Variant report

Variant	nsv879075
Chromosome Location	chr4:62124531-62354791
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	chr4:62328397-62328752	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:62309525-62309766	HepG2	liver:	n/a	n/a
3	BACH1	chr4:62261133-62261141	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr4:62328148-62328341	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:62333799-62333999	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr4:62328613-62328644	H1-hESC	embryonic stem cell:	n/a	n/a
7	BRCA1	chr4:62328229-62328683	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr4:62138881-62139192	A549	lung:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
9	CEBPB	chr4:62138834-62139260	ECC-1	luminal epithelium:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
10	CEBPB	chr4:62328072-62328751	IMR90	lung:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
11	CEBPB	chr4:62328188-62328745	ECC-1	luminal epithelium:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
12	CEBPB	chr4:62350577-62350924	HepG2	liver:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
13	CEBPB	chr4:62138888-62139158	MCF-7	breast:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
14	CEBPB	chr4:62138857-62139228	Hela-S3	cervix:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
15	CEBPB	chr4:62341665-62341906	HepG2	liver:	n/a	chr4:62341802-62341813 chr4:62341804-62341813
16	CEBPB	chr4:62350575-62350948	IMR90	lung:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
17	CEBPB	chr4:62276088-62276389	HepG2	liver:	n/a	chr4:62276236-62276247
18	CEBPB	chr4:62312650-62313007	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr4:62333775-62334143	IMR90	lung:	n/a	n/a
20	CEBPB	chr4:62260805-62261084	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:62258793-62259056	H1-hESC	embryonic stem cell:	n/a	chr4:62258908-62258919
22	CEBPB	chr4:62276180-62276412	A549	lung:	n/a	chr4:62276236-62276247
23	CEBPB	chr4:62328306-62328822	HepG2	liver:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
24	CEBPB	chr4:62350663-62351071	Hela-S3	cervix:	n/a	chr4:62350749-62350762 chr4:62350998-62351015 chr4:62350749-62350760
25	CEBPB	chr4:62239585-62240535	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr4:62328293-62328678	A549	lung:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
27	CEBPB	chr4:62328296-62328586	K562	blood:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
28	CEBPB	chr4:62262868-62263124	H1-hESC	embryonic stem cell:	n/a	chr4:62262997-62263008
29	CEBPB	chr4:62350625-62350991	A549	lung:	n/a	chr4:62350749-62350762 chr4:62350749-62350760
30	CEBPB	chr4:62138832-62139218	IMR90	lung:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
31	CEBPB	chr4:62333825-62334130	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:62323601-62323873	IMR90	lung:	n/a	chr4:62323728-62323739 chr4:62323727-62323740
33	CEBPB	chr4:62138829-62139214	H1-hESC	embryonic stem cell:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
34	CEBPB	chr4:62138840-62139215	A549	lung:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
35	CEBPB	chr4:62333760-62333999	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr4:62318701-62319033	HepG2	liver:	n/a	chr4:62318865-62318876
37	CEBPB	chr4:62328076-62328901	Hela-S3	cervix:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
38	CEBPB	chr4:62291024-62291370	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr4:62262853-62263184	IMR90	lung:	n/a	chr4:62262997-62263008
40	CEBPB	chr4:62309552-62309939	IMR90	lung:	n/a	n/a
41	CEBPB	chr4:62303375-62303869	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr4:62258772-62259055	HepG2	liver:	n/a	chr4:62258908-62258919
