Variant report

Variant	rs74038093
Chromosome Location	chr16:79921081-79921082
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:79918519..79921940-chr16:79923355..79927904,4	MCF-7	breast:
2	chr16:79891351..79893625-chr16:79919573..79921635,2	MCF-7	breast:
3	chr16:79919007..79921111-chr16:79925288..79927075,2	K562	blood:
4	chr16:79918690..79920713-chr16:79920839..79923822,2	K562	blood:

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs11641084	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs11641371	0.92[ASN][1000 genomes]
rs11644393	0.82[ASN][1000 genomes]
rs11644400	0.81[EUR][1000 genomes]
rs11646139	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11647905	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs11649114	0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12103233	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs13330024	0.97[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13330604	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13331920	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs13332408	0.84[AMR][1000 genomes]
rs13338786	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16951648	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28368255	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28384289	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs28555498	0.90[ASN][1000 genomes]
rs28580467	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs28581385	0.93[ASN][1000 genomes]
rs28613729	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs28623477	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs28680341	0.80[ASN][1000 genomes]
rs4078173	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs4473202	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4548890	0.89[ASN][1000 genomes]
rs4627365	0.94[ASN][1000 genomes]
rs58323452	0.82[ASN][1000 genomes]
rs59520813	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs60280876	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs60715095	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7188674	0.80[ASN][1000 genomes]
rs7189003	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs7191101	0.89[ASN][1000 genomes]
rs7191612	0.88[ASN][1000 genomes]
rs7193332	0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7194565	0.80[ASN][1000 genomes]
rs7195512	0.89[ASN][1000 genomes]
rs7197544	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7198844	0.80[ASN][1000 genomes]
rs7203258	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7204126	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7205649	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs73574100	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs8053565	0.93[ASN][1000 genomes]
rs8054786	0.93[ASN][1000 genomes]
rs8058927	0.93[ASN][1000 genomes]
rs8060495	0.93[ASN][1000 genomes]
rs9922138	0.85[ASN][1000 genomes]
rs9925032	0.82[ASN][1000 genomes]
rs9925120	0.93[ASN][1000 genomes]
rs9925132	0.81[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs9925837	0.83[ASN][1000 genomes]
rs9928026	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9934804	0.84[ASN][1000 genomes]
rs9935686	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9941162	0.85[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv1059511	chr16:79847882-79925436	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv542984	chr16:79847882-79925436	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv573290	chr16:79853267-79939504	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv573291	chr16:79881386-79931595	Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv906993	chr16:79883850-79923310	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv906994	chr16:79883850-79928186	Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv34919	chr16:79889959-79923310	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv457555	chr16:79893737-79926134	Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv471100	chr16:79893737-79926134	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv573292	chr16:79893737-79926134	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv2757646	chr16:79894964-79923310	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
14	esv2758662	chr16:79894964-79923310	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv457556	chr16:79896825-79926134	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
16	nsv573293	chr16:79896825-79926134	Enhancers Flanking Active TSS Weak transcription Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79908800-79931400	Weak transcription	Right Atrium	heart
2	chr16:79920400-79922000	Enhancers	Thymus	Thymus

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links