Variant report

Variant	rs7854021
Chromosome Location	chr9:71058161-71058162
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:18)

rs_ID	r²[population]
rs10125634	1.00[CEU][hapmap]
rs1389032	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1532235	1.00[CEU][hapmap]
rs61145814	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6560131	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7027250	1.00[CEU][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7028925	1.00[CEU][hapmap]
rs7038754	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7040997	0.94[AFR][1000 genomes]
rs7045327	1.00[CEU][hapmap]
rs72714328	0.86[AFR][1000 genomes]
rs7848245	1.00[CEU][hapmap]
rs7854624	0.91[AFR][1000 genomes]
rs7854926	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7862924	1.00[CEU][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7867443	1.00[CEU][hapmap]
rs7868457	0.97[AFR][1000 genomes]
rs984109	0.88[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv427847	chr9:70318730-71153527	Weak transcription Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:71045600-71061400	Weak transcription	NHLF	lung
2	chr9:71051200-71062000	Weak transcription	Left Ventricle	heart
3	chr9:71051200-71091800	Weak transcription	Psoas Muscle	Psoas
4	chr9:71051600-71066600	Weak transcription	Right Ventricle	heart
5	chr9:71053000-71058200	Weak transcription	Fetal Stomach	stomach
6	chr9:71053000-71058200	Weak transcription	Stomach Smooth Muscle	stomach
7	chr9:71053000-71061400	Weak transcription	Fetal Heart	heart
8	chr9:71053800-71058200	Weak transcription	Rectal Smooth Muscle	rectum
9	chr9:71057800-71060000	Enhancers	Fetal Lung	lung
10	chr9:71058000-71062000	Enhancers	Colon Smooth Muscle	Colon

Quick Search:

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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