Variant report

Variant rs12138711
Chromosome Location chr1:85492596-85492597
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85483600-85494800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:85485400-85513000 Weak transcription Pancreas Pancrea
3 chr1:85485800-85505200 Weak transcription Duodenum Mucosa Duodenum
4 chr1:85486000-85513000 Weak transcription Breast Myoepithelial Primary Cells Breast
5 chr1:85486400-85499200 Weak transcription NHDF-Ad bronchial
6 chr1:85486400-85500400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
7 chr1:85488000-85493000 Weak transcription HMEC breast
8 chr1:85488800-85493000 Weak transcription Primary T helper memory cells from peripheral blood 1 blood
9 chr1:85489000-85492600 Weak transcription Primary T cells fromperipheralblood blood
10 chr1:85489000-85492600 Weak transcription Primary Natural Killer cells fromperipheralblood blood
11 chr1:85489000-85500000 Weak transcription Adipose Nuclei Adipose
12 chr1:85490600-85492800 Weak transcription GM12878-XiMat blood
13 chr1:85490800-85494400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:85491400-85493000 Weak transcription Fetal Intestine Large intestine
15 chr1:85492200-85497000 Strong transcription Fetal Intestine Small intestine

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