Variant report

Variant rs115996034
Chromosome Location chr20:1550541-1550542
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:24 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:1537000-1551600 Weak transcription Primary T helper naive cells fromperipheralblood blood
2 chr20:1543800-1568000 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr20:1544600-1569000 Weak transcription Primary T regulatory cells fromperipheralblood blood
4 chr20:1546600-1551200 Enhancers Hela-S3 cervix
5 chr20:1546600-1551400 Weak transcription Spleen Spleen
6 chr20:1546800-1550800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr20:1546800-1551000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr20:1547000-1550800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr20:1547000-1551000 Enhancers HMEC breast
10 chr20:1547200-1551000 Enhancers HUVEC blood vessel
11 chr20:1548200-1551400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
12 chr20:1548600-1550600 Enhancers Primary monocytes fromperipheralblood blood
13 chr20:1548600-1550600 Enhancers A549 lung
14 chr20:1548800-1551000 Enhancers Primary hematopoietic stem cells short term culture blood
15 chr20:1548800-1551000 Enhancers NHEK skin
16 chr20:1548800-1552400 Strong transcription Primary T cells from cord blood blood
17 chr20:1549600-1550800 Weak transcription Primary B cells from cord blood blood
18 chr20:1550000-1550800 Enhancers K562 blood
19 chr20:1550000-1568200 Weak transcription Primary T helper cells fromperipheralblood blood
20 chr20:1550200-1550600 Flanking Active TSS Monocytes-CD14+_RO01746 blood
21 chr20:1550200-1551400 Weak transcription Esophagus oesophagus
22 chr20:1550400-1550600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
23 chr20:1550400-1550600 Enhancers Thymus Thymus
24 chr20:1550400-1550800 Enhancers Primary neutrophils fromperipheralblood blood

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