Variant report

Variant rs35186656
Chromosome Location chr12:9603709-9603710
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9599600-9603800 Active TSS Foreskin Melanocyte Primary Cells skin01 Skin
2 chr12:9601800-9606800 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr12:9602000-9606800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
4 chr12:9602200-9606600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr12:9602200-9606800 Weak transcription Fetal Heart heart
6 chr12:9602200-9608000 Weak transcription HUVEC blood vessel
7 chr12:9602400-9605600 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
8 chr12:9602400-9606400 Weak transcription NHEK skin
9 chr12:9602400-9606600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
10 chr12:9602400-9606600 Weak transcription K562 blood
11 chr12:9602800-9604000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr12:9603400-9606400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin

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