Variant report

Variant	rs28758224
Chromosome Location	chr2:127705284-127705285
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10168813	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10803617	0.90[ASN][1000 genomes]
rs10803618	0.96[ASN][1000 genomes]
rs11884053	0.95[EUR][1000 genomes]
rs11885353	0.95[EUR][1000 genomes]
rs11888349	0.95[EUR][1000 genomes]
rs11889584	0.95[EUR][1000 genomes]
rs11889712	0.95[EUR][1000 genomes]
rs11896939	0.98[EUR][1000 genomes]
rs11898260	0.98[EUR][1000 genomes]
rs12053575	0.96[ASN][1000 genomes]
rs12620265	0.84[ASN][1000 genomes]
rs12692123	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12997058	0.95[EUR][1000 genomes]
rs12999757	0.98[EUR][1000 genomes]
rs13010652	0.95[EUR][1000 genomes]
rs13012357	0.98[EUR][1000 genomes]
rs13013476	0.95[EUR][1000 genomes]
rs13016474	0.95[EUR][1000 genomes]
rs13024324	0.95[EUR][1000 genomes]
rs13025747	0.95[EUR][1000 genomes]
rs13026367	0.98[EUR][1000 genomes]
rs13026415	0.95[EUR][1000 genomes]
rs13026430	0.95[EUR][1000 genomes]
rs13032401	0.94[EUR][1000 genomes]
rs1510528	0.95[EUR][1000 genomes]
rs1553844	0.88[ASN][1000 genomes]
rs1553845	0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs17014691	0.98[EUR][1000 genomes]
rs17014698	0.98[EUR][1000 genomes]
rs1848902	0.95[EUR][1000 genomes]
rs1848903	0.95[EUR][1000 genomes]
rs1848904	0.95[EUR][1000 genomes]
rs1912498	0.90[ASN][1000 genomes]
rs34018781	0.95[EUR][1000 genomes]
rs34109617	0.94[EUR][1000 genomes]
rs34234549	0.92[EUR][1000 genomes]
rs34358238	0.95[EUR][1000 genomes]
rs34643552	0.95[EUR][1000 genomes]
rs34859030	0.98[EUR][1000 genomes]
rs34986734	0.95[EUR][1000 genomes]
rs35025489	0.93[EUR][1000 genomes]
rs35311329	0.95[EUR][1000 genomes]
rs35386494	0.95[EUR][1000 genomes]
rs35520257	0.95[EUR][1000 genomes]
rs35523788	0.98[EUR][1000 genomes]
rs35620035	0.95[EUR][1000 genomes]
rs4662692	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4662695	0.96[ASN][1000 genomes]
rs4662696	0.96[ASN][1000 genomes]
rs4662697	0.85[ASN][1000 genomes]
rs4662698	0.84[ASN][1000 genomes]
rs4662699	0.84[ASN][1000 genomes]
rs4663070	0.92[ASN][1000 genomes]
rs4663075	0.96[ASN][1000 genomes]
rs4663076	0.96[ASN][1000 genomes]
rs4663077	0.96[ASN][1000 genomes]
rs4663079	0.96[ASN][1000 genomes]
rs4663080	0.96[ASN][1000 genomes]
rs4663081	0.96[ASN][1000 genomes]
rs4663082	0.96[ASN][1000 genomes]
rs4663083	0.96[ASN][1000 genomes]
rs55962144	0.88[ASN][1000 genomes]
rs59366032	0.95[EUR][1000 genomes]
rs6431201	0.92[ASN][1000 genomes]
rs6431206	0.90[ASN][1000 genomes]
rs6431207	0.90[ASN][1000 genomes]
rs6431208	0.90[ASN][1000 genomes]
rs6431209	0.96[ASN][1000 genomes]
rs6431210	0.96[ASN][1000 genomes]
rs6431211	0.90[ASN][1000 genomes]
rs6431212	0.90[ASN][1000 genomes]
rs66792832	0.98[EUR][1000 genomes]
rs6732056	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6736826	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6749935	0.96[ASN][1000 genomes]
rs6753685	0.92[ASN][1000 genomes]
rs67640318	0.98[EUR][1000 genomes]
rs72976756	0.88[ASN][1000 genomes]
rs73952788	0.82[ASN][1000 genomes]
rs73952789	0.84[ASN][1000 genomes]
rs7419804	0.96[ASN][1000 genomes]
rs7420039	0.94[ASN][1000 genomes]
rs7423317	0.96[ASN][1000 genomes]
rs7424763	0.90[ASN][1000 genomes]
rs7556956	0.96[ASN][1000 genomes]
rs7557069	0.96[ASN][1000 genomes]
rs7565248	0.94[ASN][1000 genomes]
rs7586551	0.98[EUR][1000 genomes]
rs7590060	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7600840	0.98[EUR][1000 genomes]
rs870468	0.88[ASN][1000 genomes]
rs9967839	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002265	chr2:127029745-127733458	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv535919	chr2:127029745-127733458	Strong transcription Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv999422	chr2:127464647-127956543	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv1004930	chr2:127477369-127938234	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv834365	chr2:127616996-127793863	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv834366	chr2:127633714-127784692	Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	esv1797936	chr2:127653376-127717477	Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv1800233	chr2:127653376-127717477	Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	esv1823816	chr2:127653376-127717477	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	esv1828473	chr2:127653376-127717477	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv1830542	chr2:127653376-127717477	Enhancers Strong transcription Bivalent Enhancer Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	esv1837532	chr2:127653376-127717477	Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv1838997	chr2:127653376-127717477	Bivalent Enhancer Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv1843412	chr2:127653376-127717477	Bivalent Enhancer Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	esv1846050	chr2:127653376-127717477	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv2907	chr2:127669532-127709321	Weak transcription Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:127701800-127706000	Enhancers	Fetal Kidney	kidney
2	chr2:127702800-127705800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr2:127703000-127705600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr2:127704800-127705800	Enhancers	H9 Cell Line	embryonic stem cell
5	chr2:127704800-127706000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr2:127704800-127706000	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr2:127704800-127706200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
8	chr2:127704800-127706400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:127705000-127705800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
10	chr2:127705000-127706200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
11	chr2:127705000-127706400	Weak transcription	Fetal Muscle Leg	muscle

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