Variant report

Variant	nsv880254
Chromosome Location	chr4:150712923-150852782
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	chr4:150835801-150835913	HepG2	liver:	n/a	n/a
2	ATF3	chr4:150744751-150745214	HCT-116	colon:	n/a	n/a
3	BHLHE40	chr4:150835825-150836017	K562	blood:	n/a	n/a
4	BHLHE40	chr4:150716536-150716839	HepG2	liver:	n/a	n/a
5	BHLHE40	chr4:150806092-150806351	GM12878	blood:	n/a	n/a
6	BRCA1	chr4:150726652-150726925	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr4:150744822-150745206	Hela-S3	cervix:	n/a	n/a
8	CBX3	chr4:150744839-150745234	HCT-116	colon:	n/a	n/a
9	CEBPB	chr4:150731313-150731627	HepG2	liver:	n/a	chr4:150731464-150731475
10	CEBPB	chr4:150744720-150745322	HCT-116	colon:	n/a	chr4:150744896-150744908 chr4:150744987-150744995
11	CEBPB	chr4:150744814-150745151	IMR90	lung:	n/a	chr4:150744896-150744908 chr4:150744987-150744995
12	CEBPB	chr4:150811492-150811742	HepG2	liver:	n/a	n/a
13	CEBPB	chr4:150731380-150731516	H1-hESC	embryonic stem cell:	n/a	chr4:150731464-150731475
14	CEBPB	chr4:150744775-150745311	Hela-S3	cervix:	n/a	chr4:150744896-150744908 chr4:150744987-150744995
15	CEBPB	chr4:150846961-150847161	HepG2	liver:	n/a	chr4:150847080-150847091
16	CEBPB	chr4:150764636-150764897	IMR90	lung:	n/a	chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764775-150764788 chr4:150764775-150764786 chr4:150764777-150764786 chr4:150764777-150764788 chr4:150764775-150764788 chr4:150764775-150764788
17	CEBPB	chr4:150731319-150731514	A549	lung:	n/a	chr4:150731464-150731475
18	CEBPB	chr4:150717592-150717931	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:150715496-150715875	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr4:150846973-150847262	IMR90	lung:	n/a	chr4:150847080-150847091
21	CEBPB	chr4:150764617-150764914	A549	lung:	n/a	chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764775-150764788 chr4:150764775-150764786 chr4:150764777-150764786 chr4:150764777-150764788 chr4:150764775-150764788 chr4:150764775-150764788
22	CEBPB	chr4:150726588-150726979	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr4:150846178-150846212	A549	lung:	n/a	n/a
24	CEBPB	chr4:150764640-150764937	HepG2	liver:	n/a	chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764777-150764786 chr4:150764775-150764788 chr4:150764775-150764786 chr4:150764777-150764786 chr4:150764777-150764788 chr4:150764775-150764788 chr4:150764775-150764788
25	CEBPB	chr4:150731311-150731548	IMR90	lung:	n/a	chr4:150731464-150731475
26	CEBPB	chr4:150744693-150745226	HCT-116	colon:	n/a	chr4:150744896-150744908 chr4:150744987-150744995
27	CEBPB	chr4:150744874-150745113	A549	lung:	n/a	chr4:150744896-150744908 chr4:150744987-150744995
28	CEBPB	chr4:150846027-150846291	IMR90	lung:	n/a	n/a
29	CHD1	chr4:150817648-150818073	IMR90	lung:	n/a	n/a
30	CHD2	chr4:150717699-150717853	Hela-S3	cervix:	n/a	n/a
31	CHD2	chr4:150845465-150845486	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr4:150806010-150806355	GM12878	blood:	n/a	n/a
33	CTCF	chr4:150817740-150817890	GM12872	blood:	n/a	chr4:150817775-150817788
34	CTCF	chr4:150845040-150845190	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:150835780-150835930	GM12875	blood:	n/a	chr4:150835849-150835857 chr4:150835847-150835860 chr4:150835846-150835867 chr4:150835845-150835861 chr4:150835847-150835860 chr4:150835795-150835816 chr4:150835844-150835862
36	CTCF	chr4:150835775-150835909	GM19238	blood:	n/a	chr4:150835849-150835857 chr4:150835847-150835860 chr4:150835846-150835867 chr4:150835845-150835861 chr4:150835847-150835860 chr4:150835795-150835816 chr4:150835844-150835862
37	CTCF	chr4:150716513-150716524	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:150819070-150819208	SK-N-SH_RA	brain:	n/a	chr4:150819134-150819155 chr4:150819139-150819157 chr4:150819141-150819154
39	CTCF	chr4:150716462-150716617	HepG2	liver:	n/a	n/a
40	CTCF	chr4:150819000-150819150	HVMF	connective:	n/a	n/a
41	CTCF	chr4:150819043-150819207	MCF-7	breast:	n/a	chr4:150819134-150819155 chr4:150819139-150819157 chr4:150819141-150819154
42	CTCF	chr4:150819076-150819238	GM13977	blood:	n/a	chr4:150819134-150819155 chr4:150819139-150819157 chr4:150819141-150819154
43	CTCF	chr4:150835460-150835610	HMEC	breast:	n/a	n/a
44	CTCF	chr4:150817720-150817870	NHEK	skin:	n/a	chr4:150817775-150817788
45	CTCF	chr4:150817720-150817870	HMF	breast:	n/a	chr4:150817775-150817788
46	CTCF	chr4:150819003-150819010	Medullo	brain:	n/a	n/a
