Variant report

Variant rs9911414
Chromosome Location chr17:59541561-59541562
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:59539800-59541600 Enhancers HepG2 liver
2 chr17:59539800-59541800 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
3 chr17:59540000-59541600 Bivalent Enhancer iPS DF 6.9 Cell Line embryonic stem cell
4 chr17:59540000-59541600 Bivalent Enhancer Fetal Muscle Leg muscle
5 chr17:59540000-59542000 Bivalent Enhancer ES-WA7 Cell Line embryonic stem cell
6 chr17:59540000-59542000 Bivalent Enhancer H1 Cell Line embryonic stem cell
7 chr17:59540000-59544000 Transcr. at gene 5' and 3' Foreskin Fibroblast Primary Cells skin01 Skin
8 chr17:59540000-59544800 Weak transcription Pancreas Pancrea
9 chr17:59540000-59544800 Weak transcription Right Atrium heart
10 chr17:59540400-59542400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
11 chr17:59540600-59541800 Enhancers Placenta Placenta
12 chr17:59540800-59541600 Genic enhancers NHLF lung
13 chr17:59540800-59544800 Weak transcription Lung lung
14 chr17:59540800-59545400 Genic enhancers Fetal Lung lung
15 chr17:59541000-59541600 Enhancers Fetal Intestine Large intestine
16 chr17:59541000-59542200 Bivalent Enhancer HUES6 Cell Line embryonic stem cell
17 chr17:59541400-59541600 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
18 chr17:59541400-59542200 Flanking Bivalent TSS/Enh Fetal Muscle Trunk muscle

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