The 2.0 version of rSNPBase

Variant report

Variant rs11686346
Chromosome Location chr2:210363880-210363881
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210360200-210366000 Weak transcription Psoas Muscle Psoas
2 chr2:210360200-210366400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr2:210361800-210376400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr2:210362000-210365000 Weak transcription Fetal Heart heart
5 chr2:210363200-210364600 Enhancers Placenta Placenta
6 chr2:210363400-210364000 Genic enhancers H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:210363400-210364200 Enhancers A549 lung
8 chr2:210363400-210364400 Enhancers Primary monocytes fromperipheralblood blood
9 chr2:210363400-210364600 Enhancers Pancreas Pancrea
10 chr2:210363600-210365200 Strong transcription Cortex derived primary cultured neurospheres brain
11 chr2:210363600-210365400 Strong transcription Ganglion Eminence derived primary cultured neurospheres brain
12 chr2:210363600-210365800 Weak transcription Fetal Brain Female brain
13 chr2:210363600-210370800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
14 chr2:210363600-210378400 Weak transcription Brain Germinal Matrix brain
15 chr2:210363800-210364000 Enhancers HUVEC blood vessel
16 chr2:210363800-210364600 Strong transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
17 chr2:210363800-210365800 Weak transcription Pancreatic Islets Pancreatic Islet

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Last update: Aug 31, 2015