Variant report

Variant	nsv868914
Chromosome Location	chr4:98416047-98969285
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1866)
CpG islands
(count:122)
Chromatin interactive
region (count:29)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1866 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:98607042-98607171	K562	blood:	n/a	n/a
2	ATF3	chr4:98419975-98420488	HCT-116	colon:	n/a	n/a
3	ATF3	chr4:98419887-98420492	HCT-116	colon:	n/a	n/a
4	BACH1	chr4:98831268-98831463	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:98577260-98577434	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:98420053-98420303	H1-hESC	embryonic stem cell:	n/a	chr4:98420142-98420156
7	BCL3	chr4:98508998-98509375	GM12878	blood:	n/a	n/a
8	BCL3	chr4:98906959-98907234	GM12878	blood:	n/a	n/a
9	BCL3	chr4:98905816-98906082	GM12878	blood:	n/a	n/a
10	BHLHE40	chr4:98421683-98421883	GM12878	blood:	n/a	n/a
11	BRCA1	chr4:98908240-98908390	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr4:98417471-98418225	HCT-116	colon:	n/a	n/a
13	CBX3	chr4:98419861-98420515	HCT-116	colon:	n/a	n/a
14	CBX3	chr4:98419866-98420528	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:98618600-98618916	K562	blood:	n/a	n/a
16	CEBPB	chr4:98950612-98950807	HepG2	liver:	n/a	chr4:98950662-98950673
17	CEBPB	chr4:98539434-98539658	HepG2	liver:	n/a	chr4:98539512-98539523
18	CEBPB	chr4:98577269-98577808	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:98577169-98577759	HCT-116	colon:	n/a	n/a
20	CEBPB	chr4:98420213-98420360	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:98650603-98650914	HepG2	liver:	n/a	chr4:98650742-98650753 chr4:98650740-98650751 chr4:98650742-98650751
22	CEBPB	chr4:98577090-98577696	HCT-116	colon:	n/a	n/a
23	CEBPB	chr4:98586371-98586560	HepG2	liver:	n/a	chr4:98586497-98586508
24	CEBPB	chr4:98417419-98418098	A549	lung:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
25	CEBPB	chr4:98550602-98550799	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:98417464-98417940	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
27	CEBPB	chr4:98503368-98503620	HepG2	liver:	n/a	chr4:98503500-98503511 chr4:98503499-98503512
28	CEBPB	chr4:98577066-98577631	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:98417396-98418127	HCT-116	colon:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
30	CEBPB	chr4:98419984-98420473	A549	lung:	n/a	n/a
31	CEBPB	chr4:98668425-98668529	A549	lung:	n/a	n/a
32	CEBPB	chr4:98550616-98550860	A549	lung:	n/a	n/a
33	CEBPB	chr4:98417488-98417912	ECC-1	luminal epithelium:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
34	CEBPB	chr4:98419795-98420651	HCT-116	colon:	n/a	n/a
35	CEBPB	chr4:98664241-98664530	HepG2	liver:	n/a	chr4:98664382-98664393
36	CEBPB	chr4:98467950-98468187	HepG2	liver:	n/a	chr4:98468073-98468084
37	CEBPB	chr4:98577187-98577805	A549	lung:	n/a	n/a
38	CEBPB	chr4:98766860-98767235	H1-hESC	embryonic stem cell:	n/a	chr4:98767092-98767109
39	CEBPB	chr4:98863376-98863833	HCT-116	colon:	n/a	n/a
40	CEBPB	chr4:98795872-98796026	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:98539500-98539574	H1-hESC	embryonic stem cell:	n/a	chr4:98539512-98539523
42	CEBPB	chr4:98778907-98779234	IMR90	lung:	n/a	chr4:98779056-98779067
43	CEBPB	chr4:98577590-98577861	MCF-7	breast:	n/a	n/a
44	CEBPB	chr4:98420044-98420447	MCF-7	breast:	n/a	n/a
45	CEBPB	chr4:98417537-98418092	Hela-S3	cervix:	n/a	chr4:98417706-98417717 chr4:98417704-98417717 chr4:98417704-98417717
46	CEBPB	chr4:98577086-98577649	A549	lung:	n/a	n/a
47	CEBPB	chr4:98778997-98779197	K562	blood:	n/a	chr4:98779056-98779067
48	CEBPB	chr4:98832733-98832877	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:98675730-98675981	HepG2	liver:	n/a	chr4:98675830-98675841
50	CEBPB	chr4:98511464-98511776	MCF-7	breast:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:98479820-98479870	HCF	heart:	n/a
2	chr4:98479820-98479870	HNPCEpiC	eye:	n/a
3	chr4:98479820-98479870	AG09319	gingival:	n/a
4	chr4:98690072-98690122	NHDF-neo	bronchial:	n/a
5	chr4:98479820-98479870	AoSMC	blood vessel:	n/a