43	CEBPB	chr4:62138859-62139242	A549	lung:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
44	CEBPB	chr4:62163945-62164270	H1-hESC	embryonic stem cell:	n/a	chr4:62164072-62164083 chr4:62164089-62164102 chr4:62164072-62164083
45	CEBPB	chr4:62333780-62334120	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr4:62328170-62328871	A549	lung:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
47	CEBPB	chr4:62323597-62323854	HepG2	liver:	n/a	chr4:62323728-62323739 chr4:62323727-62323740
48	CEBPB	chr4:62328345-62328599	H1-hESC	embryonic stem cell:	n/a	chr4:62328457-62328468 chr4:62328456-62328467
49	CEBPB	chr4:62138820-62139176	ECC-1	luminal epithelium:	n/a	chr4:62139020-62139033 chr4:62139022-62139031 chr4:62139022-62139031 chr4:62139021-62139032 chr4:62139022-62139031 chr4:62139020-62139033
50	CEBPB	chr4:62291047-62291316	MCF-7	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:62194059-62194109	BJ	skin:	n/a
2	chr4:62238644-62238694	PrEC	prostate:	n/a
3	chr4:62238644-62238694	Caco-2	colon:	n/a
4	chr4:62194059-62194109	CMK	blood:	n/a
5	chr4:62238644-62238694	HMEC	breast:	n/a
6	chr4:62238644-62238694	Hela-S3	cervix:	n/a
7	chr4:62159885-62159935	GM19239	blood:	n/a
8	chr4:62202294-62202344	HEEpiC	esophagus:	n/a
9	chr4:62202294-62202344	HUVEC	blood vessel:	n/a
10	chr4:62253214-62253264	HL-60	blood:	n/a
11	chr4:62238644-62238694	PANC-1	pancreas:	n/a
12	chr4:62238644-62238694	A549	lung:	n/a
13	chr4:62238644-62238694	SK-N-SH_RA	brain:	n/a
14	chr4:62159885-62159935	NH-A	brain:	n/a
15	chr4:62129666-62129716	PANC-1	pancreas:	n/a
16	chr4:62253214-62253264	CMK	blood:	n/a
17	chr4:62159885-62159935	GM12878	blood:	n/a
18	chr4:62194059-62194109	K562	blood:	n/a
19	chr4:62129666-62129716	GM06990	blood:	n/a
20	chr4:62129666-62129716	HNPCEpiC	eye:	n/a
21	chr4:62238687-62238737	PrEC	prostate:	n/a
22	chr4:62194059-62194109	NT2-D1	testis:	n/a
23	chr4:62129666-62129716	HRPEpiC	eye:	n/a
24	chr4:62238644-62238694	HRCEpiC	kidney:	n/a
25	chr4:62238644-62238694	HUVEC	blood vessel:	n/a
26	chr4:62202294-62202344	T-47D	breast:	n/a
27	chr4:62194059-62194109	IMR90	lung:	fetal
28	chr4:62238687-62238737	AoSMC	blood vessel:	n/a
29	chr4:62253214-62253264	HRCEpiC	kidney:	n/a
30	chr4:62238687-62238737	SKMC	muscle:	n/a
31	chr4:62238687-62238737	AG04449	skin:	fetal
32	chr4:62194059-62194109	NHBE	bronchial:	n/a
33	chr4:62238687-62238737	Caco-2	colon:	n/a
34	chr4:62238687-62238737	SAEC	small airway:	n/a
35	chr4:62194059-62194109	HAEpiC	amniotic membrane:	n/a
36	chr4:62129666-62129716	T-47D	breast:	n/a
37	chr4:62238644-62238694	LNCaP	prostate:	n/a
38	chr4:62159885-62159935	HL-60	blood:	n/a
39	chr4:62159885-62159935	HCPEpiC	choroid plexus:	n/a
40	chr4:62238644-62238694	HL-60	blood:	n/a
41	chr4:62253214-62253264	HPAEpiC	pulmonary alveolar:	n/a
42	chr4:62238687-62238737	HAEpiC	amniotic membrane:	n/a
43	chr4:62253214-62253264	HNPCEpiC	eye:	n/a
44	chr4:62129666-62129716	HEK293	kidney:	embryo
45	chr4:62238687-62238737	T-47D	breast:	n/a
46	chr4:62253214-62253264	GM06990	blood:	n/a
47	chr4:62238644-62238694	RPTEC	kidney:	n/a
48	chr4:62129666-62129716	HCT-116	colon:	n/a
49	chr4:62238644-62238694	T-47D	breast:	n/a
50	chr4:62238687-62238737	NH-A	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:62217548..62220131-chr5:121450075..121452091,2	MCF-7	breast:
2	chr4:62340392..62342899-chr4:62384568..62386458,2	MCF-7	breast:
3	chr4:62349743..62350606-chr8:100642196..100642782,2	MCF-7	breast:
4	chr4:19583145..19583681-chr4:62195548..62196296,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-POLR2B-12	chr4:62251129-62251487	NONHSAT096609
2	lnc-POLR2B-12	chr4:62248842-62248907	NONHSAT096609

