Variant report

Variant	nsv829745
Chromosome Location	chr3:143278512-143405626
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1372)
CpG islands
(count:366)
Chromatin interactive
region (count:42)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1372 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:143309525-143309833	K562	blood:	n/a	n/a
2	ARID3A	chr3:143313181-143313335	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:143393267-143393515	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:143282652-143283036	K562	blood:	n/a	n/a
5	ATF1	chr3:143281783-143281818	K562	blood:	n/a	n/a
6	ATF2	chr3:143304895-143305357	GM12878	blood:	n/a	n/a
7	ATF2	chr3:143388131-143388675	GM12878	blood:	n/a	n/a
8	ATF2	chr3:143387972-143388789	GM12878	blood:	n/a	n/a
9	ATF2	chr3:143393275-143393545	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr3:143392915-143393592	GM12878	blood:	n/a	n/a
11	BACH1	chr3:143310178-143310180	K562	blood:	n/a	n/a
12	BACH1	chr3:143367668-143367916	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr3:143315810-143316147	K562	blood:	n/a	n/a
14	BACH1	chr3:143291707-143291717	K562	blood:	n/a	n/a
15	BACH1	chr3:143315804-143316336	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:143300878-143301093	GM12878	blood:	n/a	n/a
17	BATF	chr3:143300817-143301122	GM12878	blood:	n/a	n/a
18	BATF	chr3:143346156-143346458	GM12878	blood:	n/a	n/a
19	BATF	chr3:143346181-143346365	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:143388039-143388710	GM12878	blood:	n/a	n/a
21	BCLAF1	chr3:143363355-143363728	GM12878	blood:	n/a	n/a
22	BCLAF1	chr3:143388054-143388745	GM12878	blood:	n/a	n/a
23	BCLAF1	chr3:143393156-143393611	GM12878	blood:	n/a	n/a
24	BHLHE40	chr3:143309549-143309809	K562	blood:	n/a	n/a
25	BHLHE40	chr3:143314311-143314642	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:143282639-143283043	K562	blood:	n/a	n/a
27	BHLHE40	chr3:143284856-143285128	K562	blood:	n/a	n/a
28	BHLHE40	chr3:143393159-143393521	GM12878	blood:	n/a	n/a
29	BHLHE40	chr3:143316152-143316393	K562	blood:	n/a	n/a
30	BHLHE40	chr3:143388181-143388737	GM12878	blood:	n/a	n/a
31	BRCA1	chr3:143379673-143379709	Hela-S3	cervix:	n/a	n/a
32	BRCA1	chr3:143367638-143367972	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr3:143322708-143322908	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr3:143315819-143316436	K562	blood:	n/a	n/a
35	CBX3	chr3:143309436-143309877	K562	blood:	n/a	n/a
36	CBX3	chr3:143282617-143282985	K562	blood:	n/a	n/a
37	CBX3	chr3:143356006-143356310	K562	blood:	n/a	n/a
38	CCNT2	chr3:143282607-143282990	K562	blood:	n/a	n/a
39	CCNT2	chr3:143309573-143309891	K562	blood:	n/a	chr3:143309700-143309720
40	CCNT2	chr3:143284846-143285033	K562	blood:	n/a	n/a
41	CEBPB	chr3:143360152-143360465	H1-hESC	embryonic stem cell:	n/a	chr3:143360189-143360201 chr3:143360291-143360302
42	CEBPB	chr3:143360108-143360472	K562	blood:	n/a	chr3:143360189-143360201 chr3:143360291-143360302
43	CEBPB	chr3:143282661-143282945	K562	blood:	n/a	n/a
44	CEBPB	chr3:143309557-143309744	K562	blood:	n/a	n/a
45	CEBPB	chr3:143294771-143294996	HepG2	liver:	n/a	chr3:143294843-143294854
46	CEBPB	chr3:143360128-143360424	K562	blood:	n/a	chr3:143360189-143360201 chr3:143360291-143360302
47	CEBPB	chr3:143376370-143376529	H1-hESC	embryonic stem cell:	n/a	n/a
48	CEBPB	chr3:143360119-143360370	ECC-1	luminal epithelium:	n/a	chr3:143360189-143360201 chr3:143360291-143360302
49	CEBPB	chr3:143369589-143369666	A549	lung:	n/a	n/a
50	CEBPB	chr3:143376296-143376592	IMR90	lung:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:143316736-143316786	HRPEpiC	eye:	n/a
2	chr3:143316736-143316786	NH-A	brain:	n/a
3	chr3:143316736-143316786	AG09309	skin:	n/a
4	chr3:143321098-143321148	H1-hESC	embryonic stem cell:	embryo
5	chr3:143315342-143315392	NT2-D1	testis:	n/a
6	chr3:143318826-143318876	HCF	heart:	n/a
7	chr3:143318826-143318876	HCM	heart:	n/a
8	chr3:143321098-143321148	A549	lung:	n/a
9	chr3:143321098-143321148	ovcar-3	ovarian:	n/a
10	chr3:143321098-143321148	MCF-7	breast:	n/a
11	chr3:143317039-143317089	HNPCEpiC	eye:	n/a
12	chr3:143317039-143317089	HIPEpiC	eye:	n/a
13	chr3:143316736-143316786	T-47D	breast:	n/a
14	chr3:143317039-143317089	HEEpiC	esophagus:	n/a
15	chr3:143316736-143316786	AG04450	lung:	fetal
16	chr3:143321098-143321148	SK-N-SH	brain:	n/a
17	chr3:143316736-143316786	MCF10A-Er-Src	breast:	n/a
18	chr3:143318826-143318876	HCPEpiC	choroid plexus:	n/a
19	chr3:143316736-143316786	HCT-116	colon:	n/a
20	chr3:143321098-143321148	K562	blood:	n/a
21	chr3:143315342-143315392	GM12891	blood:	n/a
22	chr3:143316736-143316786	HUVEC	blood vessel:	n/a
23	chr3:143315342-143315392	H1-hESC	embryonic stem cell:	embryo
24	chr3:143375676-143375726	HAEpiC	amniotic membrane:	n/a
25	chr3:143318826-143318876	ECC-1	luminal epithelium:	n/a
26	chr3:143317039-143317089	GM12892	blood:	n/a
27	chr3:143316736-143316786	HepG2	liver:	n/a
28	chr3:143317039-143317089	SK-N-SH	brain:	n/a
29	chr3:143321098-143321148	Caco-2	colon:	n/a
30	chr3:143375676-143375726	H1-hESC	embryonic stem cell:	embryo
31	chr3:143317039-143317089	MCF-7	breast:	n/a
32	chr3:143316736-143316786	HEEpiC	esophagus:	n/a
33	chr3:143316736-143316786	SK-N-SH	brain:	n/a
34	chr3:143315342-143315392	SK-N-SH_RA	brain:	n/a
35	chr3:143321098-143321148	GM12891	blood:	n/a
36	chr3:143316736-143316786	HCPEpiC	choroid plexus:	n/a
37	chr3:143316736-143316786	GM12878	blood:	n/a
38	chr3:143318826-143318876	HMEC	breast:	n/a
39	chr3:143316736-143316786	PrEC	prostate:	n/a
40	chr3:143315342-143315392	HL-60	blood:	n/a
41	chr3:143317039-143317089	GM12891	blood:	n/a
42	chr3:143318826-143318876	CMK	blood:	n/a
43	chr3:143375676-143375726	BE2_C	brain:	n/a
44	chr3:143318826-143318876	GM12892	blood:	n/a
45	chr3:143375676-143375726	ovcar-3	ovarian:	n/a
46	chr3:143315342-143315392	NHDF-neo	bronchial:	n/a
47	chr3:143317039-143317089	AG04450	lung:	fetal
48	chr3:143321098-143321148	HIPEpiC	eye:	n/a
49	chr3:143317039-143317089	Hela-S3	cervix:	n/a
50	chr3:143316736-143316786	AG10803	skin:	n/a

