Variant report

Variant	nsv830156
Chromosome Location	chr4:175725040-175916435
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:734)
CpG islands
(count:1711)
Chromatin interactive
region (count:23)
LncRNA
region (count:28)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:175750407-175750888	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:175750632-175750818	K562	blood:	n/a	n/a
3	BATF	chr4:175803802-175804005	GM12878	blood:	n/a	n/a
4	BATF	chr4:175850087-175850349	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:175849333-175849694	GM12878	blood:	n/a	n/a
6	BCL11A	chr4:175850093-175850258	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:175849226-175850369	GM12878	blood:	n/a	n/a
8	BHLHE40	chr4:175854210-175854594	GM12878	blood:	n/a	n/a
9	BHLHE40	chr4:175828637-175828923	GM12878	blood:	n/a	n/a
10	CBX3	chr4:175828740-175829078	HCT-116	colon:	n/a	n/a
11	CBX3	chr4:175828689-175828929	K562	blood:	n/a	n/a
12	CBX3	chr4:175828717-175829001	K562	blood:	n/a	n/a
13	CBX3	chr4:175749887-175750279	K562	blood:	n/a	n/a
14	CEBPB	chr4:175834673-175835085	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr4:175742727-175742984	A549	lung:	n/a	chr4:175742821-175742832
16	CEBPB	chr4:175805720-175805999	A549	lung:	n/a	chr4:175805838-175805849
17	CEBPB	chr4:175805695-175805993	IMR90	lung:	n/a	chr4:175805838-175805849
18	CEBPB	chr4:175848115-175848557	MCF-7	breast:	n/a	n/a
19	CEBPB	chr4:175789121-175789332	HepG2	liver:	n/a	chr4:175789156-175789167
20	CEBPB	chr4:175897464-175897664	HepG2	liver:	n/a	chr4:175897610-175897621
21	CEBPB	chr4:175750393-175750477	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:175791814-175792305	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:175777326-175777393	K562	blood:	n/a	n/a
24	CEBPB	chr4:175902548-175902769	HepG2	liver:	n/a	chr4:175902691-175902702
25	CEBPB	chr4:175848165-175848483	MCF-7	breast:	n/a	n/a
26	CEBPB	chr4:175742736-175742981	HepG2	liver:	n/a	chr4:175742821-175742832
27	CEBPB	chr4:175791775-175792417	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:175742714-175742960	IMR90	lung:	n/a	chr4:175742821-175742832
29	CEBPB	chr4:175777349-175777510	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:175754665-175754716	K562	blood:	n/a	n/a
31	CEBPB	chr4:175805733-175805920	H1-hESC	embryonic stem cell:	n/a	chr4:175805838-175805849
32	CEBPB	chr4:175805704-175806012	HepG2	liver:	n/a	chr4:175805838-175805849
33	CHD1	chr4:175849509-175850044	GM12878	blood:	n/a	n/a
34	CHD1	chr4:175750058-175750362	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:175849189-175850449	GM12878	blood:	n/a	n/a
36	CHD2	chr4:175750152-175750594	K562	blood:	n/a	n/a
37	CHD2	chr4:175750123-175750469	GM12878	blood:	n/a	n/a
38	CHD2	chr4:175852046-175852455	GM12878	blood:	n/a	n/a
39	CHD2	chr4:175749962-175750784	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr4:175867543-175867639	GM12878	blood:	n/a	n/a
41	CHD2	chr4:175854570-175854856	GM12878	blood:	n/a	n/a
42	CTBP2	chr4:175750054-175750797	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr4:175795175-175795384	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:175795025-175795480	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:175795283-175795307	LNCaP	prostate:	n/a	n/a
46	CTCF	chr4:175795142-175795419	Medullo	brain:	n/a	n/a
47	CTCF	chr4:175750620-175750770	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr4:175795178-175795405	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:175795180-175795330	GM12866	blood:	n/a	n/a
50	CTCF	chr4:175795200-175795350	WERI-Rb-1	eye:	n/a	n/a

