Variant report

Variant rs3865306
Chromosome Location chr17:16724895-16724896
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16722800-16725200 Transcr. at gene 5' and 3' Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr17:16722800-16725200 Enhancers Esophagus oesophagus
3 chr17:16723000-16725200 Enhancers Fetal Muscle Leg muscle
4 chr17:16723200-16725200 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
5 chr17:16723800-16725200 Enhancers iPS-15b Cell Line embryonic stem cell
6 chr17:16724200-16725000 Enhancers Skeletal Muscle Male skeletal muscle
7 chr17:16724200-16725200 Enhancers ES-UCSF4 Cell Line embryonic stem cell
8 chr17:16724400-16725200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
9 chr17:16724600-16725200 Active TSS NHEK skin
10 chr17:16724800-16725200 Active TSS Placenta Amnion Placenta Amnion
11 chr17:16724800-16725800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
12 chr17:16724800-16725800 Active TSS Foreskin Keratinocyte Primary Cells skin02 Skin

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