Variant report

Variant	nsv995045
Chromosome Location	chr4:98802844-99022958
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	chr4:99014048-99014354	HepG2	liver:	n/a	n/a
2	BACH1	chr4:98831268-98831463	H1-hESC	embryonic stem cell:	n/a	n/a
3	BCL3	chr4:98906959-98907234	GM12878	blood:	n/a	n/a
4	BCL3	chr4:98905816-98906082	GM12878	blood:	n/a	n/a
5	BRCA1	chr4:98908240-98908390	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr4:98832733-98832877	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:98975792-98975954	HepG2	liver:	n/a	chr4:98975918-98975929
8	CEBPB	chr4:98967948-98968326	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:99005951-99006103	A549	lung:	n/a	chr4:99006022-99006033
10	CEBPB	chr4:98910863-98911031	A549	lung:	n/a	n/a
11	CEBPB	chr4:98973085-98973241	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr4:98849976-98850238	IMR90	lung:	n/a	n/a
13	CEBPB	chr4:98898912-98899245	HepG2	liver:	n/a	chr4:98899094-98899105
14	CEBPB	chr4:98989787-98989990	HepG2	liver:	n/a	chr4:98989872-98989883
15	CEBPB	chr4:98863376-98863833	HCT-116	colon:	n/a	n/a
16	CEBPB	chr4:98999062-98999081	K562	blood:	n/a	n/a
17	CEBPB	chr4:98998918-98999191	HepG2	liver:	n/a	chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999042-98999051 chr4:98999041-98999052 chr4:98999040-98999051 chr4:98999042-98999051 chr4:98999040-98999053
18	CEBPB	chr4:99005909-99006159	IMR90	lung:	n/a	chr4:99006022-99006033
19	CEBPB	chr4:99005881-99006191	HepG2	liver:	n/a	chr4:99006022-99006033
20	CEBPB	chr4:98950612-98950807	HepG2	liver:	n/a	chr4:98950662-98950673
21	CHD2	chr4:99001733-99001756	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr4:98949078-98949213	LNCaP	prostate:	n/a	n/a
23	CTCF	chr4:98905840-98905990	SAEC	small airway:	n/a	n/a
24	CTCF	chr4:98831260-98831410	GM12866	blood:	n/a	chr4:98831342-98831355
25	CTCF	chr4:99014120-99014270	HCFaa	heart:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
26	CTCF	chr4:99013920-99014406	HCT-116	colon:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
27	CTCF	chr4:99014160-99014310	GM12865	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
28	CTCF	chr4:98908300-98908450	HepG2	liver:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
29	CTCF	chr4:98831240-98831390	HepG2	liver:	n/a	chr4:98831342-98831355
30	CTCF	chr4:98831182-98831512	GM12878	blood:	n/a	chr4:98831342-98831355
31	CTCF	chr4:98908267-98908459	MCF-7	breast:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
32	CTCF	chr4:98949060-98949210	HBMEC	blood vessel:	n/a	n/a
33	CTCF	chr4:98908218-98908478	SK-N-SH_RA	brain:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
34	CTCF	chr4:98831260-98831410	HRPEpiC	eye:	n/a	chr4:98831342-98831355
35	CTCF	chr4:99014120-99014270	HMF	breast:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
36	CTCF	chr4:98908070-98908710	HCT-116	colon:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
37	CTCF	chr4:99014100-99014250	GM12874	blood:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
38	CTCF	chr4:98908260-98908410	GM12865	blood:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
39	CTCF	chr4:98905800-98905950	HCT-116	colon:	n/a	n/a
40	CTCF	chr4:98905840-98905990	HCFaa	heart:	n/a	n/a
41	CTCF	chr4:98905800-98905950	HVMF	connective:	n/a	n/a
42	CTCF	chr4:99014200-99014350	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr4:98831280-98831430	GM12872	blood:	n/a	chr4:98831342-98831355
44	CTCF	chr4:98977400-98977550	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:98908260-98908410	HEK293	kidney:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
46	CTCF	chr4:99014160-99014310	HCPEpiC	choroid plexus:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199
47	CTCF	chr4:98977360-98977510	HMEC	breast:	n/a	n/a
48	CTCF	chr4:98908260-98908410	HCT-116	colon:	n/a	chr4:98908367-98908388 chr4:98908372-98908390
49	CTCF	chr4:98905860-98906010	GM12872	blood:	n/a	n/a
50	CTCF	chr4:99014140-99014290	HMEC	breast:	n/a	chr4:99014180-99014201 chr4:99014185-99014203 chr4:99014186-99014202 chr4:99014192-99014199

