Variant report

Variant	rs7072577
Chromosome Location	chr10:4031002-4031003
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10795115	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10795116	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10795117	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10795118	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10904153	0.87[EUR][1000 genomes]
rs10904163	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10904164	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10904165	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11252218	0.88[EUR][1000 genomes]
rs11252222	0.86[EUR][1000 genomes]
rs11252232	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11252238	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11252240	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11252241	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs11252242	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11252243	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2031578	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2148188	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2148189	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs34133718	0.83[EUR][1000 genomes]
rs4242767	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4880652	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4880653	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7079191	0.87[EUR][1000 genomes]
rs7920244	0.87[EUR][1000 genomes]
rs7922194	0.89[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	nsv1043680	chr10:3551191-4038002	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	69 gene(s)	inside rSNPs	diseases
2	nsv1051297	chr10:3908706-4277678	Enhancers Active TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
3	nsv894784	chr10:3985194-4051081	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
4	nsv5609	chr10:4002849-4040114	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA miRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:4020200-4032600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:4022200-4036400	Weak transcription	Right Atrium	heart
3	chr10:4028200-4033800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr10:4028600-4031600	Weak transcription	Fetal Thymus	thymus
5	chr10:4028800-4032000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr10:4029200-4031200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr10:4029600-4031200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr10:4029600-4034000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr10:4030200-4037600	Weak transcription	HUVEC	blood vessel
10	chr10:4030600-4036200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr10:4030600-4037400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr10:4031000-4031800	Enhancers	Primary hematopoietic stem cells	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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