Variant report

Variant rs573173566
Chromosome Location chr4:1395784-1395785
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:1391200-1396600 Weak transcription Right Atrium heart
2 chr4:1393200-1397000 Weak transcription Gastric stomach
3 chr4:1393400-1395800 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
4 chr4:1394800-1397400 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
5 chr4:1395400-1396800 Bivalent Enhancer Primary B cells from peripheral blood blood
6 chr4:1395600-1395800 Flanking Bivalent TSS/Enh Foreskin Melanocyte Primary Cells skin01 Skin
7 chr4:1395600-1396200 Bivalent Enhancer Primary B cells from cord blood blood
8 chr4:1395600-1396200 Bivalent Enhancer Spleen Spleen
9 chr4:1395600-1396600 Bivalent Enhancer Breast Myoepithelial Primary Cells Breast
10 chr4:1395600-1398000 Bivalent Enhancer Esophagus oesophagus

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