Variant report

Variant	rs7556567
Chromosome Location	chr1:168738305-168738306
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10157677	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10918976	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11585611	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11589260	0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11591144	0.82[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs12065661	0.82[EUR][1000 genomes]
rs4656616	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs471972	0.85[EUR][1000 genomes]
rs585646	0.85[EUR][1000 genomes]
rs61801624	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61801626	0.95[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6666794	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs737608	0.89[AFR][1000 genomes];0.89[AMR][1000 genomes];0.90[EUR][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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	nsv831847	chr1:168669877-168850129	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168730400-168743600	Weak transcription	Psoas Muscle	Psoas
2	chr1:168734200-168739200	Enhancers	Fetal Lung	lung
3	chr1:168735600-168739200	Enhancers	Fetal Heart	heart
4	chr1:168736200-168741800	Weak transcription	Stomach Mucosa	stomach
5	chr1:168736200-168743000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr1:168736800-168738600	Enhancers	Colon Smooth Muscle	Colon
7	chr1:168737000-168738600	Enhancers	Fetal Muscle Leg	muscle
8	chr1:168737000-168738800	Enhancers	Fetal Stomach	stomach
9	chr1:168737200-168738800	Enhancers	Duodenum Smooth Muscle	Duodenum
10	chr1:168737200-168740400	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr1:168737400-168738800	Enhancers	Brain Germinal Matrix	brain
12	chr1:168737400-168738800	Enhancers	Fetal Brain Male	brain
13	chr1:168737600-168741000	Weak transcription	Liver	Liver
14	chr1:168737800-168741200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr1:168737800-168741800	Weak transcription	Adipose Nuclei	Adipose
16	chr1:168737800-168741800	Weak transcription	Stomach Smooth Muscle	stomach
17	chr1:168737800-168741800	Weak transcription	HepG2	liver
18	chr1:168738000-168738400	Enhancers	Fetal Muscle Trunk	muscle
19	chr1:168738000-168741200	Weak transcription	Rectal Smooth Muscle	rectum
20	chr1:168738000-168742800	Weak transcription	Skeletal Muscle Female	skeletal muscle
21	chr1:168738000-168743000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
22	chr1:168738000-168743400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr1:168738200-168738400	Enhancers	Ovary	ovary
24	chr1:168738200-168742200	Weak transcription	Left Ventricle	heart

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