Variant report

Variant rs6665321
Chromosome Location chr1:95253116-95253117
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:95242600-95268000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:95243200-95265000 Weak transcription Fetal Intestine Large intestine
3 chr1:95249200-95258000 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:95249200-95260800 Weak transcription Right Atrium heart
5 chr1:95249400-95256600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:95249400-95256800 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
7 chr1:95249600-95256400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
8 chr1:95250400-95255400 Weak transcription HUVEC blood vessel
9 chr1:95250400-95255800 Weak transcription NHLF lung
10 chr1:95250400-95256000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:95250400-95257600 Weak transcription Sigmoid Colon Sigmoid Colon
12 chr1:95250400-95257800 Weak transcription Stomach Mucosa stomach
13 chr1:95250600-95255800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
14 chr1:95250600-95258200 Weak transcription Fetal Intestine Small intestine
15 chr1:95251000-95253200 Weak transcription Breast Myoepithelial Primary Cells Breast
16 chr1:95251000-95256000 Weak transcription NHDF-Ad bronchial
17 chr1:95251000-95271600 Weak transcription Small Intestine intestine
18 chr1:95251600-95258000 Weak transcription Aorta Aorta
19 chr1:95253000-95253200 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived

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