Variant report

Variant	rs11759771
Chromosome Location	chr6:27118066-27118067
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:28)
CpG islands
(count:0)
Chromatin interactive
region (count:42)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:27117748-27118217	K562	blood:	n/a	n/a
2	MYC	chr6:27117963-27118176	K562	blood:	n/a	n/a
3	BDP1	chr6:27117831-27118145	K562	blood:	n/a	n/a
4	MYC	chr6:27118011-27118171	K562	blood:	n/a	n/a
5	ATF3	chr6:27117741-27118306	K562	blood:	n/a	n/a
6	ATF3	chr6:27117765-27118181	A549	lung:	n/a	n/a
7	ATF3	chr6:27117745-27118202	A549	lung:	n/a	n/a
8	ETS1	chr6:27117878-27118242	A549	lung:	n/a	chr6:27117990-27118003
9	CBX3	chr6:27117771-27118356	HCT-116	colon:	n/a	n/a
10	RPC155	chr6:27117872-27118259	K562	blood:	n/a	n/a
11	IRF1	chr6:27117919-27118091	K562	blood:	n/a	n/a
12	TEAD4	chr6:27117738-27118498	K562	blood:	n/a	n/a
13	CBX3	chr6:27117578-27118239	HCT-116	colon:	n/a	n/a
14	TBL1XR1	chr6:27117961-27118164	K562	blood:	n/a	n/a
15	MAX	chr6:27117730-27118388	HCT-116	colon:	n/a	n/a
16	EP300	chr6:27117803-27118182	GM12878	blood:	n/a	n/a
17	YY1	chr6:27117942-27118142	HCT-116	colon:	n/a	n/a
18	ATF3	chr6:27117772-27118383	HCT-116	colon:	n/a	n/a
19	TBP	chr6:27117915-27118069	HepG2	liver:	n/a	n/a
20	RCOR1	chr6:27118022-27118176	K562	blood:	n/a	n/a
21	TBP	chr6:27117875-27118097	H1-hESC	embryonic stem cell:	n/a	n/a
22	ZNF384	chr6:27117888-27118506	K562	blood:	n/a	n/a
23	POLR2A	chr6:27117688-27118208	K562	blood:	n/a	n/a
24	CBX3	chr6:27117889-27118262	K562	blood:	n/a	n/a
25	CEBPB	chr6:27118031-27118093	K562	blood:	n/a	n/a
26	POLR2A	chr6:27117879-27118221	HCT-116	colon:	n/a	n/a
27	GTF3C2	chr6:27117893-27118290	K562	blood:	n/a	n/a
28	ATF3	chr6:27117798-27118234	HCT-116	colon:	n/a	n/a

