Variant report

Variant	rs61233819
Chromosome Location	chr9:101312054-101312055
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs10819042	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10986744	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12347864	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2225559	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs28458297	0.87[AFR][1000 genomes];0.83[AMR][1000 genomes]
rs28546491	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs35449008	0.95[EUR][1000 genomes]
rs4507885	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs57488751	0.90[EUR][1000 genomes]
rs61565750	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7044171	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7045028	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73655489	0.95[EUR][1000 genomes]
rs73655490	0.90[EUR][1000 genomes]
rs7857537	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7876036	1.00[AMR][1000 genomes];0.95[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv430085	chr9:100928245-101339645	Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv831665	chr9:101170061-101367692	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv614936	chr9:101182698-101680380	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	esv3481710	chr9:101307131-101313629	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
5	esv3497312	chr9:101307881-101312729	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
6	nsv511424	chr9:101308111-101313371	Bivalent Enhancer Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
7	esv3481704	chr9:101308156-101313004	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
8	esv3497318	chr9:101308263-101312125	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3497323	chr9:101308331-101312679	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
10	nsv6633	chr9:101308371-101342811	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
11	esv3481706	chr9:101308831-101312179	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
12	esv3497316	chr9:101308918-101312537	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
13	esv1816890	chr9:101309058-101313371	Enhancers Bivalent Enhancer Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
14	esv1819538	chr9:101309058-101313371	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
15	esv1837372	chr9:101309058-101313371	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
16	esv1839134	chr9:101309058-101313371	Weak transcription Bivalent Enhancer Enhancers	Chromatin interactive region	n/a	inside rSNPs	n/a
17	esv1841097	chr9:101309058-101317401	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:101311800-101312200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:101311800-101315400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr9:101311800-101316600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr9:101312000-101314000	Enhancers	NH-A	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
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