Variant report

Variant	nsv876964
Chromosome Location	chr3:75202547-75437889
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1615)
CpG islands
(count:1161)
Chromatin interactive
region (count:18)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1615 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75308537-75308777	HepG2	liver:	n/a	n/a
2	ATF1	chr3:75273635-75274085	K562	blood:	n/a	n/a
3	ATF2	chr3:75229597-75230101	GM12878	blood:	n/a	n/a
4	ATF2	chr3:75241228-75241540	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr3:75229570-75230214	GM12878	blood:	n/a	n/a
6	BACH1	chr3:75390901-75391145	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr3:75229707-75230159	GM12878	blood:	n/a	n/a
8	BATF	chr3:75411604-75411874	GM12878	blood:	n/a	n/a
9	BATF	chr3:75411520-75411813	GM12878	blood:	n/a	n/a
10	BATF	chr3:75334734-75335096	GM12878	blood:	n/a	n/a
11	BATF	chr3:75386395-75386620	GM12878	blood:	n/a	n/a
12	BCL11A	chr3:75229596-75230089	GM12878	blood:	n/a	n/a
13	BCL11A	chr3:75229688-75230088	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:75334858-75335107	GM12878	blood:	n/a	n/a
15	BCL3	chr3:75229695-75230085	GM12878	blood:	n/a	n/a
16	BCL3	chr3:75395680-75395995	GM12878	blood:	n/a	n/a
17	BCL3	chr3:75429024-75429912	GM12878	blood:	n/a	n/a
18	BCL3	chr3:75417298-75417641	GM12878	blood:	n/a	n/a
19	BCL3	chr3:75416737-75417040	GM12878	blood:	n/a	n/a
20	BCL3	chr3:75407756-75407999	GM12878	blood:	n/a	n/a
21	BCL3	chr3:75428941-75429895	GM12878	blood:	n/a	n/a
22	BCL3	chr3:75417319-75417660	GM12878	blood:	n/a	n/a
23	BHLHE40	chr3:75429659-75429896	K562	blood:	n/a	n/a
24	BHLHE40	chr3:75275145-75275162	GM12878	blood:	n/a	n/a
25	BHLHE40	chr3:75226190-75226494	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:75227294-75227303	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:75229629-75230115	GM12878	blood:	n/a	n/a
28	CEBPB	chr3:75304679-75304870	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr3:75334749-75334963	IMR90	lung:	n/a	n/a
30	CEBPB	chr3:75235119-75235256	H1-hESC	embryonic stem cell:	n/a	chr3:75235211-75235224
31	CEBPB	chr3:75308521-75308803	HepG2	liver:	n/a	chr3:75308643-75308654
32	CEBPB	chr3:75298279-75298413	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr3:75273586-75274005	Hela-S3	cervix:	n/a	chr3:75273812-75273823
34	CEBPB	chr3:75273634-75273992	A549	lung:	n/a	chr3:75273812-75273823
35	CEBPB	chr3:75273652-75273997	HepG2	liver:	n/a	chr3:75273812-75273823
36	CEBPB	chr3:75242621-75242943	IMR90	lung:	n/a	chr3:75242773-75242784
