Variant report

Variant	esv2760876
Chromosome Location	chr4:165861386-165893486
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:552)
CpG islands
(count:795)
Chromatin interactive
region (count:12)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:165877669-165878118	GM12878	blood:	n/a	n/a
2	BCLAF1	chr4:165877809-165878342	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:165877987-165878027	K562	blood:	n/a	n/a
4	BHLHE40	chr4:165877853-165878275	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:165880700-165880797	HepG2	liver:	n/a	n/a
6	CBX3	chr4:165877855-165878292	K562	blood:	n/a	n/a
7	CEBPB	chr4:165893196-165893391	K562	blood:	n/a	n/a
8	CHD2	chr4:165877922-165878553	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr4:165877860-165878562	GM12878	blood:	n/a	n/a
10	CHD2	chr4:165867270-165867286	GM12878	blood:	n/a	n/a
11	CREB1	chr4:165877796-165878486	GM12878	blood:	n/a	n/a
12	CREB1	chr4:165877817-165878316	A549	lung:	n/a	n/a
13	CREB1	chr4:165877895-165878381	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTBP2	chr4:165877837-165878615	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr4:165870929-165871212	NHEK	skin:	n/a	n/a
16	CTCF	chr4:165878220-165878370	GM12865	blood:	n/a	n/a
17	CTCF	chr4:165870690-165870896	MCF-7	breast:	n/a	n/a
18	CTCF	chr4:165870700-165870850	GM12870	blood:	n/a	n/a
19	CTCF	chr4:165870709-165870882	K562	blood:	n/a	n/a
20	CTCF	chr4:165878400-165878550	GM12872	blood:	n/a	n/a
21	CTCF	chr4:165871000-165871150	HMEC	breast:	n/a	n/a
22	CTCF	chr4:165871056-165871137	MCF-7	breast:	n/a	n/a
23	CTCF	chr4:165893220-165893370	HCPEpiC	choroid plexus:	n/a	n/a
24	CTCF	chr4:165870700-165870850	GM06990	blood:	n/a	n/a
25	CTCF	chr4:165870714-165870869	MCF-7	breast:	n/a	n/a
26	CTCF	chr4:165864460-165864610	NHEK	skin:	n/a	n/a
27	CTCF	chr4:165870958-165870961	GM19239	blood:	n/a	n/a
28	CTCF	chr4:165870880-165871030	NHDF-neo	bronchial:	n/a	n/a
29	CTCF	chr4:165870693-165870910	GM19240	blood:	n/a	n/a
30	CTCF	chr4:165870700-165870850	HPF	lung:	n/a	n/a
31	CTCF	chr4:165870725-165870881	HepG2	liver:	n/a	n/a
32	CTCF	chr4:165878328-165878462	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:165870680-165870830	GM12874	blood:	n/a	n/a
34	CTCF	chr4:165870720-165870870	GM12872	blood:	n/a	n/a
35	CTCF	chr4:165870750-165870814	LNCaP	prostate:	n/a	n/a
36	CTCF	chr4:165870800-165870950	A549	lung:	n/a	n/a
37	CTCF	chr4:165870680-165870830	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:165893196-165893392	LNCaP	prostate:	n/a	n/a
39	CTCF	chr4:165878329-165878443	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:165893232-165893333	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:165870640-165870790	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr4:165870670-165870920	GM12878	blood:	n/a	n/a
43	CTCF	chr4:165870700-165870850	HPAF	blood vessel:	n/a	n/a
44	CTCF	chr4:165870640-165870790	RPTEC	kidney:	n/a	n/a
45	CTCF	chr4:165878060-165878210	AG09319	gingival:	n/a	n/a
46	CTCF	chr4:165893200-165893350	HCT-116	colon:	n/a	n/a
47	CTCF	chr4:165870700-165870850	GM12871	blood:	n/a	n/a
48	CTCF	chr4:165870633-165871252	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr4:165870760-165870910	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr4:165870680-165870830	GM12864	blood:	n/a	n/a

