Variant report

Variant	nsv1033839
Chromosome Location	chr4:186867069-186926243
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:161)
CpG islands
(count:611)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:161 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:186886708-186887142	K562	blood:	n/a	n/a
2	BACH1	chr4:186898574-186898717	K562	blood:	n/a	n/a
3	BCL11A	chr4:186920695-186920995	GM12878	blood:	n/a	n/a
4	CEBPB	chr4:186890933-186891081	HepG2	liver:	n/a	chr4:186891010-186891021
5	CEBPB	chr4:186906579-186906658	K562	blood:	n/a	n/a
6	CEBPB	chr4:186924946-186925336	Hela-S3	cervix:	n/a	chr4:186925319-186925332
7	CEBPB	chr4:186906550-186906758	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:186914203-186914400	K562	blood:	n/a	chr4:186914266-186914277 chr4:186914265-186914278
9	CEBPB	chr4:186876953-186877185	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:186916481-186916664	K562	blood:	n/a	chr4:186916572-186916583
11	CEBPB	chr4:186914173-186914373	A549	lung:	n/a	chr4:186914266-186914277 chr4:186914265-186914278
12	CEBPB	chr4:186916468-186916709	H1-hESC	embryonic stem cell:	n/a	chr4:186916572-186916583
13	CEBPB	chr4:186914154-186914409	IMR90	lung:	n/a	chr4:186914266-186914277 chr4:186914265-186914278
14	CEBPB	chr4:186890852-186891207	HepG2	liver:	n/a	chr4:186891010-186891021
15	CEBPB	chr4:186906544-186906710	IMR90	lung:	n/a	n/a
16	CEBPB	chr4:186890831-186891194	HepG2	liver:	n/a	chr4:186891010-186891021
17	CEBPB	chr4:186872870-186873096	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr4:186889081-186889445	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr4:186916431-186916776	ECC-1	luminal epithelium:	n/a	chr4:186916572-186916583
20	CEBPB	chr4:186887935-186888534	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr4:186906548-186906748	A549	lung:	n/a	n/a
22	CEBPB	chr4:186916399-186916751	A549	lung:	n/a	chr4:186916572-186916583
23	CEBPB	chr4:186916470-186916683	IMR90	lung:	n/a	chr4:186916572-186916583
24	CEBPB	chr4:186890834-186891191	HepG2	liver:	n/a	chr4:186891010-186891021
25	CEBPB	chr4:186914146-186914391	HepG2	liver:	n/a	chr4:186914266-186914277 chr4:186914265-186914278
26	CEBPB	chr4:186906563-186906763	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:186887046-186887115	K562	blood:	n/a	n/a
28	CEBPB	chr4:186916369-186916767	A549	lung:	n/a	chr4:186916572-186916583
29	CEBPB	chr4:186916423-186916743	HepG2	liver:	n/a	chr4:186916572-186916583
30	CEBPD	chr4:186890917-186891079	HepG2	liver:	n/a	n/a
31	CTCF	chr4:186906263-186906312	ProgFib	skin:	n/a	n/a
32	CTCF	chr4:186905660-186905810	GM12871	blood:	n/a	n/a
33	CTCF	chr4:186915360-186915510	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr4:186915520-186915670	HCT-116	colon:	n/a	n/a
35	CTCF	chr4:186872500-186872650	HCFaa	heart:	n/a	chr4:186872623-186872636 chr4:186872620-186872638
36	CTCF	chr4:186872560-186872710	HRE	kidney:	n/a	chr4:186872623-186872636 chr4:186872620-186872638
37	CTCF	chr4:186917100-186917250	HBMEC	blood vessel:	n/a	n/a
38	CTCF	chr4:186917040-186917190	HepG2	liver:	n/a	chr4:186917070-186917078
39	CTCF	chr4:186916960-186917110	GM12868	blood:	n/a	chr4:186917070-186917078
40	CTCF	chr4:186915320-186915470	RPTEC	kidney:	n/a	n/a
41	E2F4	chr4:186878763-186878905	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr4:186917089-186917177	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr4:186883595-186883795	MCF10A-Er-Src	breast:	n/a	n/a
44	EBF1	chr4:186887229-186887465	GM12878	blood:	n/a	chr4:186887360-186887371
45	EBF1	chr4:186887205-186887489	GM12878	blood:	n/a	chr4:186887360-186887371
46	EP300	chr4:186923725-186925406	SK-N-SH	brain:	n/a	chr4:186924953-186924963
47	EP300	chr4:186891063-186891066	HepG2	liver:	n/a	n/a
48	EP300	chr4:186924901-186925309	Hela-S3	cervix:	n/a	chr4:186924953-186924963
49	EP300	chr4:186888185-186888545	Hela-S3	cervix:	n/a	n/a
50	ESR1	chr4:186872688-186873041	ECC-1	luminal epithelium:	n/a	n/a

