Variant report

Variant	nsv1007048
Chromosome Location	chr3:21666807-21865229
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:829)
CpG islands
(count:918)
Chromatin interactive
region (count:38)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:829 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:21770932-21771044	K562	blood:	n/a	n/a
2	BACH1	chr3:21792431-21793017	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr3:21669239-21669252	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr3:21704294-21704295	K562	blood:	n/a	n/a
5	BHLHE40	chr3:21825389-21825693	K562	blood:	n/a	n/a
6	BRCA1	chr3:21782837-21782869	Hela-S3	cervix:	n/a	n/a
7	BRCA1	chr3:21779878-21779890	GM12878	blood:	n/a	n/a
8	CCNT2	chr3:21773207-21773377	K562	blood:	n/a	n/a
9	CEBPB	chr3:21744797-21745150	IMR90	lung:	n/a	chr3:21744968-21744979
10	CEBPB	chr3:21747302-21747599	IMR90	lung:	n/a	n/a
11	CEBPB	chr3:21744803-21745131	H1-hESC	embryonic stem cell:	n/a	chr3:21744968-21744979
12	CEBPB	chr3:21814548-21814749	HepG2	liver:	n/a	chr3:21814627-21814638
13	CEBPB	chr3:21781032-21781384	IMR90	lung:	n/a	chr3:21781204-21781215
14	CEBPB	chr3:21840301-21840516	A549	lung:	n/a	chr3:21840366-21840377
15	CEBPB	chr3:21840251-21840506	K562	blood:	n/a	chr3:21840366-21840377
16	CEBPB	chr3:21744802-21745144	K562	blood:	n/a	chr3:21744968-21744979
17	CEBPB	chr3:21739931-21740077	A549	lung:	n/a	n/a
18	CEBPB	chr3:21744829-21745122	Hela-S3	cervix:	n/a	chr3:21744968-21744979
19	CEBPB	chr3:21744789-21745151	HepG2	liver:	n/a	chr3:21744968-21744979
20	CEBPB	chr3:21781026-21781360	HepG2	liver:	n/a	chr3:21781204-21781215
21	CEBPB	chr3:21792339-21792940	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr3:21840231-21840551	IMR90	lung:	n/a	chr3:21840366-21840377
23	CEBPB	chr3:21747262-21747788	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr3:21744790-21745138	A549	lung:	n/a	chr3:21744968-21744979
25	CEBPB	chr3:21840207-21840516	HepG2	liver:	n/a	chr3:21840366-21840377
26	CEBPB	chr3:21758574-21758634	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr3:21713728-21714131	IMR90	lung:	n/a	n/a
28	CEBPB	chr3:21759664-21760047	IMR90	lung:	n/a	n/a
29	CEBPB	chr3:21736131-21736143	A549	lung:	n/a	n/a
30	CEBPD	chr3:21825426-21825758	K562	blood:	n/a	n/a
31	CHD1	chr3:21792005-21792065	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chr3:21730093-21730137	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chr3:21792482-21792673	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr3:21792301-21793038	H1-hESC	embryonic stem cell:	n/a	n/a
35	CREB1	chr3:21792463-21792984	H1-hESC	embryonic stem cell:	n/a	n/a
36	CREB1	chr3:21792360-21793085	H1-hESC	embryonic stem cell:	n/a	n/a
37	CTBP2	chr3:21792388-21792991	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr3:21794400-21794550	HCFaa	heart:	n/a	n/a
39	CTCF	chr3:21794320-21794470	GM12866	blood:	n/a	n/a
40	CTCF	chr3:21794340-21794490	HRPEpiC	eye:	n/a	n/a
41	CTCF	chr3:21794363-21794512	GM19239	blood:	n/a	n/a
42	CTCF	chr3:21792500-21792650	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr3:21794360-21794510	SAEC	small airway:	n/a	n/a
44	CTCF	chr3:21794317-21794600	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr3:21794340-21794490	GM06990	blood:	n/a	n/a
46	CTCF	chr3:21839520-21839670	GM12874	blood:	n/a	n/a
47	CTCF	chr3:21794360-21794510	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr3:21794340-21794490	NHLF	lung:	n/a	n/a
49	CTCF	chr3:21794309-21794580	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr3:21792520-21792670	AG04449	skin:	n/a	n/a

