The 2.0 version of rSNPBase

Variant report

Variant nsv257098
Chromosome Location chr4:45352282-45352290
allele n/a
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:45349400-45352400 Weak transcription Stomach Mucosa stomach
2 chr4:45352000-45352800 Active TSS Brain Substantia Nigra brain
3 chr4:45352000-45353200 Enhancers Fetal Heart heart
4 chr4:45352200-45352400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:45352200-45352400 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
6 chr4:45352200-45352400 Flanking Active TSS Pancreatic Islets Pancreatic Islet
7 chr4:45352200-45352400 Enhancers Dnd41 blood
8 chr4:45352200-45352800 Flanking Active TSS Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:45352200-45352800 Active TSS Brain Cingulate Gyrus brain
10 chr4:45352200-45352800 Active TSS Colon Smooth Muscle Colon
11 chr4:45352200-45352800 Active TSS GM12878-XiMat blood
12 chr4:45352200-45352800 Active TSS NHDF-Ad bronchial
13 chr4:45352200-45353000 Active TSS Muscle Satellite Cultured Cells --
14 chr4:45352200-45353200 Enhancers Cortex derived primary cultured neurospheres brain
15 chr4:45352200-45353200 Active TSS Right Atrium heart
16 chr4:45352200-45353200 Active TSS Stomach Smooth Muscle stomach

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Last update: Aug 31, 2015