(count:42 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:143325883..143327740-chr3:143333744..143335425,2	K562	blood:
2	chr3:143358392..143360810-chr3:143361757..143363354,2	MCF-7	breast:
3	chr3:143323713..143325272-chr3:143325591..143327740,2	K562	blood:
4	chr3:143296828..143299169-chr3:143301224..143303215,2	K562	blood:
5	chr3:142790255..142790841-chr3:143363451..143364029,2	MCF-7	breast:
6	chr3:143366241..143367963-chr3:143375379..143377183,2	K562	blood:
7	chr3:143310510..143312815-chr3:143313075..143315988,2	K562	blood:
8	chr3:143152268..143153220-chr3:143363059..143363930,4	MCF-7	breast:
9	chr3:143296828..143299169-chr3:143301224..143303215,2	K562	blood:
10	chr3:143367217..143368245-chr3:143392896..143393845,7	MCF-7	breast:
11	chr3:143300021..143302674-chr3:143306084..143308707,2	K562	blood:
12	chr3:143392972..143393858-chr3:143482403..143483076,2	MCF-7	breast:
13	chr3:143367288..143367898-chr3:143392977..143393650,2	MCF-7	breast:
14	chr3:143312590..143314218-chr3:143316587..143318859,2	K562	blood:
15	chr3:143301280..143303910-chr3:143308205..143310957,2	MCF-7	breast:
16	chr3:143301280..143303910-chr3:143308205..143310957,2	MCF-7	breast:
17	chr3:143312590..143314218-chr3:143316587..143318859,2	K562	blood:
18	chr3:143367249..143368125-chr3:143481961..143482742,5	MCF-7	breast:
19	chr3:142547314..142547974-chr3:143392969..143393823,2	K562	blood:
20	chr3:143302745..143305016-chr3:143310291..143312385,2	K562	blood:
21	chr3:143282773..143284390-chr3:143291030..143293531,2	K562	blood:
22	chr3:143367288..143367898-chr3:143392977..143393650,2	MCF-7	breast:
23	chr3:143287808..143289876-chr3:143292386..143294679,2	K562	blood:
24	chr3:143313566..143315859-chr3:143319839..143322453,2	K562	blood:
25	chr3:143367217..143368245-chr3:143392896..143393845,7	MCF-7	breast:
26	chr3:143302745..143305016-chr3:143310291..143312385,2	K562	blood:
27	chr3:143325883..143327740-chr3:143333744..143335425,2	K562	blood:
28	chr3:143300021..143302674-chr3:143306084..143308707,2	K562	blood:
29	chr3:143358392..143360810-chr3:143361757..143363354,2	MCF-7	breast:
30	chr3:143310510..143312815-chr3:143313075..143315988,2	K562	blood:
31	chr3:143323713..143325272-chr3:143325591..143327740,2	K562	blood:
32	chr3:143366241..143367963-chr3:143375379..143377183,2	K562	blood:
33	chr3:143049665..143050247-chr3:143392915..143393904,2	K562	blood:
34	chr3:143313566..143315859-chr3:143319839..143322453,2	K562	blood:
35	chr3:143282773..143284390-chr3:143291030..143293531,2	K562	blood:
36	chr3:142648083..142648602-chr3:143363054..143363730,2	MCF-7	breast:
37	chr3:142845393..142847101-chr3:143393090..143394841,2	K562	blood:
38	chr3:143152690..143153230-chr3:143363138..143363760,2	MCF-7	breast:
39	chr3:143287808..143289876-chr3:143292386..143294679,2	K562	blood:
40	chr3:143273534..143275942-chr3:143280274..143281956,2	K562	blood:
41	chr3:143286929..143289795-chr3:143326338..143327897,2	K562	blood:
42	chr3:143286929..143289795-chr3:143326338..143327897,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C3orf58-3	chr3:143339370-143339455	NONHSAT092528
2	lnc-C3orf58-2	chr3:143372169-143376642	NONHSAT092529
3	lnc-C3orf58-3	chr3:143345624-143345702	NONHSAT092528
4	lnc-C3orf58-3	chr3:143346014-143346532	NONHSAT092528

