Variant report

Variant	nsv427692
Chromosome Location	chr4:118262899-118437573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:557)
CpG islands
(count:0)
Chromatin interactive
region (count:33)
LncRNA
region (count:35)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:557 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:118323436-118323468	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr4:118399942-118400139	GM12878	blood:	n/a	n/a
3	CBX3	chr4:118321267-118321684	HCT-116	colon:	n/a	chr4:118321304-118321315
4	CEBPB	chr4:118388675-118388896	A549	lung:	n/a	chr4:118388751-118388762
5	CEBPB	chr4:118323728-118323964	IMR90	lung:	n/a	chr4:118323852-118323865 chr4:118323852-118323863 chr4:118323803-118323820 chr4:118323852-118323865 chr4:118323805-118323816 chr4:118323852-118323863 chr4:118323853-118323864 chr4:118323852-118323865 chr4:118323768-118323785
6	CEBPB	chr4:118321302-118321657	IMR90	lung:	n/a	n/a
7	CEBPB	chr4:118388582-118388920	IMR90	lung:	n/a	chr4:118388751-118388762
8	CEBPB	chr4:118323695-118323971	HepG2	liver:	n/a	chr4:118323852-118323865 chr4:118323852-118323863 chr4:118323803-118323820 chr4:118323852-118323865 chr4:118323805-118323816 chr4:118323852-118323863 chr4:118323853-118323864 chr4:118323852-118323865 chr4:118323768-118323785
9	CEBPB	chr4:118333842-118334173	K562	blood:	n/a	chr4:118334008-118334019
10	CEBPB	chr4:118333829-118334187	IMR90	lung:	n/a	chr4:118334008-118334019
11	CEBPB	chr4:118419554-118419881	A549	lung:	n/a	chr4:118419712-118419723
12	CEBPB	chr4:118388743-118388777	K562	blood:	n/a	chr4:118388751-118388762
13	CEBPB	chr4:118314143-118314469	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:118273357-118273662	HepG2	liver:	n/a	chr4:118273477-118273488
15	CEBPB	chr4:118339135-118339335	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:118419534-118419879	IMR90	lung:	n/a	chr4:118419712-118419723
17	CEBPB	chr4:118333852-118334143	A549	lung:	n/a	chr4:118334008-118334019
18	CEBPB	chr4:118338686-118338912	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:118333928-118334149	H1-hESC	embryonic stem cell:	n/a	chr4:118334008-118334019
20	CEBPB	chr4:118419609-118419809	H1-hESC	embryonic stem cell:	n/a	chr4:118419712-118419723
21	CEBPB	chr4:118419537-118419901	HepG2	liver:	n/a	chr4:118419712-118419723
22	CEBPB	chr4:118341771-118341971	A549	lung:	n/a	chr4:118341866-118341877 chr4:118341891-118341902 chr4:118341866-118341879 chr4:118341868-118341877 chr4:118341867-118341878 chr4:118341868-118341877 chr4:118341868-118341877 chr4:118341868-118341877
23	CEBPB	chr4:118273372-118273627	A549	lung:	n/a	chr4:118273477-118273488
24	CEBPB	chr4:118341725-118342029	HepG2	liver:	n/a	chr4:118341866-118341877 chr4:118341891-118341902 chr4:118341866-118341879 chr4:118341868-118341877 chr4:118341867-118341878 chr4:118341868-118341877 chr4:118341868-118341877 chr4:118341868-118341877
25	CEBPB	chr4:118388589-118388896	HepG2	liver:	n/a	chr4:118388751-118388762
26	CEBPB	chr4:118333846-118334182	HepG2	liver:	n/a	chr4:118334008-118334019
27	CEBPB	chr4:118338078-118338345	IMR90	lung:	n/a	n/a
28	CEBPB	chr4:118377164-118377381	HepG2	liver:	n/a	chr4:118377254-118377265
29	CTCF	chr4:118369160-118369310	RPTEC	kidney:	n/a	n/a
30	CTCF	chr4:118369200-118369350	AG04450	lung:	n/a	n/a
31	CTCF	chr4:118369080-118369462	GM12878	blood:	n/a	n/a
32	CTCF	chr4:118369160-118369310	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr4:118350380-118350530	GM12865	blood:	n/a	n/a
34	CTCF	chr4:118369100-118369250	GM12801	blood:	n/a	n/a
35	CTCF	chr4:118350360-118350510	HA-sp	spinal cord:	n/a	n/a
36	CTCF	chr4:118350347-118350525	GM12892	blood:	n/a	n/a
37	CTCF	chr4:118369201-118369337	GM10266	blood:	n/a	n/a
38	CTCF	chr4:118369220-118369370	NHEK	skin:	n/a	n/a
39	CTCF	chr4:118369180-118369330	GM12878	blood:	n/a	n/a
40	CTCF	chr4:118350420-118350570	GM12871	blood:	n/a	n/a
41	CTCF	chr4:118350359-118350503	GM12878	blood:	n/a	n/a
42	CTCF	chr4:118350360-118350510	HEK293	kidney:	n/a	n/a
43	CTCF	chr4:118350380-118350530	HepG2	liver:	n/a	n/a
44	CTCF	chr4:118369220-118369370	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:118350300-118350450	GM12871	blood:	n/a	n/a
46	CTCF	chr4:118369220-118369370	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr4:118369205-118369333	Medullo	brain:	n/a	n/a
48	CTCF	chr4:118350340-118350490	HPF	lung:	n/a	n/a
49	CTCF	chr4:118369087-118369462	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr4:118369179-118369368	HepG2	liver:	n/a	n/a

