Variant report

Variant rs10799460
Chromosome Location chr1:224257059-224257060
allele A/C
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224250600-224257800 Enhancers Rectal Mucosa Donor 31 rectum
2 chr1:224252600-224258000 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
3 chr1:224253800-224260400 Weak transcription Pancreas Pancrea
4 chr1:224255200-224259600 Enhancers K562 blood
5 chr1:224255400-224257800 Enhancers Fetal Adrenal Gland Adrenal Gland
6 chr1:224255800-224258000 Enhancers Stomach Mucosa stomach
7 chr1:224256000-224257200 Enhancers Fetal Intestine Large intestine
8 chr1:224256000-224257200 Enhancers Fetal Intestine Small intestine
9 chr1:224256200-224257200 Enhancers HepG2 liver
10 chr1:224256200-224267800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
11 chr1:224256400-224261400 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
12 chr1:224256600-224258200 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
13 chr1:224256800-224258200 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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