Variant report

Variant	rs28380048
Chromosome Location	chr4:99611535-99611536
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:99604400-99612800	Weak transcription	Fetal Heart	heart
2	chr4:99608400-99611600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
3	chr4:99608400-99611600	Enhancers	Dnd41	blood
4	chr4:99608800-99611600	Enhancers	Primary T helper cells fromperipheralblood	blood
5	chr4:99610200-99611600	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr4:99610400-99613800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr4:99610600-99611600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr4:99610600-99611800	Enhancers	HUVEC	blood vessel
9	chr4:99610800-99612000	Enhancers	Spleen	Spleen
10	chr4:99611200-99613200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr4:99611200-99615000	Weak transcription	Fetal Thymus	thymus

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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