Variant report

Variant	nsv437935
Chromosome Location	chr4:128689936-128703950
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:799)
CpG islands
(count:490)
Chromatin interactive
region (count:27)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:799 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128703288-128703855	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:128697170-128697199	K562	blood:	n/a	n/a
3	ARID3A	chr4:128699250-128699431	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:128692810-128693068	K562	blood:	n/a	n/a
5	ATF1	chr4:128692637-128692941	K562	blood:	n/a	n/a
6	ATF2	chr4:128703349-128703797	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:128703535-128703945	GM12878	blood:	n/a	n/a
8	ATF2	chr4:128703223-128704431	GM12878	blood:	n/a	n/a
9	BACH1	chr4:128703574-128704164	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL11A	chr4:128703506-128704165	GM12878	blood:	n/a	chr4:128703900-128703909
11	BCL3	chr4:128703426-128703891	A549	lung:	n/a	chr4:128703493-128703506
12	BCLAF1	chr4:128703045-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
13	BCLAF1	chr4:128703164-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
14	BHLHE40	chr4:128702794-128704390	GM12878	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
15	BHLHE40	chr4:128703316-128704638	HepG2	liver:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
16	BHLHE40	chr4:128702911-128704629	K562	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
17	BHLHE40	chr4:128697106-128697324	GM12878	blood:	n/a	n/a
18	BRCA1	chr4:128703576-128704518	HepG2	liver:	n/a	n/a
19	BRCA1	chr4:128703327-128704113	H1-hESC	embryonic stem cell:	n/a	n/a
20	BRCA1	chr4:128703299-128705533	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr4:128703553-128704042	GM12878	blood:	n/a	n/a
22	CBX3	chr4:128702501-128704742	K562	blood:	n/a	n/a
23	CCNT2	chr4:128702731-128704211	K562	blood:	n/a	n/a
24	CEBPB	chr4:128702785-128704856	Hela-S3	cervix:	n/a	chr4:128704156-128704169
25	CEBPB	chr4:128703570-128704298	K562	blood:	n/a	chr4:128704156-128704169
26	CEBPB	chr4:128703489-128704096	GM12878	blood:	n/a	n/a
27	CEBPB	chr4:128700279-128700509	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr4:128703513-128703956	MCF-7	breast:	n/a	n/a
29	CEBPB	chr4:128700370-128700522	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:128700285-128700577	K562	blood:	n/a	n/a
31	CEBPB	chr4:128703545-128704334	IMR90	lung:	n/a	chr4:128704156-128704169
32	CEBPB	chr4:128703524-128704686	HepG2	liver:	n/a	chr4:128704156-128704169
33	CEBPB	chr4:128700302-128700540	K562	blood:	n/a	n/a
34	CEBPD	chr4:128703408-128703770	HepG2	liver:	n/a	n/a
35	CHD1	chr4:128703042-128703094	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD1	chr4:128699779-128699906	GM12878	blood:	n/a	n/a
37	CHD1	chr4:128702807-128704507	GM12878	blood:	n/a	chr4:128703241-128703251
38	CHD2	chr4:128703263-128704476	HepG2	liver:	n/a	n/a
39	CHD2	chr4:128703307-128704563	K562	blood:	n/a	n/a
40	CHD2	chr4:128702732-128704749	Hela-S3	cervix:	n/a	chr4:128703241-128703251
41	CHD2	chr4:128702545-128704661	H1-hESC	embryonic stem cell:	n/a	chr4:128703241-128703251
