Variant report

Variant	rs13145010
Chromosome Location	chr4:127629723-127629724
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:127621513..127624552-chr4:127627027..127630786,3	K562	blood:
2	chr4:127628211..127630897-chr4:127699416..127701200,2	K562	blood:
3	chr4:127629211..127631287-chr4:127641916..127644046,2	K562	blood:
4	chr4:127621500..127623013-chr4:127629286..127631384,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs11098889	0.98[ASN][1000 genomes]
rs1167192	0.91[ASN][1000 genomes]
rs12650738	0.90[ASN][1000 genomes]
rs13151312	0.80[ASN][1000 genomes]
rs1491136	0.90[ASN][1000 genomes]
rs1491137	0.90[ASN][1000 genomes]
rs1503620	0.90[ASN][1000 genomes]
rs17011450	0.98[ASN][1000 genomes]
rs17011452	0.98[ASN][1000 genomes]
rs17011495	0.89[ASN][1000 genomes]
rs192855	0.87[EUR][1000 genomes]
rs2008243	0.90[ASN][1000 genomes]
rs2174183	0.80[ASN][1000 genomes]
rs220087	0.87[EUR][1000 genomes]
rs2654715	0.87[ASN][1000 genomes]
rs313068	1.00[CEU][hapmap];0.89[TSI][hapmap];0.86[EUR][1000 genomes]
rs313073	0.84[EUR][1000 genomes]
rs313108	0.86[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs313110	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs313111	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs313112	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs313113	0.87[EUR][1000 genomes]
rs313114	0.87[EUR][1000 genomes]
rs313116	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs313124	0.80[CHD][hapmap]
rs313125	0.81[EUR][1000 genomes]
rs4146615	0.82[ASN][1000 genomes]
rs433919	0.89[EUR][1000 genomes]
rs57259679	0.83[ASN][1000 genomes]
rs57840308	0.82[ASN][1000 genomes]
rs6817065	0.90[ASN][1000 genomes]
rs73846080	0.95[ASN][1000 genomes]
rs73846081	0.95[ASN][1000 genomes]
rs73846082	0.95[ASN][1000 genomes]
rs73846083	0.95[ASN][1000 genomes]
rs7660412	0.83[ASN][1000 genomes]
rs7683495	0.83[ASN][1000 genomes]
rs7697724	0.86[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.96[TSI][hapmap];0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1012833	chr4:127468474-127760933	Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv537242	chr4:127468474-127760933	Enhancers Weak transcription Genic enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv524850	chr4:127470903-127768849	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1013854	chr4:127508969-127663216	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv1009499	chr4:127532856-127659010	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
6	nsv537243	chr4:127532856-127659010	Weak transcription Active TSS Enhancers Genic enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv1007477	chr4:127561735-127726291	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv537244	chr4:127561735-127726291	Weak transcription Enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	esv2752024	chr4:127584697-127671942	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv595386	chr4:127597069-127668828	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv1028609	chr4:127597319-127664629	Enhancers Weak transcription Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13145010	INTU	cis	parietal	SCAN

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127626600-127631000	Weak transcription	K562	blood
2	chr4:127629400-127632400	Enhancers	HMEC	breast
3	chr4:127629600-127630400	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr4:127629600-127630400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:127629600-127630600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:127629600-127630600	Enhancers	NHEK	skin
7	chr4:127629600-127630800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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