Variant report

Variant rs74018303
Chromosome Location chr16:31253556-31253557
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr16:31250400-31262600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
2 chr16:31252600-31258000 Enhancers Primary monocytes fromperipheralblood blood
3 chr16:31252800-31253800 Enhancers ES-I3 Cell Line embryonic stem cell
4 chr16:31252800-31255200 Enhancers Primary neutrophils fromperipheralblood blood
5 chr16:31253200-31254400 Enhancers Spleen Spleen
6 chr16:31253400-31253600 Enhancers H9 Cell Line embryonic stem cell
7 chr16:31253400-31253600 Enhancers HUES6 Cell Line embryonic stem cell
8 chr16:31253400-31253600 Enhancers HUES64 Cell Line embryonic stem cell
9 chr16:31253400-31253600 Enhancers Primary hematopoietic stem cells short term culture blood
10 chr16:31253400-31253800 Enhancers HUES48 Cell Line embryonic stem cell
11 chr16:31253400-31253800 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr16:31253400-31253800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr16:31253400-31254000 Enhancers iPS-20b Cell Line embryonic stem cell
14 chr16:31253400-31254000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr16:31253400-31254200 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
16 chr16:31253400-31254400 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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