Variant report

Variant	nsv1013531
Chromosome Location	chr3:67917771-68070027
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:795)
Chromatin interactive
region (count:18)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:67925864-67926374	HepG2	liver:	n/a	chr3:67926095-67926111 chr3:67926096-67926112
2	ARID3A	chr3:67926647-67927182	HepG2	liver:	n/a	n/a
3	BACH1	chr3:68017186-68017276	K562	blood:	n/a	n/a
4	BHLHE40	chr3:67935315-67935332	GM12878	blood:	n/a	n/a
5	CCNT2	chr3:68033067-68033322	K562	blood:	n/a	n/a
6	CEBPB	chr3:68066177-68066441	HepG2	liver:	n/a	chr3:68066272-68066283
7	CEBPB	chr3:67974289-67974478	A549	lung:	n/a	n/a
8	CEBPB	chr3:67980779-67981121	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr3:67926813-67926954	HepG2	liver:	n/a	n/a
10	CEBPB	chr3:67997188-67997474	HepG2	liver:	n/a	chr3:67997344-67997355
11	CEBPB	chr3:67964234-67964528	HepG2	liver:	n/a	chr3:67964358-67964369
12	CEBPB	chr3:67964275-67964462	H1-hESC	embryonic stem cell:	n/a	chr3:67964358-67964369
13	CEBPB	chr3:68037023-68037308	IMR90	lung:	n/a	chr3:68037159-68037170
14	CEBPB	chr3:68037096-68037312	K562	blood:	n/a	chr3:68037159-68037170
15	CEBPB	chr3:68037035-68037272	A549	lung:	n/a	chr3:68037159-68037170
16	CEBPB	chr3:68055781-68055942	HepG2	liver:	n/a	n/a
17	CEBPB	chr3:67932535-67932706	HepG2	liver:	n/a	chr3:67932573-67932584 chr3:67932639-67932651 chr3:67932571-67932582
18	CEBPB	chr3:67985138-67985469	HepG2	liver:	n/a	chr3:67985315-67985326
19	CEBPB	chr3:67926694-67926991	A549	lung:	n/a	n/a
20	CEBPB	chr3:68033366-68033687	HepG2	liver:	n/a	chr3:68033525-68033536 chr3:68033502-68033513
21	CEBPB	chr3:68037001-68037283	HepG2	liver:	n/a	chr3:68037159-68037170
22	CEBPB	chr3:67985164-67985454	IMR90	lung:	n/a	chr3:67985315-67985326
23	CEBPB	chr3:68037007-68037284	H1-hESC	embryonic stem cell:	n/a	chr3:68037159-68037170
24	CEBPB	chr3:68030853-68031196	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr3:68030854-68031193	HepG2	liver:	n/a	n/a
26	CEBPB	chr3:67926670-67927091	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:67974240-67974550	HepG2	liver:	n/a	n/a
28	CEBPB	chr3:67926677-67927058	HepG2	liver:	n/a	n/a
29	CEBPB	chr3:67926724-67926973	HepG2	liver:	n/a	n/a
30	CHD2	chr3:67998544-67998794	H1-hESC	embryonic stem cell:	n/a	n/a
31	CHD2	chr3:68047488-68047694	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD2	chr3:68056739-68057304	H1-hESC	embryonic stem cell:	n/a	chr3:68056886-68056896
33	CTCF	chr3:67991080-67991230	GM06990	blood:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
34	CTCF	chr3:67952193-67952417	MCF-7	breast:	n/a	n/a
35	CTCF	chr3:68066342-68066488	HepG2	liver:	n/a	chr3:68066394-68066415 chr3:68066400-68066416 chr3:68066399-68066417
36	CTCF	chr3:67952200-67952350	A549	lung:	n/a	n/a
37	CTCF	chr3:68067515-68067808	IMR90	lung:	n/a	n/a
38	CTCF	chr3:68057300-68057450	GM12872	blood:	n/a	chr3:68057303-68057321
39	CTCF	chr3:68066300-68066450	HRE	kidney:	n/a	chr3:68066394-68066415 chr3:68066400-68066416 chr3:68066399-68066417
40	CTCF	chr3:67991060-67991210	NHDF-neo	bronchial:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
41	CTCF	chr3:68067540-68067690	HVMF	connective:	n/a	n/a
42	CTCF	chr3:67998714-67998790	MCF-7	breast:	n/a	n/a
43	CTCF	chr3:68067540-68067690	HMF	breast:	n/a	n/a
44	CTCF	chr3:67952206-67952414	LNCaP	prostate:	n/a	n/a
45	CTCF	chr3:67991104-67991166	LNCaP	prostate:	n/a	chr3:67991118-67991139 chr3:67991123-67991141 chr3:67991128-67991136
46	CTCF	chr3:68066436-68066438	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr3:68006188-68006235	GM20000	blood:	n/a	n/a
48	CTCF	chr3:67952180-67952330	GM12874	blood:	n/a	n/a
49	CTCF	chr3:67952284-67952331	ProgFib	skin:	n/a	n/a
50	CTCF	chr3:68067560-68067710	HVMF	connective:	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	chr3:68056706-68056756	HPAEpiC	pulmonary alveolar:	n/a
2	chr3:68047840-68047890	HCT-116	colon:	n/a
3	chr3:68056706-68056756	HPAEpiC	pulmonary alveolar:	n/a
4	chr3:68047840-68047890	HCT-116	colon:	n/a
5	chr3:68057357-68057407	HL-60	blood:	n/a
6	chr3:68056706-68056756	HL-60	blood:	n/a
