Variant report

Variant	nsv834630
Chromosome Location	chr3:21311619-21491327
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:618)
CpG islands
(count:549)
Chromatin interactive
region (count:33)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:618 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr3:21440459-21440632	K562	blood:	n/a	n/a
2	ATF2	chr3:21487560-21487918	GM12878	blood:	n/a	n/a
3	ATF3	chr3:21447160-21447359	K562	blood:	n/a	n/a
4	BATF	chr3:21487397-21487659	GM12878	blood:	n/a	n/a
5	BATF	chr3:21371872-21372123	GM12878	blood:	n/a	n/a
6	BCL11A	chr3:21487425-21487837	GM12878	blood:	n/a	chr3:21487787-21487796
7	BHLHE40	chr3:21487490-21487873	GM12878	blood:	n/a	n/a
8	BHLHE40	chr3:21360768-21360802	K562	blood:	n/a	n/a
9	BRCA1	chr3:21371738-21371763	Hela-S3	cervix:	n/a	n/a
10	BRCA1	chr3:21483405-21483415	GM12878	blood:	n/a	n/a
11	CBX3	chr3:21447117-21447403	K562	blood:	n/a	n/a
12	CCNT2	chr3:21468599-21468799	K562	blood:	n/a	n/a
13	CEBPB	chr3:21453141-21453424	A549	lung:	n/a	chr3:21453254-21453265
14	CEBPB	chr3:21365511-21365849	HepG2	liver:	n/a	chr3:21365656-21365667
15	CEBPB	chr3:21455349-21455609	IMR90	lung:	n/a	chr3:21455497-21455514 chr3:21455488-21455501
16	CEBPB	chr3:21452758-21453387	HepG2	liver:	n/a	chr3:21453014-21453025 chr3:21453014-21453025 chr3:21453014-21453027 chr3:21453254-21453265
17	CEBPB	chr3:21477297-21477706	IMR90	lung:	n/a	n/a
18	CEBPB	chr3:21362409-21362492	A549	lung:	n/a	n/a
19	CEBPB	chr3:21365546-21365830	IMR90	lung:	n/a	chr3:21365656-21365667
20	CEBPB	chr3:21403738-21403864	A549	lung:	n/a	n/a
21	CEBPB	chr3:21472353-21472390	A549	lung:	n/a	n/a
22	CEBPB	chr3:21472711-21472916	A549	lung:	n/a	chr3:21472831-21472848
23	CEBPB	chr3:21404484-21404623	K562	blood:	n/a	n/a
24	CEBPB	chr3:21372880-21373169	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr3:21461360-21461566	HepG2	liver:	n/a	chr3:21461443-21461454
26	CEBPB	chr3:21489341-21489759	IMR90	lung:	n/a	n/a
27	CEBPB	chr3:21453174-21453401	K562	blood:	n/a	chr3:21453254-21453265
28	CHD2	chr3:21487469-21487900	GM12878	blood:	n/a	n/a
29	CHD2	chr3:21368145-21368250	GM12878	blood:	n/a	n/a
30	CHD2	chr3:21371944-21372095	GM12878	blood:	n/a	n/a
31	CTCF	chr3:21332200-21332350	GM12864	blood:	n/a	n/a
32	CTCF	chr3:21332240-21332390	AG04450	lung:	n/a	n/a
33	CTCF	chr3:21332220-21332370	MCF-7	breast:	n/a	n/a
34	CTCF	chr3:21332160-21332310	AoAF	blood vessel:	n/a	n/a
35	CTCF	chr3:21332160-21332310	HRE	kidney:	n/a	n/a
36	CTCF	chr3:21368620-21368770	HRPEpiC	eye:	n/a	n/a
37	CTCF	chr3:21332160-21332310	Caco-2	colon:	n/a	n/a
38	CTCF	chr3:21332180-21332330	HRE	kidney:	n/a	n/a
39	CTCF	chr3:21332186-21332334	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr3:21332140-21332290	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr3:21332180-21332330	HVMF	connective:	n/a	n/a
42	CTCF	chr3:21332140-21332290	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr3:21332140-21332290	AG09309	skin:	n/a	n/a
44	CTCF	chr3:21332180-21332330	GM12872	blood:	n/a	n/a
45	CTCF	chr3:21332145-21332356	K562	blood:	n/a	n/a
46	CTCF	chr3:21332500-21332650	GM12872	blood:	n/a	n/a
47	CTCF	chr3:21332160-21332310	HVMF	connective:	n/a	n/a
48	CTCF	chr3:21332203-21332317	GM13976	blood:	n/a	n/a
49	CTCF	chr3:21332149-21332360	LNCaP	prostate:	n/a	n/a
50	CTCF	chr3:21332140-21332290	HBMEC	blood vessel:	n/a	n/a

