Variant report

Variant	nsv1019110
Chromosome Location	chr4:133717769-134026923
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:701)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:701 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr4:133730921-133731093	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr4:134017875-134018468	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:133748689-133748964	GM12878	blood:	n/a	n/a
4	BATF	chr4:133748694-133749057	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:133748676-133748978	GM12878	blood:	n/a	n/a
6	BHLHE40	chr4:133748778-133748970	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:133844722-133845054	HepG2	liver:	n/a	n/a
8	BRCA1	chr4:133760456-133760464	H1-hESC	embryonic stem cell:	n/a	n/a
9	CCNT2	chr4:133763893-133764093	K562	blood:	n/a	n/a
10	CEBPB	chr4:133901232-133901531	HepG2	liver:	n/a	chr4:133901381-133901392
11	CEBPB	chr4:134011897-134012080	HepG2	liver:	n/a	chr4:134011941-134011952
12	CEBPB	chr4:133732622-133732909	HepG2	liver:	n/a	chr4:133732781-133732792 chr4:133732750-133732761
13	CEBPB	chr4:133820188-133820483	Hela-S3	cervix:	n/a	chr4:133820321-133820332
14	CEBPB	chr4:133901247-133901518	K562	blood:	n/a	chr4:133901381-133901392
15	CEBPB	chr4:133820212-133820515	HepG2	liver:	n/a	chr4:133820321-133820332
16	CEBPB	chr4:133952745-133952810	HepG2	liver:	n/a	chr4:133952775-133952786
17	CEBPB	chr4:133820381-133820687	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:133850940-133850975	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:133834386-133834527	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:133723205-133723424	HepG2	liver:	n/a	chr4:133723305-133723316
21	CEBPB	chr4:133951428-133951459	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:133924382-133924703	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:133901368-133901533	A549	lung:	n/a	chr4:133901381-133901392
24	CHD2	chr4:133980020-133980175	H1-hESC	embryonic stem cell:	n/a	n/a
25	CHD2	chr4:133924510-133924519	HepG2	liver:	n/a	n/a
26	CREB1	chr4:133730886-133731169	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:133862734-133862761	GM13977	blood:	n/a	n/a
28	CTCF	chr4:133785060-133785210	BE2_C	brain:	n/a	n/a
29	CTCF	chr4:133739421-133739571	A549	lung:	n/a	n/a
30	CTCF	chr4:134023919-134024060	LNCaP	prostate:	n/a	n/a
31	CTCF	chr4:133739300-133739450	BE2_C	brain:	n/a	n/a
32	CTCF	chr4:133858940-133859090	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:134002460-134002610	HPAF	blood vessel:	n/a	n/a
34	CTCF	chr4:133730892-133731127	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr4:133730880-133731030	GM12874	blood:	n/a	n/a
36	CTCF	chr4:133730975-133731043	GM12891	blood:	n/a	n/a
37	CTCF	chr4:134002400-134002550	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:133859003-133859131	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:133730920-133731070	BE2_C	brain:	n/a	n/a
40	CTCF	chr4:133859020-133859170	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr4:133730990-133731036	GM19238	blood:	n/a	n/a
42	CTCF	chr4:133730954-133731068	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:133730776-133731094	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr4:134002520-134002790	HEEpiC	esophagus:	n/a	n/a
45	CTCF	chr4:133730900-133731050	HCT-116	colon:	n/a	n/a
46	CTCF	chr4:133739440-133739590	A549	lung:	n/a	n/a
47	CTCF	chr4:133739231-133739665	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:134002500-134002650	GM12875	blood:	n/a	n/a
49	CTCF	chr4:133739420-133739570	K562	blood:	n/a	n/a
50	CTCF	chr4:133994969-133994999	Lung_OC	lung:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:134023826-134023876	K562	blood:	n/a
2	chr4:134017922-134017972	Hepatocyte	liver:	n/a
3	chr4:133902873-133902923	LNCaP	prostate:	n/a
4	chr4:133902873-133902923	AG09319	gingival:	n/a
5	chr4:133902873-133902923	HEK293	kidney:	embryo
6	chr4:133902873-133902923	GM19239	blood:	n/a
7	chr4:133902873-133902923	Hela-S3	cervix:	n/a
8	chr4:134023826-134023876	RPTEC	kidney:	n/a
9	chr4:134023826-134023876	HL-60	blood:	n/a
10	chr4:133902873-133902923	NT2-D1	testis:	n/a
11	chr4:134017922-134017972	HMEC	breast:	n/a
12	chr4:134017922-134017972	NB4	blood:	n/a
13	chr4:134023826-134023876	HCF	heart:	n/a
14	chr4:134023826-134023876	HepG2	liver:	n/a
