Variant report

Variant	nsv880241
Chromosome Location	chr4:148411178-148461073
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	chr4:148446162-148446180	K562	blood:	n/a	n/a
2	ATF2	chr4:148413825-148414392	GM12878	blood:	n/a	n/a
3	ATF2	chr4:148413864-148414261	GM12878	blood:	n/a	n/a
4	ATF2	chr4:148439919-148440442	GM12878	blood:	n/a	n/a
5	BCL3	chr4:148413891-148414232	GM12878	blood:	n/a	n/a
6	BCL3	chr4:148413947-148414263	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:148451443-148452303	Hela-S3	cervix:	n/a	n/a
8	BRCA1	chr4:148440029-148440315	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr4:148419374-148419567	Hela-S3	cervix:	n/a	n/a
10	CCNT2	chr4:148414012-148414212	K562	blood:	n/a	n/a
11	CEBPB	chr4:148413856-148414243	IMR90	lung:	n/a	n/a
12	CEBPB	chr4:148451307-148452327	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr4:148449945-148450198	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr4:148436682-148436952	MCF-7	breast:	n/a	n/a
15	CEBPB	chr4:148438984-148439208	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:148449982-148450206	HepG2	liver:	n/a	n/a
17	CEBPB	chr4:148419189-148419536	Hela-S3	cervix:	n/a	chr4:148419356-148419369
18	CEBPB	chr4:148419119-148419552	IMR90	lung:	n/a	chr4:148419356-148419369 chr4:148419157-148419169
19	CTCF	chr4:148440120-148440270	NHLF	lung:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
20	CTCF	chr4:148447600-148447750	HVMF	connective:	n/a	n/a
21	CTCF	chr4:148440074-148440252	A549	lung:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
22	CTCF	chr4:148439941-148440315	HepG2	liver:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
23	CTCF	chr4:148447581-148447664	Fibrobl	skin:	n/a	n/a
24	CTCF	chr4:148440100-148440250	BJ	skin:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
25	CTCF	chr4:148435280-148435430	HCT-116	colon:	n/a	n/a
26	CTCF	chr4:148447640-148447790	HMF	breast:	n/a	n/a
27	CTCF	chr4:148435240-148435390	AG10803	skin:	n/a	n/a
28	CTCF	chr4:148447580-148447730	GM12865	blood:	n/a	n/a
29	CTCF	chr4:148447612-148447613	ProgFib	skin:	n/a	n/a
30	CTCF	chr4:148435420-148435570	HAc	cerebellar:	n/a	n/a
31	CTCF	chr4:148440028-148440326	MCF-7	breast:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
32	CTCF	chr4:148447580-148447730	HCM	heart:	n/a	n/a
33	CTCF	chr4:148435240-148435390	AG04450	lung:	n/a	n/a
34	CTCF	chr4:148435220-148435370	MCF-7	breast:	n/a	n/a
35	CTCF	chr4:148447560-148447710	HCFaa	heart:	n/a	n/a
36	CTCF	chr4:148440030-148440302	LNCaP	prostate:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
37	CTCF	chr4:148420620-148420770	HPF	lung:	n/a	n/a
38	CTCF	chr4:148435180-148435330	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr4:148431074-148431131	GM13976	blood:	n/a	n/a
40	CTCF	chr4:148447640-148447790	NHDF-neo	bronchial:	n/a	n/a
41	CTCF	chr4:148440100-148440250	HRE	kidney:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
42	CTCF	chr4:148447640-148447790	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr4:148435400-148435550	HCM	heart:	n/a	n/a
44	CTCF	chr4:148439790-148440560	A549	lung:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
45	CTCF	chr4:148435180-148435330	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr4:148435200-148435350	NHEK	skin:	n/a	n/a
47	CTCF	chr4:148440111-148440215	MCF-7	breast:	n/a	chr4:148440169-148440177 chr4:148440164-148440182 chr4:148440166-148440187 chr4:148440165-148440181
48	CTCF	chr4:148435240-148435390	AG09319	gingival:	n/a	n/a
49	CTCF	chr4:148447580-148447730	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:148438300-148438450	HBMEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:148413287-148413337	HUVEC	blood vessel:	n/a
2	chr4:148413287-148413337	HL-60	blood:	n/a
3	chr4:148413287-148413337	AG04450	lung:	fetal
4	chr4:148413287-148413337	PANC-1	pancreas:	n/a
5	chr4:148413287-148413337	HNPCEpiC	eye:	n/a
6	chr4:148413287-148413337	HRCEpiC	kidney:	n/a
7	chr4:148413287-148413337	HEK293	kidney:	embryo
