Variant report

Variant	rs1830028
Chromosome Location	chr7:14762355-14762356
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10228891	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10234209	0.81[AFR][1000 genomes]
rs10259838	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10278975	0.89[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11971649	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12154366	0.81[EUR][1000 genomes]
rs12533352	0.81[EUR][1000 genomes]
rs12539208	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13231864	0.80[EUR][1000 genomes]
rs13237347	0.80[EUR][1000 genomes]
rs1357856	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1357871	0.84[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1357872	0.82[EUR][1000 genomes]
rs1404615	0.80[AMR][1000 genomes]
rs1404616	0.80[AMR][1000 genomes]
rs1525099	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1568847	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17606181	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17668761	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1997040	0.80[EUR][1000 genomes]
rs34587189	0.81[EUR][1000 genomes]
rs35046572	0.82[EUR][1000 genomes]
rs35731392	0.80[EUR][1000 genomes]
rs4721360	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62448684	0.83[EUR][1000 genomes]
rs6461121	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs6947566	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6954517	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7784799	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9639212	0.90[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9691103	0.87[AMR][1000 genomes]
rs9784967	0.92[AMR][1000 genomes];0.91[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	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1031041	chr7:14624127-14999201	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv538741	chr7:14624127-14999201	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv887712	chr7:14717872-14829858	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:14712800-14775200	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr7:14758800-14763000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr7:14761200-14763000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr7:14761800-14763000	Weak transcription	Colon Smooth Muscle	Colon
5	chr7:14762000-14763800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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