Variant report

Variant	rs1364603
Chromosome Location	chr14:80020811-80020812
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	chr14:80018191..80021124-chr14:80031002..80033246,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs12433645	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs170248	0.89[CEU][hapmap];0.83[CHB][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs170255	0.85[CEU][hapmap];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs172712	0.82[CEU][hapmap];0.91[CHB][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs178348	0.85[CEU][hapmap];0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17836224	0.88[CHB][hapmap];0.80[EUR][1000 genomes]
rs17836226	0.87[CHB][hapmap];0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1834242	0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs188780	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs190092	0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs1991158	0.89[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2008380	0.89[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs221416	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs221418	0.85[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs221420	0.96[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs221421	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs221423	0.88[CEU][hapmap];0.82[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs221427	0.89[CEU][hapmap];0.84[CHB][hapmap];0.88[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs221428	0.85[CEU][hapmap]
rs221429	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs221430	0.81[CEU][hapmap];0.80[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs221431	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs221432	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs221434	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs221435	0.89[CEU][hapmap];0.84[CHB][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs221518	0.83[EUR][1000 genomes]
rs2543570	0.89[CEU][hapmap];0.88[CHB][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2543574	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2543576	0.85[CEU][hapmap];0.88[CHB][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2543577	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2543579	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2543580	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2543581	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2543582	0.84[CEU][hapmap];0.87[CHB][hapmap];0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2552407	0.83[EUR][1000 genomes]
rs2552416	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2552419	0.85[CEU][hapmap];0.88[CHB][hapmap];0.87[AMR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7140480	0.93[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs8009763	0.80[EUR][1000 genomes]
rs8013736	0.84[CEU][hapmap];0.87[CHB][hapmap];0.84[AMR][1000 genomes];0.87[EUR][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	nsv1045241	chr14:79885361-80734201	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv1039622	chr14:79908702-80266601	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv902112	chr14:79939393-80050771	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv869542	chr14:80009619-80118315	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr14:80011800-80069200	Weak transcription	Stomach Smooth Muscle	stomach
2	chr14:80014400-80037800	Weak transcription	Aorta	Aorta
3	chr14:80015800-80021000	Enhancers	Placenta Amnion	Placenta Amnion
4	chr14:80020000-80021400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr14:80020000-80027200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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