Variant report

Variant	esv3449937
Chromosome Location	chr3:75412667-75642951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2577)
CpG islands
(count:2320)
Chromatin interactive
region (count:8)
LncRNA
region (count:23)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2577 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75601426-75601483	K562	blood:	n/a	n/a
2	ARID3A	chr3:75482025-75482381	HepG2	liver:	n/a	n/a
3	ATF1	chr3:75442553-75442767	K562	blood:	n/a	n/a
4	ATF1	chr3:75482136-75482245	K562	blood:	n/a	n/a
5	ATF1	chr3:75484451-75484710	K562	blood:	n/a	n/a
6	ATF3	chr3:75482035-75482349	A549	lung:	n/a	n/a
7	ATF3	chr3:75482021-75482341	K562	blood:	n/a	n/a
8	BATF	chr3:75466555-75466915	GM12878	blood:	n/a	chr3:75466774-75466785
9	BATF	chr3:75478786-75479063	GM12878	blood:	n/a	n/a
10	BATF	chr3:75471192-75471564	GM12878	blood:	n/a	n/a
11	BATF	chr3:75483026-75483267	GM12878	blood:	n/a	n/a
12	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
13	BATF	chr3:75466554-75466845	GM12878	blood:	n/a	chr3:75466774-75466785
14	BATF	chr3:75483500-75483898	GM12878	blood:	n/a	chr3:75483518-75483528 chr3:75483514-75483524
15	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
16	BATF	chr3:75468128-75468306	GM12878	blood:	n/a	n/a
17	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
18	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
19	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
20	BATF	chr3:75484448-75484647	GM12878	blood:	n/a	n/a
21	BATF	chr3:75527612-75527941	GM12878	blood:	n/a	n/a
22	BATF	chr3:75483065-75483278	GM12878	blood:	n/a	n/a
23	BATF	chr3:75471237-75471503	GM12878	blood:	n/a	n/a
24	BATF	chr3:75483970-75484356	GM12878	blood:	n/a	n/a
25	BATF	chr3:75467667-75467909	GM12878	blood:	n/a	n/a
26	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
27	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
28	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
29	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
30	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
31	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a
32	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
33	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
34	BCL11A	chr3:75467554-75467709	GM12878	blood:	n/a	n/a
35	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
36	BCL11A	chr3:75471159-75471563	GM12878	blood:	n/a	n/a
37	BCL11A	chr3:75484021-75484296	GM12878	blood:	n/a	n/a
38	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
39	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
40	BCL11A	chr3:75466653-75466911	GM12878	blood:	n/a	chr3:75466778-75466787
41	BCL11A	chr3:75482472-75482657	GM12878	blood:	n/a	n/a
42	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
43	BCL11A	chr3:75483008-75483267	GM12878	blood:	n/a	n/a
44	BCL11A	chr3:75483449-75483810	GM12878	blood:	n/a	chr3:75483516-75483525
45	BCL11A	chr3:75471268-75471550	GM12878	blood:	n/a	n/a
46	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
47	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
48	BCL11A	chr3:75483447-75484322	GM12878	blood:	n/a	chr3:75483516-75483525
49	BCL11A	chr3:75466632-75466905	GM12878	blood:	n/a	chr3:75466778-75466787
50	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a

