Variant report

Variant	nsv1001674
Chromosome Location	chr3:75514396-75781697
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5586)
CpG islands
(count:3852)
Chromatin interactive
region (count:9)
LncRNA
region (count:27)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:5586 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75693043-75693065	K562	blood:	n/a	n/a
2	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
3	ARID3A	chr3:75770122-75770154	HepG2	liver:	n/a	n/a
4	ARID3A	chr3:75719697-75719867	HepG2	liver:	n/a	n/a
5	ARID3A	chr3:75710663-75710916	HepG2	liver:	n/a	n/a
6	ARID3A	chr3:75717896-75719229	K562	blood:	n/a	n/a
7	ARID3A	chr3:75739156-75739286	K562	blood:	n/a	n/a
8	ARID3A	chr3:75718141-75718928	HepG2	liver:	n/a	n/a
9	ARID3A	chr3:75691908-75692517	K562	blood:	n/a	n/a
10	ARID3A	chr3:75710659-75710674	K562	blood:	n/a	n/a
11	ARID3A	chr3:75754843-75755270	K562	blood:	n/a	n/a
12	ARID3A	chr3:75693851-75694060	K562	blood:	n/a	n/a
13	ARID3A	chr3:75736701-75737480	K562	blood:	n/a	n/a
14	ATF1	chr3:75777037-75777776	K562	blood:	n/a	n/a
15	ATF1	chr3:75735197-75735394	K562	blood:	n/a	n/a
16	ATF1	chr3:75691118-75692520	K562	blood:	n/a	n/a
17	ATF1	chr3:75760657-75761408	K562	blood:	n/a	n/a
18	ATF1	chr3:75747229-75747380	K562	blood:	n/a	n/a
19	ATF1	chr3:75769325-75769986	K562	blood:	n/a	n/a
20	ATF1	chr3:75733400-75734148	K562	blood:	n/a	n/a
21	ATF1	chr3:75730688-75730845	K562	blood:	n/a	n/a
22	ATF1	chr3:75695108-75700001	K562	blood:	n/a	n/a
23	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
24	ATF1	chr3:75690145-75690820	K562	blood:	n/a	n/a
25	ATF1	chr3:75743644-75744222	K562	blood:	n/a	n/a
26	ATF1	chr3:75740338-75740804	K562	blood:	n/a	n/a
27	ATF1	chr3:75759504-75760427	K562	blood:	n/a	n/a
28	ATF1	chr3:75685926-75686418	K562	blood:	n/a	n/a
29	ATF1	chr3:75779002-75782622	K562	blood:	n/a	n/a
30	ATF1	chr3:75710744-75710785	K562	blood:	n/a	n/a
31	ATF1	chr3:75735948-75736287	K562	blood:	n/a	n/a
32	ATF1	chr3:75761625-75762259	K562	blood:	n/a	n/a
33	ATF1	chr3:75773435-75776229	K562	blood:	n/a	n/a
34	ATF1	chr3:75746545-75746765	K562	blood:	n/a	n/a
35	ATF1	chr3:75771441-75772260	K562	blood:	n/a	n/a
36	ATF1	chr3:75734703-75734852	K562	blood:	n/a	n/a
37	ATF1	chr3:75763746-75764601	K562	blood:	n/a	n/a
38	ATF1	chr3:75726782-75726783	K562	blood:	n/a	n/a
39	ATF1	chr3:75745544-75745744	K562	blood:	n/a	n/a
40	ATF1	chr3:75762715-75762961	K562	blood:	n/a	n/a
41	ATF1	chr3:75703512-75703565	K562	blood:	n/a	n/a
42	ATF1	chr3:75755512-75756182	K562	blood:	n/a	n/a
43	ATF1	chr3:75693870-75694088	K562	blood:	n/a	n/a
44	ATF1	chr3:75778219-75778585	K562	blood:	n/a	n/a
45	ATF1	chr3:75736867-75738707	K562	blood:	n/a	n/a
46	ATF1	chr3:75689319-75689814	K562	blood:	n/a	n/a
47	ATF1	chr3:75728521-75728535	K562	blood:	n/a	n/a
48	ATF1	chr3:75754856-75755222	K562	blood:	n/a	n/a
49	ATF1	chr3:75765400-75768808	K562	blood:	n/a	n/a
50	ATF1	chr3:75750030-75750205	K562	blood:	n/a	n/a

(count:3852 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75653319-75653369	SK-N-SH_RA	brain:	n/a
2	chr3:75705922-75705972	HCT-116	colon:	n/a
3	chr3:75629433-75629483	GM12878	blood:	n/a
4	chr3:75555994-75556044	Jurkat	blood:	n/a
5	chr3:75668035-75668085	HCF	heart:	n/a
6	chr3:75705108-75705158	PFSK-1	brain:	n/a
7	chr3:75712695-75712745	GM19239	blood:	n/a
8	chr3:75720876-75720926	A549	lung:	n/a
9	chr3:75712695-75712745	SKMC	muscle:	n/a
10	chr3:75653319-75653369	SK-N-SH_RA	brain:	n/a
11	chr3:75705922-75705972	HCT-116	colon:	n/a
12	chr3:75629433-75629483	GM12878	blood:	n/a
13	chr3:75555994-75556044	Jurkat	blood:	n/a
14	chr3:75668035-75668085	HCF	heart:	n/a
15	chr3:75705108-75705158	PFSK-1	brain:	n/a
16	chr3:75712695-75712745	GM19239	blood:	n/a
17	chr3:75720876-75720926	A549	lung:	n/a
18	chr3:75712695-75712745	SKMC	muscle:	n/a
19	chr3:75653319-75653369	BE2_C	brain:	n/a
20	chr3:75629039-75629089	K562	blood:	n/a
21	chr3:75666381-75666431	SKMC	muscle:	n/a
22	chr3:75667994-75668044	HRCEpiC	kidney:	n/a
23	chr3:75556027-75556077	NH-A	brain:	n/a
