Variant report

Variant rs1334306
Chromosome Location chr6:12490082-12490083
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:22 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:12484400-12491400 Weak transcription Small Intestine intestine
2 chr6:12486000-12490800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr6:12486200-12490200 Weak transcription Hela-S3 cervix
4 chr6:12486200-12490800 Weak transcription HMEC breast
5 chr6:12486600-12491400 Weak transcription Placenta Amnion Placenta Amnion
6 chr6:12487200-12490600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr6:12487200-12490800 Weak transcription NHEK skin
8 chr6:12487800-12490400 Enhancers A549 lung
9 chr6:12488000-12491400 Weak transcription Aorta Aorta
10 chr6:12488200-12490800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
11 chr6:12488800-12490800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr6:12489200-12490600 Enhancers HUVEC blood vessel
13 chr6:12489400-12492400 Enhancers Fetal Adrenal Gland Adrenal Gland
14 chr6:12489600-12493000 Enhancers NHDF-Ad bronchial
15 chr6:12489800-12490800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr6:12489800-12492600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
17 chr6:12490000-12490800 Enhancers NH-A brain
18 chr6:12490000-12491400 Weak transcription Right Atrium heart
19 chr6:12490000-12492000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
20 chr6:12490000-12492200 Enhancers NHLF lung
21 chr6:12490000-12492400 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
22 chr6:12490000-12493000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin

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