Variant report

Variant rs4951763
Chromosome Location chr1:211696610-211696611
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211688200-211701200 Weak transcription Gastric stomach
2 chr1:211689400-211701200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
3 chr1:211689400-211715000 Weak transcription Placenta Amnion Placenta Amnion
4 chr1:211690200-211698400 Enhancers Liver Liver
5 chr1:211691000-211700400 Weak transcription Fetal Thymus thymus
6 chr1:211693400-211697800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
7 chr1:211694800-211698000 Weak transcription Fetal Muscle Leg muscle
8 chr1:211695000-211697400 Weak transcription K562 blood
9 chr1:211695000-211697800 Weak transcription Fetal Muscle Trunk muscle
10 chr1:211695000-211698400 Enhancers HepG2 liver
11 chr1:211695200-211701200 Weak transcription Right Atrium heart
12 chr1:211696200-211699200 Weak transcription GM12878-XiMat blood
13 chr1:211696400-211696800 Weak transcription ES-I3 Cell Line embryonic stem cell
14 chr1:211696400-211696800 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
15 chr1:211696400-211697800 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
16 chr1:211696400-211700400 Weak transcription iPS-15b Cell Line embryonic stem cell

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