24	chr3:75631426-75631476	ECC-1	luminal epithelium:	n/a
25	chr3:75717453-75717503	CMK	blood:	n/a
26	chr3:75553294-75553344	GM12892	blood:	n/a
27	chr3:75707560-75707610	HCF	heart:	n/a
28	chr3:75658735-75658785	NB4	blood:	n/a
29	chr3:75705108-75705158	GM12891	blood:	n/a
30	chr3:75553762-75553812	AG04449	skin:	fetal
31	chr3:75658735-75658785	GM12891	blood:	n/a
32	chr3:75666381-75666431	MCF10A-Er-Src	breast:	n/a
33	chr3:75668035-75668085	A549	lung:	n/a
34	chr3:75632533-75632583	HMEC	breast:	n/a
35	chr3:75629039-75629089	NB4	blood:	n/a
36	chr3:75658410-75658460	Caco-2	colon:	n/a
37	chr3:75720876-75720926	AG04449	skin:	fetal
38	chr3:75661799-75661849	HCT-116	colon:	n/a
39	chr3:75658410-75658460	SAEC	small airway:	n/a
40	chr3:75704498-75704548	AG04450	lung:	fetal
41	chr3:75668369-75668419	MCF10A-Er-Src	breast:	n/a
42	chr3:75721577-75721627	T-47D	breast:	n/a
43	chr3:75721888-75721938	HEK293	kidney:	embryo
44	chr3:75701993-75702043	AoSMC	blood vessel:	n/a
45	chr3:75553723-75553773	HNPCEpiC	eye:	n/a
46	chr3:75668758-75668808	K562	blood:	n/a
47	chr3:75667994-75668044	LNCaP	prostate:	n/a
48	chr3:75704824-75704874	HNPCEpiC	eye:	n/a
49	chr3:75720876-75720926	NT2-D1	testis:	n/a
50	chr3:75667994-75668044	CMK	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr17:56709052..56711813-chr3:75770362..75772517,2	MCF-7	breast:
2	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
3	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
4	chr3:75692090..75692596-chr7:138578273..138578773,2	K562	blood:
5	chr3:75718137..75719895-chr9:68411990..68414461,3	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	chr3:75693392..75694000-chr5:103852101..103852601,2	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF717-1	chr3:75716700-75717742	NONHSAT090545
2	lnc-FRG2C-7	chr3:75713970-75714047	NR_037925
3	lnc-ZNF717-1	chr3:75719171-75721030	NONHSAT090545
4	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
5	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
6	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
7	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
8	lnc-ZNF717-2	chr3:75695572-75695597	XLOC_003164
9	lnc-FRG2C-1	chr3:75723564-75725031	ENSG00000242516
10	lnc-FRG2C-10	chr3:75687750-75688507	NONHSAT090542
11	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540
12	lnc-ZNF717-2	chr3:75691158-75691575	XLOC_003164
13	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
14	lnc-FRG2C-1	chr3:75725119-75725776	ENSG00000242516
15	lnc-ZNF717-1	chr3:75719171-75721122	ENSG00000234317
16	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
17	lnc-ZNF717-1	chr3:75721121-75721241	NONHSAT090545
18	lnc-ZNF717-1	chr3:75716700-75717742	ENSG00000234317
19	lnc-CNTN3-1	chr3:75762167-75762465	NONHSAT090550
20	lnc-ZNF717-1	chr3:75719171-75719204	NONHSAT090540
21	lnc-FRG2C-7	chr3:75714277-75714354	NR_037925
22	lnc-FRG2C-10	chr3:75694930-75696049	NONHSAT090542
23	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
24	lnc-FRG2C-7	chr3:75714678-75716368	NR_037925
25	lnc-FRG2C-10	chr3:75691156-75691895	NONHSAT090542
26	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
27	lnc-FRG2C-7	chr3:75713481-75713708	NR_037925

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
AGGF1P3	TF binding region
LINC00960	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
RN7SL92P	TF binding region
RARRES2P1	TF binding region
ENPP7P2	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
AGGF1P3	CpG island
LINC00960	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
RN7SL92P	CpG island
RARRES2P1	CpG island
ENPP7P2	CpG island
ENSG00000236138	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000129925	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000232815	chromatin interactions
ENSG00000236829	chromatin interactions

Extended variants
information (count: 14824 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:14824 , 50 per page) page: 1 2 3 4 5 6 7 ... 297