15	chr4:134023826-134023876	ProgFib	skin:	n/a
16	chr4:133902873-133902923	AG04450	lung:	fetal
17	chr4:134023826-134023876	GM12892	blood:	n/a
18	chr4:134023826-134023876	HNPCEpiC	eye:	n/a
19	chr4:134023826-134023876	GM12891	blood:	n/a
20	chr4:134017922-134017972	NHDF-neo	bronchial:	n/a
21	chr4:133902873-133902923	HRE	kidney:	n/a
22	chr4:133902873-133902923	GM06990	blood:	n/a
23	chr4:134017922-134017972	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:134017922-134017972	ProgFib	skin:	n/a
25	chr4:134023826-134023876	NHBE	bronchial:	n/a
26	chr4:134023826-134023876	NB4	blood:	n/a
27	chr4:134017922-134017972	PrEC	prostate:	n/a
28	chr4:134017922-134017972	LNCaP	prostate:	n/a
29	chr4:134023826-134023876	H1-hESC	embryonic stem cell:	embryo
30	chr4:134017922-134017972	BE2_C	brain:	n/a
31	chr4:134023826-134023876	NHDF-neo	bronchial:	n/a
32	chr4:134023826-134023876	HMEC	breast:	n/a
33	chr4:134023826-134023876	T-47D	breast:	n/a
34	chr4:133902873-133902923	HL-60	blood:	n/a
35	chr4:134023826-134023876	HRCEpiC	kidney:	n/a
36	chr4:134023826-134023876	SKMC	muscle:	n/a
37	chr4:133902873-133902923	AG09309	skin:	n/a
38	chr4:134017922-134017972	HIPEpiC	eye:	n/a
39	chr4:133902873-133902923	GM12892	blood:	n/a
40	chr4:134023826-134023876	SK-N-SH	brain:	n/a
41	chr4:134017922-134017972	NH-A	brain:	n/a
42	chr4:134023826-134023876	PrEC	prostate:	n/a
43	chr4:134023826-134023876	HCT-116	colon:	n/a
44	chr4:134017922-134017972	HL-60	blood:	n/a
45	chr4:134017922-134017972	HRCEpiC	kidney:	n/a
46	chr4:133902873-133902923	HCM	heart:	n/a
47	chr4:133902873-133902923	MCF-7	breast:	n/a
48	chr4:134023826-134023876	AG09309	skin:	n/a
49	chr4:134023826-134023876	A549	lung:	n/a
50	chr4:134023826-134023876	AoSMC	blood vessel:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:133888553..133890099-chr4:133891528..133893270,2	MCF-7	breast:
2	chr4:134026102..134027632-chr4:134051284..134053471,2	MCF-7	breast:
3	chr4:133770404..133772149-chr4:133774462..133777277,2	MCF-7	breast:
4	chr4:133826544..133829141-chr4:133839890..133842736,2	MCF-7	breast:
5	chr4:133826904..133828729-chr4:133829382..133832081,2	MCF-7	breast:
6	chr4:133969011..133970671-chr4:133972621..133974563,2	K562	blood:
7	chr4:133843222..133845641-chr4:133850338..133852318,2	MCF-7	breast:
8	chr4:133770404..133772149-chr4:133774462..133777277,2	MCF-7	breast:
9	chr4:133820254..133821914-chr4:133825205..133827261,2	MCF-7	breast:
10	chr4:133820254..133821914-chr4:133825205..133827261,2	MCF-7	breast:
11	chr4:133843222..133845641-chr4:133850338..133852318,2	MCF-7	breast:
12	chr4:133826544..133829141-chr4:133839890..133842736,2	MCF-7	breast:
13	chr4:133888553..133890099-chr4:133891528..133893270,2	MCF-7	breast:
14	chr4:133826904..133828729-chr4:133829382..133832081,2	MCF-7	breast:
15	chr4:133969011..133970671-chr4:133972621..133974563,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-5	chr4:133998524-133998610	ENSG00000250241
2	lnc-RP11-62N21.1.1-4	chr4:133909583-133909832	ENSG00000249513
3	lnc-RP11-62N21.1.1-3	chr4:133902801-133902832	XLOC_004079
4	lnc-RP11-62N21.1.1-5	chr4:133996466-133996594	ENSG00000250241
5	lnc-RP11-62N21.1.1-4	chr4:133906667-133906763	XLOC_004080
6	lnc-RP11-62N21.1.1-3	chr4:133791541-133791672	XLOC_004079
7	lnc-RP11-62N21.1.1-5	chr4:134017891-134018038	NONHSAT098344
8	lnc-RP11-62N21.1.1-5	chr4:134017891-134017981	ENSG00000250241
9	lnc-RP11-62N21.1.1-4	chr4:133884936-133884952	XLOC_004080
10	lnc-RP11-62N21.1.1-4	chr4:133906665-133906763	ENSG00000249513
11	lnc-RP11-62N21.1.1-4	chr4:133909583-133909832	XLOC_004080
12	lnc-RP11-62N21.1.1-5	chr4:133999493-133999617	ENSG00000250241
13	lnc-RP11-62N21.1.1-5	chr4:134015015-134017105	ENSG00000250241
14	lnc-RP11-62N21.1.1-5	chr4:134017891-134018038	ENSG00000250241
15	lnc-RP11-62N21.1.1-4	chr4:133906851-133906963	XLOC_004080
16	lnc-RP11-62N21.1.1-4	chr4:133906851-133906963	ENSG00000249513
17	lnc-RP11-62N21.1.1-3	chr4:133757927-133758349	XLOC_004079
18	lnc-RP11-62N21.1.1-5	chr4:134017040-134017105	ENSG00000250241
19	lnc-RP11-62N21.1.1-5	chr4:134016687-134017105	NONHSAT098344

No data

Variant related genes	Relation type
ENSG00000251488	TF binding region
ENSG00000249513	TF binding region
ENSG00000250241	TF binding region
ENSG00000251488	CpG island
ENSG00000249513	CpG island
ENSG00000250241	CpG island
ZNF711	miRNA target sites