(count:549 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:21445979-21446029	GM12878	blood:	n/a
2	chr3:21448049-21448099	SK-N-SH	brain:	n/a
3	chr3:21447391-21447441	AG09319	gingival:	n/a
4	chr3:21447508-21447558	CMK	blood:	n/a
5	chr3:21446874-21446924	Caco-2	colon:	n/a
6	chr3:21447667-21447717	NB4	blood:	n/a
7	chr3:21447667-21447717	RPTEC	kidney:	n/a
8	chr3:21445979-21446029	GM12892	blood:	n/a
9	chr3:21445979-21446029	HCM	heart:	n/a
10	chr3:21448049-21448099	HCT-116	colon:	n/a
11	chr3:21447508-21447558	HEK293	kidney:	embryo
12	chr3:21448049-21448099	AG10803	skin:	n/a
13	chr3:21447501-21447551	AG09319	gingival:	n/a
14	chr3:21447391-21447441	H1-hESC	embryonic stem cell:	embryo
15	chr3:21446874-21446924	HepG2	liver:	n/a
16	chr3:21447667-21447717	HIPEpiC	eye:	n/a
17	chr3:21448049-21448099	GM06990	blood:	n/a
18	chr3:21448049-21448099	U87	brain:	n/a
19	chr3:21446874-21446924	PANC-1	pancreas:	n/a
20	chr3:21445979-21446029	GM12891	blood:	n/a
21	chr3:21445979-21446029	AG10803	skin:	n/a
22	chr3:21447667-21447717	BE2_C	brain:	n/a
23	chr3:21445979-21446029	HUVEC	blood vessel:	n/a
24	chr3:21447501-21447551	GM19239	blood:	n/a
25	chr3:21448012-21448062	AG10803	skin:	n/a
26	chr3:21447508-21447558	SKMC	muscle:	n/a
27	chr3:21447667-21447717	NT2-D1	testis:	n/a
28	chr3:21446874-21446924	SAEC	small airway:	n/a
29	chr3:21447667-21447717	AG10803	skin:	n/a
30	chr3:21447508-21447558	AG10803	skin:	n/a
31	chr3:21447391-21447441	HCM	heart:	n/a
32	chr3:21447667-21447717	MCF10A-Er-Src	breast:	n/a
33	chr3:21446874-21446924	AoSMC	blood vessel:	n/a
34	chr3:21447667-21447717	NHBE	bronchial:	n/a
35	chr3:21447667-21447717	HCPEpiC	choroid plexus:	n/a
36	chr3:21426059-21426109	AoSMC	blood vessel:	n/a
37	chr3:21426059-21426109	Hela-S3	cervix:	n/a
38	chr3:21447508-21447558	HCF	heart:	n/a
39	chr3:21448049-21448099	BJ	skin:	n/a
40	chr3:21447501-21447551	HAEpiC	amniotic membrane:	n/a
41	chr3:21448012-21448062	HIPEpiC	eye:	n/a
42	chr3:21446874-21446924	HPAEpiC	pulmonary alveolar:	n/a
43	chr3:21447391-21447441	Jurkat	blood:	n/a
44	chr3:21426059-21426109	BJ	skin:	n/a
45	chr3:21447508-21447558	HPAEpiC	pulmonary alveolar:	n/a
46	chr3:21448012-21448062	RPTEC	kidney:	n/a
47	chr3:21448049-21448099	T-47D	breast:	n/a
48	chr3:21448049-21448099	AG09319	gingival:	n/a
49	chr3:21447508-21447558	PANC-1	pancreas:	n/a
