Variant report

Variant	nsv834707
Chromosome Location	chr3:60005679-60184046
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	chr3:60089333-60089791	K562	blood:	n/a	n/a
2	ARID3A	chr3:60080880-60080974	K562	blood:	n/a	n/a
3	ARID3A	chr3:60039271-60039405	K562	blood:	n/a	n/a
4	ATF1	chr3:60072608-60072940	K562	blood:	n/a	n/a
5	ATF1	chr3:60175649-60176121	K562	blood:	n/a	n/a
6	ATF2	chr3:60072552-60072929	GM12878	blood:	n/a	n/a
7	ATF2	chr3:60175754-60176100	GM12878	blood:	n/a	n/a
8	ATF2	chr3:60072548-60072961	GM12878	blood:	n/a	n/a
9	ATF3	chr3:60072525-60072862	K562	blood:	n/a	n/a
10	ATF3	chr3:60039325-60039564	K562	blood:	n/a	n/a
11	BACH1	chr3:60039339-60039564	H1-hESC	embryonic stem cell:	n/a	n/a
12	BATF	chr3:60125935-60126267	GM12878	blood:	n/a	n/a
13	BATF	chr3:60178356-60178622	GM12878	blood:	n/a	n/a
14	BATF	chr3:60178290-60178695	GM12878	blood:	n/a	n/a
15	BATF	chr3:60072622-60072863	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
16	BATF	chr3:60175866-60176100	GM12878	blood:	n/a	chr3:60175916-60175929
17	BATF	chr3:60072565-60072906	GM12878	blood:	n/a	chr3:60072719-60072730 chr3:60072749-60072760
18	BATF	chr3:60066331-60066721	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:60178405-60178610	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:60178284-60178674	GM12878	blood:	n/a	n/a
21	BCL3	chr3:60178326-60178686	GM12878	blood:	n/a	n/a
22	BHLHE40	chr3:60072788-60072959	K562	blood:	n/a	n/a
23	BHLHE40	chr3:60067413-60067707	GM12878	blood:	n/a	n/a
24	BRCA1	chr3:60041707-60041710	GM12878	blood:	n/a	n/a
25	CBX3	chr3:60072440-60073038	HCT-116	colon:	n/a	n/a
26	CEBPB	chr3:60087462-60087710	HepG2	liver:	n/a	n/a
27	CEBPB	chr3:60145922-60146334	K562	blood:	n/a	n/a
28	CEBPB	chr3:60079147-60079362	IMR90	lung:	n/a	chr3:60079184-60079195
29	CEBPB	chr3:60079107-60079367	HepG2	liver:	n/a	chr3:60079184-60079195
30	CEBPB	chr3:60170978-60171261	HepG2	liver:	n/a	chr3:60171089-60171100
31	CEBPB	chr3:60153992-60154232	A549	lung:	n/a	chr3:60154095-60154108 chr3:60154095-60154106 chr3:60154096-60154107
32	CEBPB	chr3:60174380-60174479	A549	lung:	n/a	chr3:60174393-60174406
33	CEBPB	chr3:60079073-60079279	A549	lung:	n/a	chr3:60079184-60079195
34	CEBPB	chr3:60174245-60174529	K562	blood:	n/a	chr3:60174375-60174387 chr3:60174393-60174406
35	CEBPB	chr3:60048184-60048381	HepG2	liver:	n/a	chr3:60048244-60048255
36	CEBPB	chr3:60160304-60160512	K562	blood:	n/a	chr3:60160461-60160472
37	CEBPB	chr3:60153970-60154274	HepG2	liver:	n/a	chr3:60154095-60154108 chr3:60154095-60154106 chr3:60154096-60154107
38	CEBPB	chr3:60057064-60057137	A549	lung:	n/a	chr3:60057124-60057135
39	CEBPB	chr3:60087409-60087712	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr3:60146552-60146873	K562	blood:	n/a	chr3:60146695-60146708 chr3:60146696-60146707 chr3:60146694-60146711
41	CEBPB	chr3:60170971-60171214	K562	blood:	n/a	chr3:60171089-60171100
42	CEBPB	chr3:60034475-60034689	HepG2	liver:	n/a	chr3:60034603-60034614
43	CEBPB	chr3:60146575-60146881	HepG2	liver:	n/a	chr3:60146695-60146708 chr3:60146696-60146707 chr3:60146694-60146711
44	CEBPB	chr3:60057089-60057218	HepG2	liver:	n/a	chr3:60057124-60057135
45	CEBPB	chr3:60122391-60122573	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr3:60160320-60160651	HepG2	liver:	n/a	chr3:60160461-60160472
47	CEBPB	chr3:60160367-60160597	A549	lung:	n/a	chr3:60160461-60160472
48	CEBPB	chr3:60143928-60144224	K562	blood:	n/a	n/a
49	CEBPB	chr3:60146568-60146768	H1-hESC	embryonic stem cell:	n/a	chr3:60146695-60146708 chr3:60146696-60146707 chr3:60146694-60146711
50	CEBPB	chr3:60079049-60079379	K562	blood:	n/a	chr3:60079184-60079195

