Variant report

Variant rs12684893
Chromosome Location chr9:139674527-139674528
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:139668200-139682400 Weak transcription Right Atrium heart
2 chr9:139672600-139674600 Weak transcription Placenta Placenta
3 chr9:139673400-139682000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
4 chr9:139674000-139675000 Enhancers K562 blood
5 chr9:139674200-139675400 Enhancers Colonic Mucosa Colon
6 chr9:139674400-139674600 Bivalent Enhancer Ganglion Eminence derived primary cultured neurospheres brain
7 chr9:139674400-139674800 Enhancers A549 lung
8 chr9:139674400-139675000 Enhancers Fetal Intestine Small intestine
9 chr9:139674400-139676000 Enhancers Fetal Intestine Large intestine
10 chr9:139674400-139676000 Enhancers HepG2 liver
11 chr9:139674400-139676600 Enhancers Rectal Mucosa Donor 31 rectum

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