50	chr3:21448049-21448099	SAEC	small airway:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:21381102..21383225-chr3:21383828..21386655,2	MCF-7	breast:
2	chr3:21475881..21478303-chr3:21479412..21482583,3	K562	blood:
3	chr3:21448531..21452327-chr3:21453436..21457568,4	K562	blood:
4	chr3:21331844..21332737-chr5:18941538..18942038,2	MCF-7	breast:
5	chr3:21434090..21435912-chr3:21501028..21503829,2	K562	blood:
6	chr3:21357091..21358959-chr3:21367501..21369153,2	K562	blood:
7	chr3:21438293..21442012-chr3:21443506..21445713,3	K562	blood:
8	chr3:21439366..21441034-chr3:21442770..21445274,2	K562	blood:
9	chr3:21381102..21383225-chr3:21383828..21386655,2	MCF-7	breast:
10	chr3:21388598..21390467-chr3:21391576..21393925,2	K562	blood:
11	chr3:21439015..21441958-chr3:21447248..21448760,2	K562	blood:
12	chr3:20381733..20382301-chr3:21331781..21332364,2	MCF-7	breast:
13	chr3:21431277..21433806-chr3:21435047..21437239,3	K562	blood:
14	chr3:21426737..21428480-chr3:21430250..21431910,2	K562	blood:
15	chr3:21439015..21441958-chr3:21447248..21448760,2	K562	blood:
16	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
17	chr3:21388282..21390460-chr3:21398661..21400819,2	K562	blood:
18	chr3:21384888..21387310-chr3:21389573..21391520,2	K562	blood:
19	chr3:21491005..21492571-chr3:21495896..21498520,2	K562	blood:
20	chr3:21386176..21388301-chr3:21404995..21407589,2	K562	blood:
21	chr3:21434215..21436621-chr3:21438277..21440578,2	MCF-7	breast:
22	chr3:21388282..21390460-chr3:21398661..21400819,2	K562	blood:
23	chr3:21439366..21441034-chr3:21442770..21445274,2	K562	blood:
24	chr3:21357091..21358959-chr3:21367501..21369153,2	K562	blood:
25	chr3:21426737..21428480-chr3:21430250..21431910,2	K562	blood:
26	chr3:21438293..21442012-chr3:21443506..21445713,3	K562	blood:
27	chr3:21466338..21470140-chr3:21472004..21475648,4	K562	blood:
28	chr3:21475881..21478303-chr3:21479412..21482583,3	K562	blood:
29	chr3:21388598..21390467-chr3:21391576..21393925,2	K562	blood:
30	chr3:21384888..21387310-chr3:21389573..21391520,2	K562	blood:
31	chr3:21431277..21433806-chr3:21435047..21437239,3	K562	blood:
32	chr3:21446128..21447988-chr3:21449593..21451314,2	K562	blood:
33	chr3:21434215..21436621-chr3:21438277..21440578,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF385D-1	chr3:21453714-21455436	ENSG00000272511.1

