Variant report

Variant	nsv1004686
Chromosome Location	chr3:75538843-75681198
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1265)
CpG islands
(count:2259)
Chromatin interactive
region (count:2)
LncRNA
region (count:9)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1265 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

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	ATF1	chr3:75679956-75680482	K562	blood:	n/a	n/a
3	BATF	chr3:75548046-75548331	GM12878	blood:	n/a	n/a
4	BATF	chr3:75596078-75596520	GM12878	blood:	n/a	n/a
5	BATF	chr3:75551282-75551694	GM12878	blood:	n/a	n/a
6	BATF	chr3:75680489-75680800	GM12878	blood:	n/a	n/a
7	BATF	chr3:75566162-75566431	GM12878	blood:	n/a	n/a
8	BATF	chr3:75653800-75653992	GM12878	blood:	n/a	n/a
9	BATF	chr3:75544610-75544819	GM12878	blood:	n/a	chr3:75544723-75544731
10	BATF	chr3:75573541-75573863	GM12878	blood:	n/a	n/a
11	BATF	chr3:75547955-75548333	GM12878	blood:	n/a	n/a
12	BATF	chr3:75551976-75552365	GM12878	blood:	n/a	n/a
13	BATF	chr3:75551286-75551692	GM12878	blood:	n/a	n/a
14	BATF	chr3:75653770-75654057	GM12878	blood:	n/a	n/a
15	BATF	chr3:75573564-75573871	GM12878	blood:	n/a	n/a
16	BCL11A	chr3:75680425-75680736	GM12878	blood:	n/a	chr3:75680637-75680646 chr3:75680722-75680731
17	BCL11A	chr3:75573652-75573882	GM12878	blood:	n/a	chr3:75573771-75573780
18	BCL11A	chr3:75566204-75566463	GM12878	blood:	n/a	n/a
19	BCL11A	chr3:75551437-75551623	GM12878	blood:	n/a	n/a
20	BCL11A	chr3:75544573-75544904	GM12878	blood:	n/a	chr3:75544808-75544817
21	BCL11A	chr3:75680444-75680757	GM12878	blood:	n/a	chr3:75680637-75680646 chr3:75680722-75680731
22	BCL11A	chr3:75609659-75609871	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:75551326-75551720	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:75596331-75596513	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:75547956-75548367	GM12878	blood:	n/a	chr3:75548358-75548367
26	BCL11A	chr3:75615329-75615521	GM12878	blood:	n/a	n/a
27	BCL11A	chr3:75547962-75548278	GM12878	blood:	n/a	n/a
28	BHLHE40	chr3:75629343-75629581	HepG2	liver:	n/a	chr3:75629450-75629466
29	BHLHE40	chr3:75680386-75680905	K562	blood:	n/a	n/a
30	BHLHE40	chr3:75552652-75552692	K562	blood:	n/a	n/a
31	BHLHE40	chr3:75545920-75546031	K562	blood:	n/a	chr3:75546012-75546021 chr3:75546006-75546027 chr3:75546013-75546022 chr3:75546012-75546021 chr3:75546011-75546020
32	BHLHE40	chr3:75680525-75680941	GM12878	blood:	n/a	n/a
33	BHLHE40	chr3:75549695-75549729	K562	blood:	n/a	n/a
34	BHLHE40	chr3:75679465-75679715	K562	blood:	n/a	n/a
35	BRCA1	chr3:75680297-75680308	GM12878	blood:	n/a	n/a
36	CBX3	chr3:75560367-75560646	K562	blood:	n/a	n/a
37	CBX3	chr3:75552469-75552889	K562	blood:	n/a	n/a
38	CEBPB	chr3:75630628-75630820	HepG2	liver:	n/a	chr3:75630780-75630791 chr3:75630780-75630793 chr3:75630782-75630791
39	CEBPB	chr3:75552686-75552799	K562	blood:	n/a	n/a
40	CEBPB	chr3:75556758-75557165	K562	blood:	n/a	n/a
