Variant report

Variant	rs627330
Chromosome Location	chr11:66602099-66602100
allele	C/T
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:25)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:66459547..66465432-chr11:66599355..66603296,9	MCF-7	breast:
2	chr11:66466709..66469416-chr11:66599980..66602428,2	MCF-7	breast:
3	chr11:66457750..66467271-chr11:66598332..66608447,16	K562	blood:
4	chr11:66452976..66456335-chr11:66601263..66603949,4	MCF-7	breast:
5	chr11:66450885..66452663-chr11:66600474..66602578,2	MCF-7	breast:
6	chr11:66206368..66207048-chr11:66601439..66602377,2	K562	blood:
7	chr11:66175645..66176654-chr11:66601360..66602402,6	K562	blood:
8	chr11:66461759..66462938-chr11:66600504..66602873,21	MCF-7	breast:
9	chr11:66480251..66482794-chr11:66601517..66603126,2	K562	blood:
10	chr11:66490952..66495603-chr11:66599430..66602599,5	MCF-7	breast:
11	chr11:66600847..66602669-chr11:66650829..66652399,2	MCF-7	breast:
12	chr11:66407180..66409474-chr11:66600961..66602936,2	K562	blood:
13	chr11:66461811..66462859-chr11:66601414..66602394,18	K562	blood:
14	chr11:66487468..66490091-chr11:66601151..66603548,2	MCF-7	breast:
15	chr11:66443786..66447111-chr11:66599587..66602502,4	K562	blood:
16	chr11:66412034..66414807-chr11:66600460..66602396,2	MCF-7	breast:
17	chr11:66595690..66597317-chr11:66600394..66603185,2	MCF-7	breast:
18	chr11:66461004..66463732-chr11:66600353..66604002,4	K562	blood:
19	chr11:66600602..66603038-chr11:66798482..66800239,2	MCF-7	breast:
20	chr11:66445912..66446591-chr11:66601375..66602234,2	MCF-7	breast:
21	chr11:66443901..66447111-chr11:66599621..66602502,3	K562	blood:
22	chr11:66578493..66580917-chr11:66600388..66602985,2	K562	blood:
23	chr11:66460828..66465487-chr11:66600237..66603918,6	MCF-7	breast:
24	chr11:66412976..66415260-chr11:66600626..66602387,2	K562	blood:
25	chr11:66461666..66462664-chr11:66601443..66602548,9	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000173914	Chromatin interaction
ENSG00000254510	Chromatin interaction
ENSG00000239553	Chromatin interaction
ENSG00000173898	Chromatin interaction

Extended variants
information (count: 25 )
Associated
traits (count: 10 )

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs12577111	0.83[ASW][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.82[MKK][hapmap]
rs12805133	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs2276138	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs2513658	1.00[CEU][hapmap];0.95[CHB][hapmap];0.90[CHD][hapmap];0.88[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.93[TSI][hapmap];0.91[YRI][hapmap];0.81[AFR][1000 genomes];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs3741363	1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap]
rs4930387	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4930391	0.92[ASW][hapmap];1.00[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap];0.84[MKK][hapmap];0.89[TSI][hapmap];0.81[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs508443	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs543191	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs551708	0.89[TSI][hapmap]
rs569818	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs577023	0.95[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap]
rs580910	0.83[ASW][hapmap];0.91[CHB][hapmap];0.81[CHD][hapmap];0.95[JPT][hapmap];0.82[MKK][hapmap]
rs594313	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.94[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.86[MEX][hapmap];0.92[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs608248	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.90[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap]
rs682842	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7107944	0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv897789	chr11:66372390-66634397	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
2	nsv897790	chr11:66414915-66626234	Transcr. at gene 5' and 3' Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	75 gene(s)	inside rSNPs	diseases
3	nsv427891	chr11:66456140-66606701	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
4	nsv468602	chr11:66468469-66634397	Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Weak transcription 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 miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv555225	chr11:66468469-66634397	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv508638	chr11:66541653-66643634	Strong transcription Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	53 gene(s)	inside rSNPs	diseases
7	nsv897794	chr11:66579572-66744119	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	58 gene(s)	inside rSNPs	diseases
8	nsv555226	chr11:66579572-66845362	Active TSS Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	74 gene(s)	inside rSNPs	diseases

mRNA abundance (count:10)

