Variant report

Variant	nsv1006642
Chromosome Location	chr4:7786980-7811291
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:989)
CpG islands
(count:1588)
Chromatin interactive
region (count:43)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7805872-7806028	K562	blood:	n/a	n/a
2	ARID3A	chr4:7807239-7807979	HepG2	liver:	n/a	n/a
3	ATF1	chr4:7807740-7808076	K562	blood:	n/a	n/a
4	ATF1	chr4:7803976-7804198	K562	blood:	n/a	n/a
5	ATF2	chr4:7803628-7804231	GM12878	blood:	n/a	n/a
6	ATF3	chr4:7807126-7807648	A549	lung:	n/a	n/a
7	ATF3	chr4:7807123-7807688	A549	lung:	n/a	n/a
8	BACH1	chr4:7800693-7800710	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr4:7786736-7787025	GM12878	blood:	n/a	chr4:7786917-7786928
10	BCL3	chr4:7807064-7807769	A549	lung:	n/a	n/a
11	BCL3	chr4:7806961-7808222	A549	lung:	n/a	n/a
12	BCLAF1	chr4:7805703-7806161	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:7795026-7795170	GM12878	blood:	n/a	n/a
14	BHLHE40	chr4:7794370-7794529	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:7807250-7807634	HepG2	liver:	n/a	n/a
16	BHLHE40	chr4:7803867-7804084	K562	blood:	n/a	n/a
17	BHLHE40	chr4:7805782-7806052	K562	blood:	n/a	n/a
18	BHLHE40	chr4:7805827-7806112	GM12878	blood:	n/a	n/a
19	BRCA1	chr4:7803812-7804123	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:7807203-7807670	Hela-S3	cervix:	n/a	n/a
21	CBX3	chr4:7799956-7800259	K562	blood:	n/a	n/a
22	CEBPB	chr4:7808038-7808064	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:7790863-7791191	A549	lung:	n/a	chr4:7791037-7791048
24	CEBPB	chr4:7809289-7809677	IMR90	lung:	n/a	n/a
25	CEBPB	chr4:7800044-7800379	IMR90	lung:	n/a	n/a
26	CEBPB	chr4:7809377-7809549	K562	blood:	n/a	n/a
27	CEBPB	chr4:7807160-7807723	MCF-7	breast:	n/a	n/a
28	CEBPB	chr4:7805756-7806029	A549	lung:	n/a	n/a
29	CEBPB	chr4:7807223-7807587	HepG2	liver:	n/a	n/a
30	CEBPB	chr4:7807112-7807689	ECC-1	luminal epithelium:	n/a	n/a
31	CEBPB	chr4:7790862-7791209	IMR90	lung:	n/a	chr4:7791037-7791048
32	CEBPB	chr4:7809291-7809664	A549	lung:	n/a	n/a
33	CEBPB	chr4:7807208-7808160	HepG2	liver:	n/a	n/a
34	CEBPB	chr4:7805711-7806053	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:7809294-7809666	HepG2	liver:	n/a	n/a
36	CEBPB	chr4:7807080-7807726	A549	lung:	n/a	n/a
37	CEBPB	chr4:7809308-7809617	K562	blood:	n/a	n/a
38	CEBPB	chr4:7807165-7808093	A549	lung:	n/a	n/a
39	CEBPB	chr4:7807134-7807685	Hela-S3	cervix:	n/a	n/a
40	CEBPB	chr4:7806931-7808253	A549	lung:	n/a	n/a
41	CEBPB	chr4:7807814-7808189	A549	lung:	n/a	n/a
42	CEBPB	chr4:7807133-7807735	MCF-7	breast:	n/a	n/a
43	CEBPB	chr4:7807186-7807709	HepG2	liver:	n/a	n/a
44	CEBPB	chr4:7790942-7791147	K562	blood:	n/a	chr4:7791037-7791048
45	CEBPB	chr4:7809363-7809683	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr4:7807208-7807570	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr4:7805713-7806049	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr4:7805733-7806031	K562	blood:	n/a	n/a
49	CEBPB	chr4:7809301-7809631	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr4:7809276-7809703	A549	lung:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7790161-7790211	HRCEpiC	kidney:	n/a
2	chr4:7788342-7788392	HCM	heart:	n/a
3	chr4:7790161-7790211	HRCEpiC	kidney:	n/a
4	chr4:7788342-7788392	HCM	heart:	n/a
5	chr4:7788981-7789031	ECC-1	luminal epithelium:	n/a
6	chr4:7802369-7802419	ProgFib	skin:	n/a
7	chr4:7802545-7802595	HRCEpiC	kidney:	n/a
8	chr4:7788198-7788248	AG09309	skin:	n/a
9	chr4:7788198-7788248	HMEC	breast:	n/a
10	chr4:7805952-7806002	HCM	heart:	n/a
11	chr4:7790161-7790211	BE2_C	brain:	n/a
12	chr4:7802545-7802595	AG04450	lung:	fetal
13	chr4:7802238-7802288	U87	brain:	n/a
14	chr4:7799346-7799396	H1-hESC	embryonic stem cell:	embryo
15	chr4:7788342-7788392	AoSMC	blood vessel:	n/a
16	chr4:7802238-7802288	MCF10A-Er-Src	breast:	n/a
17	chr4:7801337-7801387	Hela-S3	cervix:	n/a
18	chr4:7789738-7789788	HPAEpiC	pulmonary alveolar:	n/a
19	chr4:7807438-7807488	LNCaP	prostate:	n/a
20	chr4:7805952-7806002	AG10803	skin:	n/a
21	chr4:7787960-7788010	NH-A	brain:	n/a
22	chr4:7803013-7803063	MCF10A-Er-Src	breast:	n/a
23	chr4:7801337-7801387	IMR90	lung:	fetal
