Variant report

Variant	nsv879851
Chromosome Location	chr4:120942372-120984077
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:639)
CpG islands
(count:183)
Chromatin interactive
region (count:38)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:639 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:120964875-120964999	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:120971059-120971246	K562	blood:	n/a	n/a
3	ARID3A	chr4:120977380-120977726	K562	blood:	n/a	n/a
4	BCLAF1	chr4:120970911-120971326	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:120971053-120971327	K562	blood:	n/a	n/a
6	BHLHE40	chr4:120975224-120975427	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:120971084-120971375	Hela-S3	cervix:	n/a	n/a
8	CCNT2	chr4:120977486-120977686	K562	blood:	n/a	n/a
9	CEBPB	chr4:120956410-120956619	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:120974099-120974485	ECC-1	luminal epithelium:	n/a	n/a
11	CEBPB	chr4:120955314-120955502	HepG2	liver:	n/a	chr4:120955329-120955340
12	CEBPB	chr4:120953850-120954085	HepG2	liver:	n/a	chr4:120953995-120954012
13	CEBPB	chr4:120974039-120974533	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr4:120974024-120974662	IMR90	lung:	n/a	n/a
15	CTCF	chr4:120977540-120977690	AG04450	lung:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
16	CTCF	chr4:120945900-120946050	HCM	heart:	n/a	n/a
17	CTCF	chr4:120945919-120946022	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:120971160-120971310	GM12875	blood:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
19	CTCF	chr4:120971140-120971290	HPAF	blood vessel:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
20	CTCF	chr4:120945880-120946030	GM12872	blood:	n/a	n/a
21	CTCF	chr4:120971140-120971290	HepG2	liver:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
22	CTCF	chr4:120945860-120946010	HMF	breast:	n/a	n/a
23	CTCF	chr4:120945869-120945913	Spleen_OC	spleen:	n/a	n/a
24	CTCF	chr4:120971120-120971270	HCFaa	heart:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
25	CTCF	chr4:120977560-120977710	BJ	skin:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
26	CTCF	chr4:120964100-120964250	NHEK	skin:	n/a	n/a
27	CTCF	chr4:120977540-120977690	HL-60	blood:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
28	CTCF	chr4:120945840-120945990	HPF	lung:	n/a	n/a
29	CTCF	chr4:120971160-120971310	HAc	cerebellar:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
30	CTCF	chr4:120971120-120971270	HFF-Myc	foreskin:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
31	CTCF	chr4:120970944-120971482	MCF-7	breast:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
32	CTCF	chr4:120971120-120971270	HMEC	breast:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
33	CTCF	chr4:120971160-120971310	GM12878	blood:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
34	CTCF	chr4:120946700-120946850	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr4:120977554-120977683	Pancreas_OC	pancreas:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
36	CTCF	chr4:120977520-120977670	BJ	skin:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
37	CTCF	chr4:120971140-120971290	HCM	heart:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
38	CTCF	chr4:120945900-120946050	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:120971180-120971330	GM06990	blood:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
40	CTCF	chr4:120971140-120971290	HPF	lung:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
41	CTCF	chr4:120971140-120971290	AG09309	skin:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
42	CTCF	chr4:120971005-120971397	MCF-7	breast:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
43	CTCF	chr4:120971098-120971363	A549	lung:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
44	CTCF	chr4:120945820-120945970	BJ	skin:	n/a	n/a
45	CTCF	chr4:120945935-120946004	K562	blood:	n/a	n/a
46	CTCF	chr4:120971140-120971290	GM12872	blood:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
47	CTCF	chr4:120977500-120977650	HPAF	blood vessel:	n/a	chr4:120977591-120977609 chr4:120977592-120977608 chr4:120977586-120977607
48	CTCF	chr4:120971071-120971360	A549	lung:	n/a	chr4:120971217-120971235 chr4:120971212-120971233
49	CTCF	chr4:120970040-120970190	HVMF	connective:	n/a	n/a
50	CTCF	chr4:120971140-120971290	HRPEpiC	eye:	n/a	chr4:120971217-120971235 chr4:120971212-120971233

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:120971108-120971158	HCT-116	colon:	n/a
2	chr4:120971108-120971158	SKMC	muscle:	n/a
3	chr4:120975643-120975693	HIPEpiC	eye:	n/a
