Variant report

Variant	esv1815076
Chromosome Location	chr4:68960810-69009703
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:68995505-68995878	K562	blood:	n/a	n/a
2	ATF1	chr4:68995507-68995848	K562	blood:	n/a	n/a
3	ATF3	chr4:68995610-68995980	K562	blood:	n/a	n/a
4	BACH1	chr4:68990022-68990381	H1-hESC	embryonic stem cell:	n/a	n/a
5	BHLHE40	chr4:68995560-68995938	K562	blood:	n/a	n/a
6	CBX3	chr4:68995373-68995867	HCT-116	colon:	n/a	n/a
7	CBX3	chr4:68995389-68995866	K562	blood:	n/a	n/a
8	CCNT2	chr4:68995497-68995943	K562	blood:	n/a	n/a
9	CEBPB	chr4:68995482-68995898	MCF-7	breast:	n/a	n/a
10	CEBPB	chr4:68995579-68995924	K562	blood:	n/a	n/a
11	CEBPB	chr4:68987328-68987795	H1-hESC	embryonic stem cell:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
12	CEBPB	chr4:68987327-68987697	K562	blood:	n/a	chr4:68987420-68987431 chr4:68987420-68987431 chr4:68987420-68987433 chr4:68987677-68987688
13	CEBPB	chr4:68995621-68995932	K562	blood:	n/a	n/a
14	CREB1	chr4:68989350-68989616	H1-hESC	embryonic stem cell:	n/a	n/a
15	CREB1	chr4:68989221-68989671	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr4:68989739-68989777	Lung_OC	lung:	n/a	n/a
17	CTCF	chr4:68995500-68995650	NHLF	lung:	n/a	n/a
18	CTCF	chr4:68966963-68967066	GM20000	blood:	n/a	n/a
19	CTCF	chr4:68971880-68972030	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr4:68977918-68977937	Kidney_OC	kidney:	n/a	n/a
21	CTCF	chr4:68996001-68996008	K562	blood:	n/a	n/a
22	CUX1	chr4:68995434-68996067	K562	blood:	n/a	n/a
23	E2F4	chr4:68976682-68976795	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr4:68977086-68977411	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr4:68997772-68997932	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr4:69007806-69008006	MCF10A-Er-Src	breast:	n/a	n/a
27	EGR1	chr4:68964802-68964998	K562	blood:	n/a	chr4:68964911-68964922 chr4:68964909-68964924 chr4:68964910-68964923 chr4:68964910-68964923 chr4:68964911-68964921
28	EGR1	chr4:68964795-68965018	K562	blood:	n/a	chr4:68964911-68964922 chr4:68964909-68964924 chr4:68964910-68964923 chr4:68964910-68964923 chr4:68964911-68964921
29	EGR1	chr4:68964792-68965013	H1-hESC	embryonic stem cell:	n/a	chr4:68964911-68964922 chr4:68964909-68964924 chr4:68964910-68964923 chr4:68964910-68964923 chr4:68964911-68964921
30	EP300	chr4:68985769-68985919	K562	blood:	n/a	n/a
31	EP300	chr4:68995406-68995933	MCF-7	breast:	n/a	chr4:68995882-68995896
32	EP300	chr4:68995404-68995875	MCF-7	breast:	n/a	n/a
33	EP300	chr4:69007598-69007910	SK-N-SH_RA	brain:	n/a	n/a
34	EP300	chr4:68989250-68989634	H1-hESC	embryonic stem cell:	n/a	n/a
35	EP300	chr4:68995406-68995999	K562	blood:	n/a	chr4:68995882-68995896
36	FOS	chr4:69004623-69004638	MCF10A-Er-Src	breast:	n/a	n/a
37	FOSL1	chr4:68995666-68995885	K562	blood:	n/a	n/a
38	FOSL2	chr4:68995394-68995954	MCF-7	breast:	n/a	n/a
39	FOXP2	chr4:68975544-68976137	SK-N-MC	brain:	n/a	n/a
40	GABPA	chr4:69000369-69000464	HepG2	liver:	n/a	n/a
41	GATA1	chr4:68995234-68996210	PBDE	blood:	n/a	chr4:68995841-68995857 chr4:68995835-68995852 chr4:68995686-68995702
42	GATA2	chr4:68985662-68985929	K562	blood:	n/a	n/a
43	GATA2	chr4:68995389-68996024	K562	blood:	n/a	chr4:68995841-68995857 chr4:68995835-68995852 chr4:68995686-68995702
44	GATA3	chr4:68995429-68995855	MCF-7	breast:	n/a	chr4:68995835-68995852 chr4:68995686-68995702
45	GATA3	chr4:68995435-68995790	T-47D	breast:	n/a	chr4:68995686-68995702
46	GATA3	chr4:68995416-68995763	T-47D	breast:	n/a	chr4:68995686-68995702
47	GATA3	chr4:68995114-68996131	MCF-7	breast:	n/a	chr4:68995841-68995857 chr4:68995835-68995852 chr4:68995686-68995702
48	GATA3	chr4:69007616-69007906	SH-SY5Y	brain:	n/a	n/a
49	GATA3	chr4:68995454-68995741	MCF-7	breast:	n/a	chr4:68995686-68995702
50	GATA3	chr4:68995393-68996081	MCF-7	breast:	n/a	chr4:68995841-68995857 chr4:68995835-68995852 chr4:68995686-68995702