24	chr4:7802192-7802242	HCT-116	colon:	n/a
25	chr4:7788198-7788248	AoSMC	blood vessel:	n/a
26	chr4:7787944-7787994	HEEpiC	esophagus:	n/a
27	chr4:7788981-7789031	AG04449	skin:	fetal
28	chr4:7790161-7790211	K562	blood:	n/a
29	chr4:7799701-7799751	AoSMC	blood vessel:	n/a
30	chr4:7802238-7802288	NHBE	bronchial:	n/a
31	chr4:7787983-7788033	HRCEpiC	kidney:	n/a
32	chr4:7802192-7802242	LNCaP	prostate:	n/a
33	chr4:7802238-7802288	HCPEpiC	choroid plexus:	n/a
34	chr4:7787944-7787994	BJ	skin:	n/a
35	chr4:7810640-7810690	IMR90	lung:	fetal
36	chr4:7799636-7799686	NHBE	bronchial:	n/a
37	chr4:7802369-7802419	PANC-1	pancreas:	n/a
38	chr4:7807438-7807488	AoSMC	blood vessel:	n/a
39	chr4:7807438-7807488	HEEpiC	esophagus:	n/a
40	chr4:7802238-7802288	HPAEpiC	pulmonary alveolar:	n/a
41	chr4:7810640-7810690	Jurkat	blood:	n/a
42	chr4:7788198-7788248	Hepatocyte	liver:	n/a
43	chr4:7810640-7810690	HRE	kidney:	n/a
44	chr4:7801337-7801387	NH-A	brain:	n/a
45	chr4:7787983-7788033	HMEC	breast:	n/a
46	chr4:7789542-7789592	NB4	blood:	n/a
47	chr4:7802347-7802397	SAEC	small airway:	n/a
48	chr4:7799636-7799686	T-47D	breast:	n/a
49	chr4:7789542-7789592	NHDF-neo	bronchial:	n/a
50	chr4:7802238-7802288	HL-60	blood:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7807226..7807954-chr4:7930533..7931051,2	K562	blood:
2	chr15:91414030..91415040-chr4:7788215..7789214,4	HCT-116	colon:
3	chr4:7805419..7806405-chr4:7988814..7989339,2	K562	blood:
4	chr4:7806581..7808350-chr4:8014117..8016969,2	MCF-7	breast:
5	chr4:7787308..7789396-chr4:7796554..7799014,2	K562	blood:
6	chr4:7796049..7798614-chr4:7799200..7800916,2	MCF-7	breast:
7	chr4:7804029..7806912-chr4:7851204..7853700,2	MCF-7	breast:
8	chr4:7723319..7725071-chr4:7788895..7790676,2	K562	blood:
9	chr4:7808655..7810334-chr4:7810904..7813896,2	MCF-7	breast:
10	chr4:7808655..7810334-chr4:7810904..7813896,2	MCF-7	breast:
11	chr4:7783261..7784863-chr4:7786642..7789248,2	K562	blood:
12	chr4:7805566..7806506-chr4:7851979..7852511,2	K562	blood:
13	chr4:7787308..7789396-chr4:7796554..7799014,2	K562	blood:
14	chr4:7805394..7806236-chr4:7877431..7878287,4	MCF-7	breast:
15	chr4:7771806..7772761-chr4:7803548..7804554,10	MCF-7	breast:
16	chr4:7763037..7763633-chr4:7803589..7804397,3	MCF-7	breast:
17	chr4:7784424..7786891-chr4:7788959..7792253,4	K562	blood:
18	chr4:7807434..7808952-chr4:8000439..8002438,2	MCF-7	breast:
19	chr4:7763127..7763762-chr4:7803659..7804271,2	MCF-7	breast:
20	chr4:7805890..7806402-chr4:7930617..7931480,2	MCF-7	breast:
21	chr4:7803065..7805141-chr4:7807691..7809396,2	K562	blood:
22	chr4:7044398..7046569-chr4:7804109..7805802,2	K562	blood:
23	chr15:91412162..91414947-chr4:7788716..7790216,2	MCF-7	breast:
24	chr4:7790898..7792455-chr4:7794012..7795584,2	K562	blood:
25	chr4:7799366..7802066-chr4:7938906..7941900,2	MCF-7	breast:
26	chr4:7785064..7787531-chr4:7788291..7790828,3	K562	blood:
27	chr4:7785064..7787531-chr4:7788291..7790828,3	K562	blood:
28	chr3:64223802..64226025-chr4:7789518..7791033,2	MCF-7	breast:
29	chr4:7805030..7805958-chr4:7990369..7990911,2	K562	blood:
30	chr4:7804324..7807098-chr4:7992889..7994621,2	MCF-7	breast:
31	chr4:7770365..7771286-chr4:7803447..7804040,2	MCF-7	breast:
32	chr4:7804713..7806247-chr4:7939917..7942517,2	MCF-7	breast:
33	chr4:7803065..7804892-chr4:7807691..7809470,2	K562	blood:
34	chr4:7805561..7806399-chr4:7988705..7989541,5	MCF-7	breast:
35	chr4:7773384..7775813-chr4:7806131..7807839,2	MCF-7	breast:
36	chr4:7805249..7806076-chr4:7845775..7846418,2	MCF-7	breast:
37	chr4:7803065..7805141-chr4:7807691..7809396,2	K562	blood:
38	chr4:7805902..7806736-chr4:7939845..7940494,2	MCF-7	breast:
39	chr4:7803065..7804892-chr4:7807691..7809470,2	K562	blood:
40	chr4:7793303..7795239-chr4:7800745..7802759,2	MCF-7	breast:
41	chr16:89626684..89629192-chr4:7810790..7812508,2	MCF-7	breast:
42	chr4:7805604..7807190-chr4:7845615..7846654,7	MCF-7	breast:
43	chr4:7806783..7809609-chr4:7939273..7941651,3	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SORCS2-2	chr4:7800371-7800445	NONHSAT095066
2	lnc-SORCS2-2	chr4:7809374-7809715	NONHSAT095066
3	lnc-SORCS2-3	chr4:7806717-7806786	refGeneNc_1113_NR_026892

No data