4	chr4:120975643-120975693	AG09319	gingival:	n/a
5	chr4:120974344-120974394	ProgFib	skin:	n/a
6	chr4:120971108-120971158	AG04449	skin:	fetal
7	chr4:120974344-120974394	SKMC	muscle:	n/a
8	chr4:120974344-120974394	AoSMC	blood vessel:	n/a
9	chr4:120971108-120971158	HRPEpiC	eye:	n/a
10	chr4:120975643-120975693	PANC-1	pancreas:	n/a
11	chr4:120971108-120971158	HRE	kidney:	n/a
12	chr4:120974344-120974394	NB4	blood:	n/a
13	chr4:120975643-120975693	AG10803	skin:	n/a
14	chr4:120971108-120971158	HIPEpiC	eye:	n/a
15	chr4:120971108-120971158	Hepatocyte	liver:	n/a
16	chr4:120971108-120971158	PANC-1	pancreas:	n/a
17	chr4:120974344-120974394	A549	lung:	n/a
18	chr4:120975643-120975693	T-47D	breast:	n/a
19	chr4:120974344-120974394	HIPEpiC	eye:	n/a
20	chr4:120974344-120974394	HCF	heart:	n/a
21	chr4:120974344-120974394	NHBE	bronchial:	n/a
22	chr4:120974344-120974394	HEEpiC	esophagus:	n/a
23	chr4:120975643-120975693	BE2_C	brain:	n/a
24	chr4:120975643-120975693	HCF	heart:	n/a
25	chr4:120975643-120975693	GM12891	blood:	n/a
26	chr4:120974344-120974394	U87	brain:	n/a
27	chr4:120974344-120974394	HepG2	liver:	n/a
28	chr4:120975643-120975693	HCPEpiC	choroid plexus:	n/a
29	chr4:120971108-120971158	HPAEpiC	pulmonary alveolar:	n/a
30	chr4:120974344-120974394	HEK293	kidney:	embryo
31	chr4:120971108-120971158	HL-60	blood:	n/a
32	chr4:120974344-120974394	NHDF-neo	bronchial:	n/a
33	chr4:120974344-120974394	AG04450	lung:	fetal
34	chr4:120975643-120975693	NB4	blood:	n/a
35	chr4:120975643-120975693	PFSK-1	brain:	n/a
36	chr4:120974344-120974394	ovcar-3	ovarian:	n/a
37	chr4:120975643-120975693	HMEC	breast:	n/a
38	chr4:120974344-120974394	T-47D	breast:	n/a
39	chr4:120971108-120971158	ovcar-3	ovarian:	n/a
40	chr4:120975643-120975693	AG09309	skin:	n/a
41	chr4:120971108-120971158	HNPCEpiC	eye:	n/a
42	chr4:120971108-120971158	NT2-D1	testis:	n/a
43	chr4:120975643-120975693	SK-N-MC	brain:	n/a
44	chr4:120971108-120971158	NB4	blood:	n/a
45	chr4:120971108-120971158	HEEpiC	esophagus:	n/a
46	chr4:120974344-120974394	HUVEC	blood vessel:	n/a
47	chr4:120975643-120975693	GM12892	blood:	n/a
48	chr4:120974344-120974394	HCT-116	colon:	n/a
49	chr4:120975643-120975693	HRE	kidney:	n/a
50	chr4:120974344-120974394	ECC-1	luminal epithelium:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:120966303..120968314-chr4:120969694..120972264,2	K562	blood:
2	chr4:120964367..120966016-chr4:120972622..120975603,2	K562	blood:
3	chr4:120970922..120972689-chr4:120977467..120980264,3	K562	blood:
4	chr4:120973859..120975620-chr4:120985435..120987169,2	K562	blood:
5	chr4:120965543..120968090-chr4:120982539..120985159,2	K562	blood:
6	chr4:120970925..120972723-chr4:120974695..120976845,2	MCF-7	breast:
7	chr4:120965102..120968292-chr4:120969292..120973289,4	K562	blood:
8	chr4:120549969..120550595-chr4:120970742..120971442,3	MCF-7	breast:
9	chr4:120973210..120976068-chr4:120976112..120978407,2	MCF-7	breast:
10	chr4:120965102..120968292-chr4:120969292..120973289,4	K562	blood:
11	chr4:120981267..120985179-chr4:120986108..120989816,4	MCF-7	breast:
12	chr4:120549794..120550449-chr4:120971003..120971739,4	MCF-7	breast:
13	chr4:119963061..119963691-chr4:120970722..120971258,2	K562	blood:
14	chr4:120975001..120976877-chr4:120985952..120988451,2	MCF-7	breast:
15	chr4:120568266..120570200-chr4:120973262..120975604,2	K562	blood:
16	chr4:120973210..120976068-chr4:120976112..120978407,2	MCF-7	breast:
17	chr4:120964367..120966016-chr4:120972622..120975603,2	K562	blood:
18	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
19	chr4:120973200..120974897-chr4:120987662..120990383,3	K562	blood:
20	chr4:120956553..120960562-chr4:120961898..120965735,4	K562	blood:
21	chr4:120235624..120236167-chr4:120970907..120971659,2	K562	blood:
22	chr4:120955421..120958256-chr4:120958733..120960538,2	K562	blood:
23	chr4:120970925..120972723-chr4:120974695..120976845,2	MCF-7	breast:
24	chr4:120552728..120554364-chr4:120974086..120975727,2	MCF-7	breast:
25	chr4:120692868..120695733-chr4:120948622..120950761,2	K562	blood:
26	chr4:120548059..120548579-chr4:120971160..120971673,2	K562	blood:
27	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
28	chr4:120549176..120551336-chr4:120973371..120974959,2	MCF-7	breast:
29	chr4:120979559..120981440-chr4:120988106..120989709,2	MCF-7	breast:
30	chr4:120975064..120977095-chr4:120978627..120980325,3	K562	blood:
31	chr4:120970922..120972689-chr4:120977467..120980264,3	K562	blood:
32	chr4:120550452..120551201-chr4:120970722..120971578,2	K562	blood:
33	chr4:120975064..120977095-chr4:120978627..120980325,3	K562	blood:
34	chr4:120966303..120968314-chr4:120969694..120972264,2	K562	blood:
35	chr4:120958158..120959809-chr4:120965003..120967800,2	K562	blood:
36	chr4:120965543..120968090-chr4:120982539..120985159,2	K562	blood:
37	chr4:120550305..120551270-chr4:120977378..120978356,2	MCF-7	breast:
38	chr4:120956553..120960562-chr4:120961898..120965735,4	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAD2L1-3	chr4:120945055-120945118	ucscGeneNc_uc003idk_1
2	lnc-MAD2L1-3	chr4:120943327-120943495	ucscGeneNc_uc003idk_1
3	lnc-MAD2L1-1	chr4:120956188-120956353	ENSG00000253825
4	lnc-MAD2L1-1	chr4:120961463-120961770	ENSG00000253825

No data

Variant related genes	Relation type
ENSG00000253825	TF binding region
ENSG00000250938	TF binding region
MAD2L1	TF binding region
ENSG00000253825	CpG island
ENSG00000250938	CpG island
MAD2L1	CpG island
ENSG00000164109	chromatin interactions
ENSG00000250938	chromatin interactions
ENSG00000138735	chromatin interactions

Extended variants
information (count: 903 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:903 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185259718	chr4:120943415-120943416	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs116258738	chr4:120943425-120943426	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs137972685	chr4:120943461-120943462	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs369035254	chr4:120943468-120943469	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs144324588	chr4:120943800-120943801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs116731625	chr4:120943828-120943829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs568259408	chr4:120943893-120943894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs537286715	chr4:120944019-120944020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs148344509	chr4:120944039-120944040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs141593148	chr4:120944081-120944082	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150901697	chr4:120944108-120944109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs34171123	chr4:120944125-120944126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs188842700	chr4:120944130-120944131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs139562662	chr4:120944141-120944142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs181080856	chr4:120944157-120944158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs562090292	chr4:120944246-120944247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186120370	chr4:120944258-120944259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544512742	chr4:120944267-120944268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs144176845	chr4:120944316-120944317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs76010331	chr4:120944324-120944325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs12649550	chr4:120944333-120944334	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566826131	chr4:120944342-120944343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191432978	chr4:120944380-120944381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372760258	chr4:120944384-120944385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117885852	chr4:120944409-120944410	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182461050	chr4:120944427-120944428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537222175	chr4:120944479-120944480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs556851697	chr4:120944493-120944494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs570638905	chr4:120944504-120944505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373783679	chr4:120944507-120944508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539118877	chr4:120944561-120944562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546605457	chr4:120944612-120944613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs566389033	chr4:120944613-120944614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146094211	chr4:120944616-120944617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572498990	chr4:120944674-120944675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541463931	chr4:120944694-120944695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs140058183	chr4:120944712-120944713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs187321941	chr4:120944826-120944827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs17009087	chr4:120944831-120944832	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs145022638	chr4:120944869-120944870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72686517	chr4:120944872-120944873	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533576552	chr4:120944943-120944944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs371474268	chr4:120944978-120944979	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373686414	chr4:120945057-120945058	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
