Variant report

Variant	rs11705217
Chromosome Location	chr22:23427105-23427106
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23425767..23428206-chr22:23439942..23442818,2	MCF-7	breast:
2	chr22:22899225..22902133-chr22:23425045..23427702,2	K562	blood:

Variant related genes	Relation type
ENSG00000185686	Chromatin interaction
ENSG00000220891	Chromatin interaction

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs11702939	1.00[EUR][1000 genomes]
rs11702951	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11702988	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11703018	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11703394	1.00[ASN][1000 genomes]
rs11703410	1.00[EUR][1000 genomes]
rs11703413	1.00[EUR][1000 genomes]
rs11703415	1.00[EUR][1000 genomes]
rs11703459	1.00[ASN][1000 genomes]
rs11703619	1.00[EUR][1000 genomes]
rs11703666	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11703730	1.00[AMR][1000 genomes]
rs11703839	1.00[ASN][1000 genomes]
rs11704087	1.00[AMR][1000 genomes]
rs11704126	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11704186	1.00[ASN][1000 genomes]
rs11704318	1.00[AMR][1000 genomes]
rs11704645	1.00[EUR][1000 genomes]
rs11704807	1.00[EUR][1000 genomes]
rs11704812	1.00[EUR][1000 genomes]
rs11704834	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11705141	1.00[ASN][1000 genomes]
rs11705526	1.00[EUR][1000 genomes]
rs11705531	1.00[ASN][1000 genomes]
rs11705643	1.00[EUR][1000 genomes]
rs11705661	1.00[EUR][1000 genomes]
rs11705689	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11705692	1.00[EUR][1000 genomes]
rs11913797	1.00[JPT][hapmap]
rs16997431	1.00[ASN][1000 genomes]
rs17853740	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2013551	1.00[JPT][hapmap]
rs41277287	1.00[EUR][1000 genomes]
rs41277289	1.00[EUR][1000 genomes]
rs41311051	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58182042	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5996464	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5996466	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5996468	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6003439	1.00[JPT][hapmap]
rs6003445	1.00[JPT][hapmap]
rs6003475	1.00[JPT][hapmap]
rs6003490	1.00[ASN][1000 genomes]
rs6003506	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6003508	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6003510	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6003511	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73384386	1.00[ASN][1000 genomes]
rs765744	1.00[JPT][hapmap]
rs8136486	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs915613	1.00[JPT][hapmap]
rs9612177	1.00[JPT][hapmap]
rs9612186	1.00[JPT][hapmap]
rs9612188	1.00[JPT][hapmap]
rs9612192	1.00[JPT][hapmap]
rs9624011	1.00[EUR][1000 genomes]
rs9624022	1.00[ASN][1000 genomes]
rs9624023	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9624027	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:30 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv1803110	chr22:22731758-23497674	Flanking Active TSS Bivalent Enhancer Strong transcription Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	136 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	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
9	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
10	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
11	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
12	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
13	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
14	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
15	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
16	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
17	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
18	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
19	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
20	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
21	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
22	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
23	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
24	esv34158	chr22:23216762-23499513	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	53 gene(s)	inside rSNPs	diseases
25	nsv914575	chr22:23399743-23467804	Weak transcription Active TSS Strong transcription Genic enhancers Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
26	nsv914576	chr22:23399743-23469918	Strong transcription Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
27	esv1806531	chr22:23400739-23448258	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
28	nsv544609	chr22:23400739-23455790	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
29	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
30	esv1825944	chr22:23414398-23473840	Enhancers Genic enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23413600-23430400	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr22:23413600-23440600	Strong transcription	Right Atrium	heart
3	chr22:23415000-23427800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr22:23415800-23430200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr22:23416000-23452800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr22:23416200-23427200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr22:23416800-23435000	Weak transcription	Fetal Brain Male	brain
8	chr22:23418200-23428600	Weak transcription	Primary B cells from cord blood	blood
9	chr22:23419000-23430400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr22:23420400-23430400	Weak transcription	Psoas Muscle	Psoas
11	chr22:23420600-23430200	Weak transcription	Stomach Smooth Muscle	stomach
12	chr22:23420600-23435000	Weak transcription	Brain Germinal Matrix	brain
13	chr22:23420800-23437000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr22:23421000-23430600	Weak transcription	Ovary	ovary
15	chr22:23422800-23428800	Weak transcription	Stomach Mucosa	stomach
16	chr22:23423400-23428600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr22:23423600-23428600	Weak transcription	Primary B cells from peripheral blood	blood
18	chr22:23425200-23427800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr22:23425200-23430200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr22:23425600-23427600	Weak transcription	HepG2	liver
21	chr22:23425800-23430800	Enhancers	Brain Hippocampus Middle	brain
22	chr22:23425800-23433000	Weak transcription	Fetal Brain Female	brain
23	chr22:23426200-23428000	Enhancers	Brain Substantia Nigra	brain
24	chr22:23426400-23427200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr22:23426400-23437800	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr22:23426800-23427200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr22:23426800-23427600	Enhancers	Brain Anterior Caudate	brain
28	chr22:23426800-23427600	Enhancers	Spleen	Spleen
29	chr22:23427000-23427200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr22:23427000-23427400	Weak transcription	Gastric	stomach
31	chr22:23427000-23427800	Genic enhancers	Brain Angular Gyrus	brain
32	chr22:23427000-23427800	Enhancers	Brain Cingulate Gyrus	brain

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