Variant report

Variant	rs4721042
Chromosome Location	chr7:12170496-12170497
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:12166840..12168760-chr7:12170445..12172889,2	K562	blood:

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs1003432	0.83[ASN][1000 genomes]
rs1003433	0.83[ASN][1000 genomes]
rs10236588	0.91[EUR][1000 genomes]
rs10950383	0.91[EUR][1000 genomes]
rs10950384	0.91[EUR][1000 genomes]
rs11761090	0.91[EUR][1000 genomes]
rs11771114	0.91[EUR][1000 genomes]
rs12699310	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13221968	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17165582	0.90[EUR][1000 genomes]
rs17592324	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17650986	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1861279	0.96[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2192732	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2356053	0.92[EUR][1000 genomes]
rs2356055	0.91[EUR][1000 genomes]
rs2356056	0.91[EUR][1000 genomes]
rs35649285	0.91[EUR][1000 genomes]
rs35828107	0.92[EUR][1000 genomes]
rs36014865	0.89[EUR][1000 genomes]
rs4236267	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4236268	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4719294	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4719295	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4719296	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4721038	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4721039	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4721041	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6460882	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs68113272	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6945990	0.91[EUR][1000 genomes]
rs6952511	0.90[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6956124	0.88[EUR][1000 genomes]
rs7783494	0.90[EUR][1000 genomes]
rs7790585	0.90[EUR][1000 genomes]
rs7797675	0.92[EUR][1000 genomes]
rs9638681	0.91[EUR][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	nsv606199	chr7:11506143-12486659	Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv887614	chr7:11778424-12211198	Bivalent/Poised TSS Active TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
3	nsv830906	chr7:12001764-12177869	Enhancers Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1023608	chr7:12064114-12247520	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv534432	chr7:12148960-12693032	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
6	nsv518343	chr7:12164100-12170496	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1021710	chr7:12164993-12251790	Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:11 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:12167200-12170800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
2	chr7:12167600-12170600	Weak transcription	A549	lung
3	chr7:12169600-12171400	Enhancers	Fetal Intestine Large	intestine
4	chr7:12169800-12171200	Enhancers	Rectal Mucosa Donor 31	rectum
5	chr7:12170200-12170800	Enhancers	Hela-S3	cervix
6	chr7:12170400-12171000	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr7:12170400-12171200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:12170400-12171200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
9	chr7:12170400-12171200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr7:12170400-12171400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
11	chr7:12170400-12171400	Enhancers	Primary T helper cells PMA-I stimulated	--

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