Variant report

Variant rs61553554
Chromosome Location chr2:172081649-172081650
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:172077200-172083600 Weak transcription Placenta Placenta
2 chr2:172081200-172082400 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
3 chr2:172081200-172082400 Enhancers Muscle Satellite Cultured Cells --
4 chr2:172081200-172082400 Enhancers NH-A brain
5 chr2:172081200-172082400 Enhancers Osteobl bone
6 chr2:172081200-172084000 Enhancers HMEC breast
7 chr2:172081200-172084400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr2:172081400-172082000 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
9 chr2:172081400-172082200 Flanking Active TSS A549 lung
10 chr2:172081400-172082600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr2:172081400-172082600 Enhancers NHDF-Ad bronchial
12 chr2:172081400-172084400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
13 chr2:172081600-172082000 Flanking Active TSS NHEK skin
14 chr2:172081600-172082400 Enhancers HSMM muscle
15 chr2:172081600-172082400 Enhancers HSMMtube muscle
16 chr2:172081600-172082400 Enhancers HUVEC blood vessel
17 chr2:172081600-172082400 Enhancers K562 blood
18 chr2:172081600-172083000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
19 chr2:172081600-172084000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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