Variant report

Variant	nsv1002292
Chromosome Location	chr3:93519466-93736214
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1696)
CpG islands
(count:1773)
Chromatin interactive
region (count:67)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1696 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:93560605-93560733	K562	blood:	n/a	n/a
2	ARID3A	chr3:93698649-93699202	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:93692592-93692986	K562	blood:	n/a	n/a
4	ARID3A	chr3:93690348-93690789	K562	blood:	n/a	n/a
5	ARID3A	chr3:93560633-93560810	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:93676282-93676501	HepG2	liver:	n/a	n/a
7	ARID3A	chr3:93642022-93642172	K562	blood:	n/a	n/a
8	ARID3A	chr3:93691767-93692970	HepG2	liver:	n/a	n/a
9	ATF1	chr3:93688928-93689209	K562	blood:	n/a	n/a
10	ATF1	chr3:93692661-93693084	K562	blood:	n/a	n/a
11	ATF1	chr3:93698620-93699143	K562	blood:	n/a	n/a
12	ATF3	chr3:93698831-93699098	K562	blood:	n/a	chr3:93698974-93698987
13	ATF3	chr3:93688877-93689155	K562	blood:	n/a	n/a
14	BACH1	chr3:93692288-93692715	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:93713979-93714016	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:93655969-93656191	GM12878	blood:	n/a	n/a
17	BCLAF1	chr3:93698872-93699504	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:93698741-93699514	GM12878	blood:	n/a	n/a
19	BHLHE40	chr3:93688299-93688633	K562	blood:	n/a	n/a
20	BHLHE40	chr3:93698432-93699352	K562	blood:	n/a	n/a
21	BHLHE40	chr3:93692454-93693052	K562	blood:	n/a	n/a
22	BHLHE40	chr3:93690516-93690676	K562	blood:	n/a	n/a
23	BRCA1	chr3:93698708-93699567	Hela-S3	cervix:	n/a	chr3:93699508-93699515
24	BRCA1	chr3:93692300-93692913	HepG2	liver:	n/a	n/a
25	BRCA1	chr3:93698957-93699082	HepG2	liver:	n/a	n/a
26	CBX3	chr3:93625948-93626194	K562	blood:	n/a	n/a
27	CBX3	chr3:93661017-93661284	K562	blood:	n/a	n/a
28	CBX3	chr3:93692607-93693038	K562	blood:	n/a	n/a
29	CBX3	chr3:93560363-93560688	HCT-116	colon:	n/a	n/a
30	CBX3	chr3:93700392-93700721	K562	blood:	n/a	n/a
31	CBX3	chr3:93660944-93661275	K562	blood:	n/a	n/a
32	CCNT2	chr3:93688880-93689213	K562	blood:	n/a	n/a
33	CCNT2	chr3:93692423-93693063	K562	blood:	n/a	chr3:93692940-93692949
34	CCNT2	chr3:93698783-93699452	K562	blood:	n/a	n/a
35	CEBPB	chr3:93560451-93560821	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chr3:93560459-93560814	IMR90	lung:	n/a	n/a
37	CEBPB	chr3:93574844-93574994	K562	blood:	n/a	n/a
38	CEBPB	chr3:93700376-93700715	K562	blood:	n/a	n/a
39	CEBPB	chr3:93560563-93560817	HepG2	liver:	n/a	n/a
40	CEBPB	chr3:93690689-93691261	K562	blood:	n/a	chr3:93690752-93690765 chr3:93690752-93690765 chr3:93691136-93691147 chr3:93691136-93691147
41	CEBPB	chr3:93649629-93649633	K562	blood:	n/a	n/a
42	CEBPB	chr3:93683888-93684166	A549	lung:	n/a	chr3:93684037-93684048
43	CEBPB	chr3:93560514-93560789	A549	lung:	n/a	n/a
44	CEBPB	chr3:93628924-93629461	Hela-S3	cervix:	n/a	chr3:93629160-93629171 chr3:93628939-93628950 chr3:93629159-93629172 chr3:93629159-93629170
45	CEBPB	chr3:93560562-93560819	K562	blood:	n/a	n/a
46	CEBPB	chr3:93691900-93692927	HepG2	liver:	n/a	n/a
47	CEBPB	chr3:93650513-93650709	HepG2	liver:	n/a	chr3:93650686-93650699 chr3:93650686-93650697
48	CEBPB	chr3:93629053-93629308	K562	blood:	n/a	chr3:93629160-93629171 chr3:93629159-93629172 chr3:93629159-93629170
49	CEBPB	chr3:93698943-93699110	HepG2	liver:	n/a	n/a
50	CEBPB	chr3:93577008-93577134	A549	lung:	n/a	n/a

