Variant report

Variant	rs73000002
Chromosome Location	chr3:144064183-144064184
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	chr3:144060304..144063071-chr3:144063118..144065175,2	K562	blood:

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs12486580	0.86[AFR][1000 genomes]
rs12629763	1.00[ASN][1000 genomes]
rs12630075	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12632207	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12632605	0.96[ASN][1000 genomes]
rs12633232	0.89[ASN][1000 genomes]
rs12633585	0.89[ASN][1000 genomes]
rs12634524	0.89[ASN][1000 genomes]
rs12634939	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12636393	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12637613	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1503324	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41401847	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41430844	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56247328	1.00[EUR][1000 genomes]
rs57317338	1.00[EUR][1000 genomes]
rs57444904	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59921777	0.86[AFR][1000 genomes]
rs61146072	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61200466	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6440244	1.00[EUR][1000 genomes]
rs6762994	1.00[EUR][1000 genomes]
rs6770469	0.93[ASN][1000 genomes]
rs72999924	0.86[AFR][1000 genomes]
rs72999937	0.96[ASN][1000 genomes]
rs72999962	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72999980	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72999982	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs72999985	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72999988	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72999989	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs72999991	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73000000	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73001805	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73005843	1.00[EUR][1000 genomes]
rs73873256	1.00[EUR][1000 genomes]
rs73873257	1.00[EUR][1000 genomes]
rs7622410	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010117	chr3:143750590-144093775	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv536748	chr3:143750590-144093775	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv532633	chr3:143802417-144440646	Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	nsv1002032	chr3:143848755-144065468	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv877570	chr3:143853149-144123401	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv1011685	chr3:143959237-144218424	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv536751	chr3:143959237-144218424	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv591928	chr3:144050897-144822081	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv822274	chr3:144059205-144064282	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:144062600-144065600	Enhancers	Dnd41	blood
2	chr3:144062800-144064400	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr3:144063200-144064200	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr3:144063200-144064200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr3:144063200-144064200	Bivalent Enhancer	Primary hematopoietic stem cells	blood
6	chr3:144063200-144064400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr3:144063200-144064600	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:144063200-144064600	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr3:144063200-144064600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr3:144063200-144065400	Weak transcription	Ovary	ovary
11	chr3:144063400-144068400	Weak transcription	Fetal Lung	lung
12	chr3:144063600-144064200	Enhancers	H9 Cell Line	embryonic stem cell
13	chr3:144063600-144064200	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr3:144063600-144064200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr3:144063600-144064200	Enhancers	Primary monocytes fromperipheralblood	blood
16	chr3:144063600-144064200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:144063600-144064600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr3:144063800-144064400	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr3:144063800-144064400	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr3:144063800-144064600	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr3:144063800-144064600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
22	chr3:144064000-144064400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr3:144064000-144064400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
24	chr3:144064000-144064800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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