Variant report

Variant rs11161512
Chromosome Location chr1:85496484-85496485
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:85485400-85513000 Weak transcription Pancreas Pancrea
2 chr1:85485800-85505200 Weak transcription Duodenum Mucosa Duodenum
3 chr1:85486000-85513000 Weak transcription Breast Myoepithelial Primary Cells Breast
4 chr1:85486400-85499200 Weak transcription NHDF-Ad bronchial
5 chr1:85486400-85500400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
6 chr1:85489000-85500000 Weak transcription Adipose Nuclei Adipose
7 chr1:85492200-85497000 Strong transcription Fetal Intestine Small intestine
8 chr1:85493000-85498200 Strong transcription Fetal Intestine Large intestine
9 chr1:85493000-85501000 Weak transcription HUES48 Cell Line embryonic stem cell
10 chr1:85493600-85498800 Weak transcription GM12878-XiMat blood
11 chr1:85494000-85498000 Weak transcription Osteobl bone
12 chr1:85495000-85512800 Weak transcription HMEC breast
13 chr1:85496000-85499000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr1:85496000-85500000 Weak transcription Right Atrium heart
15 chr1:85496400-85498800 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin

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