Variant report

Variant	rs61068714
Chromosome Location	chr17:59471688-59471689
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	KAP1	chr17:59471160-59471773	U2OS	brain:	n/a	n/a
2	EP300	chr17:59470910-59471902	HepG2	liver:	n/a	chr17:59471161-59471177 chr17:59471668-59471684
3	HNF4A	chr17:59471414-59471771	HepG2	liver:	n/a	chr17:59471555-59471563
4	GATA3	chr17:59470148-59472995	MCF-7	breast:	n/a	chr17:59471848-59471857
5	TEAD4	chr17:59471529-59471778	K562	blood:	n/a	n/a
6	POLR2A	chr17:59468390-59479830	ProgFib	skin:	n/a	n/a
7	POLR2A	chr17:59471617-59472179	MCF10A-Er-Src	breast:	n/a	n/a
8	RAD21	chr17:59471359-59471938	SK-N-SH_RA	brain:	n/a	chr17:59471513-59471526
9	TEAD4	chr17:59466501-59473617	A549	lung:	n/a	n/a
10	EP300	chr17:59471586-59471717	K562	blood:	n/a	chr17:59471668-59471684
11	CHD2	chr17:59471311-59471955	HepG2	liver:	n/a	n/a
12	RAD21	chr17:59471015-59471826	HepG2	liver:	n/a	chr17:59471166-59471180 chr17:59471160-59471173 chr17:59471168-59471187 chr17:59471513-59471526
13	YY1	chr17:59471576-59471945	HepG2	liver:	n/a	n/a
14	MAZ	chr17:59470841-59472805	IMR90	lung:	n/a	n/a
15	TEAD4	chr17:59471275-59471899	HepG2	liver:	n/a	n/a
16	EP300	chr17:59471366-59472012	SK-N-SH_RA	brain:	n/a	chr17:59471668-59471684
17	EP300	chr17:59471271-59472040	HepG2	liver:	n/a	chr17:59471668-59471684
18	YY1	chr17:59471297-59471936	HepG2	liver:	n/a	n/a
19	SP1	chr17:59471339-59471928	HepG2	liver:	n/a	n/a
20	GATA3	chr17:59471511-59472033	SH-SY5Y	brain:	n/a	chr17:59471848-59471857
21	MAZ	chr17:59471422-59471786	HepG2	liver:	n/a	n/a
22	POLR2A	chr17:59470805-59472166	SK-N-SH	brain:	n/a	n/a
23	RAD21	chr17:59471424-59471869	SK-N-SH_RA	brain:	n/a	chr17:59471513-59471526
24	FOSL2	chr17:59471265-59472028	HepG2	liver:	n/a	n/a
25	RAD21	chr17:59464232-59473165	MCF-7	breast:	n/a	chr17:59469180-59469190 chr17:59469147-59469157 chr17:59471166-59471180 chr17:59467970-59467984 chr17:59467474-59467493 chr17:59471160-59471173 chr17:59468503-59468516 chr17:59465088-59465102 chr17:59471168-59471187 chr17:59464507-59464519 chr17:59471513-59471526 chr17:59470903-59470917 chr17:59466182-59466196 chr17:59472703-59472713 chr17:59469179-59469192
26	ZBTB7A	chr17:59471379-59471823	HepG2	liver:	n/a	n/a
27	POLR2A	chr17:59469840-59471992	HepG2	liver:	n/a	n/a
28	HDAC2	chr17:59471315-59472178	HepG2	liver:	n/a	n/a
29	ARID3A	chr17:59471126-59472001	HepG2	liver:	n/a	n/a
30	RAD21	chr17:59471384-59471919	HepG2	liver:	n/a	chr17:59471513-59471526
31	GATA3	chr17:59471298-59472104	SK-N-SH	brain:	n/a	chr17:59471848-59471857
32	MYC	chr17:59471453-59471752	HepG2	liver:	n/a	n/a
33	ZNF217	chr17:59470926-59471897	MCF-7	breast:	n/a	n/a
34	MBD4	chr17:59471012-59472212	HepG2	liver:	n/a	n/a
35	HEY1	chr17:59471378-59471921	HepG2	liver:	n/a	n/a
36	POLR2A	chr17:59471289-59472070	HepG2	liver:	n/a	n/a
37	RCOR1	chr17:59471521-59471894	K562	blood:	n/a	n/a
38	POLR2A	chr17:59471680-59471936	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXA2	chr17:59471359-59471838	HepG2	liver:	n/a	n/a
40	NFIC	chr17:59471067-59472088	HepG2	liver:	n/a	n/a
41	POLR2A	chr17:59471162-59472873	HepG2	liver:	n/a	n/a
42	CTCF	chr17:59471560-59471710	NHLF	lung:	n/a	n/a
43	RXRA	chr17:59471410-59471889	HepG2	liver:	n/a	chr17:59471630-59471644
44	RCOR1	chr17:59470936-59471761	HepG2	liver:	n/a	n/a
45	POLR2A	chr17:59468021-59474379	Hela-S3	cervix:	n/a	n/a
46	TCF7L2	chr17:59471439-59471809	MCF-7	breast:	n/a	n/a
47	EP300	chr17:59471351-59471960	SK-N-SH_RA	brain:	n/a	chr17:59471668-59471684
48	MYBL2	chr17:59471295-59471896	HepG2	liver:	n/a	n/a
49	RAD21	chr17:59471358-59471824	HepG2	liver:	n/a	chr17:59471513-59471526
50	MYBL2	chr17:59470850-59472680	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:59470667..59471725-chr17:59488553..59489465,8	MCF-7	breast:
