Variant report

Variant rs372960941
Chromosome Location chr1:169229927-169229928
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169220600-169230000 Weak transcription Liver Liver
2 chr1:169227200-169231200 Weak transcription Primary T helper cells PMA-I stimulated --
3 chr1:169227600-169231000 Weak transcription Primary B cells from cord blood blood
4 chr1:169227600-169231800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:169227600-169233000 Weak transcription Fetal Kidney kidney
6 chr1:169227600-169257400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:169228400-169230400 Enhancers Primary monocytes fromperipheralblood blood
8 chr1:169228400-169230600 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr1:169228400-169230800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
10 chr1:169228400-169231000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
11 chr1:169228400-169257400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:169229000-169230200 Enhancers Primary neutrophils fromperipheralblood blood
13 chr1:169229000-169233000 Weak transcription Brain Angular Gyrus brain
14 chr1:169229200-169230400 Flanking Active TSS Monocytes-CD14+_RO01746 blood
15 chr1:169229800-169230200 ZNF genes & repeats Fetal Brain Female brain
16 chr1:169229800-169230400 Enhancers Primary hematopoietic stem cells blood
17 chr1:169229800-169230400 Strong transcription HUVEC blood vessel
18 chr1:169229800-169232000 Strong transcription Primary T cells from cord blood blood
19 chr1:169229800-169232000 ZNF genes & repeats Rectal Mucosa Donor 31 rectum

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