Variant report

Variant	rs17159869
Chromosome Location	chr1:146581836-146581837
allele	C/T
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	chr1:146575479..146577684-chr1:146581433..146583404,2	MCF-7	breast:
2	chr1:146580378..146582055-chr1:146607503..146610346,2	MCF-7	breast:
3	chr1:146554000..146557123-chr1:146579975..146584093,5	MCF-7	breast:
4	chr1:146580362..146583637-chr1:146585824..146588988,4	MCF-7	breast:
5	chr1:146581474..146583027-chr1:146601887..146603711,2	MCF-7	breast:
6	chr1:146563238..146565126-chr1:146580992..146583533,2	MCF-7	breast:
7	chr1:146554672..146558646-chr1:146578367..146584066,7	K562	blood:
8	chr1:146581417..146584376-chr1:146587481..146589591,2	K562	blood:
9	chr1:146580035..146583266-chr1:146583930..146586472,4	MCF-7	breast:
10	chr1:146580735..146583076-chr1:146639979..146642635,2	MCF-7	breast:
11	chr1:146554430..146558928-chr1:146575655..146584919,15	K562	blood:
12	chr1:146581119..146583919-chr1:146708299..146710988,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000230832	Chromatin interaction

Extended variants
information (count: 138 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:122)

rs_ID	r²[population]
rs10494242	1.00[CEU][hapmap]
rs10494243	1.00[CEU][hapmap]
rs11239933	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs12089108	1.00[EUR][1000 genomes]
rs17159878	1.00[CEU][hapmap];0.92[AMR][1000 genomes]
rs17159880	1.00[CEU][hapmap];0.92[AMR][1000 genomes]
rs17159882	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs17159883	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs17159890	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs17159909	0.83[AMR][1000 genomes]
rs17160790	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17355733	0.91[AMR][1000 genomes]
rs17355740	0.91[AMR][1000 genomes]
rs17355768	0.91[AMR][1000 genomes]
rs17355796	0.91[AMR][1000 genomes]
rs17355969	1.00[CEU][hapmap]
rs17356024	1.00[CEU][hapmap]
rs17359851	1.00[CEU][hapmap];0.91[AMR][1000 genomes]
rs17359865	0.91[AMR][1000 genomes]
rs17359879	0.91[AMR][1000 genomes]
rs17360003	1.00[CEU][hapmap]
rs28381225	0.91[AMR][1000 genomes]
rs28381230	0.91[AMR][1000 genomes]
rs34838459	0.91[AMR][1000 genomes]
rs41295821	0.91[AMR][1000 genomes]
rs41312712	0.91[AMR][1000 genomes]
rs55653839	0.91[AMR][1000 genomes]
rs55701100	0.83[AMR][1000 genomes]
rs55705039	0.92[AMR][1000 genomes]
rs55797044	0.83[AMR][1000 genomes]
rs55888723	0.91[AMR][1000 genomes]
rs56004039	0.92[AMR][1000 genomes]
rs56053798	0.83[AMR][1000 genomes]
rs56074784	0.83[AMR][1000 genomes]
rs56079929	0.91[AMR][1000 genomes]
rs56163155	0.92[AMR][1000 genomes]
rs56175228	0.92[AMR][1000 genomes]
rs56182581	0.91[AMR][1000 genomes]
rs56743621	0.83[AMR][1000 genomes]
rs56833520	0.83[AMR][1000 genomes]
rs57211600	1.00[AMR][1000 genomes]
rs57247303	0.91[AMR][1000 genomes]
rs57570045	0.91[AMR][1000 genomes]
rs58423612	0.83[AMR][1000 genomes]
rs58785568	0.83[AMR][1000 genomes]
rs59665085	0.85[AMR][1000 genomes]
rs60280517	0.83[AMR][1000 genomes]
rs60603428	0.92[AMR][1000 genomes]
rs61374973	0.92[AMR][1000 genomes]
rs61549987	0.91[AMR][1000 genomes]
rs62623392	0.91[AMR][1000 genomes]
rs62623395	0.91[AMR][1000 genomes]
rs6658465	0.83[AMR][1000 genomes]
rs6659191	1.00[CEU][hapmap];0.91[AMR][1000 genomes]
rs6663107	0.92[AMR][1000 genomes]
rs6665580	1.00[CEU][hapmap]
rs6665934	1.00[CEU][hapmap]
rs6668865	1.00[CEU][hapmap]
rs6678588	1.00[CEU][hapmap];0.83[AMR][1000 genomes]
rs6679406	0.83[AMR][1000 genomes]
rs6684454	1.00[CEU][hapmap]
rs6690541	0.91[AMR][1000 genomes]
rs72706446	0.92[AMR][1000 genomes]
rs72706447	0.92[AMR][1000 genomes]
rs72706448	0.83[AMR][1000 genomes]
rs72706449	0.83[AMR][1000 genomes]
rs72706450	0.83[AMR][1000 genomes]
rs72706451	0.83[AMR][1000 genomes]
rs72706452	0.83[AMR][1000 genomes]
rs72706456	0.83[AMR][1000 genomes]
rs72706457	0.83[AMR][1000 genomes]
rs72706465	0.83[AMR][1000 genomes]
rs72706469	0.83[AMR][1000 genomes]
rs72706474	0.83[AMR][1000 genomes]