42	CHD2	chr4:128702882-128704300	GM12878	blood:	n/a	chr4:128703241-128703251
43	CREB1	chr4:128703155-128704770	HepG2	liver:	n/a	n/a
44	CREB1	chr4:128703386-128703848	A549	lung:	n/a	n/a
45	CREB1	chr4:128702790-128703326	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTBP2	chr4:128702959-128704525	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr4:128703927-128703997	Hela-S3	cervix:	n/a	chr4:128703969-128703982
48	CTCF	chr4:128703880-128704030	MCF-7	breast:	n/a	chr4:128703969-128703982
49	CTCF	chr4:128703219-128704277	GM12878	blood:	n/a	chr4:128703969-128703982
50	CTCF	chr4:128703420-128703570	HEK293	kidney:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128703335-128703385	HIPEpiC	eye:	n/a
2	chr4:128703335-128703385	Jurkat	blood:	n/a
3	chr4:128703335-128703385	HIPEpiC	eye:	n/a
4	chr4:128703335-128703385	Jurkat	blood:	n/a
5	chr4:128703702-128703752	HAEpiC	amniotic membrane:	n/a
6	chr4:128703088-128703138	NH-A	brain:	n/a
7	chr4:128694731-128694781	Hepatocyte	liver:	n/a
8	chr4:128703088-128703138	SK-N-MC	brain:	n/a
9	chr4:128703702-128703752	ProgFib	skin:	n/a
10	chr4:128694731-128694781	PrEC	prostate:	n/a
11	chr4:128703335-128703385	Hepatocyte	liver:	n/a
12	chr4:128699484-128699534	ECC-1	luminal epithelium:	n/a
13	chr4:128703599-128703649	K562	blood:	n/a
14	chr4:128703702-128703752	PrEC	prostate:	n/a
15	chr4:128703180-128703230	SKMC	muscle:	n/a
16	chr4:128703599-128703649	NH-A	brain:	n/a
17	chr4:128702014-128702064	AG09309	skin:	n/a
18	chr4:128699484-128699534	GM12892	blood:	n/a
19	chr4:128703088-128703138	HNPCEpiC	eye:	n/a
20	chr4:128699484-128699534	K562	blood:	n/a
21	chr4:128703599-128703649	AG04449	skin:	fetal
22	chr4:128694731-128694781	T-47D	breast:	n/a
23	chr4:128703180-128703230	GM12891	blood:	n/a
24	chr4:128699484-128699534	H1-hESC	embryonic stem cell:	embryo
25	chr4:128703088-128703138	AG04449	skin:	fetal
26	chr4:128703335-128703385	H1-hESC	embryonic stem cell:	embryo
27	chr4:128702014-128702064	SAEC	small airway:	n/a
28	chr4:128703335-128703385	ovcar-3	ovarian:	n/a
29	chr4:128702014-128702064	NB4	blood:	n/a
30	chr4:128703599-128703649	HAEpiC	amniotic membrane:	n/a
31	chr4:128703599-128703649	SK-N-SH	brain:	n/a
32	chr4:128694731-128694781	HEEpiC	esophagus:	n/a
33	chr4:128694731-128694781	MCF10A-Er-Src	breast:	n/a
34	chr4:128703088-128703138	BJ	skin:	n/a
35	chr4:128699484-128699534	PANC-1	pancreas:	n/a
36	chr4:128703599-128703649	U87	brain:	n/a
37	chr4:128699484-128699534	SAEC	small airway:	n/a
38	chr4:128703599-128703649	GM12878	blood:	n/a
39	chr4:128702014-128702064	LNCaP	prostate:	n/a
40	chr4:128703088-128703138	AG09309	skin:	n/a
41	chr4:128703180-128703230	U87	brain:	n/a
42	chr4:128703180-128703230	A549	lung:	n/a
43	chr4:128702014-128702064	GM06990	blood:	n/a
44	chr4:128703088-128703138	IMR90	lung:	fetal
45	chr4:128703088-128703138	ECC-1	luminal epithelium:	n/a
46	chr4:128694731-128694781	BE2_C	brain:	n/a
47	chr4:128703702-128703752	AG10803	skin:	n/a
48	chr4:128699484-128699534	SK-N-MC	brain:	n/a
49	chr4:128703088-128703138	T-47D	breast:	n/a
50	chr4:128699484-128699534	HIPEpiC	eye:	n/a

