Variant report

Variant rs3845516
Chromosome Location chr1:246329014-246329015
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246314200-246369000 Weak transcription Aorta Aorta
2 chr1:246317600-246329200 Weak transcription Esophagus oesophagus
3 chr1:246321600-246344000 Weak transcription Primary hematopoietic stem cells blood
4 chr1:246323000-246329600 Weak transcription Pancreas Pancrea
5 chr1:246325600-246329800 Weak transcription Osteobl bone
6 chr1:246325600-246342000 Weak transcription Primary T cells from cord blood blood
7 chr1:246326000-246329200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr1:246326200-246339600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:246327200-246340200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
10 chr1:246327400-246329600 Weak transcription Fetal Heart heart
11 chr1:246327400-246332200 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
12 chr1:246327600-246341600 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr1:246327800-246330400 Enhancers H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
14 chr1:246328200-246329600 Enhancers K562 blood
15 chr1:246328600-246330000 Enhancers Placenta Amnion Placenta Amnion
16 chr1:246328800-246329400 Enhancers NHEK skin
17 chr1:246328800-246329600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr1:246329000-246341800 Weak transcription Monocytes-CD14+_RO01746 blood

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