Variant report

Variant	rs2537936
Chromosome Location	chr4:18963957-18963958
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 87 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:74)

rs_ID	r²[population]
rs10014091	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10020388	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10024481	0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1349668	0.97[EUR][1000 genomes]
rs1349669	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1349670	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1377155	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452558	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1452560	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452561	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452562	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452566	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452567	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452568	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452569	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1452570	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1452571	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs185936	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1901618	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1993179	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs207278	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs207279	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs207369	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs207370	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs207372	0.90[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs207373	0.80[EUR][1000 genomes]
rs207374	0.80[EUR][1000 genomes]
rs207375	0.93[AMR][1000 genomes];0.80[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs207376	0.80[EUR][1000 genomes]
rs207378	0.80[EUR][1000 genomes]
rs207379	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs207380	0.80[EUR][1000 genomes]
rs207381	0.80[EUR][1000 genomes]
rs207382	0.80[EUR][1000 genomes]
rs207383	0.85[EUR][1000 genomes]
rs207384	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs207385	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs207400	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2123315	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2123316	0.97[EUR][1000 genomes]
rs2123319	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2123320	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2123321	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2256795	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2537918	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2537919	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537924	0.97[EUR][1000 genomes]
rs2537929	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537930	0.97[EUR][1000 genomes]
rs2537931	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537932	0.97[EUR][1000 genomes]
rs2537933	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537934	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537935	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537937	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537938	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537939	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537942	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537943	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2537945	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2537946	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601562	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601563	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601574	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601575	0.97[EUR][1000 genomes]
rs2601576	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601580	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601581	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601582	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2601583	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601586	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601592	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2601595	0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs28625252	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533087	chr4:18362040-19176896	Enhancers Bivalent Enhancer ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv532708	chr4:18596861-19176896	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv878723	chr4:18668957-19005988	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Active TSS	Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
4	nsv1000054	chr4:18839588-19271261	Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv537051	chr4:18839588-19271261	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1008625	chr4:18880048-19148705	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv1010560	chr4:18892570-18968334	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv1000563	chr4:18924475-19246818	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1006775	chr4:18932671-18988369	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv1003321	chr4:18936051-19117825	Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	nsv1006650	chr4:18941726-18968334	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv999100	chr4:18941726-18975268	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv432583	chr4:18944656-18971291	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:18962800-18964400	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:18963000-18964400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:18963000-18964400	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr4:18963200-18964400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:18963600-18964400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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