Variant report

Variant rs10254886
Chromosome Location chr7:16968034-16968035
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:16961000-16973400 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
2 chr7:16963200-16972400 Weak transcription Primary T regulatory cells fromperipheralblood blood
3 chr7:16963200-16973600 Weak transcription Small Intestine intestine
4 chr7:16964800-16969600 ZNF genes & repeats H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr7:16965600-16970200 Enhancers Stomach Mucosa stomach
6 chr7:16966000-16968800 Weak transcription Fetal Thymus thymus
7 chr7:16966000-16968800 Weak transcription Thymus Thymus
8 chr7:16966400-16968800 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr7:16966600-16968400 Weak transcription Primary T cells from cord blood blood
10 chr7:16966600-16973200 Weak transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
11 chr7:16966800-16974800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
12 chr7:16967000-16968800 Weak transcription Sigmoid Colon Sigmoid Colon
13 chr7:16967200-16977600 Weak transcription Gastric stomach
14 chr7:16967600-16968200 Weak transcription A549 lung
15 chr7:16967600-16968800 Weak transcription Rectal Mucosa Donor 31 rectum
16 chr7:16967600-16974200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
17 chr7:16967800-16974200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
18 chr7:16968000-16974000 Weak transcription NHEK skin

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