No data

Variant related genes	Relation type
VENTXP7	TF binding region
ENSG00000252306	TF binding region
ZNF385D	TF binding region
ENSG00000272511	TF binding region
VENTXP7	CpG island
ENSG00000252306	CpG island
ZNF385D	CpG island
ENSG00000272511	CpG island
ENSG00000151789	chromatin interactions
ENSG00000236380	chromatin interactions
ENSG00000272511	chromatin interactions

Extended variants
information (count: 4587 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:4587 , 50 per page) page: 1 2 3 4 5 6 7 ... 92

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538656883	chr3:21311659-21311660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554092817	chr3:21311705-21311706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs572485001	chr3:21311708-21311709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543101994	chr3:21311712-21311713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561762513	chr3:21311729-21311730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs551703517	chr3:21311732-21311733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs6763061	chr3:21311787-21311788	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs116721170	chr3:21311790-21311791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs562774675	chr3:21311823-21311824	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114465977	chr3:21311833-21311834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs534741662	chr3:21311849-21311850	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs551130890	chr3:21311881-21311882	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs565135446	chr3:21311904-21311905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs149397713	chr3:21311926-21311927	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs144810671	chr3:21311973-21311974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs148163904	chr3:21311979-21311980	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs566990171	chr3:21312007-21312008	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs144102737	chr3:21312019-21312020	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs373408059	chr3:21312035-21312036	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368990418	chr3:21312091-21312092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs34223112	chr3:21312093-21312094	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs571614425	chr3:21312127-21312128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs192265212	chr3:21312155-21312156	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs536006366	chr3:21312228-21312229	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs184701990	chr3:21312237-21312238	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189151884	chr3:21312294-21312295	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147339395	chr3:21312344-21312345	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs376656262	chr3:21312347-21312348	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs139481794	chr3:21312375-21312376	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs550310774	chr3:21312381-21312382	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs1821775	chr3:21312403-21312404	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs562665067	chr3:21312481-21312482	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs578033034	chr3:21312489-21312490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545266765	chr3:21312509-21312510	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs371164673	chr3:21312517-21312518	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs559929782	chr3:21312561-21312562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs568683173	chr3:21312585-21312586	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs1821774	chr3:21312586-21312587	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs147162964	chr3:21312588-21312589	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs370383975	chr3:21312596-21312597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139532390	chr3:21312610-21312611	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9846127	chr3:21312612-21312613	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs117195320	chr3:21312613-21312614	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs182435832	chr3:21312668-21312669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs548053626	chr3:21312701-21312702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566206843	chr3:21312780-21312781	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs537599116	chr3:21312784-21312785	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375393368	chr3:21312800-21312801	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs535343674	chr3:21312815-21312816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs7650211	chr3:21312817-21312818	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:79)

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
early-passage human iPS cells	21368824	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:402 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:21309600-21314600	Weak transcription	Fetal Brain Male	brain
2	chr3:21311400-21311800	Weak transcription	NHDF-Ad	bronchial
3	chr3:21311800-21312000	Enhancers	NHDF-Ad	bronchial
4	chr3:21311800-21312200	Enhancers	Fetal Stomach	stomach
5	chr3:21311800-21312600	Enhancers	Fetal Lung	lung
6	chr3:21312000-21314000	Weak transcription	NHDF-Ad	bronchial
7	chr3:21312600-21312800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr3:21312600-21314600	Weak transcription	Fetal Lung	lung
9	chr3:21312800-21313400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr3:21313200-21313400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin01	Skin
11	chr3:21313200-21313600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr3:21313400-21314800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr3:21313600-21315800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr3:21314000-21315000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr3:21314000-21316200	Enhancers	NHDF-Ad	bronchial
16	chr3:21314400-21314600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr3:21314400-21314800	Enhancers	Colon Smooth Muscle	Colon
18	chr3:21314400-21316200	Enhancers	Fetal Stomach	stomach
19	chr3:21314400-21316200	Enhancers	NH-A	brain
20	chr3:21314400-21316400	Enhancers	HUVEC	blood vessel
21	chr3:21314600-21314800	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr3:21314600-21315000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
23	chr3:21314600-21315000	Enhancers	Fetal Brain Male	brain
24	chr3:21314600-21315200	Enhancers	HSMM	muscle
25	chr3:21314600-21315400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr3:21314600-21316000	Enhancers	Muscle Satellite Cultured Cells	--
27	chr3:21314600-21316200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr3:21314600-21316400	Enhancers	Fetal Lung	lung
29	chr3:21314800-21315000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr3:21314800-21315000	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:21314800-21315200	Enhancers	NHLF	lung
32	chr3:21314800-21315600	Enhancers	Brain Germinal Matrix	brain
33	chr3:21314800-21316000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr3:21314800-21316000	Enhancers	HMEC	breast
35	chr3:21315000-21315200	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
36	chr3:21315000-21315400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr3:21315000-21315400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr3:21315000-21315400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chr3:21315000-21316000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr3:21315000-21317200	Weak transcription	Fetal Brain Male	brain
41	chr3:21315200-21315600	Weak transcription	NHLF	lung
42	chr3:21315200-21316200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr3:21315400-21315600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr3:21315400-21316200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr3:21315400-21316200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr3:21315600-21316200	Enhancers	NHLF	lung
47	chr3:21315800-21316000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr3:21315800-21316200	Enhancers	Fetal Muscle Leg	muscle
49	chr3:21315800-21316200	Enhancers	Rectal Smooth Muscle	rectum
50	chr3:21317200-21317600	Active TSS	Fetal Brain Male	brain

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