Variant report

Variant	rs73459768
Chromosome Location	chr7:145449664-145449665
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	chr7:145449251..145450121-chr7:145786995..145787798,2	K562	blood:

Extended variants
information (count: 82 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10215152	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10215527	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10224199	0.82[ASN][1000 genomes]
rs10238054	0.85[ASN][1000 genomes]
rs10249365	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10249899	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10252033	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10255978	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10268002	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10271223	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10271257	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10280333	0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10282552	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1112676	0.88[ASN][1000 genomes]
rs11979253	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12668333	0.88[ASN][1000 genomes]
rs13243170	0.92[ASN][1000 genomes]
rs1403839	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1523729	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1523733	0.82[ASN][1000 genomes]
rs17169863	0.88[ASN][1000 genomes]
rs2030629	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2030631	0.88[ASN][1000 genomes]
rs2030632	0.88[ASN][1000 genomes]
rs2091097	0.85[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2103093	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2140472	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2372128	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2372129	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2372133	0.88[ASN][1000 genomes]
rs28459185	0.88[ASN][1000 genomes]
rs28687396	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs28816522	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28846092	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs28859574	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs28860008	0.85[ASN][1000 genomes]
rs28875289	0.88[ASN][1000 genomes]
rs28876797	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2888248	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs35095326	0.88[ASN][1000 genomes]
rs4436045	0.85[ASN][1000 genomes]
rs4534070	0.80[EUR][1000 genomes]
rs4580953	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs55788321	0.88[ASN][1000 genomes]
rs55930903	0.88[ASN][1000 genomes]
rs56295629	0.88[ASN][1000 genomes]
rs59723212	0.88[ASN][1000 genomes]
rs6464694	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6464695	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6464697	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6464698	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6464701	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6464702	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6464703	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6942501	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6943097	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6946087	0.85[ASN][1000 genomes]
rs6948800	0.88[ASN][1000 genomes]
rs6954634	0.82[ASN][1000 genomes]
rs6957646	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6966607	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6969543	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6972421	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6974953	0.88[ASN][1000 genomes]
rs6976208	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6979675	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73453054	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs73456937	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7785512	0.82[ASN][1000 genomes]
rs7799203	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7800906	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7805756	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7805880	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7806864	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7808969	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9655578	0.80[ASN][1000 genomes]
rs9655683	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9986960	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754040	chr7:145303352-145698352	Enhancers Weak transcription Active TSS Bivalent Enhancer Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	esv2755386	chr7:145303352-145698352	Genic enhancers Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv889383	chr7:145396141-145549570	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv831182	chr7:145399806-145556489	Enhancers Genic enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:145449600-145450000	Active TSS	H9 Cell Line	embryonic stem cell

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