Variant report

Variant	rs7935594
Chromosome Location	chr11:26736172-26736173
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs16916148	0.91[YRI][hapmap]
rs16916156	1.00[YRI][hapmap];0.80[AFR][1000 genomes]
rs17243650	0.91[YRI][hapmap]
rs4370890	0.91[YRI][hapmap]
rs60517765	0.92[AFR][1000 genomes]
rs61283127	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs6484246	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7112383	0.89[AMR][1000 genomes]
rs7128606	0.89[AMR][1000 genomes]
rs7130359	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]
rs7925046	0.91[YRI][hapmap]
rs7926762	1.00[AMR][1000 genomes]
rs7937138	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044544	chr11:26506962-26967285	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:26721200-26741200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr11:26731600-26736400	Weak transcription	Fetal Heart	heart
3	chr11:26732200-26736600	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr11:26734200-26736600	Weak transcription	Duodenum Mucosa	Duodenum
5	chr11:26734200-26738000	Enhancers	Fetal Intestine Small	intestine
6	chr11:26734400-26736800	Weak transcription	Fetal Lung	lung
7	chr11:26735200-26736200	Weak transcription	Fetal Intestine Large	intestine

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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