Variant report

Variant	nsv1002766
Chromosome Location	chr4:98006688-98128416
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	ATF2	chr4:98062525-98062850	H1-hESC	embryonic stem cell:	n/a	n/a
2	BCL11A	chr4:98062524-98062754	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr4:98027581-98028303	IMR90	lung:	n/a	chr4:98028170-98028181 chr4:98027683-98027694 chr4:98028169-98028180
4	CEBPB	chr4:98074165-98074537	ECC-1	luminal epithelium:	n/a	n/a
5	CEBPB	chr4:98062382-98062872	H1-hESC	embryonic stem cell:	n/a	chr4:98062395-98062406 chr4:98062393-98062406
6	CEBPB	chr4:98074319-98074479	HepG2	liver:	n/a	n/a
7	CEBPB	chr4:98028097-98028214	H1-hESC	embryonic stem cell:	n/a	chr4:98028170-98028181 chr4:98028169-98028180
8	CEBPB	chr4:98074171-98074537	A549	lung:	n/a	n/a
9	CEBPB	chr4:98074239-98074506	K562	blood:	n/a	n/a
10	CEBPB	chr4:98074224-98074678	MCF-7	breast:	n/a	n/a
11	CEBPB	chr4:98074205-98074562	HepG2	liver:	n/a	n/a
12	CEBPB	chr4:98074228-98074521	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr4:98028040-98028353	HepG2	liver:	n/a	chr4:98028170-98028181 chr4:98028169-98028180
14	CEBPB	chr4:98027598-98027822	HepG2	liver:	n/a	chr4:98027683-98027694
15	CEBPB	chr4:98074198-98074562	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:98080891-98081077	A549	lung:	n/a	chr4:98081041-98081054
17	CEBPB	chr4:98074081-98074673	HCT-116	colon:	n/a	n/a
18	CEBPB	chr4:98074135-98074528	HCT-116	colon:	n/a	n/a
19	CEBPB	chr4:98080816-98081138	MCF-7	breast:	n/a	chr4:98081041-98081054
20	CEBPB	chr4:98074215-98074555	A549	lung:	n/a	n/a
21	CEBPB	chr4:98074216-98074554	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr4:98074180-98074566	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr4:98074283-98074642	MCF-7	breast:	n/a	n/a
24	CEBPB	chr4:98028050-98028263	A549	lung:	n/a	chr4:98028170-98028181 chr4:98028169-98028180
25	CHD1	chr4:98010675-98010677	GM12878	blood:	n/a	n/a
26	CTCF	chr4:98074295-98074491	Pancreas_OC	pancreas:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
27	CTCF	chr4:98074320-98074470	HVMF	connective:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
28	CTCF	chr4:98074300-98074450	HCT-116	colon:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
29	CTCF	chr4:98028700-98028850	GM12864	blood:	n/a	n/a
30	CTCF	chr4:98074300-98074450	RPTEC	kidney:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
31	CTCF	chr4:98074320-98074470	HMEC	breast:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
32	CTCF	chr4:98074297-98074508	LNCaP	prostate:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
33	CTCF	chr4:98074320-98074478	HepG2	liver:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
34	CTCF	chr4:98074280-98074430	GM12865	blood:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
35	CTCF	chr4:98074293-98074517	MCF-7	breast:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
36	CTCF	chr4:98074128-98074589	MCF-7	breast:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
37	CTCF	chr4:98074372-98074449	GM10248	blood:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
38	CTCF	chr4:98074278-98074508	K562	blood:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
39	CTCF	chr4:98074380-98074530	GM12874	blood:	n/a	chr4:98074385-98074394
40	CTCF	chr4:98074296-98074435	HepG2	liver:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
41	CTCF	chr4:98074280-98074430	HCM	heart:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
42	CTCF	chr4:98074260-98074410	GM12866	blood:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
43	CTCF	chr4:98074340-98074490	HEK293	kidney:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
44	CTCF	chr4:98074320-98074470	HEEpiC	esophagus:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
45	CTCF	chr4:98074340-98074490	HepG2	liver:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
46	CTCF	chr4:98074282-98074527	Medullo	brain:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
47	CTCF	chr4:98074340-98074490	SAEC	small airway:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
48	CTCF	chr4:98074200-98074580	GM12878	blood:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
49	CTCF	chr4:98074300-98074450	SK-N-SH_RA	brain:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397
50	CTCF	chr4:98074298-98074456	Kidney_OC	kidney:	n/a	chr4:98074374-98074395 chr4:98074385-98074394 chr4:98074379-98074397

