Variant report

Variant	nsv1006666
Chromosome Location	chr3:431436-544279
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	chr3:534692-534822	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:455772-456068	HepG2	liver:	n/a	chr3:455850-455866
3	BACH1	chr3:516562-516874	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr3:541423-541496	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr3:505464-505768	GM12878	blood:	n/a	n/a
6	BATF	chr3:462357-462600	GM12878	blood:	n/a	chr3:462485-462494
7	BATF	chr3:515014-515376	GM12878	blood:	n/a	chr3:515252-515263
8	BATF	chr3:462277-462661	GM12878	blood:	n/a	chr3:462485-462494
9	BATF	chr3:515030-515408	GM12878	blood:	n/a	chr3:515252-515263
10	BHLHE40	chr3:462348-462658	GM12878	blood:	n/a	n/a
11	BHLHE40	chr3:543200-543216	GM12878	blood:	n/a	n/a
12	BRCA1	chr3:463605-463647	Hela-S3	cervix:	n/a	n/a
13	BRCA1	chr3:467465-468300	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr3:450741-451052	HepG2	liver:	n/a	n/a
15	CEBPB	chr3:468815-469191	Hela-S3	cervix:	n/a	chr3:468996-469009 chr3:469100-469117 chr3:468998-469009
16	CEBPB	chr3:458278-458461	A549	lung:	n/a	chr3:458369-458380 chr3:458369-458380 chr3:458369-458382 chr3:458369-458382
17	CEBPB	chr3:438022-438326	H1-hESC	embryonic stem cell:	n/a	chr3:438182-438195 chr3:438184-438193
18	CEBPB	chr3:468928-469135	H1-hESC	embryonic stem cell:	n/a	chr3:468996-469009 chr3:469100-469117 chr3:468998-469009
19	CEBPB	chr3:437995-438379	Hela-S3	cervix:	n/a	chr3:438182-438195 chr3:438184-438193
20	CEBPB	chr3:438001-438370	HepG2	liver:	n/a	chr3:438182-438195 chr3:438184-438193
21	CEBPB	chr3:450708-451032	IMR90	lung:	n/a	n/a
22	CEBPB	chr3:438003-438367	A549	lung:	n/a	chr3:438182-438195 chr3:438184-438193
23	CEBPB	chr3:459160-459210	K562	blood:	n/a	chr3:459185-459196
24	CEBPB	chr3:450769-450941	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:526407-526558	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr3:450750-451019	A549	lung:	n/a	n/a
27	CEBPB	chr3:534600-534964	HepG2	liver:	n/a	chr3:534767-534778
28	CEBPB	chr3:452366-452605	IMR90	lung:	n/a	chr3:452447-452458
29	CEBPB	chr3:438085-438248	K562	blood:	n/a	chr3:438182-438195 chr3:438184-438193
30	CEBPB	chr3:473256-473490	A549	lung:	n/a	chr3:473347-473358
31	CEBPB	chr3:494829-495089	A549	lung:	n/a	n/a
32	CEBPB	chr3:452335-452549	HepG2	liver:	n/a	chr3:452447-452458
33	CEBPB	chr3:526427-526685	HepG2	liver:	n/a	n/a
34	CEBPB	chr3:438012-438371	IMR90	lung:	n/a	chr3:438182-438195 chr3:438184-438193
35	CEBPB	chr3:466898-468265	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr3:473205-473536	HepG2	liver:	n/a	chr3:473347-473358
37	CEBPB	chr3:534354-535027	Hela-S3	cervix:	n/a	chr3:534767-534778
38	CHD1	chr3:503173-503210	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr3:509878-510131	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr3:509922-510119	H1-hESC	embryonic stem cell:	n/a	chr3:510034-510052 chr3:510037-510050 chr3:510036-510057
41	CTCF	chr3:523440-523590	GM12874	blood:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
42	CTCF	chr3:455840-455990	GM12872	blood:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
43	CTCF	chr3:509980-510130	NHEK	skin:	n/a	chr3:510034-510052 chr3:510037-510050 chr3:510036-510057
44	CTCF	chr3:455777-456107	IMR90	lung:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
45	CTCF	chr3:455867-455992	Kidney_OC	kidney:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943
46	CTCF	chr3:523480-523630	NHEK	skin:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
47	CTCF	chr3:509902-510157	Hela-S3	cervix:	n/a	chr3:510034-510052 chr3:510037-510050 chr3:510036-510057
48	CTCF	chr3:523420-523570	HEEpiC	esophagus:	n/a	chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
49	CTCF	chr3:523460-523668	LNCaP	prostate:	n/a	chr3:523551-523572 chr3:523550-523566 chr3:523552-523565 chr3:523549-523567
50	CTCF	chr3:455860-456010	HMEC	breast:	n/a	chr3:455932-455953 chr3:455930-455948 chr3:455935-455943

