Variant report

Variant	rs11757754
Chromosome Location	chr6:26219744-26219745
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:26219725-26222587	K562	blood:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr6:26219518..26221470-chr6:26568147..26570701,2	K562	blood:
2	chr6:26217931..26220550-chr6:26594492..26597110,4	K562	blood:
3	chr6:26215032..26220721-chr6:27098305..27106549,21	K562	blood:
4	chr6:26215488..26220486-chr6:27788576..27794997,7	K562	blood:
5	chr6:26215418..26221672-chr6:27112268..27118117,18	K562	blood:
6	chr6:26020264..26023736-chr6:26216792..26220704,4	MCF-7	breast:
7	chr6:26217037..26219945-chr6:26536626..26539021,2	K562	blood:
8	chr6:26055764..26057537-chr6:26219301..26220936,2	MCF-7	breast:
9	chr6:26219007..26221610-chr6:26537432..26539647,2	MCF-7	breast:
10	chr6:26210558..26220469-chr6:27093552..27103796,28	K562	blood:
11	chr6:26215236..26220335-chr6:27112505..27117796,8	MCF-7	breast:
12	chr6:26217116..26219858-chr6:26520988..26523268,4	K562	blood:

No data

Variant related genes	Relation type
HIST1H2BG	TF binding region
ENSG00000196787	Chromatin interaction
ENSG00000182952	Chromatin interaction
ENSG00000187837	Chromatin interaction
ENSG00000184825	Chromatin interaction
ENSG00000198366	Chromatin interaction
ENSG00000124635	Chromatin interaction
ENSG00000197238	Chromatin interaction
ENSG00000197903	Chromatin interaction
ENSG00000228223	Chromatin interaction
ENSG00000265565	Chromatin interaction
ENSG00000196176	Chromatin interaction

