Variant report

Variant	rs73181905
Chromosome Location	chr7:103466018-103466019
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:103458610..103460709-chr7:103463601..103466082,3	K562	blood:
2	chr7:103466010..103468744-chr7:103470404..103473260,3	K562	blood:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10215861	0.85[EUR][1000 genomes]
rs10233074	0.85[EUR][1000 genomes]
rs10244283	0.85[EUR][1000 genomes]
rs10250074	0.85[EUR][1000 genomes]
rs10262803	0.85[EUR][1000 genomes]
rs10266261	0.85[EUR][1000 genomes]
rs10267445	0.83[EUR][1000 genomes]
rs10272530	0.85[EUR][1000 genomes]
rs10275624	0.82[EUR][1000 genomes]
rs10276941	0.86[EUR][1000 genomes]
rs10279423	0.85[EUR][1000 genomes]
rs12534629	0.85[EUR][1000 genomes]
rs1404431	0.81[ASN][1000 genomes]
rs1510855	0.85[EUR][1000 genomes]
rs1510857	0.86[EUR][1000 genomes]
rs17156394	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1848959	0.86[EUR][1000 genomes]
rs1877109	0.82[EUR][1000 genomes]
rs2237645	0.81[EUR][1000 genomes]
rs262375	0.86[ASN][1000 genomes]
rs28374422	0.85[EUR][1000 genomes]
rs28417410	0.83[EUR][1000 genomes]
rs28418870	0.85[EUR][1000 genomes]
rs28513620	0.85[EUR][1000 genomes]
rs28529490	0.85[EUR][1000 genomes]
rs28628152	0.85[EUR][1000 genomes]
rs28658324	0.84[EUR][1000 genomes]
rs28710358	0.85[EUR][1000 genomes]
rs28760395	0.82[EUR][1000 genomes]
rs28803202	0.85[EUR][1000 genomes]
rs28841308	0.85[EUR][1000 genomes]
rs28880083	0.85[EUR][1000 genomes]
rs3819484	0.82[ASN][1000 genomes]
rs3819489	0.82[ASN][1000 genomes]
rs4729931	0.81[ASN][1000 genomes]
rs56106813	0.83[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs56673287	0.85[EUR][1000 genomes]
rs56739105	0.85[EUR][1000 genomes]
rs57559907	0.85[EUR][1000 genomes]
rs60861793	0.85[EUR][1000 genomes]
rs67342215	0.81[ASN][1000 genomes]
rs67399010	0.82[ASN][1000 genomes]
rs67649823	0.81[ASN][1000 genomes]
rs6951263	0.85[EUR][1000 genomes]
rs73180201	1.00[ASN][1000 genomes]
rs73181915	0.85[EUR][1000 genomes]
rs73412894	0.81[ASN][1000 genomes]
rs745540	0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1843940	chr7:103421702-103590285	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	nsv523031	chr7:103457789-103470499	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv934055	chr7:103462527-103473944	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103457800-103472000	Weak transcription	HepG2	liver
2	chr7:103461200-103482400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr7:103465800-103466600	Strong transcription	K562	blood

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