Variant report

Variant rs57302235
Chromosome Location chr1:211692956-211692957
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:211688200-211701200 Weak transcription Gastric stomach
2 chr1:211689400-211694400 Weak transcription Right Atrium heart
3 chr1:211689400-211701200 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr1:211689400-211715000 Weak transcription Placenta Amnion Placenta Amnion
5 chr1:211690200-211693400 Enhancers Primary B cells from cord blood blood
6 chr1:211690200-211693400 Enhancers Primary B cells from peripheral blood blood
7 chr1:211690200-211698400 Enhancers Liver Liver
8 chr1:211690400-211695800 Weak transcription H9 Cell Line embryonic stem cell
9 chr1:211690800-211694000 Weak transcription Placenta Placenta
10 chr1:211690800-211694400 Weak transcription K562 blood
11 chr1:211690800-211694600 Weak transcription A549 lung
12 chr1:211691000-211700400 Weak transcription Fetal Thymus thymus
13 chr1:211691200-211694400 Weak transcription Hela-S3 cervix
14 chr1:211691400-211693000 Enhancers Primary monocytes fromperipheralblood blood
15 chr1:211691800-211693600 Flanking Active TSS HepG2 liver
16 chr1:211692000-211693200 Weak transcription Primary hematopoietic stem cells short term culture blood
17 chr1:211692400-211694200 Enhancers GM12878-XiMat blood
18 chr1:211692800-211693000 Enhancers Fetal Muscle Leg muscle
19 chr1:211692800-211693400 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived

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