No data

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	4:118357351-118360885..4:118437019-118438281	H1-hESC	embryonic stem cell:	embryo
2	4:118357351-118360885..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo
3	4:118291537-118294071..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
4	chr4:118377487..118379398-chr4:119198520..119200981,2	K562	blood:
5	4:118383653-118385442..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo
6	4:118357351-118360885..4:118437019-118438281	H1-hESC	embryonic stem cell:	embryo
7	4:118313000-118315008..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
8	4:118357351-118360885..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
9	4:118424109-118425531..4:118428948-118429401	K562	blood:
10	4:118312235-118312291..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
11	4:118320200-118324249..4:118559839-118566258	GM12878	blood:
12	4:118320200-118324249..4:118414019-118416561	Hela-S3	cervix:
13	chr4:118373648..118376261-chr4:118378262..118380604,2	K562	blood:
14	4:118357351-118360885..4:118559839-118566258	GM12878	blood:
15	4:118428948-118429401..4:118429401-118431437	H1-hESC	embryonic stem cell:	embryo
16	4:118320200-118324249..4:118722741-118723956	H1-hESC	embryonic stem cell:	embryo
17	4:118428948-118429401..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
18	4:118387398-118387878..4:118667424-118683756	Hela-S3	cervix:
19	4:118319405-118319911..4:118454469-118464115	H1-hESC	embryonic stem cell:	embryo
20	4:118319405-118319911..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo
21	4:118320200-118324249..4:118735152-118737645	GM12878	blood:
22	chr4:118373648..118376261-chr4:118378262..118380604,2	K562	blood:
23	4:118320200-118324249..4:118414019-118416561	Hela-S3	cervix:
24	4:118424109-118425531..4:118428948-118429401	K562	blood:
25	4:118312235-118312291..4:118636913-118638401	H1-hESC	embryonic stem cell:	embryo
26	4:118312235-118312291..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
27	4:118301798-118302725..4:118541860-118551269	H1-hESC	embryonic stem cell:	embryo
28	4:118414019-118416561..4:118706981-118715929	Hela-S3	cervix:
29	4:118291537-118294071..4:118559839-118566258	H1-hESC	embryonic stem cell:	embryo
30	4:118428948-118429401..4:118429401-118431437	H1-hESC	embryonic stem cell:	embryo
31	4:118327401-118331084..4:118559839-118566258	GM12878	blood:
32	4:118313000-118315008..4:118319405-118319911	H1-hESC	embryonic stem cell:	embryo
33	4:118319405-118319911..4:118687551-118689447	H1-hESC	embryonic stem cell:	embryo