(count:2320 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75483803-75483853	AG09319	gingival:	n/a
2	chr3:75415561-75415611	ovcar-3	ovarian:	n/a
3	chr3:75483803-75483853	AG09319	gingival:	n/a
4	chr3:75415561-75415611	ovcar-3	ovarian:	n/a
5	chr3:75484213-75484263	Hela-S3	cervix:	n/a
6	chr3:75444752-75444802	SAEC	small airway:	n/a
7	chr3:75481281-75481331	AG09319	gingival:	n/a
8	chr3:75487529-75487579	LNCaP	prostate:	n/a
9	chr3:75414693-75414743	HUVEC	blood vessel:	n/a
10	chr3:75443047-75443097	HEK293	kidney:	embryo
11	chr3:75483803-75483853	SKMC	muscle:	n/a
12	chr3:75415526-75415576	HCPEpiC	choroid plexus:	n/a
13	chr3:75484516-75484566	Hepatocyte	liver:	n/a
14	chr3:75484516-75484566	PFSK-1	brain:	n/a
15	chr3:75553723-75553773	A549	lung:	n/a
16	chr3:75414486-75414536	GM12891	blood:	n/a
17	chr3:75484516-75484566	IMR90	lung:	fetal
18	chr3:75441804-75441854	H1-hESC	embryonic stem cell:	embryo
19	chr3:75445738-75445788	ProgFib	skin:	n/a
20	chr3:75448983-75449033	AG04450	lung:	fetal
21	chr3:75416171-75416221	PANC-1	pancreas:	n/a
22	chr3:75445502-75445552	NB4	blood:	n/a
23	chr3:75441804-75441854	MCF10A-Er-Src	breast:	n/a
24	chr3:75553723-75553773	SAEC	small airway:	n/a
25	chr3:75415561-75415611	HMEC	breast:	n/a
26	chr3:75448983-75449033	SK-N-SH	brain:	n/a
27	chr3:75631426-75631476	HUVEC	blood vessel:	n/a
28	chr3:75485110-75485160	NH-A	brain:	n/a
29	chr3:75416171-75416221	HL-60	blood:	n/a
30	chr3:75414486-75414536	SK-N-SH	brain:	n/a
31	chr3:75628819-75628869	PFSK-1	brain:	n/a
32	chr3:75629039-75629089	HEK293	kidney:	embryo
33	chr3:75414486-75414536	NT2-D1	testis:	n/a
34	chr3:75484213-75484263	PFSK-1	brain:	n/a
35	chr3:75555994-75556044	HCPEpiC	choroid plexus:	n/a
36	chr3:75413083-75413133	CMK	blood:	n/a
37	chr3:75485448-75485498	HCM	heart:	n/a
38	chr3:75414693-75414743	NB4	blood:	n/a
39	chr3:75414486-75414536	SK-N-SH_RA	brain:	n/a
40	chr3:75556027-75556077	ProgFib	skin:	n/a
41	chr3:75482182-75482232	MCF-7	breast:	n/a
42	chr3:75416171-75416221	PFSK-1	brain:	n/a
43	chr3:75445095-75445145	HL-60	blood:	n/a
44	chr3:75556027-75556077	HRCEpiC	kidney:	n/a
45	chr3:75415591-75415641	GM06990	blood:	n/a
46	chr3:75484213-75484263	SK-N-SH_RA	brain:	n/a
47	chr3:75482182-75482232	AG04450	lung:	fetal
48	chr3:75485110-75485160	ECC-1	luminal epithelium:	n/a
49	chr3:75556027-75556077	AG04450	lung:	fetal
50	chr3:75628819-75628869	SKMC	muscle:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr11:71498107..71498639-chr3:75483883..75484386,2	Hela-S3	cervix:
2	chr3:75466672..75467412-chr3:129812592..129813394,2	NB4	blood:
3	chr3:75343052..75344300-chr3:75470848..75471840,6	MCF-7	breast:
4	chr3:75343035..75343810-chr3:75470999..75471871,7	MCF-7	breast:
5	chr3:75390707..75391392-chr3:75471007..75471537,3	MCF-7	breast:
6	chr3:75484863..75485638-chr6:26156199..26156944,2	HCT-116	colon:
7	chr3:75343239..75343917-chr3:75478470..75479360,2	MCF-7	breast:
8	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:

(count:23 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
2	lnc-FRG2C-3	chr3:75492659-75492797	ENSG00000272690.1
3	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
4	lnc-FRG2C-3	chr3:75492659-75492775	XLOC_002710
5	lnc-FRG2C-3	chr3:75496316-75496447	ENSG00000272690.1
6	lnc-FRG2C-3	chr3:75501683-75501794	NONHSAT090533
7	lnc-FRG2C-3	chr3:75485928-75486426	XLOC_002710
8	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
9	lnc-FRG2C-3	chr3:75485367-75485503	XLOC_002710
10	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
11	lnc-FRG2C-3	chr3:75505768-75506637	ENSG00000272690.1
12	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
13	lnc-FRG2C-3	chr3:75497520-75500553	NONHSAT090533
14	lnc-FRG2C-3	chr3:75484499-75484564	ENSG00000272690.1
15	lnc-FRG2C-3	chr3:75486207-75486426	XLOC_002710
16	lnc-FRG2C-3	chr3:75501348-75501809	ENSG00000272690.1
17	lnc-FRG2C-3	chr3:75500361-75500553	ENSG00000272690.1
18	lnc-FRG2C-3	chr3:75488905-75488997	XLOC_002710
19	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
20	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
21	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
22	lnc-FRG2C-3	chr3:75488905-75488988	XLOC_002710
23	lnc-FRG2C-3	chr3:75501683-75501802	ENSG00000272690.1

No data

Variant related genes	Relation type
ENSG00000239383	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
ENSG00000272690	TF binding region
FAM86DP	TF binding region
ENSG00000266685	TF binding region
ENSG00000242953	TF binding region
OR7E55P	TF binding region
ENSG00000221602	TF binding region
LSP1P2	TF binding region
ENPP7P2	TF binding region
ALG1L6P	TF binding region
ENSG00000244699	TF binding region
ENSG00000272710	TF binding region
ENSG00000239383	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
ENSG00000272690	CpG island
FAM86DP	CpG island
ENSG00000266685	CpG island
ENSG00000242953	CpG island
OR7E55P	CpG island
ENSG00000221602	CpG island
LSP1P2	CpG island
ENPP7P2	CpG island
ALG1L6P	CpG island
ENSG00000244699	CpG island
ENSG00000272710	CpG island
ENSG00000168298	chromatin interactions
ENSG00000251287	chromatin interactions
ENSG00000158483	chromatin interactions
ENSG00000248243	chromatin interactions
ITGB1	miRNA target sites
SFRS5	miRNA target sites

