Variant report

Variant	rs61477394
Chromosome Location	chr1:226990500-226990501
allele	A/G
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	chr1:226987200-227001400	Weak transcription	Right Atrium	heart
2	chr1:226987400-226991400	Weak transcription	Lung	lung
3	chr1:226987400-226992000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr1:226987400-226997400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:226988600-226990800	Weak transcription	Thymus	Thymus
6	chr1:226988600-226992800	Weak transcription	Primary T cells fromperipheralblood	blood
7	chr1:226989400-227002800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
8	chr1:226989600-226994200	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr1:226989800-226991400	Weak transcription	K562	blood
10	chr1:226990000-226992600	Weak transcription	Primary T cells from cord blood	blood
11	chr1:226990000-226995000	Enhancers	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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