Variant report

Variant rs7551957
Chromosome Location chr1:161470042-161470043
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:161466600-161471400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:161467800-161471600 Enhancers Primary monocytes fromperipheralblood blood
3 chr1:161467800-161471600 Enhancers Primary hematopoietic stem cells short term culture blood
4 chr1:161468600-161470200 Enhancers Primary hematopoietic stem cells blood
5 chr1:161468600-161472400 Enhancers K562 blood
6 chr1:161469000-161470200 Flanking Active TSS Primary neutrophils fromperipheralblood blood
7 chr1:161469200-161470600 Enhancers HUVEC blood vessel
8 chr1:161469200-161475200 Weak transcription Brain Substantia Nigra brain
9 chr1:161469400-161470200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr1:161469600-161470400 Enhancers Primary B cells from cord blood blood
11 chr1:161469600-161470400 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
12 chr1:161469600-161475000 Weak transcription Primary Natural Killer cells fromperipheralblood blood
13 chr1:161469800-161470200 Enhancers GM12878-XiMat blood
14 chr1:161470000-161470200 Enhancers Fetal Adrenal Gland Adrenal Gland
15 chr1:161470000-161470600 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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