Variant report

Variant rs72869664
Chromosome Location chr2:33267873-33267874
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:33250600-33273000 Weak transcription K562 blood
2 chr2:33259200-33276200 Weak transcription Right Ventricle heart
3 chr2:33260200-33268000 Weak transcription Fetal Muscle Leg muscle
4 chr2:33260200-33268400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
5 chr2:33260200-33273400 Weak transcription HUVEC blood vessel
6 chr2:33260200-33276400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr2:33260200-33295400 Weak transcription Right Atrium heart
8 chr2:33264200-33276200 Weak transcription Left Ventricle heart
9 chr2:33264200-33276600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr2:33265800-33273200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
11 chr2:33267200-33268200 Enhancers Colon Smooth Muscle Colon
12 chr2:33267400-33268200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr2:33267400-33268200 Genic enhancers IMR90 fetal lung fibroblasts Cell Line lung
14 chr2:33267400-33268200 Enhancers Breast Myoepithelial Primary Cells Breast
15 chr2:33267400-33268200 Enhancers Aorta Aorta
16 chr2:33267400-33268200 Enhancers Rectal Smooth Muscle rectum
17 chr2:33267600-33269000 Flanking Active TSS Liver Liver
18 chr2:33267600-33269000 Enhancers Stomach Smooth Muscle stomach
19 chr2:33267800-33270200 Weak transcription Cortex derived primary cultured neurospheres brain

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