Variant report

Variant rs150678927
Chromosome Location chr7:22000295-22000296
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:21999400-22002800 Weak transcription Primary B cells from peripheral blood blood
2 chr7:21999800-22001200 Enhancers HUVEC blood vessel
3 chr7:21999800-22002200 Enhancers Muscle Satellite Cultured Cells --
4 chr7:22000000-22001000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr7:22000000-22001000 Enhancers HMEC breast
6 chr7:22000000-22001000 Enhancers NH-A brain
7 chr7:22000000-22001000 Enhancers Osteobl bone
8 chr7:22000000-22001600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
9 chr7:22000200-22000400 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
10 chr7:22000200-22000800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr7:22000200-22000800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr7:22000200-22000800 Enhancers Hela-S3 cervix
13 chr7:22000200-22001000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr7:22000200-22001000 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
15 chr7:22000200-22001000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
16 chr7:22000200-22001000 Enhancers HSMM muscle
17 chr7:22000200-22001000 Enhancers NHEK skin
18 chr7:22000200-22001000 Enhancers NHLF lung
19 chr7:22000200-22001200 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
20 chr7:22000200-22002400 Weak transcription A549 lung

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