2	chr17:59415713..59496229-chr20:49401322..49431802,760	MCF-7	breast:
3	chr17:57917973..57919820-chr17:59471106..59472896,2	MCF-7	breast:
4	chr17:59468937..59480240-chr20:49340039..49356868,49	MCF-7	breast:
5	chr17:59470884..59471787-chr20:49411053..49411955,4	MCF-7	breast:
6	chr17:59468469..59482635-chr20:45977748..45992950,51	MCF-7	breast:
7	chr17:56736472..56738107-chr17:59470143..59472768,3	MCF-7	breast:
8	chr17:59470592..59472862-chr9:115912081..115913641,2	MCF-7	breast:
9	chr17:59470525..59474011-chr17:59486288..59490375,89	MCF-7	breast:
10	chr17:57914768..57917622-chr17:59471234..59472961,2	MCF-7	breast:
11	chr17:59470522..59472690-chr20:55839093..55841752,2	MCF-7	breast:
12	chr17:59468167..59483990-chr20:49341590..49352501,35	MCF-7	breast:
13	chr17:59471651..59472334-chr8:145581802..145582762,2	MCF-7	breast:
14	chr17:59470609..59471850-chr20:49410193..49412110,32	MCF-7	breast:
15	chr17:59447417..59500105-chr20:49391742..49424382,639	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NACA2-2	chr17:59470242-59472935	ucscGeneNc_uc002jdy_1

Variant related genes	Relation type
ENSG00000267280	TF binding region
ENSG00000185803	Chromatin interaction
ENSG00000199004	Chromatin interaction
ENSG00000231119	Chromatin interaction
ENSG00000202077	Chromatin interaction
ENSG00000267280	Chromatin interaction
ENSG00000136867	Chromatin interaction
ENSG00000124243	Chromatin interaction
ENSG00000062716	Chromatin interaction
ENSG00000101040	Chromatin interaction
ENSG00000101144	Chromatin interaction
ENSG00000187013	Chromatin interaction
ENSG00000273451	Chromatin interaction
ENSG00000124171	Chromatin interaction
ENSG00000182325	Chromatin interaction

Extended variants
information (count: 27 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs4459608	0.83[ASN][1000 genomes]
rs55663968	0.83[AFR][1000 genomes]
rs57045595	0.83[ASN][1000 genomes]
rs58036240	0.83[ASN][1000 genomes]
rs58832799	0.83[ASN][1000 genomes]
rs59382073	0.83[ASN][1000 genomes]
rs59430864	0.83[ASN][1000 genomes]
rs60549606	0.83[ASN][1000 genomes]
rs61764069	0.83[ASN][1000 genomes]
rs7211156	0.81[AFR][1000 genomes]
rs7215875	0.81[AFR][1000 genomes]
rs734375	0.83[ASN][1000 genomes]
rs73991913	0.83[ASN][1000 genomes]
rs758600	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1065939	chr17:59283350-59517730	Enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	331 gene(s)	inside rSNPs	diseases
2	nsv833505	chr17:59323466-59518007	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	326 gene(s)	inside rSNPs	diseases
3	nsv833506	chr17:59362377-59562984	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	334 gene(s)	inside rSNPs	diseases
4	nsv518130	chr17:59456589-59491281	Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	265 gene(s)	inside rSNPs	diseases
5	esv1796927	chr17:59460119-59495319	Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	270 gene(s)	inside rSNPs	diseases
6	nsv908663	chr17:59464069-59521310	Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	278 gene(s)	inside rSNPs	diseases
7	nsv908664	chr17:59465697-59491030	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	261 gene(s)	inside rSNPs	diseases
8	nsv908665	chr17:59470193-59494574	Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Weak transcription Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	264 gene(s)	inside rSNPs	diseases
9	nsv908666	chr17:59470842-59489822	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS Weak transcription Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	253 gene(s)	inside rSNPs	diseases
