Variant report

Variant	rs3764352
Chromosome Location	chr17:37790939-37790940
allele	A/G
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	chr17:37790820-37790970	HRPEpiC	eye:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
2	CTCF	chr17:37790643-37790959	Hela-S3	cervix:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
3	CTCF	chr17:37790689-37790989	ECC-1	luminal epithelium:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
4	CTCF	chr17:37790718-37790959	LNCaP	prostate:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
5	RAD21	chr17:37790696-37790977	HepG2	liver:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
6	MAZ	chr17:37790652-37790968	K562	blood:	n/a	n/a
7	CTCF	chr17:37790492-37791033	K562	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
8	CTCF	chr17:37790633-37790985	ECC-1	luminal epithelium:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
9	CTCF	chr17:37790415-37791047	H1-hESC	embryonic stem cell:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
10	CTCF	chr17:37790710-37790961	Pancreas_OC	pancreas:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
11	CTCF	chr17:37790679-37790993	SK-N-SH_RA	brain:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
12	CTCF	chr17:37790933-37791020	GM19238	blood:	n/a	n/a
13	CTCF	chr17:37790597-37791001	Medullo	brain:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
14	CTCF	chr17:37790366-37791140	K562	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
15	CTCF	chr17:37790557-37791020	GM12878	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
16	CTCF	chr17:37789741-37791243	A549	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
17	CTCF	chr17:37790603-37791055	IMR90	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
18	CTCF	chr17:37790405-37791127	MCF-7	breast:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
19	CTCF	chr17:37790322-37791165	HCT-116	colon:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
20	CTCF	chr17:37790466-37790992	H1-hESC	embryonic stem cell:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
21	RAD21	chr17:37790397-37791202	HCT-116	colon:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
22	RAD21	chr17:37790616-37791038	H1-hESC	embryonic stem cell:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
23	CTCF	chr17:37790612-37790958	MCF-7	breast:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
24	CTCF	chr17:37790463-37791093	A549	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
25	CTCF	chr17:37790582-37790978	GM10266	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
26	RAD21	chr17:37790652-37790978	H1-hESC	embryonic stem cell:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
27	CTCF	chr17:37790800-37790950	HVMF	connective:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
28	CTCF	chr17:37790574-37791032	A549	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
29	CTCF	chr17:37790482-37791037	GM12878	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
30	NFYA	chr17:37790609-37791014	Hela-S3	cervix:	n/a	n/a
31	ZNF143	chr17:37790564-37791044	GM12878	blood:	n/a	n/a
32	CTCF	chr17:37790532-37791118	T-47D	breast:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
33	CTCF	chr17:37790391-37791233	HepG2	liver:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
34	SMC3	chr17:37790726-37791038	K562	blood:	n/a	chr17:37790837-37790851
35	BCL3	chr17:37790526-37791199	A549	lung:	n/a	n/a
36	RAD21	chr17:37790656-37791012	IMR90	lung:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
37	RAD21	chr17:37790660-37790986	SK-N-SH_RA	brain:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
38	RAD21	chr17:37790655-37790966	Hela-S3	cervix:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
39	SMC3	chr17:37790631-37791025	GM12878	blood:	n/a	chr17:37790837-37790851
40	CTCF	chr17:37790636-37790961	Lung_OC	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
41	POLR2A	chr17:37790868-37791223	HepG2	liver:	n/a	n/a
42	MYBL2	chr17:37790469-37791013	HepG2	liver:	n/a	n/a
43	CTCF	chr17:37790701-37790946	Kidney_OC	kidney:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
44	ARID3A	chr17:37790617-37791026	HepG2	liver:	n/a	n/a
45	RAD21	chr17:37790451-37791078	H1-hESC	embryonic stem cell:	n/a	chr17:37790752-37790765 chr17:37790839-37790848 chr17:37790754-37790766 chr17:37790833-37790852 chr17:37790836-37790849
46	CTCF	chr17:37790800-37790950	HL-60	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
47	CTCF	chr17:37790222-37791292	HCT-116	colon:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
48	CTCF	chr17:37790731-37791004	A549	lung:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851
49	ZNF143	chr17:37790657-37791013	K562	blood:	n/a	n/a
50	CTCF	chr17:37790729-37790963	GM13977	blood:	n/a	chr17:37790836-37790852 chr17:37790835-37790853 chr17:37790840-37790848 chr17:37790830-37790851

