Variant report

Variant	nsv829996
Chromosome Location	chr4:85016673-85173300
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:874)
CpG islands
(count:489)
Chromatin interactive
region (count:22)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:874 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:85152699-85153034	K562	blood:	n/a	n/a
2	ATF1	chr4:85158186-85158535	K562	blood:	n/a	n/a
3	ATF1	chr4:85165754-85165952	K562	blood:	n/a	n/a
4	ATF2	chr4:85156731-85157066	GM12878	blood:	n/a	n/a
5	ATF3	chr4:85158247-85158485	K562	blood:	n/a	n/a
6	BATF	chr4:85067531-85067809	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:85152697-85152993	K562	blood:	n/a	n/a
8	BHLHE40	chr4:85165637-85165726	K562	blood:	n/a	n/a
9	BHLHE40	chr4:85158275-85158640	K562	blood:	n/a	n/a
10	BHLHE40	chr4:85067585-85067821	GM12878	blood:	n/a	n/a
11	CBX3	chr4:85088813-85089099	HCT-116	colon:	n/a	n/a
12	CEBPB	chr4:85119744-85120477	HepG2	liver:	n/a	chr4:85119904-85119915
13	CEBPB	chr4:85163228-85163479	A549	lung:	n/a	n/a
14	CEBPB	chr4:85135957-85136188	A549	lung:	n/a	n/a
15	CEBPB	chr4:85163236-85163510	HepG2	liver:	n/a	n/a
16	CEBPB	chr4:85119769-85120419	A549	lung:	n/a	chr4:85119904-85119915
17	CEBPB	chr4:85079965-85080234	A549	lung:	n/a	n/a
18	CEBPB	chr4:85017533-85017825	IMR90	lung:	n/a	chr4:85017666-85017677
19	CEBPB	chr4:85148336-85148471	HepG2	liver:	n/a	chr4:85148391-85148402
20	CEBPB	chr4:85119744-85120069	IMR90	lung:	n/a	chr4:85119904-85119915
21	CEBPB	chr4:85080088-85080249	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:85057686-85057780	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:85108449-85108714	H1-hESC	embryonic stem cell:	n/a	chr4:85108566-85108577
24	CEBPB	chr4:85163346-85163549	K562	blood:	n/a	n/a
25	CEBPB	chr4:85135969-85136221	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:85017500-85017839	HepG2	liver:	n/a	chr4:85017666-85017677
27	CEBPB	chr4:85017568-85017768	K562	blood:	n/a	chr4:85017666-85017677
28	CEBPB	chr4:85156460-85156708	H1-hESC	embryonic stem cell:	n/a	chr4:85156584-85156595
29	CEBPB	chr4:85159385-85159752	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:85148398-85148410	K562	blood:	n/a	n/a
31	CEBPB	chr4:85108520-85108554	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:85159377-85159684	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:85084572-85084750	HepG2	liver:	n/a	chr4:85084721-85084730 chr4:85084719-85084730
34	CEBPB	chr4:85079993-85080193	HepG2	liver:	n/a	n/a
35	CHD2	chr4:85152628-85152944	K562	blood:	n/a	n/a
36	CREB1	chr4:85080957-85081224	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTCF	chr4:85081024-85081286	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:85081040-85081190	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr4:85088380-85088530	BE2_C	brain:	n/a	chr4:85088420-85088441 chr4:85088425-85088443
40	CTCF	chr4:85072780-85072930	GM12865	blood:	n/a	n/a
41	CTCF	chr4:85159700-85159850	RPTEC	kidney:	n/a	n/a
42	CTCF	chr4:85159720-85159870	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:85088799-85089104	K562	blood:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
44	CTCF	chr4:85088420-85088570	BE2_C	brain:	n/a	chr4:85088420-85088441 chr4:85088425-85088443
45	CTCF	chr4:85088753-85089113	HepG2	liver:	n/a	chr4:85088908-85088924 chr4:85088907-85088925
46	CTCF	chr4:85081020-85081170	GM12865	blood:	n/a	n/a
47	CTCF	chr4:85072880-85073030	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr4:85081020-85081170	RPTEC	kidney:	n/a	n/a
49	CTCF	chr4:85072679-85073170	MCF-7	breast:	n/a	n/a
50	CTCF	chr4:85072817-85072980	GM19238	blood:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:85048240-85048290	RPTEC	kidney:	n/a
2	chr4:85048240-85048290	RPTEC	kidney:	n/a
3	chr4:85048240-85048290	LNCaP	prostate:	n/a
4	chr4:85145324-85145374	BJ	skin:	n/a
5	chr4:85165491-85165541	GM19239	blood:	n/a
6	chr4:85165491-85165541	SK-N-MC	brain:	n/a
