Variant report

Variant	rs2267010
Chromosome Location	chr22:23534366-23534367
allele	A/G
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:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr22:23533010..23534823-chr22:23562883..23564469,2	MCF-7	breast:
2	chr22:23532493..23535088-chr22:23609980..23612908,2	MCF-7	breast:
3	chr22:23534227..23534938-chr22:23611497..23612086,2	MCF-7	breast:
4	chr22:23520992..23525924-chr22:23533484..23536719,11	MCF-7	breast:
5	chr22:23534323..23535865-chr22:23538315..23540375,2	MCF-7	breast:
6	chr22:23533236..23535920-chr22:23537412..23541871,4	MCF-7	breast:
7	chr22:23534219..23534727-chr22:23611586..23612126,2	MCF-7	breast:
8	chr22:23533495..23535148-chr22:23585840..23588084,2	MCF-7	breast:
9	chr22:23533489..23536061-chr22:23622372..23624122,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000236794	Chromatin interaction
ENSG00000186716	Chromatin interaction

Extended variants
information (count: 70 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11704365	0.86[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11912218	0.82[YRI][hapmap]
rs12167308	0.81[JPT][hapmap]
rs2071431	0.85[JPT][hapmap]
rs2267007	0.81[JPT][hapmap]
rs2267009	0.85[JPT][hapmap]
rs2267011	0.85[JPT][hapmap]
rs2267012	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2267014	1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2330361	0.81[JPT][hapmap]
rs3761418	0.85[JPT][hapmap]
rs4820541	0.81[JPT][hapmap]
rs4820542	0.85[JPT][hapmap]
rs4822369	0.81[JPT][hapmap]
rs5751583	1.00[ASW][hapmap];1.00[CEU][hapmap];0.90[MEX][hapmap];0.91[TSI][hapmap]
rs5751593	0.81[JPT][hapmap]
rs5751596	0.81[JPT][hapmap]
rs5751603	0.85[JPT][hapmap]
rs5751605	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5751606	0.85[JPT][hapmap]
rs5759607	0.81[JPT][hapmap]
rs5759608	0.81[JPT][hapmap]
rs5759611	0.81[JPT][hapmap]
rs5759612	0.81[JPT][hapmap]
rs5759613	0.81[JPT][hapmap]
rs5759614	0.81[JPT][hapmap]
rs5759615	0.81[JPT][hapmap]
rs5759619	0.81[JPT][hapmap]
rs5759620	0.81[JPT][hapmap]
rs5759621	0.81[JPT][hapmap]
rs5759631	0.85[JPT][hapmap]
rs5759639	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5996483	0.85[JPT][hapmap]
rs60054645	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62220914	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs713617	0.85[JPT][hapmap]
rs713682	0.81[JPT][hapmap]
rs737819	0.81[JPT][hapmap]
rs756633	0.81[JPT][hapmap]
rs768513	0.86[CHB][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs8142746	0.81[JPT][hapmap]
rs9612237	0.84[JPT][hapmap]
rs9612248	0.85[JPT][hapmap]
rs9612252	0.80[JPT][hapmap]
rs9612257	0.90[JPT][hapmap];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv915235	chr22:22971768-23650987	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	101 gene(s)	inside rSNPs	diseases
2	esv3388845	chr22:22973346-23652447	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	100 gene(s)	inside rSNPs	diseases
3	nsv531799	chr22:22993679-23642142	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
4	nsv1061433	chr22:22997799-23649107	Enhancers Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
5	nsv521695	chr22:22998337-23648009	Weak transcription Strong transcription Genic enhancers Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
6	nsv915236	chr22:22998337-23650987	Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
7	nsv588512	chr22:22998337-23667731	Flanking Active TSS Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	99 gene(s)	inside rSNPs	diseases
8	nsv531800	chr22:23002708-23648163	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
9	nsv916593	chr22:23002709-23648790	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
10	nsv993496	chr22:23002709-23654222	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
11	nsv1067002	chr22:23007167-23643363	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
12	nsv1067324	chr22:23007367-23654223	Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
13	nsv533839	chr22:23012013-23643223	Flanking Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
14	nsv916933	chr22:23012069-23654237	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	97 gene(s)	inside rSNPs	diseases
15	nsv531801	chr22:23028586-23657804	Enhancers Weak transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	92 gene(s)	inside rSNPs	diseases
16	nsv531802	chr22:23046186-23627391	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	85 gene(s)	inside rSNPs	diseases
17	nsv1060509	chr22:23055148-23648719	Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS 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	83 gene(s)	inside rSNPs	diseases
