Variant report

Variant	nsv834737
Chromosome Location	chr3:75558251-75761573
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4781)
CpG islands
(count:3485)
Chromatin interactive
region (count:8)
LncRNA
region (count:26)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:4781 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
2	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
3	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
4	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
5	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
6	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
7	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
8	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
10	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
11	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
12	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
13	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
14	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
15	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
16	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
17	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
18	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
19	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
20	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
21	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
22	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
23	ATF1	chr3:75728107-75728162	K562	blood:	n/a	n/a
24	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
25	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
26	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
27	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
28	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a
29	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
30	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
31	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
32	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
33	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
34	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
35	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
36	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
37	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
38	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
39	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
40	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
41	ATF3	chr3:75718289-75718505	K562	blood:	n/a	n/a
42	ATF3	chr3:75717987-75718165	K562	blood:	n/a	n/a
43	BACH1	chr3:75682306-75682660	K562	blood:	n/a	n/a
44	BACH1	chr3:75691900-75692752	K562	blood:	n/a	n/a
45	BACH1	chr3:75717886-75719337	K562	blood:	n/a	n/a
46	BACH1	chr3:75734445-75734852	K562	blood:	n/a	n/a
47	BACH1	chr3:75710659-75710761	K562	blood:	n/a	n/a
48	BACH1	chr3:75735200-75735345	K562	blood:	n/a	n/a
49	BACH1	chr3:75739253-75739499	K562	blood:	n/a	n/a
50	BACH1	chr3:75744812-75745060	K562	blood:	n/a	n/a

(count:3485 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75721888-75721938	HUVEC	blood vessel:	n/a
2	chr3:75668035-75668085	NHDF-neo	bronchial:	n/a
3	chr3:75717248-75717298	HIPEpiC	eye:	n/a
4	chr3:75712695-75712745	SK-N-SH	brain:	n/a
5	chr3:75668758-75668808	SK-N-SH_RA	brain:	n/a
6	chr3:75705108-75705158	GM12878	blood:	n/a
7	chr3:75721888-75721938	SAEC	small airway:	n/a
8	chr3:75666392-75666442	AG10803	skin:	n/a
9	chr3:75721888-75721938	HUVEC	blood vessel:	n/a
10	chr3:75668035-75668085	NHDF-neo	bronchial:	n/a
11	chr3:75717248-75717298	HIPEpiC	eye:	n/a
12	chr3:75712695-75712745	SK-N-SH	brain:	n/a
13	chr3:75668758-75668808	SK-N-SH_RA	brain:	n/a
14	chr3:75705108-75705158	GM12878	blood:	n/a
15	chr3:75721888-75721938	SAEC	small airway:	n/a
16	chr3:75666392-75666442	AG10803	skin:	n/a
17	chr3:75659629-75659679	HAEpiC	amniotic membrane:	n/a
18	chr3:75628819-75628869	A549	lung:	n/a
19	chr3:75721577-75721627	CMK	blood:	n/a
20	chr3:75720876-75720926	HEK293	kidney:	embryo
21	chr3:75717453-75717503	A549	lung:	n/a
22	chr3:75690456-75690506	HCPEpiC	choroid plexus:	n/a
23	chr3:75668369-75668419	ovcar-3	ovarian:	n/a
24	chr3:75661320-75661370	LNCaP	prostate:	n/a
25	chr3:75666381-75666431	BJ	skin:	n/a
26	chr3:75712404-75712454	NB4	blood:	n/a
27	chr3:75653319-75653369	K562	blood:	n/a
28	chr3:75632533-75632583	HNPCEpiC	eye:	n/a
29	chr3:75707560-75707610	AG04450	lung:	fetal
30	chr3:75632533-75632583	BJ	skin:	n/a
31	chr3:75707805-75707855	ProgFib	skin:	n/a
32	chr3:75690456-75690506	GM12878	blood:	n/a
33	chr3:75671115-75671165	AG09309	skin:	n/a
34	chr3:75721434-75721484	LNCaP	prostate:	n/a
35	chr3:75717453-75717503	ovcar-3	ovarian:	n/a
36	chr3:75720199-75720249	SAEC	small airway:	n/a
37	chr3:75717248-75717298	HL-60	blood:	n/a
38	chr3:75705922-75705972	HRE	kidney:	n/a
39	chr3:75707805-75707855	NH-A	brain:	n/a
40	chr3:75657183-75657233	PANC-1	pancreas:	n/a
41	chr3:75690456-75690506	ECC-1	luminal epithelium:	n/a
42	chr3:75657758-75657808	HRE	kidney:	n/a
43	chr3:75721888-75721938	Caco-2	colon:	n/a
44	chr3:75712404-75712454	U87	brain:	n/a
45	chr3:75658735-75658785	ProgFib	skin:	n/a
46	chr3:75712404-75712454	AG10803	skin:	n/a
47	chr3:75714447-75714497	SK-N-SH	brain:	n/a
48	chr3:75653319-75653369	HCM	heart:	n/a
49	chr3:75666392-75666442	Jurkat	blood:	n/a
50	chr3:75720199-75720249	HL-60	blood:	n/a