(count:35 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDST3-5	chr4:118281822-118281965	XLOC_003658
2	lnc-NDST3-5	chr4:118282495-118282662	XLOC_003658
3	lnc-TRAM1L1-1	chr4:118280884-118280965	XLOC_004051
4	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
5	lnc-NDST3-4	chr4:118389305-118389388	ENSG00000236922
6	lnc-NDST3-10	chr4:118334618-118335435	NONHSAT097958
7	lnc-NDST3-5	chr4:118293914-118293973	XLOC_003658
8	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
9	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
10	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
11	lnc-NDST3-5	chr4:118293752-118293891	XLOC_003658
12	lnc-NDST3-5	chr4:118281781-118281965	XLOC_003658
13	lnc-NDST3-5	chr4:118282557-118282662	XLOC_003658
14	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
15	lnc-NDST3-5	chr4:118293520-118293627	XLOC_003658
16	lnc-NDST3-5	chr4:118282566-118282662	XLOC_003658
17	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
18	lnc-NDST3-5	chr4:118282556-118282662	XLOC_003658
19	lnc-NDST3-5	chr4:118293520-118293891	XLOC_003658
20	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
21	lnc-NDST3-5	chr4:118293520-118293754	XLOC_003658
22	lnc-NDST3-4	chr4:118349853-118349923	ENSG00000236922.5
23	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
24	lnc-NDST3-4	chr4:118385627-118385693	ENSG00000236922
25	lnc-NDST3-5	chr4:118292748-118292818	XLOC_003658
26	lnc-NDST3-4	chr4:118349552-118349639	ENSG00000236922.5
27	lnc-NDST3-4	chr4:118349559-118349639	ENSG00000236922
28	lnc-NDST3-5	chr4:118282505-118282662	XLOC_003658
29	lnc-TRAM1L1-1	chr4:118272349-118272394	XLOC_004051
30	lnc-NDST3-5	chr4:118282557-118282662	XLOC_003658
31	lnc-NDST3-5	chr4:118281779-118281965	XLOC_003658
32	lnc-NDST3-4	chr4:118349850-118349923	ENSG00000236922
33	lnc-TRAM1L1-1	chr4:118281720-118281795	XLOC_004051
34	lnc-NDST3-5	chr4:118293752-118293858	XLOC_003658
35	lnc-NDST3-5	chr4:118293914-118294008	XLOC_003658

No data

Variant related genes	Relation type
ENSG00000236922	TF binding region
ENSG00000224932	TF binding region
ENSG00000228358	TF binding region
RPSAP35	TF binding region
ENSG00000269893	chromatin interactions
ZCCHC14	miRNA target sites
CD46	miRNA target sites
C5orf24	miRNA target sites
EIF4G2	miRNA target sites
ARID3B	miRNA target sites
KIAA0528	miRNA target sites
ARF4	miRNA target sites