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:99008595-99008645	Hepatocyte	liver:	n/a
2	chr4:99008595-99008645	GM19239	blood:	n/a
3	chr4:99008595-99008645	HRPEpiC	eye:	n/a
4	chr4:99008595-99008645	GM12878	blood:	n/a
5	chr4:99008595-99008645	HAEpiC	amniotic membrane:	n/a
6	chr4:99008595-99008645	NT2-D1	testis:	n/a
7	chr4:99008595-99008645	SK-N-SH	brain:	n/a
8	chr4:99008595-99008645	NHDF-neo	bronchial:	n/a
9	chr4:99008595-99008645	PFSK-1	brain:	n/a
10	chr4:99008595-99008645	HRCEpiC	kidney:	n/a
11	chr4:99008595-99008645	Caco-2	colon:	n/a
12	chr4:99008595-99008645	IMR90	lung:	fetal
13	chr4:99008595-99008645	T-47D	breast:	n/a
14	chr4:99008595-99008645	PrEC	prostate:	n/a
15	chr4:99008595-99008645	Hela-S3	cervix:	n/a
16	chr4:99008595-99008645	LNCaP	prostate:	n/a
17	chr4:99008595-99008645	HCT-116	colon:	n/a
18	chr4:99008595-99008645	SK-N-SH_RA	brain:	n/a
19	chr4:99008595-99008645	HNPCEpiC	eye:	n/a
20	chr4:99008595-99008645	SAEC	small airway:	n/a
21	chr4:99008595-99008645	K562	blood:	n/a
22	chr4:99008595-99008645	NB4	blood:	n/a
23	chr4:99008595-99008645	ECC-1	luminal epithelium:	n/a
24	chr4:99008595-99008645	HEK293	kidney:	embryo
25	chr4:99008595-99008645	H1-hESC	embryonic stem cell:	embryo
26	chr4:99008595-99008645	ProgFib	skin:	n/a
27	chr4:99008595-99008645	HUVEC	blood vessel:	n/a
28	chr4:99008595-99008645	PANC-1	pancreas:	n/a
29	chr4:99008595-99008645	HCF	heart:	n/a
30	chr4:99008595-99008645	HepG2	liver:	n/a
31	chr4:99008595-99008645	AG04449	skin:	fetal
32	chr4:99008595-99008645	MCF-7	breast:	n/a
33	chr4:99008595-99008645	GM12892	blood:	n/a
34	chr4:99008595-99008645	HEEpiC	esophagus:	n/a
35	chr4:99008595-99008645	MCF10A-Er-Src	breast:	n/a
36	chr4:99008595-99008645	CMK	blood:	n/a
37	chr4:99008595-99008645	NH-A	brain:	n/a
38	chr4:99008595-99008645	AG10803	skin:	n/a
39	chr4:99008595-99008645	HRE	kidney:	n/a
40	chr4:99008595-99008645	Jurkat	blood:	n/a
41	chr4:99008595-99008645	A549	lung:	n/a
42	chr4:99008595-99008645	GM06990	blood:	n/a
43	chr4:99008595-99008645	BJ	skin:	n/a
44	chr4:99008595-99008645	AG09309	skin:	n/a
45	chr4:99008595-99008645	HMEC	breast:	n/a
46	chr4:99008595-99008645	HCPEpiC	choroid plexus:	n/a
47	chr4:99008595-99008645	HCM	heart:	n/a
48	chr4:99008595-99008645	ovcar-3	ovarian:	n/a
49	chr4:99008595-99008645	GM12891	blood:	n/a
50	chr4:99008595-99008645	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
2	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
3	chr4:99001766..99003673-chr4:99063340..99066059,2	MCF-7	breast:
4	chr4:99002780..99005606-chr4:99010089..99012416,2	MCF-7	breast:
5	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
6	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
7	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
8	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
9	chr4:99012356..99014792-chr4:99062792..99064417,2	MCF-7	breast:
10	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
11	chr4:98995356..98997429-chr4:98998775..99000432,2	MCF-7	breast:
12	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
13	chr4:97404242..97405044-chr4:98905771..98906367,3	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477
2	lnc-RAP1GDS1-6	chr4:98969706-98970194	NONHSAT097481

Variant related genes	Relation type
STPG2	TF binding region
RPL5P12	TF binding region
CRYZP2	TF binding region
DUTP8	TF binding region
STPG2	CpG island
RPL5P12	CpG island
CRYZP2	CpG island
DUTP8	CpG island
ENSG00000163116	chromatin interactions

