Variant report

Variant rs13355813
Chromosome Location chr5:147723018-147723019
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:147709400-147749200 Weak transcription Psoas Muscle Psoas
2 chr5:147713000-147728800 Weak transcription Aorta Aorta
3 chr5:147714800-147731200 Weak transcription Pancreas Pancrea
4 chr5:147721600-147723600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr5:147721600-147729000 Weak transcription Left Ventricle heart
6 chr5:147721800-147723800 Enhancers HMEC breast
7 chr5:147722000-147723400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr5:147722200-147723400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr5:147722200-147723400 Enhancers NHEK skin
10 chr5:147722400-147723600 Enhancers Stomach Mucosa stomach
11 chr5:147722600-147723400 Enhancers Monocytes-CD14+_RO01746 blood
12 chr5:147722600-147723800 Enhancers Primary monocytes fromperipheralblood blood
13 chr5:147722600-147723800 Enhancers Rectal Mucosa Donor 31 rectum
14 chr5:147722600-147724200 Enhancers K562 blood
15 chr5:147722800-147723200 Enhancers iPS-15b Cell Line embryonic stem cell
16 chr5:147722800-147723200 Enhancers Esophagus oesophagus
17 chr5:147722800-147723200 Flanking Active TSS Hela-S3 cervix
18 chr5:147722800-147723400 Enhancers Sigmoid Colon Sigmoid Colon
19 chr5:147723000-147723200 Enhancers Colon Smooth Muscle Colon

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