Variant report

Variant	rs66482609
Chromosome Location	chr17:37779599-37779600
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	CTCF	chr17:37779471-37779641	GM12892	blood:	n/a	n/a
2	POLR2A	chr17:37779337-37780207	K562	blood:	n/a	n/a
3	CTCF	chr17:37779480-37779630	AG04449	skin:	n/a	n/a
4	CTCF	chr17:37777426-37780368	A549	lung:	n/a	chr17:37777636-37777645 chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
5	POU2F2	chr17:37779505-37780016	GM12891	blood:	n/a	n/a
6	CTCF	chr17:37779489-37779632	GM12891	blood:	n/a	n/a
7	CHD1	chr17:37779189-37780165	IMR90	lung:	n/a	n/a
8	CTCF	chr17:37779574-37780126	MCF-7	breast:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
9	RAD21	chr17:37779522-37780149	ECC-1	luminal epithelium:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
10	RAD21	chr17:37779496-37780341	HCT-116	colon:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
11	HEY1	chr17:37779292-37780270	K562	blood:	n/a	n/a
12	ELF1	chr17:37779463-37779946	GM12878	blood:	n/a	chr17:37779714-37779723 chr17:37779713-37779724
13	BCL3	chr17:37779519-37780047	A549	lung:	n/a	chr17:37779578-37779587
14	POLR2A	chr17:37779373-37780227	K562	blood:	n/a	n/a
15	CTCF	chr17:37779506-37779604	GM12878	blood:	n/a	n/a
16	ZNF263	chr17:37779510-37780300	HEK293-T-REx	kidney:	n/a	chr17:37780132-37780141
17	MTA3	chr17:37779315-37780113	GM12878	blood:	n/a	n/a
18	CTCF	chr17:37779586-37780088	GM12878	blood:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
19	RAD21	chr17:37779445-37780268	HCT-116	colon:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
20	ELF1	chr17:37779549-37779925	K562	blood:	n/a	chr17:37779714-37779723 chr17:37779713-37779724
21	CTCF	chr17:37779524-37780219	HCT-116	colon:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
22	RAD21	chr17:37779584-37780076	ECC-1	luminal epithelium:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
23	GABPA	chr17:37779519-37779950	K562	blood:	n/a	n/a
24	CTCF	chr17:37779476-37780016	GM19238	blood:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
25	RAD21	chr17:37779515-37780150	H1-hESC	embryonic stem cell:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
26	POLR2A	chr17:37779390-37780215	K562	blood:	n/a	n/a
27	NR2F2	chr17:37779465-37780062	MCF-7	breast:	n/a	n/a
28	CTCF	chr17:37779471-37779626	GM19239	blood:	n/a	n/a
29	RAD21	chr17:37779578-37780147	A549	lung:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
30	RCOR1	chr17:37779576-37779793	K562	blood:	n/a	n/a
31	RAD21	chr17:37779264-37780255	SK-N-SH	brain:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
32	CTCF	chr17:37779562-37780126	A549	lung:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
33	RAD21	chr17:37779555-37779965	MCF-7	breast:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
34	PML	chr17:37779386-37780259	K562	blood:	n/a	n/a
35	CTCF	chr17:37779460-37780288	HCT-116	colon:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
36	POLR2A	chr17:37779407-37780199	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr17:37779542-37779637	GM19240	blood:	n/a	n/a
38	TCF12	chr17:37779410-37780081	A549	lung:	n/a	n/a
39	TAF7	chr17:37779575-37780223	K562	blood:	n/a	n/a
40	POLR2A	chr17:37779571-37780147	K562	blood:	n/a	n/a
41	EBF1	chr17:37779595-37779993	GM12878	blood:	n/a	n/a
42	RAD21	chr17:37779575-37780068	H1-hESC	embryonic stem cell:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
43	CTCF	chr17:37779584-37780009	H1-hESC	embryonic stem cell:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866
44	RAD21	chr17:37779594-37780046	SK-N-SH_RA	brain:	n/a	chr17:37779820-37779834 chr17:37779850-37779862 chr17:37779852-37779866 chr17:37779848-37779867
45	CTCF	chr17:37779343-37780268	SK-N-SH	brain:	n/a	chr17:37779850-37779868 chr17:37779852-37779865 chr17:37779851-37779867 chr17:37779845-37779866

