Variant report

Variant	nsv1012036
Chromosome Location	chr4:56963544-57106642
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:984)
CpG islands
(count:427)
Chromatin interactive
region (count:35)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:984 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56970225-56970838	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:57081401-57082148	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:57000348-57000651	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:56999175-56999293	HepG2	liver:	n/a	n/a
5	ATF1	chr4:57024759-57024993	K562	blood:	n/a	n/a
6	ATF1	chr4:57047391-57048010	K562	blood:	n/a	n/a
7	ATF3	chr4:57024757-57024966	K562	blood:	n/a	chr4:57024888-57024901 chr4:57024887-57024902
8	ATF3	chr4:56995656-56995891	K562	blood:	n/a	n/a
9	ATF3	chr4:57049527-57049775	K562	blood:	n/a	n/a
10	BACH1	chr4:57013663-57013995	K562	blood:	n/a	n/a
11	BACH1	chr4:56973718-56973985	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:57013668-57013991	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr4:57019003-57019017	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr4:56995571-56995985	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr4:56996934-56997217	GM12878	blood:	n/a	n/a
16	BHLHE40	chr4:56995704-56995850	K562	blood:	n/a	n/a
17	BHLHE40	chr4:57049526-57049852	K562	blood:	n/a	n/a
18	BHLHE40	chr4:57049712-57050079	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:56978643-56978678	GM12878	blood:	n/a	n/a
20	CBX3	chr4:57081976-57082493	HCT-116	colon:	n/a	n/a
21	CBX3	chr4:57049542-57049915	K562	blood:	n/a	n/a
22	CBX3	chr4:57049530-57049892	K562	blood:	n/a	n/a
23	CCNT2	chr4:56976554-56976654	K562	blood:	n/a	n/a
24	CEBPB	chr4:56999163-56999259	HepG2	liver:	n/a	n/a
25	CEBPB	chr4:57081527-57081945	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:57015861-57016083	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:57047457-57047670	K562	blood:	n/a	n/a
28	CEBPB	chr4:56970276-56970637	HepG2	liver:	n/a	chr4:56970510-56970521
29	CEBPB	chr4:57081439-57081670	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:57079886-57079990	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:56988264-56988535	K562	blood:	n/a	chr4:56988369-56988382 chr4:56988370-56988381 chr4:56988369-56988380
32	CEBPB	chr4:57001102-57001512	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:57047438-57047638	K562	blood:	n/a	n/a
34	CEBPB	chr4:57014675-57014942	Hela-S3	cervix:	n/a	chr4:57014827-57014844
35	CEBPB	chr4:56970352-56970690	HepG2	liver:	n/a	chr4:56970510-56970521
36	CEBPB	chr4:57000044-57000083	HepG2	liver:	n/a	chr4:57000051-57000062
37	CEBPB	chr4:57057024-57057162	HepG2	liver:	n/a	chr4:57057099-57057110
38	CEBPB	chr4:56970322-56970651	HepG2	liver:	n/a	chr4:56970510-56970521
39	CEBPB	chr4:57096927-57097147	HepG2	liver:	n/a	n/a
40	CEBPB	chr4:56993785-56994037	HepG2	liver:	n/a	chr4:56993883-56993894 chr4:56993882-56993895
41	CEBPB	chr4:56970397-56970620	HepG2	liver:	n/a	chr4:56970510-56970521
42	CEBPB	chr4:56988231-56988504	HepG2	liver:	n/a	chr4:56988369-56988382 chr4:56988370-56988381 chr4:56988369-56988380
43	CEBPB	chr4:57078179-57078320	H1-hESC	embryonic stem cell:	n/a	n/a
44	CEBPD	chr4:56970270-56970564	HepG2	liver:	n/a	n/a
45	CHD2	chr4:57059327-57059448	K562	blood:	n/a	n/a
46	CREB1	chr4:57024765-57024992	GM12878	blood:	n/a	n/a
47	CREB1	chr4:57024724-57025026	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr4:57049620-57049770	GM12875	blood:	n/a	chr4:57049725-57049741
49	CTCF	chr4:56995600-56995750	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr4:56995760-56995910	HFF-Myc	foreskin:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:57036403-57036453	HCM	heart:	n/a
2	chr4:56978667-56978717	HCF	heart:	n/a
3	chr4:57082806-57082856	HUVEC	blood vessel:	n/a
4	chr4:57035957-57036007	IMR90	lung:	fetal
5	chr4:57035957-57036007	MCF-7	breast:	n/a
6	chr4:57035957-57036007	NHDF-neo	bronchial:	n/a
7	chr4:57035957-57036007	MCF10A-Er-Src	breast:	n/a
8	chr4:57036403-57036453	GM12891	blood:	n/a
9	chr4:57035957-57036007	PANC-1	pancreas:	n/a
10	chr4:57092248-57092298	HMEC	breast:	n/a
11	chr4:57036403-57036453	AG09319	gingival:	n/a
12	chr4:57036298-57036348	GM12891	blood:	n/a
13	chr4:57035957-57036007	SAEC	small airway:	n/a
14	chr4:57092248-57092298	AoSMC	blood vessel:	n/a
15	chr4:57036298-57036348	SK-N-SH	brain:	n/a
16	chr4:57092248-57092298	IMR90	lung:	fetal
