Variant report

Variant	esv1827424
Chromosome Location	chr4:9324644-9514568
allele	n/a
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	ARID3A	chr4:9454189-9454353	HepG2	liver:	n/a	n/a
2	BATF	chr4:9382976-9383219	GM12878	blood:	n/a	n/a
3	BATF	chr4:9390689-9391024	GM12878	blood:	n/a	n/a
4	BATF	chr4:9456872-9457051	GM12878	blood:	n/a	n/a
5	BATF	chr4:9431784-9432036	GM12878	blood:	n/a	n/a
6	BATF	chr4:9496997-9497347	GM12878	blood:	n/a	n/a
7	BATF	chr4:9511928-9512224	GM12878	blood:	n/a	n/a
8	BATF	chr4:9481131-9481403	GM12878	blood:	n/a	n/a
9	BATF	chr4:9383032-9383262	GM12878	blood:	n/a	n/a
10	BATF	chr4:9481132-9481453	GM12878	blood:	n/a	n/a
11	BATF	chr4:9511904-9512243	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:9382943-9383169	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:9390633-9391020	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:9390780-9390984	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:9497025-9497432	GM12878	blood:	n/a	chr4:9497121-9497129
16	BHLHE40	chr4:9390742-9390935	GM12878	blood:	n/a	n/a
17	BRCA1	chr4:9352626-9352812	HepG2	liver:	n/a	n/a
18	CEBPB	chr4:9405864-9406123	A549	lung:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
19	CEBPB	chr4:9405910-9406125	K562	blood:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
20	CEBPB	chr4:9430641-9430768	HepG2	liver:	n/a	chr4:9430673-9430686 chr4:9430674-9430685
21	CEBPB	chr4:9405866-9406215	HepG2	liver:	n/a	chr4:9406025-9406038 chr4:9406027-9406036 chr4:9406027-9406038 chr4:9406025-9406036 chr4:9406027-9406036 chr4:9406027-9406036 chr4:9406027-9406036
22	CEBPB	chr4:9453481-9453664	HepG2	liver:	n/a	chr4:9453618-9453629
23	CEBPB	chr4:9387057-9387237	HepG2	liver:	n/a	chr4:9387117-9387128
24	CTCF	chr4:9497200-9497350	HepG2	liver:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
25	CTCF	chr4:9481156-9481418	K562	blood:	n/a	n/a
26	CTCF	chr4:9383220-9383370	NHEK	skin:	n/a	n/a
27	CTCF	chr4:9497181-9497421	HepG2	liver:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
28	CTCF	chr4:9499229-9499280	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr4:9497160-9497420	MCF-7	breast:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
30	CTCF	chr4:9456833-9457043	K562	blood:	n/a	n/a
31	CTCF	chr4:9431928-9431985	GM10266	blood:	n/a	n/a
32	CTCF	chr4:9383240-9383390	AG10803	skin:	n/a	n/a
33	CTCF	chr4:9435204-9435316	GM19238	blood:	n/a	n/a
34	CTCF	chr4:9497200-9497350	HRE	kidney:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
35	CTCF	chr4:9383220-9383370	HAc	cerebellar:	n/a	n/a
36	CTCF	chr4:9383051-9383271	K562	blood:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
37	CTCF	chr4:9431877-9431978	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:9383032-9383322	LNCaP	prostate:	n/a	chr4:9383162-9383180 chr4:9383144-9383165 chr4:9383150-9383166 chr4:9383149-9383167 chr4:9383164-9383185
39	CTCF	chr4:9497197-9497421	GM10248	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
40	CTCF	chr4:9497220-9497370	GM12866	blood:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
41	CTCF	chr4:9427033-9427103	Medullo	brain:	n/a	n/a
42	CTCF	chr4:9431689-9432238	A549	lung:	n/a	n/a
43	CTCF	chr4:9481140-9481290	GM06990	blood:	n/a	n/a
44	CTCF	chr4:9435180-9435330	HEK293	kidney:	n/a	n/a
45	CTCF	chr4:9431901-9432078	HepG2	liver:	n/a	n/a
46	CTCF	chr4:9497200-9497350	HRPEpiC	eye:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
47	CTCF	chr4:9497207-9497411	Hela-S3	cervix:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
48	CTCF	chr4:9497220-9497370	MCF-7	breast:	n/a	chr4:9497303-9497313 chr4:9497301-9497310 chr4:9497300-9497321 chr4:9497301-9497314 chr4:9497298-9497316
49	CTCF	chr4:9431835-9432103	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:9401465-9401565	LNCaP	prostate:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:9382066-9382116	K562	blood:	n/a
2	chr4:9382953-9383003	GM19239	blood:	n/a
3	chr4:9453084-9453134	HCT-116	colon:	n/a
4	chr4:9507499-9507549	GM19239	blood:	n/a
