Variant report

Variant	esv3393088
Chromosome Location	chr4:56484073-56503988
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:1221)
Chromatin interactive
region (count:15)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:56493426-56493494	K562	blood:	n/a	n/a
2	ARID3A	chr4:56503388-56504015	K562	blood:	n/a	n/a
3	ARID3A	chr4:56501495-56501827	K562	blood:	n/a	n/a
4	ATF1	chr4:56501416-56501837	K562	blood:	n/a	n/a
5	ATF1	chr4:56498147-56498454	K562	blood:	n/a	n/a
6	BACH1	chr4:56502324-56502563	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr4:56483945-56484132	K562	blood:	n/a	n/a
8	BACH1	chr4:56502806-56503160	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:56503675-56503978	K562	blood:	n/a	n/a
10	BACH1	chr4:56503593-56503801	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr4:56483933-56484337	GM12878	blood:	n/a	n/a
12	BATF	chr4:56483976-56484328	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:56502266-56502629	K562	blood:	n/a	n/a
14	BHLHE40	chr4:56501226-56501818	K562	blood:	n/a	n/a
15	CCNT2	chr4:56501265-56503172	K562	blood:	n/a	chr4:56501740-56501760
16	CEBPB	chr4:56500114-56500405	A549	lung:	n/a	n/a
17	CEBPB	chr4:56493333-56493439	A549	lung:	n/a	n/a
18	CEBPB	chr4:56500141-56500429	HepG2	liver:	n/a	n/a
19	CEBPB	chr4:56493262-56493575	K562	blood:	n/a	n/a
20	CEBPB	chr4:56493264-56493488	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:56500092-56500438	K562	blood:	n/a	n/a
22	CEBPB	chr4:56498999-56499040	K562	blood:	n/a	n/a
23	CEBPB	chr4:56500139-56500401	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:56500146-56500378	K562	blood:	n/a	n/a
25	CEBPB	chr4:56498129-56498435	K562	blood:	n/a	n/a
26	CEBPB	chr4:56490400-56490597	K562	blood:	n/a	n/a
27	CEBPB	chr4:56500041-56500445	K562	blood:	n/a	n/a
28	CEBPD	chr4:56500094-56500488	K562	blood:	n/a	n/a
29	CHD1	chr4:56502755-56502917	H1-hESC	embryonic stem cell:	n/a	n/a
30	CHD2	chr4:56502183-56502449	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr4:56502112-56503096	K562	blood:	n/a	n/a
32	CTBP2	chr4:56501652-56502510	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr4:56502354-56502525	GM12878	blood:	n/a	chr4:56502419-56502432
34	CTCF	chr4:56502340-56502490	GM12873	blood:	n/a	chr4:56502419-56502432
35	CTCF	chr4:56502340-56502490	HMEC	breast:	n/a	chr4:56502419-56502432
36	CTCF	chr4:56502284-56502549	MCF-7	breast:	n/a	chr4:56502419-56502432
37	CTCF	chr4:56502116-56502538	T-47D	breast:	n/a	chr4:56502419-56502432
38	CTCF	chr4:56502323-56502544	LNCaP	prostate:	n/a	chr4:56502419-56502432
39	CTCF	chr4:56502338-56502506	H1-hESC	embryonic stem cell:	n/a	chr4:56502419-56502432
40	CTCF	chr4:56502380-56502530	HBMEC	blood vessel:	n/a	chr4:56502419-56502432
41	CTCF	chr4:56502357-56502493	ProgFib	skin:	n/a	chr4:56502419-56502432
42	CTCF	chr4:56502369-56502500	Spleen_OC	spleen:	n/a	chr4:56502419-56502432
43	CTCF	chr4:56502300-56502450	SK-N-SH_RA	brain:	n/a	chr4:56502419-56502432
44	CTCF	chr4:56494460-56494610	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:56502380-56502530	GM12874	blood:	n/a	chr4:56502419-56502432
46	CTCF	chr4:56502360-56502510	GM12871	blood:	n/a	chr4:56502419-56502432
47	CTCF	chr4:56502321-56502509	Fibrobl	skin:	n/a	chr4:56502419-56502432
48	CTCF	chr4:56502321-56502518	MCF-7	breast:	n/a	chr4:56502419-56502432
49	CTCF	chr4:56502380-56502530	GM06990	blood:	n/a	chr4:56502419-56502432
50	CTCF	chr4:56502300-56502450	GM12872	blood:	n/a	chr4:56502419-56502432

