Variant report

Variant	rs11733424
Chromosome Location	chr4:126300933-126300934
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10012726	1.00[AMR][1000 genomes]
rs10029125	1.00[AMR][1000 genomes]
rs11942648	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12711125	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1396700	1.00[AMR][1000 genomes]
rs1509288	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2055768	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2102461	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2457262	1.00[AMR][1000 genomes]
rs2663253	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2663258	1.00[AMR][1000 genomes]
rs2663262	1.00[AMR][1000 genomes]
rs2663284	1.00[AMR][1000 genomes]
rs2710537	1.00[AMR][1000 genomes]
rs2710565	1.00[AMR][1000 genomes]
rs2710577	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2710581	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2710585	1.00[AMR][1000 genomes]
rs2710586	1.00[AMR][1000 genomes]
rs2710588	1.00[AMR][1000 genomes]
rs28470542	1.00[AMR][1000 genomes]
rs28871071	1.00[AMR][1000 genomes]
rs4834029	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6844307	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906793	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs906794	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs925244	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1006068	chr4:126103233-126497467	Enhancers ZNF genes & repeats Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830051	chr4:126234895-126403426	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv470070	chr4:126299145-126408586	Flanking Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:126290400-126309200	Weak transcription	HSMM	muscle
2	chr4:126290600-126303400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr4:126290800-126317600	Weak transcription	Fetal Brain Male	brain
4	chr4:126291000-126304000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr4:126291400-126303600	Weak transcription	HUVEC	blood vessel
6	chr4:126291600-126305000	Weak transcription	Fetal Lung	lung
7	chr4:126296000-126311200	Weak transcription	Aorta	Aorta
8	chr4:126300800-126301000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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