47	CTCF	chr4:150835730-150835976	GM10248	blood:	n/a	chr4:150835849-150835857 chr4:150835847-150835860 chr4:150835846-150835867 chr4:150835845-150835861 chr4:150835847-150835860 chr4:150835795-150835816 chr4:150835844-150835862
48	CTCF	chr4:150819040-150819190	GM12874	blood:	n/a	chr4:150819134-150819155 chr4:150819139-150819157 chr4:150819141-150819154
49	CTCF	chr4:150817704-150817904	K562	blood:	n/a	chr4:150817775-150817788
50	CTCF	chr4:150817643-150817934	Gliobla	brain:	n/a	chr4:150817775-150817788

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:150806283-150806333	ProgFib	skin:	n/a
2	chr4:150832003-150832053	HCM	heart:	n/a
3	chr4:150737126-150737176	MCF10A-Er-Src	breast:	n/a
4	chr4:150714071-150714121	H1-hESC	embryonic stem cell:	embryo
5	chr4:150806283-150806333	HRCEpiC	kidney:	n/a
6	chr4:150806283-150806333	SK-N-SH_RA	brain:	n/a
7	chr4:150832003-150832053	T-47D	breast:	n/a
8	chr4:150806283-150806333	Hela-S3	cervix:	n/a
9	chr4:150714071-150714121	K562	blood:	n/a
10	chr4:150832003-150832053	AG09319	gingival:	n/a
11	chr4:150714071-150714121	HIPEpiC	eye:	n/a
12	chr4:150806283-150806333	HCT-116	colon:	n/a
13	chr4:150832003-150832053	Caco-2	colon:	n/a
14	chr4:150806283-150806333	HCF	heart:	n/a
15	chr4:150806283-150806333	SK-N-MC	brain:	n/a
16	chr4:150832003-150832053	HCF	heart:	n/a
17	chr4:150714071-150714121	HNPCEpiC	eye:	n/a
18	chr4:150832003-150832053	HMEC	breast:	n/a
19	chr4:150714071-150714121	SK-N-SH_RA	brain:	n/a
20	chr4:150832003-150832053	AG04449	skin:	fetal
21	chr4:150714071-150714121	NH-A	brain:	n/a
22	chr4:150737126-150737176	GM19239	blood:	n/a
23	chr4:150806283-150806333	NHBE	bronchial:	n/a
24	chr4:150714071-150714121	HRCEpiC	kidney:	n/a
25	chr4:150714071-150714121	Jurkat	blood:	n/a
26	chr4:150737126-150737176	AoSMC	blood vessel:	n/a
27	chr4:150737126-150737176	NH-A	brain:	n/a
28	chr4:150714071-150714121	AG04449	skin:	fetal
29	chr4:150737126-150737176	PFSK-1	brain:	n/a
30	chr4:150737126-150737176	ovcar-3	ovarian:	n/a
31	chr4:150714071-150714121	SAEC	small airway:	n/a
32	chr4:150832003-150832053	NH-A	brain:	n/a
33	chr4:150832003-150832053	U87	brain:	n/a
34	chr4:150737126-150737176	Hepatocyte	liver:	n/a
35	chr4:150714071-150714121	T-47D	breast:	n/a
36	chr4:150714071-150714121	HRE	kidney:	n/a
37	chr4:150832003-150832053	BJ	skin:	n/a
38	chr4:150714071-150714121	AG09319	gingival:	n/a
39	chr4:150806283-150806333	H1-hESC	embryonic stem cell:	embryo
40	chr4:150806283-150806333	IMR90	lung:	fetal
41	chr4:150832003-150832053	HNPCEpiC	eye:	n/a
42	chr4:150714071-150714121	IMR90	lung:	fetal
43	chr4:150806283-150806333	PrEC	prostate:	n/a
44	chr4:150806283-150806333	PFSK-1	brain:	n/a
45	chr4:150714071-150714121	LNCaP	prostate:	n/a
46	chr4:150806283-150806333	CMK	blood:	n/a
47	chr4:150737126-150737176	U87	brain:	n/a
48	chr4:150806283-150806333	ECC-1	luminal epithelium:	n/a
49	chr4:150737126-150737176	LNCaP	prostate:	n/a
50	chr4:150714071-150714121	NT2-D1	testis:	n/a

No.	Distal block	Cell Line	Cell type
1	chr14:96048737..96049315-chr4:150789320..150789840,2	MCF-7	breast:
2	chr4:150291870..150292862-chr4:150818587..150819565,7	MCF-7	breast:
3	chr4:150748708..150749209-chr4:150780113..150780775,2	MCF-7	breast:
4	chr4:150704577..150707428-chr4:150761140..150764079,2	MCF-7	breast:
5	chr4:150748708..150749209-chr4:150780113..150780775,2	MCF-7	breast:
6	chr4:150716192..150716942-chr4:150818465..150819264,2	MCF-7	breast:
7	chr4:150293228..150293911-chr4:150818686..150819650,2	MCF-7	breast:
8	chr4:150716192..150716942-chr4:150818465..150819264,2	MCF-7	breast:
9	chr4:150835279..150836290-chr4:150844620..150845340,3	MCF-7	breast:
10	chr4:150835531..150836236-chr4:150901791..150902666,2	MCF-7	breast:
11	chr4:150815194..150816071-chr7:136849876..136850472,2	MCF-7	breast:
12	chr4:150835352..150836296-chr4:151130289..151131265,2	K562	blood:
13	chr4:150746312..150747926-chr4:150748033..150750862,2	K562	blood:
14	chr4:150835279..150836290-chr4:150844620..150845340,3	MCF-7	breast:
15	chr4:150746312..150747926-chr4:150748033..150750862,2	K562	blood:
16	chr4:150567133..150567704-chr4:150817712..150818389,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRBA-2	chr4:150736752-150736966	ENSG00000234828
2	lnc-LRBA-2	chr4:150736463-150736500	ENSG00000234828
3	lnc-LRBA-2	chr4:150736752-150736980	ENSG00000234828
4	lnc-LRBA-2	chr4:150817286-150817385	ENSG00000234828
5	lnc-LRBA-2	chr4:150714812-150714868	ENSG00000234828
