Variant report

Variant rs188843152
Chromosome Location chr1:169230738-169230739
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169227200-169231200 Weak transcription Primary T helper cells PMA-I stimulated --
2 chr1:169227600-169231000 Weak transcription Primary B cells from cord blood blood
3 chr1:169227600-169231800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
4 chr1:169227600-169233000 Weak transcription Fetal Kidney kidney
5 chr1:169227600-169257400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:169228400-169230800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
7 chr1:169228400-169231000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr1:169228400-169257400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:169229000-169233000 Weak transcription Brain Angular Gyrus brain
10 chr1:169229800-169232000 Strong transcription Primary T cells from cord blood blood
11 chr1:169229800-169232000 ZNF genes & repeats Rectal Mucosa Donor 31 rectum
12 chr1:169230400-169230800 Enhancers Monocytes-CD14+_RO01746 blood
13 chr1:169230400-169232200 Weak transcription HUVEC blood vessel
14 chr1:169230400-169235400 Weak transcription Primary hematopoietic stem cells blood
15 chr1:169230600-169231200 Genic enhancers Primary hematopoietic stem cells short term culture blood

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