17	chr4:57082806-57082856	IMR90	lung:	fetal
18	chr4:57035948-57035998	PANC-1	pancreas:	n/a
19	chr4:57092248-57092298	SK-N-SH_RA	brain:	n/a
20	chr4:57092248-57092298	HCT-116	colon:	n/a
21	chr4:57036403-57036453	ovcar-3	ovarian:	n/a
22	chr4:56978667-56978717	HEK293	kidney:	embryo
23	chr4:57035948-57035998	HMEC	breast:	n/a
24	chr4:57092248-57092298	AG04449	skin:	fetal
25	chr4:56978667-56978717	AG04450	lung:	fetal
26	chr4:57035948-57035998	HRCEpiC	kidney:	n/a
27	chr4:57035957-57036007	HRPEpiC	eye:	n/a
28	chr4:57035948-57035998	T-47D	breast:	n/a
29	chr4:57092248-57092298	SKMC	muscle:	n/a
30	chr4:57082806-57082856	HepG2	liver:	n/a
31	chr4:57035957-57036007	AG04449	skin:	fetal
32	chr4:57035948-57035998	AG04449	skin:	fetal
33	chr4:57036298-57036348	NT2-D1	testis:	n/a
34	chr4:57082806-57082856	SAEC	small airway:	n/a
35	chr4:57082806-57082856	U87	brain:	n/a
36	chr4:57035948-57035998	AG04450	lung:	fetal
37	chr4:57036298-57036348	HAEpiC	amniotic membrane:	n/a
38	chr4:57035957-57036007	GM12892	blood:	n/a
39	chr4:57036403-57036453	NHDF-neo	bronchial:	n/a
40	chr4:57082806-57082856	NB4	blood:	n/a
41	chr4:57035948-57035998	AG09309	skin:	n/a
42	chr4:56978667-56978717	HUVEC	blood vessel:	n/a
43	chr4:57036403-57036453	NHBE	bronchial:	n/a
44	chr4:57082806-57082856	HCPEpiC	choroid plexus:	n/a
45	chr4:57092248-57092298	NT2-D1	testis:	n/a
46	chr4:57036403-57036453	CMK	blood:	n/a
47	chr4:56978667-56978717	ECC-1	luminal epithelium:	n/a
48	chr4:57035948-57035998	HCPEpiC	choroid plexus:	n/a
49	chr4:57082806-57082856	Jurkat	blood:	n/a
50	chr4:57082806-57082856	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:57026944..57028463-chr4:57029397..57031028,2	K562	blood:
2	chr4:57097502..57100938-chr4:57102922..57104816,3	K562	blood:
3	chr4:56996872..56999249-chr4:57000156..57002361,2	K562	blood:
4	chr4:56986755..56988749-chr4:56988899..56991340,2	MCF-7	breast:
5	chr4:57054944..57056829-chr4:57061059..57063842,2	MCF-7	breast:
6	chr4:57093123..57095590-chr4:57097803..57099999,2	K562	blood:
7	chr4:57093123..57095590-chr4:57097803..57099999,2	K562	blood:
8	chr4:57024723..57027325-chr4:57027371..57029147,2	MCF-7	breast:
9	chr4:57021309..57023973-chr4:57025557..57028531,2	K562	blood:
10	chr4:57054944..57056829-chr4:57061059..57063842,2	MCF-7	breast:
11	chr4:57097502..57100938-chr4:57102922..57104816,3	K562	blood:
12	chr4:57046901..57049380-chr4:57055137..57059248,3	K562	blood:
13	chr4:56990498..56992393-chr4:56995607..56997336,2	K562	blood:
14	chr4:56990498..56992393-chr4:56995607..56997336,2	K562	blood:
15	chr4:56986755..56988749-chr4:56988899..56991340,2	MCF-7	breast:
16	chr4:57021309..57023973-chr4:57025557..57028531,2	K562	blood:
17	chr4:57007519..57009026-chr4:57014142..57015746,2	K562	blood:
18	chr4:57020491..57022913-chr4:57025333..57027120,2	K562	blood:
19	chr4:57007519..57009026-chr4:57014142..57015746,2	K562	blood:
20	chr4:57024723..57027325-chr4:57027371..57029147,2	MCF-7	breast:
21	chr4:56960470..56963101-chr4:56964832..56967339,3	MCF-7	breast:
22	chr4:56995263..56996196-chr4:57049303..57050160,2	K562	blood:
23	chr4:56791515..56793046-chr4:56992694..56994388,2	K562	blood:
24	chr4:56994960..56996210-chr4:57167032..57168215,14	MCF-7	breast:
25	chr4:57009940..57012315-chr4:57015568..57017810,2	K562	blood:
26	chr4:57026944..57028463-chr4:57029397..57031028,2	K562	blood:
27	chr4:57009940..57012315-chr4:57015568..57017810,2	K562	blood:
28	chr4:56915544..56917169-chr4:56971414..56974217,2	K562	blood:
29	chr4:57020491..57022913-chr4:57025333..57027120,2	K562	blood:
30	chr4:57046901..57049380-chr4:57055137..57059248,3	K562	blood:
31	chr4:56996872..56999249-chr4:57000156..57002361,2	K562	blood:
32	chr4:56995235..56996245-chr4:57167093..57168027,4	MCF-7	breast:
33	chr4:56995263..56996196-chr4:57049303..57050160,2	K562	blood:
34	chr4:56995303..56996217-chr4:57702535..57703041,2	MCF-7	breast:
35	chr4:57097271..57099309-chr4:57112147..57113822,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AASDH-1	chr4:57095800-57097193	NONHSAT096490

No data

Variant related genes	Relation type
KIAA1211	TF binding region
RNA5SP161	TF binding region
KIAA1211	CpG island
RNA5SP161	CpG island
ENSG00000109265	chromatin interactions

Extended variants
