Variant report

Variant	rs73163600
Chromosome Location	chr7:150504090-150504091
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs17173637	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs28657958	0.86[EUR][1000 genomes]
rs55947915	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56321085	0.84[EUR][1000 genomes]
rs73165503	0.86[EUR][1000 genomes]
rs73165507	0.86[EUR][1000 genomes]
rs73165523	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73165526	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73165531	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73165540	0.86[EUR][1000 genomes]
rs73165545	0.86[EUR][1000 genomes]
rs7787577	0.86[EUR][1000 genomes]
rs7794403	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv608990	chr7:149961274-150707488	Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	90 gene(s)	inside rSNPs	diseases
2	nsv1017368	chr7:150016952-150655773	Bivalent Enhancer ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
3	nsv539195	chr7:150016952-150655773	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv1030109	chr7:150312916-150701010	Enhancers Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv967475	chr7:150323577-150610034	Enhancers Bivalent Enhancer Weak transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:150502600-150504200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
2	chr7:150502600-150505200	Weak transcription	Colonic Mucosa	Colon
3	chr7:150502800-150504200	ZNF genes & repeats	Duodenum Mucosa	Duodenum
4	chr7:150502800-150504200	ZNF genes & repeats	Fetal Intestine Small	intestine
5	chr7:150503400-150504800	Weak transcription	Rectal Smooth Muscle	rectum
6	chr7:150503400-150528000	Weak transcription	Ovary	ovary
7	chr7:150503600-150504600	Weak transcription	Fetal Intestine Large	intestine
8	chr7:150503600-150504800	Weak transcription	Rectal Mucosa Donor 31	rectum
9	chr7:150503800-150504200	ZNF genes & repeats	Liver	Liver
10	chr7:150504000-150504600	Weak transcription	Stomach Mucosa	stomach

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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