Variant report

Variant	rs12403889
Chromosome Location	chr1:76327428-76327429
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:76327097..76328864-chr1:76332786..76334905,2	K562	blood:

Extended variants
information (count: 95 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:86)

rs_ID	r²[population]
rs10873724	0.90[ASN][1000 genomes]
rs10873727	0.92[ASN][1000 genomes]
rs10873728	0.92[ASN][1000 genomes]
rs10873735	0.83[ASN][1000 genomes]
rs10873738	0.92[ASN][1000 genomes]
rs10873739	0.92[ASN][1000 genomes]
rs11161600	0.81[ASN][1000 genomes]
rs11161700	0.92[ASN][1000 genomes]
rs11161704	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11161790	0.90[ASN][1000 genomes]
rs11161795	0.90[ASN][1000 genomes]
rs1144328	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1144331	0.96[ASN][1000 genomes]
rs1144333	0.96[ASN][1000 genomes]
rs1144337	0.96[ASN][1000 genomes]
rs1144338	0.92[ASN][1000 genomes]
rs1144339	0.96[ASN][1000 genomes]
rs1144341	0.96[ASN][1000 genomes]
rs1144342	0.96[ASN][1000 genomes]
rs1146572	0.80[ASN][1000 genomes]
rs1146592	0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1146593	0.92[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1146602	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1146613	0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1146616	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1146625	0.86[ASN][1000 genomes]
rs1146645	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1146647	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1146648	0.91[ASN][1000 genomes]
rs1146649	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1146651	0.96[ASN][1000 genomes]
rs1146652	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1146656	0.92[ASN][1000 genomes]
rs11579355	0.91[ASN][1000 genomes]
rs12021750	0.82[ASN][1000 genomes]
rs12024086	0.90[ASN][1000 genomes]
rs12031600	0.80[ASN][1000 genomes]
rs12049212	0.80[ASN][1000 genomes]
rs12076093	0.92[ASN][1000 genomes]
rs12078151	0.92[ASN][1000 genomes]
rs12081710	0.92[ASN][1000 genomes]
rs12090712	0.92[ASN][1000 genomes]
rs12385715	0.92[ASN][1000 genomes]
rs12401729	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12405178	0.92[ASN][1000 genomes]
rs1250875	0.80[ASN][1000 genomes]
rs1250877	0.80[ASN][1000 genomes]
rs1250878	0.84[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1250881	0.87[ASN][1000 genomes]
rs1250882	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1251065	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1251270	1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1251272	0.92[ASN][1000 genomes]
rs1251273	0.96[ASN][1000 genomes]
rs1251274	0.96[ASN][1000 genomes]
rs1251275	0.92[ASN][1000 genomes]
rs12703	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs12728962	0.81[ASN][1000 genomes]
rs12756349	0.81[ASN][1000 genomes]
rs12757213	0.80[ASN][1000 genomes]
rs1631498	0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17097681	0.84[EUR][1000 genomes]
rs1767459	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1770513	0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1812589	0.90[ASN][1000 genomes]
rs2012536	0.95[ASN][1000 genomes]
rs34045364	0.91[ASN][1000 genomes]
rs34177389	0.91[ASN][1000 genomes]
rs35290302	0.80[ASN][1000 genomes]
rs35591768	0.91[ASN][1000 genomes]
rs36054685	0.95[ASN][1000 genomes]
rs3765682	0.86[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4949884	0.92[ASN][1000 genomes]
rs5019550	0.92[ASN][1000 genomes]
rs56350137	0.92[ASN][1000 genomes]
rs5745327	0.95[ASN][1000 genomes]
rs5745343	0.96[ASN][1000 genomes]
rs5745353	0.82[ASN][1000 genomes]
rs5745354	0.96[ASN][1000 genomes]
rs5745392	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs5745429	0.80[ASN][1000 genomes]
rs61676733	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs699683	0.81[ASN][1000 genomes]
rs7514912	0.91[ASN][1000 genomes]
rs7548391	0.91[ASN][1000 genomes]
rs815309	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519329	chr1:75830438-76358591	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1014072	chr1:76200531-76460726	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	nsv535005	chr1:76200531-76460726	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
4	esv1795237	chr1:76268573-76383565	Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv1800125	chr1:76269439-76379497	Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	esv1799260	chr1:76269439-76383297	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	esv1847721	chr1:76269439-76383565	Weak transcription ZNF genes & repeats Enhancers Strong transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
8	nsv1004669	chr1:76301198-76409451	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv871671	chr1:76304215-76391646	Enhancers Active TSS Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:76327200-76327800	Enhancers	ES-I3 Cell Line	embryonic stem cell
2	chr1:76327400-76327800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr1:76327400-76327800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr1:76327400-76328000	Enhancers	H1 Cell Line	embryonic stem cell
5	chr1:76327400-76328000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr1:76327400-76328000	Strong transcription	Aorta	Aorta

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