Variant report

Variant	rs35107776
Chromosome Location	chr4:33742386-33742387
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:33723604..33726474-chr4:33740549..33743079,2	K562	blood:
2	chr4:33741662..33743292-chr4:33747301..33749148,2	K562	blood:

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:94)

rs_ID	r²[population]
rs10011550	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10021740	0.89[ASN][1000 genomes]
rs10025016	0.89[ASN][1000 genomes]
rs10030710	0.89[ASN][1000 genomes]
rs10033461	0.89[ASN][1000 genomes]
rs10033782	0.96[ASN][1000 genomes]
rs10034901	0.89[ASN][1000 genomes]
rs10050065	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10470879	0.89[ASN][1000 genomes]
rs11945628	0.89[ASN][1000 genomes]
rs12640941	0.98[ASN][1000 genomes]
rs12642628	0.90[ASN][1000 genomes]
rs13110392	0.89[ASN][1000 genomes]
rs13111438	0.98[ASN][1000 genomes]
rs13112341	0.98[ASN][1000 genomes]
rs13113238	0.98[ASN][1000 genomes]
rs13131261	0.89[ASN][1000 genomes]
rs13136846	0.89[ASN][1000 genomes]
rs13137090	0.89[ASN][1000 genomes]
rs13139622	0.89[ASN][1000 genomes]
rs13142161	0.89[ASN][1000 genomes]
rs13142365	0.89[ASN][1000 genomes]
rs13147878	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13150067	0.89[ASN][1000 genomes]
rs1373494	0.98[ASN][1000 genomes]
rs1378039	0.89[ASN][1000 genomes]
rs1444377	0.89[ASN][1000 genomes]
rs1444378	0.89[ASN][1000 genomes]
rs1596581	0.89[ASN][1000 genomes]
rs16989167	0.89[ASN][1000 genomes]
rs16989187	0.89[ASN][1000 genomes]
rs16989190	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs16995875	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2120677	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2166108	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2166109	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2166110	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs2338361	0.98[ASN][1000 genomes]
rs28394002	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28489645	0.91[ASN][1000 genomes]
rs28558465	0.89[ASN][1000 genomes]
rs28588941	0.89[ASN][1000 genomes]
rs28613726	0.89[ASN][1000 genomes]
rs28661791	0.89[ASN][1000 genomes]
rs28696054	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28744428	0.80[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs28814696	0.89[ASN][1000 genomes]
rs28819970	0.98[ASN][1000 genomes]
rs28830587	0.89[ASN][1000 genomes]
rs28848573	0.89[ASN][1000 genomes]
rs28855206	0.89[ASN][1000 genomes]
rs28859331	0.89[ASN][1000 genomes]
rs28872587	0.89[ASN][1000 genomes]
rs28877976	0.89[ASN][1000 genomes]
rs28880369	0.89[ASN][1000 genomes]
rs28884892	0.89[ASN][1000 genomes]
rs28893243	0.89[ASN][1000 genomes]
rs34003616	0.88[ASN][1000 genomes]
rs34151233	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34365744	0.89[ASN][1000 genomes]
rs35041609	0.85[AMR][1000 genomes]
rs35437107	0.88[ASN][1000 genomes]
rs35639548	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35664299	0.89[ASN][1000 genomes]
rs36051778	0.90[ASN][1000 genomes]
rs3863828	0.96[ASN][1000 genomes]
rs3910837	0.81[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4444815	0.98[ASN][1000 genomes]
rs4475134	0.89[ASN][1000 genomes]
rs57420599	0.88[ASN][1000 genomes]
rs59660596	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67441316	0.82[AFR][1000 genomes];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs67906834	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6810417	0.98[ASN][1000 genomes]
rs6858079	0.82[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs71602006	0.89[ASN][1000 genomes]
rs73127077	0.89[ASN][1000 genomes]
rs7660710	0.87[ASN][1000 genomes]
rs7661640	0.89[ASN][1000 genomes]
rs7665615	0.80[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7667563	0.89[ASN][1000 genomes]
rs7674046	0.80[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7684329	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7688152	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7691370	0.81[ASN][1000 genomes]
rs7693464	0.98[ASN][1000 genomes]
rs7694031	0.89[ASN][1000 genomes]
rs7694226	0.98[ASN][1000 genomes]
rs9990714	0.88[ASN][1000 genomes]
rs9992483	0.89[ASN][1000 genomes]
rs9993419	0.89[ASN][1000 genomes]
rs9995588	0.89[ASN][1000 genomes]
rs9995797	0.89[ASN][1000 genomes]
rs9997046	0.80[EUR][1000 genomes];0.96[ASN][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	nsv1012155	chr4:33203447-33798612	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv537059	chr4:33203447-33798612	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	nsv1005061	chr4:33366334-33894491	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv878876	chr4:33653757-34000455	Flanking Active TSS Active TSS Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	esv1819154	chr4:33658459-33774322	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:33741800-33743000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr4:33741800-33743000	Enhancers	Dnd41	blood
3	chr4:33742000-33743000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr4:33742200-33743200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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