No data

Variant related genes	Relation type
ENSG00000248374	TF binding region
ENSG00000248374	CpG island

Extended variants
information (count: 4702 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:4702 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs559214736	chr3:143278517-143278518	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs577550856	chr3:143278555-143278556	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs201680681	chr3:143278599-143278600	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541623009	chr3:143278620-143278621	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556945231	chr3:143278626-143278627	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs185429957	chr3:143278723-143278724	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs541472709	chr3:143278742-143278743	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553796605	chr3:143278800-143278801	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572069016	chr3:143278818-143278819	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs189555802	chr3:143278827-143278828	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs563924031	chr3:143278902-143278903	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs531442304	chr3:143278938-143278939	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543309314	chr3:143278955-143278956	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs561836266	chr3:143278966-143278967	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs113445117	chr3:143278984-143278985	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs141477177	chr3:143279033-143279034	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs548305030	chr3:143279057-143279058	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs566926807	chr3:143279112-143279113	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs147502103	chr3:143279123-143279124	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs76584616	chr3:143279129-143279130	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs571055328	chr3:143279162-143279163	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs180794645	chr3:143279164-143279165	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs185615445	chr3:143279170-143279171	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192668043	chr3:143279272-143279273	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs140114485	chr3:143279435-143279436	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372450397	chr3:143279489-143279490	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs190077165	chr3:143279491-143279492	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs572041723	chr3:143279499-143279500	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs373430842	chr3:143279513-143279514	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs114876149	chr3:143279535-143279536	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs11431519	chr3:143279571-143279572	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs200025374	chr3:143279579-143279580	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs59305072	chr3:143279581-143279582	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs370756339	chr3:143279682-143279683	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs557475902	chr3:143279720-143279721	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs575784515	chr3:143279743-143279744	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs543220205	chr3:143279748-143279749	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561981455	chr3:143279761-143279762	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs534083807	chr3:143279775-143279776	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs144080065	chr3:143279776-143279777	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541343285	chr3:143279821-143279822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs200235812	chr3:143279852-143279853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs1967350	chr3:143279879-143279880	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552658436	chr3:143279880-143279881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181714232	chr3:143279895-143279896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs6779379	chr3:143279896-143279897	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs550128922	chr3:143280104-143280105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375306039	chr3:143280131-143280132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568667609	chr3:143280168-143280169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs535757845	chr3:143280194-143280195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Melanoma	18172304	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
Cervical Cancer	21857958	CNVD
Melanoma	21693616	CNVD
Lung cancer	21426551	CNVD
Cancer	21637783	CNVD
Cervical cancer	21063398	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
microdeletion syndrome	22180640	CNVD
Basal cell lymphoma	21115979	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	18645599	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Hepatocellular carcinoma	16750200	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Myelodysplastic syndrome	21251322	CNVD
Blepharophimosis-ptosis-epicanthus inversus syndrome	22067867	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
abnormal development	18461090	CNVD
Cancer	21129771	CNVD
Ovarian cancer	23621864	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17847001	CNVD
Basal cell lymphoma	17170743	CNVD
Adrenocortical carcinoma	18281524	CNVD
Congenital anomalies of the kidney and urinary tract	20605837	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
early-passage human iPS cells	21368824	CNVD
Schizophrenia	20967226	CNVD
Autism	22495309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD

