Variant report

Variant rs35199438
Chromosome Location chr11:16630779-16630780
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:16629800-16634200 Weak transcription Pancreas Pancrea
2 chr11:16630000-16633200 Weak transcription Right Atrium heart
3 chr11:16630000-16633600 Weak transcription Left Ventricle heart
4 chr11:16630000-16633600 Weak transcription Right Ventricle heart
5 chr11:16630000-16634200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
6 chr11:16630000-16634200 Weak transcription Psoas Muscle Psoas
7 chr11:16630000-16634400 Weak transcription K562 blood
8 chr11:16630200-16630800 Enhancers Fetal Heart heart
9 chr11:16630200-16631200 Enhancers Cortex derived primary cultured neurospheres brain
10 chr11:16630200-16631600 Enhancers Brain Germinal Matrix brain
11 chr11:16630600-16631000 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
12 chr11:16630600-16633200 Weak transcription Pancreatic Islets Pancreatic Islet
13 chr11:16630600-16633800 Bivalent/Poised TSS iPS-15b Cell Line embryonic stem cell

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