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:175750373-175750423	PANC-1	pancreas:	n/a
2	chr4:175751001-175751051	ECC-1	luminal epithelium:	n/a
3	chr4:175887842-175887892	SAEC	small airway:	n/a
4	chr4:175750373-175750423	PANC-1	pancreas:	n/a
5	chr4:175751001-175751051	ECC-1	luminal epithelium:	n/a
6	chr4:175887842-175887892	SAEC	small airway:	n/a
7	chr4:175839604-175839654	ECC-1	luminal epithelium:	n/a
8	chr4:175839468-175839518	HCPEpiC	choroid plexus:	n/a
9	chr4:175789139-175789189	NB4	blood:	n/a
10	chr4:175839604-175839654	GM12892	blood:	n/a
11	chr4:175897327-175897377	IMR90	lung:	fetal
12	chr4:175839423-175839473	HUVEC	blood vessel:	n/a
13	chr4:175897327-175897377	SK-N-MC	brain:	n/a
14	chr4:175839604-175839654	HepG2	liver:	n/a
15	chr4:175895177-175895227	AG04450	lung:	fetal
16	chr4:175887842-175887892	IMR90	lung:	fetal
17	chr4:175841091-175841141	HCPEpiC	choroid plexus:	n/a
18	chr4:175841091-175841141	HRPEpiC	eye:	n/a
19	chr4:175851052-175851102	HMEC	breast:	n/a
20	chr4:175750507-175750557	AG09309	skin:	n/a
21	chr4:175838768-175838818	NHBE	bronchial:	n/a
22	chr4:175750583-175750633	HCT-116	colon:	n/a
23	chr4:175750802-175750852	HIPEpiC	eye:	n/a
24	chr4:175838768-175838818	GM12892	blood:	n/a
25	chr4:175887842-175887892	GM06990	blood:	n/a
26	chr4:175750507-175750557	RPTEC	kidney:	n/a
27	chr4:175887842-175887892	NHDF-neo	bronchial:	n/a
28	chr4:175750583-175750633	H1-hESC	embryonic stem cell:	embryo
29	chr4:175839423-175839473	NT2-D1	testis:	n/a
30	chr4:175750510-175750560	U87	brain:	n/a
31	chr4:175838768-175838818	AG09309	skin:	n/a
32	chr4:175752781-175752831	BJ	skin:	n/a
33	chr4:175750109-175750159	BJ	skin:	n/a
34	chr4:175750637-175750687	LNCaP	prostate:	n/a
35	chr4:175750109-175750159	GM12892	blood:	n/a
36	chr4:175750792-175750842	AG09319	gingival:	n/a
37	chr4:175897327-175897377	GM19239	blood:	n/a
38	chr4:175839610-175839660	MCF10A-Er-Src	breast:	n/a
39	chr4:175750373-175750423	HMEC	breast:	n/a
40	chr4:175838768-175838818	HAEpiC	amniotic membrane:	n/a
41	chr4:175752696-175752746	HEK293	kidney:	embryo
42	chr4:175851052-175851102	HIPEpiC	eye:	n/a
43	chr4:175750527-175750577	HCPEpiC	choroid plexus:	n/a
44	chr4:175750802-175750852	LNCaP	prostate:	n/a
45	chr4:175897327-175897377	SAEC	small airway:	n/a
46	chr4:175750527-175750577	MCF-7	breast:	n/a
47	chr4:175751001-175751051	HEEpiC	esophagus:	n/a
48	chr4:175899203-175899253	LNCaP	prostate:	n/a
49	chr4:175750507-175750557	MCF-7	breast:	n/a
50	chr4:175750637-175750687	A549	lung:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:175795214..175795815-chr4:176031046..176031911,2	MCF-7	breast:
2	chr4:175741383..175744501-chr4:175747246..175749375,3	MCF-7	breast:
3	chr4:175824252..175826749-chr4:175827509..175829887,2	K562	blood:
4	chr4:175730873..175733814-chr4:175736376..175738792,2	MCF-7	breast:
5	chr4:175889489..175891812-chr4:175895689..175898573,2	MCF-7	breast:
6	chr4:175752218..175753789-chr4:175757146..175759391,2	K562	blood:
7	chr4:175842803..175844474-chr4:175850265..175852682,2	MCF-7	breast:
8	chr4:175824252..175826749-chr4:175827509..175829887,2	K562	blood:
9	chr4:175749505..175752528-chr4:175753322..175755968,3	K562	blood:
10	chr4:175722667..175724604-chr4:175731422..175734130,2	MCF-7	breast:
11	chr4:175752218..175753789-chr4:175757146..175759391,2	K562	blood:
12	chr4:175741383..175744501-chr4:175747246..175749375,3	MCF-7	breast:
13	chr4:175750658..175752347-chr4:175791168..175793959,2	MCF-7	breast:
14	chr4:175748664..175750520-chr4:175777181..175779077,2	MCF-7	breast:
15	chr4:175889489..175891812-chr4:175895689..175898573,2	MCF-7	breast:
16	chr4:175842803..175844474-chr4:175850265..175852682,2	MCF-7	breast:
17	chr4:175730873..175733814-chr4:175736376..175738792,2	MCF-7	breast:
18	chr4:175863834..175867164-chr4:175868876..175871904,3	MCF-7	breast:
19	chr4:175732826..175734634-chr4:175741566..175744026,2	K562	blood:
20	chr4:175863834..175867164-chr4:175868876..175871904,3	MCF-7	breast:
21	chr4:175750746..175753052-chr4:175753645..175755940,3	MCF-7	breast:
22	chr4:175794804..175795498-chr4:176173944..176174819,2	MCF-7	breast:
23	chr4:175732826..175734634-chr4:175741566..175744026,2	K562	blood:

(count:28 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CEP44-5	chr4:175777682-175777758	NONHSAT099327
2	lnc-GLRA3-2	chr4:175844964-175845189	NONHSAT099333
3	lnc-CEP44-5	chr4:175750876-175751017	XLOC_003789
4	lnc-CEP44-5	chr4:175752879-175753037	XLOC_003789
5	lnc-CEP44-5	chr4:175777682-175777760	XLOC_003789
6	lnc-CEP44-5	chr4:175750819-175751017	XLOC_003789
7	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
8	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
9	lnc-CEP44-5	chr4:175839509-175839622	NONHSAT099331
10	lnc-GLRA3-1	chr4:175900489-175900532	ENSG00000250431.1
11	lnc-CEP44-5	chr4:175789957-175791938	XLOC_003789
12	lnc-CEP44-5	chr4:175777682-175777758	XLOC_003789
13	lnc-CEP44-5	chr4:175756000-175756088	NONHSAT099327
14	lnc-CEP44-5	chr4:175789966-175790300	XLOC_003789
15	lnc-CEP44-5	chr4:175841838-175841943	NONHSAT099331
16	lnc-CEP44-5	chr4:175796946-175797115	XLOC_003789
17	lnc-CEP44-5	chr4:175841838-175841943	NONHSAT099332
18	lnc-CEP44-5	chr4:175852137-175852325	NONHSAT099327
19	lnc-CEP44-5	chr4:175858084-175858128	NONHSAT099332
20	lnc-CEP44-5	chr4:175852137-175852549	NONHSAT099331
21	lnc-CEP44-5	chr4:175852137-175852454	NONHSAT099332
22	lnc-CEP44-5	chr4:175839526-175839622	NONHSAT099332
23	lnc-GLRA3-1	chr4:175899439-175899532	ENSG00000250431.1
24	lnc-CEP44-5	chr4:175789957-175791186	XLOC_003789
25	lnc-CEP44-5	chr4:175802504-175802532	XLOC_003789
26	lnc-GLRA3-1	chr4:175898722-175898816	ENSG00000250431.1
27	lnc-CEP44-5	chr4:175756000-175756088	XLOC_003789
28	lnc-CEP44-5	chr4:175750840-175751017	NONHSAT099327

No data

Variant related genes	Relation type
ENSG00000250431	TF binding region
ENSG00000250200	TF binding region
GLRA3	TF binding region
ADAM29	TF binding region
ENSG00000265493	TF binding region
ENSG00000250431	CpG island
ENSG00000250200	CpG island
GLRA3	CpG island
ADAM29	CpG island
ENSG00000265493	CpG island
ENSG00000168594	chromatin interactions
ENSG00000145451	chromatin interactions
ALDH1B1	miRNA target sites
RBM15	miRNA target sites

