Variant report

Variant rs3765604
Chromosome Location chr6:29976024-29976025
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:29974800-29981000 Weak transcription Hela-S3 cervix
2 chr6:29974800-30002400 Weak transcription Dnd41 blood
3 chr6:29975200-29976600 Bivalent Enhancer Foreskin Melanocyte Primary Cells skin01 Skin
4 chr6:29975200-30027800 Weak transcription Aorta Aorta
5 chr6:29975400-29976200 Bivalent Enhancer ES-UCSF4 Cell Line embryonic stem cell
6 chr6:29975400-29978800 Weak transcription Sigmoid Colon Sigmoid Colon
7 chr6:29975400-29985200 Weak transcription Lung lung
8 chr6:29975600-29976200 Bivalent/Poised TSS Skeletal Muscle Male skeletal muscle
9 chr6:29975600-29976200 Bivalent Enhancer Skeletal Muscle Female skeletal muscle
10 chr6:29975600-29979200 Weak transcription Ovary ovary
11 chr6:29975600-29979200 Weak transcription Pancreas Pancrea
12 chr6:29975600-29985000 Weak transcription Liver Liver
13 chr6:29975600-29985200 Weak transcription Primary B cells from cord blood blood
14 chr6:29975600-29987200 Weak transcription Breast Myoepithelial Primary Cells Breast
15 chr6:29975600-29987600 Weak transcription HepG2 liver
16 chr6:29975600-30027800 Weak transcription Right Ventricle heart
17 chr6:29975800-29976400 Bivalent Enhancer iPS DF 19.11 Cell Line embryonic stem cell
18 chr6:29975800-29976400 Weak transcription Spleen Spleen
19 chr6:29975800-29986600 Weak transcription Esophagus oesophagus
20 chr6:29975800-30027800 Weak transcription Gastric stomach

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