information (count: 5299 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:5299 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189959050	chr4:56963573-56963574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs182194296	chr4:56963586-56963587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117821501	chr4:56963592-56963593	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185293135	chr4:56963606-56963607	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs578194147	chr4:56963653-56963654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537616376	chr4:56963739-56963740	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536705394	chr4:56963743-56963744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140629542	chr4:56963783-56963784	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs573758935	chr4:56963823-56963824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201624230	chr4:56963948-56963949	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs542780022	chr4:56963974-56963975	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs73164244	chr4:56964085-56964086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75257334	chr4:56964100-56964101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs114224526	chr4:56964123-56964124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200278985	chr4:56964222-56964223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528799700	chr4:56964317-56964318	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs530732750	chr4:56964324-56964325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550725237	chr4:56964456-56964457	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs17086281	chr4:56964458-56964459	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs564071082	chr4:56964518-56964519	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs375555829	chr4:56964519-56964520	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs564445722	chr4:56964529-56964530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs4864569	chr4:56964544-56964545	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs377101298	chr4:56964545-56964546	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs148092925	chr4:56964590-56964591	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs534976381	chr4:56964651-56964652	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs367898733	chr4:56964657-56964658	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs138188856	chr4:56964671-56964672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs567068151	chr4:56964683-56964684	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs180712992	chr4:56964686-56964687	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs369811716	chr4:56964689-56964690	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs557515758	chr4:56964722-56964723	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs574325814	chr4:56964728-56964729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs111672551	chr4:56964745-56964746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536350348	chr4:56964772-56964773	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs56105986	chr4:56964858-56964859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs56109611	chr4:56964859-56964860	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs183802261	chr4:56964870-56964871	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558292211	chr4:56964873-56964874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575477442	chr4:56964899-56964900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs141769798	chr4:56964950-56964951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs531127031	chr4:56964953-56964954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs560744676	chr4:56964957-56964958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs529790008	chr4:56964968-56964969	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs540047079	chr4:56964981-56964982	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs551133825	chr4:56964988-56964989	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs35798357	chr4:56964997-56964998	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs371706529	chr4:56965002-56965003	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs138781484	chr4:56965033-56965034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs566718387	chr4:56965048-56965049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	19435819	CNVD
Multiple myeloma	16616336	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
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
