Variant report

Variant	esv1811886
Chromosome Location	chr4:68725776-68780041
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	chr4:68776107-68776264	HepG2	liver:	n/a	n/a
2	BATF	chr4:68727274-68727575	GM12878	blood:	n/a	n/a
3	BATF	chr4:68727253-68727571	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:68775659-68776005	Hela-S3	cervix:	n/a	chr4:68775829-68775840
5	CEBPB	chr4:68775665-68776273	K562	blood:	n/a	chr4:68775829-68775840
6	CEBPB	chr4:68775691-68776000	A549	lung:	n/a	chr4:68775829-68775840
7	CEBPB	chr4:68751495-68752334	IMR90	lung:	n/a	chr4:68752041-68752054
8	CEBPB	chr4:68739494-68739757	HepG2	liver:	n/a	chr4:68739607-68739620 chr4:68739608-68739619 chr4:68739634-68739645
9	CEBPB	chr4:68775720-68775923	H1-hESC	embryonic stem cell:	n/a	chr4:68775829-68775840
10	CEBPB	chr4:68739532-68739750	A549	lung:	n/a	chr4:68739607-68739620 chr4:68739608-68739619 chr4:68739634-68739645
11	CEBPB	chr4:68775674-68776023	HepG2	liver:	n/a	chr4:68775829-68775840
12	CEBPB	chr4:68775653-68776022	IMR90	lung:	n/a	chr4:68775829-68775840
13	CHD1	chr4:68751078-68752771	IMR90	lung:	n/a	n/a
14	CTCF	chr4:68776106-68776355	Spleen_OC	spleen:	n/a	n/a
15	CTCF	chr4:68758760-68758910	Caco-2	colon:	n/a	n/a
16	CTCF	chr4:68758752-68758963	Fibrobl	skin:	n/a	n/a
17	CTCF	chr4:68758742-68758960	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:68737680-68737830	NB4	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
19	CTCF	chr4:68776061-68776336	K562	blood:	n/a	n/a
20	CTCF	chr4:68737620-68737770	HAc	cerebellar:	n/a	n/a
21	CTCF	chr4:68737660-68737910	GM12878	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
22	CTCF	chr4:68737700-68737850	GM12865	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
23	CTCF	chr4:68776205-68776235	Kidney_OC	kidney:	n/a	n/a
24	CTCF	chr4:68758800-68758950	BJ	skin:	n/a	n/a
25	CTCF	chr4:68737740-68737890	HA-sp	spinal cord:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
26	CTCF	chr4:68737678-68737925	K562	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
27	CTCF	chr4:68776026-68776320	H1-hESC	embryonic stem cell:	n/a	n/a
28	CTCF	chr4:68737686-68737866	MCF-7	breast:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
29	CTCF	chr4:68758740-68758890	AG04450	lung:	n/a	n/a
30	CTCF	chr4:68776160-68776310	HVMF	connective:	n/a	n/a
31	CTCF	chr4:68737680-68737830	GM12868	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
32	CTCF	chr4:68776560-68776710	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr4:68737657-68738040	HCT-116	colon:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
34	CTCF	chr4:68737720-68737870	HCT-116	colon:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
35	CTCF	chr4:68737660-68737810	K562	blood:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
36	CTCF	chr4:68776120-68776270	GM12873	blood:	n/a	n/a
37	CTCF	chr4:68737676-68737861	A549	lung:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
38	CTCF	chr4:68776200-68776350	HCT-116	colon:	n/a	n/a
39	CTCF	chr4:68776120-68776270	AG09309	skin:	n/a	n/a
40	CTCF	chr4:68776180-68776330	NHLF	lung:	n/a	n/a
41	CTCF	chr4:68776160-68776310	HBMEC	blood vessel:	n/a	n/a
42	CTCF	chr4:68737760-68737910	HVMF	connective:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
43	CTCF	chr4:68775939-68776594	SK-N-SH	brain:	n/a	n/a
44	CTCF	chr4:68758807-68758898	MCF-7	breast:	n/a	n/a
45	CTCF	chr4:68737740-68737890	AG10803	skin:	n/a	chr4:68737784-68737805 chr4:68737782-68737800
46	CTCF	chr4:68776120-68776270	HEK293	kidney:	n/a	n/a
47	CTCF	chr4:68758740-68758890	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr4:68758760-68758910	HCFaa	heart:	n/a	n/a
49	CTCF	chr4:68776122-68776303	LNCaP	prostate:	n/a	n/a
50	CTCF	chr4:68758780-68758930	RPTEC	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:68750080-68750130	HNPCEpiC	eye:	n/a
2	chr4:68776652-68776702	NT2-D1	testis:	n/a
3	chr4:68751711-68751761	T-47D	breast:	n/a
4	chr4:68751711-68751761	MCF10A-Er-Src	breast:	n/a
5	chr4:68750080-68750130	HMEC	breast:	n/a
6	chr4:68776652-68776702	HEEpiC	esophagus:	n/a
7	chr4:68776652-68776702	HAEpiC	amniotic membrane:	n/a
8	chr4:68750080-68750130	MCF-7	breast:	n/a
9	chr4:68750080-68750130	Caco-2	colon:	n/a
10	chr4:68776652-68776702	NH-A	brain:	n/a
11	chr4:68750080-68750130	ovcar-3	ovarian:	n/a
12	chr4:68776652-68776702	Jurkat	blood:	n/a
13	chr4:68751711-68751761	SKMC	muscle:	n/a
14	chr4:68751711-68751761	CMK	blood:	n/a
15	chr4:68776652-68776702	MCF-7	breast:	n/a
16	chr4:68751711-68751761	NB4	blood:	n/a
17	chr4:68750080-68750130	AG10803	skin:	n/a
18	chr4:68750080-68750130	ECC-1	luminal epithelium:	n/a
19	chr4:68751711-68751761	Caco-2	colon:	n/a
20	chr4:68750080-68750130	NH-A	brain:	n/a
21	chr4:68750080-68750130	BJ	skin:	n/a
22	chr4:68750080-68750130	HL-60	blood:	n/a
23	chr4:68750080-68750130	HepG2	liver:	n/a
24	chr4:68751711-68751761	HRE	kidney:	n/a
25	chr4:68751711-68751761	ovcar-3	ovarian:	n/a
26	chr4:68750080-68750130	PrEC	prostate:	n/a
27	chr4:68776652-68776702	GM19239	blood:	n/a
28	chr4:68776652-68776702	AG04449	skin:	fetal
29	chr4:68751711-68751761	HepG2	liver:	n/a
30	chr4:68751711-68751761	MCF-7	breast:	n/a
