Variant report

Variant	esv3486585
Chromosome Location	chr4:166565013-166680227
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	chr4:166575722-166576063	HepG2	liver:	n/a	n/a
2	BCL11A	chr4:166589947-166590167	H1-hESC	embryonic stem cell:	n/a	chr4:166590134-166590143
3	BHLHE40	chr4:166673516-166673879	HepG2	liver:	n/a	n/a
4	BRCA1	chr4:166578253-166578381	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr4:166615715-166615918	HepG2	liver:	n/a	chr4:166615830-166615841
6	CEBPB	chr4:166630613-166631155	ECC-1	luminal epithelium:	n/a	chr4:166630912-166630923 chr4:166630912-166630925
7	CEBPB	chr4:166662058-166662414	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:166575776-166576093	HepG2	liver:	n/a	n/a
9	CEBPB	chr4:166664959-166665063	K562	blood:	n/a	chr4:166665034-166665045
10	CEBPB	chr4:166644938-166645043	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr4:166615688-166615921	A549	lung:	n/a	chr4:166615830-166615841
12	CEBPB	chr4:166665902-166666168	HepG2	liver:	n/a	chr4:166666057-166666068
13	CEBPB	chr4:166627604-166627964	HepG2	liver:	n/a	chr4:166627780-166627793 chr4:166627781-166627792
14	CEBPB	chr4:166630723-166631116	ECC-1	luminal epithelium:	n/a	chr4:166630912-166630923 chr4:166630912-166630925
15	CEBPB	chr4:166627679-166627907	H1-hESC	embryonic stem cell:	n/a	chr4:166627780-166627793 chr4:166627781-166627792
16	CEBPB	chr4:166627646-166627954	IMR90	lung:	n/a	chr4:166627780-166627793 chr4:166627781-166627792
17	CEBPB	chr4:166627646-166627907	K562	blood:	n/a	chr4:166627780-166627793 chr4:166627781-166627792
18	CEBPB	chr4:166644271-166644581	A549	lung:	n/a	chr4:166644449-166644460
19	CEBPB	chr4:166630897-166630957	K562	blood:	n/a	chr4:166630912-166630923 chr4:166630912-166630925
20	CEBPB	chr4:166583455-166583750	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:166644320-166644573	IMR90	lung:	n/a	chr4:166644449-166644460
22	CEBPB	chr4:166644297-166644592	HepG2	liver:	n/a	chr4:166644449-166644460
23	CEBPB	chr4:166644208-166644650	Hela-S3	cervix:	n/a	chr4:166644449-166644460
24	CEBPB	chr4:166627634-166627884	A549	lung:	n/a	chr4:166627780-166627793 chr4:166627781-166627792
25	CEBPB	chr4:166644450-166644569	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr4:166678669-166678970	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:166667771-166667827	Hela-S3	cervix:	n/a	chr4:166667783-166667800 chr4:166667784-166667795
28	CEBPB	chr4:166592039-166592049	HepG2	liver:	n/a	n/a
29	CEBPB	chr4:166623743-166623929	A549	lung:	n/a	n/a
30	CEBPB	chr4:166613417-166613543	HepG2	liver:	n/a	chr4:166613480-166613491
31	CEBPB	chr4:166644910-166645125	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chr4:166630771-166631085	HepG2	liver:	n/a	chr4:166630912-166630923 chr4:166630912-166630925
33	CEBPB	chr4:166630760-166631086	IMR90	lung:	n/a	chr4:166630912-166630923 chr4:166630912-166630925
34	CHD1	chr4:166678822-166678929	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:166622118-166622250	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:166622107-166622277	HepG2	liver:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
37	CTCF	chr4:166622120-166622270	GM12873	blood:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
38	CTCF	chr4:166622120-166622270	HEK293	kidney:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
39	CTCF	chr4:166622060-166622210	GM12870	blood:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
40	CTCF	chr4:166622080-166622230	AG04450	lung:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
41	CTCF	chr4:166622120-166622270	HVMF	connective:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
42	CTCF	chr4:166622120-166622270	RPTEC	kidney:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
43	CTCF	chr4:166622120-166622270	HCT-116	colon:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
44	CTCF	chr4:166622080-166622316	NHEK	skin:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
45	CTCF	chr4:166622180-166622330	HCT-116	colon:	n/a	chr4:166622181-166622194
46	CTCF	chr4:166622175-166622236	GM10266	blood:	n/a	chr4:166622179-166622197 chr4:166622181-166622194
47	CTCF	chr4:166580480-166580524	Fibrobl	skin:	n/a	n/a
48	CTCF	chr4:166622119-166622233	SK-N-SH_RA	brain:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
49	CTCF	chr4:166622092-166622274	LNCaP	prostate:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194
50	CTCF	chr4:166622080-166622230	HPF	lung:	n/a	chr4:166622174-166622195 chr4:166622179-166622197 chr4:166622181-166622194

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:166631112-166631162	NH-A	brain:	n/a