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10452600	0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10484436	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11753131	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][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]
rs11753625	0.88[EUR][1000 genomes]
rs11753655	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11754744	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11755210	0.86[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11755943	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[YRI][hapmap];0.85[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11757394	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11758351	0.82[YRI][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11759904	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1341759	0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891378	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891397	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891401	0.89[CHB][hapmap];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16891405	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs16891443	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891446	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891455	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891456	0.99[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891466	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891467	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16891474	0.92[AFR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16891481	0.89[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17598927	0.89[CHB][hapmap];0.86[EUR][1000 genomes]
rs1997768	1.00[CEU][hapmap];0.89[CHB][hapmap];0.82[YRI][hapmap];0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2022448	0.85[CEU][hapmap];0.89[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2050948	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2050950	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2069018	0.85[CEU][hapmap];0.89[CHB][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2069019	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2069020	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2143345	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2143346	0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2143347	0.89[CHB][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2183948	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs3734530	0.88[CHB][hapmap]
rs3757135	0.89[CHB][hapmap];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs41266801	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs41266807	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs55643278	1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55815656	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs55848726	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56186759	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56220351	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56398712	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029920	chr6:25638507-26585842	Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
2	nsv538162	chr6:25638507-26585842	Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Weak transcription Strong transcription Enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1215 gene(s)	inside rSNPs	diseases
3	nsv1030351	chr6:25813178-26352046	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1189 gene(s)	inside rSNPs	diseases
4	nsv1023453	chr6:25853830-26528250	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	1201 gene(s)	inside rSNPs	diseases
5	nsv1025237	chr6:25874326-26280867	Flanking Active TSS Active TSS Enhancers Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
6	nsv538163	chr6:25874326-26280867	Enhancers Flanking Active TSS Strong transcription Active TSS Weak transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1166 gene(s)	inside rSNPs	diseases
7	nsv428137	chr6:25987413-26351920	Enhancers Flanking Active TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1181 gene(s)	inside rSNPs	diseases
8	nsv916992	chr6:25991630-26280921	Active TSS Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1159 gene(s)	inside rSNPs	diseases
9	nsv1028232	chr6:26005449-26319756	Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1171 gene(s)	inside rSNPs	diseases
10	nsv870314	chr6:26008435-26280807	Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1151 gene(s)	inside rSNPs	diseases
11	nsv1023457	chr6:26014014-26305407	Active TSS Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1170 gene(s)	inside rSNPs	diseases
12	nsv1025493	chr6:26026870-26223838	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1001 gene(s)	inside rSNPs	diseases
13	nsv1023979	chr6:26026870-26287399	Flanking Active TSS Enhancers Bivalent/Poised TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1113 gene(s)	inside rSNPs	diseases
14	nsv1015782	chr6:26026870-26323895	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1114 gene(s)	inside rSNPs	diseases
15	nsv1018665	chr6:26026870-26352046	Flanking Active TSS Weak transcription Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1116 gene(s)	inside rSNPs	diseases
16	nsv482348	chr6:26082709-26261136	Enhancers Flanking Active TSS Active TSS Weak transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	799 gene(s)	inside rSNPs	diseases
17	nsv883490	chr6:26172219-26231608	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	316 gene(s)	inside rSNPs	diseases
18	nsv1021294	chr6:26190316-26246784	Active TSS Flanking Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	309 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:85 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:26217600-26224000	Weak transcription	Pancreas	Pancrea
2	chr6:26217800-26225400	Weak transcription	Spleen	Spleen
3	chr6:26218000-26223600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr6:26218000-26223600	Weak transcription	Right Atrium	heart
5	chr6:26218200-26222800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
6	chr6:26218200-26222800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
7	chr6:26218200-26223000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr6:26218400-26220000	Weak transcription	NHEK	skin
9	chr6:26218400-26222600	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr6:26218400-26222800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr6:26218400-26222800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
12	chr6:26218400-26222800	Weak transcription	Primary T helper cells fromperipheralblood	blood
13	chr6:26218400-26223200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
14	chr6:26218400-26223200	Weak transcription	Fetal Stomach	stomach
15	chr6:26218400-26223600	Weak transcription	Liver	Liver
16	chr6:26218400-26223800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:26218600-26220000	Weak transcription	Primary hematopoietic stem cells	blood
18	chr6:26218600-26220400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr6:26218600-26221000	Enhancers	Dnd41	blood
20	chr6:26218600-26222600	Weak transcription	Primary B cells from peripheral blood	blood
21	chr6:26218600-26222600	Weak transcription	HUVEC	blood vessel
22	chr6:26218600-26222800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
23	chr6:26218600-26222800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr6:26218600-26222800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr6:26218600-26222800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr6:26218600-26222800	Weak transcription	Fetal Lung	lung
27	chr6:26218600-26223000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:26218600-26223000	Weak transcription	Osteobl	bone
29	chr6:26218600-26223200	Weak transcription	Duodenum Mucosa	Duodenum
30	chr6:26218600-26223200	Weak transcription	NH-A	brain
31	chr6:26218600-26223200	Weak transcription	NHLF	lung
32	chr6:26218600-26223400	Weak transcription	Primary neutrophils fromperipheralblood	blood
33	chr6:26218600-26223800	Weak transcription	Placenta	Placenta
34	chr6:26218800-26220600	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr6:26218800-26220600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr6:26218800-26221000	Enhancers	GM12878-XiMat	blood
37	chr6:26218800-26221200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr6:26218800-26222000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr6:26218800-26222600	Weak transcription	Primary T cells fromperipheralblood	blood
40	chr6:26218800-26222600	Weak transcription	HMEC	breast
41	chr6:26218800-26222800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr6:26218800-26222800	Weak transcription	Primary T cells from cord blood	blood
43	chr6:26218800-26222800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr6:26218800-26222800	Weak transcription	Fetal Brain Female	brain
45	chr6:26218800-26222800	Weak transcription	Sigmoid Colon	Sigmoid Colon
46	chr6:26218800-26223000	Enhancers	Fetal Thymus	thymus
47	chr6:26219000-26220000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr6:26219000-26220200	Weak transcription	Primary B cells from cord blood	blood
49	chr6:26219000-26220200	Weak transcription	Brain Germinal Matrix	brain
50	chr6:26219000-26221800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links