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7653202	chr3:75514396-75514397	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs553268459	chr3:75514397-75514398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574749443	chr3:75514410-75514411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147291394	chr3:75514412-75514413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371685952	chr3:75514436-75514437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs557389000	chr3:75514442-75514443	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575643427	chr3:75514469-75514470	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs116655152	chr3:75514475-75514476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531446946	chr3:75514500-75514501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs547930779	chr3:75514506-75514507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564249599	chr3:75514541-75514542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573106799	chr3:75514583-75514584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs7374535	chr3:75514604-75514605	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs561854378	chr3:75514613-75514614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140922772	chr3:75514619-75514620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs149787659	chr3:75514628-75514629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs562545817	chr3:75514645-75514646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs7374358	chr3:75514646-75514647	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs374582071	chr3:75514686-75514687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570679037	chr3:75514692-75514693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs148507372	chr3:75514701-75514702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs547227358	chr3:75514702-75514703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568672224	chr3:75514712-75514713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs57225284	chr3:75514730-75514731	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs557071779	chr3:75514734-75514735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs59092908	chr3:75514743-75514744	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs539922954	chr3:75514745-75514746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs558297109	chr3:75514754-75514755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs573045482	chr3:75514775-75514776	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs540430415	chr3:75514777-75514778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs140376652	chr3:75514836-75514837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573843745	chr3:75514837-75514838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544523464	chr3:75514847-75514848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145586995	chr3:75514857-75514858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs72885134	chr3:75514942-75514943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs183144315	chr3:75514967-75514968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373101699	chr3:75514981-75514982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34044963	chr3:75515026-75515027	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs546867364	chr3:75515038-75515039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs535944630	chr3:75515048-75515049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs140836466	chr3:75515078-75515079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs150112468	chr3:75515111-75515112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62259153	chr3:75515112-75515113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs569242421	chr3:75515140-75515141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs149240153	chr3:75515159-75515160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs146921500	chr3:75515177-75515178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs137927887	chr3:75515178-75515179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs534343149	chr3:75515210-75515211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369570188	chr3:75515245-75515246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201358293	chr3:75515271-75515272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Non-syndromic sensorineural hearing loss	18451855	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