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:165881424-165881474	GM12891	blood:	n/a
2	chr4:165877045-165877095	GM12892	blood:	n/a
3	chr4:165881424-165881474	GM12891	blood:	n/a
4	chr4:165877045-165877095	GM12892	blood:	n/a
5	chr4:165878136-165878186	K562	blood:	n/a
6	chr4:165875543-165875593	PFSK-1	brain:	n/a
7	chr4:165875543-165875593	PrEC	prostate:	n/a
8	chr4:165877875-165877925	Jurkat	blood:	n/a
9	chr4:165877875-165877925	HCF	heart:	n/a
10	chr4:165877875-165877925	BJ	skin:	n/a
11	chr4:165877875-165877925	LNCaP	prostate:	n/a
12	chr4:165878317-165878367	NHDF-neo	bronchial:	n/a
13	chr4:165881424-165881474	HEK293	kidney:	embryo
14	chr4:165876955-165877005	SKMC	muscle:	n/a
15	chr4:165877875-165877925	SK-N-MC	brain:	n/a
16	chr4:165878085-165878135	GM19239	blood:	n/a
17	chr4:165878136-165878186	HIPEpiC	eye:	n/a
18	chr4:165881424-165881474	NHBE	bronchial:	n/a
19	chr4:165878317-165878367	ECC-1	luminal epithelium:	n/a
20	chr4:165878091-165878141	IMR90	lung:	fetal
21	chr4:165875543-165875593	NHBE	bronchial:	n/a
22	chr4:165878317-165878367	IMR90	lung:	fetal
23	chr4:165878742-165878792	HepG2	liver:	n/a
24	chr4:165881424-165881474	AG09319	gingival:	n/a
25	chr4:165878136-165878186	SK-N-SH_RA	brain:	n/a
26	chr4:165878085-165878135	NHBE	bronchial:	n/a
27	chr4:165878055-165878105	AG04449	skin:	fetal
28	chr4:165878037-165878087	AG09319	gingival:	n/a
29	chr4:165877045-165877095	ovcar-3	ovarian:	n/a
30	chr4:165878037-165878087	NHBE	bronchial:	n/a
31	chr4:165878219-165878269	BJ	skin:	n/a
32	chr4:165878037-165878087	BJ	skin:	n/a
33	chr4:165881424-165881474	BE2_C	brain:	n/a
34	chr4:165878317-165878367	ProgFib	skin:	n/a
35	chr4:165876955-165877005	HPAEpiC	pulmonary alveolar:	n/a
36	chr4:165876955-165877005	NHBE	bronchial:	n/a
37	chr4:165878219-165878269	PANC-1	pancreas:	n/a
38	chr4:165878317-165878367	HEK293	kidney:	embryo
39	chr4:165878317-165878367	SAEC	small airway:	n/a
40	chr4:165878742-165878792	HNPCEpiC	eye:	n/a
41	chr4:165875543-165875593	HEK293	kidney:	embryo
42	chr4:165878091-165878141	GM06990	blood:	n/a
43	chr4:165875543-165875593	HRE	kidney:	n/a
44	chr4:165881424-165881474	GM19239	blood:	n/a
45	chr4:165878219-165878269	HepG2	liver:	n/a
46	chr4:165878085-165878135	A549	lung:	n/a
47	chr4:165878037-165878087	HEEpiC	esophagus:	n/a
48	chr4:165877045-165877095	PANC-1	pancreas:	n/a
49	chr4:165878317-165878367	GM12878	blood:	n/a
50	chr4:165876955-165877005	HepG2	liver:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
2	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
3	chr1:11966992..11968590-chr4:165867023..165868624,2	K562	blood:
4	chr4:165866322..165867965-chr4:165877072..165879577,2	MCF-7	breast:
5	chr4:165877284..165881205-chr4:165885674..165889440,5	MCF-7	breast:
6	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
7	chr4:165877542..165879531-chr4:165880684..165882237,2	MCF-7	breast:
8	chr4:165874581..165877460-chr4:165878651..165880772,2	K562	blood:
9	chr4:165876074..165878048-chr4:165892405..165894471,2	MCF-7	breast:
10	chr4:165868972..165872041-chr4:165876298..165879460,3	MCF-7	breast:
11	chr4:165868495..165870203-chr4:165872665..165874987,2	MCF-7	breast:
12	chr4:165876835..165879626-chr4:165882281..165885476,4	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C4orf39-3	chr4:165883229-165883240	NONHSAT099093
2	lnc-TMEM192-4	chr4:165889739-165891154	NONHSAT099094
3	lnc-C4orf39-3	chr4:165882287-165882345	NONHSAT099093
4	lnc-C4orf39-3	chr4:165869231-165869699	NONHSAT099093

No data

Variant related genes	Relation type
ENSG00000236941	TF binding region
NACA3P	TF binding region
ENSG00000248632	TF binding region
FAM218A	TF binding region
ENSG00000248645	TF binding region
ENSG00000236941	CpG island
NACA3P	CpG island
ENSG00000248632	CpG island
FAM218A	CpG island
ENSG00000248645	CpG island
ENSG00000236941	chromatin interactions
ENSG00000199347	chromatin interactions
ENSG00000250486	chromatin interactions