No data

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:27112142..27119511-chr6:27439134..27442830,9	K562	blood:
2	chr6:27117048..27119900-chr6:27858885..27861711,3	MCF-7	breast:
3	chr6:26229487..26231711-chr6:27116350..27119197,2	K562	blood:
4	chr6:27116267..27118681-chr6:27586916..27588668,2	K562	blood:
5	chr6:26123361..26125092-chr6:27117190..27119549,2	MCF-7	breast:
6	chr6:27047436..27049044-chr6:27116652..27118353,2	K562	blood:
7	chr20:52210047..52212145-chr6:27116560..27119327,2	MCF-7	breast:
8	chr6:27094943..27118570-chr6:27854106..27868030,101	K562	blood:
9	chr6:26030074..26034864-chr6:27112849..27118591,14	K562	blood:
10	chr6:27117077..27118620-chr6:27811336..27813416,2	K562	blood:
11	chr6:27115470..27118070-chr6:27629887..27631658,2	K562	blood:
12	chr6:26026480..26028197-chr6:27116538..27118082,2	K562	blood:
13	chr6:27111360..27127716-chr6:27768319..27787545,69	MCF-7	breast:
14	chr6:27093465..27120217-chr6:27768366..27817187,256	K562	blood:
15	chr6:26060606..26062295-chr6:27115552..27118165,2	K562	blood:
16	chr6:27113591..27118417-chr6:27832860..27835856,7	K562	blood:
17	chr6:27112528..27118803-chr6:27787647..27794623,16	K562	blood:
18	chr6:27117530..27120483-chr6:27722122..27723771,2	K562	blood:
19	chr6:26985479..26987950-chr6:27115470..27119189,3	K562	blood:
20	chr6:27117733..27121878-chr6:27773539..27777847,4	MCF-7	breast:
21	chr6:27116703..27118888-chr6:27241856..27243743,2	MCF-7	breast:
22	chr6:26205006..26206607-chr6:27116862..27119170,2	K562	blood:
23	chr14:49046971..49048491-chr6:27116511..27118075,2	K562	blood:
24	chr6:26587627..26591087-chr6:27116064..27118804,3	K562	blood:
25	chr6:27113131..27119021-chr6:27794877..27801018,12	K562	blood:
26	chr1:145381347..145383315-chr6:27115404..27118202,2	K562	blood:
27	chr6:27116381..27118425-chr6:27261911..27264171,2	K562	blood:
28	chr6:26215418..26221672-chr6:27112268..27118117,18	K562	blood:
29	chr6:26025629..26034912-chr6:27111740..27118591,16	K562	blood:
30	chr6:27116861..27118975-chr6:27145251..27147249,2	MCF-7	breast:
31	chr6:27105394..27120060-chr6:27855994..27866393,42	K562	blood:
32	chr6:27111807..27118148-chr6:27215986..27222524,9	K562	blood:
33	chr6:27111071..27119431-chr6:27801399..27810552,22	K562	blood:
34	chr6:26020714..26025029-chr6:27113708..27118688,4	K562	blood:
35	chr6:26322042..26323682-chr6:27115726..27118257,2	K562	blood:
36	chr6:26212467..26219073-chr6:27112587..27119625,13	MCF-7	breast:
37	chr6:26102393..26107181-chr6:27115545..27120891,6	K562	blood:
38	chr6:27116662..27118391-chr6:27520872..27522438,2	K562	blood:
39	chr6:27116132..27118211-chr9:130212545..130214193,2	K562	blood:
40	chr6:27116303..27118476-chr6:27504825..27506956,2	K562	blood:
41	chr6:27111749..27120986-chr6:27774460..27781468,38	K562	blood:
42	chr6:26593150..26599498-chr6:27112360..27118946,12	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HIST1H2AH-1	chr6:27117671-27118618	NONHSAT108347

No data

Variant related genes	Relation type
HIST1H2BK	TF binding region
ENSG00000203813	Chromatin interaction
ENSG00000196331	Chromatin interaction
ENSG00000168274	Chromatin interaction
ENSG00000124693	Chromatin interaction
ENSG00000197061	Chromatin interaction
ENSG00000220875	Chromatin interaction
ENSG00000233224	Chromatin interaction
ENSG00000171940	Chromatin interaction
ENSG00000196176	Chromatin interaction
ENSG00000197958	Chromatin interaction
ENSG00000185130	Chromatin interaction
ENSG00000182611	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000201558	Chromatin interaction
ENSG00000233822	Chromatin interaction
ENSG00000146109	Chromatin interaction
ENSG00000180596	Chromatin interaction
ENSG00000196374	Chromatin interaction
ENSG00000124529	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000184348	Chromatin interaction
ENSG00000196747	Chromatin interaction
ENSG00000137259	Chromatin interaction
ENSG00000217862	Chromatin interaction
ENSG00000180573	Chromatin interaction
ENSG00000198374	Chromatin interaction
ENSG00000233396	Chromatin interaction
ENSG00000184357	Chromatin interaction
ENSG00000148356	Chromatin interaction
ENSG00000187990	Chromatin interaction
ENSG00000238610	Chromatin interaction
ENSG00000197153	Chromatin interaction
ENSG00000197914	Chromatin interaction
ENSG00000112812	Chromatin interaction
ENSG00000096654	Chromatin interaction