Extended variants
information (count: 9400 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:9400 , 50 per page) page: 1 2 3 4 5 6 7 ... 188

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574956253	chr3:75412667-75412668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs549006299	chr3:75412673-75412674	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180698842	chr3:75412679-75412680	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs117321175	chr3:75412695-75412696	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185519739	chr3:75412696-75412697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564531464	chr3:75412703-75412704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs528489183	chr3:75412709-75412710	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs567247061	chr3:75412715-75412716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs568754574	chr3:75412789-75412790	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs535760094	chr3:75412825-75412826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550792018	chr3:75412833-75412834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs140184232	chr3:75412835-75412836	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200582428	chr3:75412844-75412845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs539185806	chr3:75412854-75412855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs557438955	chr3:75412855-75412856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs572800969	chr3:75412862-75412863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs189985125	chr3:75412865-75412866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs560653417	chr3:75412866-75412867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs377672076	chr3:75412867-75412868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs573911829	chr3:75412877-75412878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs182959192	chr3:75412898-75412899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs185977771	chr3:75412907-75412908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs577922828	chr3:75412922-75412923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs191779496	chr3:75412983-75412984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs368434183	chr3:75412989-75412990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs564629725	chr3:75412992-75412993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs2142076	chr3:75412995-75412996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs552605462	chr3:75413002-75413003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs540658521	chr3:75413015-75413016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184071806	chr3:75413022-75413023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs529587743	chr3:75413052-75413053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs189037669	chr3:75413057-75413058	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569165450	chr3:75413058-75413059	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs533349083	chr3:75413066-75413067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192328945	chr3:75413083-75413084	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146860089	chr3:75413084-75413085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs376464500	chr3:75413092-75413093	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555368951	chr3:75413096-75413097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs139618991	chr3:75413097-75413098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537801633	chr3:75413100-75413101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182120528	chr3:75413108-75413109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577978794	chr3:75413112-75413113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545242855	chr3:75413125-75413126	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2875203	chr3:75413136-75413137	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs573317684	chr3:75413173-75413174	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540370533	chr3:75413195-75413196	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562151429	chr3:75413214-75413215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529257859	chr3:75413236-75413237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs187232326	chr3:75413238-75413239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs115397069	chr3:75413268-75413269	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Melanoma	20877625	CNVD
Ollier disease	21235737	CNVD
Non-syndromic sensorineural hearing loss	22297974	CNVD

Chromatin state (count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75411000-75413400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr3:75411600-75412800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr3:75412000-75413400	Enhancers	Stomach Mucosa	stomach
4	chr3:75413000-75413200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr3:75420200-75421800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr3:75421400-75423000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:75421800-75422600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr3:75422000-75422200	Flanking Active TSS	Osteobl	bone
9	chr3:75422000-75422400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr3:75422000-75422400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr3:75422000-75423000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr3:75422200-75422800	Enhancers	Osteobl	bone
13	chr3:75422600-75423000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chr3:75423000-75423600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:75427600-75427800	Enhancers	Fetal Lung	lung
16	chr3:75427800-75428000	Enhancers	Fetal Heart	heart
17	chr3:75427800-75428200	Enhancers	Fetal Muscle Leg	muscle
18	chr3:75427800-75429000	Weak transcription	Fetal Lung	lung
19	chr3:75428000-75429000	Weak transcription	Fetal Heart	heart
20	chr3:75429000-75429200	Enhancers	Fetal Lung	lung
21	chr3:75429000-75429600	Enhancers	Fetal Heart	heart
22	chr3:75429000-75429600	Enhancers	Gastric	stomach
23	chr3:75429000-75429800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr3:75429000-75429800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:75429000-75429800	ZNF genes & repeats	Fetal Kidney	kidney
26	chr3:75429000-75429800	Enhancers	Pancreas	Pancrea
27	chr3:75429200-75429800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr3:75429200-75429800	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr3:75429200-75429800	Active TSS	Fetal Lung	lung
30	chr3:75429200-75429800	ZNF genes & repeats	Dnd41	blood
31	chr3:75429400-75429800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr3:75429600-75429800	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr3:75429800-75430200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr3:75429800-75445600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr3:75430000-75430200	Weak transcription	Fetal Kidney	kidney
36	chr3:75431600-75431800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr3:75431800-75432600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr3:75432000-75432200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr3:75432200-75433000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr3:75432600-75432800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr3:75432600-75433000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr3:75432800-75433400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr3:75435800-75436000	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chr3:75435800-75436400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr3:75436400-75437400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:75437400-75437600	Enhancers	Muscle Satellite Cultured Cells	--
47	chr3:75437400-75437600	Enhancers	Osteobl	bone
48	chr3:75437400-75437800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr3:75437400-75438200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr3:75437400-75438200	Enhancers	Ovary	ovary

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