No.	Distal block	Cell Line	Cell type
1	chr17:37785506..37788397-chr17:37788916..37793369,4	K562	blood:
2	chr17:37789471..37791960-chr17:37905766..37908053,2	MCF-7	breast:
3	chr17:37790905..37794856-chr17:37820000..37822270,4	K562	blood:
4	chr17:37790730..37792254-chr17:37891251..37894000,2	K562	blood:
5	chr17:37789742..37792172-chr17:37795424..37797567,2	MCF-7	breast:
6	chr17:37789315..37792571-chr17:37910228..37913282,4	K562	blood:

Variant related genes	Relation type
STARD3	TF binding region
ENSG00000131771	Chromatin interaction
ENSG00000173991	Chromatin interaction

Extended variants
information (count: 93 )
Associated
traits (count: 6 )

rSNPs within LD-proxies of this variant (count:80)

rs_ID	r²[population]
rs1018246	0.87[ASN][1000 genomes]
rs1053651	0.87[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs10852934	0.83[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs11651497	0.90[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11657058	0.83[CEU][hapmap]
rs11657153	0.83[CEU][hapmap]
rs11658786	0.89[ASN][1000 genomes]
rs11869286	0.81[ASW][hapmap];0.87[CHB][hapmap];0.86[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.91[ASN][1000 genomes]
rs12150047	0.83[CEU][hapmap]
rs12150298	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs12150603	0.82[ASW][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs12453682	0.82[CHB][hapmap];0.85[CHD][hapmap];0.82[GIH][hapmap];0.85[JPT][hapmap];0.85[LWK][hapmap];0.93[MKK][hapmap];0.90[ASN][1000 genomes]
rs12937013	0.83[CEU][hapmap]
rs12938099	0.83[CEU][hapmap]
rs12940986	0.82[ASW][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs12947506	0.83[CEU][hapmap]
rs14050	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs1476278	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs1495099	0.99[ASN][1000 genomes]
rs1495100	0.87[ASN][1000 genomes]
rs1495101	0.87[ASN][1000 genomes]
rs1495102	0.87[ASN][1000 genomes]
rs1565920	0.87[ASN][1000 genomes]
rs1565922	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs1874228	0.82[ASW][hapmap];0.95[CHB][hapmap];0.98[CHD][hapmap];0.87[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.87[MKK][hapmap];0.97[ASN][1000 genomes]
rs1877031	0.88[ASW][hapmap];0.87[CHB][hapmap];0.86[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.92[LWK][hapmap];0.95[MKK][hapmap];0.91[ASN][1000 genomes]
rs2247862	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2271308	0.83[CHB][hapmap];0.84[CHD][hapmap];0.86[GIH][hapmap];0.82[JPT][hapmap];0.89[ASN][1000 genomes]
rs2271309	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2313171	0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs2517952	0.80[ASN][1000 genomes]
rs2517953	0.82[ASN][1000 genomes]
rs2517954	0.81[ASN][1000 genomes]
rs2517955	0.82[ASW][hapmap];0.80[ASN][1000 genomes]
rs2517956	0.80[ASN][1000 genomes]
rs2517957	0.89[JPT][hapmap];0.89[ASN][1000 genomes]
rs2517958	0.81[JPT][hapmap];0.89[ASN][1000 genomes]
rs2517959	0.81[ASN][1000 genomes]
rs2934951	0.87[ASN][1000 genomes]
rs2934952	0.87[ASN][1000 genomes]
rs2934953	0.85[JPT][hapmap];0.87[ASN][1000 genomes]
rs2934956	0.87[ASN][1000 genomes]
rs2941503	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2941504	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs2941505	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2941506	0.87[ASN][1000 genomes]
rs2952151	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs2952152	0.86[ASN][1000 genomes]
rs33953566	0.99[ASN][1000 genomes]
rs3751903	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3764353	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3794712	0.97[ASN][1000 genomes]
rs3817160	0.90[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs407307	0.84[ASN][1000 genomes]
rs4794817	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4795379	0.83[CEU][hapmap]
rs4795388	0.95[CHB][hapmap];0.93[CHD][hapmap];0.95[JPT][hapmap];0.92[ASN][1000 genomes]
rs4795389	0.97[ASN][1000 genomes]
rs4795390	0.99[ASN][1000 genomes]
rs732083	0.87[ASN][1000 genomes]
rs732084	0.87[ASN][1000 genomes]
rs7503377	0.83[CEU][hapmap]
rs8069074	0.83[CEU][hapmap]
rs8077172	0.87[ASN][1000 genomes]
rs8078228	0.81[JPT][hapmap];0.87[ASN][1000 genomes]
rs879606	0.83[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs881844	0.83[CHB][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs903501	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs903502	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs907087	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs907088	0.87[ASN][1000 genomes]
rs907089	0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs907090	0.87[ASN][1000 genomes]
rs907094	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];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9303274	0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs931992	0.88[ASW][hapmap];0.83[CHB][hapmap];0.84[CHD][hapmap];0.90[GIH][hapmap];0.82[JPT][hapmap];0.92[LWK][hapmap];0.95[MKK][hapmap]
rs9646419	0.83[CEU][hapmap]
rs9675194	0.81[GIH][hapmap];0.82[JPT][hapmap];0.87[ASN][1000 genomes]
rs9915323	0.91[CHB][hapmap];0.85[JPT][hapmap];0.92[ASN][1000 genomes]
rs9972882	0.87[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];0.91[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	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	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
12	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
13	nsv516757	chr17:37781849-37834541	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	16 gene(s)	inside rSNPs	diseases