2	chr4:166678822-166678872	HRCEpiC	kidney:	n/a
3	chr4:166631112-166631162	GM12878	blood:	n/a
4	chr4:166678822-166678872	U87	brain:	n/a
5	chr4:166631112-166631162	Caco-2	colon:	n/a
6	chr4:166678822-166678872	SKMC	muscle:	n/a
7	chr4:166678822-166678872	HRPEpiC	eye:	n/a
8	chr4:166678822-166678872	Hela-S3	cervix:	n/a
9	chr4:166678822-166678872	AG09319	gingival:	n/a
10	chr4:166678822-166678872	HepG2	liver:	n/a
11	chr4:166678822-166678872	NT2-D1	testis:	n/a
12	chr4:166631112-166631162	NHBE	bronchial:	n/a
13	chr4:166631112-166631162	U87	brain:	n/a
14	chr4:166678822-166678872	HIPEpiC	eye:	n/a
15	chr4:166678822-166678872	Caco-2	colon:	n/a
16	chr4:166678822-166678872	SK-N-SH	brain:	n/a
17	chr4:166631112-166631162	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:166678822-166678872	MCF-7	breast:	n/a
19	chr4:166678822-166678872	SK-N-SH_RA	brain:	n/a
20	chr4:166678822-166678872	HAEpiC	amniotic membrane:	n/a
21	chr4:166678822-166678872	GM12892	blood:	n/a
22	chr4:166678822-166678872	LNCaP	prostate:	n/a
23	chr4:166631112-166631162	HCM	heart:	n/a
24	chr4:166631112-166631162	GM12891	blood:	n/a
25	chr4:166678822-166678872	Hepatocyte	liver:	n/a
26	chr4:166631112-166631162	ovcar-3	ovarian:	n/a
27	chr4:166678822-166678872	ProgFib	skin:	n/a
28	chr4:166678822-166678872	ECC-1	luminal epithelium:	n/a
29	chr4:166631112-166631162	A549	lung:	n/a
30	chr4:166678822-166678872	HL-60	blood:	n/a
31	chr4:166678822-166678872	HCPEpiC	choroid plexus:	n/a
32	chr4:166631112-166631162	HAEpiC	amniotic membrane:	n/a
33	chr4:166678822-166678872	GM12891	blood:	n/a
34	chr4:166678822-166678872	HCT-116	colon:	n/a
35	chr4:166631112-166631162	MCF10A-Er-Src	breast:	n/a
36	chr4:166631112-166631162	ProgFib	skin:	n/a
37	chr4:166678822-166678872	PANC-1	pancreas:	n/a
38	chr4:166678822-166678872	HMEC	breast:	n/a
39	chr4:166678822-166678872	HCM	heart:	n/a
40	chr4:166631112-166631162	H1-hESC	embryonic stem cell:	embryo
41	chr4:166678822-166678872	SAEC	small airway:	n/a
42	chr4:166678822-166678872	NHBE	bronchial:	n/a
43	chr4:166631112-166631162	HMEC	breast:	n/a
44	chr4:166631112-166631162	HepG2	liver:	n/a
45	chr4:166631112-166631162	K562	blood:	n/a
46	chr4:166678822-166678872	NHDF-neo	bronchial:	n/a
47	chr4:166631112-166631162	AoSMC	blood vessel:	n/a
48	chr4:166631112-166631162	HCT-116	colon:	n/a
49	chr4:166631112-166631162	NHDF-neo	bronchial:	n/a
50	chr4:166631112-166631162	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:166621893..166624500-chr4:166635086..166637348,2	K562	blood:
2	chr4:166634808..166637865-chr4:166643527..166646451,3	K562	blood:
3	chr4:166644382..166646352-chr4:166648144..166651480,3	K562	blood:
4	chr4:166635415..166637271-chr4:166637684..166639309,2	K562	blood:
5	chr4:166635414..166637271-chr4:166637362..166639309,3	K562	blood:
6	chr19:13262110..13263957-chr4:166671160..166673024,2	MCF-7	breast:
7	chr4:166635415..166637271-chr4:166637684..166639309,2	K562	blood:
8	chr4:166457869..166458829-chr4:166621749..166622649,2	MCF-7	breast:
9	chr11:1792562..1794476-chr4:166674340..166677025,2	MCF-7	breast:
10	chr4:166621893..166624500-chr4:166635086..166637348,2	K562	blood:
11	chr4:166669810..166671344-chr4:166671766..166673848,2	K562	blood:
12	chr4:166638909..166642014-chr4:166642942..166645668,3	K562	blood:
13	chr4:166669810..166671344-chr4:166671766..166673848,2	K562	blood:
14	chr4:166551503..166553353-chr4:166596803..166598460,2	MCF-7	breast:
15	chr4:166634808..166637865-chr4:166643527..166646451,3	K562	blood:
16	chr4:166643419..166645366-chr4:166645827..166649777,4	MCF-7	breast:
17	chr4:166658631..166660297-chr4:166687744..166690707,2	K562	blood:
18	chr4:166638909..166642014-chr4:166642942..166645668,3	K562	blood:
19	chr4:166644382..166646352-chr4:166648144..166651480,3	K562	blood:
20	chr4:166643419..166645366-chr4:166645827..166649777,4	MCF-7	breast:
21	chr4:166030684..166033525-chr4:166643977..166646390,2	K562	blood:
22	chr4:166635414..166637271-chr4:166637362..166639309,3	K562	blood:
23	chr4:166552860..166555630-chr4:166591074..166593334,2	MCF-7	breast:
24	chr4:166678013..166679693-chr4:166681397..166683849,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TLL1-1	chr4:166613328-166613497	XLOC_003770
2	lnc-TMEM192-1	chr4:166655825-166656055	ENSG00000248358
3	lnc-TMEM192-1	chr4:166664171-166664223	ENSG00000248358
4	lnc-TMEM192-1	chr4:166651932-166652836	ENSG00000248358
5	lnc-TLL1-1	chr4:166654247-166654332	XLOC_003770
6	lnc-TLL1-1	chr4:166605791-166605905	XLOC_003770
7	lnc-TLL1-1	chr4:166606936-166607018	XLOC_003770
8	lnc-TMEM192-1	chr4:166659483-166659847	ENSG00000248358