Variant related genes	Relation type
ENSG00000205682	TF binding region
ENSG00000205682	CpG island

Extended variants
information (count: 8341 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:8341 , 50 per page) page: 1 2 3 4 5 6 7 ... 167

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10446793	chr4:62124531-62124532	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs201829974	chr4:62124537-62124538	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs565068950	chr4:62124538-62124539	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376290604	chr4:62124553-62124554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs532350122	chr4:62124635-62124636	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs370368030	chr4:62124642-62124643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541279171	chr4:62124659-62124660	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs75936984	chr4:62124696-62124697	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527658169	chr4:62124698-62124699	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs549514831	chr4:62124750-62124751	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs3860622	chr4:62124771-62124772	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9685980	chr4:62124776-62124777	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs550153192	chr4:62124779-62124780	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs66717947	chr4:62124807-62124808	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs188442266	chr4:62124811-62124812	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192176581	chr4:62124815-62124816	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145594310	chr4:62124878-62124879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs565362085	chr4:62124908-62124909	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs146019071	chr4:62124913-62124914	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184018722	chr4:62124927-62124928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs565045445	chr4:62124969-62124970	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs575759703	chr4:62124985-62124986	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187812899	chr4:62125010-62125011	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs531303130	chr4:62125070-62125071	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550502512	chr4:62125097-62125098	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs558512356	chr4:62125112-62125113	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576922070	chr4:62125113-62125114	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs562561935	chr4:62125115-62125116	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191454249	chr4:62125119-62125120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540988786	chr4:62125141-62125142	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201220469	chr4:62125142-62125143	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs58289743	chr4:62125176-62125177	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs559652160	chr4:62125181-62125182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs563558807	chr4:62125184-62125185	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397993630	chr4:62125187-62125188	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs548352284	chr4:62125208-62125209	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558173539	chr4:62125212-62125213	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs564025144	chr4:62125218-62125219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs151107944	chr4:62125234-62125235	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs141111255	chr4:62125358-62125359	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372377346	chr4:62125369-62125370	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183985034	chr4:62125472-62125473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77516628	chr4:62125618-62125619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs371536390	chr4:62125624-62125625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs565343201	chr4:62125645-62125646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532713361	chr4:62125663-62125664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs527905272	chr4:62125673-62125674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs547793131	chr4:62125694-62125695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs72633459	chr4:62125729-62125730	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs536527382	chr4:62125783-62125784	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

Disease	PMID	Source
Gastrointestinal stromal cancer	16982739	CNVD
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
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Multiple myeloma	16616336	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
Colorectal cancer	16272173	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute monocytic leukemia	16498392	CNVD
Prostate cancer	16573809	CNVD
Osteoporosis	18992858	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	20369283	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Cancer	20164919	CNVD
Lung cancer	20668451	CNVD
Intellectual disability	21811512	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Myelodysplastic syndrome	21251322	CNVD

Chromatin state (count:1245 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:62111400-62129400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:62116000-62127000	Weak transcription	Brain Cingulate Gyrus	brain
3	chr4:62119800-62127400	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr4:62120600-62126000	Weak transcription	Brain Substantia Nigra	brain
5	chr4:62120600-62126600	Weak transcription	Brain Anterior Caudate	brain
6	chr4:62121000-62125400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:62122000-62128200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr4:62122400-62126200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:62123400-62124600	Enhancers	Fetal Heart	heart
10	chr4:62124400-62127000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr4:62124400-62127800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr4:62124600-62129200	Weak transcription	Fetal Heart	heart
13	chr4:62125400-62126600	Weak transcription	Brain Angular Gyrus	brain
14	chr4:62125400-62127200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr4:62126000-62126400	Active TSS	Brain Substantia Nigra	brain
16	chr4:62126400-62128000	Enhancers	Brain Substantia Nigra	brain
17	chr4:62126600-62126800	Enhancers	Brain Anterior Caudate	brain
18	chr4:62126600-62127400	Enhancers	Brain Hippocampus Middle	brain
19	chr4:62126600-62128000	Enhancers	Brain Angular Gyrus	brain
20	chr4:62126800-62127200	Weak transcription	Brain Anterior Caudate	brain
21	chr4:62127000-62128000	Enhancers	Brain Cingulate Gyrus	brain
22	chr4:62127000-62128000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr4:62127200-62127600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr4:62127200-62128200	Active TSS	Brain Anterior Caudate	brain
25	chr4:62127400-62127800	Flanking Active TSS	Brain Hippocampus Middle	brain
26	chr4:62127400-62127800	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr4:62127600-62128400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr4:62127600-62129400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr4:62127800-62128000	Enhancers	Brain Inferior Temporal Lobe	brain
30	chr4:62127800-62128200	Enhancers	Brain Hippocampus Middle	brain
31	chr4:62127800-62128200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
32	chr4:62128000-62129400	Weak transcription	Brain Inferior Temporal Lobe	brain
33	chr4:62128000-62129400	Weak transcription	Brain Substantia Nigra	brain
34	chr4:62128000-62129800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
35	chr4:62128000-62131000	Weak transcription	Brain Angular Gyrus	brain
36	chr4:62128000-62133000	Weak transcription	Brain Cingulate Gyrus	brain
37	chr4:62128200-62128400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:62128200-62128400	Flanking Active TSS	Brain Hippocampus Middle	brain
39	chr4:62128200-62129200	Weak transcription	Brain Anterior Caudate	brain
40	chr4:62128200-62143600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
41	chr4:62128400-62129200	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr4:62128400-62130200	Weak transcription	Brain Hippocampus Middle	brain
43	chr4:62128400-62133400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:62128600-62131000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr4:62128800-62130800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:62129000-62129400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr4:62129200-62130600	Enhancers	Fetal Heart	heart
48	chr4:62129200-62131200	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr4:62129200-62134000	Enhancers	Brain Anterior Caudate	brain
50	chr4:62129400-62129600	Enhancers	H9 Cell Line	embryonic stem cell

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