No.	Distal block	Cell Line	Cell type
1	chr17:37778895..37779929-chr17:37824753..37825581,4	K562	blood:
2	chr17:37776626..37780124-chr17:37818606..37821377,4	K562	blood:
3	chr17:37703730..37705624-chr17:37777887..37780361,14	K562	blood:
4	chr17:37777309..37780105-chr17:37909118..37911531,3	MCF-7	breast:
5	chr17:37777123..37780362-chr17:37909816..37911514,36	K562	blood:
6	chr17:37777435..37780800-chr17:37803920..37808668,4	K562	blood:
7	chr17:37704896..37707478-chr17:37777687..37780191,2	MCF-7	breast:
8	chr17:37703620..37705488-chr17:37779313..37780378,12	MCF-7	breast:
9	chr17:37732171..37732825-chr17:37779402..37780361,2	K562	blood:
10	chr17:37777756..37783081-chr17:37819129..37825010,9	K562	blood:
11	chr17:37776845..37781693-chr17:37790426..37796554,9	K562	blood:
12	chr17:37769208..37773729-chr17:37777189..37781252,6	K562	blood:
13	chr17:37779426..37780039-chr17:37828512..37829091,2	K562	blood:
14	chr17:37778539..37780288-chr17:37893179..37895344,2	K562	blood:
15	chr17:37779395..37780335-chr17:37811349..37811933,2	K562	blood:
16	chr17:37778774..37780358-chr17:37893179..37896235,3	K562	blood:
17	chr17:37778202..37782049-chr17:37783082..37786622,6	K562	blood:
18	chr17:37778310..37780085-chr17:37905969..37908685,2	K562	blood:
19	chr17:37775807..37781695-chr17:37822673..37828377,10	K562	blood:
20	chr17:37779307..37779994-chr17:37809757..37810305,2	K562	blood:

Variant related genes	Relation type
PPP1R1B	TF binding region
ENSG00000131748	Chromatin interaction
ENSG00000141738	Chromatin interaction
ENSG00000173991	Chromatin interaction
ENSG00000131771	Chromatin interaction
ENSG00000141744	Chromatin interaction
ENSG00000167258	Chromatin interaction

