Variant report

Variant rs4722735
Chromosome Location chr7:3410591-3410592
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3407200-3411800 Enhancers Fetal Brain Male brain
2 chr7:3408800-3426200 Weak transcription Aorta Aorta
3 chr7:3409400-3410800 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr7:3409400-3410800 Enhancers Fetal Brain Female brain
5 chr7:3409400-3412200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
6 chr7:3409600-3412800 Enhancers Primary neutrophils fromperipheralblood blood
7 chr7:3410200-3411200 Enhancers Pancreatic Islets Pancreatic Islet
8 chr7:3410200-3412400 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr7:3410400-3410600 Genic enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
10 chr7:3410400-3410600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
11 chr7:3410400-3410600 Enhancers Lung lung
12 chr7:3410400-3410800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
13 chr7:3410400-3410800 Enhancers Pancreas Pancrea
14 chr7:3410400-3410800 Enhancers Spleen Spleen
15 chr7:3410400-3412200 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr7:3410400-3412400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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