18	nsv1056324	chr22:23055148-23750989	Active TSS Weak transcription Genic enhancers Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
19	nsv1062780	chr22:23060449-23648719	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
20	nsv948942	chr22:23063178-23645718	Enhancers Weak transcription Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	82 gene(s)	inside rSNPs	diseases
21	nsv1063200	chr22:23097177-23643224	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	80 gene(s)	inside rSNPs	diseases
22	nsv949250	chr22:23157485-23645718	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	69 gene(s)	inside rSNPs	diseases
23	nsv1057659	chr22:23400739-24138788	Enhancers Weak transcription Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
24	nsv1058604	chr22:23497533-23545751	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
25	nsv588598	chr22:23530168-23638025	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:120 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23526000-23535200	Weak transcription	Stomach Mucosa	stomach
2	chr22:23526000-23546000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr22:23526200-23535800	Weak transcription	Aorta	Aorta
4	chr22:23526200-23546800	Weak transcription	Colonic Mucosa	Colon
5	chr22:23526400-23535000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr22:23526400-23536000	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr22:23526400-23560800	Weak transcription	A549	lung
8	chr22:23527000-23535600	Strong transcription	NHEK	skin
9	chr22:23527000-23536000	Weak transcription	HMEC	breast
10	chr22:23527000-23541400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr22:23527000-23547200	Weak transcription	Fetal Kidney	kidney
12	chr22:23527200-23534400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr22:23527200-23535600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr22:23527200-23535600	Strong transcription	Fetal Stomach	stomach
15	chr22:23527200-23536000	Weak transcription	HSMM	muscle
16	chr22:23527200-23545400	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr22:23527200-23547000	Weak transcription	Rectal Mucosa Donor 31	rectum
18	chr22:23527400-23535200	Weak transcription	Fetal Lung	lung
19	chr22:23527400-23535400	Weak transcription	Hela-S3	cervix
20	chr22:23527400-23545400	Weak transcription	Duodenum Mucosa	Duodenum
21	chr22:23527600-23541200	Weak transcription	Cortex derived primary cultured neurospheres	brain
22	chr22:23527600-23544200	Strong transcription	Fetal Intestine Small	intestine
23	chr22:23528400-23540600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
24	chr22:23528600-23534400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr22:23529000-23542400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
26	chr22:23529400-23536400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr22:23529600-23552800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr22:23530000-23536200	Strong transcription	Monocytes-CD14+_RO01746	blood
29	chr22:23530000-23536400	Genic enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr22:23530200-23545200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
31	chr22:23530400-23535800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr22:23530400-23545600	Weak transcription	Liver	Liver
33	chr22:23530400-23558800	Weak transcription	Small Intestine	intestine
34	chr22:23530600-23535400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr22:23530600-23535800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr22:23530600-23535800	Weak transcription	HSMMtube	muscle
37	chr22:23530600-23536000	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr22:23530600-23545400	Weak transcription	Colon Smooth Muscle	Colon
39	chr22:23530600-23557200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
40	chr22:23530800-23534400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr22:23530800-23534800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr22:23530800-23534800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr22:23530800-23535000	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr22:23530800-23535000	Weak transcription	Fetal Brain Female	brain
45	chr22:23530800-23535600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr22:23530800-23535800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr22:23530800-23535800	Weak transcription	Brain Substantia Nigra	brain
48	chr22:23530800-23536000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr22:23530800-23536000	Weak transcription	NHLF	lung
50	chr22:23530800-23536400	Strong transcription	Dnd41	blood

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