Variant related genes	Relation type
AFAP1	TF binding region
AFAP1	CpG island
ENSG00000200084	chromatin interactions
ENSG00000228919	chromatin interactions
ENSG00000196526	chromatin interactions
ENSG00000167526	chromatin interactions
ENSG00000173011	chromatin interactions
ENSG00000173013	chromatin interactions

Extended variants
information (count: 1359 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:1359 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7675797	chr4:7786980-7786981	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs565924921	chr4:7787011-7787012	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73084412	chr4:7787015-7787016	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377750197	chr4:7787031-7787032	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs76533672	chr4:7787040-7787041	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs13128495	chr4:7787049-7787050	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs115530757	chr4:7787100-7787101	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568263094	chr4:7787115-7787116	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs535683807	chr4:7787136-7787137	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs7699923	chr4:7787205-7787206	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs142944269	chr4:7787211-7787212	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs16841240	chr4:7787262-7787263	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs58790280	chr4:7787305-7787306	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs573232380	chr4:7787356-7787357	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs374176894	chr4:7787360-7787361	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs117634673	chr4:7787374-7787375	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113360052	chr4:7787375-7787376	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs556532947	chr4:7787401-7787402	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs529552084	chr4:7787433-7787434	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544823762	chr4:7787492-7787493	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs111577016	chr4:7787510-7787511	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs529309811	chr4:7787539-7787540	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs56922435	chr4:7787543-7787544	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs545333128	chr4:7787544-7787545	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs570117523	chr4:7787579-7787580	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs115168070	chr4:7787580-7787581	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs535994824	chr4:7787616-7787617	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs34466235	chr4:7787637-7787638	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs371998907	chr4:7787641-7787642	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs546270829	chr4:7787674-7787675	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs140791670	chr4:7787698-7787699	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs535367535	chr4:7787760-7787761	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557139553	chr4:7787763-7787764	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs13136890	chr4:7787768-7787769	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs182118247	chr4:7787769-7787770	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs558235523	chr4:7787834-7787835	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185778425	chr4:7787836-7787837	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs144595018	chr4:7787841-7787842	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs555460211	chr4:7787851-7787852	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs574298304	chr4:7787857-7787858	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189498200	chr4:7787875-7787876	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs16841246	chr4:7787899-7787900	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs561051799	chr4:7787921-7787922	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371401645	