(count:918 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21792684-21792734	T-47D	breast:	n/a
2	chr3:21714788-21714838	HUVEC	blood vessel:	n/a
3	chr3:21792684-21792734	PFSK-1	brain:	n/a
4	chr3:21792684-21792734	T-47D	breast:	n/a
5	chr3:21714788-21714838	HUVEC	blood vessel:	n/a
6	chr3:21792684-21792734	PFSK-1	brain:	n/a
7	chr3:21792857-21792907	AG09319	gingival:	n/a
8	chr3:21792857-21792907	GM19239	blood:	n/a
9	chr3:21792938-21792988	HUVEC	blood vessel:	n/a
10	chr3:21792857-21792907	GM12878	blood:	n/a
11	chr3:21761217-21761267	ovcar-3	ovarian:	n/a
12	chr3:21792434-21792484	HMEC	breast:	n/a
13	chr3:21792991-21793041	K562	blood:	n/a
14	chr3:21720400-21720450	A549	lung:	n/a
15	chr3:21790232-21790282	HMEC	breast:	n/a
16	chr3:21792543-21792593	AG09319	gingival:	n/a
17	chr3:21792543-21792593	GM06990	blood:	n/a
18	chr3:21720400-21720450	Caco-2	colon:	n/a
19	chr3:21792434-21792484	PrEC	prostate:	n/a
20	chr3:21793557-21793607	PFSK-1	brain:	n/a
21	chr3:21792857-21792907	SK-N-SH_RA	brain:	n/a
22	chr3:21761217-21761267	HAEpiC	amniotic membrane:	n/a
23	chr3:21793557-21793607	GM12891	blood:	n/a
24	chr3:21792991-21793041	AG09309	skin:	n/a
25	chr3:21792684-21792734	HL-60	blood:	n/a
26	chr3:21714788-21714838	SKMC	muscle:	n/a
27	chr3:21792965-21793015	A549	lung:	n/a
28	chr3:21792991-21793041	HRCEpiC	kidney:	n/a
29	chr3:21720400-21720450	MCF-7	breast:	n/a
30	chr3:21792857-21792907	HRPEpiC	eye:	n/a
31	chr3:21792965-21793015	IMR90	lung:	fetal
32	chr3:21792434-21792484	HIPEpiC	eye:	n/a
33	chr3:21792991-21793041	AG04450	lung:	fetal
34	chr3:21793557-21793607	HAEpiC	amniotic membrane:	n/a
35	chr3:21792857-21792907	BE2_C	brain:	n/a
36	chr3:21792991-21793041	HEEpiC	esophagus:	n/a
37	chr3:21792965-21793015	SK-N-SH_RA	brain:	n/a
38	chr3:21792684-21792734	HCF	heart:	n/a
39	chr3:21790232-21790282	PFSK-1	brain:	n/a
40	chr3:21792991-21793041	T-47D	breast:	n/a
41	chr3:21720400-21720450	ovcar-3	ovarian:	n/a
42	chr3:21792684-21792734	GM06990	blood:	n/a
43	chr3:21790232-21790282	U87	brain:	n/a
44	chr3:21792857-21792907	ProgFib	skin:	n/a
45	chr3:21792991-21793041	SK-N-SH	brain:	n/a
46	chr3:21714788-21714838	MCF-7	breast:	n/a
47	chr3:21790232-21790282	RPTEC	kidney:	n/a
48	chr3:21792543-21792593	ECC-1	luminal epithelium:	n/a
49	chr3:21792684-21792734	SK-N-MC	brain:	n/a
50	chr3:21792684-21792734	MCF-7	breast:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:21721634..21724337-chr3:21728946..21730736,2	K562	blood:
2	chr3:21664828..21666953-chr3:21672242..21674310,2	K562	blood:
3	chr3:21731209..21733494-chr3:21734239..21737036,2	K562	blood:
4	chr3:21705075..21707006-chr3:21711502..21714008,3	K562	blood:
5	chr3:21700043..21701909-chr3:21703783..21705920,2	K562	blood:
6	chr3:21696094..21698231-chr3:21699619..21701912,2	K562	blood:
7	chr3:21693828..21695393-chr3:21699216..21701060,2	K562	blood:
8	chr3:21664828..21666953-chr3:21672242..21674310,2	K562	blood:
9	chr3:21731209..21733494-chr3:21734239..21737036,2	K562	blood:
10	chr3:21794398..21795153-chr3:22159350..22159975,2	MCF-7	breast:
11	chr3:21734569..21736577-chr3:21736842..21738820,2	K562	blood:
12	chr3:21793963..21794585-chr3:21876272..21877179,2	MCF-7	breast:
13	chr3:21834699..21836749-chr3:21841872..21843616,2	K562	blood:
14	chr3:21820384..21822203-chr3:21834742..21836819,2	K562	blood:
15	chr3:21705075..21707006-chr3:21711502..21714008,3	K562	blood:
16	chr3:21680949..21682612-chr3:21687713..21689448,2	K562	blood:
17	chr3:21827028..21830015-chr3:21877815..21880748,2	K562	blood:
18	chr3:21835216..21837652-chr3:21840366..21842817,3	K562	blood:
19	chr3:21709988..21712111-chr3:21717387..21720312,2	K562	blood:
20	chr3:21709988..21712111-chr3:21717387..21720312,2	K562	blood:
21	chr3:21834699..21836749-chr3:21841872..21843616,2	K562	blood:
22	chr3:21705697..21707746-chr3:21710936..21713423,2	MCF-7	breast:
23	chr3:21835216..21837652-chr3:21840366..21842817,3	K562	blood:
24	chr3:21721634..21724337-chr3:21728946..21730736,2	K562	blood:
25	chr3:21693828..21695393-chr3:21699216..21701060,2	K562	blood:
26	chr3:21734569..21736577-chr3:21736842..21738820,2	K562	blood:
27	chr3:21680949..21682612-chr3:21687713..21689448,2	K562	blood:
28	chr3:21700043..21701909-chr3:21703783..21705920,2	K562	blood:
29	chr3:21820384..21822203-chr3:21834742..21836819,2	K562	blood:
30	chr3:21660057..21662035-chr3:21669557..21671867,2	MCF-7	breast:
31	chr3:21829102..21831903-chr3:21833288..21835106,2	MCF-7	breast:
32	chr3:21661677..21663876-chr3:21672087..21673595,2	K562	blood:
33	chr3:21696094..21698231-chr3:21699619..21701912,2	K562	blood:
34	chr3:21793981..21794891-chr3:21935742..21936689,4	MCF-7	breast:
35	chr3:21699534..21701543-chr3:21703590..21705283,2	K562	blood:
36	chr3:21699534..21701543-chr3:21703590..21705283,2	K562	blood:
37	chr3:21829102..21831903-chr3:21833288..21835106,2	MCF-7	breast:
38	chr3:21705697..21707746-chr3:21710936..21713423,2	MCF-7	breast:

No data

Variant related genes	Relation type
ZNF385D	TF binding region
ZNF385D	CpG island

Extended variants
information (count: 7959 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:7959 , 50 per page) page: 1 2 3 4 5 6 7 ... 160

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546528305	chr3:21666809-21666810	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs142820422	chr3:21666816-21666817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114696146	chr3:21666883-21666884	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs550393130	chr3:21666893-21666894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs568589471	chr3:21666915-21666916	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs10780010	chr3:21666926-21666927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs557851809	chr3:21666969-21666970	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs367553175	chr3:21666985-21666986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs572710251	chr3:21667015-21667016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114944101	chr3:21667091-21667092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527477361	chr3:21667161-21667162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs555784460	chr3:21667163-21667164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182772028	chr3:21667164-21667165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs74355354	chr3:21667212-21667213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150622914	chr3:21667290-21667291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs200665638	chr3:21667329-21667330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs556826516	chr3:21667353-21667354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549573623	chr3:21667363-21667364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs74484305	chr3:21667372-21667373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs73138804	chr3:21667376-21667377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs73819365	chr3:21667387-21667388	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs77576381	chr3:21667401-21667402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543047057	chr3:21667414-21667415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs372290440	chr3:21667481-21667482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs529179043	chr3:21667487-21667488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs60982953	chr3:21667543-21667544	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs548603045	chr3:21667586-21667587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs139763365	chr3:21667592-21667593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs556478124	chr3:21667593-21667594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376408040	chr3:21667630-21667631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs185635983	chr3:21667667-21667668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1532129	chr3:21667698-21667699	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs190731081	chr3:21667701-21667702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533547638	chr3:21667702-21667703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62237376	chr3:21667736-21667737	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs567940755	chr3:21667749-21667750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs547494932	chr3:21667781-21667782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531989634	chr3:21667806-21667807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149809367	chr3:21667817-21667818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182870544	chr3:21667842-21667843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs34237405	chr3:21667845-21667846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77498131	chr3:21667856-21667857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs545628433	chr3:21667872-21667873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs74830267	chr3:21667892-21667893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542657188	chr3:21667897-21667898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570678951	chr3:21667910-21667911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs146846173	chr3:21667948-21667949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79101985	chr3:21667972-21667973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561306546	chr3:21667990-21667991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187943179	chr3:21668007-21668008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Melanoma	20688739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1131 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21646200-21669000	Weak transcription	Fetal Lung	lung
2	chr3:21651600-21686600	Weak transcription	Fetal Stomach	stomach
3	chr3:21664000-21683800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:21665000-21667000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr3:21665000-21685200	Weak transcription	Aorta	Aorta
6	chr3:21669000-21670000	Enhancers	Fetal Lung	lung
7	chr3:21669200-21670000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr3:21670000-21681600	Weak transcription	Fetal Lung	lung
9	chr3:21674000-21674400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:21681000-21683600	Weak transcription	Fetal Muscle Trunk	muscle
11	chr3:21681400-21681800	Weak transcription	Fetal Muscle Leg	muscle
12	chr3:21681600-21682600	ZNF genes & repeats	Fetal Lung	lung
13	chr3:21681800-21682200	Active TSS	Fetal Brain Male	brain
14	chr3:21681800-21682200	ZNF genes & repeats	Fetal Muscle Leg	muscle
15	chr3:21682200-21684000	Weak transcription	Fetal Brain Male	brain
16	chr3:21682600-21682800	Enhancers	Psoas Muscle	Psoas
17	chr3:21682600-21683400	Weak transcription	Fetal Muscle Leg	muscle
18	chr3:21682600-21686400	Weak transcription	Fetal Lung	lung
19	chr3:21682800-21686800	Weak transcription	Psoas Muscle	Psoas
20	chr3:21683000-21683200	Weak transcription	Pancreatic Islets	Pancreatic Islet
21	chr3:21683400-21683800	Enhancers	H9 Cell Line	embryonic stem cell
22	chr3:21683400-21683800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr3:21683400-21684000	Enhancers	H1 Cell Line	embryonic stem cell
24	chr3:21683600-21683800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr3:21683600-21684000	Enhancers	iPS-20b Cell Line	embryonic stem cell
26	chr3:21683600-21684200	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr3:21683600-21684200	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr3:21683600-21686600	Weak transcription	Brain Hippocampus Middle	brain
29	chr3:21683800-21684000	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr3:21683800-21686400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr3:21683800-21686600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr3:21683800-21686600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr3:21683800-21706600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr3:21684000-21684400	Enhancers	Fetal Brain Male	brain
35	chr3:21684000-21684600	Weak transcription	Pancreatic Islets	Pancreatic Islet
36	chr3:21684000-21686800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chr3:21684200-21686200	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr3:21684200-21687000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr3:21684600-21684800	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr3:21684800-21685000	Enhancers	NHLF	lung
41	chr3:21684800-21685400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr3:21684800-21686400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr3:21684800-21687200	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr3:21685000-21686000	Enhancers	Right Ventricle	heart
45	chr3:21685200-21686200	Enhancers	Aorta	Aorta
46	chr3:21685200-21686200	Weak transcription	NHLF	lung
47	chr3:21685200-21687000	Enhancers	Right Atrium	heart
48	chr3:21685200-21687200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr3:21685200-21688400	Enhancers	Left Ventricle	heart
50	chr3:21685400-21685600	Enhancers	Pancreatic Islets	Pancreatic Islet

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