Variant report

Variant	rs587808
Chromosome Location	chr11:68151713-68151714
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:21)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:67980044..67980579-chr11:68151208..68151793,2	MCF-7	breast:
2	chr11:68080045..68083223-chr11:68150219..68153957,3	K562	blood:
3	chr11:68038206..68039086-chr11:68150710..68152161,6	MCF-7	breast:
4	chr11:68024595..68025560-chr11:68151108..68152097,7	MCF-7	breast:
5	chr11:68064937..68065691-chr11:68151319..68152084,2	MCF-7	breast:
6	chr11:68079123..68084573-chr11:68146394..68152402,13	MCF-7	breast:
7	chr11:68135719..68138627-chr11:68149871..68152730,2	MCF-7	breast:
8	chr11:68151096..68151778-chr3:64009115..64009628,2	MCF-7	breast:
9	chr11:68079549..68080757-chr11:68151168..68151894,3	MCF-7	breast:
10	chr11:68108161..68113775-chr11:68145002..68152027,11	MCF-7	breast:
11	chr11:68025463..68028062-chr11:68150558..68152096,2	MCF-7	breast:
12	chr11:68036771..68039513-chr11:68151035..68153879,2	K562	blood:
13	chr11:68106405..68113140-chr11:68145593..68153963,20	MCF-7	breast:
14	chr11:68151226..68152155-chr11:68214483..68215186,2	MCF-7	breast:
15	chr11:68079577..68083546-chr11:68146426..68152842,7	MCF-7	breast:
16	chr11:68150498..68154117-chr11:68165017..68167539,3	MCF-7	breast:
17	chr11:68025022..68025803-chr11:68151109..68152026,3	K562	blood:
18	chr11:68064797..68065836-chr11:68150982..68152139,9	MCF-7	breast:
19	chr11:68024643..68025542-chr11:68151241..68152008,2	MCF-7	breast:
20	chr11:68151217..68154169-chr11:68155729..68159223,3	MCF-7	breast:
21	chr11:68065987..68066914-chr11:68151516..68152265,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000110066	Chromatin interaction
ENSG00000163636	Chromatin interaction
ENSG00000171067	Chromatin interaction
ENSG00000162337	Chromatin interaction

Extended variants
information (count: 47 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10896321	0.80[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs11228225	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11602256	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11823032	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs11826287	1.00[CHB][hapmap]
rs12222261	0.80[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs160607	0.86[JPT][hapmap]
rs1784237	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2508838	0.95[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs312780	0.81[AMR][1000 genomes]
rs312782	0.81[AMR][1000 genomes]
rs312783	0.86[JPT][hapmap];0.83[AMR][1000 genomes]
rs312784	0.82[AMR][1000 genomes]
rs312785	0.83[AMR][1000 genomes]
rs312788	0.86[JPT][hapmap];0.83[AMR][1000 genomes]
rs312790	0.83[AMR][1000 genomes]
rs312791	0.85[AMR][1000 genomes]
rs312792	0.86[JPT][hapmap];0.84[AMR][1000 genomes]
rs314761	0.81[AMR][1000 genomes]
rs314773	0.88[EUR][1000 genomes]
rs314775	0.86[JPT][hapmap];0.80[YRI][hapmap];0.85[AMR][1000 genomes]
rs314776	0.83[AMR][1000 genomes]
rs3781590	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57197891	0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs628115	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs629012	0.90[EUR][1000 genomes]
rs643892	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs643981	0.81[AMR][1000 genomes]
rs659605	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs66787665	0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs671191	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs74744	0.86[JPT][hapmap];0.81[AMR][1000 genomes]
rs91285	0.83[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	nsv825963	chr11:67763676-68197054	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	149 gene(s)	inside rSNPs	diseases
2	esv3347272	chr11:67969427-68218997	Strong transcription Flanking Active TSS Genic enhancers Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	78 gene(s)	inside rSNPs	diseases
3	nsv897857	chr11:68056770-68231240	Enhancers Genic enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	22 gene(s)	inside rSNPs	diseases
4	nsv897858	chr11:68077238-68293545	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
5	nsv897859	chr11:68102000-68231240	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
6	nsv897860	chr11:68102000-68293545	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
7	nsv1047532	chr11:68103330-68239242	Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv541082	chr11:68103330-68239242	Weak transcription Enhancers Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
9	nsv1039671	chr11:68120571-68206630	Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv1036561	chr11:68123135-68315685	Weak transcription Strong transcription Genic enhancers Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv897861	chr11:68129606-68196830	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
12	nsv897862	chr11:68129606-68236389	Strong transcription Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
13	nsv469965	chr11:68140781-68217420	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
14	nsv555285	chr11:68144283-68231240	Strong transcription Weak transcription Active TSS Flanking Active TSS Genic enhancers Enhancers 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	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:68121800-68156400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
2	chr11:68128200-68153800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
3	chr11:68129800-68153600	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr11:68135200-68153400	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr11:68135200-68153600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr11:68136200-68153400	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr11:68136800-68152800	Weak transcription	Dnd41	blood
8	chr11:68137000-68156400	Weak transcription	K562	blood
9	chr11:68139600-68156400	Weak transcription	Hela-S3	cervix
10	chr11:68140000-68153400	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr11:68140200-68153600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
12	chr11:68141400-68153400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr11:68142600-68179000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr11:68142800-68153400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr11:68143000-68156400	Weak transcription	NHEK	skin
16	chr11:68143400-68153200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr11:68143600-68153400	Weak transcription	Brain Germinal Matrix	brain
18	chr11:68144400-68152800	Weak transcription	Thymus	Thymus
19	chr11:68145600-68152200	Enhancers	Stomach Mucosa	stomach
20	chr11:68145600-68153600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr11:68145600-68153600	Enhancers	Liver	Liver
22	chr11:68147400-68152000	Enhancers	Right Ventricle	heart
23	chr11:68147400-68181600	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr11:68147800-68151800	Enhancers	Left Ventricle	heart
25	chr11:68148000-68152200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr11:68148400-68153600	Weak transcription	Fetal Brain Female	brain
27	chr11:68148400-68153800	Weak transcription	Placenta Amnion	Placenta Amnion
28	chr11:68148600-68152400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr11:68148600-68153600	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr11:68148600-68165600	Weak transcription	Small Intestine	intestine
31	chr11:68148600-68196800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr11:68148800-68153200	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr11:68148800-68153400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr11:68148800-68156400	Weak transcription	Fetal Kidney	kidney
35	chr11:68149000-68152000	Enhancers	Adipose Nuclei	Adipose
36	chr11:68149000-68152000	Enhancers	Rectal Smooth Muscle	rectum
37	chr11:68149000-68152600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr11:68149000-68153600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr11:68149000-68156200	Weak transcription	Primary T cells from cord blood	blood
40	chr11:68149000-68165200	Weak transcription	Psoas Muscle	Psoas
41	chr11:68149200-68151800	Enhancers	Skeletal Muscle Male	skeletal muscle
42	chr11:68149200-68153400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr11:68149200-68155600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:68149200-68156400	Weak transcription	HMEC	breast
45	chr11:68149200-68156600	Weak transcription	Osteobl	bone
46	chr11:68149200-68156800	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr11:68149200-68174000	Weak transcription	Primary B cells from cord blood	blood
48	chr11:68149400-68152000	Genic enhancers	Fetal Muscle Trunk	muscle
49	chr11:68149400-68153400	Weak transcription	Fetal Lung	lung
50	chr11:68149400-68156400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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