Variant report

Variant rs61825421
Chromosome Location chr1:224137928-224137929
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:224135800-224149800 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
2 chr1:224136200-224139400 Weak transcription Fetal Intestine Small intestine
3 chr1:224136400-224179800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
4 chr1:224136600-224149200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:224137200-224138600 Weak transcription Fetal Stomach stomach
6 chr1:224137600-224139200 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin
7 chr1:224137800-224139400 Weak transcription Adipose Nuclei Adipose
8 chr1:224137800-224139400 Weak transcription Fetal Adrenal Gland Adrenal Gland
9 chr1:224137800-224139400 Weak transcription Fetal Muscle Trunk muscle
10 chr1:224137800-224139400 Weak transcription Placenta Placenta
11 chr1:224137800-224139400 Weak transcription Skeletal Muscle Female skeletal muscle
12 chr1:224137800-224139400 Weak transcription Spleen Spleen
13 chr1:224137800-224160600 Weak transcription Brain Inferior Temporal Lobe brain

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