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68995759-68995809	PFSK-1	brain:	n/a
2	chr4:68995995-68996045	ProgFib	skin:	n/a
3	chr4:68995995-68996045	HRPEpiC	eye:	n/a
4	chr4:68995759-68995809	HPAEpiC	pulmonary alveolar:	n/a
5	chr4:68995759-68995809	BJ	skin:	n/a
6	chr4:68995759-68995809	ProgFib	skin:	n/a
7	chr4:68995995-68996045	RPTEC	kidney:	n/a
8	chr4:68995759-68995809	RPTEC	kidney:	n/a
9	chr4:68995759-68995809	AG09309	skin:	n/a
10	chr4:68995995-68996045	PrEC	prostate:	n/a
11	chr4:68995759-68995809	ECC-1	luminal epithelium:	n/a
12	chr4:68995995-68996045	NT2-D1	testis:	n/a
13	chr4:68995995-68996045	ECC-1	luminal epithelium:	n/a
14	chr4:68995995-68996045	GM19239	blood:	n/a
15	chr4:68995759-68995809	IMR90	lung:	fetal
16	chr4:68995995-68996045	SK-N-SH_RA	brain:	n/a
17	chr4:68995759-68995809	ovcar-3	ovarian:	n/a
18	chr4:68995759-68995809	HEEpiC	esophagus:	n/a
19	chr4:68995759-68995809	SAEC	small airway:	n/a
20	chr4:68995995-68996045	HIPEpiC	eye:	n/a
21	chr4:68995995-68996045	AG04449	skin:	fetal
22	chr4:68995995-68996045	MCF-7	breast:	n/a
23	chr4:68995759-68995809	GM12891	blood:	n/a
24	chr4:68995995-68996045	SAEC	small airway:	n/a
25	chr4:68995995-68996045	LNCaP	prostate:	n/a
26	chr4:68995995-68996045	GM12891	blood:	n/a
27	chr4:68995995-68996045	IMR90	lung:	fetal
28	chr4:68995759-68995809	PANC-1	pancreas:	n/a
29	chr4:68995759-68995809	HCT-116	colon:	n/a
30	chr4:68995759-68995809	HAEpiC	amniotic membrane:	n/a
31	chr4:68995759-68995809	LNCaP	prostate:	n/a
32	chr4:68995995-68996045	AG09309	skin:	n/a
33	chr4:68995995-68996045	HRCEpiC	kidney:	n/a
34	chr4:68995759-68995809	HCF	heart:	n/a
35	chr4:68995759-68995809	H1-hESC	embryonic stem cell:	embryo
36	chr4:68995995-68996045	PANC-1	pancreas:	n/a
37	chr4:68995759-68995809	GM12892	blood:	n/a
38	chr4:68995759-68995809	Hela-S3	cervix:	n/a
39	chr4:68995759-68995809	NHBE	bronchial:	n/a
40	chr4:68995759-68995809	NB4	blood:	n/a
41	chr4:68995995-68996045	HepG2	liver:	n/a
42	chr4:68995759-68995809	U87	brain:	n/a
43	chr4:68995995-68996045	PFSK-1	brain:	n/a
44	chr4:68995995-68996045	HCT-116	colon:	n/a
45	chr4:68995759-68995809	PrEC	prostate:	n/a
46	chr4:68995759-68995809	NT2-D1	testis:	n/a
47	chr4:68995759-68995809	MCF-7	breast:	n/a
48	chr4:68995759-68995809	HEK293	kidney:	embryo
49	chr4:68995995-68996045	SK-N-MC	brain:	n/a
50	chr4:68995759-68995809	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
2	chr4:68994438..68997123-chr4:69006589..69008746,2	K562	blood:
3	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
4	chr4:68989293..68991883-chr4:68991970..68993905,2	MCF-7	breast:
5	chr4:68987951..68990702-chr4:68992647..68994699,2	K562	blood:
6	chr4:68588334..68590985-chr4:68982055..68983628,2	K562	blood:

Variant related genes	Relation type
TMPRSS11F	TF binding region
TMPRSS11F	CpG island
ENSG00000198092	chromatin interactions
ENSG00000270228	chromatin interactions

