Variant report

Variant rs60957338
Chromosome Location chr1:246546617-246546618
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:246514400-246554200 Weak transcription Primary T cells from cord blood blood
2 chr1:246520600-246563800 Weak transcription Osteobl bone
3 chr1:246538000-246547200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
4 chr1:246545800-246561000 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
5 chr1:246546000-246547400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
6 chr1:246546000-246547400 Enhancers HMEC breast
7 chr1:246546200-246546800 Enhancers H1 Cell Line embryonic stem cell
8 chr1:246546200-246547200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
9 chr1:246546200-246547600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
10 chr1:246546400-246546800 Enhancers iPS-15b Cell Line embryonic stem cell
11 chr1:246546400-246547000 Enhancers Fetal Lung lung
12 chr1:246546400-246547000 Enhancers NH-A brain
13 chr1:246546400-246547200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
14 chr1:246546400-246547600 Enhancers HUVEC blood vessel
15 chr1:246546400-246547600 Enhancers NHEK skin
16 chr1:246546600-246547000 Enhancers A549 lung
17 chr1:246546600-246547200 Enhancers HepG2 liver
18 chr1:246546600-246561400 Weak transcription Ovary ovary

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