Variant report

Variant rs12639909
Chromosome Location chr4:187138801-187138802
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:187117600-187140600 Weak transcription Aorta Aorta
2 chr4:187125800-187149200 Weak transcription Colon Smooth Muscle Colon
3 chr4:187130400-187144200 Weak transcription Esophagus oesophagus
4 chr4:187130600-187149400 Weak transcription Gastric stomach
5 chr4:187130800-187145000 Weak transcription Pancreas Pancrea
6 chr4:187131000-187139800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr4:187131400-187139000 Weak transcription Small Intestine intestine
8 chr4:187131600-187146000 Weak transcription Brain Dorsolateral Prefrontal Cortex brain
9 chr4:187131600-187148400 Weak transcription Fetal Kidney kidney
10 chr4:187131800-187149000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
11 chr4:187131800-187159000 Weak transcription Skeletal Muscle Male skeletal muscle
12 chr4:187131800-187181600 Weak transcription Brain Hippocampus Middle brain
13 chr4:187132600-187139200 Weak transcription Fetal Intestine Small intestine
14 chr4:187134000-187139800 Weak transcription Liver Liver
15 chr4:187134000-187149000 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr4:187138400-187139000 Weak transcription Fetal Lung lung
17 chr4:187138400-187139400 Enhancers Fetal Intestine Large intestine
18 chr4:187138800-187139400 Enhancers iPS-15b Cell Line embryonic stem cell

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