Variant report

Variant rs71484711
Chromosome Location chr11:16356803-16356804
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16319400-16377600 Weak transcription Psoas Muscle Psoas
2 chr11:16340800-16357600 Weak transcription Cortex derived primary cultured neurospheres brain
3 chr11:16345800-16367000 Weak transcription Skeletal Muscle Female skeletal muscle
4 chr11:16348400-16362600 Weak transcription Left Ventricle heart
5 chr11:16348800-16368600 Weak transcription Brain Germinal Matrix brain
6 chr11:16349400-16357400 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr11:16349600-16357800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
8 chr11:16351000-16360000 Weak transcription Fetal Heart heart
9 chr11:16353000-16361400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr11:16354800-16360400 Enhancers Pancreatic Islets Pancreatic Islet
11 chr11:16356400-16358200 Enhancers Fetal Intestine Small intestine
12 chr11:16356600-16358200 Enhancers Rectal Mucosa Donor 31 rectum
13 chr11:16356800-16357400 Weak transcription Fetal Intestine Large intestine
14 chr11:16356800-16357600 Enhancers Duodenum Mucosa Duodenum
15 chr11:16356800-16357800 Enhancers Rectal Mucosa Donor 29 rectum
16 chr11:16356800-16358200 Enhancers HepG2 liver
17 chr11:16356800-16360800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain

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