(count:1221 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:56502392-56502442	BE2_C	brain:	n/a
2	chr4:56502392-56502442	BE2_C	brain:	n/a
3	chr4:56502544-56502594	IMR90	lung:	fetal
4	chr4:56501718-56501768	HRCEpiC	kidney:	n/a
5	chr4:56502392-56502442	HCF	heart:	n/a
6	chr4:56502529-56502579	RPTEC	kidney:	n/a
7	chr4:56502116-56502166	AG09319	gingival:	n/a
8	chr4:56501727-56501777	K562	blood:	n/a
9	chr4:56500362-56500412	AG09319	gingival:	n/a
10	chr4:56502116-56502166	IMR90	lung:	fetal
11	chr4:56502544-56502594	HIPEpiC	eye:	n/a
12	chr4:56500362-56500412	HepG2	liver:	n/a
13	chr4:56503521-56503571	AoSMC	blood vessel:	n/a
14	chr4:56502898-56502948	NHDF-neo	bronchial:	n/a
15	chr4:56502664-56502714	U87	brain:	n/a
16	chr4:56503521-56503571	HCF	heart:	n/a
17	chr4:56499522-56499572	AG10803	skin:	n/a
18	chr4:56501727-56501777	HCF	heart:	n/a
19	chr4:56502116-56502166	AG10803	skin:	n/a
20	chr4:56502598-56502648	HCPEpiC	choroid plexus:	n/a
21	chr4:56501727-56501777	Hepatocyte	liver:	n/a
22	chr4:56502788-56502838	T-47D	breast:	n/a
23	chr4:56501441-56501491	U87	brain:	n/a
24	chr4:56502664-56502714	AG09309	skin:	n/a
25	chr4:56502849-56502899	MCF10A-Er-Src	breast:	n/a
26	chr4:56502544-56502594	AG09319	gingival:	n/a
27	chr4:56496836-56496886	HCT-116	colon:	n/a
28	chr4:56501441-56501491	NT2-D1	testis:	n/a
29	chr4:56502864-56502914	AG09319	gingival:	n/a
30	chr4:56503521-56503571	RPTEC	kidney:	n/a
31	chr4:56502392-56502442	AG04449	skin:	fetal
32	chr4:56502469-56502519	HAEpiC	amniotic membrane:	n/a
33	chr4:56502534-56502584	Caco-2	colon:	n/a
34	chr4:56502534-56502584	MCF10A-Er-Src	breast:	n/a
35	chr4:56502392-56502442	HL-60	blood:	n/a
36	chr4:56500362-56500412	GM19239	blood:	n/a
37	chr4:56502529-56502579	AG04450	lung:	fetal
38	chr4:56502598-56502648	NT2-D1	testis:	n/a
39	chr4:56502598-56502648	K562	blood:	n/a
40	chr4:56500362-56500412	ProgFib	skin:	n/a
41	chr4:56501978-56502028	HIPEpiC	eye:	n/a
42	chr4:56500362-56500412	MCF10A-Er-Src	breast:	n/a
43	chr4:56502529-56502579	GM19239	blood:	n/a
44	chr4:56502534-56502584	HCF	heart:	n/a
45	chr4:56502529-56502579	HCPEpiC	choroid plexus:	n/a
46	chr4:56502849-56502899	PrEC	prostate:	n/a
47	chr4:56496836-56496886	HEEpiC	esophagus:	n/a
48	chr4:56501727-56501777	NHDF-neo	bronchial:	n/a
49	chr4:56502864-56502914	HCM	heart:	n/a
50	chr4:56502534-56502584	HIPEpiC	eye:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:56408119..56414507-chr4:56501105..56505595,8	K562	blood:
2	chr4:56492253..56496567-chr4:56500430..56503372,5	K562	blood:
3	chr4:56469856..56472454-chr4:56489855..56491752,2	K562	blood:
4	chr4:56410839..56413778-chr4:56501227..56505067,4	K562	blood:
5	chr4:56412329..56414161-chr4:56494486..56496762,2	K562	blood:
6	chr4:56211245..56214093-chr4:56502603..56505420,3	K562	blood:
7	chr4:56479641..56481239-chr4:56491828..56493480,2	K562	blood:
8	chr4:56474369..56476951-chr4:56481028..56484786,4	K562	blood:
9	chr4:56481534..56484408-chr4:56607415..56610057,2	K562	blood:
10	chr4:56500129..56502345-chr4:56579313..56582236,2	K562	blood:
11	chr4:56411599..56413538-chr4:56502547..56504625,2	MCF-7	breast:
12	chr4:56479641..56482011-chr4:56491746..56493328,2	K562	blood:
13	chr4:56407970..56411777-chr4:56498734..56501001,3	K562	blood:
14	chr4:56480747..56484464-chr4:56594012..56597947,4	K562	blood:
15	chr4:56492997..56495090-chr4:56501850..56503549,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMU-1	chr4:56496569-56496629	NONHSAT096476
2	lnc-NMU-2	chr4:56501440-56501555	l_2648_chr4:56499345-56508927_adipose
3	lnc-NMU-1	chr4:56502711-56502865	NONHSAT096475
4	lnc-NMU-1	chr4:56496569-56496627	NONHSAT096475
5	lnc-NMU-2	chr4:56499346-56499878	l_2648_chr4:56499345-56508927_adipose

