Variant report

Variant rs6903613
Chromosome Location chr6:4688031-4688032
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:4669000-4695600 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
2 chr6:4684400-4688200 Weak transcription Primary hematopoietic stem cells short term culture blood
3 chr6:4687600-4688200 Enhancers Hela-S3 cervix
4 chr6:4687600-4688400 Enhancers Primary monocytes fromperipheralblood blood
5 chr6:4687600-4688400 Enhancers HMEC breast
6 chr6:4687800-4688400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
7 chr6:4688000-4688200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
8 chr6:4688000-4688200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
9 chr6:4688000-4688200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
10 chr6:4688000-4688200 Enhancers NHEK skin
11 chr6:4688000-4688400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr6:4688000-4688400 Enhancers HUVEC blood vessel
13 chr6:4688000-4688400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
14 chr6:4688000-4688400 Enhancers NH-A brain
15 chr6:4688000-4688400 Enhancers NHDF-Ad bronchial
16 chr6:4688000-4688400 Enhancers NHLF lung
17 chr6:4688000-4688400 Enhancers Osteobl bone
18 chr6:4688000-4688600 Active TSS A549 lung
19 chr6:4688000-4688800 Enhancers Placenta Amnion Placenta Amnion
20 chr6:4688000-4688800 Enhancers HSMM muscle
21 chr6:4688000-4689000 Flanking Active TSS K562 blood

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