(count:1773 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:93646432-93646482	HRPEpiC	eye:	n/a
2	chr3:93692564-93692614	AG09309	skin:	n/a
3	chr3:93698864-93698914	GM12891	blood:	n/a
4	chr3:93692925-93692975	Caco-2	colon:	n/a
5	chr3:93646432-93646482	HRPEpiC	eye:	n/a
6	chr3:93692564-93692614	AG09309	skin:	n/a
7	chr3:93698864-93698914	GM12891	blood:	n/a
8	chr3:93692925-93692975	Caco-2	colon:	n/a
9	chr3:93733689-93733739	Jurkat	blood:	n/a
10	chr3:93692764-93692814	Hela-S3	cervix:	n/a
11	chr3:93692773-93692823	HAEpiC	amniotic membrane:	n/a
12	chr3:93698928-93698978	NHDF-neo	bronchial:	n/a
13	chr3:93699352-93699402	HAEpiC	amniotic membrane:	n/a
14	chr3:93698864-93698914	RPTEC	kidney:	n/a
15	chr3:93698864-93698914	MCF10A-Er-Src	breast:	n/a
16	chr3:93698533-93698583	NHBE	bronchial:	n/a
17	chr3:93693147-93693197	HRPEpiC	eye:	n/a
18	chr3:93698533-93698583	PANC-1	pancreas:	n/a
19	chr3:93694020-93694070	SK-N-SH_RA	brain:	n/a
20	chr3:93698964-93699014	SK-N-SH_RA	brain:	n/a
21	chr3:93693147-93693197	HCPEpiC	choroid plexus:	n/a
22	chr3:93698864-93698914	AG10803	skin:	n/a
23	chr3:93677738-93677788	HL-60	blood:	n/a
24	chr3:93692952-93693002	Hela-S3	cervix:	n/a
25	chr3:93702658-93702708	PANC-1	pancreas:	n/a
26	chr3:93698768-93698818	AoSMC	blood vessel:	n/a
27	chr3:93698231-93698281	BE2_C	brain:	n/a
28	chr3:93698928-93698978	Hepatocyte	liver:	n/a
29	chr3:93692773-93692823	GM19239	blood:	n/a
30	chr3:93698461-93698511	T-47D	breast:	n/a
31	chr3:93647007-93647057	SK-N-SH	brain:	n/a
32	chr3:93698461-93698511	HRCEpiC	kidney:	n/a
33	chr3:93692952-93693002	H1-hESC	embryonic stem cell:	embryo
34	chr3:93646378-93646428	HCPEpiC	choroid plexus:	n/a
35	chr3:93699019-93699069	NT2-D1	testis:	n/a
36	chr3:93689422-93689472	Hela-S3	cervix:	n/a
37	chr3:93647605-93647655	HCT-116	colon:	n/a
38	chr3:93698768-93698818	AG10803	skin:	n/a
39	chr3:93646432-93646482	HUVEC	blood vessel:	n/a
40	chr3:93698932-93698982	HEEpiC	esophagus:	n/a
41	chr3:93698231-93698281	PANC-1	pancreas:	n/a
42	chr3:93698461-93698511	SK-N-SH	brain:	n/a
43	chr3:93698932-93698982	PANC-1	pancreas:	n/a
44	chr3:93647007-93647057	HCF	heart:	n/a
45	chr3:93689422-93689472	H1-hESC	embryonic stem cell:	embryo
46	chr3:93699352-93699402	ovcar-3	ovarian:	n/a
47	chr3:93694020-93694070	MCF10A-Er-Src	breast:	n/a
48	chr3:93733689-93733739	Hela-S3	cervix:	n/a
49	chr3:93646432-93646482	PANC-1	pancreas:	n/a
50	chr3:93698966-93699016	HCPEpiC	choroid plexus:	n/a