8	chr4:148413287-148413337	CMK	blood:	n/a
9	chr4:148413287-148413337	HRPEpiC	eye:	n/a
10	chr4:148413287-148413337	GM12892	blood:	n/a
11	chr4:148413287-148413337	Hela-S3	cervix:	n/a
12	chr4:148413287-148413337	AoSMC	blood vessel:	n/a
13	chr4:148413287-148413337	HCM	heart:	n/a
14	chr4:148413287-148413337	AG10803	skin:	n/a
15	chr4:148413287-148413337	PFSK-1	brain:	n/a
16	chr4:148413287-148413337	SK-N-MC	brain:	n/a
17	chr4:148413287-148413337	HepG2	liver:	n/a
18	chr4:148413287-148413337	GM12891	blood:	n/a
19	chr4:148413287-148413337	MCF-7	breast:	n/a
20	chr4:148413287-148413337	BE2_C	brain:	n/a
21	chr4:148413287-148413337	NHDF-neo	bronchial:	n/a
22	chr4:148413287-148413337	HAEpiC	amniotic membrane:	n/a
23	chr4:148413287-148413337	GM06990	blood:	n/a
24	chr4:148413287-148413337	ovcar-3	ovarian:	n/a
25	chr4:148413287-148413337	GM19239	blood:	n/a
26	chr4:148413287-148413337	HMEC	breast:	n/a
27	chr4:148413287-148413337	K562	blood:	n/a
28	chr4:148413287-148413337	ProgFib	skin:	n/a
29	chr4:148413287-148413337	SK-N-SH	brain:	n/a
30	chr4:148413287-148413337	HCT-116	colon:	n/a
31	chr4:148413287-148413337	H1-hESC	embryonic stem cell:	embryo
32	chr4:148413287-148413337	GM12878	blood:	n/a
33	chr4:148413287-148413337	A549	lung:	n/a
34	chr4:148413287-148413337	HCF	heart:	n/a
35	chr4:148413287-148413337	AG04449	skin:	fetal
36	chr4:148413287-148413337	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:148413287-148413337	AG09319	gingival:	n/a
38	chr4:148413287-148413337	HEEpiC	esophagus:	n/a
39	chr4:148413287-148413337	SK-N-SH_RA	brain:	n/a
40	chr4:148413287-148413337	Caco-2	colon:	n/a
41	chr4:148413287-148413337	T-47D	breast:	n/a
42	chr4:148413287-148413337	MCF10A-Er-Src	breast:	n/a
43	chr4:148413287-148413337	IMR90	lung:	fetal
44	chr4:148413287-148413337	LNCaP	prostate:	n/a
45	chr4:148413287-148413337	NH-A	brain:	n/a
46	chr4:148413287-148413337	HCPEpiC	choroid plexus:	n/a
47	chr4:148413287-148413337	HRE	kidney:	n/a
48	chr4:148413287-148413337	U87	brain:	n/a
49	chr4:148413287-148413337	HIPEpiC	eye:	n/a
50	chr4:148413287-148413337	Jurkat	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:148427685..148429776-chr4:148434169..148436838,2	MCF-7	breast:
2	chr4:148440067..148441110-chr4:148510925..148512204,7	MCF-7	breast:
3	chr4:148427685..148429776-chr4:148434169..148436838,2	MCF-7	breast:
4	chr4:148400462..148402309-chr4:148413592..148415499,2	K562	blood:
5	chr4:148439745..148440641-chr4:148511561..148512087,2	K562	blood:
6	chr4:148438170..148441036-chr4:148443723..148446840,3	K562	blood:
7	chr4:148447258..148447941-chr4:148845761..148846516,2	MCF-7	breast:
8	chr4:148438170..148441036-chr4:148443723..148446840,3	K562	blood:
9	chr4:148444121..148446101-chr4:148450428..148453338,2	K562	blood:
10	chr4:148439722..148440301-chr4:148788057..148788672,2	MCF-7	breast:
11	chr4:148439062..148441461-chr4:148511763..148514115,2	MCF-7	breast:
12	chr4:148439677..148440826-chr4:148787272..148788626,10	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TMEM184C-2	chr4:148407981-148413807	NONHSAT098682
2	lnc-TMEM184C-1	chr4:148427243-148427917	NONHSAT098683

Variant related genes	Relation type
GTF2F2P1	TF binding region
EDNRA	TF binding region
GTF2F2P1	CpG island
EDNRA	CpG island
ENSG00000151617	chromatin interactions

Extended variants
information (count: 1811 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:1811 , 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	rs11942855	chr4:148411178-148411179	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs570748493	chr4:148411196-148411197	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
3	rs537336206	chr4:148411198-148411199	Weak transcription Strong transcription Flanking Active TSS Genic enhancers Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
4	rs191296295	chr4:148411218-148411219	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
5	rs111778857	chr4:148411230-148411231	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