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:2712 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75502800-75517600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr3:75517800-75518600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr3:75520200-75521200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr3:75523000-75523400	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr3:75524200-75524600	Active TSS	H9 Cell Line	embryonic stem cell
6	chr3:75538400-75540400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr3:75539800-75540400	ZNF genes & repeats	Fetal Intestine Small	intestine
8	chr3:75539800-75542400	Weak transcription	Ovary	ovary
9	chr3:75540200-75540600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:75542600-75551400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr3:75544400-75552000	Weak transcription	Ovary	ovary
12	chr3:75545800-75562400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr3:75546200-75550800	Weak transcription	Fetal Intestine Small	intestine
14	chr3:75546800-75551400	Weak transcription	Fetal Lung	lung
15	chr3:75548000-75548200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr3:75548200-75552000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr3:75549000-75551600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr3:75549200-75549800	Enhancers	Fetal Intestine Large	intestine
19	chr3:75549200-75550200	Enhancers	K562	blood
20	chr3:75549800-75550800	Weak transcription	Fetal Intestine Large	intestine
21	chr3:75550200-75550800	Weak transcription	K562	blood
22	chr3:75550200-75553600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr3:75550600-75552800	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr3:75550800-75551000	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr3:75550800-75551200	Enhancers	Fetal Heart	heart
26	chr3:75550800-75551200	Enhancers	Stomach Mucosa	stomach
27	chr3:75550800-75551400	Enhancers	Fetal Intestine Large	intestine
28	chr3:75550800-75551400	Enhancers	Fetal Intestine Small	intestine
29	chr3:75550800-75552000	Enhancers	K562	blood
30	chr3:75550800-75552800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr3:75551000-75551400	Enhancers	Small Intestine	intestine
32	chr3:75551000-75552400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
33	chr3:75551400-75551600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr3:75551400-75551600	Weak transcription	Small Intestine	intestine
35	chr3:75551400-75552000	Enhancers	Fetal Lung	lung
36	chr3:75551400-75552200	Active TSS	Fetal Heart	heart
37	chr3:75551400-75552400	Active TSS	Skeletal Muscle Female	skeletal muscle
38	chr3:75551400-75552400	Active TSS	Stomach Mucosa	stomach
39	chr3:75551400-75552600	Enhancers	H9 Cell Line	embryonic stem cell
40	chr3:75551400-75552600	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr3:75551400-75552600	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr3:75551400-75552600	Active TSS	Duodenum Mucosa	Duodenum
43	chr3:75551400-75552800	Active TSS	Fetal Intestine Small	intestine
44	chr3:75551400-75552800	Active TSS	Right Atrium	heart
45	chr3:75551400-75553000	Active TSS	Rectal Mucosa Donor 29	rectum
46	chr3:75551400-75554000	Active TSS	Fetal Intestine Large	intestine
47	chr3:75551600-75551800	Active TSS	Small Intestine	intestine
48	chr3:75551600-75552000	Enhancers	Fetal Muscle Leg	muscle
49	chr3:75551600-75552400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr3:75551600-75552600	Active TSS	Left Ventricle	heart

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