(count:8 , 50 per page) page: 1

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
2	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925
3	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
4	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
5	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
6	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
7	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
8	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
9	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
10	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
11	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
12	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
13	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
14	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
15	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
16	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
17	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
18	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
19	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
20	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
21	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
22	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
23	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
24	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
25	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
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
LINC00960	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
RARRES2P1	TF binding region
ENSG00000221602	TF binding region
AGGF1P3	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
LINC00960	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RARRES2P1	CpG island
ENSG00000221602	CpG island
AGGF1P3	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000236829	chromatin interactions
ENSG00000232815	chromatin interactions
ENSG00000129925	chromatin interactions

Extended variants
information (count: 10910 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:10910 , 50 per page) page: 1 2 3 4 5 6 7 ... 219

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542589394	chr3:75558304-75558305	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs560535309	chr3:75558310-75558311	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs192852236	chr3:75558313-75558314	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs543064587	chr3:75558318-75558319	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs564645682	chr3:75558331-75558332	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs2944654	chr3:75558346-75558347	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs115212056	chr3:75558351-75558352	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs185208901	chr3:75558354-75558355	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs9682226	chr3:75558356-75558357	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs144891567	chr3:75558385-75558386	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs567618862	chr3:75558414-75558415	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs116357195	chr3:75558431-75558432	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs550265110	chr3:75558432-75558433	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs571790148	chr3:75558455-75558456	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs149043722	chr3:75558467-75558468	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs190535775	chr3:75558486-75558487	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs3895034	chr3:75558498-75558499	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs1711613	chr3:75558522-75558523	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs192501775	chr3:75558524-75558525	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs554443658	chr3:75558525-75558526	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs1711612	chr3:75558532-75558533	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs9682241	chr3:75558551-75558552	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs558160843	chr3:75558587-75558588	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs576858152	chr3:75558606-75558607	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs183778324	chr3:75558608-75558609	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs9682091	chr3:75558622-75558623	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs527884995	chr3:75558628-75558629	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs543302542	chr3:75558645-75558646	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs188119230	chr3:75558659-75558660	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs1810328	chr3:75558666-75558667	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs71627430	chr3:75558668-75558669	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs76590685	chr3:75558695-75558696	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs9681430	chr3:75558696-75558697	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs571701290	chr3:75558715-75558716	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs3895033	chr3:75558728-75558729	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs3895032	chr3:75558733-75558734	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs1711611	chr3:75558749-75558750	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1711610	chr3:75558767-75558768	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs12631335	chr3:75558811-75558812	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370977622	chr3:75558818-75558819	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs536063710	chr3:75558874-75558875	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs2459508	chr3:75558876-75558877	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs184631670	chr3:75558897-75558898	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs139685809	chr3:75558909-75558910	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs558122045	chr3:75558915-75558916	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs115199110	chr3:75558958-75558959	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs541076199	chr3:75559011-75559012	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs552804633	chr3:75559016-75559017	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs572565456	chr3:75559022-75559023	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs543265650	chr3:75559033-75559034	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2339 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75545800-75562400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:75558200-75558400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr3:75560600-75562200	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
4	chr3:75561200-75561600	Active TSS	Fetal Heart	heart
5	chr3:75561800-75562200	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
6	chr3:75562200-75574200	Weak transcription	Skeletal Muscle Female	skeletal muscle
7	chr3:75562400-75562800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr3:75562800-75566000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr3:75563400-75564600	ZNF genes & repeats	Rectal Mucosa Donor 31	rectum
10	chr3:75564200-75564600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr3:75566000-75567000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:75567000-75571400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr3:75571400-75573400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:75573400-75575600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr3:75574200-75575800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr3:75575600-75575800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr3:75581000-75585800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr3:75586600-75586800	ZNF genes & repeats	Ovary	ovary
19	chr3:75586800-75587400	Weak transcription	Ovary	ovary
20	chr3:75599400-75601200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr3:75600600-75601200	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr3:75608000-75608600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr3:75625600-75626000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
24	chr3:75625600-75628000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr3:75625800-75626800	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr3:75626000-75627400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr3:75626800-75628200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr3:75627400-75628200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr3:75628000-75629000	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr3:75628200-75628400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr3:75628200-75628400	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
32	chr3:75628200-75628400	Bivalent Enhancer	Fetal Kidney	kidney
33	chr3:75628200-75629400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
35	chr3:75628400-75628600	Bivalent/Poised TSS	H9 Cell Line	embryonic stem cell
36	chr3:75628400-75628600	Flanking Bivalent TSS/Enh	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr3:75628400-75628600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
38	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
39	chr3:75628400-75628600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr3:75628400-75629400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr3:75628400-75629400	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
43	chr3:75628400-75629400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
44	chr3:75628400-75629600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
45	chr3:75628400-75629600	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
46	chr3:75628400-75629600	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
47	chr3:75628400-75629600	Active TSS	Breast Myoepithelial Primary Cells	Breast
48	chr3:75628400-75629600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr3:75628400-75629800	Active TSS	Brain Cingulate Gyrus	brain
50	chr3:75628600-75628800	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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