Variant report

Variant rs7528902
Chromosome Location chr1:209869121-209869122
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:209863200-209869600 Weak transcription Fetal Heart heart
2 chr1:209863200-209870000 Weak transcription Fetal Adrenal Gland Adrenal Gland
3 chr1:209866200-209872200 Weak transcription Thymus Thymus
4 chr1:209866400-209869200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
5 chr1:209866400-209869200 Weak transcription NHEK skin
6 chr1:209866400-209870800 Weak transcription Stomach Mucosa stomach
7 chr1:209866600-209870000 Weak transcription Brain Cingulate Gyrus brain
8 chr1:209866800-209870000 Weak transcription HMEC breast
9 chr1:209866800-209870400 Weak transcription Primary T helper memory cells from peripheral blood 2 blood
10 chr1:209866800-209870600 Weak transcription Primary T helper cells PMA-I stimulated --
11 chr1:209867000-209870000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr1:209867000-209875400 Weak transcription Brain Anterior Caudate brain
13 chr1:209867200-209869200 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin

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