41	CEBPB	chr3:75556273-75556580	K562	blood:	n/a	n/a
42	CEBPB	chr3:75632584-75632615	K562	blood:	n/a	n/a
43	CEBPB	chr3:75556865-75557134	K562	blood:	n/a	n/a
44	CEBPB	chr3:75607016-75607045	HepG2	liver:	n/a	chr3:75607021-75607032
45	CEBPD	chr3:75673790-75674085	K562	blood:	n/a	n/a
46	CHD2	chr3:75680122-75680478	GM12878	blood:	n/a	n/a
47	CHD2	chr3:75629407-75629419	GM12878	blood:	n/a	n/a
48	CHD2	chr3:75680135-75680142	HepG2	liver:	n/a	n/a
49	CHD2	chr3:75681053-75681088	GM12878	blood:	n/a	n/a
50	CHD2	chr3:75668910-75668924	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2259 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75555994-75556044	AG10803	skin:	n/a
2	chr3:75669109-75669159	MCF-7	breast:	n/a
3	chr3:75555994-75556044	AG10803	skin:	n/a
4	chr3:75669109-75669159	MCF-7	breast:	n/a
5	chr3:75553723-75553773	AG04450	lung:	fetal
6	chr3:75555938-75555988	AG04450	lung:	fetal
7	chr3:75556027-75556077	AG10803	skin:	n/a
8	chr3:75659629-75659679	MCF-7	breast:	n/a
9	chr3:75632533-75632583	NB4	blood:	n/a
10	chr3:75671115-75671165	GM12892	blood:	n/a
11	chr3:75661320-75661370	NH-A	brain:	n/a
12	chr3:75669109-75669159	HEK293	kidney:	embryo
13	chr3:75661320-75661370	T-47D	breast:	n/a
14	chr3:75679454-75679504	HepG2	liver:	n/a
15	chr3:75629433-75629483	Jurkat	blood:	n/a
16	chr3:75631426-75631476	HUVEC	blood vessel:	n/a
17	chr3:75555994-75556044	Hela-S3	cervix:	n/a
18	chr3:75669109-75669159	HIPEpiC	eye:	n/a
19	chr3:75553762-75553812	ECC-1	luminal epithelium:	n/a
20	chr3:75668758-75668808	ProgFib	skin:	n/a
21	chr3:75661320-75661370	BE2_C	brain:	n/a
22	chr3:75666392-75666442	SK-N-SH	brain:	n/a
23	chr3:75653319-75653369	HL-60	blood:	n/a
24	chr3:75631426-75631476	MCF10A-Er-Src	breast:	n/a
25	chr3:75666392-75666442	HEEpiC	esophagus:	n/a
26	chr3:75632533-75632583	PANC-1	pancreas:	n/a
27	chr3:75668627-75668677	AG04450	lung:	fetal
28	chr3:75658410-75658460	AG04449	skin:	fetal
29	chr3:75668627-75668677	CMK	blood:	n/a
30	chr3:75555938-75555988	GM12892	blood:	n/a
31	chr3:75629039-75629089	GM12892	blood:	n/a
32	chr3:75661206-75661256	SK-N-SH	brain:	n/a
33	chr3:75671793-75671843	HEK293	kidney:	embryo
34	chr3:75671793-75671843	ProgFib	skin:	n/a
35	chr3:75631426-75631476	AG04450	lung:	fetal
36	chr3:75666381-75666431	SAEC	small airway:	n/a
37	chr3:75671115-75671165	Hela-S3	cervix:	n/a
38	chr3:75629433-75629483	GM19239	blood:	n/a
39	chr3:75632533-75632583	HEK293	kidney:	embryo
40	chr3:75631426-75631476	MCF-7	breast:	n/a
41	chr3:75555938-75555988	Jurkat	blood:	n/a
42	chr3:75659629-75659679	Jurkat	blood:	n/a
43	chr3:75658552-75658602	GM12878	blood:	n/a
44	chr3:75628819-75628869	HCT-116	colon:	n/a
45	chr3:75657183-75657233	HEK293	kidney:	embryo
46	chr3:75553762-75553812	BE2_C	brain:	n/a
47	chr3:75664059-75664109	Caco-2	colon:	n/a
48	chr3:75668035-75668085	IMR90	lung:	fetal
49	chr3:75657183-75657233	AG04450	lung:	fetal
50	chr3:75658490-75658540	AG04450	lung:	fetal

