Variant report

Variant	rs765861
Chromosome Location	chr1:47709201-47709202
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:47705200-47766400	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:47705600-47766400	Weak transcription	Primary T cells from cord blood	blood
3	chr1:47705800-47709400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr1:47705800-47714800	Weak transcription	Fetal Thymus	thymus
5	chr1:47706800-47709800	Enhancers	Spleen	Spleen
6	chr1:47707400-47709400	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr1:47707600-47716600	Weak transcription	Hela-S3	cervix
8	chr1:47707600-47722800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr1:47707800-47711400	Enhancers	K562	blood
10	chr1:47708000-47715200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr1:47708200-47709600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr1:47708200-47709600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:47709200-47709600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
14	chr1:47709200-47709600	Bivalent Enhancer	HepG2	liver
15	chr1:47709200-47710000	Enhancers	HUVEC	blood vessel

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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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