Variant report

Variant	rs71591558
Chromosome Location	chr4:120238918-120238919
allele	AAATTACA/CAATTATG
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10003567	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10005237	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10023641	0.82[AFR][1000 genomes]
rs10024933	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10212714	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10212719	0.84[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs10212775	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10213158	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10213267	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10518300	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11098501	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11098502	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11724409	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs11732087	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11732686	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12498994	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12506610	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12507565	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12509621	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12510269	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12511640	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12513083	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs12711071	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13108589	0.83[EUR][1000 genomes]
rs1511017	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1511025	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1546503	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1546506	0.90[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs17049949	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs17595608	0.87[EUR][1000 genomes]
rs1814814	0.85[AFR][1000 genomes]
rs1980024	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1980025	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1980026	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs1980027	0.87[EUR][1000 genomes]
rs2002047	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2002049	0.86[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs2036856	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2036857	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2036860	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28363929	0.84[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs28369503	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs28373117	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs28502463	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs28643450	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs28652763	0.90[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs28713555	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs2964	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs34425882	0.83[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs34685788	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs3864141	0.83[EUR][1000 genomes]
rs4107728	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs4422403	0.81[AFR][1000 genomes]
rs4443261	0.86[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4472123	0.87[EUR][1000 genomes]
rs66900435	0.87[EUR][1000 genomes]
rs714899	0.88[EUR][1000 genomes]
rs72676046	0.85[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7671978	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs7672129	0.88[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7672372	0.83[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs7672594	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7672778	0.88[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7673476	0.86[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs7689729	0.85[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs878372	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs878376	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs907204	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs907205	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs938056	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs9991166	0.92[AFR][1000 genomes];0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9991959	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs9993347	0.87[EUR][1000 genomes]
rs9996494	0.92[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9996644	0.91[AFR][1000 genomes];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9999724	0.87[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916641	chr4:119780023-120777320	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv1012868	chr4:120014630-120464880	Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
3	nsv537232	chr4:120014630-120464880	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
4	nsv428769	chr4:120205572-120363323	Strong transcription Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
5	nsv879840	chr4:120227419-120257417	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120222000-120251000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr4:120222200-120244600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr4:120222400-120240800	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr4:120222800-120240800	Weak transcription	Rectal Mucosa Donor 31	rectum
5	chr4:120235000-120239400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr4:120235600-120251000	Weak transcription	Left Ventricle	heart
7	chr4:120235800-120241800	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chr4:120238000-120239000	Weak transcription	NHDF-Ad	bronchial
9	chr4:120238400-120239200	Strong transcription	Duodenum Mucosa	Duodenum
10	chr4:120238600-120239000	Genic enhancers	Fetal Intestine Large	intestine
11	chr4:120238800-120239000	Enhancers	Fetal Intestine Small	intestine
12	chr4:120238800-120240000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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