Variant report

Variant rs73431697
Chromosome Location chr11:16414412-16414413
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16406800-16415200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr11:16409000-16419200 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr11:16410000-16418800 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr11:16414200-16414600 Enhancers Muscle Satellite Cultured Cells --
5 chr11:16414200-16414600 Enhancers Fetal Intestine Large intestine
6 chr11:16414200-16416400 Enhancers Fetal Intestine Small intestine
7 chr11:16414400-16414600 Enhancers K562 blood
8 chr11:16414400-16414800 Weak transcription Pancreatic Islets Pancreatic Islet
9 chr11:16414400-16414800 Enhancers NHDF-Ad bronchial
10 chr11:16414400-16415200 Enhancers Small Intestine intestine
11 chr11:16414400-16415400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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