7	chr3:68053371-68053421	AG04450	lung:	fetal
8	chr3:68047840-68047890	A549	lung:	n/a
9	chr3:68053949-68053999	HCM	heart:	n/a
10	chr3:68057357-68057407	HRPEpiC	eye:	n/a
11	chr3:68057322-68057372	MCF-7	breast:	n/a
12	chr3:68057025-68057075	HRCEpiC	kidney:	n/a
13	chr3:68053273-68053323	PFSK-1	brain:	n/a
14	chr3:68057306-68057356	AG04450	lung:	fetal
15	chr3:68057025-68057075	HAEpiC	amniotic membrane:	n/a
16	chr3:68060925-68060975	GM19239	blood:	n/a
17	chr3:68060925-68060975	SK-N-SH	brain:	n/a
18	chr3:68057306-68057356	SKMC	muscle:	n/a
19	chr3:68057322-68057372	MCF10A-Er-Src	breast:	n/a
20	chr3:68053484-68053534	HepG2	liver:	n/a
21	chr3:68060925-68060975	H1-hESC	embryonic stem cell:	embryo
22	chr3:68053371-68053421	PANC-1	pancreas:	n/a
23	chr3:68056976-68057026	MCF10A-Er-Src	breast:	n/a
24	chr3:68039483-68039533	U87	brain:	n/a
25	chr3:68053949-68053999	ProgFib	skin:	n/a
26	chr3:68057025-68057075	Hela-S3	cervix:	n/a
27	chr3:68039483-68039533	GM12892	blood:	n/a
28	chr3:68053949-68053999	Hela-S3	cervix:	n/a
29	chr3:68047840-68047890	HRCEpiC	kidney:	n/a
30	chr3:68053273-68053323	PrEC	prostate:	n/a
31	chr3:68057025-68057075	HCM	heart:	n/a
32	chr3:68057322-68057372	A549	lung:	n/a
33	chr3:68057306-68057356	AG09309	skin:	n/a
34	chr3:68053484-68053534	Jurkat	blood:	n/a
35	chr3:68056976-68057026	AG04449	skin:	fetal
36	chr3:68053273-68053323	HCF	heart:	n/a
37	chr3:68047840-68047890	NB4	blood:	n/a
38	chr3:68056976-68057026	GM12892	blood:	n/a
39	chr3:68053273-68053323	MCF-7	breast:	n/a
40	chr3:68057025-68057075	ECC-1	luminal epithelium:	n/a
41	chr3:68060925-68060975	T-47D	breast:	n/a
42	chr3:68056706-68056756	HCT-116	colon:	n/a
43	chr3:68053949-68053999	CMK	blood:	n/a
44	chr3:68053371-68053421	MCF-7	breast:	n/a
45	chr3:68056976-68057026	HIPEpiC	eye:	n/a
46	chr3:68057322-68057372	T-47D	breast:	n/a
47	chr3:68053273-68053323	SKMC	muscle:	n/a
48	chr3:68053273-68053323	HAEpiC	amniotic membrane:	n/a
49	chr3:68057357-68057407	HPAEpiC	pulmonary alveolar:	n/a
50	chr3:68053371-68053421	NT2-D1	testis:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
2	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
3	chr3:67951890..67952870-chr3:68066397..68066948,2	MCF-7	breast:
4	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
5	chr3:67840426..67841246-chr3:68065943..68066794,2	MCF-7	breast:
6	chr3:67991529..67993327-chr3:67994469..67996433,2	MCF-7	breast:
7	chr17:56159704..56161633-chr3:67919204..67920724,2	MCF-7	breast:
8	chr3:67160040..67160708-chr3:68065971..68066562,2	MCF-7	breast:
9	chr3:67869894..67870930-chr3:68066062..68066983,4	MCF-7	breast:
10	chr3:67991094..67994023-chr3:67995213..67998211,2	MCF-7	breast:
11	chr3:67951890..67952870-chr3:68066397..68066948,2	MCF-7	breast:
12	chr3:67951881..67952772-chr3:68305559..68306337,2	MCF-7	breast:
13	chr17:56160421..56161299-chr3:67919204..67919724,3	HCT-116	colon:
14	chr17:56159655..56161786-chr3:67919204..67920724,2	MCF-7	breast:
15	chr3:68045575..68047988-chr3:68059342..68060872,2	MCF-7	breast:
16	chr3:67951814..67952581-chr3:68255379..68256164,2	MCF-7	breast:
17	chr3:68058440..68060357-chr3:68076381..68078551,2	K562	blood:
18	chr3:67952201..67952773-chr3:68925063..68925992,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM19A1-1	chr3:67939434-67939460	XLOC_002693
2	lnc-FAM19A1-1	chr3:67939433-67939460	NONHSAT090326
3	lnc-FAM19A1-1	chr3:67997565-67998137	ENSG00000241316
4	lnc-FAM19A1-1	chr3:67997565-67998136	NR_109992
5	lnc-FAM19A1-1	chr3:67939434-67939533	NR_109992
6	lnc-FAM19A1-1	chr3:67939434-67939533	ENSG00000241316

No data

Variant related genes	Relation type
FAM19A1	TF binding region
FAM19A1	CpG island
ENSG00000266290	chromatin interactions
ENSG00000264364	chromatin interactions
E2F3	miRNA target sites

Extended variants
information (count: 2740 )
Associated
traits (count: 83 )

