Variant report

Variant rs35035962
Chromosome Location chr1:175006195-175006196
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:174993200-175013800 Weak transcription Spleen Spleen
2 chr1:174999400-175006400 Weak transcription Primary monocytes fromperipheralblood blood
3 chr1:175004800-175006200 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
4 chr1:175005000-175006200 Enhancers ES-I3 Cell Line embryonic stem cell
5 chr1:175005000-175006200 Enhancers HUES48 Cell Line embryonic stem cell
6 chr1:175005000-175006400 Enhancers HUES6 Cell Line embryonic stem cell
7 chr1:175005200-175006400 Enhancers HUES64 Cell Line embryonic stem cell
8 chr1:175005200-175006600 Enhancers iPS-15b Cell Line embryonic stem cell
9 chr1:175005200-175010000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:175005400-175006400 Enhancers ES-WA7 Cell Line embryonic stem cell
11 chr1:175005400-175006400 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:175005800-175006400 Enhancers iPS-20b Cell Line embryonic stem cell
13 chr1:175006000-175006200 Enhancers iPS DF 6.9 Cell Line embryonic stem cell

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