No data

Variant related genes	Relation type
NMU	TF binding region
NMU	CpG island
ENSG00000128039	chromatin interactions
ENSG00000109255	chromatin interactions
ENSG00000272969	chromatin interactions
ENSG00000134852	chromatin interactions

Extended variants
information (count: 626 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:626 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35233725	chr4:56484183-56484184	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs571094873	chr4:56484205-56484206	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs567424193	chr4:56484237-56484238	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529980925	chr4:56484238-56484239	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546865137	chr4:56484293-56484294	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565989402	chr4:56484297-56484298	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs534703074	chr4:56484311-56484312	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs538587236	chr4:56484332-56484333	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62308667	chr4:56484402-56484403	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs112552644	chr4:56484406-56484407	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575409464	chr4:56484416-56484417	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs112220654	chr4:56484463-56484464	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192897953	chr4:56484552-56484553	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs574161447	chr4:56484553-56484554	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs368210069	chr4:56484622-56484623	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs376526804	chr4:56484623-56484624	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542990220	chr4:56484625-56484626	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs369040295	chr4:56484629-56484630	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs553626860	chr4:56484658-56484659	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543816817	chr4:56484663-56484664	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573530084	chr4:56484664-56484665	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545028989	chr4:56484682-56484683	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546822849	chr4:56484732-56484733	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35651967	chr4:56484739-56484740	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs564831374	chr4:56484740-56484741	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs369539946	chr4:56484775-56484776	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199856537	chr4:56484807-56484808	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs144412161	chr4:56484811-56484812	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs145314077	chr4:56484841-56484842	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533864547	chr4:56484842-56484843	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs200004974	chr4:56484847-56484848	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs141124691	chr4:56484848-56484849	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs200806133	chr4:56484856-56484857	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs530643221	chr4:56484857-56484858	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs10017514	chr4:56484866-56484867	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs140966291	chr4:56484888-56484889	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs372546521	chr4:56484889-56484890	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs529897802	chr4:56484897-56484898	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs546434094	chr4:56484898-56484899	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs140656774	chr4:56484926-56484927	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs200063310	chr4:56484930-56484931	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs58664028	chr4:56484931-56484932	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200281588	chr4:56484955-56484956	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs572471118	chr4:56484980-56484981	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs28865997	chr4:56484983-56484984	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs375029664	chr4:56484995-56484996	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs11946388	chr4:56485005-56485006	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs11940682	chr4:56485006-56485007	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11946390	chr4:56485014-56485015	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541524577	chr4:56485033-56485034	Active TSS Strong transcription Weak transcription Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Autism	22543975	CNVD
Breast cancer	21785460	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:513 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:56473600-56491600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
2	chr4:56476200-56485000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:56478200-56491600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr4:56478600-56485000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:56481600-56485200	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:56483400-56484200	Enhancers	K562	blood
7	chr4:56483600-56484200	Enhancers	GM12878-XiMat	blood
8	chr4:56484200-56491600	Weak transcription	K562	blood
9	chr4:56484400-56484800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:56484800-56485000	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr4:56485000-56485200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:56485000-56485400	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chr4:56485000-56485400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
14	chr4:56485000-56485400	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr4:56485000-56485400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
16	chr4:56485000-56485400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:56485200-56485400	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:56485200-56487600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:56485200-56491400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:56485400-56491800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:56485400-56491800	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:56485400-56498000	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr4:56485400-56498400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:56489400-56493800	Weak transcription	HUES48 Cell Line	embryonic stem cell
25	chr4:56489400-56498000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr4:56489800-56498200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:56491400-56492200	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:56491600-56492400	ZNF genes & repeats	K562	blood
29	chr4:56491600-56492600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
30	chr4:56491600-56496200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr4:56491800-56492200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr4:56491800-56493400	Strong transcription	H1 Cell Line	embryonic stem cell
33	chr4:56492000-56492200	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr4:56492000-56492200	Enhancers	Esophagus	oesophagus
35	chr4:56492000-56496400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:56492200-56495800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr4:56492200-56498200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr4:56492200-56498200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr4:56492400-56496600	Strong transcription	K562	blood
40	chr4:56492600-56498400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
41	chr4:56493400-56500200	Weak transcription	H1 Cell Line	embryonic stem cell
42	chr4:56493800-56494600	Strong transcription	HUES48 Cell Line	embryonic stem cell
43	chr4:56494000-56500600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chr4:56494600-56495200	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr4:56495200-56496200	Strong transcription	HUES48 Cell Line	embryonic stem cell
46	chr4:56495800-56499000	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr4:56496200-56498200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chr4:56496200-56498800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:56496600-56497000	Transcr. at gene 5' and 3'	K562	blood
50	chr4:56497000-56498000	Active TSS	K562	blood

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