Chromatin state (count:1021 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143256000-143305600	Weak transcription	Brain Cingulate Gyrus	brain
2	chr3:143262000-143279200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr3:143270600-143304800	Weak transcription	Duodenum Smooth Muscle	Duodenum
4	chr3:143273800-143279800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:143277400-143279600	Weak transcription	Gastric	stomach
6	chr3:143277400-143282400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
7	chr3:143277400-143292400	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:143277400-143301200	Weak transcription	Esophagus	oesophagus
9	chr3:143277400-143303600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr3:143277400-143310200	Weak transcription	Primary T helper cells PMA-I stimulated	--
11	chr3:143277600-143284200	Weak transcription	Brain Substantia Nigra	brain
12	chr3:143277600-143292400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
13	chr3:143277800-143279200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:143278000-143279000	Enhancers	Fetal Lung	lung
15	chr3:143278200-143284000	Weak transcription	Monocytes-CD14+_RO01746	blood
16	chr3:143278600-143285200	Weak transcription	Primary B cells from cord blood	blood
17	chr3:143278800-143279000	ZNF genes & repeats	Primary T helper cells fromperipheralblood	blood
18	chr3:143279000-143281800	Weak transcription	Fetal Lung	lung
19	chr3:143279000-143296200	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr3:143279800-143280800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:143280600-143283000	Enhancers	Dnd41	blood
22	chr3:143280800-143282600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:143281000-143281400	Enhancers	Stomach Mucosa	stomach
24	chr3:143281000-143282000	Enhancers	Fetal Thymus	thymus
25	chr3:143281400-143281800	Weak transcription	Stomach Mucosa	stomach
26	chr3:143281400-143292200	Weak transcription	Primary T cells from cord blood	blood
27	chr3:143281600-143283400	Enhancers	K562	blood
28	chr3:143281800-143282000	Enhancers	Stomach Mucosa	stomach
29	chr3:143281800-143282200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:143281800-143282800	Enhancers	Fetal Lung	lung
31	chr3:143282200-143284000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr3:143282600-143284600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:143282800-143284400	Weak transcription	Fetal Lung	lung
34	chr3:143283200-143286200	Weak transcription	HUVEC	blood vessel
35	chr3:143283800-143284000	Enhancers	Spleen	Spleen
36	chr3:143283800-143285000	Enhancers	Brain Anterior Caudate	brain
37	chr3:143283800-143286200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr3:143284000-143284200	Enhancers	Monocytes-CD14+_RO01746	blood
39	chr3:143284000-143287200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr3:143284000-143306400	Weak transcription	Spleen	Spleen
41	chr3:143284200-143284400	Enhancers	Brain Substantia Nigra	brain
42	chr3:143284200-143285600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
43	chr3:143284400-143285200	Enhancers	Fetal Lung	lung
44	chr3:143284400-143285400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:143284400-143285800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr3:143284400-143287400	Enhancers	Fetal Intestine Small	intestine
47	chr3:143284400-143292600	Weak transcription	Brain Substantia Nigra	brain
48	chr3:143284400-143299200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr3:143284600-143285400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:143284600-143286800	Enhancers	Primary B cells from peripheral blood	blood

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