Variant report

Variant	rs17154414
Chromosome Location	chr7:103338217-103338218
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:103331525..103333505-chr7:103337273..103339840,2	K562	blood:
2	chr7:103337945..103339542-chr7:103340287..103342669,2	K562	blood:
3	chr7:103335628..103338296-chr7:103339379..103341676,2	K562	blood:

Extended variants
information (count: 40 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10487167	0.82[CEU][hapmap];1.00[CHB][hapmap];0.88[CHD][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12533612	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12539423	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1541328	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17153784	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17153873	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17154011	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs17154172	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs17155063	0.82[CEU][hapmap];1.00[CHB][hapmap];0.81[YRI][hapmap];0.87[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs17155341	0.82[CEU][hapmap]
rs2072402	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs2072403	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs2072404	1.00[CEU][hapmap];0.82[CHB][hapmap];0.84[MEX][hapmap]
rs2073552	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2073553	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[MEX][hapmap];0.85[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2073554	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2075042	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2215536	0.80[ASN][1000 genomes]
rs2237634	0.82[CEU][hapmap];0.81[YRI][hapmap]
rs2299351	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2299352	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs28784650	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3025970	1.00[CEU][hapmap];1.00[MEX][hapmap];0.87[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34196791	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs362685	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs362704	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3757737	1.00[CEU][hapmap];0.90[JPT][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs3757739	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3757740	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3757741	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3808022	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs3808023	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3808025	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3808028	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs3819466	0.82[CEU][hapmap];0.83[GIH][hapmap];0.84[MEX][hapmap];0.81[YRI][hapmap]
rs7803243	0.81[JPT][hapmap]

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	nsv491911	chr7:102967150-103403622	Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Genic enhancers 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
2	nsv831085	chr7:103140672-103342388	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv427799	chr7:103250733-103454202	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	esv1835816	chr7:103255144-103354223	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:103331200-103342400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr7:103333200-103339400	Weak transcription	Liver	Liver
3	chr7:103334200-103342400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr7:103335800-103339200	Strong transcription	HepG2	liver
5	chr7:103337400-103339000	Strong transcription	K562	blood

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