Variant report

Variant	rs4129736
Chromosome Location	chr11:26671418-26671419
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:26318438..26319350-chr11:26670793..26671982,7	MCF-7	breast:
2	chr11:26544159..26545613-chr11:26671003..26672359,7	MCF-7	breast:

Extended variants
information (count: 43 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:36)

rs_ID	r²[population]
rs10734380	0.92[AFR][1000 genomes]
rs10742149	0.86[JPT][hapmap];0.81[ASN][1000 genomes]
rs10742151	0.82[ASN][1000 genomes]
rs10767556	0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs10767567	0.91[CHB][hapmap]
rs10835005	0.91[ASN][1000 genomes]
rs10835006	0.92[CHB][hapmap];0.93[JPT][hapmap];0.93[ASN][1000 genomes]
rs10835007	0.87[JPT][hapmap]
rs10835019	0.87[JPT][hapmap];0.82[ASN][1000 genomes]
rs10835021	0.82[JPT][hapmap];0.82[ASN][1000 genomes]
rs11029629	0.87[JPT][hapmap]
rs12420230	0.91[CHB][hapmap]
rs1389455	0.93[JPT][hapmap]
rs1567351	0.87[JPT][hapmap]
rs211066	1.00[CHB][hapmap]
rs2298	0.94[JPT][hapmap];0.88[YRI][hapmap];0.92[AFR][1000 genomes]
rs28622575	0.82[ASN][1000 genomes]
rs4254034	1.00[CHB][hapmap]
rs4293085	0.92[CHB][hapmap]
rs4390308	0.94[JPT][hapmap]
rs4447134	0.80[ASN][1000 genomes]
rs4576775	0.93[JPT][hapmap];0.81[ASN][1000 genomes]
rs4603259	0.94[JPT][hapmap]
rs4922765	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4922766	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6484233	0.81[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs6484234	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7101498	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7121838	0.86[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.88[YRI][hapmap]
rs7928737	0.94[JPT][hapmap];0.89[YRI][hapmap];0.93[AFR][1000 genomes]
rs7930308	0.87[JPT][hapmap]
rs7931282	0.87[JPT][hapmap]
rs7934757	0.94[JPT][hapmap]
rs7936525	0.94[JPT][hapmap]
rs7938949	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7948089	0.94[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1044544	chr11:26506962-26967285	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
2	nsv1050121	chr11:26532655-26675303	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	nsv540974	chr11:26532655-26675303	Weak transcription Enhancers Active TSS Strong transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
4	nsv916187	chr11:26576875-27328603	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
5	nsv897141	chr11:26659406-26674033	Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv467779	chr11:26661690-26674033	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv553908	chr11:26661690-26674033	Enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription	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	chr11:26645200-26671600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
2	chr11:26671400-26671800	Enhancers	Colon Smooth Muscle	Colon

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