(count:611 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:186877657-186877707	HCM	heart:	n/a
2	chr4:186877657-186877707	HCM	heart:	n/a
3	chr4:186877916-186877966	NHBE	bronchial:	n/a
4	chr4:186921299-186921349	ProgFib	skin:	n/a
5	chr4:186876457-186876507	SKMC	muscle:	n/a
6	chr4:186921299-186921349	GM12878	blood:	n/a
7	chr4:186877550-186877600	HEK293	kidney:	embryo
8	chr4:186877601-186877651	HCM	heart:	n/a
9	chr4:186921049-186921099	IMR90	lung:	fetal
10	chr4:186877497-186877547	PrEC	prostate:	n/a
11	chr4:186877916-186877966	HCM	heart:	n/a
12	chr4:186877550-186877600	K562	blood:	n/a
13	chr4:186877601-186877651	HIPEpiC	eye:	n/a
14	chr4:186877601-186877651	HUVEC	blood vessel:	n/a
15	chr4:186921299-186921349	PrEC	prostate:	n/a
16	chr4:186877778-186877828	H1-hESC	embryonic stem cell:	embryo
17	chr4:186877657-186877707	HRE	kidney:	n/a
18	chr4:186877550-186877600	AG04450	lung:	fetal
19	chr4:186879260-186879310	IMR90	lung:	fetal
20	chr4:186876457-186876507	GM19239	blood:	n/a
21	chr4:186877657-186877707	ovcar-3	ovarian:	n/a
22	chr4:186877657-186877707	ProgFib	skin:	n/a
23	chr4:186877497-186877547	NHDF-neo	bronchial:	n/a
24	chr4:186877497-186877547	HUVEC	blood vessel:	n/a
25	chr4:186879260-186879310	H1-hESC	embryonic stem cell:	embryo
26	chr4:186877601-186877651	AG04449	skin:	fetal
27	chr4:186921049-186921099	AG09309	skin:	n/a
28	chr4:186877657-186877707	AoSMC	blood vessel:	n/a
29	chr4:186877916-186877966	PrEC	prostate:	n/a
30	chr4:186879260-186879310	T-47D	breast:	n/a
31	chr4:186876457-186876507	SK-N-SH	brain:	n/a
32	chr4:186877497-186877547	GM12878	blood:	n/a
33	chr4:186876457-186876507	BE2_C	brain:	n/a
34	chr4:186877550-186877600	GM12892	blood:	n/a
35	chr4:186877550-186877600	AG09309	skin:	n/a
36	chr4:186876457-186876507	AG04449	skin:	fetal
37	chr4:186877601-186877651	CMK	blood:	n/a
38	chr4:186877550-186877600	Hepatocyte	liver:	n/a
39	chr4:186877601-186877651	GM12878	blood:	n/a
40	chr4:186879260-186879310	AG09309	skin:	n/a
41	chr4:186877778-186877828	CMK	blood:	n/a
42	chr4:186876457-186876507	SK-N-SH_RA	brain:	n/a
43	chr4:186877657-186877707	SAEC	small airway:	n/a
44	chr4:186921299-186921349	MCF-7	breast:	n/a
45	chr4:186877657-186877707	HNPCEpiC	eye:	n/a
46	chr4:186921299-186921349	Jurkat	blood:	n/a
47	chr4:186877778-186877828	GM19239	blood:	n/a
48	chr4:186876457-186876507	HMEC	breast:	n/a
49	chr4:186879260-186879310	RPTEC	kidney:	n/a
50	chr4:186877916-186877966	SK-N-SH_RA	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:186895004..186896872-chr4:186900773..186902842,2	K562	blood:
2	chr4:186884071..186886436-chr4:186886448..186888967,3	K562	blood:
3	chr4:186911301..186912971-chr4:186916620..186919384,2	K562	blood:
4	chr4:186884071..186886436-chr4:186886448..186888967,3	K562	blood:
5	chr4:186895004..186896872-chr4:186900773..186902842,2	K562	blood:
6	chr4:186911301..186912971-chr4:186916620..186919384,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PDLIM3-6	chr4:186877350-186877522	NONHSAT099625
2	lnc-PDLIM3-6	chr4:186877350-186877502	NONHSAT099627

No data

Variant related genes	Relation type
SORBS2	TF binding region
ENSG00000239034	TF binding region
SORBS2	CpG island
ENSG00000239034	CpG island