9	lnc-TLL1-1	chr4:166675953-166676138	XLOC_003770

Variant related genes	Relation type
ENSG00000250725	TF binding region
ENSG00000249500	TF binding region
ENSG00000250725	CpG island
ENSG00000249500	CpG island
ENSG00000160888	chromatin interactions
BDH2	miRNA target sites
TESK2	miRNA target sites
CEP97	miRNA target sites
GPD1L	miRNA target sites

Extended variants
information (count: 4056 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:4056 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540294583	chr4:166565026-166565027	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs562097012	chr4:166565111-166565112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs529598437	chr4:166565122-166565123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs180719572	chr4:166565177-166565178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563076824	chr4:166565180-166565181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs533524557	chr4:166565210-166565211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185976648	chr4:166565222-166565223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370595872	chr4:166565223-166565224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6536926	chr4:166565277-166565278	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs564471113	chr4:166565280-166565281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs530434897	chr4:166565290-166565291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs544150356	chr4:166565292-166565293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs564050364	chr4:166565299-166565300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546315525	chr4:166565308-166565309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs367873592	chr4:166565311-166565312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs7675632	chr4:166565361-166565362	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs535408910	chr4:166565366-166565367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs556792845	chr4:166565406-166565407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs4511957	chr4:166565409-166565410	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs201706109	chr4:166565472-166565473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79242517	chr4:166565473-166565474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs557909994	chr4:166565480-166565481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs531290935	chr4:166565486-166565487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573288358	chr4:166565527-166565528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs540711600	chr4:166565598-166565599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547990239	chr4:166565605-166565606	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs17588412	chr4:166565626-166565627	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs368558412	chr4:166565639-166565640	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534025456	chr4:166565644-166565645	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573931478	chr4:166565645-166565646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs138009682	chr4:166565661-166565662	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs555381156	chr4:166565666-166565667	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs563142244	chr4:166565667-166565668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs562074297	chr4:166565699-166565700	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116477142	chr4:166565758-166565759	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191179801	chr4:166565800-166565801	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs149539314	chr4:166565804-166565805	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs75976015	chr4:166565830-166565831	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs528216625	chr4:166565834-166565835	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs2714828	chr4:166565849-166565850	Weak transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs182468781	chr4:166565859-166565860	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs528821692	chr4:166565884-166565885	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs550479524	chr4:166565885-166565886	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs147216703	chr4:166565901-166565902	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs539329962	chr4:166565919-166565920	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs138683824	chr4:166565923-166565924	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs566654222	chr4:166565942-166565943	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372703417	chr4:166565997-166565998	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs534038222	chr4:166565998-166565999	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs187101446	chr4:166566018-166566019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	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