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:501673-501723	RPTEC	kidney:	n/a
2	chr3:501673-501723	RPTEC	kidney:	n/a
3	chr3:523012-523062	HCPEpiC	choroid plexus:	n/a
4	chr3:447414-447464	PFSK-1	brain:	n/a
5	chr3:447414-447464	HEK293	kidney:	embryo
6	chr3:523012-523062	PANC-1	pancreas:	n/a
7	chr3:491979-492029	AG09319	gingival:	n/a
8	chr3:447414-447464	HAEpiC	amniotic membrane:	n/a
9	chr3:491979-492029	Hepatocyte	liver:	n/a
10	chr3:523375-523425	HRE	kidney:	n/a
11	chr3:501673-501723	Caco-2	colon:	n/a
12	chr3:501673-501723	NB4	blood:	n/a
13	chr3:501673-501723	PFSK-1	brain:	n/a
14	chr3:447414-447464	PrEC	prostate:	n/a
15	chr3:523012-523062	CMK	blood:	n/a
16	chr3:447414-447464	BJ	skin:	n/a
17	chr3:447414-447464	SKMC	muscle:	n/a
18	chr3:491979-492029	HRE	kidney:	n/a
19	chr3:501673-501723	IMR90	lung:	fetal
20	chr3:523375-523425	PrEC	prostate:	n/a
21	chr3:447414-447464	HCPEpiC	choroid plexus:	n/a
22	chr3:523375-523425	HCF	heart:	n/a
23	chr3:523012-523062	HUVEC	blood vessel:	n/a
24	chr3:501673-501723	Hela-S3	cervix:	n/a
25	chr3:501673-501723	GM19239	blood:	n/a
26	chr3:523012-523062	NHDF-neo	bronchial:	n/a
27	chr3:447414-447464	MCF10A-Er-Src	breast:	n/a
28	chr3:501673-501723	Hepatocyte	liver:	n/a
29	chr3:501673-501723	SK-N-SH_RA	brain:	n/a
30	chr3:447414-447464	GM12878	blood:	n/a
31	chr3:523012-523062	HCT-116	colon:	n/a
32	chr3:491979-492029	U87	brain:	n/a
33	chr3:447414-447464	HCT-116	colon:	n/a
34	chr3:523012-523062	AoSMC	blood vessel:	n/a
35	chr3:523375-523425	CMK	blood:	n/a
36	chr3:501673-501723	GM12892	blood:	n/a
37	chr3:491979-492029	HL-60	blood:	n/a
38	chr3:523012-523062	HEEpiC	esophagus:	n/a
39	chr3:501673-501723	HL-60	blood:	n/a
40	chr3:491979-492029	PFSK-1	brain:	n/a
41	chr3:523012-523062	GM19239	blood:	n/a
42	chr3:523012-523062	GM12892	blood:	n/a
43	chr3:501673-501723	MCF10A-Er-Src	breast:	n/a
44	chr3:447414-447464	HCF	heart:	n/a
45	chr3:491979-492029	NB4	blood:	n/a
46	chr3:501673-501723	SK-N-SH	brain:	n/a
47	chr3:491979-492029	NT2-D1	testis:	n/a
48	chr3:491979-492029	HepG2	liver:	n/a
49	chr3:523375-523425	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:491979-492029	NHDF-neo	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
2	chr3:522873..523625-chr3:674344..674995,2	MCF-7	breast:
3	chr3:496434..499262-chr3:500586..502601,2	K562	blood:
4	chr3:496434..499262-chr3:500586..502601,2	K562	blood:
5	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
6	chr3:457571..459756-chr3:462210..465015,2	K562	blood:
7	chr3:512741..514299-chr3:528430..530623,2	K562	blood:
8	chr3:453296..456199-chr3:456966..458950,2	K562	blood:
9	chr3:455533..456082-chr3:893341..894026,2	MCF-7	breast:
10	chr3:457571..459756-chr3:462210..465015,2	K562	blood:
11	chr3:426526..428688-chr3:432686..435480,2	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	CHL1	hsa-miR-10a-5p	chr3:450171-450192
2	CHL1	hsa-miR-10a-5p	chr3:450185-450191
3	CHL1	hsa-miR-181a-5p	chr3:448562-448584

Variant related genes	Relation type
CHL1-AS1	TF binding region
CHL1-AS1	CpG island
ENSG00000234661	chromatin interactions

Extended variants
information (count: 3977 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:3977 , 50 per page) page: 1 2 3 4 5 6 7 ... 80