SNP	Gene	Cis/trans	Tissue	Source
rs627330	CTD-3074O7.2	cis	Muscle Skeletal	GTEx
rs627330	ACTN3	cis	Muscle Skeletal	GTEx
rs627330	SYT12	cis	parietal	SCAN
rs627330	LRFN4	Cis_1M	lymphoblastoid	RTeQTL
rs627330	EHBP1L1	cis	cerebellum	SCAN
rs627330	MACROD1	cis	parietal	SCAN
rs627330	CCS	cis	lymphoblastoid	seeQTL
rs627330	ESRRA	cis	cerebellum	SCAN
rs627330	ACTN3	cis	lymphoblastoid	seeQTL
rs627330	SLC25A45	cis	parietal	SCAN

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:66513400-66606800	Weak transcription	Brain Angular Gyrus	brain
2	chr11:66530000-66605400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr11:66544000-66609600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
4	chr11:66554600-66605800	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr11:66556200-66603000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr11:66556800-66607400	Weak transcription	Fetal Lung	lung
7	chr11:66560400-66605400	Weak transcription	Duodenum Mucosa	Duodenum
8	chr11:66561600-66609400	Weak transcription	Colonic Mucosa	Colon
9	chr11:66565000-66605400	Weak transcription	Gastric	stomach
10	chr11:66567000-66606800	Weak transcription	Brain Anterior Caudate	brain
11	chr11:66567000-66609800	Weak transcription	Ovary	ovary
12	chr11:66568000-66609400	Weak transcription	Rectal Smooth Muscle	rectum
13	chr11:66568800-66609600	Weak transcription	Fetal Kidney	kidney
14	chr11:66570000-66605400	Weak transcription	HSMMtube	muscle
15	chr11:66570000-66606800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr11:66571000-66609400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr11:66571600-66609600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr11:66571800-66605400	Weak transcription	Lung	lung
19	chr11:66572000-66606600	Weak transcription	Brain Inferior Temporal Lobe	brain
20	chr11:66572000-66609200	Weak transcription	Colon Smooth Muscle	Colon
21	chr11:66576000-66605400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr11:66576000-66609600	Weak transcription	Esophagus	oesophagus
23	chr11:66576000-66609800	Weak transcription	Aorta	Aorta
24	chr11:66576200-66605200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
25	chr11:66577000-66609400	Weak transcription	Small Intestine	intestine
26	chr11:66580600-66606600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr11:66580800-66609600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr11:66581200-66609800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr11:66583200-66605200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr11:66583400-66609200	Weak transcription	NH-A	brain
31	chr11:66583600-66603000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr11:66583600-66603000	Weak transcription	NHDF-Ad	bronchial
33	chr11:66583800-66605200	Weak transcription	NHEK	skin
34	chr11:66585200-66609000	Weak transcription	HepG2	liver
35	chr11:66586800-66606600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr11:66588000-66605400	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr11:66588200-66605600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr11:66588600-66605200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr11:66590200-66605200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr11:66590600-66609200	Weak transcription	Brain Cingulate Gyrus	brain
41	chr11:66591000-66605600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr11:66591600-66606400	Weak transcription	GM12878-XiMat	blood
43	chr11:66593600-66603000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr11:66594000-66605200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr11:66594000-66605400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr11:66594000-66609000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr11:66594200-66603400	Weak transcription	NHLF	lung
48	chr11:66594200-66605200	Weak transcription	Dnd41	blood
49	chr11:66595400-66605400	Weak transcription	Spleen	Spleen
50	chr11:66596000-66603000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin

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