Variant report

Variant	rs11205128
Chromosome Location	chr1:152844142-152844143
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:152717789..152718414-chr1:152843679..152844506,2	MCF-7	breast:
2	chr1:152843289..152844260-chr1:153005064..153006050,2	MCF-7	breast:
3	chr1:152842063..152844434-chr1:153164775..153166274,11	MCF-7	breast:
4	chr1:152843652..152844300-chr1:153003266..153003806,2	MCF-7	breast:
5	chr1:152843080..152844798-chr1:153164828..153166213,18	MCF-7	breast:
6	chr1:152843310..152844245-chr1:152890638..152891212,2	MCF-7	breast:
7	chr1:152843263..152844168-chr1:153005237..153006058,6	MCF-7	breast:
8	chr1:152843206..152844266-chr1:152889921..152890796,3	MCF-7	breast:
9	chr1:152843390..152844417-chr1:152898307..152899295,4	MCF-7	breast:
10	chr1:152843518..152844203-chr8:96897506..96898026,2	MCF-7	breast:
11	chr1:152843341..152844548-chr1:152897786..152899223,16	MCF-7	breast:
12	chr1:152843532..152844154-chr1:152896678..152897196,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000169469	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs11205127	1.00[CEU][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11205129	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.80[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11205131	0.85[JPT][hapmap]
rs11801996	1.00[CEU][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.80[GIH][hapmap];0.86[JPT][hapmap];1.00[MEX][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12021601	0.95[CHB][hapmap];0.98[CHD][hapmap];0.80[GIH][hapmap];0.86[JPT][hapmap];0.85[MEX][hapmap];0.92[ASN][1000 genomes]
rs12022319	0.87[CHB][hapmap];0.88[CHD][hapmap];0.81[MEX][hapmap]
rs12022349	1.00[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.96[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs12022870	0.90[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs12026193	1.00[CEU][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12047888	0.92[ASN][1000 genomes]
rs12048655	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.83[YRI][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12239808	0.81[JPT][hapmap]
rs12239814	0.86[JPT][hapmap]
rs12568299	0.92[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];0.93[GIH][hapmap];0.95[LWK][hapmap];0.93[MEX][hapmap];0.86[MKK][hapmap];0.86[YRI][hapmap];0.84[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16834715	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs16834728	0.87[CHB][hapmap];0.88[CHD][hapmap];0.86[MEX][hapmap]
rs16834734	0.95[CHB][hapmap];0.85[JPT][hapmap];0.91[ASN][1000 genomes]
rs2339383	0.95[CHB][hapmap];0.86[JPT][hapmap];0.92[ASN][1000 genomes]
rs2339398	0.85[ASW][hapmap];1.00[CEU][hapmap];0.80[CHD][hapmap];0.88[LWK][hapmap];0.92[MEX][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2879485	0.81[JPT][hapmap]
rs3737861	0.87[CHB][hapmap];0.86[CHD][hapmap]
rs3737862	0.95[CHB][hapmap];0.98[CHD][hapmap];0.80[GIH][hapmap];0.86[JPT][hapmap];0.85[MEX][hapmap];0.91[ASN][1000 genomes]
rs4240862	1.00[CEU][hapmap];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4363387	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs4845489	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4845490	0.87[CHB][hapmap]
rs4845491	0.86[CHB][hapmap]
rs4845492	0.87[CHB][hapmap];0.86[CHD][hapmap];0.81[MEX][hapmap]
rs4845494	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs60566199	0.91[ASN][1000 genomes]
rs73006590	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7542656	0.86[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs7553755	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7556490	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757755	chr1:152472839-152898153	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	esv2758970	chr1:152472839-152898153	ZNF genes & repeats Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv427786	chr1:152572990-152898153	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
4	nsv1013433	chr1:152619305-153262215	Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
5	nsv535170	chr1:152619305-153262215	Enhancers Bivalent Enhancer Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
6	nsv1001834	chr1:152648853-153279143	Enhancers Weak transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
7	nsv547899	chr1:152672005-153245082	Enhancers Weak transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	42 gene(s)	inside rSNPs	diseases
8	nsv999918	chr1:152749733-152861866	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1009885	chr1:152762750-152851273	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv1000159	chr1:152809514-152853766	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1008447	chr1:152811171-152853748	Enhancers Weak transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	esv2761937	chr1:152811183-152853760	Weak transcription Enhancers Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv831592	chr1:152815054-152997162	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:152838800-152846000	Weak transcription	HMEC	breast
2	chr1:152843800-152844200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:152844000-152844200	Enhancers	Fetal Stomach	stomach
4	chr1:152844000-152845000	Flanking Active TSS	GM12878-XiMat	blood
5	chr1:152844000-152846000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:152844000-152850800	Weak transcription	NHEK	skin

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