Variant report

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1004477	1.00[CEU][hapmap]
rs10145775	1.00[CEU][hapmap]
rs17115503	1.00[CEU][hapmap]
rs17115530	1.00[CEU][hapmap]
rs17115684	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs17115708	1.00[CEU][hapmap]
rs17115950	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17116023	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17116029	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17116069	1.00[CEU][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17116212	1.00[CEU][hapmap]
rs17116237	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17116276	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17116292	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17116396	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs17116464	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs2238178	1.00[EUR][1000 genomes]
rs2238190	1.00[CEU][hapmap]
rs2239211	1.00[CEU][hapmap]
rs45601334	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56884598	1.00[EUR][1000 genomes]
rs59189869	1.00[EUR][1000 genomes]
rs59884363	1.00[EUR][1000 genomes]
rs61303255	1.00[EUR][1000 genomes]
rs740536	1.00[CEU][hapmap]
rs8022670	1.00[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530794	chr14:72113818-73034008	Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
2	nsv948800	chr14:72462557-73150701	Enhancers Bivalent Enhancer Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72891000-72908600	Weak transcription	Left Ventricle	heart
2	chr14:72900800-72904400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr14:72901200-72906800	Enhancers	Dnd41	blood
4	chr14:72901400-72904600	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr14:72901800-72904400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr14:72902200-72905600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr14:72902400-72905800	Weak transcription	Primary T cells from cord blood	blood
8	chr14:72902600-72905200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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