5	chr4:9355372-9355422	Caco-2	colon:	n/a
6	chr4:9510286-9510336	Caco-2	colon:	n/a
7	chr4:9382953-9383003	HEK293	kidney:	embryo
8	chr4:9382066-9382116	K562	blood:	n/a
9	chr4:9382953-9383003	GM19239	blood:	n/a
10	chr4:9453084-9453134	HCT-116	colon:	n/a
11	chr4:9507499-9507549	GM19239	blood:	n/a
12	chr4:9355372-9355422	Caco-2	colon:	n/a
13	chr4:9510286-9510336	Caco-2	colon:	n/a
14	chr4:9382953-9383003	HEK293	kidney:	embryo
15	chr4:9493231-9493281	Jurkat	blood:	n/a
16	chr4:9352827-9352877	Hela-S3	cervix:	n/a
17	chr4:9507285-9507335	AG10803	skin:	n/a
18	chr4:9494907-9494957	GM06990	blood:	n/a
19	chr4:9352827-9352877	HMEC	breast:	n/a
20	chr4:9484735-9484785	HRCEpiC	kidney:	n/a
21	chr4:9382066-9382116	Jurkat	blood:	n/a
22	chr4:9453084-9453134	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:9453084-9453134	HEK293	kidney:	embryo
24	chr4:9505698-9505748	H1-hESC	embryonic stem cell:	embryo
25	chr4:9509787-9509837	HL-60	blood:	n/a
26	chr4:9494487-9494537	K562	blood:	n/a
27	chr4:9500293-9500343	A549	lung:	n/a
28	chr4:9500465-9500515	AG09319	gingival:	n/a
29	chr4:9497357-9497407	T-47D	breast:	n/a
30	chr4:9508254-9508304	HL-60	blood:	n/a
31	chr4:9508890-9508940	PrEC	prostate:	n/a
32	chr4:9382066-9382116	SK-N-SH	brain:	n/a
33	chr4:9445586-9445636	HepG2	liver:	n/a
34	chr4:9475346-9475396	SAEC	small airway:	n/a
35	chr4:9500174-9500224	SK-N-SH_RA	brain:	n/a
36	chr4:9382953-9383003	PANC-1	pancreas:	n/a
37	chr4:9478126-9478176	HCT-116	colon:	n/a
38	chr4:9446084-9446134	Jurkat	blood:	n/a
39	chr4:9445158-9445208	SK-N-MC	brain:	n/a
40	chr4:9453010-9453060	Hela-S3	cervix:	n/a
41	chr4:9509830-9509880	U87	brain:	n/a
42	chr4:9508890-9508940	BJ	skin:	n/a
43	chr4:9505191-9505241	NB4	blood:	n/a
44	chr4:9500293-9500343	GM06990	blood:	n/a
45	chr4:9499367-9499417	SAEC	small airway:	n/a
46	chr4:9352827-9352877	Caco-2	colon:	n/a
47	chr4:9481822-9481872	HCT-116	colon:	n/a
48	chr4:9382765-9382815	IMR90	lung:	fetal
49	chr4:9493231-9493281	NH-A	brain:	n/a
50	chr4:9382961-9383011	SKMC	muscle:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:4147498..4148004-chr4:9497288..9497793,2	MCF-7	breast:
2	chr4:4147469..4148009-chr4:9497278..9497791,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DEFB131-1	chr4:9470746-9471694	NONHSAT095133
2	lnc-RP11-1396O13.13.1-1	chr4:9376809-9376876	XLOC_003878
3	lnc-RP11-1396O13.13.1-1	chr4:9387384-9387466	XLOC_003878
4	lnc-RP11-1396O13.13.1-2	chr4:9390589-9390785	l_2601_chr4:9381878-9390785_kidney
5	lnc-RP11-1396O13.13.1-2	chr4:9381879-9382091	l_2601_chr4:9381878-9390785_kidney
6	lnc-RP11-1396O13.13.1-1	chr4:9388003-9388085	XLOC_003878

Variant related genes	Relation type
RNA5SP153	TF binding region
OR7E85P	TF binding region
ENSG00000266246	TF binding region
USP17L24	TF binding region
ENSG00000232773	TF binding region
OR7E84P	TF binding region
USP17L29	TF binding region
OR7E86P	TF binding region
ENSG00000219492	TF binding region
DEFB131	TF binding region
USP17L9P	TF binding region
USP17L5	TF binding region
USP17L30	TF binding region
UNC93B7	TF binding region
ENSG00000188438	TF binding region
OR7E83P	TF binding region
USP17L26	TF binding region
USP17L25	TF binding region
USP17L6P	TF binding region
USP17L27	TF binding region
USP17L28	TF binding region
RNA5SP153	CpG island
OR7E85P	CpG island
ENSG00000266246	CpG island
USP17L24	CpG island
ENSG00000232773	CpG island
OR7E84P	CpG island
USP17L29	CpG island
OR7E86P	CpG island
ENSG00000219492	CpG island
DEFB131	CpG island
USP17L9P	CpG island
USP17L5	CpG island
USP17L30	CpG island
UNC93B7	CpG island
ENSG00000188438	CpG island
OR7E83P	CpG island
USP17L26	CpG island
USP17L25	CpG island
USP17L6P	CpG island
USP17L27	CpG island
USP17L28	CpG island

Extended variants
