Variant report

Variant rs10202553
Chromosome Location chr2:186996576-186996577
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:186992200-186999200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr2:186993400-186996800 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr2:186993400-186997600 Enhancers HepG2 liver
4 chr2:186993400-186998000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
5 chr2:186993600-186997000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
6 chr2:186994200-186996800 Enhancers Cortex derived primary cultured neurospheres brain
7 chr2:186994400-186996600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr2:186994800-186996800 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr2:186995000-186997000 Enhancers HUVEC blood vessel
10 chr2:186995200-186996600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr2:186996000-187000400 Weak transcription Colon Smooth Muscle Colon
12 chr2:186996200-186996600 Enhancers H9 Cell Line embryonic stem cell
13 chr2:186996200-186996600 Weak transcription Breast Myoepithelial Primary Cells Breast
14 chr2:186996400-186996600 Enhancers ES-I3 Cell Line embryonic stem cell
15 chr2:186996400-186996600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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