37	CEBPB	chr3:75236445-75236543	K562	blood:	n/a	n/a
38	CEBPB	chr3:75236311-75236614	IMR90	lung:	n/a	chr3:75236334-75236347
39	CEBPB	chr3:75341243-75341447	IMR90	lung:	n/a	n/a
40	CEBPB	chr3:75242648-75242901	A549	lung:	n/a	chr3:75242773-75242784
41	CEBPB	chr3:75236305-75236610	HepG2	liver:	n/a	chr3:75236334-75236347
42	CEBPB	chr3:75298676-75298908	IMR90	lung:	n/a	chr3:75298746-75298757
43	CEBPB	chr3:75308543-75308721	HepG2	liver:	n/a	chr3:75308643-75308654
44	CEBPB	chr3:75224080-75224265	IMR90	lung:	n/a	chr3:75224186-75224195 chr3:75224184-75224195 chr3:75224186-75224195 chr3:75224184-75224197 chr3:75224186-75224195 chr3:75224186-75224195 chr3:75224184-75224197
45	CEBPB	chr3:75298607-75298890	HepG2	liver:	n/a	chr3:75298746-75298757
46	CEBPB	chr3:75336625-75336889	IMR90	lung:	n/a	n/a
47	CEBPB	chr3:75321899-75322205	IMR90	lung:	n/a	n/a
48	CEBPB	chr3:75242606-75242929	HepG2	liver:	n/a	chr3:75242773-75242784
49	CEBPB	chr3:75223799-75223857	IMR90	lung:	n/a	n/a
50	CEBPB	chr3:75236452-75236563	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75263641-75263691	HCPEpiC	choroid plexus:	n/a
2	chr3:75263641-75263691	ovcar-3	ovarian:	n/a
3	chr3:75263641-75263691	HCPEpiC	choroid plexus:	n/a
4	chr3:75263641-75263691	ovcar-3	ovarian:	n/a
5	chr3:75411217-75411267	HIPEpiC	eye:	n/a
6	chr3:75416171-75416221	AG04449	skin:	fetal
7	chr3:75263641-75263691	PANC-1	pancreas:	n/a
8	chr3:75411421-75411471	HIPEpiC	eye:	n/a
9	chr3:75411421-75411471	GM12892	blood:	n/a
10	chr3:75411421-75411471	PFSK-1	brain:	n/a
11	chr3:75263626-75263676	ovcar-3	ovarian:	n/a
12	chr3:75415526-75415576	PFSK-1	brain:	n/a
13	chr3:75263685-75263735	AG09319	gingival:	n/a
14	chr3:75410747-75410797	AG04450	lung:	fetal
15	chr3:75413083-75413133	RPTEC	kidney:	n/a
16	chr3:75263626-75263676	A549	lung:	n/a
17	chr3:75411217-75411267	ECC-1	luminal epithelium:	n/a
18	chr3:75414486-75414536	ovcar-3	ovarian:	n/a
19	chr3:75411038-75411088	GM12892	blood:	n/a
20	chr3:75415526-75415576	HCT-116	colon:	n/a
21	chr3:75410789-75410839	GM06990	blood:	n/a
22	chr3:75328275-75328325	MCF10A-Er-Src	breast:	n/a
23	chr3:75263691-75263741	NH-A	brain:	n/a
24	chr3:75412866-75412916	GM12891	blood:	n/a
25	chr3:75411217-75411267	NHBE	bronchial:	n/a
26	chr3:75411421-75411471	U87	brain:	n/a
27	chr3:75263619-75263669	ovcar-3	ovarian:	n/a
28	chr3:75263619-75263669	HCT-116	colon:	n/a
29	chr3:75416171-75416221	HNPCEpiC	eye:	n/a
30	chr3:75411038-75411088	HL-60	blood:	n/a
31	chr3:75416171-75416221	HRPEpiC	eye:	n/a
