Variant report

Variant	rs3016759
Chromosome Location	chr11:64412725-64412726
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr11:64411167-64429413	U87	brain:	n/a	n/a
2	POLR2A	chr11:64411167-64414430	U87	brain:	n/a	n/a
3	CTCF	chr11:64412383-64412808	K562	blood:	n/a	n/a
4	RAD21	chr11:64412149-64412813	SK-N-SH	brain:	n/a	chr11:64412470-64412479 chr11:64412596-64412609
5	TEAD4	chr11:64412366-64412757	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr11:64412640-64412790	GM12873	blood:	n/a	n/a
7	POLR2A	chr11:64412359-64412736	U87	brain:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:64411217..64413501-chr11:64452044..64454513,2	K562	blood:
2	chr11:64411039..64413414-chr11:64416751..64419165,4	K562	blood:
3	11:64187725-64189071..11:64402707-64415880	K562	blood:
4	chr11:64320459..64321631-chr11:64411779..64413112,6	MCF-7	breast:

Variant related genes	Relation type
ENSG00000237410	TF binding region
NRXN2	TF binding region
ENSG00000231492	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs1212539	1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs1212851	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17146100	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17146110	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17146119	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs1787671	1.00[AMR][1000 genomes]
rs2022049	0.85[AMR][1000 genomes]
rs2518908	1.00[AMR][1000 genomes]
rs2666561	1.00[AMR][1000 genomes]
rs2666562	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2904961	1.00[AMR][1000 genomes]
rs2959651	1.00[AMR][1000 genomes]
rs3016758	0.96[AFR][1000 genomes]
rs475704	1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs512926	0.92[YRI][hapmap]
rs516041	1.00[AMR][1000 genomes]
rs534052	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs534073	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs535606	1.00[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs541305	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs545167	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs545819	1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs546323	1.00[AMR][1000 genomes]
rs550930	1.00[AMR][1000 genomes]
rs553618	1.00[AMR][1000 genomes]
rs559095	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs559977	1.00[AMR][1000 genomes]
rs565688	0.83[AMR][1000 genomes]
rs573545	1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs579175	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492134	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492139	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492140	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73492144	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7948607	1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897693	chr11:64305452-64440920	Enhancers Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
2	esv2422214	chr11:64312491-64483418	Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
3	nsv832188	chr11:64315368-64485209	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
4	nsv468596	chr11:64334114-64527080	Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
5	nsv555195	chr11:64334114-64527080	Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
6	nsv897694	chr11:64334114-64584959	Weak transcription Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
7	nsv818842	chr11:64345448-64546391	Bivalent Enhancer Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
8	nsv528506	chr11:64345448-64701030	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Active TSS Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
9	nsv555196	chr11:64357072-64559898	Enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	77 gene(s)	inside rSNPs	diseases
10	nsv897695	chr11:64357072-64701030	Weak transcription Genic enhancers Enhancers Active TSS Transcr. at gene 5' and 3' Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	1075 gene(s)	inside rSNPs	diseases
11	nsv897696	chr11:64365796-64412877	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv1051350	chr11:64372906-64533632	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
13	nsv555198	chr11:64373899-64573589	Weak transcription Transcr. at gene 5' and 3' Genic enhancers Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
14	esv1804443	chr11:64386453-64534785	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:64411400-64412800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
2	chr11:64411400-64413000	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr11:64411400-64413000	Bivalent Enhancer	Fetal Thymus	thymus
4	chr11:64411400-64413200	Bivalent Enhancer	NHDF-Ad	bronchial
5	chr11:64411400-64413400	Bivalent Enhancer	Fetal Intestine Large	intestine
6	chr11:64411400-64413600	Bivalent Enhancer	Fetal Intestine Small	intestine
7	chr11:64411600-64412800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
8	chr11:64411600-64412800	Bivalent Enhancer	Fetal Stomach	stomach
9	chr11:64411600-64413200	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr11:64411600-64427800	Weak transcription	Aorta	Aorta
11	chr11:64411800-64412800	Enhancers	Primary hematopoietic stem cells	blood
12	chr11:64411800-64412800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
13	chr11:64411800-64412800	Enhancers	Fetal Brain Male	brain
14	chr11:64411800-64413000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr11:64411800-64413800	Bivalent Enhancer	Fetal Muscle Leg	muscle
16	chr11:64411800-64414200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr11:64411800-64416800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr11:64411800-64420000	Weak transcription	Brain Substantia Nigra	brain
19	chr11:64411800-64420200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr11:64411800-64420400	Weak transcription	Brain Angular Gyrus	brain
21	chr11:64412000-64413800	Enhancers	Primary hematopoietic stem cells short term culture	blood
22	chr11:64412000-64416400	Weak transcription	Ovary	ovary
23	chr11:64412200-64412800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
24	chr11:64412200-64412800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
25	chr11:64412200-64412800	Enhancers	Fetal Kidney	kidney
26	chr11:64412200-64413000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
27	chr11:64412200-64413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr11:64412200-64413000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:64412200-64415200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr11:64412200-64416800	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr11:64412400-64412800	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
32	chr11:64412400-64414800	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr11:64412400-64428200	Weak transcription	Right Atrium	heart
34	chr11:64412600-64412800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
35	chr11:64412600-64412800	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
36	chr11:64412600-64412800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr11:64412600-64412800	Bivalent Enhancer	Adipose Nuclei	Adipose
38	chr11:64412600-64413000	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
39	chr11:64412600-64413600	Weak transcription	Fetal Brain Female	brain
40	chr11:64412600-64413800	Weak transcription	Brain Germinal Matrix	brain
41	chr11:64412600-64419800	Weak transcription	Brain Hippocampus Middle	brain
42	chr11:64412600-64420000	Weak transcription	Brain Anterior Caudate	brain
43	chr11:64412600-64425600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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