7	chr4:85048240-85048290	BE2_C	brain:	n/a
8	chr4:85139232-85139282	ProgFib	skin:	n/a
9	chr4:85145324-85145374	HAEpiC	amniotic membrane:	n/a
10	chr4:85048240-85048290	GM06990	blood:	n/a
11	chr4:85163562-85163612	HepG2	liver:	n/a
12	chr4:85076551-85076601	Jurkat	blood:	n/a
13	chr4:85165491-85165541	PFSK-1	brain:	n/a
14	chr4:85076551-85076601	SK-N-SH	brain:	n/a
15	chr4:85048240-85048290	A549	lung:	n/a
16	chr4:85165689-85165739	HRPEpiC	eye:	n/a
17	chr4:85145324-85145374	SKMC	muscle:	n/a
18	chr4:85139232-85139282	GM06990	blood:	n/a
19	chr4:85139232-85139282	PFSK-1	brain:	n/a
20	chr4:85139232-85139282	HNPCEpiC	eye:	n/a
21	chr4:85076551-85076601	H1-hESC	embryonic stem cell:	embryo
22	chr4:85048240-85048290	PrEC	prostate:	n/a
23	chr4:85163562-85163612	HRE	kidney:	n/a
24	chr4:85145324-85145374	HCF	heart:	n/a
25	chr4:85139232-85139282	HRPEpiC	eye:	n/a
26	chr4:85145324-85145374	HCT-116	colon:	n/a
27	chr4:85020829-85020879	GM12891	blood:	n/a
28	chr4:85145324-85145374	K562	blood:	n/a
29	chr4:85076551-85076601	A549	lung:	n/a
30	chr4:85139232-85139282	Hepatocyte	liver:	n/a
31	chr4:85139232-85139282	GM19239	blood:	n/a
32	chr4:85165491-85165541	NB4	blood:	n/a
33	chr4:85076551-85076601	HAEpiC	amniotic membrane:	n/a
34	chr4:85020829-85020879	NB4	blood:	n/a
35	chr4:85076551-85076601	IMR90	lung:	fetal
36	chr4:85139232-85139282	GM12891	blood:	n/a
37	chr4:85076551-85076601	NH-A	brain:	n/a
38	chr4:85163562-85163612	SK-N-SH	brain:	n/a
39	chr4:85048240-85048290	NH-A	brain:	n/a
40	chr4:85165689-85165739	HAEpiC	amniotic membrane:	n/a
41	chr4:85139232-85139282	AG04449	skin:	fetal
42	chr4:85076551-85076601	SKMC	muscle:	n/a
43	chr4:85048240-85048290	T-47D	breast:	n/a
44	chr4:85165689-85165739	PrEC	prostate:	n/a
45	chr4:85020829-85020879	PFSK-1	brain:	n/a
46	chr4:85139232-85139282	U87	brain:	n/a
47	chr4:85165689-85165739	H1-hESC	embryonic stem cell:	embryo
48	chr4:85020829-85020879	HNPCEpiC	eye:	n/a
49	chr4:85139232-85139282	HCPEpiC	choroid plexus:	n/a
50	chr4:85165491-85165541	AoSMC	blood vessel:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
2	chr4:84827046..84827675-chr4:85088517..85089246,2	MCF-7	breast:
3	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
4	chr4:84882460..84883415-chr4:85088632..85089152,2	MCF-7	breast:
5	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:
6	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
7	chr4:85080701..85081585-chr4:85425136..85425979,2	MCF-7	breast:
8	chr4:85072631..85073368-chr4:85450368..85450912,2	MCF-7	breast:
9	chr4:85080575..85081559-chr4:85180120..85181416,6	MCF-7	breast:
10	chr4:85072431..85073209-chr4:85424476..85425190,3	MCF-7	breast:
11	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
12	chr4:84565617..84566470-chr4:85088713..85089282,2	MCF-7	breast:
13	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
14	chr4:85024708..85027047-chr4:85028536..85030200,2	K562	blood:
15	chr4:85071031..85073190-chr4:85079864..85082804,2	MCF-7	breast:
16	chr4:85139303..85141304-chr4:85144022..85145808,2	K562	blood:
17	chr20:52481552..52482195-chr4:85078491..85079377,2	MCF-7	breast:
18	chr4:85159698..85160208-chr4:85372408..85372912,2	MCF-7	breast:
19	chr4:85072451..85073423-chr4:85180134..85180901,4	MCF-7	breast:
20	chr4:85143338..85145421-chr4:85146842..85148891,2	K562	blood:
21	chr4:85103034..85104935-chr4:85113026..85114643,2	K562	blood:
22	chr4:85143892..85145421-chr4:85147391..85149801,2	K562	blood:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NKX6-1-3	chr4:85152232-85152296	ucscGeneNc_uc010ikd_1
2	lnc-NKX6-1-2	chr4:85070372-85070409	ENSG00000250546
3	lnc-NKX6-1-2	chr4:85068886-85069283	ENSG00000250546
4	lnc-NKX6-1-2	chr4:85164264-85164369	ENSG00000250546
5	lnc-NKX6-1-2	chr4:85164264-85164369	NONHSAT097229
6	lnc-NKX6-1-3	chr4:85075800-85075907	ucscGeneNc_uc010ikd_1
7	lnc-NKX6-1-2	chr4:85070372-85070441	ENSG00000250546
8	lnc-NKX6-1-2	chr4:85069200-85069283	ENSG00000250546

