Variant report

Variant	nsv876984
Chromosome Location	chr3:75589320-75786440
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5332)
CpG islands
(count:3482)
Chromatin interactive
region (count:9)
LncRNA
region (count:26)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:5332 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
2	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
4	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
5	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
6	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
7	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
8	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
9	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
10	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
11	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
12	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
13	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
14	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
15	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
16	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
17	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
18	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
19	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
20	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
21	ATF1	chr3:75785062-75787392	K562	blood:	n/a	n/a
22	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
23	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
24	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
25	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
26	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
27	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
28	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
29	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
30	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
31	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
32	ATF1	chr3:75783726-75784839	K562	blood:	n/a	n/a
33	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
34	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
35	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
36	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
37	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
38	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
39	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
40	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
41	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
42	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
43	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
44	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
45	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
46	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
47	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
48	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
49	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
50	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a

(count:3482 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75705922-75705972	MCF-7	breast:	n/a
2	chr3:75679454-75679504	H1-hESC	embryonic stem cell:	embryo
3	chr3:75661799-75661849	NB4	blood:	n/a
4	chr3:75668758-75668808	SK-N-SH	brain:	n/a
5	chr3:75628819-75628869	SK-N-SH	brain:	n/a
6	chr3:75705922-75705972	MCF-7	breast:	n/a
7	chr3:75679454-75679504	H1-hESC	embryonic stem cell:	embryo
8	chr3:75661799-75661849	NB4	blood:	n/a
9	chr3:75668758-75668808	SK-N-SH	brain:	n/a
10	chr3:75628819-75628869	SK-N-SH	brain:	n/a
11	chr3:75664059-75664109	HIPEpiC	eye:	n/a
12	chr3:75658735-75658785	AoSMC	blood vessel:	n/a
13	chr3:75658410-75658460	SAEC	small airway:	n/a
14	chr3:75704498-75704548	HNPCEpiC	eye:	n/a
15	chr3:75701993-75702043	GM12892	blood:	n/a
16	chr3:75720199-75720249	HepG2	liver:	n/a
17	chr3:75712695-75712745	HEEpiC	esophagus:	n/a
18	chr3:75701993-75702043	GM12878	blood:	n/a
19	chr3:75632533-75632583	MCF10A-Er-Src	breast:	n/a
20	chr3:75668758-75668808	HIPEpiC	eye:	n/a
21	chr3:75707805-75707855	HAEpiC	amniotic membrane:	n/a
22	chr3:75661320-75661370	HEK293	kidney:	embryo
23	chr3:75708197-75708247	NHDF-neo	bronchial:	n/a
24	chr3:75717453-75717503	AG04449	skin:	fetal
25	chr3:75712404-75712454	ProgFib	skin:	n/a
26	chr3:75715783-75715833	AG04450	lung:	fetal
27	chr3:75721434-75721484	GM12891	blood:	n/a
28	chr3:75701993-75702043	HepG2	liver:	n/a
29	chr3:75720199-75720249	HCM	heart:	n/a
30	chr3:75628819-75628869	ProgFib	skin:	n/a
31	chr3:75715783-75715833	HIPEpiC	eye:	n/a
32	chr3:75668369-75668419	T-47D	breast:	n/a
33	chr3:75658490-75658540	MCF-7	breast:	n/a
34	chr3:75659629-75659679	HRE	kidney:	n/a
35	chr3:75721577-75721627	Jurkat	blood:	n/a
36	chr3:75720876-75720926	AoSMC	blood vessel:	n/a
37	chr3:75669109-75669159	K562	blood:	n/a
38	chr3:75721434-75721484	HAEpiC	amniotic membrane:	n/a
39	chr3:75719149-75719199	Jurkat	blood:	n/a
40	chr3:75704824-75704874	AG04450	lung:	fetal
41	chr3:75720876-75720926	NH-A	brain:	n/a
42	chr3:75628819-75628869	NHDF-neo	bronchial:	n/a
43	chr3:75707990-75708040	HCF	heart:	n/a
44	chr3:75629433-75629483	T-47D	breast:	n/a
45	chr3:75667994-75668044	HCT-116	colon:	n/a
46	chr3:75701993-75702043	ProgFib	skin:	n/a
47	chr3:75657183-75657233	HEK293	kidney:	embryo
48	chr3:75708104-75708154	A549	lung:	n/a
49	chr3:75658552-75658602	NHBE	bronchial:	n/a
50	chr3:75668924-75668974	HEEpiC	esophagus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
2	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
3	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
4	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
5	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:
6	chr3:75717548..75719836-chr9:68411784..68414340,4	MCF-7	breast:
7	chr19:22025273..22026773-chr3:75695462..75697658,2	MCF-7	breast:
8	chr16:33943186..33943816-chr3:75719164..75719883,2	MCF-7	breast:
9	chr3:75718137..75719895-chr9:68411990..68414461,3	MCF-7	breast:

(count:26 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
2	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
3	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
4	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
5	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
6	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
7	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
8	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
9	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
10	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
11	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
12	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
13	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
14	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
15	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
16	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
17	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
18	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
19	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
20	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
21	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
22	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
23	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
24	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
25	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
26	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545

miRNA name	Chromosome Location	mirBase accession
hsa-miR-1324	chr3:75679974-75679997	MIMAT0005956

