Variant report

Variant rs531554898
Chromosome Location chr4:187092191-187092192
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187080000-187092200 Weak transcription Brain Cingulate Gyrus brain
2 chr4:187080000-187092200 Weak transcription Spleen Spleen
3 chr4:187080000-187094000 Weak transcription Rectal Mucosa Donor 31 rectum
4 chr4:187080200-187094000 Weak transcription Rectal Mucosa Donor 29 rectum
5 chr4:187081000-187099200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr4:187082000-187095000 Weak transcription Fetal Brain Male brain
7 chr4:187085000-187093200 Weak transcription Duodenum Mucosa Duodenum
8 chr4:187087400-187093000 Weak transcription Brain Germinal Matrix brain
9 chr4:187090000-187092400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
10 chr4:187090200-187094800 Weak transcription Brain Hippocampus Middle brain
11 chr4:187090400-187092600 Weak transcription Stomach Smooth Muscle stomach
12 chr4:187090600-187095000 Weak transcription Fetal Brain Female brain
13 chr4:187090800-187092200 Weak transcription Fetal Intestine Large intestine
14 chr4:187090800-187092200 Weak transcription Pancreas Pancrea
15 chr4:187090800-187092400 Weak transcription Gastric stomach
16 chr4:187091000-187092200 Weak transcription Lung lung
17 chr4:187091000-187092800 Weak transcription Ovary ovary
18 chr4:187091200-187092200 Enhancers HepG2 liver
19 chr4:187091600-187093000 Weak transcription Fetal Stomach stomach

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