31	chr4:68776652-68776702	A549	lung:	n/a
32	chr4:68750080-68750130	HCM	heart:	n/a
33	chr4:68751711-68751761	HL-60	blood:	n/a
34	chr4:68751711-68751761	SK-N-SH_RA	brain:	n/a
35	chr4:68776652-68776702	BE2_C	brain:	n/a
36	chr4:68751711-68751761	GM12892	blood:	n/a
37	chr4:68776652-68776702	SK-N-MC	brain:	n/a
38	chr4:68776652-68776702	NB4	blood:	n/a
39	chr4:68750080-68750130	HRCEpiC	kidney:	n/a
40	chr4:68776652-68776702	SAEC	small airway:	n/a
41	chr4:68751711-68751761	A549	lung:	n/a
42	chr4:68751711-68751761	HNPCEpiC	eye:	n/a
43	chr4:68750080-68750130	CMK	blood:	n/a
44	chr4:68750080-68750130	AG04449	skin:	fetal
45	chr4:68750080-68750130	HAEpiC	amniotic membrane:	n/a
46	chr4:68776652-68776702	HRCEpiC	kidney:	n/a
47	chr4:68776652-68776702	Caco-2	colon:	n/a
48	chr4:68750080-68750130	AG04450	lung:	fetal
49	chr4:68750080-68750130	HRPEpiC	eye:	n/a
50	chr4:68750080-68750130	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:68734136..68735963-chr4:68740619..68742852,2	K562	blood:
2	chr4:68737272..68738257-chr4:68775113..68776602,5	MCF-7	breast:
3	chr4:68737272..68738257-chr4:68775113..68776602,5	MCF-7	breast:
4	chr4:68747971..68750609-chr4:68750969..68752547,2	MCF-7	breast:
5	chr4:68738395..68739969-chr4:68740984..68743038,2	K562	blood:
6	chr4:68414627..68415373-chr4:68775821..68776638,2	MCF-7	breast:
7	chr4:68737188..68737967-chr4:68783944..68784741,2	MCF-7	breast:
8	chr4:68774616..68776298-chr4:68783211..68785677,2	K562	blood:
9	chr4:68734136..68735963-chr4:68740619..68742852,2	K562	blood:
10	chr4:68738395..68739969-chr4:68740984..68743038,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GNRHR-5	chr4:68749644-68749716	NONHSAT096714
2	lnc-GNRHR-5	chr4:68749644-68749678	NONHSAT096715
3	lnc-GNRHR-5	chr4:68749644-68749719	NONHSAT096713
4	lnc-GNRHR-5	chr4:68726105-68726154	NONHSAT096715

Variant related genes	Relation type
TMPRSS11D	TF binding region
TMPRSS11D	CpG island
ENSG00000153802	chromatin interactions

Extended variants
information (count: 1885 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1542664	chr4:68725776-68725777	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553801461	chr4:68725789-68725790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs563163414	chr4:68726105-68726106	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs189638582	chr4:68726143-68726144	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs565584052	chr4:68726804-68726805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148863051	chr4:68726819-68726820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs3838850	chr4:68726820-68726821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs34702150	chr4:68726821-68726822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs3037023	chr4:68726822-68726823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs201046325	chr4:68726823-68726824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs78768579	chr4:68726861-68726862	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs4582201	chr4:68726885-68726886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9999435	chr4:68726924-68726925	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs371889111	chr4:68726980-68726981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs567351121	chr4:68726998-68726999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs375198101	chr4:68727063-68727064	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs145074498	chr4:68727072-68727073	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs549746308	chr4:68727151-68727152	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs369363579	chr4:68727196-68727197	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs371744411	chr4:68727243-68727244	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs181357333	chr4:68727246-68727247	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs558524902	chr4:68727248-68727249	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs186847030	chr4:68727271-68727272	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576397378	chr4:68727347-68727348	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368836818	chr4:68727353-68727354	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs149124900	chr4:68727356-68727357	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs568107416	chr4:68727392-68727393	Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs534476305	chr4:68727428-68727429	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554378323	chr4:68727454-68727455	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573775477	chr4:68727458-68727459	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs7689160	chr4:68727465-68727466	Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs556513391	chr4:68727506-68727507	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs199768061	chr4:68727512-68727513	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs142162348	chr4:68727514-68727515	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs576320158	chr4:68727531-68727532	Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs11131729	