Variant report

Variant rs2836568
Chromosome Location chr21:39977435-39977436
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr21:39973000-39982000 Weak transcription Breast Myoepithelial Primary Cells Breast
2 chr21:39975400-39977600 Enhancers HUES48 Cell Line embryonic stem cell
3 chr21:39976400-39977800 Enhancers iPS-20b Cell Line embryonic stem cell
4 chr21:39976600-39977600 Enhancers iPS-15b Cell Line embryonic stem cell
5 chr21:39976600-39977800 Enhancers H1 Cell Line embryonic stem cell
6 chr21:39976600-39977800 Enhancers H9 Cell Line embryonic stem cell
7 chr21:39976600-39977800 Enhancers Foreskin Melanocyte Primary Cells skin01 Skin
8 chr21:39976600-39978000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
9 chr21:39976800-39977800 Enhancers iPS-18 Cell Line embryonic stem cell
10 chr21:39977000-39977800 Enhancers HUES64 Cell Line embryonic stem cell
11 chr21:39977200-39977600 Enhancers ES-WA7 Cell Line embryonic stem cell
12 chr21:39977200-39977600 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr21:39977200-39977600 Active TSS Aorta Aorta
14 chr21:39977200-39977600 Enhancers Fetal Brain Male brain
15 chr21:39977200-39978000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
16 chr21:39977400-39977800 Enhancers HUES6 Cell Line embryonic stem cell

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