6	chr4:98479820-98479870	GM12891	blood:	n/a
7	chr4:98690072-98690122	Hela-S3	cervix:	n/a
8	chr4:98479820-98479870	U87	brain:	n/a
9	chr4:98690072-98690122	ovcar-3	ovarian:	n/a
10	chr4:98479820-98479870	HL-60	blood:	n/a
11	chr4:98690072-98690122	HepG2	liver:	n/a
12	chr4:98690072-98690122	HRE	kidney:	n/a
13	chr4:98690072-98690122	HMEC	breast:	n/a
14	chr4:98479820-98479870	HMEC	breast:	n/a
15	chr4:98479820-98479870	RPTEC	kidney:	n/a
16	chr4:98479820-98479870	NHDF-neo	bronchial:	n/a
17	chr4:98690072-98690122	MCF10A-Er-Src	breast:	n/a
18	chr4:98479820-98479870	GM12892	blood:	n/a
19	chr4:98479820-98479870	Caco-2	colon:	n/a
20	chr4:98690072-98690122	SK-N-SH	brain:	n/a
21	chr4:98690072-98690122	PrEC	prostate:	n/a
22	chr4:98690072-98690122	BE2_C	brain:	n/a
23	chr4:98479820-98479870	HRE	kidney:	n/a
24	chr4:98479820-98479870	H1-hESC	embryonic stem cell:	embryo
25	chr4:98690072-98690122	T-47D	breast:	n/a
26	chr4:98690072-98690122	HL-60	blood:	n/a
27	chr4:98479820-98479870	PFSK-1	brain:	n/a
28	chr4:98479820-98479870	T-47D	breast:	n/a
29	chr4:98690072-98690122	SKMC	muscle:	n/a
30	chr4:98690072-98690122	GM12891	blood:	n/a
31	chr4:98479820-98479870	HEK293	kidney:	embryo
32	chr4:98690072-98690122	NH-A	brain:	n/a
33	chr4:98479820-98479870	ECC-1	luminal epithelium:	n/a
34	chr4:98690072-98690122	SK-N-SH_RA	brain:	n/a
35	chr4:98479820-98479870	PrEC	prostate:	n/a
36	chr4:98479820-98479870	CMK	blood:	n/a
37	chr4:98479820-98479870	GM06990	blood:	n/a
38	chr4:98479820-98479870	GM12878	blood:	n/a
39	chr4:98479820-98479870	HCM	heart:	n/a
40	chr4:98479820-98479870	BJ	skin:	n/a
41	chr4:98479820-98479870	Hepatocyte	liver:	n/a
42	chr4:98479820-98479870	Hela-S3	cervix:	n/a
43	chr4:98479820-98479870	GM19239	blood:	n/a
44	chr4:98690072-98690122	HCPEpiC	choroid plexus:	n/a
45	chr4:98479820-98479870	HIPEpiC	eye:	n/a
46	chr4:98479820-98479870	AG04450	lung:	fetal
47	chr4:98479820-98479870	PANC-1	pancreas:	n/a
48	chr4:98690072-98690122	GM06990	blood:	n/a
49	chr4:98690072-98690122	H1-hESC	embryonic stem cell:	embryo
50	chr4:98479820-98479870	HAEpiC	amniotic membrane:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
2	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
3	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
4	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:
5	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
6	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
7	chr4:98600978..98604672-chr4:98609268..98612042,3	MCF-7	breast:
8	chr4:97091475..97092009-chr4:98641981..98642501,2	MCF-7	breast:
9	chr4:98588787..98591250-chr4:98592135..98594195,2	MCF-7	breast:
10	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
11	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
12	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
13	chr4:98522959..98525428-chr4:98528956..98531903,2	K562	blood:
14	chr4:98401691..98403419-chr4:98441466..98443377,2	K562	blood:
15	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
16	chr4:98505232..98506917-chr4:98508304..98511467,3	MCF-7	breast:
17	chr4:98967509..98968412-chr4:99013843..99014513,4	MCF-7	breast:
18	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
19	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:
20	chr4:98417634..98419230-chr4:98419373..98421465,2	MCF-7	breast:
21	chr4:98687863..98690416-chr4:98692655..98695152,2	MCF-7	breast:
22	chr4:98790810..98793729-chr4:98795373..98798047,2	K562	blood:
23	chr4:98562115..98565020-chr4:98567699..98570313,2	MCF-7	breast:
24	chr4:97404242..97405044-chr4:98905771..98906367,3	MCF-7	breast:
25	chr4:98576156..98578566-chr4:98579040..98581603,2	MCF-7	breast:
26	chr4:98641928..98642827-chr4:98905748..98906362,2	MCF-7	breast:
27	chr4:98547951..98550382-chr4:98550750..98552792,2	MCF-7	breast:
28	chr4:98765331..98767165-chr4:99012892..99015543,2	K562	blood:
29	chr4:98896668..98898608-chr4:98901811..98903490,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSPAN5-3	chr4:98814203-98814354	NONHSAT097477
2	lnc-TSPAN5-3	chr4:98633850-98633965	NONHSAT097477