Variant overlapped rSNPs/rCNVs (count:2740 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565740849	chr3:67917791-67917792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs536912825	chr3:67917792-67917793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs547658995	chr3:67917803-67917804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs377509920	chr3:67917833-67917834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140787709	chr3:67917836-67917837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551745199	chr3:67917865-67917866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs150120986	chr3:67917871-67917872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs539873087	chr3:67917925-67917926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs7612447	chr3:67917959-67917960	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556609764	chr3:67917962-67917963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564445711	chr3:67917971-67917972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs576576010	chr3:67918002-67918003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs558609635	chr3:67918025-67918026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs117334398	chr3:67918111-67918112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs555890751	chr3:67918127-67918128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572594704	chr3:67918137-67918138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs138433477	chr3:67918146-67918147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs79695728	chr3:67918274-67918275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs185490068	chr3:67918304-67918305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs572138924	chr3:67918310-67918311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs542980800	chr3:67918347-67918348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs55884224	chr3:67918419-67918420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189565686	chr3:67918437-67918438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528936782	chr3:67918449-67918450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs114499999	chr3:67918491-67918492	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533531879	chr3:67918519-67918520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs559495778	chr3:67918528-67918529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs75717325	chr3:67918634-67918635	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs551685364	chr3:67918735-67918736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571529121	chr3:67918737-67918738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537362838	chr3:67918739-67918740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs182263126	chr3:67918749-67918750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs148834157	chr3:67918759-67918760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs550151144	chr3:67918781-67918782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs568909697	chr3:67918786-67918787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs6801973	chr3:67918792-67918793	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs555629692	chr3:67918798-67918799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs566243908	chr3:67918870-67918871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs12636542	chr3:67918879-67918880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs111498214	chr3:67918905-67918906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs145195277	chr3:67918914-67918915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs377393179	chr3:67918916-67918917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577889711	chr3:67918917-67918918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543710585	chr3:67918920-67918921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs541129186	chr3:67918921-67918922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114638084	chr3:67918948-67918949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs573600143	chr3:67919079-67919080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs62254930	chr3:67919081-67919082	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs559216063	chr3:67919108-67919109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs542872886	chr3:67919113-67919114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:83)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	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
