Variant report

Variant rs185485696
Chromosome Location chr20:1557036-1557037
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:1543800-1568000 Weak transcription Primary T helper cells PMA-I stimulated --
2 chr20:1544600-1569000 Weak transcription Primary T regulatory cells fromperipheralblood blood
3 chr20:1550000-1568200 Weak transcription Primary T helper cells fromperipheralblood blood
4 chr20:1552400-1558000 Weak transcription Primary T cells from cord blood blood
5 chr20:1552400-1568000 Weak transcription Primary T helper naive cells fromperipheralblood blood
6 chr20:1552600-1569000 Weak transcription Spleen Spleen
7 chr20:1552800-1558400 Weak transcription Primary mononuclear cells fromperipheralblood Blood
8 chr20:1556800-1557200 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
9 chr20:1556800-1557400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr20:1556800-1557600 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
11 chr20:1556800-1557600 Enhancers NHEK skin
12 chr20:1556800-1558200 Enhancers Hela-S3 cervix
13 chr20:1556800-1558600 Genic enhancers Primary neutrophils fromperipheralblood blood
14 chr20:1556800-1560000 Genic enhancers Primary monocytes fromperipheralblood blood
15 chr20:1556800-1560000 Genic enhancers Monocytes-CD14+_RO01746 blood
16 chr20:1557000-1557400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin

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