Variant report

Variant rs11023919
Chromosome Location chr11:16357754-16357755
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16319400-16377600 Weak transcription Psoas Muscle Psoas
2 chr11:16345800-16367000 Weak transcription Skeletal Muscle Female skeletal muscle
3 chr11:16348400-16362600 Weak transcription Left Ventricle heart
4 chr11:16348800-16368600 Weak transcription Brain Germinal Matrix brain
5 chr11:16349600-16357800 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr11:16351000-16360000 Weak transcription Fetal Heart heart
7 chr11:16353000-16361400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr11:16354800-16360400 Enhancers Pancreatic Islets Pancreatic Islet
9 chr11:16356400-16358200 Enhancers Fetal Intestine Small intestine
10 chr11:16356600-16358200 Enhancers Rectal Mucosa Donor 31 rectum
11 chr11:16356800-16357800 Enhancers Rectal Mucosa Donor 29 rectum
12 chr11:16356800-16358200 Enhancers HepG2 liver
13 chr11:16356800-16360800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
14 chr11:16357000-16358400 Enhancers Fetal Kidney kidney
15 chr11:16357200-16357800 Enhancers K562 blood
16 chr11:16357400-16360200 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr11:16357400-16360200 Enhancers Fetal Intestine Large intestine
18 chr11:16357600-16358000 Genic enhancers Cortex derived primary cultured neurospheres brain
19 chr11:16357600-16358200 Flanking Active TSS Duodenum Mucosa Duodenum

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