Extended variants
information (count: 1225 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1225 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569881616	chr4:165861386-165861387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs71641128	chr4:165861388-165861389	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs71641127	chr4:165861397-165861398	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550791213	chr4:165861422-165861423	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs569172088	chr4:165861424-165861425	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs117428490	chr4:165861425-165861426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185062274	chr4:165861437-165861438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs140672728	chr4:165861451-165861452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs149713303	chr4:165861452-165861453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558005602	chr4:165861496-165861497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs114303274	chr4:165861498-165861499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs533918115	chr4:165861559-165861560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs555469420	chr4:165861613-165861614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573795733	chr4:165861620-165861621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs4443238	chr4:165861678-165861679	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs377320524	chr4:165861684-165861685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs371196021	chr4:165861702-165861703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs370909633	chr4:165861711-165861712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs578090283	chr4:165861740-165861741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs190305849	chr4:165861757-165861758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182193899	chr4:165861794-165861795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs144773489	chr4:165861802-165861803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527561124	chr4:165861843-165861844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs540211682	chr4:165861879-165861880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186719996	chr4:165861923-165861924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs528987522	chr4:165861975-165861976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs73000592	chr4:165861986-165861987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs375456140	chr4:165862041-165862042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs34508937	chr4:165862077-165862078	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs533116218	chr4:165862099-165862100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570478553	chr4:165862149-165862150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs376204026	chr4:165862173-165862174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551421051	chr4:165862250-165862251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs138764859	chr4:165862251-165862252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533980985	chr4:165862308-165862309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181213312	chr4:165862377-165862378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567283544	chr4:165862378-165862379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537954989	chr4:165862383-165862384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556590782	chr4:165862408-165862409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs367753012	chr4:165862425-165862426	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs539204633	chr4:165862447-165862448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs554193888	chr4:165862454-165862455	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572772843	chr4:165862463-165862464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs570166875	chr4:165862470-165862471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140367773	chr4:165862524-165862525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs561674958	chr4:165862540-165862541	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573631787	chr4:165862542-165862543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543988685	chr4:165862577-165862578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs562590326	chr4:165862578-165862579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs4383571	chr4:165862591-165862592	Weak transcription	n/a	n/a	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
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
Non-syndromic sensorineural hearing loss	18451855	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:165859200-165864400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr4:165859200-165869200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:165861200-165861400	Enhancers	Fetal Muscle Leg	muscle
4	chr4:165864200-165864600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr4:165864200-165864800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr4:165864400-165864600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:165864400-165864600	Bivalent Enhancer	Fetal Muscle Leg	muscle
8	chr4:165864400-165864800	Enhancers	NHEK	skin
9	chr4:165864600-165864800	Enhancers	Fetal Muscle Leg	muscle
10	chr4:165864600-165865000	Enhancers	HSMMtube	muscle
11	chr4:165864600-165865200	Enhancers	Placenta Amnion	Placenta Amnion
12	chr4:165864600-165869200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr4:165864800-165869000	Weak transcription	Fetal Muscle Leg	muscle
14	chr4:165864800-165869200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:165865800-165867000	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:165866200-165866600	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr4:165866200-165866800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr4:165866200-165866800	Enhancers	iPS-20b Cell Line	embryonic stem cell
19	chr4:165866600-165866800	Enhancers	HMEC	breast
20	chr4:165866600-165868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr4:165866800-165869200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chr4:165866800-165870800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr4:165867000-165870800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr4:165867600-165869400	Enhancers	GM12878-XiMat	blood
25	chr4:165869000-165869600	Enhancers	Fetal Muscle Trunk	muscle
26	chr4:165869000-165871200	Enhancers	Fetal Muscle Leg	muscle
27	chr4:165869200-165869400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:165869200-165869400	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr4:165869200-165869600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr4:165869200-165869600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr4:165869200-165869600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:165869400-165870200	Weak transcription	GM12878-XiMat	blood
33	chr4:165869600-165870200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:165869600-165870800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
35	chr4:165870200-165871200	Enhancers	GM12878-XiMat	blood
36	chr4:165870800-165871000	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:165870800-165871000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr4:165870800-165871200	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:165870800-165871200	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr4:165870800-165871200	Bivalent Enhancer	Psoas Muscle	Psoas
41	chr4:165870800-165871400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr4:165870800-165871400	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:165871000-165874800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr4:165871000-165877800	Weak transcription	Spleen	Spleen
45	chr4:165871200-165875000	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr4:165871200-165877600	Weak transcription	GM12878-XiMat	blood
47	chr4:165873400-165875000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr4:165873800-165874000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr4:165873800-165874000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr4:165874000-165874200	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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