6	rs577117270	chr4:148411238-148411239	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
7	rs182433443	chr4:148411275-148411276	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
8	rs138746457	chr4:148411300-148411301	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
9	rs538283328	chr4:148411306-148411307	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
10	rs562003749	chr4:148411328-148411329	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
11	rs554445096	chr4:148411332-148411333	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
12	rs554311068	chr4:148411364-148411365	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
13	rs33985171	chr4:148411365-148411366	Weak transcription Enhancers Flanking Active TSS Genic enhancers	lncRNA	n/a	Overlapped CNVs	n/a
14	rs552806692	chr4:148411423-148411424	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
15	rs572865534	chr4:148411480-148411481	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
16	rs187072467	chr4:148411505-148411506	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
17	rs561331233	chr4:148411514-148411515	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
18	rs192026655	chr4:148411549-148411550	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
19	rs147801070	chr4:148411587-148411588	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
20	rs17023360	chr4:148411672-148411673	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs72959547	chr4:148411723-148411724	Weak transcription Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs547144186	chr4:148411726-148411727	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
23	rs560411661	chr4:148411776-148411777	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
24	rs77246688	chr4:148411779-148411780	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
25	rs77582717	chr4:148411780-148411781	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
26	rs34450591	chr4:148411791-148411792	Weak transcription Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
27	rs35139018	chr4:148411851-148411852	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
28	rs529374644	chr4:148411864-148411865	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
29	rs549151413	chr4:148411898-148411899	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
30	rs185394918	chr4:148411906-148411907	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
31	rs538199259	chr4:148411990-148411991	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
32	rs531782339	chr4:148411994-148411995	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
33	rs118112612	chr4:148412023-148412024	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
34	rs570722539	chr4:148412070-148412071	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
35	rs139117129	chr4:148412072-148412073	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
36	rs553108550	chr4:148412099-148412100	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
37	rs117084549	chr4:148412132-148412133	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
38	rs550251365	chr4:148412135-148412136	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
39	rs568736959	chr4:148412137-148412138	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
40	rs190369051	chr4:148412145-148412146	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
41	rs535736435	chr4:148412161-148412162	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
42	rs72959548	chr4:148412163-148412164	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
43	rs554154011	chr4:148412193-148412194	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
44	rs371719136	chr4:148412250-148412251	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
45	rs566052566	chr4:148412279-148412280	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
46	rs193292236	chr4:148412280-148412281	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
47	rs578181290	chr4:148412306-148412307	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
