Variant report

Variant rs1038566
Chromosome Location chr2:173060756-173060757
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:173059400-173061000 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
2 chr2:173060200-173061000 Enhancers Hela-S3 cervix
3 chr2:173060200-173061000 Enhancers HMEC breast
4 chr2:173060200-173061400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr2:173060200-173061400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr2:173060200-173061800 Enhancers Breast Myoepithelial Primary Cells Breast
7 chr2:173060200-173061800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:173060400-173061200 Enhancers Rectal Mucosa Donor 29 rectum
9 chr2:173060400-173062400 Enhancers Stomach Mucosa stomach
10 chr2:173060600-173060800 Enhancers Monocytes-CD14+_RO01746 blood
11 chr2:173060600-173061000 ZNF genes & repeats Foreskin Melanocyte Primary Cells skin01 Skin
12 chr2:173060600-173061600 Flanking Active TSS NHEK skin
13 chr2:173060600-173062000 Enhancers Thymus Thymus
14 chr2:173060600-173063800 Enhancers Placenta Amnion Placenta Amnion
15 chr2:173060600-173064400 Enhancers Primary monocytes fromperipheralblood blood
16 chr2:173060600-173064400 Enhancers Fetal Thymus thymus

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