(count:67 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:93690937..93695495-chr3:93697759..93704969,13	K562	blood:
2	chr3:93686048..93689439-chr3:93690333..93693840,4	K562	blood:
3	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
4	chr3:93723191..93723797-chr3:93786247..93787199,2	MCF-7	breast:
5	chr3:93699087..93699759-chr6:33167964..33168678,2	Hela-S3	cervix:
6	chr3:93650076..93652154-chr3:93653341..93655975,2	K562	blood:
7	chr3:93666897..93669716-chr3:93698788..93701503,2	K562	blood:
8	chr3:93722817..93723819-chr3:93787860..93788816,4	MCF-7	breast:
9	chr3:93708802..93710855-chr3:93729063..93731672,2	MCF-7	breast:
10	chr3:93571786..93573423-chr3:93699770..93701438,2	K562	blood:
11	chr3:93719015..93720527-chr3:93726108..93727920,2	K562	blood:
12	chr3:93679066..93681793-chr3:93685442..93688192,2	K562	blood:
13	chr3:93700627..93702647-chr3:93720581..93722935,2	MCF-7	breast:
14	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
15	chr3:93695644..93698458-chr3:93698499..93700134,2	K562	blood:
16	chr3:93682608..93685138-chr3:93687218..93690057,2	K562	blood:
17	chr3:93725914..93728188-chr3:93784613..93787224,2	K562	blood:
18	chr3:93690937..93695495-chr3:93697759..93704969,13	K562	blood:
19	chr3:93719824..93725075-chr3:93780190..93785120,6	MCF-7	breast:
20	chr3:93719015..93720527-chr3:93726108..93727920,2	K562	blood:
21	chr3:93677775..93680053-chr3:93699785..93701689,2	K562	blood:
22	chr3:93691441..93695260-chr3:93696863..93699033,5	MCF-7	breast:
23	chr3:93675612..93678506-chr3:93691202..93693980,2	K562	blood:
24	chr3:93700627..93702647-chr3:93720581..93722935,2	MCF-7	breast:
25	chr3:93688772..93690676-chr3:93696447..93698454,2	MCF-7	breast:
26	chr3:93722783..93723665-chr3:93787777..93788798,5	MCF-7	breast:
27	chr3:93666583..93669103-chr3:93690628..93693616,3	MCF-7	breast:
28	chr3:93614459..93614996-chr5:160095807..160096625,2	MCF-7	breast:
29	chr3:93720983..93723390-chr3:93739905..93741891,2	K562	blood:
30	chr3:93571786..93573423-chr3:93699770..93701438,2	K562	blood:
31	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
32	chr16:85780887..85783274-chr3:93688561..93690081,2	MCF-7	breast:
33	chr3:93675612..93678506-chr3:93691202..93693980,2	K562	blood:
34	chr3:93685719..93688188-chr3:93691422..93694022,3	MCF-7	breast:
35	chr3:93722234..93724634-chr3:93733108..93735943,2	K562	blood:
36	chr3:93713936..93716429-chr3:93717357..93719541,2	K562	blood:
37	chr3:93685719..93688188-chr3:93691422..93694022,3	MCF-7	breast:
38	chr3:57582642..57583494-chr3:93698783..93699437,2	Hela-S3	cervix:
39	chr3:93654201..93655762-chr3:93660898..93663750,2	MCF-7	breast:
40	chr3:93644215..93645979-chr3:93647690..93649933,2	K562	blood:
41	chr3:93734850..93736362-chr3:93780454..93782213,2	MCF-7	breast:
42	chr3:93722902..93723801-chr3:93787301..93788704,3	K562	blood:
43	chr3:93699718..93702695-chr3:93774813..93776691,2	K562	blood:
44	chr3:93682608..93685138-chr3:93687218..93690057,2	K562	blood:
45	chr3:93691277..93692824-chr3:93694719..93696283,2	K562	blood:
46	chr3:93699508..93701266-chr3:93779921..93782891,2	K562	blood:
47	chr3:93695644..93698458-chr3:93698499..93700134,2	K562	blood:
48	chr12:120906986..120907695-chr3:93698981..93699682,2	Hela-S3	cervix:
49	chr3:93700112..93701767-chr3:93770731..93773671,2	K562	blood:
50	chr3:93690925..93693157-chr3:93696535..93699093,2	MCF-7	breast:

(count:3 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PROS1-1	chr3:93707478-93707790	NONHSAT090724
2	lnc-STX19-1	chr3:93624884-93624987	NONHSAT090718
3	lnc-STX19-1	chr3:93629463-93630001	NONHSAT090718

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PROS1	hsa-miR-335-5p	chr3:93592888-93592909

Variant related genes	Relation type
ENSG00000201339	TF binding region
RNU6-488P	TF binding region
ARL13B	TF binding region
PROS1	TF binding region
RNU6-511P	TF binding region
HMGN1P7	TF binding region
ENSG00000201339	CpG island
RNU6-488P	CpG island
ARL13B	CpG island
PROS1	CpG island
RNU6-511P	CpG island
HMGN1P7	CpG island
ENSG00000111786	chromatin interactions
ENSG00000088986	chromatin interactions
ENSG00000112473	chromatin interactions
ENSG00000201339	chromatin interactions
ENSG00000168374	chromatin interactions
ENSG00000169379	chromatin interactions
ENSG00000204231	chromatin interactions
ENSG00000272146	chromatin interactions
ENSG00000184500	chromatin interactions
ENSG00000178700	chromatin interactions
ENSG00000200366	chromatin interactions
ENSG00000178694	chromatin interactions

Extended variants
information (count: 6287 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:6287 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144226673	chr3:93540604-93540605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144416914	chr3:93540605-93540606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558503716	chr3:93540614-93540615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs533411777	chr3:93540659-93540660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs552192612	chr3:93540670-93540671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs9799126	chr3:93540674-93540675	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs374039602	chr3:93540696-93540697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs537578116	chr3:93540702-93540703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181364085	chr3:93540750-93540751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574152495	chr3:93540795-93540796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs185498590	chr3:93540804-93540805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs376932104	chr3:93540822-93540823	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190061182	chr3:93540827-93540828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs142584610	chr3:93540832-93540833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534002798	chr3:93540837-93540838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553640592	chr3:93540853-93540854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577115392	chr3:93540856-93540857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs202018185	chr3:93540864-93540865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs545768050	chr3:93540865-93540866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs150955988	chr3:93540882-93540883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs563029705	chr3:93540884-93540885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs533682543	chr3:93540888-93540889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182968563	chr3:93540893-93540894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs116541937	chr3:93540894-93540895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562179150	chr3:93540901-93540902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34058845	chr3:93540911-93540912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs527745409	chr3:93540920-93540921	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs140677534	chr3:93540949-93540950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs185900749	chr3:93540965-93540966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs533716416	chr3:93540971-93540972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs372304580	chr3:93540977-93540978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190907429	chr3:93541020-93541021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs146639451	chr3:93541026-93541027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs375770521	chr3:93541031-93541032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs531222004	chr3:93541083-93541084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9283577	chr3:93541117-93541118	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs376584233	chr3:93541152-93541153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369789060	chr3:93541159-93541160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183991727	chr3:93541175-93541176	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34511846	chr3:93541180-93541181	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs570536154	chr3:93541209-93541210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539747031	chr3:93541219-93541220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs374682996	chr3:93541224-93541225	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs576370985	chr3:93541345-93541346	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535859051	chr3:93541377-93541378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555750794	chr3:93541394-93541395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572617405	chr3:93541399-93541400	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs567912798	chr3:93558033-93558034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140702281	chr3:93558043-93558044	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs184339702	chr3:93558076-93558077	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
Oral cancer	21386901	CNVD
Renal cell carcinoma	21668985	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Hirschsprung''s Disease	21712996	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
Prostate cancer	21965145	CNVD
Cancer	21129771	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
Neurodevelopmental disorder	22521361	CNVD
Cancer	20164920	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	16461572	CNVD
Neuroblastoma	17533364	CNVD
microdeletion syndrome	22180640	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
Renal cell carcinoma	19461508	CNVD
Cancer	22065749	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Myelofibrosis	22110671	CNVD
Epilepsy	21858020	CNVD