Oral squamous cell carcinoma	17134496	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
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Breast cancer	21509527	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Autism	22102821	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Prostate cancer	17217626	CNVD
Urothelial cell carcinoma	18451213	CNVD
Alzheimer''s disease	22166940	CNVD
Mental retardation	20848658	CNVD
Breast cancer	17142309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:67909800-67920800	Weak transcription	Liver	Liver
2	chr3:67917200-67919800	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr3:67920800-67922000	Enhancers	Liver	Liver
4	chr3:67922000-67925400	Weak transcription	Liver	Liver
5	chr3:67925400-67925800	Enhancers	A549	lung
6	chr3:67925400-67927000	Enhancers	Liver	Liver
7	chr3:67925400-67927600	Enhancers	HepG2	liver
8	chr3:67925600-67926000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr3:67925600-67926800	Enhancers	Hela-S3	cervix
10	chr3:67925800-67926400	Flanking Active TSS	A549	lung
11	chr3:67925800-67937400	Weak transcription	Aorta	Aorta
12	chr3:67926000-67926400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr3:67926400-67926600	Active TSS	A549	lung
14	chr3:67926400-67927000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr3:67926400-67927000	Enhancers	Ovary	ovary
16	chr3:67926400-67928000	Enhancers	Fetal Intestine Large	intestine
17	chr3:67926600-67926800	Flanking Active TSS	A549	lung
18	chr3:67926600-67927200	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr3:67926600-67928000	Enhancers	Fetal Intestine Small	intestine
20	chr3:67927000-67927400	Flanking Active TSS	Liver	Liver
21	chr3:67927200-67927600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr3:67927400-67928000	Enhancers	Liver	Liver
23	chr3:67927600-67928000	Enhancers	Rectal Mucosa Donor 31	rectum
24	chr3:67934400-67934800	Enhancers	Fetal Brain Female	brain
25	chr3:67946200-67947400	Enhancers	Fetal Intestine Small	intestine
26	chr3:67946200-67947600	Enhancers	Fetal Intestine Large	intestine
27	chr3:67946400-67946600	Enhancers	Fetal Brain Male	brain
28	chr3:67946400-67947800	Enhancers	Liver	Liver
29	chr3:67946600-67947200	Weak transcription	Fetal Brain Male	brain
30	chr3:67947200-67948600	Enhancers	Fetal Brain Male	brain
31	chr3:67948000-67948400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr3:67948000-67948800	Enhancers	Fetal Kidney	kidney
33	chr3:67948000-67949600	Enhancers	Fetal Brain Female	brain
34	chr3:67948200-67948800	Enhancers	Primary B cells from peripheral blood	blood
35	chr3:67949200-67949600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr3:67956400-67957400	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr3:67956400-67958200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
38	chr3:67956600-67957200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr3:67956600-67957400	Enhancers	Primary T helper cells PMA-I stimulated	--
40	chr3:67956600-67957600	Enhancers	Primary hematopoietic stem cells	blood
41	chr3:67956600-67958000	Enhancers	Primary T cells from cord blood	blood
42	chr3:67956600-67958000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
43	chr3:67956800-67957200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
44	chr3:67956800-67957200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
45	chr3:67956800-67957600	Enhancers	Primary T helper cells fromperipheralblood	blood
46	chr3:67956800-67957800	Enhancers	Primary T helper naive cells from peripheral blood	blood
47	chr3:67957400-67957600	Enhancers	Primary T cells fromperipheralblood	blood
48	chr3:67958000-67958400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr3:67958000-67958400	Enhancers	Brain Substantia Nigra	brain
50	chr3:67966000-67966800	Enhancers	Colon Smooth Muscle	Colon

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