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98064236-98064286	AG09319	gingival:	n/a
2	chr4:98064236-98064286	HRCEpiC	kidney:	n/a
3	chr4:98064236-98064286	HMEC	breast:	n/a
4	chr4:98064236-98064286	CMK	blood:	n/a
5	chr4:98064236-98064286	ovcar-3	ovarian:	n/a
6	chr4:98064236-98064286	SK-N-SH	brain:	n/a
7	chr4:98064236-98064286	SAEC	small airway:	n/a
8	chr4:98064236-98064286	AG04449	skin:	fetal
9	chr4:98064236-98064286	GM06990	blood:	n/a
10	chr4:98064236-98064286	GM12891	blood:	n/a
11	chr4:98064236-98064286	HCPEpiC	choroid plexus:	n/a
12	chr4:98064236-98064286	HCM	heart:	n/a
13	chr4:98064236-98064286	AG09309	skin:	n/a
14	chr4:98064236-98064286	MCF10A-Er-Src	breast:	n/a
15	chr4:98064236-98064286	RPTEC	kidney:	n/a
16	chr4:98064236-98064286	K562	blood:	n/a
17	chr4:98064236-98064286	A549	lung:	n/a
18	chr4:98064236-98064286	GM12878	blood:	n/a
19	chr4:98064236-98064286	IMR90	lung:	fetal
20	chr4:98064236-98064286	HIPEpiC	eye:	n/a
21	chr4:98064236-98064286	BJ	skin:	n/a
22	chr4:98064236-98064286	T-47D	breast:	n/a
23	chr4:98064236-98064286	HRPEpiC	eye:	n/a
24	chr4:98064236-98064286	MCF-7	breast:	n/a
25	chr4:98064236-98064286	AG04450	lung:	fetal
26	chr4:98064236-98064286	HepG2	liver:	n/a
27	chr4:98064236-98064286	ECC-1	luminal epithelium:	n/a
28	chr4:98064236-98064286	Hepatocyte	liver:	n/a
29	chr4:98064236-98064286	U87	brain:	n/a
30	chr4:98064236-98064286	NH-A	brain:	n/a
31	chr4:98064236-98064286	PrEC	prostate:	n/a
32	chr4:98064236-98064286	Hela-S3	cervix:	n/a
33	chr4:98064236-98064286	HCF	heart:	n/a
34	chr4:98064236-98064286	HAEpiC	amniotic membrane:	n/a
35	chr4:98064236-98064286	HUVEC	blood vessel:	n/a
36	chr4:98064236-98064286	NB4	blood:	n/a
37	chr4:98064236-98064286	AG10803	skin:	n/a
38	chr4:98064236-98064286	PFSK-1	brain:	n/a
39	chr4:98064236-98064286	HRE	kidney:	n/a
40	chr4:98064236-98064286	SK-N-SH_RA	brain:	n/a
41	chr4:98064236-98064286	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:98064236-98064286	SK-N-MC	brain:	n/a
43	chr4:98064236-98064286	GM12892	blood:	n/a
44	chr4:98064236-98064286	H1-hESC	embryonic stem cell:	embryo
45	chr4:98064236-98064286	LNCaP	prostate:	n/a
46	chr4:98064236-98064286	HEEpiC	esophagus:	n/a
47	chr4:98064236-98064286	HEK293	kidney:	embryo
48	chr4:98064236-98064286	HL-60	blood:	n/a
49	chr4:98064236-98064286	NHDF-neo	bronchial:	n/a
50	chr4:98064236-98064286	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:98092499..98095381-chr4:98096517..98098591,2	MCF-7	breast:
2	chr4:98121338..98122914-chr4:98123026..98125277,2	MCF-7	breast:
3	chr4:98102707..98104208-chr4:98112967..98114585,2	MCF-7	breast:
4	chr4:98123649..98126373-chr4:98396261..98399179,2	MCF-7	breast:
5	chr4:98102707..98104208-chr4:98112967..98114585,2	MCF-7	breast:
6	chr4:98025635..98028062-chr4:98029788..98032302,2	K562	blood:
7	chr4:98092499..98095381-chr4:98096517..98098591,2	MCF-7	breast:
8	chr4:98071711..98073412-chr4:98074732..98076478,2	MCF-7	breast:
9	chr4:97997425..97999591-chr4:98017375..98019216,2	MCF-7	breast:
10	chr4:98071711..98073412-chr4:98074732..98076478,2	MCF-7	breast:
11	chr4:98121338..98122914-chr4:98123026..98125277,2	MCF-7	breast:
12	chr4:98025635..98028062-chr4:98029788..98032302,2	K562	blood:
13	chr4:98075243..98078105-chr4:98081885..98084700,2	MCF-7	breast:
14	chr4:98075243..98078105-chr4:98081885..98084700,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RAP1GDS1-5	chr4:98041852-98041916	ENSG00000253170
2	lnc-RAP1GDS1-5	chr4:98055751-98056210	ENSG00000253170

