Variant report

Variant rs28559933
Chromosome Location chr7:20785633-20785634
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:20782400-20788000 Strong transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr7:20782800-20796200 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
3 chr7:20784600-20785800 Enhancers Fetal Kidney kidney
4 chr7:20784800-20785800 Enhancers H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:20784800-20785800 Enhancers iPS-18 Cell Line embryonic stem cell
6 chr7:20784800-20785800 Enhancers Fetal Muscle Leg muscle
7 chr7:20784800-20786000 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
8 chr7:20785000-20785800 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr7:20785200-20785800 Enhancers Fetal Muscle Trunk muscle
10 chr7:20785200-20786000 Enhancers H1 Cell Line embryonic stem cell
11 chr7:20785400-20785800 Enhancers HUES64 Cell Line embryonic stem cell
12 chr7:20785400-20786000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr7:20785400-20787200 Weak transcription ES-WA7 Cell Line embryonic stem cell
14 chr7:20785600-20785800 Enhancers H9 Cell Line embryonic stem cell

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