Variant report

Variant rs3014224
Chromosome Location chr1:46002358-46002359
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:45992800-46002400 Weak transcription Fetal Intestine Small intestine
2 chr1:45999200-46004600 Weak transcription Monocytes-CD14+_RO01746 blood
3 chr1:45999600-46003000 Enhancers Liver Liver
4 chr1:45999800-46006400 Weak transcription Primary monocytes fromperipheralblood blood
5 chr1:46000800-46016000 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
6 chr1:46001200-46003400 Enhancers HepG2 liver
7 chr1:46001600-46002600 Enhancers NHEK skin
8 chr1:46001600-46003200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr1:46001600-46003400 Enhancers K562 blood
10 chr1:46001800-46002400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:46001800-46002400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr1:46001800-46002400 Enhancers HMEC breast
13 chr1:46001800-46002600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
14 chr1:46001800-46003000 Enhancers Hela-S3 cervix
15 chr1:46002000-46003200 Enhancers ES-I3 Cell Line embryonic stem cell

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