No data

Variant related genes	Relation type
ENSG00000250546	TF binding region
RNU6-774P	TF binding region
ENSG00000214980	TF binding region
ENSG00000250546	CpG island
RNU6-774P	CpG island
ENSG00000214980	CpG island
FOXP1	miRNA target sites
VAMP2	miRNA target sites
FAM3C	miRNA target sites
F3	miRNA target sites
USP25	miRNA target sites

Extended variants
information (count: 2743 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2743 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs199680484	chr4:85016693-85016694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563043745	chr4:85016703-85016704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs533161184	chr4:85016817-85016818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs140335041	chr4:85016881-85016882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs1921858	chr4:85016898-85016899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs560392066	chr4:85016904-85016905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs527950692	chr4:85016934-85016935	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs549279694	chr4:85016993-85016994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186894461	chr4:85017005-85017006	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs531980506	chr4:85017014-85017015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs374553808	chr4:85017042-85017043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs79799569	chr4:85017076-85017077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568968314	chr4:85017080-85017081	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs539044934	chr4:85017152-85017153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs557760978	chr4:85017160-85017161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs532919577	chr4:85017206-85017207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs73833621	chr4:85017235-85017236	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs62301631	chr4:85017244-85017245	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs62301632	chr4:85017247-85017248	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs73833622	chr4:85017261-85017262	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs556364376	chr4:85017276-85017277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578069028	chr4:85017325-85017326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs191742027	chr4:85017330-85017331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs560080770	chr4:85017337-85017338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs562576110	chr4:85017353-85017354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs527687156	chr4:85017356-85017357	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs542911599	chr4:85017396-85017397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs561288756	chr4:85017406-85017407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs28438793	chr4:85017413-85017414	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs550378161	chr4:85017456-85017457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs551232290	chr4:85017492-85017493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs73833623	chr4:85017555-85017556	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs533014227	chr4:85017584-85017585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183700261	chr4:85017622-85017623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530466473	chr4:85017629-85017630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs566430310	chr4:85017697-85017698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs187827114	chr4:85017709-85017710	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs191758386	chr4:85017756-85017757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs182116593	chr4:85017799-85017800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371381962	chr4:85017874-85017875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537619879	chr4:85017882-85017883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs556294567	chr4:85017940-85017941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186753926	chr4:85017958-85017959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs60422578	chr4:85017996-85017997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553895923	chr4:85017999-85018000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146486695	chr4:85018012-85018013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367641103	chr4:85018018-85018019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs542647543	chr4:85018051-85018052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561225546	chr4:85018105-85018106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367746039	chr4:85018161-85018162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
lymphocytic leukemia	21291569	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
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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Prostate cancer	16573809	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:247 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:85015200-85020800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr4:85020000-85020800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:85020400-85021800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:85020600-85021200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr4:85020600-85021200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr4:85020600-85021600	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:85020600-85021800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr4:85020800-85021000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:85020800-85021200	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:85020800-85021200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr4:85020800-85021600	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr4:85020800-85021600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:85020800-85021800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:85020800-85021800	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:85021000-85021400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr4:85021000-85021400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
17	chr4:85021200-85021600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
18	chr4:85021200-85022000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:85021400-85021800	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr4:85021600-85021800	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr4:85025800-85026400	Enhancers	Pancreatic Islets	Pancreatic Islet
22	chr4:85026400-85030200	Weak transcription	Pancreatic Islets	Pancreatic Islet
23	chr4:85030200-85032800	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr4:85030400-85031600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:85031200-85031400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:85031200-85031600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chr4:85031400-85031600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:85047000-85047600	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chr4:85047200-85047400	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:85047200-85047600	Enhancers	H1 Cell Line	embryonic stem cell
31	chr4:85047200-85047600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr4:85047200-85048400	Active TSS	iPS-15b Cell Line	embryonic stem cell
33	chr4:85047400-85047600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:85047400-85047600	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr4:85047400-85047800	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
36	chr4:85047400-85047800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:85047600-85047800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr4:85047600-85047800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:85047600-85048000	Active TSS	H1 Cell Line	embryonic stem cell
40	chr4:85047600-85048000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
41	chr4:85047600-85048400	Active TSS	ES-I3 Cell Line	embryonic stem cell
42	chr4:85047600-85048400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
43	chr4:85047600-85048400	Active TSS	iPS-18 Cell Line	embryonic stem cell
44	chr4:85047600-85048400	Active TSS	iPS-20b Cell Line	embryonic stem cell
45	chr4:85047600-85048400	Active TSS	K562	blood
46	chr4:85047800-85048400	Active TSS	HUES48 Cell Line	embryonic stem cell
47	chr4:85047800-85048400	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr4:85047800-85048400	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:85047800-85048400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:85047800-85048400	Active TSS	NHEK	skin

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