Extended variants
information (count: 1818 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1818 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553862246	chr4:175731206-175731207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567007893	chr4:175731249-175731250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs28664890	chr4:175731369-175731370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72708276	chr4:175731450-175731451	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs540853729	chr4:175731476-175731477	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114497219	chr4:175731491-175731492	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535721816	chr4:175731494-175731495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs548586145	chr4:175731550-175731551	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568475251	chr4:175731555-175731556	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560682285	chr4:175731564-175731565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575786567	chr4:175731565-175731566	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6816364	chr4:175731572-175731573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376658505	chr4:175731737-175731738	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557555771	chr4:175731742-175731743	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs577799938	chr4:175731766-175731767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533722692	chr4:175731768-175731769	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs553981127	chr4:175731868-175731869	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184791749	chr4:175731869-175731870	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs573999889	chr4:175731882-175731883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs539585273	chr4:175731883-175731884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs558543272	chr4:175731933-175731934	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542902475	chr4:175731950-175731951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs76897840	chr4:175731968-175731969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575708170	chr4:175731971-175731972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188163671	chr4:175732025-175732026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564409093	chr4:175732056-175732057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533605571	chr4:175732079-175732080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs546902423	chr4:175732087-175732088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs79834472	chr4:175732112-175732113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs529554699	chr4:175732131-175732132	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs78127666	chr4:175732198-175732199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34393605	chr4:175732238-175732239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs367625302	chr4:175732249-175732250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs557862758	chr4:175732265-175732266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs143695330	chr4:175732266-175732267	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1385841	chr4:175732267-175732268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs202242243	chr4:175732272-175732273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs545696543	chr4:175732337-175732338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs76452779	chr4:175732352-175732353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs570060073	chr4:175732354-175732355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571275641	chr4:175732374-175732375	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533851128	chr4:175732375-175732376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs554018009	chr4:175732387-175732388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs1388341	chr4:175732395-175732396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567420610	chr4:175732419-175732420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs536597624	chr4:175732424-175732425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs556489602	chr4:175732428-175732429	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs146294356	chr4:175732461-175732462	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs544258819	chr4:175732512-175732513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs17300019	chr4:175732576-175732577	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Cancer	20164919	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175731200-175731400	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:175731200-175732200	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr4:175731400-175732000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr4:175731800-175732600	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr4:175732000-175732400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:175732000-175732800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:175732000-175732800	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:175732000-175732800	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr4:175732200-175732800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr4:175732200-175732800	Enhancers	iPS-20b Cell Line	embryonic stem cell
11	chr4:175747000-175747200	Enhancers	Pancreatic Islets	Pancreatic Islet
12	chr4:175747200-175751600	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr4:175749200-175751000	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr4:175749400-175749600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:175749400-175749600	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr4:175749400-175749800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr4:175749400-175751200	Active TSS	Brain Angular Gyrus	brain
18	chr4:175749400-175751200	Active TSS	Brain Anterior Caudate	brain
19	chr4:175749400-175751400	Active TSS	HUES48 Cell Line	embryonic stem cell
20	chr4:175749600-175749800	Enhancers	ES-I3 Cell Line	embryonic stem cell
21	chr4:175749600-175749800	Active TSS	Brain Hippocampus Middle	brain
22	chr4:175749600-175750000	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
23	chr4:175749600-175751000	Active TSS	Brain Cingulate Gyrus	brain
24	chr4:175749600-175751000	Active TSS	Brain Germinal Matrix	brain
25	chr4:175749600-175751200	Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr4:175749600-175751200	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr4:175749600-175751200	Active TSS	Fetal Brain Male	brain
28	chr4:175749600-175751200	Active TSS	Fetal Brain Female	brain
29	chr4:175749600-175751200	Active TSS	K562	blood
30	chr4:175749600-175751800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:175749800-175750000	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
32	chr4:175749800-175750000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr4:175749800-175750000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:175749800-175750000	Enhancers	Duodenum Smooth Muscle	Duodenum
35	chr4:175749800-175750000	Enhancers	Fetal Intestine Large	intestine
36	chr4:175749800-175750200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:175749800-175750200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
38	chr4:175749800-175750200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
39	chr4:175749800-175750200	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
40	chr4:175749800-175750200	Enhancers	Placenta	Placenta
41	chr4:175749800-175750400	Enhancers	Pancreas	Pancrea
42	chr4:175749800-175750400	Active TSS	Rectal Smooth Muscle	rectum
43	chr4:175749800-175750800	Active TSS	Brain Substantia Nigra	brain
44	chr4:175749800-175751000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:175749800-175751200	Active TSS	H1 Cell Line	embryonic stem cell
46	chr4:175749800-175751200	Active TSS	H9 Cell Line	embryonic stem cell
47	chr4:175749800-175751200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:175749800-175751200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:175749800-175751200	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
50	chr4:175749800-175751200	Active TSS	A549	lung

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