32	chr3:75411038-75411088	ECC-1	luminal epithelium:	n/a
33	chr3:75263619-75263669	HepG2	liver:	n/a
34	chr3:75415526-75415576	HCM	heart:	n/a
35	chr3:75328275-75328325	SK-N-SH_RA	brain:	n/a
36	chr3:75413083-75413133	GM12878	blood:	n/a
37	chr3:75414486-75414536	Hepatocyte	liver:	n/a
38	chr3:75415591-75415641	HNPCEpiC	eye:	n/a
39	chr3:75413083-75413133	BJ	skin:	n/a
40	chr3:75410747-75410797	A549	lung:	n/a
41	chr3:75263685-75263735	MCF10A-Er-Src	breast:	n/a
42	chr3:75328275-75328325	HCPEpiC	choroid plexus:	n/a
43	chr3:75416171-75416221	AoSMC	blood vessel:	n/a
44	chr3:75411038-75411088	GM19239	blood:	n/a
45	chr3:75263685-75263735	PFSK-1	brain:	n/a
46	chr3:75263626-75263676	Caco-2	colon:	n/a
47	chr3:75415561-75415611	NB4	blood:	n/a
48	chr3:75415591-75415641	PANC-1	pancreas:	n/a
49	chr3:75413083-75413133	MCF-7	breast:	n/a
50	chr3:75328275-75328325	HMEC	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:75343455..75344253-chr3:75389889..75390567,2	MCF-7	breast:
2	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:
3	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
4	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
5	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
6	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
7	chr3:75308414..75309217-chr3:75343438..75343942,2	MCF-7	breast:
8	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:
9	chr3:75308414..75309217-chr3:75343438..75343942,2	MCF-7	breast:
10	chr3:75343455..75344253-chr3:75389889..75390567,2	MCF-7	breast:
11	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
12	chr3:75248466..75250220-chr3:75254434..75257051,2	K562	blood:
13	chr3:75225822..75228445-chr3:75228843..75230349,2	MCF-7	breast:
14	chr3:75105526..75106181-chr3:75220559..75221295,2	MCF-7	breast:
15	chr3:75215422..75217161-chr3:75220288..75221815,2	K562	blood:
16	chr3:75215422..75217161-chr3:75220288..75221815,2	K562	blood:
17	chr3:75299981..75301854-chr3:75306203..75307918,2	MCF-7	breast:
18	chr3:75299981..75301854-chr3:75306203..75307918,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-4	chr3:75273648-75273709	NONHSAT090505
2	lnc-FRG2C-4	chr3:75273688-75273709	XLOC_002709
3	lnc-FRG2C-4	chr3:75289336-75289618	XLOC_002709
4	lnc-ZNF717-7	chr3:75264644-75264868	NONHSAT090504
5	lnc-ZNF717-7	chr3:75264616-75264635	NONHSAT090504
6	lnc-FRG2C-4	chr3:75289333-75289869	NONHSAT090505
7	lnc-ZNF717-7	chr3:75264310-75264481	NONHSAT090504
8	lnc-ZNF717-8	chr3:75231907-75232199	NONHSAT090502
9	lnc-FRG2C-4	chr3:75289122-75289170	NONHSAT090505

