Variant report

Variant	rs34420020
Chromosome Location	chr22:30558499-30558500
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	chr22:30523289..30525993-chr22:30557345..30559122,2	K562	blood:

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

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

rs_ID	r²[population]
rs1160671	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12233358	0.89[EUR][1000 genomes]
rs12484547	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13053765	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13054837	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13055998	0.89[EUR][1000 genomes]
rs13056332	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13056990	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13057204	0.89[EUR][1000 genomes]
rs13057580	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13057878	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1476514	0.89[EUR][1000 genomes]
rs2010916	0.85[EUR][1000 genomes]
rs2012308	0.89[EUR][1000 genomes]
rs2106430	0.95[EUR][1000 genomes]
rs2106722	0.89[ASN][1000 genomes]
rs2214047	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2412977	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2412979	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34391152	0.95[EUR][1000 genomes]
rs34474867	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs34545612	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35067150	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs35539897	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs35710453	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs36018230	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4820829	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4823067	0.89[EUR][1000 genomes]
rs4823071	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4823080	0.89[EUR][1000 genomes]
rs4823081	0.89[EUR][1000 genomes]
rs4823082	0.95[EUR][1000 genomes]
rs5753002	0.89[EUR][1000 genomes]
rs5753007	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs5753013	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753014	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753015	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753019	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753020	0.81[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753022	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5753027	0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs5753028	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5753029	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5753030	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5753046	0.95[EUR][1000 genomes]
rs5763701	0.89[EUR][1000 genomes]
rs5763734	0.89[EUR][1000 genomes]
rs5763742	0.89[EUR][1000 genomes]
rs5763746	0.89[EUR][1000 genomes]
rs5763748	0.89[EUR][1000 genomes]
rs5763750	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs5763758	0.85[ASN][1000 genomes]
rs5763759	0.89[EUR][1000 genomes]
rs5763763	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763766	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763769	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763774	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763782	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763787	0.85[ASN][1000 genomes]
rs5763788	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5763801	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs5763805	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5763810	0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5763825	0.91[ASN][1000 genomes]
rs5763852	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5763854	0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5763861	0.82[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs5763872	0.95[EUR][1000 genomes]
rs718773	0.85[ASN][1000 genomes]
rs7286304	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7286681	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7288576	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs739616	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs757026	0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs766011	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs975704	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.94[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	nsv1064081	chr22:29826745-30623965	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	nsv544677	chr22:29826745-30623965	Weak transcription Bivalent/Poised TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
3	nsv588884	chr22:30494371-30590026	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv834173	chr22:30515092-30658277	Enhancers ZNF genes & repeats Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
5	nsv527188	chr22:30529741-30581722	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:30555400-30558600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
2	chr22:30557600-30563400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr22:30558200-30560800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
4	chr22:30558200-30563000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
5	chr22:30558200-30563000	Weak transcription	Thymus	Thymus
6	chr22:30558200-30563800	Weak transcription	Dnd41	blood
7	chr22:30558400-30564400	Weak transcription	Fetal Thymus	thymus

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