Chromatin state (count:1641 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:93540600-93541400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:93558000-93558400	Enhancers	Osteobl	bone
3	chr3:93558200-93559200	Enhancers	Muscle Satellite Cultured Cells	--
4	chr3:93558400-93558800	Weak transcription	Osteobl	bone
5	chr3:93558600-93560200	Weak transcription	Psoas Muscle	Psoas
6	chr3:93558800-93559000	Enhancers	Osteobl	bone
7	chr3:93559000-93560200	Weak transcription	Osteobl	bone
8	chr3:93559200-93560200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:93560000-93560200	Enhancers	Adipose Nuclei	Adipose
10	chr3:93560000-93560200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr3:93560000-93560200	Enhancers	Fetal Muscle Trunk	muscle
12	chr3:93560200-93560400	Enhancers	Primary B cells from peripheral blood	blood
13	chr3:93560200-93560400	Enhancers	Primary T cells fromperipheralblood	blood
14	chr3:93560200-93560400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
15	chr3:93560200-93560400	Enhancers	HUVEC	blood vessel
16	chr3:93560200-93560600	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:93560200-93560600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
18	chr3:93560200-93560600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
19	chr3:93560200-93560600	Active TSS	Muscle Satellite Cultured Cells	--
20	chr3:93560200-93560600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr3:93560200-93560600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr3:93560200-93560600	Flanking Active TSS	Adipose Nuclei	Adipose
23	chr3:93560200-93560600	Active TSS	Aorta	Aorta
24	chr3:93560200-93560600	Flanking Active TSS	Liver	Liver
25	chr3:93560200-93560600	Active TSS	Brain Anterior Caudate	brain
26	chr3:93560200-93560600	Active TSS	Brain Inferior Temporal Lobe	brain
27	chr3:93560200-93560600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
28	chr3:93560200-93560600	Active TSS	Colon Smooth Muscle	Colon
29	chr3:93560200-93560600	Active TSS	Duodenum Mucosa	Duodenum
30	chr3:93560200-93560600	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
31	chr3:93560200-93560600	Active TSS	Fetal Intestine Small	intestine
32	chr3:93560200-93560600	Flanking Active TSS	Fetal Muscle Trunk	muscle
33	chr3:93560200-93560600	Enhancers	Placenta	Placenta
34	chr3:93560200-93560600	Active TSS	Psoas Muscle	Psoas
35	chr3:93560200-93560600	Active TSS	Rectal Mucosa Donor 31	rectum
36	chr3:93560200-93560600	Active TSS	Rectal Smooth Muscle	rectum
37	chr3:93560200-93560600	Active TSS	Right Atrium	heart
38	chr3:93560200-93560600	Active TSS	Right Ventricle	heart
39	chr3:93560200-93560600	Active TSS	HMEC	breast
40	chr3:93560200-93560600	Active TSS	NH-A	brain
41	chr3:93560200-93560600	Active TSS	NHDF-Ad	bronchial
42	chr3:93560200-93560800	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr3:93560200-93560800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr3:93560200-93560800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr3:93560200-93560800	Active TSS	Primary T helper naive cells fromperipheralblood	blood
46	chr3:93560200-93560800	Active TSS	Primary T helper cells fromperipheralblood	blood
47	chr3:93560200-93560800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr3:93560200-93560800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr3:93560200-93560800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr3:93560200-93560800	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin

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