Variant report

Variant rs66663429
Chromosome Location chr17:16776956-16776957
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr17:16775400-16777600 Enhancers Fetal Intestine Small intestine
2 chr17:16775600-16777000 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
3 chr17:16775600-16777800 Enhancers Fetal Intestine Large intestine
4 chr17:16775800-16777400 Enhancers Liver Liver
5 chr17:16775800-16777800 Enhancers Duodenum Mucosa Duodenum
6 chr17:16776200-16777000 Enhancers Gastric stomach
7 chr17:16776400-16777200 Enhancers Colonic Mucosa Colon
8 chr17:16776600-16777000 Enhancers HepG2 liver
9 chr17:16776600-16777200 Enhancers Fetal Brain Male brain
10 chr17:16776600-16777200 Enhancers Rectal Mucosa Donor 29 rectum
11 chr17:16776600-16777200 Enhancers Rectal Mucosa Donor 31 rectum
12 chr17:16776800-16777000 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
13 chr17:16776800-16777000 Bivalent Enhancer Fetal Muscle Leg muscle
14 chr17:16776800-16777000 Bivalent Enhancer Skeletal Muscle Male skeletal muscle
15 chr17:16776800-16777200 Enhancers Lung lung
16 chr17:16776800-16777200 Enhancers Pancreas Pancrea
17 chr17:16776800-16777200 Enhancers Small Intestine intestine
18 chr17:16776800-16777400 ZNF genes & repeats iPS DF 19.11 Cell Line embryonic stem cell
19 chr17:16776800-16777400 Bivalent Enhancer Fetal Adrenal Gland Adrenal Gland
20 chr17:16776800-16777400 Bivalent Enhancer Fetal Muscle Trunk muscle

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