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4444	chr3:75263669-75263686	MIMAT0018962_1

No data

Variant related genes	Relation type
ENSG00000266685	TF binding region
OR7E55P	TF binding region
RN7SL294P	TF binding region
OR7E66P	TF binding region
MYLKP1	TF binding region
OR7E22P	TF binding region
HNRNPA3P6	TF binding region
MIR4444-1	TF binding region
ENSG00000263782	TF binding region
ENSG00000266685	CpG island
OR7E55P	CpG island
RN7SL294P	CpG island
OR7E66P	CpG island
MYLKP1	CpG island
OR7E22P	CpG island
HNRNPA3P6	CpG island
MIR4444-1	CpG island
ENSG00000263782	CpG island
FAM20C	miRNA target sites
FAM199X	miRNA target sites

Extended variants
information (count: 6759 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6759 , 50 per page) page: 1 2 3 4 5 6 7 ... 136

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566967877	chr3:75214610-75214611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs567298261	chr3:75214679-75214680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145684548	chr3:75214688-75214689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556536726	chr3:75214711-75214712	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs34094450	chr3:75214718-75214719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs540695561	chr3:75214727-75214728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs372710362	chr3:75214744-75214745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs77594192	chr3:75214753-75214754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs538456465	chr3:75214768-75214769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143183495	chr3:75214788-75214789	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs7427152	chr3:75214789-75214790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188995739	chr3:75214804-75214805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148283408	chr3:75214845-75214846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs559268266	chr3:75214854-75214855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs141728864	chr3:75214856-75214857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs530026845	chr3:75214866-75214867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs563085623	chr3:75214882-75214883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs145482574	chr3:75214910-75214911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs537942474	chr3:75214965-75214966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs138043819	chr3:75214969-75214970	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs117644571	chr3:75214992-75214993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192960175	chr3:75215015-75215016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs117394356	chr3:75215028-75215029	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs118181881	chr3:75215049-75215050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs527861253	chr3:75215075-75215076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184618986	chr3:75215153-75215154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs117166648	chr3:75215231-75215232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530759199	chr3:75215241-75215242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs7431394	chr3:75215245-75215246	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs571584677	chr3:75215249-75215250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs74527889	chr3:75215254-75215255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs113244737	chr3:75215260-75215261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs553764862	chr3:75215262-75215263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs7429678	chr3:75215307-75215308	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs372111955	chr3:75215363-75215364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs529551251	chr3:75215396-75215397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530930603	chr3:75220026-75220027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552637109	chr3:75220060-75220061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35790348	chr3:75220067-75220068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs571085858	chr3:75220113-75220114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187375829	chr3:75220152-75220153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547141979	chr3:75220160-75220161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs147326052	chr3:75220211-75220212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs535207856	chr3:75220221-75220222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs564665707	chr3:75220267-75220268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs61241357	chr3:75220269-75220270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs75850438	chr3:75220288-75220289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574938277	chr3:75220294-75220295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140914617	chr3:75220353-75220354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs4677483	chr3:75220468-75220469	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

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	21364760	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	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Ovarian cancer	21720365	CNVD

Chromatin state (count:486 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75214600-75215400	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr3:75220000-75220800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr3:75220600-75222600	Enhancers	Brain Germinal Matrix	brain
4	chr3:75220800-75226000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr3:75222600-75224600	Weak transcription	Brain Germinal Matrix	brain
6	chr3:75224200-75225400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr3:75224600-75225200	Enhancers	Brain Germinal Matrix	brain
8	chr3:75225200-75228200	Weak transcription	Brain Germinal Matrix	brain
9	chr3:75226000-75226600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr3:75226000-75226800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr3:75226200-75226600	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr3:75226200-75226600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr3:75226200-75226600	Enhancers	HUES6 Cell Line	embryonic stem cell
14	chr3:75226200-75226600	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr3:75226200-75226800	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr3:75226600-75229200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:75227200-75227600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr3:75228200-75228800	Enhancers	Brain Germinal Matrix	brain
19	chr3:75229200-75229400	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr3:75229600-75230000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
21	chr3:75229600-75230400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr3:75230000-75230400	Enhancers	NH-A	brain
23	chr3:75234800-75235200	Enhancers	H9 Cell Line	embryonic stem cell
24	chr3:75235200-75237800	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr3:75235800-75236800	Enhancers	Brain Germinal Matrix	brain
26	chr3:75236600-75238400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr3:75236800-75237600	Weak transcription	Brain Germinal Matrix	brain
28	chr3:75237600-75239200	Enhancers	Brain Germinal Matrix	brain
29	chr3:75237800-75238200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:75237800-75238400	Enhancers	H9 Cell Line	embryonic stem cell
31	chr3:75238000-75238400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr3:75238000-75238800	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr3:75238200-75238400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr3:75238200-75239000	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr3:75238200-75240200	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr3:75238400-75239400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr3:75238400-75241600	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr3:75239000-75240000	Weak transcription	HUES64 Cell Line	embryonic stem cell
39	chr3:75239400-75239800	Enhancers	H1 Cell Line	embryonic stem cell
40	chr3:75239400-75239800	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr3:75240000-75240200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr3:75240800-75244600	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chr3:75241400-75241600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr3:75241400-75242000	Enhancers	HMEC	breast
45	chr3:75241600-75241800	Enhancers	H9 Cell Line	embryonic stem cell
46	chr3:75242600-75243600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr3:75250200-75250400	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr3:75250400-75251800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr3:75250400-75257800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
50	chr3:75251400-75251800	Enhancers	Brain Germinal Matrix	brain

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