Variant report

Variant	rs11704365
Chromosome Location	chr22:23506826-23506827
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr22:23505806..23510284-chr22:23519945..23523267,5	MCF-7	breast:
2	chr22:23435451..23438238-chr22:23506678..23508386,2	K562	blood:

Variant related genes	Relation type
ENSG00000186716	Chromatin interaction
ENSG00000236794	Chromatin interaction

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:67)

rs_ID	r²[population]
rs1051875	0.84[JPT][hapmap]
rs12167308	0.85[JPT][hapmap]
rs13054985	0.84[JPT][hapmap]
rs2157710	0.85[JPT][hapmap]
rs2267001	0.80[JPT][hapmap]
rs2267004	0.85[JPT][hapmap]
rs2267005	0.80[JPT][hapmap]
rs2267006	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs2267007	0.85[JPT][hapmap]
rs2267010	0.86[CHB][hapmap];0.95[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267012	0.87[CHB][hapmap];0.90[JPT][hapmap];0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2267014	0.86[JPT][hapmap];0.82[EUR][1000 genomes]
rs2283803	0.85[JPT][hapmap]
rs2283804	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs2301554	0.85[JPT][hapmap]
rs2330361	0.85[JPT][hapmap]
rs3788347	0.84[JPT][hapmap]
rs3788348	0.85[JPT][hapmap]
rs4820537	0.84[JPT][hapmap]
rs4820539	0.84[JPT][hapmap]
rs4820541	0.85[JPT][hapmap]
rs4822357	0.84[JPT][hapmap]
rs4822359	0.85[JPT][hapmap]
rs4822360	0.84[JPT][hapmap]
rs4822361	0.84[JPT][hapmap]
rs4822362	0.84[JPT][hapmap]
rs4822369	0.85[JPT][hapmap]
rs5751587	0.82[JPT][hapmap]
rs5751589	0.84[JPT][hapmap]
rs5751593	0.85[JPT][hapmap]
rs5751596	0.85[JPT][hapmap]
rs5751605	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs5759593	0.85[JPT][hapmap]
rs5759598	0.84[JPT][hapmap]
rs5759600	0.85[JPT][hapmap]
rs5759603	0.87[CHB][hapmap];0.84[JPT][hapmap]
rs5759604	0.82[JPT][hapmap]
rs5759607	0.85[JPT][hapmap]
rs5759608	0.85[JPT][hapmap]
rs5759611	0.85[JPT][hapmap]
rs5759612	0.85[JPT][hapmap]
rs5759613	0.85[JPT][hapmap]
rs5759614	0.85[JPT][hapmap]
rs5759615	0.85[JPT][hapmap]
rs5759619	0.85[JPT][hapmap]
rs5759620	0.85[JPT][hapmap]
rs5759621	0.85[JPT][hapmap]
rs5759639	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6003518	0.85[JPT][hapmap]
rs60054645	0.82[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs62220914	0.83[ASN][1000 genomes]
rs713682	0.85[JPT][hapmap]
rs737818	0.84[JPT][hapmap]
rs737819	0.85[JPT][hapmap]
rs756633	0.85[JPT][hapmap]
rs768513	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs8142746	0.85[JPT][hapmap]
rs885963	0.80[JPT][hapmap]
rs885964	0.85[JPT][hapmap]
rs916583	0.85[JPT][hapmap]
rs916584	0.85[JPT][hapmap]
rs916585	0.81[JPT][hapmap]
rs9612234	0.84[JPT][hapmap]
rs9612237	0.89[JPT][hapmap]
rs9612248	0.91[CHB][hapmap];0.90[JPT][hapmap];0.82[ASN][1000 genomes]
rs9612252	0.85[JPT][hapmap]
rs9612257	0.91[CHB][hapmap];0.95[JPT][hapmap];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 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

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:23490400-23522000	Weak transcription	Aorta	Aorta
2	chr22:23491200-23512000	Strong transcription	Right Atrium	heart
3	chr22:23492400-23509000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr22:23492400-23518000	Weak transcription	Esophagus	oesophagus
5	chr22:23493600-23510800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr22:23498400-23509200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr22:23500000-23508600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr22:23500000-23510800	Weak transcription	Gastric	stomach
9	chr22:23501000-23509200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr22:23501200-23509000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr22:23501400-23508600	Weak transcription	Pancreas	Pancrea
12	chr22:23504600-23508800	Enhancers	Liver	Liver
13	chr22:23504800-23509400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr22:23504800-23516200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr22:23505800-23507000	Enhancers	Colonic Mucosa	Colon
16	chr22:23505800-23507000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
17	chr22:23505800-23507000	Enhancers	Lung	lung
18	chr22:23505800-23507000	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr22:23506200-23507400	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr22:23506200-23507400	Enhancers	Rectal Mucosa Donor 29	rectum
21	chr22:23506400-23507000	Enhancers	Fetal Muscle Leg	muscle
22	chr22:23506400-23508400	Weak transcription	Fetal Intestine Small	intestine
23	chr22:23506600-23510400	Weak transcription	Stomach Smooth Muscle	stomach
24	chr22:23506800-23507000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr22:23506800-23509600	Weak transcription	Fetal Brain Male	brain
26	chr22:23506800-23509600	Enhancers	HepG2	liver
27	chr22:23506800-23510200	Weak transcription	Fetal Brain Female	brain
28	chr22:23506800-23511600	Weak transcription	Brain Germinal Matrix	brain
29	chr22:23506800-23520600	Weak transcription	Brain Anterior Caudate	brain

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