Variant report

Variant rs558904040
Chromosome Location chr1:169231257-169231258
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169227600-169231800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr1:169227600-169233000 Weak transcription Fetal Kidney kidney
3 chr1:169227600-169257400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
4 chr1:169228400-169257400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr1:169229000-169233000 Weak transcription Brain Angular Gyrus brain
6 chr1:169229800-169232000 Strong transcription Primary T cells from cord blood blood
7 chr1:169229800-169232000 ZNF genes & repeats Rectal Mucosa Donor 31 rectum
8 chr1:169230400-169232200 Weak transcription HUVEC blood vessel
9 chr1:169230400-169235400 Weak transcription Primary hematopoietic stem cells blood
10 chr1:169231000-169234000 ZNF genes & repeats Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:169231200-169231400 ZNF genes & repeats Primary T helper cells PMA-I stimulated --
12 chr1:169231200-169232000 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood

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