Variant related genes	Relation type
ENSG00000253170	TF binding region
ENSG00000253170	CpG island

Extended variants
information (count: 2950 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2950 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529466951	chr4:98017800-98017801	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs541393220	chr4:98017876-98017877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs193281182	chr4:98017895-98017896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559983086	chr4:98017899-98017900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs78504299	chr4:98017900-98017901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs570571072	chr4:98017921-98017922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572039717	chr4:98017950-98017951	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9997830	chr4:98017954-98017955	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs375953184	chr4:98017983-98017984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs568290361	chr4:98017988-98017989	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184255828	chr4:98018060-98018061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139271617	chr4:98018069-98018070	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs374425664	chr4:98018077-98018078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539456017	chr4:98018080-98018081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557692014	chr4:98018090-98018091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs139177534	chr4:98018133-98018134	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187924938	chr4:98018134-98018135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373260625	chr4:98018135-98018136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs149980790	chr4:98018148-98018149	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368483535	chr4:98018163-98018164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs56312920	chr4:98018184-98018185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75166271	chr4:98018413-98018414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183989998	chr4:98018417-98018418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552674709	chr4:98018429-98018430	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568138816	chr4:98018440-98018441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs11737190	chr4:98018459-98018460	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs188767839	chr4:98018504-98018505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565848511	chr4:98018532-98018533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374935114	chr4:98018548-98018549	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181499406	chr4:98018550-98018551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546172013	chr4:98018553-98018554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs62315804	chr4:98018564-98018565	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs569746753	chr4:98018593-98018594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185484835	chr4:98018646-98018647	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs77429167	chr4:98018681-98018682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs555485328	chr4:98018693-98018694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs113327398	chr4:98018712-98018713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534914739	chr4:98018716-98018717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190309744	chr4:98018723-98018724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs56784394	chr4:98018756-98018757	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs151006657	chr4:98018764-98018765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs140745999	chr4:98018765-98018766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376299353	chr4:98018778-98018779	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs182540718	chr4:98018791-98018792	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185825357	chr4:98018829-98018830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs79068358	chr4:98018842-98018843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565830942	chr4:98018865-98018866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs13149484	chr4:98018892-98018893	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs547292467	chr4:98018894-98018895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs112087036	chr4:98018931-98018932	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	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
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Hirschsprung''s Disease	21712996	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Cancer	19907438	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	19197363	CNVD
Melanoma	20688739	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98017800-98018200	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr4:98018400-98018800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
3	chr4:98018400-98019200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr4:98018400-98019200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:98018800-98019200	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr4:98023200-98023400	Enhancers	NHEK	skin
7	chr4:98023400-98024400	Weak transcription	NHEK	skin
8	chr4:98024200-98025000	Enhancers	Primary hematopoietic stem cells short term culture	blood
9	chr4:98024200-98026000	Enhancers	HMEC	breast
10	chr4:98024200-98027200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
11	chr4:98024200-98027600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:98024400-98026800	Enhancers	NHEK	skin
13	chr4:98030200-98036800	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr4:98035800-98036400	Enhancers	Fetal Intestine Large	intestine
15	chr4:98036000-98037400	Enhancers	Fetal Intestine Small	intestine
16	chr4:98036400-98036800	Weak transcription	Fetal Intestine Large	intestine
17	chr4:98036800-98037400	Enhancers	Fetal Intestine Large	intestine
18	chr4:98040000-98040400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr4:98040400-98042000	Strong transcription	HUES6 Cell Line	embryonic stem cell
20	chr4:98040600-98042800	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr4:98042000-98042600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:98042000-98043800	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chr4:98042200-98043800	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr4:98042200-98044000	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr4:98042400-98042600	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr4:98042600-98042800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
27	chr4:98042600-98043400	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr4:98042600-98043400	Enhancers	Fetal Intestine Small	intestine
29	chr4:98042600-98043600	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr4:98042800-98043000	Active TSS	iPS-20b Cell Line	embryonic stem cell
31	chr4:98042800-98043600	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:98043000-98043200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
33	chr4:98043200-98043400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr4:98043200-98043400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:98043200-98043600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr4:98043400-98044600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr4:98043400-98045000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr4:98043600-98044800	Weak transcription	H1 Cell Line	embryonic stem cell
39	chr4:98043800-98048600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
40	chr4:98044000-98044600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:98044600-98044800	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr4:98044800-98045200	Enhancers	H9 Cell Line	embryonic stem cell
43	chr4:98044800-98045200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:98044800-98045200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr4:98044800-98045200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:98044800-98045400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr4:98045000-98045200	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
48	chr4:98045000-98045200	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr4:98045000-98045200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
50	chr4:98045000-98045200	ZNF genes & repeats	Gastric	stomach

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