TMEM33	miRNA target sites
RBM9	miRNA target sites
BCL2	miRNA target sites
CNOT4	miRNA target sites
MAP3K3	miRNA target sites
CA13	miRNA target sites
OSBPL8	miRNA target sites

Extended variants
information (count: 4842 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:4842 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574417168	chr4:133719002-133719003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs141780581	chr4:133719004-133719005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs75002957	chr4:133719056-133719057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375432007	chr4:133719105-133719106	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs187291303	chr4:133719110-133719111	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs531828744	chr4:133719162-133719163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545770548	chr4:133719164-133719165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562868871	chr4:133719202-133719203	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs191967327	chr4:133719212-133719213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs74477274	chr4:133719248-133719249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs77254354	chr4:133719267-133719268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369784705	chr4:133719282-133719283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs527738032	chr4:133719339-133719340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547957870	chr4:133719366-133719367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533782048	chr4:133730215-133730216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs56165460	chr4:133730243-133730244	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs199718719	chr4:133730245-133730246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs374971311	chr4:133730249-133730250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs57234102	chr4:133730256-133730257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550976934	chr4:133730257-133730258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs567377995	chr4:133730258-133730259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs536356960	chr4:133730324-133730325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs555135015	chr4:133730340-133730341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs567599917	chr4:133730365-133730366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs34744826	chr4:133730385-133730386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35735925	chr4:133730393-133730394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs565586321	chr4:133730396-133730397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs566352323	chr4:133730400-133730401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs148479540	chr4:133730438-133730439	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs181357506	chr4:133730452-133730453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs375731614	chr4:133730464-133730465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs75203997	chr4:133730494-133730495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557644185	chr4:133730497-133730498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs556918119	chr4:133730501-133730502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs573736053	chr4:133730509-133730510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs575816209	chr4:133730538-133730539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs185044919	chr4:133730552-133730553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs542783937	chr4:133730578-133730579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1597122	chr4:133730607-133730608	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs80035535	chr4:133730637-133730638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs73856559	chr4:133730666-133730667	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs1839079	chr4:133730687-133730688	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs182306939	chr4:133730696-133730697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs187090387	chr4:133730736-133730737	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560988788	chr4:133730746-133730747	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs111808777	chr4:133730765-133730766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533687218	chr4:133730784-133730785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76933305	chr4:133730935-133730936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs78626080	chr4:133730938-133730939	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs35706425	chr4:133730960-133730961	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