Extended variants
information (count: 2093 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:2093 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550783142	chr4:186867082-186867083	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs76424085	chr4:186867086-186867087	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs536247633	chr4:186867097-186867098	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs547605155	chr4:186867113-186867114	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs553444750	chr4:186867139-186867140	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs566883632	chr4:186867146-186867147	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs535139036	chr4:186867152-186867153	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs538695785	chr4:186867156-186867157	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs534868989	chr4:186867182-186867183	Enhancers Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs143269947	chr4:186867217-186867218	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs577727083	chr4:186867274-186867275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543634557	chr4:186867276-186867277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs150827936	chr4:186867291-186867292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs573725049	chr4:186867306-186867307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs184177405	chr4:186867341-186867342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs537408728	chr4:186867342-186867343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs370429724	chr4:186867368-186867369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs114259265	chr4:186867458-186867459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575338713	chr4:186867459-186867460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs1378150	chr4:186867469-186867470	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs528077588	chr4:186867474-186867475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575966294	chr4:186867493-186867494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545267187	chr4:186867501-186867502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs1378151	chr4:186867513-186867514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs190212442	chr4:186867514-186867515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370655564	chr4:186867594-186867595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs74520673	chr4:186867596-186867597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567646186	chr4:186867739-186867740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117567687	chr4:186867774-186867775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35510709	chr4:186867776-186867777	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs547120193	chr4:186867793-186867794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193001395	chr4:186867797-186867798	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs959584	chr4:186867803-186867804	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs542515385	chr4:186867824-186867825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs558066110	chr4:186867848-186867849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559501946	chr4:186867875-186867876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs79786522	chr4:186867886-186867887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs35447862	chr4:186867902-186867903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs370681809	chr4:186867917-186867918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185605292	chr4:186867922-186867923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs573762552	chr4:186867954-186867955	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs535895471	chr4:186867956-186867957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552671569	chr4:186868028-186868029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs959585	chr4:186868062-186868063	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs114850766	chr4:186868107-186868108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530453000	chr4:186868136-186868137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565436778	chr4:186868141-186868142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs959586	chr4:186868146-186868147	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs544588551	chr4:186868173-186868174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs57468116	chr4:186868227-186868228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:77)

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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	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
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
Lung adenocarcinoma	17086460	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Lung cancer	17086460	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	22341455	CNVD
Cancer	20164920	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:186847800-186872400	Weak transcription	Right Atrium	heart
2	chr4:186865800-186867200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
3	chr4:186866000-186867200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:186866000-186867200	Enhancers	Osteobl	bone
5	chr4:186866200-186867200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr4:186866800-186867200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr4:186866800-186867200	Enhancers	Adipose Nuclei	Adipose
8	chr4:186867000-186872200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr4:186867200-186871800	Weak transcription	Osteobl	bone
10	chr4:186867200-186872000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:186870200-186871200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr4:186870600-186870800	Enhancers	Fetal Brain Male	brain
13	chr4:186870800-186873400	Weak transcription	Fetal Brain Male	brain
14	chr4:186871800-186872200	Enhancers	Osteobl	bone
15	chr4:186871800-186872800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
16	chr4:186872000-186872200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr4:186872000-186872800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr4:186872200-186872600	Enhancers	Muscle Satellite Cultured Cells	--
19	chr4:186872200-186872800	Enhancers	Fetal Brain Female	brain
20	chr4:186872400-186872600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:186872400-186872600	Enhancers	Right Atrium	heart
22	chr4:186872600-186872800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr4:186872600-186873000	Enhancers	Fetal Thymus	thymus
24	chr4:186872800-186873800	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr4:186872800-186874400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:186872800-186874600	Weak transcription	Fetal Brain Female	brain
27	chr4:186873400-186876000	Enhancers	Fetal Brain Male	brain
28	chr4:186873800-186876800	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr4:186874000-186874200	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr4:186874000-186874200	Enhancers	Hela-S3	cervix
31	chr4:186874400-186875000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:186874600-186874800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr4:186874600-186874800	Active TSS	Fetal Brain Female	brain
34	chr4:186874800-186875200	Flanking Active TSS	Fetal Brain Female	brain
35	chr4:186874800-186875800	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr4:186875000-186875800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:186875200-186877200	Active TSS	Fetal Brain Female	brain
38	chr4:186875800-186876200	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr4:186875800-186876400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:186875800-186877400	Active TSS	Brain Germinal Matrix	brain
41	chr4:186875800-186879000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr4:186876000-186876200	Flanking Active TSS	Fetal Brain Male	brain
43	chr4:186876000-186877000	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr4:186876000-186877200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:186876000-186877800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr4:186876000-186878000	Active TSS	Brain Angular Gyrus	brain
47	chr4:186876200-186876400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr4:186876200-186877400	Active TSS	Fetal Adrenal Gland	Adrenal Gland
49	chr4:186876200-186877600	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:186876200-186877800	Enhancers	iPS-15b Cell Line	embryonic stem cell

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