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:60065489-60065539	HIPEpiC	eye:	n/a
2	chr3:60133085-60133135	AG10803	skin:	n/a
3	chr3:60066405-60066455	BE2_C	brain:	n/a
4	chr3:60065489-60065539	SK-N-SH_RA	brain:	n/a
5	chr3:60066405-60066455	NT2-D1	testis:	n/a
6	chr3:60065489-60065539	H1-hESC	embryonic stem cell:	embryo
7	chr3:60066405-60066455	Hela-S3	cervix:	n/a
8	chr3:60066405-60066455	HEEpiC	esophagus:	n/a
9	chr3:60065489-60065539	GM12892	blood:	n/a
10	chr3:60066405-60066455	HRPEpiC	eye:	n/a
11	chr3:60133085-60133135	AoSMC	blood vessel:	n/a
12	chr3:60065489-60065539	AG10803	skin:	n/a
13	chr3:60066405-60066455	NHDF-neo	bronchial:	n/a
14	chr3:60065489-60065539	ovcar-3	ovarian:	n/a
15	chr3:60066405-60066455	HL-60	blood:	n/a
16	chr3:60065489-60065539	HCF	heart:	n/a
17	chr3:60066405-60066455	U87	brain:	n/a
18	chr3:60065489-60065539	Caco-2	colon:	n/a
19	chr3:60133085-60133135	GM12892	blood:	n/a
20	chr3:60066405-60066455	IMR90	lung:	fetal
21	chr3:60133085-60133135	PrEC	prostate:	n/a
22	chr3:60133085-60133135	H1-hESC	embryonic stem cell:	embryo
23	chr3:60133085-60133135	SAEC	small airway:	n/a
24	chr3:60066405-60066455	GM06990	blood:	n/a
25	chr3:60066405-60066455	MCF10A-Er-Src	breast:	n/a
26	chr3:60066405-60066455	PrEC	prostate:	n/a
27	chr3:60133085-60133135	GM19239	blood:	n/a
28	chr3:60133085-60133135	HEK293	kidney:	embryo
29	chr3:60066405-60066455	GM12878	blood:	n/a
30	chr3:60065489-60065539	GM12891	blood:	n/a
31	chr3:60065489-60065539	HNPCEpiC	eye:	n/a
32	chr3:60065489-60065539	HL-60	blood:	n/a
33	chr3:60133085-60133135	HCT-116	colon:	n/a
34	chr3:60133085-60133135	GM12891	blood:	n/a
35	chr3:60066405-60066455	SK-N-SH_RA	brain:	n/a
36	chr3:60065489-60065539	NB4	blood:	n/a
37	chr3:60066405-60066455	ECC-1	luminal epithelium:	n/a
38	chr3:60065489-60065539	PrEC	prostate:	n/a
39	chr3:60133085-60133135	BE2_C	brain:	n/a
40	chr3:60133085-60133135	HCF	heart:	n/a
41	chr3:60133085-60133135	HCPEpiC	choroid plexus:	n/a
42	chr3:60066405-60066455	AG04449	skin:	fetal
43	chr3:60065489-60065539	HPAEpiC	pulmonary alveolar:	n/a
44	chr3:60065489-60065539	IMR90	lung:	fetal
45	chr3:60066405-60066455	PFSK-1	brain:	n/a
46	chr3:60066405-60066455	K562	blood:	n/a
47	chr3:60066405-60066455	MCF-7	breast:	n/a
48	chr3:60065489-60065539	AG09309	skin:	n/a
49	chr3:60065489-60065539	GM19239	blood:	n/a
50	chr3:60133085-60133135	ProgFib	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr3:60101310..60104205-chr3:60104357..60107292,2	K562	blood:
2	chr3:60044792..60047333-chr3:60050018..60052719,2	MCF-7	breast:
3	chr3:60165952..60167759-chr3:60170117..60173099,2	K562	blood:
4	chr3:60092867..60094612-chr3:60094796..60097247,2	K562	blood:
5	chr3:60052745..60054653-chr3:60055819..60059567,3	MCF-7	breast:
6	chr3:60183906..60185619-chr3:60186648..60189161,2	K562	blood:
7	chr3:60101310..60104205-chr3:60104357..60107292,2	K562	blood:
8	chr3:60120417..60123350-chr3:60125419..60128034,2	K562	blood:
9	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
10	chr3:60044792..60047333-chr3:60050018..60052719,2	MCF-7	breast:
11	chr3:60165952..60167759-chr3:60170117..60173099,2	K562	blood:
12	chr3:60052745..60054653-chr3:60055819..60059567,3	MCF-7	breast:
13	chr3:60169452..60171383-chr3:60172881..60175585,3	K562	blood:
14	chr3:60120417..60123350-chr3:60125419..60128034,2	K562	blood:
15	chr3:59988215..59988997-chr3:60152321..60153153,2	MCF-7	breast:
16	chr3:60092867..60094612-chr3:60094796..60097247,2	K562	blood:

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

Extended variants
information (count: 8886 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:8886 , 50 per page) page: 1 2 3 4 5 6 7 ... 178

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs374222631	chr3:60005758-60005759	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs530342810	chr3:60005759-60005760	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs80337919	chr3:60005775-60005776	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs532482092	chr3:60005797-60005798	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs200771349	chr3:60005801-60005802	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs146060823	chr3:60005802-60005803	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549565428	chr3:60005807-60005808	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76062469	chr3:60005816-60005817	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182019007	chr3:60005881-60005882	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs529998124	chr3:60005918-60005919	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548555512	chr3:60005938-60005939	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs550454634	chr3:60005967-60005968	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs187336426	chr3:60006002-60006003	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs568184281	chr3:60006008-60006009	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544119543	chr3:60006021-60006022	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs546430271	chr3:60006029-60006030	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs116484665	chr3:60006035-60006036	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs139677447	chr3:60006050-60006051	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs571022705	chr3:60006053-60006054	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563872280	chr3:60006105-60006106	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs538761585	chr3:60006111-60006112	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs548835948	chr3:60006123-60006124	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149749176	chr3:60006148-60006149	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191651798	chr3:60006160-60006161	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs536298889	chr3:60006211-60006212	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181699441	chr3:60006213-60006214	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11130746	chr3:60006232-60006233	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs540483733	chr3:60006283-60006284	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558491872	chr3:60006318-60006319	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs145609424	chr3:60006330-60006331	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs114329546	chr3:60006374-60006375	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs562685824	chr3:60006381-60006382	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs148468075	chr3:60006384-60006385	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs564794078	chr3:60006395-60006396	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs114885333	chr3:60006453-60006454	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs560525963	chr3:60006459-60006460	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527993103	chr3:60006463-60006464	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs534264259	chr3:60006481-60006482	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs552808597	chr3:60006533-60006534	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532748213	chr3:60006555-60006556	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs145227003	chr3:60006566-60006567	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs17321950	chr3:60006588-60006589	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs569001858	chr3:60006595-60006596	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs536328903	chr3:60006596-60006597	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs17061825	chr3:60006600-60006601	Weak transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs147604200	chr3:60006618-60006619	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs371259580	chr3:60006624-60006625	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs367554411	chr3:60006675-60006676	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs577116391	chr3:60006696-60006697	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs212025	chr3:60006708-60006709	Weak transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21785460	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
Prostate cancer	18632612	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Cancer	18162546	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Myxofibrosarcoma	16751306	CNVD
Non-small cell lung cancer	21829676	CNVD
Urothelial cell carcinoma	18451213	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Colorectal cancer	16272173	CNVD
Mental retardation	17847001	CNVD
Neuroticism	17667963	CNVD
Squamous cell cancer	19047905	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Cancer	20164920	CNVD
Schizophrenia	23813976	CNVD
Autism	22102821	CNVD
Prostate cancer	19363497	CNVD
Malaria	21533027	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Colorectal cancer	21518781	CNVD
Esophageal cancer	21518781	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Glioblastoma multiforme	21569311	CNVD
Hepatocellular carcinoma	22267523	CNVD
Acute lymphoblastic leukemia	19100363	CNVD

