Variant report

Variant rs71484394
Chromosome Location chr11:104980515-104980516
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:104972200-104980600 Weak transcription Adipose Nuclei Adipose
2 chr11:104972600-104981000 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
3 chr11:104975000-104983400 Weak transcription H9 Cell Line embryonic stem cell
4 chr11:104977000-104980800 Enhancers Hela-S3 cervix
5 chr11:104979000-104982600 Enhancers Breast Myoepithelial Primary Cells Breast
6 chr11:104979400-104980600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
7 chr11:104979400-104981600 Weak transcription Placenta Placenta
8 chr11:104979800-104980800 Enhancers NHEK skin
9 chr11:104980000-104980800 Enhancers Primary monocytes fromperipheralblood blood
10 chr11:104980000-104980800 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr11:104980200-104980800 Enhancers Primary neutrophils fromperipheralblood blood
12 chr11:104980200-104980800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr11:104980200-104980800 Enhancers Fetal Intestine Large intestine
14 chr11:104980200-104980800 Enhancers HUVEC blood vessel
15 chr11:104980200-104981200 Enhancers HMEC breast
16 chr11:104980200-104981800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
17 chr11:104980200-104982200 Enhancers Cortex derived primary cultured neurospheres brain
18 chr11:104980400-104981200 Enhancers Brain Anterior Caudate brain
19 chr11:104980400-104981200 Enhancers Fetal Intestine Small intestine
20 chr11:104980400-104981600 Flanking Active TSS Monocytes-CD14+_RO01746 blood

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