(count:27 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:128702265..128705282-chr4:128884841..128889213,7	K562	blood:
2	chr4:128697244..128699961-chr4:128704246..128706827,2	MCF-7	breast:
3	chr4:128691903..128693530-chr4:128709934..128712766,2	K562	blood:
4	chr4:128701911..128705042-chr4:128800160..128804699,6	K562	blood:
5	chr4:128699357..128701844-chr4:128885755..128888672,2	K562	blood:
6	chr4:128701934..128705815-chr4:128979420..128984468,5	K562	blood:
7	chr4:128696482..128698537-chr4:128884403..128886306,2	K562	blood:
8	chr11:76155451..76155958-chr4:128703322..128703844,2	Hela-S3	cervix:
9	chr4:128701934..128705815-chr4:128979420..128985014,7	K562	blood:
10	chr19:41222374..41223187-chr4:128703821..128704556,2	Hela-S3	cervix:
11	chr11:47206754..47207663-chr4:128703485..128704269,2	Hela-S3	cervix:
12	chr4:128702203..128705505-chr4:128800773..128804170,4	MCF-7	breast:
13	chr4:128684329..128686101-chr4:128689330..128691100,2	MCF-7	breast:
14	chr4:128701212..128704782-chr4:128885853..128888301,4	MCF-7	breast:
15	chr4:128697060..128698600-chr4:128725159..128726803,2	K562	blood:
16	chr20:33865366..33866126-chr4:128702884..128703646,2	Hela-S3	cervix:
17	chr4:128689601..128691361-chr4:128702000..128704848,2	K562	blood:
18	chr4:128703531..128705249-chr4:130014655..130017577,2	K562	blood:
19	chr3:156871327..156871960-chr4:128702865..128703820,2	Hela-S3	cervix:
20	chr4:128701663..128704492-chr4:128800560..128804784,7	MCF-7	breast:
21	chr4:128695077..128697905-chr4:128698575..128703396,7	K562	blood:
22	chr4:128702304..128707255-chr4:128884841..128889595,9	K562	blood:
23	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
24	chr4:128702580..128705894-chr4:128810025..128813296,3	K562	blood:
25	chr4:128702147..128704685-chr4:128980177..128982661,2	MCF-7	breast:
26	chr4:128695663..128697275-chr4:128706487..128708747,2	K562	blood:
27	chr12:120729413..120730207-chr4:128703177..128703844,2	Hela-S3	cervix:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	SLC25A31	hsa-miR-335-5p	chr4:128695378-128695400

Variant related genes	Relation type
HSPA4L	TF binding region
HSPA4L	CpG island
ENSG00000251821	chromatin interactions
ENSG00000165912	chromatin interactions
ENSG00000126005	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000151466	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000088298	chromatin interactions
ENSG00000164073	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000201778	chromatin interactions
ENSG00000164074	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000151470	chromatin interactions
ENSG00000142731	chromatin interactions
ENSG00000164070	chromatin interactions