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs138908196	chr3:431455-431456	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs560694168	chr3:431509-431510	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs527917650	chr3:431512-431513	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187026469	chr3:431524-431525	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371355114	chr3:431536-431537	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142027076	chr3:431537-431538	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs193048522	chr3:431602-431603	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs550173127	chr3:431655-431656	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs374794274	chr3:431661-431662	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571674005	chr3:431670-431671	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs539095387	chr3:431696-431697	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs76300119	chr3:431725-431726	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183488362	chr3:431739-431740	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs12488723	chr3:431740-431741	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs188787306	chr3:431767-431768	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs193055497	chr3:431775-431776	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs60921148	chr3:431776-431777	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs146344100	chr3:431791-431792	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs17036953	chr3:431824-431825	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs71619456	chr3:431850-431851	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs375329815	chr3:431851-431852	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs368985771	chr3:431856-431857	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9836576	chr3:431862-431863	Strong transcription Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs559225792	chr3:431867-431868	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs527862265	chr3:431886-431887	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542822279	chr3:431942-431943	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561554780	chr3:431977-431978	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185083167	chr3:431990-431991	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs188135658	chr3:431994-431995	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550506892	chr3:432079-432080	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs139510178	chr3:432116-432117	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144176694	chr3:432176-432177	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547847724	chr3:432185-432186	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs372849126	chr3:432191-432192	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs566075679	chr3:432240-432241	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536766092	chr3:432285-432286	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371560188	chr3:432339-432340	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs563306729	chr3:432347-432348	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377111536	chr3:432373-432374	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs151121953	chr3:432400-432401	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs191451500	chr3:432401-432402	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs374112825	chr3:432404-432405	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs377752260	chr3:432418-432419	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs536905194	chr3:432427-432428	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141032064	chr3:432433-432434	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201024315	chr3:432437-432438	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs370425791	chr3:432443-432444	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs113253448	chr3:432455-432456	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576424714	chr3:432477-432478	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs373196122	chr3:432482-432483	Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Cancer	20164920	CNVD
Lung cancer	16618734	CNVD
Autism	18349135	CNVD
Breast cancer	20409316	CNVD
Myelofibrosis	22110671	CNVD
Autism	22241247	CNVD
Intellectual disability	22045946	CNVD
Squamous cell cancer	19607727	CNVD
Gastric adenocarcinoma	19115996	CNVD
sporadic birth defects	19047251	CNVD
Mental retardation	17124404	CNVD
abnormal development	18461090	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Sudden cardiac death	19188705	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian cancer	21720365	CNVD
Neuroblastoma	18923191	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21364760	CNVD
Schizophrenia	20967226	CNVD
Autism	22543975	CNVD
Attention deficit hyperactivity disorder	19546859	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Tetralogy of Fallot	22912587	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Autism	20685689	CNVD
Multiple myeloma	17550852	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:397600-453400	Weak transcription	Brain Angular Gyrus	brain
2	chr3:416200-447400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr3:421000-453600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr3:424200-453600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr3:426000-446400	Weak transcription	Adipose Nuclei	Adipose
6	chr3:427600-442200	Weak transcription	Brain Substantia Nigra	brain
7	chr3:429000-453000	Weak transcription	Cortex derived primary cultured neurospheres	brain
8	chr3:429800-431600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr3:430400-431800	Strong transcription	Fetal Brain Female	brain
10	chr3:430600-431600	Strong transcription	Ovary	ovary
11	chr3:430600-434200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
12	chr3:430600-434400	Strong transcription	Brain Germinal Matrix	brain
13	chr3:430600-451600	Weak transcription	Pancreatic Islets	Pancreatic Islet
14	chr3:430800-434000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr3:431000-434600	Strong transcription	Brain Anterior Caudate	brain
16	chr3:431600-433600	Weak transcription	Ovary	ovary
17	chr3:431600-443600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr3:431800-451400	Weak transcription	Fetal Brain Female	brain
19	chr3:433400-434200	Weak transcription	HSMM	muscle
20	chr3:433600-434000	Strong transcription	Ovary	ovary
21	chr3:434000-439200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:434000-443800	Weak transcription	Ovary	ovary
23	chr3:434200-436400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr3:434400-449400	Weak transcription	Brain Germinal Matrix	brain
25	chr3:434600-443400	Weak transcription	Brain Anterior Caudate	brain
26	chr3:434800-435400	Weak transcription	HSMM	muscle
27	chr3:435400-435600	Enhancers	HSMMtube	muscle
28	chr3:435400-436600	Enhancers	HSMM	muscle
29	chr3:435600-438200	Weak transcription	HSMMtube	muscle
30	chr3:435800-436800	Enhancers	Muscle Satellite Cultured Cells	--
31	chr3:436400-438200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr3:438200-438600	Enhancers	HSMMtube	muscle
33	chr3:438200-443400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
34	chr3:439200-447800	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr3:443400-444000	Strong transcription	Brain Anterior Caudate	brain
36	chr3:443400-447200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr3:443600-445600	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr3:443800-444800	Strong transcription	Ovary	ovary
39	chr3:444000-444400	Weak transcription	Brain Anterior Caudate	brain
40	chr3:444400-445000	Strong transcription	Brain Anterior Caudate	brain
41	chr3:444800-445000	ZNF genes & repeats	Ovary	ovary
42	chr3:445000-446600	Weak transcription	Ovary	ovary
43	chr3:445000-449600	Weak transcription	Brain Anterior Caudate	brain
44	chr3:445600-446800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr3:446800-448200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:447200-451400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr3:447800-449800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr3:448200-450000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr3:452200-452800	Active TSS	Aorta	Aorta
50	chr3:452800-453400	Enhancers	Aorta	Aorta

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