Variant report

Variant rs10085568
Chromosome Location chr7:3900810-3900811
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:3894800-3901600 Weak transcription Aorta Aorta
2 chr7:3898200-3901000 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
3 chr7:3900200-3902600 Enhancers iPS-18 Cell Line embryonic stem cell
4 chr7:3900600-3901000 Enhancers Right Atrium heart
5 chr7:3900600-3901200 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
6 chr7:3900600-3901200 Enhancers Lung lung
7 chr7:3900600-3901600 Enhancers Fetal Lung lung
8 chr7:3900600-3902000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
9 chr7:3900600-3902200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
10 chr7:3900600-3902200 Enhancers Muscle Satellite Cultured Cells --
11 chr7:3900600-3902400 Enhancers Colon Smooth Muscle Colon
12 chr7:3900600-3902800 Enhancers H9 Cell Line embryonic stem cell
13 chr7:3900600-3902800 Enhancers HUES48 Cell Line embryonic stem cell
14 chr7:3900800-3901200 Enhancers Skeletal Muscle Female skeletal muscle
15 chr7:3900800-3901800 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
16 chr7:3900800-3902200 Enhancers H9 Derived Neuronal Progenitor Cultured Cells ES cell derived

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