chr4:68727562-68727563	Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs369540817	chr4:68727624-68727625	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs151185713	chr4:68727625-68727626	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs572807672	chr4:68727640-68727641	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs557416055	chr4:68727679-68727680	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs190036336	chr4:68727712-68727713	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs574335635	chr4:68727819-68727820	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs529813225	chr4:68727867-68727868	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs7694467	chr4:68727930-68727931	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs563406695	chr4:68727980-68727981	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181723188	chr4:68728013-68728014	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543349518	chr4:68728028-68728029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs140303125	chr4:68728050-68728051	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs77018226	chr4:68728170-68728171	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs534634993	chr4:68728199-68728200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
small cell lung cancer	20016488	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
Depressive disorder	21152026	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
Non-syndromic sensorineural hearing loss	17122850	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:248 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:68725400-68725800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:68726800-68727000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr4:68726800-68727000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:68726800-68727000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:68726800-68727000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:68726800-68727000	Enhancers	NHEK	skin
7	chr4:68726800-68727200	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr4:68727000-68727200	Flanking Active TSS	HMEC	breast
9	chr4:68727000-68727400	Enhancers	Muscle Satellite Cultured Cells	--
10	chr4:68727000-68727600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:68727000-68727600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
12	chr4:68727000-68727600	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:68727000-68727600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr4:68727000-68727600	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr4:68727000-68727800	Flanking Active TSS	NHEK	skin
16	chr4:68727200-68727400	Active TSS	HMEC	breast
17	chr4:68727200-68727600	Enhancers	HSMM	muscle
18	chr4:68727400-68727600	Flanking Active TSS	HMEC	breast
19	chr4:68727600-68727800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:68727600-68727800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:68727600-68727800	Enhancers	HMEC	breast
22	chr4:68727600-68728200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:68727800-68728000	Enhancers	NHEK	skin
24	chr4:68727800-68735400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr4:68734200-68735000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:68735200-68735600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr4:68735400-68735800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:68735400-68735800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:68735600-68740800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr4:68735800-68738400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr4:68735800-68738400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr4:68737800-68739600	Enhancers	NHEK	skin
33	chr4:68737800-68741200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr4:68738400-68739600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:68738400-68739600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr4:68738400-68740200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:68738600-68739000	Enhancers	ES-I3 Cell Line	embryonic stem cell
38	chr4:68738600-68739200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr4:68738600-68739200	Enhancers	HMEC	breast
40	chr4:68738800-68739000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr4:68738800-68739200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:68739000-68739400	Enhancers	Adipose Nuclei	Adipose
43	chr4:68739000-68747000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr4:68739200-68740800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr4:68739200-68740800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr4:68739400-68741000	Weak transcription	Adipose Nuclei	Adipose
47	chr4:68739600-68740800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:68739600-68747400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr4:68740200-68740600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:68740600-68741200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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