Variant report

Variant rs10863811
Chromosome Location chr1:210297597-210297598
allele A/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:210283000-210298000 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
2 chr1:210295600-210298600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
3 chr1:210295800-210298000 Enhancers HUES64 Cell Line embryonic stem cell
4 chr1:210296200-210299800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
5 chr1:210296600-210298000 Enhancers HMEC breast
6 chr1:210296600-210298400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr1:210296600-210298800 Enhancers NH-A brain
8 chr1:210296600-210299400 Enhancers NHDF-Ad bronchial
9 chr1:210296800-210298000 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
10 chr1:210296800-210298200 Enhancers NHEK skin
11 chr1:210297000-210297600 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
12 chr1:210297200-210298000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr1:210297200-210298200 Enhancers Muscle Satellite Cultured Cells --
14 chr1:210297200-210298200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
15 chr1:210297200-210298200 Bivalent Enhancer HUVEC blood vessel
16 chr1:210297200-210298400 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
17 chr1:210297400-210298000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
18 chr1:210297400-210298000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
19 chr1:210297400-210298200 Enhancers iPS-15b Cell Line embryonic stem cell

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