chr4:7787922-7787923	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577770152	chr4:7787956-7787957	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370469870	chr4:7787960-7787961	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs141071297	chr4:7787983-7787984	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138509764	chr4:7787991-7787992	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs367862961	chr4:7787998-7787999	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs372059550	chr4:7788007-7788008	Strong transcription Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7758400-7795400	Weak transcription	Hela-S3	cervix
2	chr4:7759400-7790400	Weak transcription	Psoas Muscle	Psoas
3	chr4:7762000-7788000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr4:7762000-7805800	Weak transcription	Stomach Mucosa	stomach
5	chr4:7770800-7828400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr4:7776400-7787200	Weak transcription	Fetal Brain Male	brain
7	chr4:7776400-7790000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr4:7776400-7799000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr4:7776400-7800000	Weak transcription	H1 Cell Line	embryonic stem cell
10	chr4:7776400-7806800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr4:7780200-7794400	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr4:7780600-7788000	Genic enhancers	Osteobl	bone
13	chr4:7780600-7800200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr4:7780800-7790600	Weak transcription	Pancreas	Pancrea
15	chr4:7781000-7800000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr4:7781200-7796000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr4:7781400-7800400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr4:7781400-7801000	Weak transcription	Brain Substantia Nigra	brain
19	chr4:7781400-7801200	Weak transcription	Brain Anterior Caudate	brain
20	chr4:7781600-7789400	Strong transcription	Muscle Satellite Cultured Cells	--
21	chr4:7781600-7791400	Strong transcription	Fetal Intestine Large	intestine
22	chr4:7781600-7807400	Weak transcription	Brain Angular Gyrus	brain
23	chr4:7781800-7790000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr4:7782000-7790600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr4:7782200-7791000	Strong transcription	Stomach Smooth Muscle	stomach
26	chr4:7782600-7790800	Strong transcription	Cortex derived primary cultured neurospheres	brain
27	chr4:7783200-7788200	Enhancers	GM12878-XiMat	blood
28	chr4:7783400-7794000	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr4:7783400-7798800	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr4:7783400-7799200	Weak transcription	HepG2	liver
31	chr4:7783600-7789200	Strong transcription	HSMM	muscle
32	chr4:7783800-7806200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
33	chr4:7784000-7791000	Weak transcription	Spleen	Spleen
34	chr4:7784000-7792800	Weak transcription	Primary T cells from cord blood	blood
35	chr4:7784000-7794200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr4:7784000-7794400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:7784000-7801800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
38	chr4:7784000-7821200	Weak transcription	Small Intestine	intestine
39	chr4:7784200-7788800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr4:7784200-7790600	Weak transcription	Primary monocytes fromperipheralblood	blood
41	chr4:7784200-7797800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
42	chr4:7784200-7800600	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:7784200-7800600	Weak transcription	Esophagus	oesophagus
44	chr4:7784200-7802200	Weak transcription	Aorta	Aorta
45	chr4:7784200-7802800	Strong transcription	Fetal Muscle Trunk	muscle
46	chr4:7784400-7791800	Strong transcription	Fetal Stomach	stomach
47	chr4:7784400-7794000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr4:7784600-7791400	Strong transcription	A549	lung
49	chr4:7784800-7789200	Strong transcription	Fetal Lung	lung
50	chr4:7784800-7789400	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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