6	lnc-LRBA-2	chr4:150736463-150736500	NONHSAT098722
7	lnc-LRBA-2	chr4:150736463-150736500	ENSG00000234828
8	lnc-LRBA-2	chr4:150736463-150736500	ENSG00000234828
9	lnc-LRBA-2	chr4:150736463-150736500	ENSG00000234828
10	lnc-LRBA-2	chr4:150736752-150736952	NONHSAT098722
11	lnc-LRBA-2	chr4:150736752-150736966	ENSG00000234828

Variant related genes	Relation type
RNU6-1230P	TF binding region
ENSG00000234828	TF binding region
RNA5SP167	TF binding region
RNU6-1230P	CpG island
ENSG00000234828	CpG island
RNA5SP167	CpG island
ENSG00000238721	chromatin interactions

Extended variants
information (count: 3464 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:3464 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1394845	chr4:150712923-150712924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576609252	chr4:150712940-150712941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs553565224	chr4:150712957-150712958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs115640064	chr4:150712993-150712994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs113286308	chr4:150713005-150713006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145530628	chr4:150713014-150713015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs1394846	chr4:150713021-150713022	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs561232050	chr4:150713085-150713086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs545143599	chr4:150713100-150713101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs574869314	chr4:150713132-150713133	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115285140	chr4:150713133-150713134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs115488971	chr4:150713137-150713138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs532244788	chr4:150713240-150713241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147281970	chr4:150713283-150713284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559224402	chr4:150713299-150713300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528338890	chr4:150713328-150713329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs374742757	chr4:150713329-150713330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs142300525	chr4:150713331-150713332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557387011	chr4:150713348-150713349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs28461665	chr4:150713376-150713377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs550446976	chr4:150713437-150713438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs570487202	chr4:150713471-150713472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538862208	chr4:150713655-150713656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs559081765	chr4:150713677-150713678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567418051	chr4:150713689-150713690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs78054726	chr4:150713695-150713696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115949248	chr4:150713736-150713737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549785049	chr4:150713744-150713745	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72728514	chr4:150713797-150713798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs117671509	chr4:150713814-150713815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs79654312	chr4:150713834-150713835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs562936551	chr4:150713840-150713841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74762973	chr4:150713843-150713844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs10010177	chr4:150713866-150713867	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs117098169	chr4:150713874-150713875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs188658231	chr4:150713898-150713899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs117362625	chr4:150713918-150713919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530434743	chr4:150713938-150713939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs550503398	chr4:150714073-150714074	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs79295545	chr4:150714082-150714083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs539486235	chr4:150714091-150714092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17026442	chr4:150714094-150714095	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs566303463	