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:436504..437180-chr3:75674246..75674764,2	MCF-7	breast:
2	chr3:75343397..75343923-chr3:75600934..75601577,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-11	chr3:75570954-75571163	NONHSAT090534
2	lnc-FRG2C-2	chr3:75608026-75608433	XLOC_002712
3	lnc-FRG2C-2	chr3:75608026-75608398	XLOC_002712
4	lnc-FRG2C-2	chr3:75606223-75606260	XLOC_002712
5	lnc-ZNF717-3	chr3:75629129-75629150	ENSG00000272710.1
6	lnc-FRG2C-2	chr3:75606117-75606146	XLOC_002712
7	lnc-ZNF717-1	chr3:75674122-75674304	NONHSAT090540
8	lnc-ZNF717-3	chr3:75589200-75589378	ENSG00000272710.1
9	lnc-ZNF717-1	chr3:75679231-75679352	NONHSAT090540

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

No data

Variant related genes	Relation type
UNC93B3	TF binding region
ENSG00000243422	TF binding region
ENSG00000239383	TF binding region
RPS3AP15	TF binding region
ENSG00000243794	TF binding region
OR7E121P	TF binding region
ENSG00000221602	TF binding region
ENPP7P2	TF binding region
ENSG00000272710	TF binding region
MIR1324	TF binding region
UNC93B3	CpG island
ENSG00000243422	CpG island
ENSG00000239383	CpG island
RPS3AP15	CpG island
ENSG00000243794	CpG island
OR7E121P	CpG island
ENSG00000221602	CpG island
ENPP7P2	CpG island
ENSG00000272710	CpG island
MIR1324	CpG island
ENSG00000129925	chromatin interactions
ENSG00000236829	chromatin interactions

Extended variants
information (count: 4159 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:4159 , 50 per page) page: 1 2 3 4 5 6 7 ... 84

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9799287	chr3:75538843-75538844	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs551373164	chr3:75538885-75538886	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs72628696	chr3:75538932-75538933	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs139389427	chr3:75538952-75538953	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs143324743	chr3:75538972-75538973	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs572658440	chr3:75538982-75538983	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs538069412	chr3:75538991-75538992	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs556180517	chr3:75539043-75539044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs374533353	chr3:75539049-75539050	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs578028216	chr3:75539059-75539060	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs533557485	chr3:75539101-75539102	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs553805478	chr3:75539130-75539131	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs190815017	chr3:75539134-75539135	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs143749645	chr3:75539141-75539142	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs112723911	chr3:75539153-75539154	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs561067814	chr3:75539159-75539160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs529462893	chr3:75539161-75539162	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs544833626	chr3:75539162-75539163	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs550038211	chr3:75539173-75539174	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs533451444	chr3:75539182-75539183	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs551336359	chr3:75539194-75539195	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs566540998	chr3:75539195-75539196	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs563772234	chr3:75539207-75539208	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs527712021	chr3:75539210-75539211	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs549185885	chr3:75539213-75539214	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs112930033	chr3:75539228-75539229	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs112714040	chr3:75539243-75539244	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs372168655	chr3:75539269-75539270	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs74819559	chr3:75539283-75539284	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs529348190	chr3:75539285-75539286	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs77656976	chr3:75539287-75539288	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs150649050	chr3:75539309-75539310	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs375324628	chr3:75539321-75539322	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs186630832	chr3:75539331-75539332	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs367881744	chr3:75539340-75539341	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs538951419	chr3:75539348-75539349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs554142304	chr3:75539359-75539360	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs201106381	chr3:75539362-75539363	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs202060561	chr3:75539384-75539385	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs193010143	chr3:75539402-75539403	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs200167463	chr3:75539410-75539411	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs201140037	chr3:75539420-75539421	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs182798309	chr3:75539426-75539427	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs200413081	chr3:75539441-75539442	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs569826707	chr3:75539475-75539476	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs117965637	chr3:75539490-75539491	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs576098762	chr3:75539564-75539565	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs372267084	chr3:75539567-75539568	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs199692160	chr3:75539580-75539581	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs544435312	chr3:75539594-75539595	ZNF genes & repeats	n/a	n/a	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
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

Chromatin state (count:589 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

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

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