Extended variants
information (count: 28 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12103674	0.83[AFR][1000 genomes]
rs1877032	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs28533242	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs33938012	0.86[AFR][1000 genomes]
rs34695955	0.84[AFR][1000 genomes]
rs72827166	0.93[EUR][1000 genomes]
rs734645	0.83[AFR][1000 genomes]
rs9892853	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs9899652	0.82[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9899653	0.97[AFR][1000 genomes];0.95[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs9907501	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:17 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv932024	chr17:37192290-37850932	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	92 gene(s)	inside rSNPs	diseases
2	nsv1066033	chr17:37333956-37795617	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Bivalent Enhancer 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	78 gene(s)	inside rSNPs	diseases
3	nsv543340	chr17:37333956-37795617	Flanking Active TSS Strong transcription Enhancers Active TSS Weak transcription Genic enhancers Bivalent Enhancer 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	78 gene(s)	inside rSNPs	diseases
4	esv1825702	chr17:37487168-37876767	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	nsv833442	chr17:37692880-37861291	Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases
6	nsv521294	chr17:37694709-37804858	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	26 gene(s)	inside rSNPs	diseases
7	nsv908205	chr17:37709422-37830900	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv908206	chr17:37709422-37866005	Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
9	nsv908207	chr17:37709422-37922259	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
10	nsv833443	chr17:37725640-37882864	Weak transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Strong transcription Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
11	nsv908208	chr17:37749259-37781849	Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
12	nsv908209	chr17:37749259-37790340	Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Enhancers Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
13	nsv908210	chr17:37761202-37781849	Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
14	nsv908211	chr17:37765047-37782410	Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
15	nsv908212	chr17:37765047-37790340	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
16	nsv457738	chr17:37770005-37831035	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
17	nsv574991	chr17:37770005-37831035	Bivalent Enhancer Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers 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	18 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37775000-37782400	Weak transcription	Gastric	stomach
2	chr17:37775200-37779600	Weak transcription	Spleen	Spleen
3	chr17:37775200-37781200	Weak transcription	Sigmoid Colon	Sigmoid Colon
4	chr17:37775200-37782600	Weak transcription	Lung	lung
5	chr17:37775200-37782800	Weak transcription	Right Atrium	heart
6	chr17:37775400-37782800	Weak transcription	Right Ventricle	heart
7	chr17:37777200-37781200	Enhancers	Fetal Brain Male	brain
8	chr17:37777400-37780200	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr17:37777800-37780200	Enhancers	Primary B cells from peripheral blood	blood
10	chr17:37777800-37780400	Enhancers	Primary B cells from cord blood	blood
11	chr17:37778000-37779800	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr17:37778000-37780200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
13	chr17:37778000-37780200	Enhancers	Primary T helper cells PMA-I stimulated	--
14	chr17:37778000-37780200	Enhancers	Adipose Nuclei	Adipose
15	chr17:37778000-37780200	Enhancers	Fetal Intestine Small	intestine
16	chr17:37778000-37780400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
17	chr17:37778200-37780000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr17:37778200-37780000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
19	chr17:37778200-37780000	Enhancers	Fetal Thymus	thymus
20	chr17:37778200-37780200	Enhancers	Brain Germinal Matrix	brain
21	chr17:37778200-37780200	Enhancers	Dnd41	blood
22	chr17:37778400-37779600	Enhancers	Brain Cingulate Gyrus	brain
23	chr17:37778400-37779600	Enhancers	Fetal Heart	heart
24	chr17:37778400-37779800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
25	chr17:37778400-37779800	Enhancers	Brain Angular Gyrus	brain
26	chr17:37778400-37780000	Enhancers	Pancreas	Pancrea
27	chr17:37778400-37780200	Enhancers	Brain Anterior Caudate	brain
28	chr17:37778400-37780200	Enhancers	Brain Inferior Temporal Lobe	brain
29	chr17:37778400-37780200	Enhancers	Stomach Mucosa	stomach
30	chr17:37778400-37780400	Enhancers	Esophagus	oesophagus
31	chr17:37778400-37782600	Enhancers	Breast Myoepithelial Primary Cells	Breast
32	chr17:37778600-37779600	Enhancers	Skeletal Muscle Female	skeletal muscle
33	chr17:37778600-37779800	Enhancers	Primary neutrophils fromperipheralblood	blood
34	chr17:37778600-37779800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr17:37778600-37779800	Enhancers	Skeletal Muscle Male	skeletal muscle
36	chr17:37778600-37780200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr17:37778800-37779600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr17:37778800-37779600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr17:37778800-37779600	Enhancers	Rectal Mucosa Donor 29	rectum
40	chr17:37778800-37779800	Enhancers	Duodenum Smooth Muscle	Duodenum
41	chr17:37778800-37780000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr17:37778800-37780000	Enhancers	Brain Substantia Nigra	brain
43	chr17:37778800-37780000	Enhancers	Hela-S3	cervix
44	chr17:37778800-37780200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr17:37778800-37780200	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr17:37778800-37780200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
47	chr17:37778800-37780200	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr17:37778800-37780200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
49	chr17:37778800-37780200	Enhancers	Primary T killer memory cells from peripheral blood	blood
50	chr17:37778800-37780200	Enhancers	GM12878-XiMat	blood

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