Variant report

Variant rs562441822
Chromosome Location chr1:169235378-169235379
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:7 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:169227600-169257400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
2 chr1:169228400-169257400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr1:169230400-169235400 Weak transcription Primary hematopoietic stem cells blood
4 chr1:169234600-169240800 Weak transcription Primary T cells from cord blood blood
5 chr1:169235000-169235400 Enhancers HepG2 liver
6 chr1:169235200-169235400 ZNF genes & repeats Fetal Intestine Large intestine
7 chr1:169235200-169240200 Weak transcription Rectal Mucosa Donor 31 rectum

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