information (count: 3845 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:3845 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369977695	chr4:9325935-9325936	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs145207877	chr4:9325940-9325941	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs142143794	chr4:9325956-9325957	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs151223510	chr4:9325957-9325958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs139186150	chr4:9325967-9325968	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs144636811	chr4:9325968-9325969	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs147642755	chr4:9325984-9325985	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs147873271	chr4:9325987-9325988	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs142231502	chr4:9326041-9326042	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111262992	chr4:9326046-9326047	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs141676001	chr4:9326095-9326096	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs147061553	chr4:9326109-9326110	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs145375663	chr4:9326117-9326118	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs149194340	chr4:9326122-9326123	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs138657043	chr4:9326127-9326128	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs143326501	chr4:9326137-9326138	ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs201683960	chr4:9326153-9326154	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
18	rs57310149	chr4:9326159-9326160	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
19	rs148380449	chr4:9326160-9326161	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
20	rs142230279	chr4:9326169-9326170	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
21	rs564748731	chr4:9326177-9326178	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
22	rs528771909	chr4:9326178-9326179	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
23	rs374931243	chr4:9326185-9326186	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
24	rs145274378	chr4:9326187-9326188	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
25	rs137880374	chr4:9326188-9326189	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
26	rs142496046	chr4:9326199-9326200	ZNF genes & repeats Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
27	rs141165282	chr4:9328902-9328903	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs144874970	chr4:9328911-9328912	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs138736333	chr4:9328921-9328922	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs141220871	chr4:9328923-9328924	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs139077567	chr4:9333308-9333309	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs149514246	chr4:9333320-9333321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs144019747	chr4:9333355-9333356	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs148697909	chr4:9333392-9333393	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs144512985	chr4:9333398-9333399	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs147677639	chr4:9333469-9333470	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs140724755	chr4:9333495-9333496	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs144572851	chr4:9333528-9333529	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs150045455	chr4:9333648-9333649	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs145329033	chr4:9333657-9333658	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs149231486	chr4:9333667-9333668	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs145166844	chr4:9333669-9333670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs201282879	chr4:9352692-9352693	ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs199777440	chr4:9352801-9352802	Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs538004740	chr4:9355388-9355389	Inactive region	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs528711746	chr4:9361104-9361105	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs148542026	chr4:9361112-9361113	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs546949225	chr4:9361123-9361124	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs562382092	chr4:9361166-9361167	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs200909464	chr4:9361177-9361178	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Melanoma	20688739	CNVD
