Variant report

Variant rs374290744
Chromosome Location chr4:187091877-187091878
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 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 chr4:187082200-187092000 Weak transcription Fetal Lung lung
8 chr4:187085000-187093200 Weak transcription Duodenum Mucosa Duodenum
9 chr4:187087400-187093000 Weak transcription Brain Germinal Matrix brain
10 chr4:187090000-187092400 Genic enhancers iPS DF 19.11 Cell Line embryonic stem cell
11 chr4:187090200-187094800 Weak transcription Brain Hippocampus Middle brain
12 chr4:187090400-187092600 Weak transcription Stomach Smooth Muscle stomach
13 chr4:187090600-187095000 Weak transcription Fetal Brain Female brain
14 chr4:187090800-187092200 Weak transcription Fetal Intestine Large intestine
15 chr4:187090800-187092200 Weak transcription Pancreas Pancrea
16 chr4:187090800-187092400 Weak transcription Gastric stomach
17 chr4:187091000-187092000 Weak transcription Fetal Intestine Small intestine
18 chr4:187091000-187092200 Weak transcription Lung lung
19 chr4:187091000-187092800 Weak transcription Ovary ovary
20 chr4:187091200-187092200 Enhancers HepG2 liver
21 chr4:187091600-187093000 Weak transcription Fetal Stomach stomach

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