Variant report

Variant rs67249415
Chromosome Location chr15:52744160-52744161
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:21 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr15:52730400-52744600 Weak transcription Primary T regulatory cells fromperipheralblood blood
2 chr15:52732600-52750600 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr15:52734600-52753200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr15:52734800-52747400 Weak transcription HSMM muscle
5 chr15:52738800-52744600 Weak transcription Primary T helper cells fromperipheralblood blood
6 chr15:52739000-52751800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr15:52739000-52753600 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
8 chr15:52740400-52756200 Weak transcription Primary T cells effector/memory enriched fromperipheralblood blood
9 chr15:52740600-52744200 Weak transcription Brain Hippocampus Middle brain
10 chr15:52740600-52753200 Weak transcription Monocytes-CD14+_RO01746 blood
11 chr15:52742000-52755800 Weak transcription Primary T helper naive cells fromperipheralblood blood
12 chr15:52742200-52751600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
13 chr15:52742200-52753000 Weak transcription NHEK skin
14 chr15:52742400-52744400 Weak transcription Skeletal Muscle Male skeletal muscle
15 chr15:52742400-52744600 Weak transcription Left Ventricle heart
16 chr15:52743200-52744200 Genic enhancers Foreskin Melanocyte Primary Cells skin03 Skin
17 chr15:52743400-52744800 Enhancers Right Atrium heart
18 chr15:52743600-52744800 Enhancers Brain Cingulate Gyrus brain
19 chr15:52743600-52744800 Enhancers Skeletal Muscle Female skeletal muscle
20 chr15:52743800-52758200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
21 chr15:52744000-52744200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin

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