chr4:150714095-150714096	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535227434	chr4:150714138-150714139	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191159454	chr4:150714162-150714163	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs575143598	chr4:150714206-150714207	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183322861	chr4:150714225-150714226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs187765803	chr4:150714308-150714309	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577280247	chr4:150714367-150714368	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191505467	chr4:150714370-150714371	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Intellectual disability	22102821	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
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	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
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:255 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:150703000-150714400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:150707600-150714200	Weak transcription	HSMM	muscle
3	chr4:150707600-150714400	Weak transcription	HMEC	breast
4	chr4:150707600-150715000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr4:150712200-150714200	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr4:150712800-150714000	Weak transcription	Hela-S3	cervix
7	chr4:150714000-150716400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr4:150714000-150718000	Enhancers	Hela-S3	cervix
9	chr4:150714200-150715600	Enhancers	HSMM	muscle
10	chr4:150714200-150715800	Enhancers	Muscle Satellite Cultured Cells	--
11	chr4:150714400-150715200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:150714400-150715200	Enhancers	HMEC	breast
13	chr4:150714400-150715400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:150714400-150715800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:150714600-150715400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:150715000-150715400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
17	chr4:150715000-150715600	Enhancers	NHDF-Ad	bronchial
18	chr4:150715000-150716800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr4:150715800-150717200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:150715800-150720800	Weak transcription	Muscle Satellite Cultured Cells	--
21	chr4:150716400-150722200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:150716600-150717000	Enhancers	Right Ventricle	heart
23	chr4:150717400-150717600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:150717400-150717600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:150718000-150726400	Weak transcription	Hela-S3	cervix
26	chr4:150720800-150721400	Enhancers	Muscle Satellite Cultured Cells	--
27	chr4:150722200-150723000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:150723400-150723800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:150726400-150727000	Enhancers	Hela-S3	cervix
30	chr4:150731200-150731400	Enhancers	Left Ventricle	heart
31	chr4:150743400-150743600	Enhancers	NHEK	skin
32	chr4:150743400-150743600	Enhancers	Osteobl	bone
33	chr4:150743600-150744600	Weak transcription	NHEK	skin
34	chr4:150743600-150744600	Weak transcription	Osteobl	bone
35	chr4:150744000-150744600	Enhancers	Hela-S3	cervix
36	chr4:150744000-150745800	Enhancers	HUVEC	blood vessel
37	chr4:150744200-150744600	Enhancers	NHDF-Ad	bronchial
38	chr4:150744200-150744800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:150744200-150744800	Enhancers	Muscle Satellite Cultured Cells	--
40	chr4:150744400-150747000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:150744600-150744800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:150744600-150745000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:150744600-150745000	Weak transcription	Hela-S3	cervix
44	chr4:150744600-150745000	Weak transcription	NHDF-Ad	bronchial
45	chr4:150744600-150745000	Enhancers	Osteobl	bone
46	chr4:150744600-150745600	Enhancers	NHEK	skin
47	chr4:150744800-150745000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
48	chr4:150744800-150745200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
49	chr4:150744800-150745400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:150744800-150745400	Flanking Active TSS	Muscle Satellite Cultured Cells	--

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