
5 chr6:167661200-167663600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
6 chr6:167661200-167663600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
7 chr6:167661200-167663600 Enhancers HepG2 liver
8 chr6:167661200-167664000 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
9 chr6:167662800-167663800 Weak transcription HUES6 Cell Line embryonic stem cell
10 chr6:167663200-167663400 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin

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