10	nsv908667	chr17:59471151-59491030	Flanking Active TSS Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	256 gene(s)	inside rSNPs	diseases
11	nsv908668	chr17:59471151-59494574	Weak transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	263 gene(s)	inside rSNPs	diseases
12	nsv908669	chr17:59471372-59491030	Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Weak transcription Enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	255 gene(s)	inside rSNPs	diseases
13	nsv908670	chr17:59471372-59494574	Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	262 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:59444600-59473400	Weak transcription	Right Atrium	heart
2	chr17:59447000-59473400	Weak transcription	Pancreas	Pancrea
3	chr17:59464000-59474000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr17:59467400-59471800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr17:59467400-59474000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr17:59467600-59472800	Weak transcription	Adipose Nuclei	Adipose
7	chr17:59467800-59472800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr17:59467800-59473800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr17:59468000-59472200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr17:59470000-59471800	Weak transcription	Right Ventricle	heart
11	chr17:59470600-59472000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr17:59470600-59472200	Enhancers	Fetal Lung	lung
13	chr17:59470600-59472400	Weak transcription	Spleen	Spleen
14	chr17:59470600-59472800	Enhancers	Hela-S3	cervix
15	chr17:59470600-59473600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr17:59470800-59472000	Enhancers	HSMMtube	muscle
17	chr17:59470800-59472200	Enhancers	Osteobl	bone
18	chr17:59470800-59472400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr17:59470800-59472400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr17:59470800-59472800	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
21	chr17:59470800-59473200	Enhancers	Placenta	Placenta
22	chr17:59470800-59476000	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr17:59471000-59471800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr17:59471000-59471800	Enhancers	Fetal Heart	heart
25	chr17:59471000-59471800	Enhancers	Lung	lung
26	chr17:59471000-59471800	Enhancers	Ovary	ovary
27	chr17:59471000-59471800	Enhancers	A549	lung
28	chr17:59471000-59472200	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr17:59471000-59472200	Enhancers	Muscle Satellite Cultured Cells	--
30	chr17:59471000-59472200	Enhancers	Gastric	stomach
31	chr17:59471000-59472800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
32	chr17:59471000-59473200	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr17:59471200-59471800	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
34	chr17:59471200-59472200	Enhancers	HSMM	muscle
35	chr17:59471200-59472400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr17:59471200-59472800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr17:59471200-59472800	Flanking Active TSS	HepG2	liver
38	chr17:59471200-59472800	Enhancers	NHDF-Ad	bronchial
39	chr17:59471200-59473400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
40	chr17:59471400-59472600	Enhancers	NH-A	brain
41	chr17:59471400-59474000	Bivalent Enhancer	Fetal Muscle Leg	muscle
42	chr17:59471600-59472000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr17:59471600-59472000	Transcr. at gene 5' and 3'	NHLF	lung
44	chr17:59471600-59472400	Weak transcription	Esophagus	oesophagus
45	chr17:59471600-59472600	Weak transcription	Brain Substantia Nigra	brain
46	chr17:59471600-59472800	Bivalent Enhancer	Fetal Stomach	stomach

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