Wilms tumour	21544195	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Sezary syndrome	18413736	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Urothelial carcinoma	21177765	CNVD
Neuroblastoma	20406844	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:267 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:9326000-9326200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:9326000-9326200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:9326000-9326200	ZNF genes & repeats	Adipose Nuclei	Adipose
4	chr4:9326000-9326200	ZNF genes & repeats	Aorta	Aorta
5	chr4:9326000-9326200	ZNF genes & repeats	Brain Cingulate Gyrus	brain
6	chr4:9326000-9326200	ZNF genes & repeats	Brain Hippocampus Middle	brain
7	chr4:9326000-9326200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
8	chr4:9326000-9326200	Flanking Bivalent TSS/Enh	Duodenum Mucosa	Duodenum
9	chr4:9326000-9326200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
10	chr4:9326000-9326200	ZNF genes & repeats	Gastric	stomach
11	chr4:9326000-9326200	ZNF genes & repeats	Left Ventricle	heart
12	chr4:9326000-9326200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
13	chr4:9326000-9326200	ZNF genes & repeats	Stomach Mucosa	stomach
14	chr4:9326000-9326200	ZNF genes & repeats	Spleen	Spleen
15	chr4:9352600-9352800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:9352600-9353000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:9352600-9353000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr4:9352600-9353000	ZNF genes & repeats	Gastric	stomach
19	chr4:9352600-9353000	ZNF genes & repeats	Pancreas	Pancrea
20	chr4:9352600-9353000	ZNF genes & repeats	Spleen	Spleen
21	chr4:9352800-9353000	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:9382400-9382600	Enhancers	Breast Myoepithelial Primary Cells	Breast
23	chr4:9382400-9382600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
24	chr4:9382400-9382600	Enhancers	Colonic Mucosa	Colon
25	chr4:9382400-9382600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
26	chr4:9382400-9382600	Enhancers	Pancreas	Pancrea
27	chr4:9382400-9382600	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr4:9382400-9382800	Enhancers	Cortex derived primary cultured neurospheres	brain
29	chr4:9382400-9383000	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr4:9382400-9383200	Active TSS	HUES6 Cell Line	embryonic stem cell
31	chr4:9382400-9383200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:9382400-9383200	Active TSS	Duodenum Mucosa	Duodenum
33	chr4:9382600-9382800	Enhancers	Primary T cells fromperipheralblood	blood
34	chr4:9382600-9382800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr4:9382600-9382800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr4:9382600-9382800	Enhancers	Fetal Muscle Leg	muscle
37	chr4:9382600-9382800	Enhancers	Lung	lung
38	chr4:9382600-9382800	Enhancers	Psoas Muscle	Psoas
39	chr4:9382600-9383000	Active TSS	iPS-15b Cell Line	embryonic stem cell
40	chr4:9382600-9383000	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
41	chr4:9382600-9383000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
42	chr4:9382600-9383000	Enhancers	Adipose Nuclei	Adipose
43	chr4:9382600-9383000	Active TSS	Brain Angular Gyrus	brain
44	chr4:9382600-9383000	Active TSS	Brain Inferior Temporal Lobe	brain
45	chr4:9382600-9383000	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr4:9382600-9383000	Flanking Active TSS	Colonic Mucosa	Colon
47	chr4:9382600-9383000	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
48	chr4:9382600-9383000	Flanking Active TSS	Pancreas	Pancrea
49	chr4:9382600-9383000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
50	chr4:9382600-9383000	Active TSS	NH-A	brain

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