Variant report

Variant	rs4712818
Chromosome Location	chr6:24308896-24308897
allele	A/G
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]
rs10806987	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1087289	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10946689	1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs10946690	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12055879	0.80[AFR][1000 genomes]
rs1340695	0.88[ASN][1000 genomes]
rs2185599	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2296539	0.80[AFR][1000 genomes]
rs3846829	0.85[ASN][1000 genomes]
rs3846831	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3846832	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3857542	0.90[ASN][1000 genomes]
rs3895346	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4712817	0.80[AFR][1000 genomes]
rs7752761	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7770593	0.91[ASN][1000 genomes]
rs793836	0.81[AMR][1000 genomes]
rs9295619	0.81[EUR][1000 genomes]
rs9393540	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:24294600-24312000	Weak transcription	Fetal Intestine Small	intestine
2	chr6:24303000-24310000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:24308000-24309200	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr6:24308400-24313600	Weak transcription	Fetal Kidney	kidney
5	chr6:24308400-24313800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:24308600-24309400	Enhancers	HepG2	liver
7	chr6:24308600-24309800	Weak transcription	A549	lung
8	chr6:24308600-24311000	Weak transcription	HUES64 Cell Line	embryonic stem cell
9	chr6:24308600-24311200	Weak transcription	HSMMtube	muscle
10	chr6:24308600-24311800	Weak transcription	HUES6 Cell Line	embryonic stem cell

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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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