Extended variants
information (count: 374 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:374 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2305958	chr4:128689936-128689937	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs34538293	chr4:128689953-128689954	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557204804	chr4:128689994-128689995	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs377425288	chr4:128690005-128690006	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs150542608	chr4:128690006-128690007	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs372171427	chr4:128690007-128690008	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs200720529	chr4:128690019-128690020	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs542822232	chr4:128690033-128690034	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs140557219	chr4:128690046-128690047	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs573155910	chr4:128690082-128690083	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs185390518	chr4:128690090-128690091	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs564530720	chr4:128690094-128690095	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs55685174	chr4:128690099-128690100	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs547593144	chr4:128690107-128690108	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs550629383	chr4:128690111-128690112	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs76227179	chr4:128690169-128690170	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs529810943	chr4:128690179-128690180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs145684397	chr4:128690218-128690219	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs566674400	chr4:128690291-128690292	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs527539556	chr4:128690320-128690321	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs138339483	chr4:128690326-128690327	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs187807162	chr4:128690391-128690392	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs569628466	chr4:128690431-128690432	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs538694976	chr4:128690445-128690446	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs557341714	chr4:128690470-128690471	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs75981796	chr4:128690514-128690515	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs368620204	chr4:128690570-128690571	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs57786091	chr4:128690599-128690600	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs191160478	chr4:128690637-128690638	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs142918275	chr4:128690689-128690690	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs375568085	chr4:128690781-128690782	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs540522088	chr4:128690782-128690783	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs183546104	chr4:128690810-128690811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs368919281	chr4:128690848-128690849	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs80076337	chr4:128690889-128690890	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs543825806	chr4:128690901-128690902	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs77755630	chr4:128690924-128690925	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs529707442	chr4:128690991-128690992	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs538753209	chr4:128690995-128690996	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371830853	chr4:128691050-128691051	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541916867	chr4:128691098-128691099	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560376588	chr4:128691119-128691120	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs527513708	chr4:128691151-128691152	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs375121363	chr4:128691185-128691186	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117415525	chr4:128691239-128691240	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs71612137	chr4:128691315-128691316	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs565758642	chr4:128691316-128691317	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs10026828	chr4:128691333-128691334	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs188283042	chr4:128691344-128691345	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs571980392	chr4:128691350-128691351	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

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
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
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	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
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD

Chromatin state (count:332 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128692600-128693200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:128692600-128693400	Enhancers	NHEK	skin
3	chr4:128692800-128693600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:128693000-128693400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr4:128693000-128693400	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr4:128693000-128693600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr4:128693600-128694600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:128693600-128702200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:128694600-128694800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr4:128694800-128695200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:128695200-128697200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:128695800-128696000	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chr4:128696200-128697400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:128696800-128699400	Enhancers	GM12878-XiMat	blood
15	chr4:128697200-128697400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr4:128697200-128697400	Enhancers	K562	blood
17	chr4:128697200-128698600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr4:128697400-128698000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr4:128697600-128698000	Enhancers	HMEC	breast
20	chr4:128697600-128698800	Weak transcription	K562	blood
21	chr4:128697600-128699400	Enhancers	HepG2	liver
22	chr4:128697600-128701800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr4:128697800-128698000	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:128698000-128698800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr4:128698000-128702400	Weak transcription	HMEC	breast
26	chr4:128698200-128699000	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr4:128698600-128699000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:128698600-128699800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:128698600-128700000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:128698800-128699000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr4:128698800-128699000	Enhancers	Gastric	stomach
32	chr4:128698800-128699800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:128698800-128699800	Enhancers	K562	blood
34	chr4:128699000-128699800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:128699000-128702800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr4:128699000-128702800	Weak transcription	Gastric	stomach
37	chr4:128699400-128699600	Flanking Active TSS	GM12878-XiMat	blood
38	chr4:128699400-128699800	Flanking Active TSS	HepG2	liver
39	chr4:128699600-128699800	Enhancers	GM12878-XiMat	blood
40	chr4:128699800-128700000	Flanking Active TSS	GM12878-XiMat	blood
41	chr4:128699800-128700000	Enhancers	HepG2	liver
42	chr4:128699800-128701000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr4:128699800-128702600	Weak transcription	K562	blood
44	chr4:128699800-128703000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr4:128700000-128700200	Enhancers	GM12878-XiMat	blood
46	chr4:128700000-128700600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood
47	chr4:128700000-128702800	Weak transcription	HepG2	liver
48	chr4:128700200-128700600	Weak transcription	GM12878-XiMat	blood
49	chr4:128700600-128700800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr4:128700600-128701000	Flanking Bivalent TSS/Enh	Monocytes-CD14+_RO01746	blood

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