Variant report

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs10131300	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1155166	1.00[CHB][hapmap];0.87[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs12433564	0.92[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12436059	0.82[ASN][1000 genomes]
rs1548686	0.92[CEU][hapmap]
rs2159194	0.96[CEU][hapmap];1.00[CHB][hapmap];0.84[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2238189	0.82[ASN][1000 genomes]
rs2332835	0.90[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs4903025	0.91[ASN][1000 genomes]
rs4903026	0.96[CEU][hapmap];1.00[CHB][hapmap];0.92[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4903028	0.85[CEU][hapmap]
rs6574077	0.96[CEU][hapmap];1.00[CHB][hapmap];0.83[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7143154	0.80[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs7143912	1.00[CHB][hapmap];0.93[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs7155105	0.82[ASN][1000 genomes]
rs7158962	1.00[CHB][hapmap];0.92[AFR][1000 genomes];0.82[ASN][1000 genomes]
rs7159439	1.00[CHB][hapmap];0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs758265	0.96[CEU][hapmap];1.00[CHB][hapmap];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8012037	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9989171	0.82[ASN][1000 genomes]

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:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:72918000-72930000	Weak transcription	Right Atrium	heart
2	chr14:72918200-72929000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr14:72918200-72930000	Weak transcription	Left Ventricle	heart
4	chr14:72919000-72931400	Weak transcription	Adipose Nuclei	Adipose
5	chr14:72919400-72926800	Weak transcription	Fetal Intestine Small	intestine
6	chr14:72919400-72945200	Weak transcription	Brain Germinal Matrix	brain
7	chr14:72919800-72927400	Weak transcription	Fetal Muscle Leg	muscle
8	chr14:72923800-72946200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr14:72924200-72927400	Strong transcription	Cortex derived primary cultured neurospheres	brain
10	chr14:72924400-72926000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr14:72924400-72927800	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:72924800-72930000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr14:72924800-72930000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr14:72925200-72930000	Weak transcription	NH-A	brain
15	chr14:72925400-72930200	Weak transcription	NHLF	lung

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