Variant report

Variant rs577683822
Chromosome Location chr12:9606304-9606305
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr12:9601800-9606800 Weak transcription Fetal Adrenal Gland Adrenal Gland
2 chr12:9602000-9606800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
3 chr12:9602200-9606600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
4 chr12:9602200-9606800 Weak transcription Fetal Heart heart
5 chr12:9602200-9608000 Weak transcription HUVEC blood vessel
6 chr12:9602400-9606400 Weak transcription NHEK skin
7 chr12:9602400-9606600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
8 chr12:9602400-9606600 Weak transcription K562 blood
9 chr12:9603400-9606400 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
10 chr12:9603800-9606600 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
11 chr12:9604000-9606600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
12 chr12:9606200-9607400 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin

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