Variant report

Variant	rs6576743
Chromosome Location	chr1:85501052-85501053
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:85494419..85496418-chr1:85499652..85502502,2	K562	blood:
2	chr1:85494641..85496503-chr1:85499761..85501491,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000055732	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10782535	1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs10873675	1.00[ASN][1000 genomes]
rs1458401	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17371429	1.00[EUR][1000 genomes]
rs2028304	0.90[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2039814	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs486647	1.00[ASN][1000 genomes]
rs4907122	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs496561	1.00[ASN][1000 genomes]
rs499579	1.00[ASN][1000 genomes]
rs511765	1.00[ASN][1000 genomes]
rs517156	1.00[ASN][1000 genomes]
rs531169	1.00[ASN][1000 genomes]
rs534908	1.00[ASN][1000 genomes]
rs562126	1.00[ASN][1000 genomes]
rs586403	1.00[ASN][1000 genomes]
rs589227	1.00[ASN][1000 genomes]
rs599137	1.00[ASN][1000 genomes]
rs599888	1.00[ASN][1000 genomes]
rs607298	1.00[ASN][1000 genomes]
rs614194	0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs61769365	1.00[ASN][1000 genomes]
rs641427	1.00[ASN][1000 genomes]
rs6576737	1.00[ASN][1000 genomes]
rs6576740	1.00[ASW][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6576742	1.00[ASN][1000 genomes]
rs664763	1.00[ASN][1000 genomes]
rs6679539	0.90[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap]
rs6684210	1.00[ASN][1000 genomes]
rs679932	1.00[ASN][1000 genomes]
rs680330	1.00[ASN][1000 genomes]
rs7519717	1.00[ASW][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7522239	0.90[LWK][hapmap];0.83[MKK][hapmap];1.00[YRI][hapmap]
rs7533496	1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[ASN][1000 genomes]
rs7537692	1.00[ASN][1000 genomes]
rs920340	1.00[ASN][1000 genomes]
rs9804097	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv470724	chr1:85334788-85585260	Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv462383	chr1:85334788-85594466	Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	nsv546700	chr1:85334788-85594466	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
4	nsv947434	chr1:85334915-85594135	Bivalent/Poised TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv1006994	chr1:85454304-86327679	Active TSS Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	72 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:85485400-85513000	Weak transcription	Pancreas	Pancrea
2	chr1:85485800-85505200	Weak transcription	Duodenum Mucosa	Duodenum
3	chr1:85486000-85513000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr1:85495000-85512800	Weak transcription	HMEC	breast
5	chr1:85496800-85512400	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr1:85497000-85501800	Weak transcription	Fetal Intestine Small	intestine
7	chr1:85498600-85506000	Weak transcription	Aorta	Aorta
8	chr1:85499000-85501200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:85499400-85501200	Strong transcription	Fetal Intestine Large	intestine
10	chr1:85499600-85506000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr1:85500000-85501200	Enhancers	Adipose Nuclei	Adipose
12	chr1:85501000-85501200	Enhancers	Right Atrium	heart
13	chr1:85501000-85501400	Enhancers	Fetal Heart	heart

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