Variant report

Variant rs10486701
Chromosome Location chr7:41051036-41051037
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:41047800-41052800 Weak transcription NH-A brain
2 chr7:41048000-41051400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr7:41048600-41065600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
4 chr7:41049000-41051600 Enhancers Primary neutrophils fromperipheralblood blood
5 chr7:41049200-41052000 Enhancers Primary monocytes fromperipheralblood blood
6 chr7:41049600-41051600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr7:41049600-41052000 Enhancers Fetal Muscle Leg muscle
8 chr7:41049800-41051600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:41049800-41051800 Enhancers NHDF-Ad bronchial
10 chr7:41049800-41053200 Enhancers Muscle Satellite Cultured Cells --
11 chr7:41050000-41051200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
12 chr7:41050000-41052000 Enhancers HSMM muscle
13 chr7:41050200-41051200 Enhancers HUVEC blood vessel
14 chr7:41050200-41051200 Enhancers Monocytes-CD14+_RO01746 blood
15 chr7:41051000-41052800 Weak transcription Osteobl bone
16 chr7:41051000-41060400 Weak transcription HSMMtube muscle

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