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian neoplasms	16753589	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Glioblastoma	17504929	CNVD
Glioblastoma	16823502	CNVD
Melanoma	16908931	CNVD
Glioblastoma	20031968	CNVD
Medulloblastoma	19270706	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Olfactory neuroblastoma	18408657	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Rhabdomyosarcoma	16790082	CNVD
Gastrointestinal stromal cancer	17438095	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Glioblastoma multiforme	19115005	CNVD
Wilms tumour	21544195	CNVD
Glioblastoma multiforme	21138945	CNVD
Cancer	22183965	CNVD
Breast cancer	21785460	CNVD
Medullary thyroid carcinoma	18765511	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1213 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56945600-56965200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:56948800-56972200	Weak transcription	Fetal Stomach	stomach
3	chr4:56949000-56965200	Weak transcription	Primary hematopoietic stem cells	blood
4	chr4:56952000-57024400	Weak transcription	Fetal Intestine Small	intestine
5	chr4:56952600-56965200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr4:56952800-56968400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr4:56952800-56978200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:56953000-56965200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr4:56953600-56965200	Weak transcription	Brain Germinal Matrix	brain
10	chr4:56955800-56963800	Weak transcription	Cortex derived primary cultured neurospheres	brain
11	chr4:56957600-56971800	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr4:56962000-56965400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr4:56962000-56968200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr4:56962400-56965200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr4:56962400-56966800	Weak transcription	Fetal Brain Female	brain
16	chr4:56963200-56963800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr4:56963800-56964000	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr4:56963800-56974600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:56964000-56964400	Weak transcription	Cortex derived primary cultured neurospheres	brain
20	chr4:56964400-56969400	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr4:56965000-56965800	Enhancers	GM12878-XiMat	blood
22	chr4:56965200-56965400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr4:56965200-56965800	Enhancers	Primary hematopoietic stem cells	blood
24	chr4:56965200-56966000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:56965200-56966000	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr4:56965200-56966000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr4:56965200-56966000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:56965200-56966000	Enhancers	HMEC	breast
29	chr4:56965200-56966000	Enhancers	NH-A	brain
30	chr4:56965200-56966200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr4:56965200-56966200	Enhancers	Brain Anterior Caudate	brain
32	chr4:56965200-56967800	Enhancers	Brain Germinal Matrix	brain
33	chr4:56965400-56966000	Enhancers	Breast Myoepithelial Primary Cells	Breast
34	chr4:56965400-56966000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr4:56965400-56966000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr4:56965400-56966800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr4:56965600-56966000	Enhancers	Left Ventricle	heart
38	chr4:56965600-56966000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr4:56965600-56966000	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chr4:56965600-56966000	Enhancers	HSMM	muscle
41	chr4:56965600-56966000	Enhancers	HSMMtube	muscle
42	chr4:56965800-56974000	Weak transcription	Primary hematopoietic stem cells	blood
43	chr4:56966000-56966200	Enhancers	Fetal Brain Male	brain
44	chr4:56966000-56971600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:56966000-56973200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr4:56966000-56973800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr4:56966000-56981200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr4:56966200-56966600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:56966200-56968200	Weak transcription	Fetal Brain Male	brain
50	chr4:56966400-56967000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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