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
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
small cell lung cancer	20016488	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:298 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:133719000-133719400	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr4:133730200-133732600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:133730600-133731000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr4:133734800-133738600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr4:133736000-133738600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr4:133738600-133738800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
7	chr4:133738600-133739800	Active TSS	ES-I3 Cell Line	embryonic stem cell
8	chr4:133738800-133739600	Active TSS	ES-WA7 Cell Line	embryonic stem cell
9	chr4:133738800-133739600	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr4:133738800-133739800	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr4:133739000-133739400	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr4:133739000-133739600	Active TSS	HUES48 Cell Line	embryonic stem cell
13	chr4:133739200-133739600	Active TSS	H9 Cell Line	embryonic stem cell
14	chr4:133739600-133739800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr4:133740200-133740600	Active TSS	Fetal Heart	heart
16	chr4:133740400-133740600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:133746000-133747400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:133746200-133747400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr4:133748400-133748600	Active TSS	Brain Anterior Caudate	brain
20	chr4:133748600-133749000	Enhancers	Brain Angular Gyrus	brain
21	chr4:133748600-133749000	Enhancers	Brain Anterior Caudate	brain
22	chr4:133748800-133749000	Enhancers	Brain Inferior Temporal Lobe	brain
23	chr4:133749000-133749200	Active TSS	Brain Anterior Caudate	brain
24	chr4:133759400-133760000	ZNF genes & repeats	Aorta	Aorta
25	chr4:133759600-133759800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:133759600-133760000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:133767000-133767400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr4:133774000-133774200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr4:133774200-133785600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:133774600-133775000	Enhancers	HMEC	breast
31	chr4:133782000-133782400	Enhancers	HMEC	breast
32	chr4:133782400-133785600	Weak transcription	HMEC	breast
33	chr4:133785600-133786200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:133785600-133786600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
35	chr4:133785600-133787400	Enhancers	HMEC	breast
36	chr4:133786200-133788200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:133786600-133786800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr4:133786800-133788000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr4:133787800-133788000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr4:133788200-133788600	Enhancers	Brain Hippocampus Middle	brain
41	chr4:133788200-133788600	Enhancers	Brain Substantia Nigra	brain
42	chr4:133804400-133804600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:133814800-133815200	Enhancers	HUVEC	blood vessel
44	chr4:133825000-133825400	Enhancers	Dnd41	blood
45	chr4:133825000-133825600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr4:133825200-133825800	Enhancers	Primary hematopoietic stem cells short term culture	blood
47	chr4:133831200-133831400	Enhancers	Pancreatic Islets	Pancreatic Islet
48	chr4:133831400-133831800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:133831400-133832200	Weak transcription	Pancreatic Islets	Pancreatic Islet
50	chr4:133832200-133833000	Enhancers	Pancreatic Islets	Pancreatic Islet

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