rs72706496	0.83[AMR][1000 genomes]
rs72706497	0.83[AMR][1000 genomes]
rs72706499	0.83[AMR][1000 genomes]
rs72706501	0.91[AMR][1000 genomes]
rs72706502	0.91[AMR][1000 genomes]
rs72708503	0.91[AMR][1000 genomes]
rs72708504	0.91[AMR][1000 genomes]
rs72708505	0.91[AMR][1000 genomes]
rs72708508	0.91[AMR][1000 genomes]
rs72708509	0.91[AMR][1000 genomes]
rs72708510	0.91[AMR][1000 genomes]
rs72708511	0.91[AMR][1000 genomes]
rs72708514	0.91[AMR][1000 genomes]
rs72708515	0.91[AMR][1000 genomes]
rs72708517	0.91[AMR][1000 genomes]
rs72708518	0.91[AMR][1000 genomes]
rs72708519	0.91[AMR][1000 genomes]
rs72708520	0.91[AMR][1000 genomes]
rs72708521	0.91[AMR][1000 genomes]
rs72708526	0.83[AMR][1000 genomes]
rs72708527	0.91[AMR][1000 genomes]
rs72708529	0.91[AMR][1000 genomes]
rs72708530	0.91[AMR][1000 genomes]
rs72708535	0.91[AMR][1000 genomes]
rs72708537	0.91[AMR][1000 genomes]
rs72708538	0.91[AMR][1000 genomes]
rs72708539	0.91[AMR][1000 genomes]
rs72708544	0.91[AMR][1000 genomes]
rs72708545	0.91[AMR][1000 genomes]
rs72708547	0.91[AMR][1000 genomes]
rs72708548	0.83[AMR][1000 genomes]
rs72708553	0.91[AMR][1000 genomes]
rs72708554	0.91[AMR][1000 genomes]
rs72708555	0.91[AMR][1000 genomes]
rs72708556	0.91[AMR][1000 genomes]
rs72708558	0.91[AMR][1000 genomes]
rs72708563	0.91[AMR][1000 genomes]
rs72708564	0.91[AMR][1000 genomes]
rs72708565	0.91[AMR][1000 genomes]
rs74119827	0.92[AMR][1000 genomes]
rs7519713	1.00[CEU][hapmap]
rs7521249	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs7528172	1.00[CEU][hapmap]
rs7532458	1.00[CEU][hapmap]
rs7541245	1.00[CEU][hapmap]
rs7547138	0.91[AMR][1000 genomes]
rs7547698	1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7556347	0.91[AMR][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	esv2757753	chr1:145883119-146697542	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
2	nsv872251	chr1:146152553-146803630	Weak transcription Bivalent Enhancer Strong transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	95 gene(s)	inside rSNPs	diseases
3	nsv872252	chr1:146471863-147398135	Weak transcription Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	112 gene(s)	inside rSNPs	diseases
4	nsv999546	chr1:146507577-147356574	Weak transcription Genic enhancers Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
5	nsv535123	chr1:146507577-147356574	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
6	nsv492188	chr1:146507649-147381479	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
7	nsv916754	chr1:146507711-147417736	Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	113 gene(s)	inside rSNPs	diseases
8	nsv547673	chr1:146510112-147398135	Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
9	nsv547674	chr1:146522722-147396797	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	111 gene(s)	inside rSNPs	diseases
10	nsv998341	chr1:146531446-147384720	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
11	nsv535124	chr1:146531446-147384720	Flanking Active TSS Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
12	nsv1003493	chr1:146531446-147389944	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
13	nsv998209	chr1:146543722-147384720	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
14	nsv535126	chr1:146543722-147384720	Flanking Active TSS Bivalent Enhancer Weak transcription Strong transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	110 gene(s)	inside rSNPs	diseases
15	nsv872255	chr1:146550780-146969712	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	93 gene(s)	inside rSNPs	diseases
16	nsv872256	chr1:146556596-147410973	Flanking Active TSS Weak transcription Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:146579200-146585400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:146580200-146582600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:146580800-146582000	Flanking Active TSS	Liver	Liver
4	chr1:146581000-146583400	Enhancers	HepG2	liver

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