Extended variants
information (count: 96 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10484392	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10484393	0.82[AFR][1000 genomes]
rs10484394	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1102566	1.00[AMR][1000 genomes]
rs1102568	1.00[AMR][1000 genomes]
rs11753245	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11753378	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11753580	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11753970	0.82[AFR][1000 genomes]
rs11755519	1.00[YRI][hapmap];0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11755651	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11755813	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11756304	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11757483	0.82[AFR][1000 genomes]
rs11757963	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs11758093	1.00[YRI][hapmap];0.82[AFR][1000 genomes]
rs11759167	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12110621	0.82[AFR][1000 genomes]
rs12111326	0.82[AFR][1000 genomes]
rs16894241	1.00[AMR][1000 genomes]
rs16894325	1.00[YRI][hapmap]
rs16894520	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16895602	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs16897417	1.00[AMR][1000 genomes]
rs16897529	1.00[YRI][hapmap]
rs2021278	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2022271	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2092113	1.00[AMR][1000 genomes]
rs55656206	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55867104	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55925824	1.00[AMR][1000 genomes]
rs56141916	1.00[AMR][1000 genomes]
rs56156722	1.00[AMR][1000 genomes]
rs57603020	1.00[AMR][1000 genomes]
rs58130043	1.00[AMR][1000 genomes]
rs58265076	1.00[AMR][1000 genomes]
rs58900251	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58977511	1.00[AMR][1000 genomes]
rs59757260	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60259667	1.00[AMR][1000 genomes]
rs61185098	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs61392315	1.00[AMR][1000 genomes]
rs73737997	1.00[AMR][1000 genomes]
rs73737999	1.00[AMR][1000 genomes]
rs73738226	1.00[AMR][1000 genomes]
rs73738236	1.00[AMR][1000 genomes]
rs73738237	1.00[AMR][1000 genomes]
rs73738707	1.00[AMR][1000 genomes]
rs73738713	1.00[AMR][1000 genomes]
rs73738717	1.00[AMR][1000 genomes]
rs73738718	1.00[AMR][1000 genomes]
rs73738731	1.00[AMR][1000 genomes]
rs73738732	1.00[AMR][1000 genomes]
rs73738733	1.00[AMR][1000 genomes]
rs73738734	1.00[AMR][1000 genomes]
rs73738738	1.00[AMR][1000 genomes]
rs73738739	1.00[AMR][1000 genomes]
rs73738741	1.00[AMR][1000 genomes]
rs73738749	1.00[AMR][1000 genomes]
rs73739510	1.00[AMR][1000 genomes]
rs73739515	1.00[AMR][1000 genomes]
rs73739517	1.00[AMR][1000 genomes]
rs73739519	1.00[AMR][1000 genomes]
rs73739521	1.00[AMR][1000 genomes]
rs73739522	1.00[AMR][1000 genomes]
rs73739531	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739532	0.83[AFR][1000 genomes]
rs73739534	1.00[AMR][1000 genomes]
rs73739545	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739557	1.00[AMR][1000 genomes]
rs73739578	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739581	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739582	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739586	0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739587	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739589	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739591	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739594	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739595	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739598	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739600	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73739601	0.82[AFR][1000 genomes]
rs73740278	1.00[AMR][1000 genomes]
rs73740404	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73740405	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73740406	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73740409	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73740414	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73740432	1.00[AMR][1000 genomes]
rs7449898	1.00[AMR][1000 genomes]
rs7755679	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs858966	1.00[AMR][1000 genomes]
rs858971	1.00[AMR][1000 genomes]
rs9366681	1.00[AMR][1000 genomes]
rs996246	1.00[AMR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948921	chr6:26556890-27443957	Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	472 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:27115600-27124800	Weak transcription	Primary B cells from cord blood	blood
2	chr6:27115600-27125000	Weak transcription	Right Atrium	heart
3	chr6:27116000-27123000	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:27116200-27122600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:27117200-27122200	Weak transcription	GM12878-XiMat	blood
6	chr6:27117200-27122800	Weak transcription	Primary hematopoietic stem cells	blood
7	chr6:27117200-27124800	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr6:27117400-27122000	Weak transcription	Dnd41	blood
9	chr6:27117400-27122600	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr6:27117400-27122800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr6:27117400-27123000	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr6:27118000-27118600	Enhancers	K562	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links