Extended variants
information (count: 3021 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:3021 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190179997	chr4:98813607-98813608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529472039	chr4:98813611-98813612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181564955	chr4:98813617-98813618	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs566544787	chr4:98813621-98813622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs117326936	chr4:98813668-98813669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs116323494	chr4:98813669-98813670	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs75625170	chr4:98813695-98813696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs569586771	chr4:98813801-98813802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs573777757	chr4:98813827-98813828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs556137510	chr4:98813835-98813836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs568254495	chr4:98813848-98813849	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535235702	chr4:98813870-98813871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs72686449	chr4:98813931-98813932	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs148164702	chr4:98813956-98813957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9307215	chr4:98813965-98813966	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs577582444	chr4:98813969-98813970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs559972984	chr4:98814269-98814270	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs143125712	chr4:98814281-98814282	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs527424238	chr4:98814293-98814294	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs150846770	chr4:98814321-98814322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs17468481	chr4:98814334-98814335	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs550064432	chr4:98814382-98814383	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs567982809	chr4:98814389-98814390	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs138048523	chr4:98814392-98814393	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs547222598	chr4:98814409-98814410	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs376998841	chr4:98814425-98814426	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs572439144	chr4:98814436-98814437	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs76363341	chr4:98814448-98814449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs539551546	chr4:98814530-98814531	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs190729867	chr4:98814533-98814534	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs183241003	chr4:98814577-98814578	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs543163918	chr4:98816471-98816472	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs555013241	chr4:98816479-98816480	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs11731549	chr4:98816494-98816495	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs114325235	chr4:98816510-98816511	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs558907857	chr4:98816518-98816519	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs536779990	chr4:98816545-98816546	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs114855957	chr4:98816587-98816588	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs555317962	chr4:98816624-98816625	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs11731605	chr4:98816627-98816628	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs201455374	chr4:98816654-98816655	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs561102511	chr4:98816658-98816659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs140573538	chr4:98816684-98816685	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs530688843	chr4:98816704-98816705	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs72881499	chr4:98816721-98816722	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs543685897	chr4:98816723-98816724	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs565366559	chr4:98816776-98816777	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs567734170	chr4:98816780-98816781	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs370594906	chr4:98818610-98818611	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs534093320	chr4:98818669-98818670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
Chronic lymphocytic leukemia	21546498	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:125 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98813600-98814000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:98813600-98814000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr4:98820800-98821200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr4:98821000-98821400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:98821000-98822000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:98821200-98821600	Weak transcription	H1 Cell Line	embryonic stem cell
7	chr4:98821200-98822000	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:98821400-98821800	Enhancers	iPS-20b Cell Line	embryonic stem cell
9	chr4:98821600-98821800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr4:98821600-98821800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:98821600-98822000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:98821800-98824800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr4:98821800-98832400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr4:98822000-98824600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:98822000-98824800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
16	chr4:98824200-98824600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:98824400-98824800	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr4:98824600-98825200	Active TSS	ES-I3 Cell Line	embryonic stem cell
19	chr4:98824600-98825200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
20	chr4:98824600-98825200	Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr4:98824600-98825200	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr4:98824800-98825000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
23	chr4:98824800-98825000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr4:98824800-98825200	Active TSS	H9 Cell Line	embryonic stem cell
25	chr4:98824800-98825200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:98824800-98825200	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr4:98824800-98825200	Active TSS	iPS-18 Cell Line	embryonic stem cell
28	chr4:98825000-98825200	Active TSS	HUES64 Cell Line	embryonic stem cell
29	chr4:98825200-98825400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr4:98825200-98825600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
31	chr4:98825400-98825800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr4:98825600-98825800	Enhancers	iPS-15b Cell Line	embryonic stem cell
33	chr4:98825800-98831400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:98830600-98830800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr4:98831000-98831400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr4:98831000-98831600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:98831200-98831400	Enhancers	Pancreas	Pancrea
38	chr4:98831400-98831600	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr4:98831400-98831800	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:98831400-98832600	Weak transcription	Pancreas	Pancrea
41	chr4:98831600-98832400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
42	chr4:98831600-98839200	Weak transcription	Gastric	stomach
43	chr4:98832200-98832800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
44	chr4:98832200-98832800	Enhancers	Fetal Muscle Trunk	muscle
45	chr4:98832200-98833000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:98832200-98833200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr4:98832400-98832800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:98832400-98832800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:98832400-98832800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:98832400-98833200	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast

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