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Glioblastoma multiforme	22286061	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16750200	CNVD
Colorectal cancer	16774939	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Myelofibrosis	22110671	CNVD
intellectual deficit	22127048	CNVD
abnormal development	18461090	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:405 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:166556600-166569200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:166565600-166565800	Enhancers	Spleen	Spleen
3	chr4:166565800-166566000	ZNF genes & repeats	Spleen	Spleen
4	chr4:166569200-166570000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr4:166569400-166569600	ZNF genes & repeats	Muscle Satellite Cultured Cells	--
6	chr4:166569600-166570200	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr4:166570000-166584200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr4:166570200-166571000	Enhancers	HUVEC	blood vessel
9	chr4:166570200-166572200	Enhancers	Muscle Satellite Cultured Cells	--
10	chr4:166574200-166578600	Enhancers	HepG2	liver
11	chr4:166575400-166576400	Enhancers	Liver	Liver
12	chr4:166575800-166576000	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr4:166575800-166579000	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr4:166576000-166576600	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr4:166576200-166578800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:166576400-166578000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:166576400-166578000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:166576600-166579200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr4:166576800-166578600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr4:166576800-166578800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr4:166576800-166579000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr4:166577400-166578400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:166577400-166579000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:166577400-166579600	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr4:166577600-166578200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr4:166577600-166578200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:166577600-166578200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:166577600-166578800	Enhancers	HUVEC	blood vessel
29	chr4:166578000-166578400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr4:166578000-166578600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:166578000-166578600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr4:166578000-166578800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr4:166578000-166578800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
34	chr4:166578000-166579000	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
35	chr4:166578200-166581800	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:166578400-166583600	Weak transcription	Muscle Satellite Cultured Cells	--
37	chr4:166578600-166583600	Weak transcription	HepG2	liver
38	chr4:166578800-166579000	Active TSS	iPS-20b Cell Line	embryonic stem cell
39	chr4:166579000-166583800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
40	chr4:166579600-166583800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr4:166581800-166582000	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:166582000-166582200	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr4:166583200-166583600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
44	chr4:166583400-166585400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr4:166583600-166584000	Enhancers	HepG2	liver
46	chr4:166583600-166584200	Enhancers	Liver	Liver
47	chr4:166583600-166584600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr4:166583600-166585200	Enhancers	Muscle Satellite Cultured Cells	--
49	chr4:166583800-166584000	Enhancers	iPS-20b Cell Line	embryonic stem cell
50	chr4:166583800-166584600	Enhancers	Primary hematopoietic stem cells short term culture	blood

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