Variant report

Variant rs6902566
Chromosome Location chr6:167571048-167571049
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:167534000-167573400 Weak transcription Right Atrium heart
2 chr6:167565800-167575600 Weak transcription iPS-18 Cell Line embryonic stem cell
3 chr6:167566000-167575600 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
4 chr6:167567800-167571600 Weak transcription Primary T helper 17 cells PMA-I stimulated --
5 chr6:167569600-167571400 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
6 chr6:167570400-167571400 Enhancers iPS DF 19.11 Cell Line embryonic stem cell
7 chr6:167570800-167571400 Enhancers Esophagus oesophagus
8 chr6:167570800-167571600 Enhancers Primary B cells from cord blood blood
9 chr6:167570800-167572200 Enhancers Primary B cells from peripheral blood blood
10 chr6:167571000-167571400 Flanking Active TSS Breast Myoepithelial Primary Cells Breast
11 chr6:167571000-167571400 Enhancers Primary monocytes fromperipheralblood blood
12 chr6:167571000-167571400 Enhancers Primary Natural Killer cells fromperipheralblood blood
13 chr6:167571000-167571400 Enhancers Spleen Spleen
14 chr6:167571000-167571600 Enhancers GM12878-XiMat blood
15 chr6:167571000-167571800 Enhancers Monocytes-CD14+_RO01746 blood

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