Variant report

Variant	rs7937268
Chromosome Location	chr11:83841831-83841832
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs11824023	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55929556	0.89[AFR][1000 genomes]
rs57093812	1.00[AMR][1000 genomes]
rs57208469	0.96[AFR][1000 genomes]
rs60861772	1.00[AMR][1000 genomes]
rs61021804	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1039924	chr11:83662904-83993497	Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv541102	chr11:83662904-83993497	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv898029	chr11:83717887-83939591	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv1051279	chr11:83818647-83872815	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv555609	chr11:83822181-83842498	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a
6	esv2760422	chr11:83828680-83845579	Weak transcription Enhancers	n/a	n/a	inside rSNPs	diseases
7	nsv516717	chr11:83831259-83842498	Enhancers Weak transcription	n/a	n/a	inside rSNPs	n/a
8	nsv555610	chr11:83831922-83842498	Weak transcription Enhancers	n/a	n/a	inside rSNPs	n/a

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:83835400-83842000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr11:83840400-83845000	Weak transcription	Brain Hippocampus Middle	brain
3	chr11:83840600-83842000	Weak transcription	Brain Angular Gyrus	brain
4	chr11:83840800-83842000	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr11:83840800-83847800	Weak transcription	Brain Anterior Caudate	brain
6	chr11:83841400-83845200	Weak transcription	Fetal Heart	heart
7	chr11:83841800-83842600	Enhancers	Brain Substantia Nigra	brain

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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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