Variant report

Variant	rs7556650
Chromosome Location	chr1:71490362-71490363
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:71484257..71486555-chr1:71489083..71490597,2	MCF-7	breast:
2	chr1:71128661..71130608-chr1:71489552..71491952,2	K562	blood:
3	chr1:71488605..71491550-chr1:71545533..71547496,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTH-13	chr1:71489933-71490390	NONHSAT003876

Variant related genes	Relation type
ENSG00000132485	Chromatin interaction
ENSG00000229956	Chromatin interaction

Extended variants
information (count: 65 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1022527	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1022529	0.94[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10399632	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs10399704	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10399705	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10399706	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10399797	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10399806	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs10749799	0.81[AMR][1000 genomes]
rs10789316	0.81[AMR][1000 genomes]
rs11209733	0.81[AMR][1000 genomes]
rs11209736	0.91[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11209739	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11209740	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11209743	0.83[AMR][1000 genomes]
rs12120041	0.92[AFR][1000 genomes];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12130153	0.81[AMR][1000 genomes]
rs12134962	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12139719	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12139935	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12739047	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12739685	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12756951	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs12757161	0.92[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1988080	0.81[AMR][1000 genomes]
rs2143157	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2179412	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2206345	0.82[AMR][1000 genomes]
rs2206346	0.83[AMR][1000 genomes]
rs2223502	0.83[AMR][1000 genomes]
rs2268056	0.83[AMR][1000 genomes]
rs2268058	0.83[AMR][1000 genomes]
rs2268059	0.80[AMR][1000 genomes]
rs2268060	0.83[AMR][1000 genomes]
rs2268061	0.83[AMR][1000 genomes]
rs2268062	0.83[AMR][1000 genomes]
rs2300169	0.83[AMR][1000 genomes]
rs2300170	0.81[AMR][1000 genomes]
rs2300171	0.81[AMR][1000 genomes]
rs2300175	0.81[AMR][1000 genomes]
rs2300178	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2817864	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2901523	0.93[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs33936437	0.81[AMR][1000 genomes]
rs3765892	0.81[AMR][1000 genomes]
rs3765894	0.81[AMR][1000 genomes]
rs4361943	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4425937	0.87[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4437828	0.83[AMR][1000 genomes]
rs4439319	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4511057	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs4549988	0.89[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs5682	0.81[AMR][1000 genomes]
rs7525785	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs8179367	0.92[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs8179390	0.83[AMR][1000 genomes]
rs8179408	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs997997	0.81[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1845198	chr1:71274759-71514969	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
2	nsv546472	chr1:71432984-71541003	Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	555 gene(s)	inside rSNPs	diseases
3	nsv461851	chr1:71442626-71507541	Enhancers Genic enhancers Strong transcription Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
4	nsv546473	chr1:71442626-71507541	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	n/a
5	esv1850593	chr1:71444149-71514969	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Bivalent Enhancer Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv871242	chr1:71481050-71519326	Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv871147	chr1:71484567-71494365	Enhancers Weak transcription Active TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7556650	PTGER3	cis	Skin Sun Exposed Lower leg	GTEx

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:71481800-71501000	Weak transcription	K562	blood
2	chr1:71483800-71491400	Weak transcription	Aorta	Aorta
3	chr1:71485800-71494000	Weak transcription	Adipose Nuclei	Adipose
4	chr1:71487000-71491200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr1:71487200-71495200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:71489600-71493800	Weak transcription	NHDF-Ad	bronchial

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