48	rs540506483	chr4:148412313-148412314	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
49	rs376776437	chr4:148412321-148412322	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
50	rs11946826	chr4:148412327-148412328	Weak transcription Enhancers Flanking Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:68)

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
T-cell prolymphocytic leukemia	19278963	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

Chromatin state (count:453 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:148403800-148417600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:148404200-148412000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr4:148404200-148413000	Weak transcription	Osteobl	bone
4	chr4:148404200-148413200	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr4:148404200-148418800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr4:148404200-148419000	Weak transcription	HMEC	breast
7	chr4:148404600-148412000	Weak transcription	Fetal Kidney	kidney
8	chr4:148404600-148413000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr4:148404600-148413000	Weak transcription	Stomach Smooth Muscle	stomach
10	chr4:148404600-148413200	Weak transcription	Fetal Muscle Leg	muscle
11	chr4:148404600-148419000	Weak transcription	NHLF	lung
12	chr4:148405800-148416000	Weak transcription	Spleen	Spleen
13	chr4:148407000-148413200	Weak transcription	Right Atrium	heart
14	chr4:148407400-148411200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:148408200-148413200	Weak transcription	Fetal Stomach	stomach
16	chr4:148408400-148413200	Weak transcription	Aorta	Aorta
17	chr4:148408400-148416800	Weak transcription	Right Ventricle	heart
18	chr4:148410000-148413200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr4:148410000-148414000	Weak transcription	NHEK	skin
20	chr4:148410200-148413000	Weak transcription	NH-A	brain
21	chr4:148410200-148413400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr4:148410200-148413400	Weak transcription	Fetal Intestine Small	intestine
23	chr4:148410200-148413600	Weak transcription	NHDF-Ad	bronchial
24	chr4:148410600-148411400	Flanking Active TSS	Fetal Heart	heart
25	chr4:148410600-148411400	Genic enhancers	Fetal Lung	lung
26	chr4:148410600-148413000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
27	chr4:148410600-148413200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr4:148410800-148411200	Enhancers	Left Ventricle	heart
29	chr4:148410800-148411200	Enhancers	Ovary	ovary
30	chr4:148411000-148411200	Weak transcription	Adipose Nuclei	Adipose
31	chr4:148411200-148411400	Enhancers	Adipose Nuclei	Adipose
32	chr4:148411200-148412000	Weak transcription	Ovary	ovary
33	chr4:148411200-148415400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:148411200-148415600	Weak transcription	Left Ventricle	heart
35	chr4:148411400-148411800	Enhancers	Fetal Lung	lung
36	chr4:148411400-148413400	Enhancers	Fetal Heart	heart
37	chr4:148411400-148414000	Weak transcription	Adipose Nuclei	Adipose
38	chr4:148411800-148412400	Flanking Active TSS	Fetal Lung	lung
39	chr4:148412000-148412200	Enhancers	Fetal Kidney	kidney
40	chr4:148412000-148414000	Enhancers	Ovary	ovary
41	chr4:148412200-148412600	Weak transcription	Fetal Kidney	kidney
42	chr4:148412400-148414000	Enhancers	Fetal Lung	lung
43	chr4:148412600-148414600	Enhancers	Fetal Kidney	kidney
44	chr4:148413000-148413400	Enhancers	Stomach Smooth Muscle	stomach
45	chr4:148413000-148413600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr4:148413000-148414200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr4:148413000-148414400	Enhancers	Osteobl	bone
48	chr4:148413000-148414600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr4:148413000-148414600	Enhancers	NH-A	brain
50	chr4:148413200-148413400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung

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