Variant report

Variant	rs610447
Chromosome Location	chr7:18357192-18357193
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10253810	0.88[ASN][1000 genomes]
rs2791299	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2960781	0.89[ASN][1000 genomes]
rs2960783	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs581438	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs581820	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs582937	0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs587325	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs590099	0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs596844	0.87[ASN][1000 genomes]
rs600846	0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs602349	0.91[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs604804	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs605866	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs606064	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs612977	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs613852	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs614304	1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs621573	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs621939	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs627060	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs628095	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs636246	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs638521	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs638620	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs639387	0.90[ASN][1000 genomes]
rs639424	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs661144	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs667764	0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs669164	0.84[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs680437	0.81[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs683693	0.87[ASN][1000 genomes]
rs687748	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6950126	0.83[ASN][1000 genomes]
rs6956566	0.83[ASN][1000 genomes]
rs708127	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs880519	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
4	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
5	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
6	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv606358	chr7:18084843-18416097	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
8	nsv887810	chr7:18193589-18391557	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv830914	chr7:18196730-18376047	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv1029901	chr7:18205779-18387956	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv830916	chr7:18254299-18433349	Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Weak transcription Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
12	esv2755157	chr7:18337660-18805860	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:18349200-18358600	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:18352600-18359400	Weak transcription	Primary hematopoietic stem cells	blood
3	chr7:18352800-18359600	Weak transcription	Primary B cells from peripheral blood	blood
4	chr7:18353000-18357200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr7:18353000-18358200	Enhancers	Fetal Heart	heart
6	chr7:18354000-18360000	Weak transcription	K562	blood
7	chr7:18355600-18357200	Weak transcription	Primary B cells from cord blood	blood
8	chr7:18355800-18360600	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr7:18356000-18357200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr7:18356600-18360200	Weak transcription	Left Ventricle	heart
11	chr7:18356800-18357200	Active TSS	Primary monocytes fromperipheralblood	blood
12	chr7:18356800-18357200	Active TSS	Monocytes-CD14+_RO01746	blood
13	chr7:18356800-18358600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr7:18357000-18357600	Enhancers	Hela-S3	cervix
15	chr7:18357000-18357800	Enhancers	Primary neutrophils fromperipheralblood	blood
16	chr7:18357000-18358600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:18357000-18359000	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr7:18357000-18359000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr7:18357000-18359200	Enhancers	iPS-20b Cell Line	embryonic stem cell

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