Variant report

Variant rs1354322
Chromosome Location chr11:105015887-105015888
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:105010600-105026400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:105013200-105016000 Enhancers HUVEC blood vessel
3 chr11:105015200-105016000 Enhancers HMEC breast
4 chr11:105015200-105016400 Enhancers NHLF lung
5 chr11:105015200-105016600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
6 chr11:105015400-105016000 Enhancers NH-A brain
7 chr11:105015600-105016000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr11:105015600-105016000 Enhancers NHDF-Ad bronchial
9 chr11:105015600-105016000 Enhancers NHEK skin
10 chr11:105015600-105016200 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr11:105015600-105016400 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
12 chr11:105015600-105016600 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
13 chr11:105015600-105016600 Enhancers Hela-S3 cervix
14 chr11:105015800-105016000 Flanking Active TSS Muscle Satellite Cultured Cells --
15 chr11:105015800-105016200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr11:105015800-105016400 Enhancers Rectal Mucosa Donor 31 rectum
17 chr11:105015800-105016600 Enhancers Duodenum Mucosa Duodenum
18 chr11:105015800-105016600 Enhancers Fetal Intestine Large intestine
19 chr11:105015800-105016600 Enhancers HepG2 liver
20 chr11:105015800-105016800 Enhancers Fetal Intestine Small intestine

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