mRNA abundance (count:6)

SNP	Gene	Cis/trans	Tissue	Source
rs3764352	SLFN14	cis	parietal	SCAN
rs3764352	SPACA3	cis	parietal	SCAN
rs3764352	ORMDL3	Cis_1M	lymphoblastoid	RTeQTL
rs3764352	PGAP3	cis	Heart Left Ventricle	GTEx
rs3764352	DHRS11	cis	cerebellum	SCAN
rs3764352	IGFBP4	cis	parietal	SCAN

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:37783400-37792200	Weak transcription	Lung	lung
2	chr17:37784600-37792800	Weak transcription	Right Atrium	heart
3	chr17:37785000-37791000	Weak transcription	Esophagus	oesophagus
4	chr17:37785200-37792800	Enhancers	H1 Cell Line	embryonic stem cell
5	chr17:37785200-37792800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:37785400-37792600	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr17:37785800-37792400	Weak transcription	Fetal Lung	lung
8	chr17:37786600-37791400	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr17:37786800-37792000	Weak transcription	Spleen	Spleen
10	chr17:37787000-37792600	Enhancers	Primary neutrophils fromperipheralblood	blood
11	chr17:37787400-37791200	Enhancers	Fetal Intestine Large	intestine
12	chr17:37787400-37792800	Enhancers	Fetal Thymus	thymus
13	chr17:37787600-37791200	Enhancers	Stomach Mucosa	stomach
14	chr17:37787800-37791200	Enhancers	Brain Angular Gyrus	brain
15	chr17:37787800-37791200	Enhancers	Brain Hippocampus Middle	brain
16	chr17:37788000-37791800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr17:37788000-37792600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr17:37788200-37791000	Enhancers	Brain Cingulate Gyrus	brain
19	chr17:37788200-37791200	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr17:37788200-37792400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr17:37788200-37792600	Enhancers	Brain Substantia Nigra	brain
22	chr17:37788200-37792600	Weak transcription	HMEC	breast
23	chr17:37788200-37793000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr17:37788200-37793400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr17:37788400-37791800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr17:37788400-37792600	Weak transcription	NHEK	skin
27	chr17:37788400-37793000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr17:37788600-37792800	Weak transcription	Fetal Brain Female	brain
29	chr17:37788800-37791000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr17:37788800-37791200	Enhancers	Adipose Nuclei	Adipose
31	chr17:37788800-37792200	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr17:37788800-37792800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr17:37789000-37791000	Weak transcription	A549	lung
34	chr17:37789000-37791200	Enhancers	Pancreas	Pancrea
35	chr17:37789000-37791600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr17:37789000-37792000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr17:37789200-37791200	Genic enhancers	Fetal Intestine Small	intestine
38	chr17:37789200-37792000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr17:37789400-37791000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr17:37789400-37791800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
41	chr17:37789400-37791800	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr17:37789400-37793000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr17:37789600-37792400	Weak transcription	Rectal Smooth Muscle	rectum
44	chr17:37789800-37792600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr17:37789800-37792600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr17:37789800-37792600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr17:37790000-37791000	Enhancers	Stomach Smooth Muscle	stomach
48	chr17:37790000-37791600	Enhancers	Duodenum Mucosa	Duodenum
49	chr17:37790000-37792600	Enhancers	Duodenum Smooth Muscle	Duodenum
50	chr17:37790000-37792600	Genic enhancers	Rectal Mucosa Donor 29	rectum

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