45	rs548810579	chr4:120945077-120945078	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
46	rs560610669	chr4:120945117-120945118	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
47	rs116571628	chr4:120945159-120945160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs192220022	chr4:120945171-120945172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562893980	chr4:120945192-120945193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs114402100	chr4:120945193-120945194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Myelofibrosis	22110671	CNVD
Myelodysplastic syndrome	18508791	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD

Chromatin state (count:462 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:120943800-120946800	Weak transcription	Psoas Muscle	Psoas
2	chr4:120955600-120956000	Enhancers	Pancreas	Pancrea
3	chr4:120955800-120956200	Enhancers	Fetal Heart	heart
4	chr4:120956000-120956600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:120956200-120956400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr4:120956200-120956800	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr4:120957000-120957200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr4:120958400-120958800	Enhancers	Fetal Kidney	kidney
9	chr4:120959200-120959600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:120959200-120959600	Enhancers	HepG2	liver
11	chr4:120959200-120959800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:120959200-120959800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr4:120959200-120960600	Enhancers	Colon Smooth Muscle	Colon
14	chr4:120959400-120959600	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr4:120961600-120962200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr4:120961600-120962200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:120961800-120962200	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:120962200-120962600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr4:120962200-120987200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:120962400-120963200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:120962600-120963400	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:120962800-120963200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr4:120966000-120975600	Weak transcription	Dnd41	blood
24	chr4:120966400-120976200	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:120967400-120970200	Weak transcription	Aorta	Aorta
26	chr4:120969800-120970000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:120970000-120970200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:120970000-120971000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr4:120970000-120979600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:120970200-120970400	Active TSS	NHDF-Ad	bronchial
31	chr4:120970200-120970600	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr4:120970200-120970800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr4:120970200-120971200	Active TSS	Aorta	Aorta
34	chr4:120970400-120970600	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:120970400-120970600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr4:120970400-120970600	Enhancers	Adipose Nuclei	Adipose
37	chr4:120970400-120970600	Enhancers	Brain Angular Gyrus	brain
38	chr4:120970400-120970600	Enhancers	Brain Hippocampus Middle	brain
39	chr4:120970400-120970600	Enhancers	Colon Smooth Muscle	Colon
40	chr4:120970400-120970600	Enhancers	Rectal Smooth Muscle	rectum
41	chr4:120970400-120970600	Enhancers	NH-A	brain
42	chr4:120970400-120970600	Enhancers	Osteobl	bone
43	chr4:120970400-120970800	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr4:120970400-120970800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr4:120970400-120970800	Enhancers	Brain Cingulate Gyrus	brain
46	chr4:120970400-120970800	Flanking Active TSS	NHDF-Ad	bronchial
47	chr4:120970400-120971000	Active TSS	Brain Anterior Caudate	brain
48	chr4:120970400-120971000	Active TSS	NHLF	lung
49	chr4:120970400-120971200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr4:120970400-120971200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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