Variant report

Variant rs28495181
Chromosome Location chr14:65291798-65291799
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr14:65289600-65293600 Enhancers Fetal Heart heart
2 chr14:65289800-65295200 Enhancers Left Ventricle heart
3 chr14:65290000-65295200 Enhancers Psoas Muscle Psoas
4 chr14:65290400-65292000 Weak transcription Colon Smooth Muscle Colon
5 chr14:65290400-65292000 Enhancers Right Atrium heart
6 chr14:65290400-65292400 Bivalent Enhancer Fetal Muscle Trunk muscle
7 chr14:65290400-65292800 Weak transcription Gastric stomach
8 chr14:65290400-65293400 Weak transcription Spleen Spleen
9 chr14:65290600-65292000 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
10 chr14:65290600-65294400 Weak transcription Breast Myoepithelial Primary Cells Breast
11 chr14:65291000-65295600 Enhancers Fetal Muscle Leg muscle
12 chr14:65291200-65292200 Flanking Active TSS Skeletal Muscle Male skeletal muscle
13 chr14:65291400-65292200 Flanking Active TSS Skeletal Muscle Female skeletal muscle
14 chr14:65291400-65292400 Bivalent Enhancer HepG2 liver
15 chr14:65291600-65291800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
16 chr14:65291600-65291800 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
17 chr14:65291600-65292400 Enhancers Right Ventricle heart
18 chr14:65291600-65296000 Enhancers K562 blood

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