Chromatin state (count:1222 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59996800-60011600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr3:59997200-60005800	Enhancers	Primary T helper cells fromperipheralblood	blood
3	chr3:60000800-60012600	Enhancers	Primary T killer memory cells from peripheral blood	blood
4	chr3:60002200-60005800	Enhancers	Primary T cells fromperipheralblood	blood
5	chr3:60002200-60005800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
6	chr3:60003600-60009400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:60003600-60012800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr3:60003800-60011200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
9	chr3:60003800-60021200	Weak transcription	Thymus	Thymus
10	chr3:60004200-60007400	Genic enhancers	Primary T helper cells PMA-I stimulated	--
11	chr3:60004400-60007000	Weak transcription	Primary T cells from cord blood	blood
12	chr3:60004400-60009000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
13	chr3:60004600-60008000	Weak transcription	Fetal Heart	heart
14	chr3:60004800-60005800	Genic enhancers	Dnd41	blood
15	chr3:60004800-60009000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr3:60004800-60009000	Weak transcription	Fetal Thymus	thymus
17	chr3:60005000-60008800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
18	chr3:60005400-60007600	Enhancers	Primary T helper naive cells from peripheral blood	blood
19	chr3:60005800-60006000	Enhancers	Dnd41	blood
20	chr3:60005800-60007000	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr3:60005800-60009000	Weak transcription	Primary T cells fromperipheralblood	blood
22	chr3:60006000-60008000	Weak transcription	Dnd41	blood
23	chr3:60007000-60007200	Enhancers	Primary T cells from cord blood	blood
24	chr3:60007000-60014600	Enhancers	Primary T helper cells fromperipheralblood	blood
25	chr3:60007200-60008600	Weak transcription	Primary T cells from cord blood	blood
26	chr3:60007400-60016400	Enhancers	Primary T helper cells PMA-I stimulated	--
27	chr3:60007600-60008800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
28	chr3:60008000-60008400	Enhancers	Left Ventricle	heart
29	chr3:60008000-60008400	Enhancers	Right Atrium	heart
30	chr3:60008000-60009000	Enhancers	Fetal Heart	heart
31	chr3:60008000-60014800	Enhancers	Dnd41	blood
32	chr3:60008200-60009400	Enhancers	Aorta	Aorta
33	chr3:60008400-60009400	Enhancers	Colon Smooth Muscle	Colon
34	chr3:60008600-60009400	Enhancers	Rectal Smooth Muscle	rectum
35	chr3:60008600-60016400	Enhancers	Primary T cells from cord blood	blood
36	chr3:60008800-60010600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
37	chr3:60008800-60017400	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr3:60009000-60009400	Enhancers	Primary T cells fromperipheralblood	blood
39	chr3:60009000-60009400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
40	chr3:60009000-60009400	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr3:60009000-60009400	Enhancers	Fetal Thymus	thymus
42	chr3:60009000-60009600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
43	chr3:60009200-60009400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr3:60009200-60009600	Enhancers	Primary hematopoietic stem cells	blood
45	chr3:60009400-60010400	Weak transcription	Primary T cells fromperipheralblood	blood
46	chr3:60009400-60010400	Weak transcription	Fetal Thymus	thymus
47	chr3:60009400-60010600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
48	chr3:60009400-60010600	Weak transcription	Aorta	Aorta
49	chr3:60009400-60011200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr3:60009400-60011200	Weak transcription	Colon Smooth Muscle	Colon

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