No data

Variant related genes	Relation type
STPG2	TF binding region
RPL5P12	TF binding region
CRYZP2	TF binding region
DUTP8	TF binding region
ENSG00000254044	TF binding region
STPG2	CpG island
RPL5P12	CpG island
CRYZP2	CpG island
DUTP8	CpG island
ENSG00000254044	CpG island

Extended variants
information (count: 7230 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:7230 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185241402	chr4:98416048-98416049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111866919	chr4:98416067-98416068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs28671600	chr4:98416109-98416110	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs570394736	chr4:98416158-98416159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188556642	chr4:98416215-98416216	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs35131479	chr4:98416216-98416217	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192351584	chr4:98416242-98416243	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539540376	chr4:98416290-98416291	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs112090370	chr4:98416310-98416311	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368751329	chr4:98416389-98416390	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569682918	chr4:98416400-98416401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs536917575	chr4:98416403-98416404	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs555613837	chr4:98416445-98416446	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10000637	chr4:98416446-98416447	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs143049610	chr4:98416473-98416474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536170156	chr4:98416493-98416494	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs184941832	chr4:98416571-98416572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs530195799	chr4:98416601-98416602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs548735409	chr4:98416632-98416633	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs188143011	chr4:98416634-98416635	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545109801	chr4:98416680-98416681	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs563309667	chr4:98416698-98416699	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs112755548	chr4:98416806-98416807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs542685752	chr4:98416853-98416854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537251618	chr4:98416861-98416862	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35288994	chr4:98416862-98416863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs561614867	chr4:98416876-98416877	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs397994636	chr4:98416877-98416878	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571117310	chr4:98416958-98416959	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs372061166	chr4:98417045-98417046	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs528827195	chr4:98417060-98417061	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547123378	chr4:98417079-98417080	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs375143720	chr4:98417132-98417133	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs369401732	chr4:98417192-98417193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs138657178	chr4:98417205-98417206	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs180938716	chr4:98417213-98417214	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs551522070	chr4:98417253-98417254	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs552580819	chr4:98417337-98417338	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs569794712	chr4:98417360-98417361	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs572354244	chr4:98417370-98417371	Enhancers Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs548744884	chr4:98417445-98417446	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs567548780	chr4:98417471-98417472	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs534617865	chr4:98417491-98417492	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs184499901	chr4:98417510-98417511	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs552710362	chr4:98417518-98417519	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs78717368	chr4:98417533-98417534	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs34830960	chr4:98417562-98417563	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs72887269	chr4:98417622-98417623	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs553927530	chr4:98417636-98417637	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs116701421	chr4:98417676-98417677	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	23813976	CNVD
Gastric cancer	16891809	CNVD

Chromatin state (count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:98414200-98416200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr4:98414200-98420600	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr4:98414600-98420400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr4:98415200-98419000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr4:98415400-98419400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr4:98415600-98417400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:98415600-98417400	Weak transcription	NH-A	brain
8	chr4:98415800-98417200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:98415800-98417200	Weak transcription	A549	lung
10	chr4:98415800-98417400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:98415800-98417600	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr4:98415800-98420400	Weak transcription	NHEK	skin
13	chr4:98416000-98417000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
14	chr4:98416000-98417200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr4:98416000-98417200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr4:98416000-98417400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr4:98416000-98417400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr4:98416000-98417400	Weak transcription	HMEC	breast
19	chr4:98416000-98417600	Weak transcription	H1 Cell Line	embryonic stem cell
20	chr4:98416000-98417600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr4:98416000-98417600	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:98416000-98417600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:98416000-98420400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr4:98416200-98417400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chr4:98417000-98418000	Enhancers	Cortex derived primary cultured neurospheres	brain
26	chr4:98417000-98420600	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:98417200-98417400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr4:98417200-98417800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:98417200-98418000	Active TSS	A549	lung
30	chr4:98417200-98419200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr4:98417400-98417600	Enhancers	Liver	Liver
32	chr4:98417400-98417800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:98417400-98417800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr4:98417400-98417800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:98417400-98418000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr4:98417400-98418000	Enhancers	HMEC	breast
37	chr4:98417400-98418200	Enhancers	NH-A	brain
38	chr4:98417400-98418400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:98417400-98420600	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr4:98417600-98417800	Enhancers	H9 Cell Line	embryonic stem cell
41	chr4:98417600-98418000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr4:98417600-98418000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr4:98417600-98418000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr4:98417600-98418000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:98417600-98418000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:98417600-98418000	Flanking Active TSS	Liver	Liver
47	chr4:98417600-98418200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:98417600-98418200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:98417800-98418800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:98417800-98419400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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