Extended variants
information (count: 4161 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:4161 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563998377	chr4:118262948-118262949	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs138050284	chr4:118262986-118262987	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs540164502	chr4:118262990-118262991	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs189875949	chr4:118262997-118262998	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs532542013	chr4:118263004-118263005	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529313013	chr4:118263007-118263008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs28944770	chr4:118263099-118263100	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs62313487	chr4:118263107-118263108	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs531902537	chr4:118263166-118263167	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs17867347	chr4:118263207-118263208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182518148	chr4:118263214-118263215	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs138658902	chr4:118263233-118263234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs560952527	chr4:118263253-118263254	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs187034986	chr4:118263322-118263323	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs142701125	chr4:118263371-118263372	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs566452973	chr4:118263395-118263396	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs535150500	chr4:118263413-118263414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs555393674	chr4:118263414-118263415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575004788	chr4:118263466-118263467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543974945	chr4:118263472-118263473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111941708	chr4:118263515-118263516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs577451268	chr4:118263519-118263520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs548055873	chr4:118263560-118263561	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191930662	chr4:118263565-118263566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs17867183	chr4:118263593-118263594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367982986	chr4:118263623-118263624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185238742	chr4:118263655-118263656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs542667332	chr4:118263666-118263667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371452034	chr4:118263678-118263679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531861930	chr4:118263730-118263731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs147368513	chr4:118263759-118263760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571851483	chr4:118263800-118263801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs371573136	chr4:118263851-118263852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs548065229	chr4:118263874-118263875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536862479	chr4:118264005-118264006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536151617	chr4:118264007-118264008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140337794	chr4:118264010-118264011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs148434231	chr4:118264024-118264025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17875128	chr4:118264043-118264044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs569501199	chr4:118264052-118264053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs535387169	chr4:118264075-118264076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs114085557	chr4:118264168-118264169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568541085	chr4:118264175-118264176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537531794	chr4:118264224-118264225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs188952046	chr4:118264283-118264284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577413788	chr4:118264309-118264310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533752717	chr4:118264315-118264316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148569473	chr4:118264326-118264327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs193054377	chr4:118264351-118264352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573870481	chr4:118264428-118264429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	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
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
small cell lung cancer	20016488	CNVD
Renal cell carcinoma	18194544	CNVD
Autism	19246517	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Schizophrenia	23813976	CNVD
Pancreatic cancer	17952125	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:118250000-118272600	Weak transcription	NH-A	brain
2	chr4:118255200-118272800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:118258800-118278600	Weak transcription	HMEC	breast
4	chr4:118262400-118267200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:118262600-118263000	Active TSS	Spleen	Spleen
6	chr4:118262800-118263400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr4:118267200-118273200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:118272600-118272800	Active TSS	NH-A	brain
9	chr4:118273200-118274200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:118274200-118274800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:118274800-118275200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:118275200-118277200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:118276800-118277200	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:118277200-118278600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr4:118277800-118280000	Weak transcription	HSMMtube	muscle
16	chr4:118278600-118279400	Strong transcription	HMEC	breast
17	chr4:118278600-118282800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr4:118278800-118279000	Enhancers	NHEK	skin
19	chr4:118278800-118279200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr4:118278800-118279800	Enhancers	Fetal Lung	lung
21	chr4:118279400-118281200	Weak transcription	HMEC	breast
22	chr4:118281200-118282000	Strong transcription	HMEC	breast
23	chr4:118282000-118302000	Weak transcription	HMEC	breast
24	chr4:118282800-118284400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:118284400-118285200	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:118285200-118292200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr4:118292200-118292800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:118292200-118292800	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:118292200-118292800	Active TSS	Brain Inferior Temporal Lobe	brain
30	chr4:118292200-118295800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:118294000-118294400	Enhancers	Fetal Brain Male	brain
32	chr4:118294400-118297400	Weak transcription	Fetal Brain Male	brain
33	chr4:118295800-118306200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:118297400-118297800	Enhancers	Fetal Brain Male	brain
35	chr4:118302000-118302400	Enhancers	HMEC	breast
36	chr4:118303800-118304600	Weak transcription	Fetal Brain Male	brain
37	chr4:118304600-118306000	Enhancers	Fetal Brain Male	brain
38	chr4:118306000-118307200	Weak transcription	Fetal Brain Male	brain
39	chr4:118306200-118307200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr4:118306600-118307800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr4:118306800-118307200	Enhancers	Brain Anterior Caudate	brain
42	chr4:118307000-118307600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:118307200-118307600	Enhancers	Fetal Brain Male	brain
44	chr4:118307200-118308000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
45	chr4:118307200-118309200	Weak transcription	Brain Anterior Caudate	brain
46	chr4:118307200-118321000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr4:118309200-118309800	Enhancers	Brain Anterior Caudate	brain
48	chr4:118309400-118309600	Enhancers	Fetal Brain Male	brain
49	chr4:118313800-118322200	Weak transcription	Pancreas	Pancrea
50	chr4:118320600-118321000	Enhancers	HSMM	muscle

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