Variant report

Variant	rs74120707
Chromosome Location	chr1:165496387-165496388
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs57131010	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58101983	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120705	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120708	1.00[AMR][1000 genomes]
rs74120732	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120733	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120736	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120737	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120738	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120739	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120740	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120742	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120743	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120744	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120746	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120747	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120748	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs74120749	1.00[AMR][1000 genomes]
rs74120751	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165493200-165496600	Enhancers	HepG2	liver
2	chr1:165494800-165496400	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chr1:165495000-165496400	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr1:165495200-165496600	Weak transcription	Fetal Muscle Leg	muscle
5	chr1:165496000-165496400	Enhancers	H9 Cell Line	embryonic stem cell
6	chr1:165496000-165496800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr1:165496000-165497000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr1:165496000-165497400	Flanking Active TSS	Fetal Heart	heart
9	chr1:165496200-165496400	Flanking Active TSS	Right Ventricle	heart
10	chr1:165496200-165496400	Enhancers	K562	blood
11	chr1:165496200-165497000	Enhancers	Left Ventricle	heart

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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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