Variant report

Variant rs17011141
Chromosome Location chr1:222112634-222112635
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:222095400-222117800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr1:222098000-222118800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
3 chr1:222111800-222114400 Enhancers Primary B cells from peripheral blood blood
4 chr1:222112000-222114400 Enhancers Primary B cells from cord blood blood
5 chr1:222112200-222114600 Enhancers Fetal Brain Male brain
6 chr1:222112200-222114600 Enhancers GM12878-XiMat blood
7 chr1:222112400-222113400 Enhancers Adipose Nuclei Adipose
8 chr1:222112600-222113000 Flanking Active TSS Dnd41 blood
9 chr1:222112600-222113200 Enhancers HSMMtube muscle
10 chr1:222112600-222113400 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr1:222112600-222113400 Enhancers Fetal Thymus thymus
12 chr1:222112600-222113600 Enhancers Primary hematopoietic stem cells short term culture blood
13 chr1:222112600-222113800 Enhancers Fetal Brain Female brain

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