Variant report

Variant	rs11909011
Chromosome Location	chr21:45255650-45255651
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:45254673..45257223-chr21:45369004..45371482,2	K562	blood:
2	chr21:45249509..45251897-chr21:45254038..45257016,3	K562	blood:
3	chr21:45254709..45256717-chr21:45274155..45276543,2	MCF-7	breast:
4	chr21:45255403..45257134-chr21:45257477..45260096,2	MCF-7	breast:
5	chr21:45248939..45255746-chr21:45272255..45276727,7	K562	blood:
6	chr21:45255011..45256838-chr21:45256879..45259867,3	K562	blood:
7	chr21:45254192..45256838-chr21:45256879..45259867,3	K562	blood:

Variant related genes	Relation type
ENSG00000160216	Chromatin interaction
ENSG00000226543	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs12397630	0.81[ASN][1000 genomes]
rs17004612	0.83[ASN][1000 genomes]
rs2838405	0.82[ASN][1000 genomes]
rs2838414	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2838422	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4818870	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4819326	0.82[ASN][1000 genomes]
rs4819330	0.82[ASN][1000 genomes]
rs4819331	0.82[ASN][1000 genomes]
rs4819332	0.82[ASN][1000 genomes]
rs4819333	0.81[ASN][1000 genomes]
rs56240646	0.82[ASN][1000 genomes]
rs56928276	0.88[ASN][1000 genomes]
rs58660555	0.82[ASN][1000 genomes]
rs58859690	0.82[ASN][1000 genomes]
rs6518328	1.00[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66912549	0.82[ASN][1000 genomes]
rs67618547	0.82[ASN][1000 genomes]
rs7276547	0.81[ASN][1000 genomes]
rs7277520	0.82[ASN][1000 genomes]
rs7279644	0.85[ASN][1000 genomes]
rs7279993	0.87[ASN][1000 genomes]
rs73224999	0.88[ASN][1000 genomes]
rs762413	0.97[ASN][1000 genomes]
rs762416	0.85[ASN][1000 genomes]
rs8132053	0.87[ASN][1000 genomes]
rs9306162	0.81[ASN][1000 genomes]
rs9974080	0.82[ASN][1000 genomes]
rs9974122	0.81[ASN][1000 genomes]
rs9974624	0.82[ASN][1000 genomes]
rs9978185	0.82[ASN][1000 genomes]
rs9978333	0.82[ASN][1000 genomes]
rs9978624	0.82[ASN][1000 genomes]
rs9982899	0.81[ASN][1000 genomes]
rs9982908	0.81[ASN][1000 genomes]
rs9983217	0.82[ASN][1000 genomes]
rs9983861	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv531545	chr21:45095397-45395904	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription 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 target site	49 gene(s)	inside rSNPs	diseases
2	nsv913876	chr21:45119629-45267193	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
3	esv2830066	chr21:45133868-45258047	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	44 gene(s)	inside rSNPs	diseases
4	nsv913880	chr21:45145286-45263920	Flanking Active TSS Transcr. at gene 5' and 3' Weak transcription Strong transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
5	nsv913881	chr21:45145286-45267193	Flanking Active TSS Strong transcription Active TSS Weak transcription Enhancers 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 target site	31 gene(s)	inside rSNPs	diseases
6	nsv470904	chr21:45151045-45258047	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
7	nsv913882	chr21:45151874-45370715	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
8	nsv834107	chr21:45155325-45294546	Enhancers Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
9	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
10	nsv834108	chr21:45178037-45369641	Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
11	nsv913884	chr21:45191139-45255836	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
12	nsv544469	chr21:45194085-45257959	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
13	nsv1065007	chr21:45212880-45257959	Weak transcription Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
14	nsv544470	chr21:45212880-45257959	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
15	nsv459292	chr21:45218440-45269841	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
16	nsv587719	chr21:45218440-45269841	Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
17	nsv913886	chr21:45220483-45267193	Active TSS Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
18	nsv587720	chr21:45232322-45263920	Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
19	nsv519385	chr21:45237039-45263920	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
20	nsv1066284	chr21:45249549-45343314	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
21	esv20693	chr21:45254689-45264263	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45211000-45257200	Weak transcription	Right Atrium	heart
2	chr21:45250600-45256400	Weak transcription	K562	blood
3	chr21:45253800-45256000	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
4	chr21:45254000-45255800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr21:45254000-45256200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
6	chr21:45254200-45256200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr21:45254400-45255800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
8	chr21:45254400-45255800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr21:45254400-45255800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
10	chr21:45254600-45255800	Enhancers	Primary B cells from cord blood	blood
11	chr21:45254600-45255800	Enhancers	Adipose Nuclei	Adipose
12	chr21:45254600-45255800	Bivalent Enhancer	Fetal Muscle Leg	muscle
13	chr21:45254600-45256000	Enhancers	Lung	lung
14	chr21:45254800-45255800	Bivalent Enhancer	Primary B cells from peripheral blood	blood
15	chr21:45254800-45255800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr21:45255000-45255800	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
17	chr21:45255200-45256400	Enhancers	Primary hematopoietic stem cells	blood
18	chr21:45255400-45256000	Enhancers	Spleen	Spleen
19	chr21:45255600-45255800	Enhancers	Brain Hippocampus Middle	brain
20	chr21:45255600-45255800	Enhancers	Esophagus	oesophagus
21	chr21:45255600-45255800	Bivalent Enhancer	Placenta	Placenta
22	chr21:45255600-45256000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood

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