The 2.0 version of rSNPBase

Variant report

Variant rs16843034
Chromosome Location chr2:210385810-210385811
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210364600-210387600 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
2 chr2:210364600-210392200 Weak transcription Pancreas Pancrea
3 chr2:210366600-210387800 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
4 chr2:210371400-210391000 Weak transcription Aorta Aorta
5 chr2:210378800-210390200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:210382200-210391600 Enhancers Cortex derived primary cultured neurospheres brain
7 chr2:210383000-210391000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
8 chr2:210383200-210386200 Enhancers Brain Germinal Matrix brain
9 chr2:210384000-210386000 Bivalent Enhancer iPS-15b Cell Line embryonic stem cell
10 chr2:210384000-210386000 Enhancers Fetal Brain Female brain
11 chr2:210384000-210386600 Enhancers Pancreatic Islets Pancreatic Islet
12 chr2:210384000-210388600 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:210385200-210387000 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
14 chr2:210385800-210386000 Bivalent Enhancer H1 Cell Line embryonic stem cell
15 chr2:210385800-210386200 Enhancers HUVEC blood vessel
16 chr2:210385800-210386400 Enhancers Fetal Brain Male brain

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Last update: Aug 31, 2015