Variant report

Variant	rs28527307
Chromosome Location	chr4:7462656-7462657
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10006748	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10015399	1.00[EUR][1000 genomes]
rs10028552	1.00[EUR][1000 genomes]
rs10028710	1.00[EUR][1000 genomes]
rs11939818	1.00[EUR][1000 genomes]
rs11942787	1.00[EUR][1000 genomes]
rs13353773	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28566581	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28631017	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28650405	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28662355	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28670447	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28671671	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28733922	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28740815	1.00[EUR][1000 genomes]
rs57175617	1.00[AMR][1000 genomes]
rs57744041	1.00[AMR][1000 genomes]
rs60573952	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73093607	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73798904	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9685358	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
6	nsv878560	chr4:7402284-7475114	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
7	nsv878561	chr4:7402284-7544610	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
8	nsv878563	chr4:7420785-7529367	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
9	nsv878564	chr4:7421007-7535214	Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
10	nsv878566	chr4:7456717-7529367	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	diseases
11	nsv878567	chr4:7456717-7544610	Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7459000-7463200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr4:7460800-7466000	Enhancers	Ovary	ovary
3	chr4:7461000-7466000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
4	chr4:7461800-7463000	Enhancers	Fetal Muscle Leg	muscle
5	chr4:7462000-7464800	Enhancers	Stomach Smooth Muscle	stomach
6	chr4:7462000-7465400	Enhancers	Brain Substantia Nigra	brain
7	chr4:7462000-7465600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:7462200-7462800	Bivalent Enhancer	Placenta	Placenta
9	chr4:7462200-7462800	Enhancers	HSMMtube	muscle
10	chr4:7462200-7463000	Bivalent Enhancer	HepG2	liver
11	chr4:7462200-7464000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
12	chr4:7462200-7464400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:7462200-7464800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr4:7462200-7464800	Enhancers	Fetal Intestine Small	intestine
15	chr4:7462200-7465800	Enhancers	Brain Cingulate Gyrus	brain
16	chr4:7462200-7466000	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr4:7462400-7462800	Bivalent Enhancer	HSMM	muscle
18	chr4:7462400-7463400	Enhancers	Brain Germinal Matrix	brain
19	chr4:7462400-7464200	Bivalent Enhancer	Skeletal Muscle Female	skeletal muscle
20	chr4:7462400-7465000	Enhancers	Brain Angular Gyrus	brain
21	chr4:7462400-7466000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr4:7462600-7462800	Enhancers	Brain Anterior Caudate	brain
23	chr4:7462600-7462800	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
24	chr4:7462600-7463400	Bivalent Enhancer	Fetal Stomach	stomach
25	chr4:7462600-7463600	Enhancers	Fetal Brain Male	brain
26	chr4:7462600-7463800	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:7462600-7463800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr4:7462600-7464000	Weak transcription	Liver	Liver
29	chr4:7462600-7464600	Enhancers	H1 Cell Line	embryonic stem cell

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