Extended variants
information (count: 740 )
Associated
traits (count: 90 )

Variant overlapped rSNPs/rCNVs (count:740 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558009421	chr4:68964227-68964228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs376277612	chr4:68964247-68964248	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs542062355	chr4:68964288-68964289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs79007303	chr4:68964360-68964361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs531736169	chr4:68964384-68964385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571655376	chr4:68964394-68964395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs374474710	chr4:68964415-68964416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537238926	chr4:68964421-68964422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs560199850	chr4:68964470-68964471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs557093096	chr4:68964472-68964473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs574180204	chr4:68964526-68964527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs527733440	chr4:68964530-68964531	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs547766493	chr4:68964540-68964541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs567967050	chr4:68964552-68964553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs76699618	chr4:68964555-68964556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550126768	chr4:68964580-68964581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs371230146	chr4:68964587-68964588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374062874	chr4:68964593-68964594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs367983349	chr4:68964621-68964622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs372140845	chr4:68964635-68964636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140054355	chr4:68964683-68964684	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs111465468	chr4:68964687-68964688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs146311461	chr4:68964716-68964717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs145530248	chr4:68964724-68964725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376493432	chr4:68964741-68964742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs369447469	chr4:68964748-68964749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs146923688	chr4:68964752-68964753	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs372811524	chr4:68964755-68964756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs201360819	chr4:68964763-68964764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12503814	chr4:68964768-68964769	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs72855016	chr4:68964784-68964785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550257497	chr4:68964794-68964795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs374107153	chr4:68964799-68964800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75301633	chr4:68964818-68964819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57237742	chr4:68964823-68964824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs188637342	chr4:68964825-68964826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs58731278	chr4:68964908-68964909	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs192952490	chr4:68964926-68964927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568885071	chr4:68964928-68964929	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs73825379	chr4:68964978-68964979	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs545675891	chr4:68964995-68964996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs137925648	chr4:68965016-68965017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs58006789	chr4:68965038-68965039	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs547824358	chr4:68965053-68965054	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs370123469	chr4:68965120-68965121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs541073690	chr4:68965191-68965192	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs59256773	chr4:68965198-68965199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs184566053	chr4:68972005-68972006	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs550370068	chr4:68972035-68972036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs149761147	chr4:68972044-68972045	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:90)

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	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	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
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
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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
Graft versus host disease	20877625	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Osteoporosis	20877625	CNVD
Osteoporosis	19737800	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Glioblastoma multiforme	21138945	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Alcoholism	21790672	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
early-passage human iPS cells	21368824	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68964200-68964600	Enhancers	iPS-18 Cell Line	embryonic stem cell
2	chr4:68964400-68964800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr4:68964400-68965200	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:68964600-68965000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr4:68964600-68965000	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr4:68964600-68965200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr4:68964600-68965200	Enhancers	iPS-15b Cell Line	embryonic stem cell
8	chr4:68972000-68972400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr4:68979000-68979600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:68983400-68988000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:68987400-68989400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:68987400-68989400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:68987400-68989800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:68988000-68989600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr4:68988200-68989400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:68988600-68989600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:68989800-68995400	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:68991400-68991600	Enhancers	K562	blood
19	chr4:68991600-68991800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr4:68991600-68994600	Weak transcription	K562	blood
21	chr4:68993600-68993800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:68993600-68994000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:68994000-68994400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:68994400-68995000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:68994400-68995000	Enhancers	Placenta Amnion	Placenta Amnion
26	chr4:68994600-68995400	Enhancers	K562	blood
27	chr4:68995000-68995400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:68995000-68995400	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr4:68995200-68995400	Enhancers	NHEK	skin
30	chr4:68995400-68995600	Active TSS	Esophagus	oesophagus
31	chr4:68995400-68995800	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:68995400-68995800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:68995400-68995800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
34	chr4:68995400-68996000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:68995400-68996000	Enhancers	H9 Cell Line	embryonic stem cell
36	chr4:68995400-68996000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr4:68995400-68996000	Enhancers	HMEC	breast
38	chr4:68995400-68996000	Flanking Active TSS	K562	blood
39	chr4:68995400-68996200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr4:68995400-68996200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr4:68995400-68996200	Enhancers	Placenta Amnion	Placenta Amnion
42	chr4:68995400-68996200	Flanking Active TSS	NHEK	skin
43	chr4:68995600-68995800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:68995600-68995800	Flanking Active TSS	Esophagus	oesophagus
45	chr4:68995600-68996200	Enhancers	Placenta	Placenta
46	chr4:68995800-68998000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr4:68995800-68998200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
48	chr4:68996000-68996200	Enhancers	K562	blood
49	chr4:68996200-68996600	Enhancers	NHEK	skin
50	chr4:68996200-68998200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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