No data

Variant related genes	Relation type
UNC93B3	TF binding region
FRG2C	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
ENSG00000221602	TF binding region
MIR4273	TF binding region
AGGF1P3	TF binding region
LINC00960	TF binding region
RPS3AP15	TF binding region
OR7E121P	TF binding region
RN7SL92P	TF binding region
RARRES2P1	TF binding region
ENSG00000236138	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
FRG2C	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
ENSG00000221602	CpG island
MIR4273	CpG island
AGGF1P3	CpG island
LINC00960	CpG island
RPS3AP15	CpG island
OR7E121P	CpG island
RN7SL92P	CpG island
RARRES2P1	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000232815	chromatin interactions
ENSG00000236829	chromatin interactions
ENSG00000129925	chromatin interactions
ENSG00000212195	chromatin interactions

Extended variants
information (count: 12090 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:12090 , 50 per page) page: 1 2 3 4 5 6 7 ... 242

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4677536	chr3:75589320-75589321	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373452902	chr3:75589341-75589342	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs187564994	chr3:75589350-75589351	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs199761947	chr3:75589355-75589356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs55705970	chr3:75589359-75589360	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs139962270	chr3:75594909-75594910	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs201123528	chr3:75594946-75594947	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs78168426	chr3:75594947-75594948	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs188531370	chr3:75594948-75594949	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs199572933	chr3:75594990-75594991	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs181745514	chr3:75595010-75595011	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs186771921	chr3:75595011-75595012	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs564898407	chr3:75595046-75595047	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs532359174	chr3:75595056-75595057	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs547664951	chr3:75595059-75595060	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs372900524	chr3:75595061-75595062	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs141301938	chr3:75595464-75595465	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs201473906	chr3:75595475-75595476	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs59249015	chr3:75595481-75595482	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs10470600	chr3:75595493-75595494	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs554252688	chr3:75595496-75595497	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs185192156	chr3:75595503-75595504	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs536514755	chr3:75595509-75595510	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs143322336	chr3:75595541-75595542	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs555254463	chr3:75595552-75595553	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs576311904	chr3:75595558-75595559	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs577310375	chr3:75595572-75595573	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs79039305	chr3:75595592-75595593	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs543848527	chr3:75595602-75595603	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs186999254	chr3:75595605-75595606	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs10470601	chr3:75595640-75595641	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs143025160	chr3:75595645-75595646	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs541206908	chr3:75595652-75595653	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
34	rs201044726	chr3:75595658-75595659	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
35	rs144748463	chr3:75595659-75595660	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
36	rs144172223	chr3:75595660-75595661	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
37	rs147922761	chr3:75595715-75595716	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
38	rs189809187	chr3:75595718-75595719	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs200442518	chr3:75595770-75595771	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs530420715	chr3:75595773-75595774	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs182103204	chr3:75595803-75595804	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs4080300	chr3:75595808-75595809	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs28566971	chr3:75595823-75595824	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs79056913	chr3:75595889-75595890	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs4108676	chr3:75595901-75595902	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs4108677	chr3:75595902-75595903	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs376916946	chr3:75595907-75595908	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs76355224	chr3:75595929-75595930	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs3896095	chr3:75595930-75595931	Inactive region	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs76291779	chr3:75595935-75595936	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	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
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
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	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
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2648 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75599400-75601200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:75600600-75601200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr3:75608000-75608600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr3:75625600-75626000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr3:75625600-75628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr3:75625800-75626800	Enhancers	Breast Myoepithelial Primary Cells	Breast
7	chr3:75626000-75627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr3:75626800-75628200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
9	chr3:75627400-75628200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr3:75628000-75629000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:75628200-75628400	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr3:75628200-75628400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
13	chr3:75628200-75628400	Bivalent Enhancer	Fetal Kidney	kidney
14	chr3:75628200-75629400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
16	chr3:75628400-75628600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
17	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr3:75628400-75628600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
20	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr3:75628400-75629400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
22	chr3:75628400-75629400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
23	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
24	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
25	chr3:75628400-75629600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
26	chr3:75628400-75629600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
27	chr3:75628400-75629600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chr3:75628400-75629600	Active TSS	Breast Myoepithelial Primary Cells	Breast
29	chr3:75628400-75629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
30	chr3:75628400-75629800	Active TSS	Brain Cingulate Gyrus	brain
31	chr3:75628600-75628800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr3:75628600-75628800	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr3:75628600-75628800	Flanking Bivalent TSS/Enh	ES-UCSF4 Cell Line	embryonic stem cell
34	chr3:75628600-75628800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr3:75628600-75628800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
36	chr3:75628600-75628800	Enhancers	Brain Hippocampus Middle	brain
37	chr3:75628600-75628800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
38	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr3:75628600-75629000	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr3:75628600-75629000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr3:75628600-75629000	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
42	chr3:75628600-75629200	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
43	chr3:75628600-75629200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
44	chr3:75628600-75629200	Bivalent/Poised TSS	Fetal Intestine Large	intestine
45	chr3:75628600-75629400	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr3:75628600-75629600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell
47	chr3:75628600-75629600	Active TSS	H9 Cell Line	embryonic stem cell
48	chr3:75628600-75629600	Active TSS	Cortex derived primary cultured neurospheres	brain
49	chr3:75628600-75629600	Active TSS	Fetal Brain Female	brain
50	chr3:75628600-75629800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived

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